Clinical Chemistry: Fundamentals and

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Part 1 : Laboratory Principles 20 Gastrointestinal Disease,334

1 Laboratory Essentials, 1 21 Diseases of the Liver,346

2 Practical Laboratory Safety,25 22 Pancreatic Diseases and Disorders,363

3 Principles of Laboratory Instrumentation, 41 23 Endocrinology,379

4 lmmunoassays,78 24 Kidney and Urinary Tract Diseases,412

5 Molecular Diagnostics, 97 25 Reproductive Diseases and Disorders,432

6 Automation in the Laboratory,114 26 Pregnancy, 446

7 Laboratory Quality Management Systems,124 27 Bone,Joint,and Skeletal Muscle Diseases,458

8 Enzymes,156 28 Nervous System Diseases,474

29 Skin, Hair,and Nail Diseases,488

Part 2: Pathophysiology and Analytes
30 Eye and Ear Diseases,497
9 Clinical Chemistry and Disease,171
31 Nutritional and Metabolic Diseases,504
10 Cell Injury and Its Relationship to Disease,179
32 Immune System Diseases,529
11 Inflammation,187

12 Body Fluids and Electrolytes,204

Part 3: Other Aspects of Clinical Chemistry

13 Blood Gases and Acid-Base Balance,219 33 Therapeutic Drug Monitoring,552

14 Blood Diseases,234 34 Toxicology,584

15 Proteins, 251 35 Transplantation,616

16 Cancer and Tumor Markers,268 36 Emergency Preparedness,634

17 Blood Vessel Diseases,289 Glossary,661

18 Heart Disease,306 Answer Key,683

19 Respiratory Diseases,318 Index,707

 Clinical Chemistry
Fundamentals and Laboratory
Techniques
Clinical Chemistry
Fundamentals and Laboratory Techniques

Author

Donna Larson, EdD, MT (ASCP), DLM

Vice President for Academic and Student Affairs
Clatsop Community College
Astoria, Oregon

Consulting Editors

Joshua Hayden, PhD, DABCC

Assistant Professor of Pathology and Laboratory Medicine
Weill Cornell Medical College
Director, Toxicology and Therapeutic Drug Monitoring
Assistant Director, Central Laboratory
New York Presbyterian Hospital-Cornell Campus
New York, New York

Hari Nair, PhD, DABCC

Technical Director
Boston Heart Diagnostics
Framingham, Massachusetts

ELSEVIER
ELSEVIER
325 1 Riverporr Lane
St. Louis, Missouri 63043

CLINICAL CHEMISTRY: FUNDAMENTALS AND

LABORATORY TECHNIQUES ISBN: 978- 1 -4 5 57-42 1 4 - 1

Copyright© 2017 by Elsevier, Inc. All rights reserved.

No part of this publication may b e reproduced or rransmirred i n any form or b y any means, electronic or mechanical,
including photocopying, recording, or any information storage and retrieval system, without permission in writing
from the publisher. Details on how to seek permission, further information about the Publisher's permissions poli­
cies and our arrangements wirh organizations such as the Copyright Clearance Center and the Copyright Licensing
Agency, can be found at our website: www.elsevier.com/permissions.

This book and the individual contributions contained in it are protected under copyright by the Publisher (other than
as may be noted herein) .

Notices

Knowledge and best practice in this field are constantly changing. As new research and experience broaden our
understanding, changes in research methods, professional practices, or medical treatment may become necessary.
Practitioners and researchers must always rely on their own experience and knowledge in evaluating and using
any information, methods, compounds, or experiments described herein. In using such information or methods
they should be mindful of their own safety and the safety of others, including parties for whom they have a profes­
sional responsibility.
With respect to any drug or pharmaceutical products identified, readers are advised to check the most current
information provided (i) on procedures featured or (ii) by the manufacturer of each product to be administered,
to verify the recommended dose or formula, the method and duration of administration, and contraindications.
It is the responsibility of practitioners, relying on their own experience and knowledge of their patients, to make
diagnoses, to determine dosages and the best treatment for each individual patient, and to take all appropriate
safety precautions.
To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors, assume any liabil­
ity for any injury and/or damage to persons or property as a matter of products liability, negligence or otherwise,
or from any use or operation of any methods, products, instructions, or ideas contained in the material herein.

Library of Congress Cataloging-in-Publication Data

Clinical chemistry : fundamentals and laboratory techniques I edited by Donna Larson ; consulting editors,
Larson, Donna, editor. I Hayden, Joshua Uoshua A.) , editor. I Nair, Hari, editor.

Joshua Hayden, Hari Nair.

Clinical chemistry (Larson)

Includes bibliographical references and index.

St. Louis, Missouri : Elsevier/Saunders, [20 1 7] 1

LCCN 20 1 5 0440741 ISBN 978 1 4 5 5742 1 4 1 (paperback : alk. paper)

I MESH: Clinical Chemistry Tests.
LCC RB40 I NLM QY 90 I DOC 6 1 6. 07/5 6--dc23 LC record
available at http :/ /lccn.loc.gov/20 1 5044074

Executive Content Strategist: Kellie White

Content Development Manager: Jean Sims Fornango
Content Development Specialist: Beth LoGiudice, Spring Hollow Press
Publishing Services Manager: Catherine Jackson
Senior Project Manager: Daniel Fitzgerald
Designer: Margaret Reid

Working together

Printed in Canada
IJ!Jr- W\\"W
BookAid
[nl emational

clsc:v1cr
to grow libraries in
developing countries
<:om • www. hooka1J org
Last digit is the print number: 9 8 7 6 5 4 3 2
 To my mom and dad, Donald and Barbara Bedard (I wish they could have been here
to see this); to my husband, Earl, and my son, Adrian, for their love and support; to my
sister and her family for their warmth and love; to the Allards for their support during
my clinical year and college years; and to all the friends and colleagues I worked with at
Wentworth-Douglass Hospital (NH), 509th Strategic Hospital (NH), RAF Lakenheath
Regional Hospital (UK), Winston-Salem State University (NC), Mt Hood Community
College (OR), Portland Community College (OR), and Clatsop Community College (OR).
Donna Larson
I appreciate the opportunity Elsevier provided for me to
write the first edition of this clinical chemistry book for
medical laboratory technology students. The process was
exciting, exhausting, challenging, and an educational expe­
rience like no other. I would like to thank the contributors
for their hard work to help make this book possible.
I would like to thank the Elsevier staff for the assistance,
guidance, encouragement, and experience that they shared
with me throughout the development of the book. Thank
you to Ellen Wurm-Cutter, who helped me through the
proposal and beginning stages of manuscript development.
vi
A big thank you to Kellie White, Jean Sims Fornango, and
Beth LoGiudice for joining the team and seeing this proj­
ect through to completion. The final product has been a
long time coming. My Thursday mornings will never be
the same! Thanks also to Dan Fitzgerald and his team for
putting everything together in a beautiful full-color book.
Everyone was understanding, patient, compassionate,
empathetic, and truly amazing.
Donna Larson
Sheryl Berman, PhD
Division Dean of Health Professions
Lane Community College
Eugene, Oregon
Jimmy L. Boyd, CLS (NCA), MS/MHS
Assistant Professor, Department Head
Medical Laboratory Technology
Arkansas State University, Beebe
Beebe, Arkansas
Craig Foreback, PhD
Senior Consultant
Clear Medical Solutions, LLC
Bradenton, Florida
Senior Lecturer Emeritus
University of Wisconsin School of Medicine
and Public Health
Madison, Wisconsin
Danielle Fortuna, MD
Department of Pathology, Anatomy, and
Cell Biology
Sidney Kimmel Medical College
Thomas Jefferson University
Philadelphia, Pennsylvania
Thomas Kampfrath, PhD, DABCC
Clinical Biochemist
Santa Clara Valley Medical Center
Department of Pathology and Laboratory Medicine
San Jose, California
Laura J. McCloskey, PhD
Department of Pathology, Anatomy, and Cell Biology
Sidney Kimmel Medical College
Thomas Jefferson University
Philadelphia, Pennsylvania
M. Laura Parnas, PhD, DABCC, FACB
Director of Clinical Science
Sutter Health Shared Laboratory
Livermore, California
John W. Ridley, PhD, RN, MT (ASCP)
Formerly, Director of Medical Laboratory Technology
West Central Technical College
Waco, Georgia
Laird C. Sheldahl, PhD
Instructor, Anatomy and Physiology, Biology
Mount Hood Community College
Gresham, Oregon
Douglas F. Stickle, PhD, DABCC, FACB
Department of Pathology, Anatomy, and Cell Biology
Sidney Kimmel Medical College
Thomas Jefferson University
Philadelphia, Pennsylvania
Zi-Xuan Wang, PhD
Department of Pathology, Anatomy, and Cell Biology
Sidney Kimmel Medical College
Thomas Jefferson University
Philadelphia, Pennsylvania
vii
This page intentionally left blank
Keith Bellinger, PBT (ASCP) Amy Gatautis, MBA, MT (ASCP), SC
Medical Technologist Program Director, Medical Laboratory Technology
The United States Department of Veterans Affairs New Cuyahoga Community College
Jersey Health Care System Cleveland, Ohio
East Orange, New Jersey
Assistant Professor, Phlebotomy Kristine Hayes, MAT, MLS (ASCP)
Rutgers-The State University of New Jersey MLT and Phlebotomy Program Coordinator
Newark, New Jersey Moberly Area Community College
Moberly, Missouri
Stephanie Bielas, PhD
Assistant Professor of Human Genetics Candy Hill, MEd, MT (ASCP)
University of Michigan CLT Program Coordinator
Ann Arbor, Michigan Jefferson State Community College
Birmingham, Alabama
Jimmy L. Boyd, CLS (NCA), MS/MHS
Assistant Professor, Department Head Lorri Huffard, PhD, MT (ASCP), SBB
Medical Laboratory Technology Dean, Science & Health Programs
Arkansas State University, Beebe Wytheville Community College
Beebe, Arkansas Wytheville, Virginia

Russell Cheadle, MS, MLS (ASCP) Phyllis Ingham, EdD, MEd, MT (ASCP)
Professor, Clinical Laboratory Technology Director Clinical Laboratory Technology Program
Macomb Community College West Georgia Technical College
Warren, Michigan Waco, Georgia

Cathy Crawford, BS, MT (ASCP) Stephen M. Johnson, MS, MT (ASCP)

Clinical Courses Instructor and MLT Teaching Assistant Program Director
Mount Aloysius College Saint Vincent Health Center School of Medical
Cresson, Pennsylvania Technology
Erie, Pennsylvania
Karen M. Escolas, EdD, MT (ASCP)
Chair, Department of Medical Laboratory Technology Haywood Joiner Jr., EdD, MT (ASCP)
Farmingdale State College, State University of New York Chair, Department of Allied Health
Farmingdale, New York Louisiana State University at Alexandria
Alexandria, Louisiana
Roger Fortin, MS, MBA, MLS (ASCP)
Program Director Stephanie Jordan, BS, MLS (ASCP), CM
Bunker Hill Community College Assistant Professor
Charlestown, Massachusetts Pierpont Community and Technical College
Fairmont, West Virginia
Trent Freeman, MA, BS, MLS (ASCP)
Education Coordinator Jeffrey Josifek, MS, MLS (ASCP), CLS (NCA)
Medical Education and Training Campus Department of Medical Laboratory Technology
The George Washington University Portland Community College
Fort Sam Houston, Texas Portland, Oregon
ix
 Reviewers

Minh Kosfeld, PhD, MLT (ASCP) Ryan Rowe, MLS (ASCP)

Assistant Professor Weber State University
Department of Biomedical Laboratory Science Ogden, Utah
Doisy College of Health Sciences
St. Louis University Mary Sadlowski, MT (ASCP)
St. Louis, Missouri Medical Technologist
Greater Baltimore Medical Center and Community
Marc L. Meyers, MBA, MT (ASCP) College of Baltimore County
PM Laboratory Coordinator Towson, Maryland
Centegra Clinical Laboratories
McHenry, Illinois Cheryl Selvage, MS, MT (ASCP)
Associate Professor
Constance Moore, MS, MT (ASCP) Lorain County Community College
Program Director, Laboratory Sciences Elyria, Ohio
Eastern Gateway Community College
Steubenville, Ohio Anita Marie Smith, MT (AMT), MBA
Laboratory Administrative Director
Richard C. Mroz Jr., DA, MS, BSMT, MT (ASCP) Moberly Regional Medical Center
MLT Program Director Moberly, Missouri
Fortis Institute
Fort Lauderdale, Florida Angela Sparkman, MEd, MT (ASCP)
Program Director, Assistant Professor of the Medical
Dawn Nelson, MA, MT (ASCP) Laboratory Technology Program
MLT Program Director Ivy Tech Community College
Florence-Darlington Technical College Sellersburg, Indiana
Florence, South Carolina
Andrea Thompson, BS, MLT (ASCP)
Kathleen C. Perlmutter, MBA, MT (ASCP) MLT Instructor
Phlebotomy Coordinator, MLT Faculty Barton Community College
Montgomery County Community College Great Bend, Kansas
Blue Bell, Pennsylvania
Dionne M. Thompson, MSE, MT (ASCP)
Jennifer D. Perry, MS, BSMT (ASCP) MLT Program Director/Instructor
Associate Professor and Chairperson Three Rivers College
Clinical Laboratory Sciences Department Poplar Bluff, Missouri
Marshall University
Huntington, West Virginia

Ellen F. Romani, AAS (MLT), MS

Department Chair
Medical Laboratory Technology/Phlebotomy/Therapeutic
Massage
Spartanburg Community College
Spartanburg, South Carolina
Clinical Chemistry: Fundamentals and Laboratory Techniques
is a comprehensive, readable, and student-friendly text for
2-year medical laboratory technology programs. The text­
book has a full-color design along with detailed illustrations
and diagrams to help students with complex chemistry
concepts. Pathophysiologic concepts are included to help
students understand the clinical relevance of clinical chem­
istry assays.
Purpose and Organization
As I look back at my journey in clinical laboratory science,
I cannot help but marvel at how laboratory test methods
rapidly changed over the course of the 20th century and
into the 2 1 st century. While researching my dissertation,
The Structure of Knowledge in Clinical Laboratory Science, I
was amazed to read articles in laboratory journals ( 1 940s)
concerning how to build a better cage for laboratory ani­
mals. (Pregnancy tests during that time used rabbits to
determine whether a woman was pregnant.) The radioim­
munoassays that were popular in the 1 970s and into the
1 980s were largely replaced by colorimetric immunoassays
in the late 1 980s and 1 990s. Looking back, there was always
new information in the expanding discipline of clinical lab­
oratory science. The more the knowledge base expands, the
more the students are asked to learn. This is especially true
of medical laboratory technology (MLT) students.
MLT students have a mere 2 years to learn all the clinical
laboratory science (CLS) knowledge (with few prerequisite
and general education courses) on which to build a solid
knowledge foundation. Pieces from various disciplines are
incorporated or embedded in their CLS . When writing this
book, I envisioned a clinical chemistry book that would
incorporate j ust-in-time learning concepts for which the
material would be fortified with additional material when
needed. Building on this approach, Part 1 , Laboratory Prin­
ciples, covers laboratory principles, safety, quality assur­
ance, and other fundamentals of laboratory techniques.
The concepts are essential for anyone working in a clini­
cal laboratory, and this section provides a good reference
for beginning MLT students. For example, the students
do not take a statistics course, but statistical concepts and
calculations are included in Chapter 7, Laboratory Qual­
ity Management Systems. Quality management methods,
including the applications of Westgard rules for control
charts and the calculation of the mean, mode, and standard
deviation, are explained and practiced in that chapter.
Part 2, Pathophysiology and Analytes, covers the dis­
eases, broken down by body system, that are commonly
diagnosed through chemical tests. Each chapter in this sec­
tion contains information about anatomy and physiology
of a specific body system, disease mechanisms of common
conditions that require clinical chemistry testing, and how
laboratory results correlate with clinical disorders. This is a
key section of the book because MLT students usually do
not have room in their program for a separate pathophysiol­
ogy class, unlike other health science students, for whom it
is part of the program paradigm.
Pathophysiologic mechanisms of diseases and the resul­
tant effects on clinical chemistry tests are discussed in each
of the chapters. For example, it is easier to remember test
results that are elevated after an acute myocardial infarction
(MI) if it is known that the muscle is damaged and that
the dying cells release specific chemicals into the blood. If
blood is drawn at timed intervals after the MI, the person
who understands the pathophysiologic mechanism behind
the infarct will know what types of clinical chemistry results
to expect from each specimen.
When diseases are discussed that do not use laboratory
tests for diagnoses or when laboratory tests are used to
rule out other disorders, this information is given so that
students can understand the laboratory test ordering pat­
terns of health care providers. This information also helps
students better understand reflex testing and how the algo­
rithms are developed.
Part 3, Other Aspects of Clinical Chemistry, covers
therapeutic drug monitoring, toxicology, transplantation,
and emergency preparedness. The clinical laboratory has a
critical role in these areas, providing ongoing testing and
assistance.
To complement the organization, the book is writ­
ten in the active voice to help students better understand
the material. Although this may be unconventional for a
textbook at this level, I believe it helps students to better
understand complex clinical chemistry concepts and mas­
ter the material.
Most individuals are visual learners. To that end, many
figures, photographs, tables, and flowcharts are included
xi
 Preface
to help students better understand concepts. Many figures
summarize complex and complicated processes or pathways
to provide better comprehension of the material by students.
Key Features
Cha pter Outl i n e
Each chapter starts with a chapter outline that shows the
main topics that are covered. It provides students and
instructors with a roadmap to the chapter and can be easily
referenced at any time.
Objectives
The textbook format facilitates the learning process by pro­
viding students and educators with detailed objectives that
address the knowledge required to master each chapter's
content. The learning objectives are listed at the beginning
of each chapter, giving students and instructors definitive
evaluation tools to use as the chapter's content is covered.
Objectives are provided at various cognitive mastery lev­
els: comprehension, application, analysis, synthesis, and
evaluation.
Key Terms
Key terms are identified at the beginning of each chapter
and highlighted in the chapter, putting valuable terminol­
ogy at students' fingertips. The key terms are also included
in the Glossary at the back of the book.
Case in Point
A key clinical case study is provided at the beginning of every
appropriate chapter. The Case in Point feature provides appli­
cation of the student's knowledge for correlating the clinical
side of test results. Students are asked to think about impor­
tant questions related to each scenario and to use fundamen­
tal information from the chapter to determine the answers.
Poi nts to Remember
A bulleted list of important concepts is included in the first part
of the chapter, providing an overview of the chapter content.
This list gives students a simple study tool for easy reference.
Summary
A short summary at the end of the chapter highlights
key information from the chapter. Students can revisit
the various chapter topics in short form for review and
reinforcement.
Review Questions
Multiple-choice review questions at the end of every chap­
ter provide students with a unique tool as they prepare for
classroom examinations and certification examinations. The
review questions give students a chance to quiz themselves
on the chapter content, assess their knowledge of important
chapter topics, and evaluate which topics need follow-up
review.
Critica l Th i n king Questions
The Critical Thinking Questions allow students and instruc­
tors to discuss the chapter topics in a broader way. Although
these questions have correct answers, they require more in­
depth thinking, analysis, evaluation, and reflection than
other questions in the chapter.
Case Stud ies
Additional Case Studies round out each most chapters,
giving students another opportunity to apply the knowl­
edge gained from the chapter. The scenarios are meant to
stimulate interest and critical thinking and to encourage
discussion of chapter topics with other students.
Evolve Companion Website
Clinical Chemistry comes with a companion website, found
on Evolve (evolve.elsevier.com/Larson) . This website con­
tains helpful ancillaries for instructors and additional mate­
rials for students.
For the I n structor
The Evolve website has multiple features for the instructor:
• A test bank with multiple-choice questions and ratio­
nales.
• PowerPoint presentations for every chapter that can be
used as is or as a template to prepare lectures.
• A detailed Answer Key with rationales for all in-text
questions.
• The Image Collection that provides electronic files of all
the chapter figures that can be downloaded into Power­
Point presentations.
For the Student
Additional content is available for the student:
• High-definition animations to illustrate key physiologic
and pathophysiologic processes.
• Extra Case Studies for certain chapters for more practical
application of textbook content.
Part 1 : Laboratory Principles 5 Molecular Diagnostics,97

Introduction, 98
Donna Larson
1 Laboratory Essentials, 1
Nucleic Acid Structure and Function, 98
Introduction, 3
Donna Larson
Laboratory Methods, 106
History of Clinical Laboratories, 3 Diagnostic Applications, 110
Types of Clinical Laboratories, 4

Laboratories, 8
Regulation and Accreditation of Clinical 6 Automation in the Laboratory,114

Laboratory Materials, 9 Introduction, 115

Donna Larson

Chemistry Review, 10 Goal of Automation, 115

Laboratory Mathematics, 14 History of Automated Analyzers, 115
Automating Clinical ChemistryTests, 117
2 Practical Laboratory Safety,25 Total Laboratory Automation, 119

Introduction, 26
Donna Larson

Safety Regulations, 26
7 Laboratory Quality Management Systems,124
John W. Ridley and Donna Larson
The Laboratory Safety Program, 29 Introduction, 126
Introduction to Quality, 126
3 Principles of Laboratory Instrumentation, 41 Facilities and Safety Overview, 128
Purchasing and Inventory, 130
Introduction, 43
Craig Foreback and Donna Larson
Process Control, 131
Properties of Light, 43 Assessment, 148
Spectrophotometry, 44 Personnel, 149
Fluorometry, 48 Customer Service, 149
Luminometry, 51 Occurrence Management, 149
Nephelometry andTurbidimetry, 51 Process Improvement, 149
Electrochemistry and Chemical Sensors, 52 Documents and Records, 151
Chromatography, 56 Organization, 152
Mass Spectrometry, 62
Electrophoresis, 67
Colligative Properties, 71
8 Enzymes,156

Point-of-CareTesting, 72 Introduction, 158

M. Laura Parnas and Thomas Kampfrath

Flow Cytometry, 74 The Nature of Enzymes, 158

Kinetics, 159
4 lmmunoassays,78 Enzyme Reaction Conditions, 162
lsoenzymes, 163
Introduction, 80
Donna Larson
Specific Enzymes, 163
Antibodies, Antigens, and Analytes, 80
lmmunochemical Methods, 82
Label Methods, 84
Part 2: Pathophysiology and Analytes

Particle Methods, 88
Light-Scattering Methods, 92
9 Clinical Chemistry and Disease,171

Introduction, 172
Donna Larson

Performance, 93
Factors Affecting Immunoassay Analytical
Definition of Disease, 172

xiii
 Contents

Pathology, 172
Disease Mechanisms, 175
17 Blood Vessel Diseases,289

Biochemistry of Disease, 175 Introduction, 291

Donna Larson

Lipids, 291
10 Cell Injury and Its Relationship to Lipoproteins, 293
Disease,179 Normal Lipoprotein Metabolism, 294
Abnormal Lipoprotein Metabolism, 296
Introduction, 180 Laboratory Procedures and Limitations, 299
Donna Larson

Overview of Cellular Injury, 180 Lipoproteins and Clinical Vascular Disease, 301
Causes of Cellular Injury, 181
Changes in Body Chemistry, 183
LaboratoryTests, 184
18 Heart Disease,306

Introduction, 307
Sheryl Berman

11 Inflammation,187 Heart Structure and Blood Flow, 307

Myocardial Infarction, 307
Introduction, 188 Congestive Heart Failure, 311
Donna Larson

Defense Mechanisms, 188 Congenital Heart Defects, 312

The Inflammation Process, 188 Endocarditis, Myocarditis, and Pericarditis, 314
Acute Inflammation, 195
Chronic Inflammation, 196
Laboratory Procedures and Limitations, 198
19 Respiratory Diseases,318

Introduction, 319
Donna Larson

12 Body Fluids and Electrolytes,204 Structure and Function of the Respiratory System, 320
Respiratory Diseases and Pathophysiology, 320
Introduction, 205
Donna Larson

Fluid Balance and Body Fluid Compartments, 205

Electrolytes, 206
20 Gastrointestinal Disease,334

Colligative Properties, 213 Introduction, 335

Sheryl Berman

Fluid Imbalances, 215 Gastrointestinal System, 335

Gastrointestinal FunctionTests, 342
13 Blood Gases and Acid-Base Balance,219

Introduction, 220
Donna Larson 21 Diseases of the Liver,346

Blood Gases, 220 Introduction, 347

Donna Larson

Acid-Base Theory, 224 Liver and BiliaryTract, 348

Acid-Base Disorders, 226 Liver Diseases, 350
Interpreting Blood Gas Analyses, 230
22 Pancreatic Diseases and Disorders,363
14 Blood Diseases,234
Introduction, 365
Donna Larson

Introduction, 236 Overview of the Pancreas, 365

Sheryl Berman

Hematopoiesis, 236 Pancreatitis, 366

White Blood Cells, 236 Diabetes, 368
Red Blood Cells, 240 Cystic Fibrosis, 375
Malabsorption and Maldigestion, 375
15 Proteins,251

Introduction, 252
Donna Larson 23 Endocrinology,379

Biochemistry of Proteins, 252 Introduction, 382

Jimmy L. Boyd and Donna Larson

Plasma Proteins, 255 Overview of the Endocrine System, 382

Proteins in Other Body Fluids, 264
Testing, 385
Anatomy, Pathophysiology, and Laboratory

16 Cancer and Tumor Markers,268

Introduction, 269
Donna Larson 24 Kidney and Urinary Tract Diseases,412

Cancer andTumor Markers, 269 Introduction, 413

Sheryl Berman

Clinical Correlations, 280 Kidney Anatomy, 414

 Contents

Normal Physiology, 416 32 Immune System Diseases,529

Disease States, 419 Sheryl Berman
Laboratory Procedures, 425 Introduction, 531
Normal Immune System, 531
25 Reproductive Diseases and Disorders,432 Disease States, 538
Donna Larson
Introduction, 433 Part 3: Other Aspects of Clinical Chemistry
Reproductive System Structure and Function, 433
Diseases and Disorders, 435 33 Therapeutic Drug Monitoring,552
Laboratory Procedures and Limitations, 442 Laird C. Sheldahl and Donna Larson
Introduction, 554
26 Pregnancy, 446 Drug Disposition, 554
Sheryl Berman Administration of Drugs, 558
Introduction, 448 Drug Levels, 560
Pregnancy, 448 Cardiovascular Drugs, 562
Complications of Pregnancy, 450 Antibiotics, 567
Fetal Complications, 453 Antiepileptic Drugs, 571
Laboratory Diagnosis of Fetal Abnormalities, 455 Psychoactive Drugs, 576
Bronchodilators, 579
27 Bone,Joint,and Skeletal Muscle Diseases,458 Immunosuppressant Drugs, 580
Donna Larson
Introduction, 459 34 Toxicology,584
Normal Anatomy and Physiology of Bones, 459 Laird C. Sheldahl and Donna Larson
Bone Diseases, 460 Introduction, 586
Normal Anatomy and Physiology of Joints, 466 Routes of Exposure, 587
Joint Diseases, 466 Dose-Response Relationship, 588
Normal Anatomy and Physiology of Muscles, 468 Acute and ChronicToxicity, 588
Muscle Diseases, 469 Specimen Collecting and Handling, 589
Conditions Caused by Pollutants, 590
28 Nervous System Diseases,474 Toxic Agents, 592
Donna Larson Household Products, 597
Introduction, 475 Toxic Metals, 599
Nervous System Anatomy and Physiology, 476 Drugs of Abuse, 602
Nervous System Diseases, 477
Cerebrospinal Fluid Analysis, 483 35 Transplantation,616

Douglas F. Stickle
Daniel/e Fortuna, Laura J. McCloskey, Zi-Xuan Wang,
29 Skin, Hair,and Nail Diseases,488
Donna Larson Introduction, 617
Introduction, 489 Overview ofTransplantation, 617
Skin Diseases, 489 Role of Medical Laboratories inTransplantation, 619
Effects of Systemic Disease on Skin, 491 Overview of the Immune System, 619
Hair Diseases, 492 Role of the Immune System inTransplantation, 622
Nail Diseases, 493 Immunosuppression, 624
Exceptional Cases inTransplantation, 628
30 Eye and Ear Diseases,497 Future ofTransplantation, 629
Donna Larson
Introduction, 497 36 Emergency Preparedness,634
Eyes, 498 Donna Larson
Ears, 501 Introduction, 636
Emergency Preparedness, 636
31 Nutritional and Metabolic Diseases,504 Emergency Response, 637
Donna Larson Laboratory Response Network, 654
Introduction, 507
General Concepts of Health and Disease, 507 Glossary,661
Cold Injuries, 507
Heat Illnesses, 508 Answer Key,683
Nutritional Conditions, 509
Metabolic Diseases, 518 Index,707
Inborn Errors of Metabolism, 520
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 Laboratory Principles

CHAPTER OUTLI N E
I ntrod uction Chemistry Review
H i story of C l i n ical Laboratories Atomic Theory

Types of C l i n ical Laboratories

Chemical Bonds

I n patient Laboratories Factors Affecting Chemical Reactions

Outpatient C l i nics and Physicia ns' Office La boratories Acid, Bases, and Salts
Reference Laboratories Orga nic Chemistry

State and Federal La boratories Biochemistry

M i l itary Laboratories La boratory Mathematics

Reg u l ation and Accreditation of C l i n ical Laboratories

Mola rity

Reg u lation Molal ity

Accreditation Norma l ity

Di l utions
La boratory Materials
Conversions
Glasswa re and Plasticwa re
pH
Centrifuges
Beer's Law
Bala nces
Sta ndard Cu rves
Pi pettes
S u m mary
Reagents
Water

O BJ ECTIVES
At the completion of this chapter, the reader will be able to:
1. Describe the history of the clinical laboratory. 1 0. Describe the types of ba lances and their use i n the
2. List the typica l depa rtments of a clinica l laboratory. laboratory.
3. List the personnel employed in a clinica l la boratory. 1 1 . Compa re a n d contrast serologic a n d vo l u metric
4. List the characteristics of reference, federal, and m i l itary pi pettes.
la boratories. 1 2. Describe the various methods used to ca librate pi pettes.
5. Briefly describe The Joint Com mission and the Col lege of 1 3. Defi ne mola rity and mole and perform the calcu lations
American Pathologists and their roles i n clinical laboratory needed for prepa ring and worki ng with molar solutions.
oversig ht. 1 4. Defi ne molality and perform the ca lcu lations needed for
6. Describe the types of water and the uses for each. prepa ring and worki ng with molal solutions.
7. Com pa re and contrast the types of glasswa re and 1 5. Defi ne normal ity, equivalent weig ht, and m i l l iequ iva lent
plasticwa re. weight and perform the calcu lations needed for prepa ring
8. Describe the types of centrifuges used in the and worki ng with normal solutions.
laboratory. 1 6. Defi ne g/d L and mg/d L u n its and perform ca lculations
9. Describe the operating instructions and precautions for necessa ry to prepa re solutions of a desired g/d L and mg/d L
centrifuges. concentration.
2 PA R T 1 Laboratory Principles

1 7. Solve d i l ution problems for fi n a l vol ume and 1 9. Convert metric u n its from one u n it to another, the th ree

between 51 u nits and conventiona l u nits, a bsorbance to

concentration g iven the i n itial vol u mes and tem perature sca les (i.e., Fa h renheit, Celsius, and Kelvin),
concentrations.
1 8. Describe how serial d i l utions a re prepared. transm itta nce and transmitta nce to a bsorba nce, and a bsor­
bance va l ues to concentration of the u n known.

KEY TERMS
Accred iting Bureau of Health Education C l i n ical Laboratory Mole
Schools I m p rovement Act Nalgene
Acid C l i n ical la boratory scientists Needlestick Safety and Prevention Act
Alcohols C l i n ical la boratory technicians of 2000
Aldehyde C l i n ical pathology Neutral ization reaction
American Society for C l i nical Col lege of American Pathologists Normal ity
Pathologists Com m ission on Accred itation of All ied Nucleic acids
Ami nes Health Ed ucation Prog ra ms Outpatient c l i n i c
Anatomic pathology Cova lent bond Pathologist
Anion Ester pH
Aromatic ring Governing board Phenol
Atomic theory Gram per deci l iter concentration Phlebotomists
Automated pi pettes Haza rd com m u n ication Physicians' office la boratories
Bala nces Hazardous chemica l s Pi pettes
Base Hematology Proficiency testing
Beer's law Hyd rocarbons Protein
Biochemistry I nternational u n its Pyrex
Blood bank Ionic bond Reagent-g rade water
Bloodborne pathogens Ions Reagents
Board of Reg istry Ketone Reference la boratories
Carbohyd rates La boratory manager Serial d i l ution
Cations Lipids Serologic g lass pi pette
Centers for Disease Control and Medical laboratory assistants Sta ndard cu rve
Prevention Medical staff Sterols
Centrifuge Medical technologist The Joint Com m ission
Chemical sym bols Microbiology department Vol u metric pi pette
C l i n ical chemistry Molal ity Va lence
Molarity

Points to Remember • Hospitals have an organizational structure consisting of a

• The American Society for Clinical Pathologists (ASCP)
was formed in 1 922 to meet the needs of the growing
pathology profession.
• The ASCP created the Board of Registry in 1928 to cer­
tify laboratory technicians and then the Board of Schools
to accredit laboratory training schools.
• In 1933, clinical laboratory technicians formed a pro­
fessional society, the American Society for Clinical
Laboratory Technicians, to provide autonomy and a
voice for the growing profession of clinical laboratory
science.
• Laboratories produce 80% of the objective data that health
care providers use to diagnose and rule out diseases, and
they provide blood for transfusion and determine the sus­
ceptibility of pathogenic bacteria to antibiotics.
• Clinical laboratories began as part of a hospital in the
early 20th century and remain a critical part of hospitals
today.
governing board, medical staff, and management.
• Anatomic pathology comprises surgical pathology, his­
tology, and cytology.
• Clinical pathology is the largest portion of the clinical
laboratory, and it is composed of hematology, clinical
chemistry, microbiology, immunohematology, toxicol­
ogy, immunology and serology, urinalysis, specimen col­
lection, and customer service.
• Pathologists are medical doctors who oversee laboratory
testing.
• A laboratory manager is responsible for the daily activi­
ties of the laboratory.
• Clinical laboratory scientists possess a bachelor's degree
in clinical, medical, or laboratory science; 3 years of aca­
demic course work; and 6 months to 1 year of clinical
experience.
• Clinical laboratory technicians or medical laboratory
technicians have a 2-year associate degree, and they per­
form all the routine testing in the laboratory.

• Medical laboratory assistants are trained to perform or
assist in performing routine laboratory testing allowed by
law and administrative tasks.
• Phlebotomists draw blood from patients.
• An outpatient clinic or a physician's office is a location
where patients receive medical care.
• Public health laboratories are responsible for health refer­
ence tests; disease prevention, control, and surveillance;
population-based interventions; and emergency response
efforts.
• The Department of Defense operates many clinical labo­
ratories across the world.
• Federal regulations that affect clinical laboratories include
the Clinical Laboratory Improvement Act (CLIA) of
1 967 and 1 988, the Needlestick Safety and Prevention
Act of 2000, and regulations for bloodborne pathogens,
hazardous chemicals, and hazard communication.
• The Health Insurance Portability and Accountability Act
affects the laboratory as it relates to patient privacy.
• Accreditation is a voluntary process with which laborato­
ries maintain standards of quality.
• The Joint Commission accredits hospitals and many
other health care organizations.
• The College of American Pathologists is an internation­
ally known agency that accredits clinical laboratories.
• Competency testing involves testing the ability of the
laboratory professionals that perform the diagnostic
tests.
• Characteristics of glassware include thermal durability;
alkali, zinc, or heavy metal content; chemical stability;
electrical conduction; optical qualities; and color.
• Plasticware can be made from polystyrene, polypropyl­
ene, polycarbonate, Teflon, and nylon.
• The four basic types of centrifuges are horizontal head
or swinging bucket, angle-head or fixed angle, axial, and
ultracentrifuge.
• Pipettes are classified as manual, semiautomated, and
automated.
• The volumetric pipette is a long glass tube with a bubble
in the middle.
• There are two types of serologic pipettes-those used to
deliver and to contain.
• Reagents must be monitored for reliability and repro­
ducibility.
• To ensure high-quality laboratory results, high-quality
chemicals and high-quality water must be used.
• The term gram molecular weight is often used as a defini­
tion of mole.
• Molarity = (grams of compound/gram molecular weight)/
liters of solution.
• The molal concentration of a solution is equal to the
number of moles of solute per 1 000 g of solvent.
• The definition of normality is 1 gram equivalent weight
of a compound dissolved in a liter of solution.
• The g/dL concentration is defined as the number of
grams of a com pound dissolved in 1 00 mL of water.
• A percent (o/o) solution can be written as g/dL or go/o.
CHAPTER 1 Laboratory Essentials
• volume1 x concentration1 = volume 2 x concentration 2 .
• Remember:
grams ---> milligrams, multiply by 1 000
decigrams ___, milligrams, multiply by 1 00
centigrams ___, milligrams, multiply by 1 0
mm 3 ---> m L (cc), divide by 1 000
milligrams ___, grams, divide by 1 000
• Conversion of Celsius to Fahrenheit: C = 5/9 x (F 32) -
• Conversion of Fahrenheit to Celsius: F = (9/5 x C) + 32
• Conversion of Celsius to Kelvin: K = C + 273 .
• The amount of dissociation that occurs and the number
of hydrogen ions (H+) in the solution correlate with the
strength of the acid and the pH of the solution.
• Beer's law: A = 2 log o/o T
-
• Aunknown/Asrandard = Cunknown / C srandard
• Standard curves are constructed by plotting points for at
least three standards for a test procedure.
Introduction
This chapter provides a short history of the clinical labora­
tory, various practice sites for laboratories and their organi­
zational structures, levels oflaboratory personnel, laboratory
departments, and accreditation agencies. Chemistry princi­
ples and essential laboratory mathematics are also reviewed.
History of Clinical Laboratories
The first clinical laboratory in the United States opened in
1 896 at Johns Hopkins Hospital. Laboratories were small
rooms with very little equipment where pathologists per­
formed tests on patients' specimens. After the discovery of
causative agents of tuberculosis, diphtheria, and cholera,
laboratories became more important in medicine. As the
volume of laboratory tests increased, pathologists trained
young women to perform some of the simpler laboratory
tests to free the pathologist to do more complex testing.
The American Society for Clinical Pathologists (ASCP)
was formed in 1 922 to meet the needs of the growing pathol­
ogy profession. In 1 926, the accrediting body for hospitals,
the American College of Surgeons, mandated hospitals to
have a pathologist on staff. During World War I, hospi­
tals experienced a critical shortage of laboratory assistants.
Pathologists viewed this as an opportunity to standardize
educational programs for laboratory assistants, now called
technologists or scientists. To meet this need, the ASCP cre­
ated the Board of Registry in 1 928 to certifY laboratory
workers and the Board of Schools to accredit laboratory
training schools. When an individual completed an accred­
ited program, she could take the Board of Registry exami­
nation. Successful completion of the examination conferred
the ASCP tide of medical technologist (MT) .
The ASCP played a major role in the formation of the
clinical laboratory science profession by approving edu­
cation programs and certifYing laboratory workers. The
National Credentialing Agency (NCA) was an independent
4 PA R T 1 Laboratory Principles
certification agency created by laboratory professionals in
the 1 970s to credential laboratory professionals. The ASCP
Board of Registry and the NCA merged in 2009 to create
the ASCP Board of Certification.
Another organization that certifies laboratory profession­
als and other medical professionals is the American Medical
Technologists (AMT) . The AMT was founded in 1 939 and
is a nationally and internationally recognized certification
and membership society for medical technologists, medi­
cal laboratory technicians, phlebotomy technicians, medical
laboratory assistants, clinical laboratory consultants, medi­
cal assistants, medical administrative specialists, dental assis­
tants, and allied health instructors.
In 1 933, clinical laboratory technicians formed a profes­
sional society, the American Society for Clinical Laboratory
Technicians, to provide autonomy and a voice for the grow­
ing profession of clinical laboratory science. Years later, the
organization changed its name to the American Society for
Medical Technology and then to the American Society for
Clinical Laboratory Science (ASCLS) .
In the 1 940s and 1 950s, clinical laboratory testing analyzed
specimens such as blood and urine. Laboratories also housed
and used animals in the test procedures. An example is the
pregnancy test where urine from a woman suspected of being
pregnant was injected into a rabbit. After a specific time period,
the rabbit's ovaries were examined for ovulation. If the ovaries
were swollen and ovulating, the woman was pregnant. In the
1 960s, laboratories used frogs to detect pregnancy in women.
By the 1 970s, more reliable and valid test procedures were
introduced into the clinical laboratory for pregnancy testing.
More sensitive test procedures were introduced in the 1 970s
(e.g., radioimmunoassay) and 1 980s (e.g., enzyme immunoas­
says) . Bioluminescence assays attained widespread use in the
1 990s. As more sensitive test procedures were introduced in the
clinical laboratory, more test analyses were added.
Types of Clinical Laboratories
Clinical laboratories are a dynamic area in health care. Lab­
oratories produce 80% of the objective data that health care
providers use to diagnose and rule out diseases, to provide
blood for transfusion, and to determine the susceptibility of
pathogenic bacteria to antibiotics. Clinical laboratories are
found in hospitals, outpatient clinics, and physicians' offices
and as stand-alone reference laboratories. Laboratories are
constantly integrating new technology and instruments to
better meet the needs of health care providers and patients.
The following sections describe the types of clinical labora­
tories, structures of organizations and laboratories, labora­
tory personnel, and laboratory departments.
I n patient la boratories
Clinical laboratories began as part of a hospital in the early
20th century and remain a critical part of hospitals today.
Although the clinical laboratory may be located in the hos­
pital, work from outpatient clinics, nursing homes, and
other settings may be sent to the hospital's clinical labora­
tory for analysis. Clinical laboratory workers are hospital
employees, and they are an important part of the health
care team.
Organizational Structure
Hospitals are an invention of the 20th century. Hospitals
were known as almshouses before the 20th century. Alms­
houses were places where poor people or people without fam­
ily members to care for them would go to receive care. These
facilities provided food, shelter, and rest. Before the 20th cen­
tury, the best medical care was received at home; even opera­
tions were performed in the home. As medical procedures
and equipment became more advanced, the patient went to
see the doctor instead of the doctor coming to see the patient.
Hospital
There are approximately 6500 hospitals in the United States.
They are classified as public, private, specialty, community,
federal, military, or other types.
Hospitals are organized in three distinct parts: govern­
ing board, medical staff, and management. The governing
board is the body responsible for the financial health of the
organization and for setting institutional policies and goals.
The governing board appoints the medical staff as the party
responsible for quality patient care.
The medical staff members of the hospital are not usu­
ally considered to be employees; however, more hospitals
and hospital systems are employing health care providers.
In the traditional structure, the medical staff is granted
the right to admit patients and perform procedures in the
hospital.
The management portion of the hospital consists of
the hospital administrator as the chief executive officer
who is responsible for managing all hospital departments.
Figure 1 - 1 shows the relationships among the three parts
of the hospital and shows where the laboratory fits into the
organizational structure.
Clinical Laboratory
Clinical laboratories are composed of many different depart­
ments. The laboratory services department is usually sepa­
rated into anatomic and clinical pathology. The anatomic
pathology department examines all tissues, fluids, organs,
and limbs removed from the body. This discipline com­
prises surgical pathology, histology, and cytology. Personnel
in the anatomic pathology department include pathologists,
pathologists' assistants, histology technicians, and cytology
technicians. In the anatomic pathology department, tis­
sues are described by pathologists, cut into sections, fixed
with chemicals, sliced very thin, placed on glass slides, and
stained with special chemicals. After the slides are stained
and cover slipped, the pathologist examines the tissue for
abnormalities.
Clinical pathology is the largest portion of the clinical
laboratory. This section is composed of hematology, clinical
chemistry, microbiology, immunohematology, toxicology,

MediAdmicalsRecords
sions ClRadi
i n icoalloLab
I maging Rehabil itation
• Figure 1-1 Hospital organ izational chart.
Hematology
• Figure 1-2 Clinical laboratory organizational chart .
immunology and serology, urinalysis, specimen collection,
and customer service. The individual laboratory sections are
described later (Fig. 1 -2) .
Departments and Their Functions
Clinical Chemistry
Clinical chemistry is the medical discipline that uses various
methods of analysis and instrumentation to determine val­
ues for chemical components in normal and diseased states,
types and concentrations of blood toxins, and therapeutic
drug levels. Routine tests run by the clinical chemistry section
analyze levels of glucose, blood urea nitrogen (BUN), electro­
lytes, calcium, phosphorus, magnesium, lipids, liver function
values, alkaline phosphatase, creatinine kinase, creatinine,
protein, albumin, and hemoglobin A1c. The clinical chem­
istry department also runs hepatitis panels, tests for rubella
and human immunodeficiency virus (HIV) , and determines
levels of antibodies in the blood. Hormone levels (e.g., thy­
roid-stimulating hormone, prolactin, follicle-stimulating
hormone) are tested in another section of this laboratory.
The routine tests are usually run in the main clinical
chemistry department. The antibody and hormone levels
are usually considered subspecialties. Other subspecialty
departments include the toxicology, therapeutic drug mon­
itoring, molecular diagnostics, and fecal analysis. Some
clinical chemistry laboratories have a section that analyzes
blood gases.
CHAPTER 1 Laboratory Essentials
AdmiHospi tal
n istrator
BusiOffincesse
gy Respi ratory
Pharmacy AdmiFaci
n i s ies ve Bil ing CodiAccounti
l ittrati &
ng ng
Support Human Resources
Immunol
Serologyogy/ Microbiology Toxicology II Uri nalysis
Hematology
Hematology is the study of blood cells. Blood cells include
erythrocytes (i.e., red blood cells) , leukocytes (i.e., white
blood cells) , and thrombocytes (i.e., platelets) . The most
common test performed in this department is the com­
plete blood count (CBC) , which is a summary of cell
counts (i.e., red, white, and platelet) , total hemoglobin
level, red blood cell size, and hematocrit. A CBC usually
includes a differential count, which reports the percentage
of each type of white blood cell in the blood sample. Cell
counts for body fluids are also performed in this depart­
ment. Other tests include reticulocyte counts and erythro­
cyte sedimentation rates.
In many laboratories, coagulation testing is performed
in the hematology department. Routine coagulation tests
include the prothrombin time (PT) and the activated par­
tial thromboplastin time (aPTT) . These tests assess the two
major clotting pathways in the body.
Microbiology
The microbiology department identifies microorgan­
isms that cause disease and determine the most effective
antibiotic to destroy bacterial pathogens. This department
grows cultures from major body systems such as the throat,
urine, stool, wound, blood, eyes, ears, body fluids, nasal,
abscesses, vagina, urethra, and tissues. Surgeons often per­
form a culture after they drain or debride an infected area.
6 PA R T 1 Laboratory Principles
Routine cultures include aerobic and anaerobic incubation
environments. This department also performs identifica­
tion or presumptive identification of fungi, parasites, and
bacteria.
Specim en Collection
The specimen collection department collects tissue, blood,
and urine samples from patients. In the outpatient area of
the laboratory, phlebotomists also educate patients about
collection of 24-hour urine, fecal fat, dean-catch urine, and
other specimens.
U rinalysis
The urinalysis department performs chemical tests on urine
specimens and analyzes formed elements that may be present
in specimens. Urine is tested for color, clarity, specific grav­
ity, glucose, protein, ketones, occult blood, and pH. These
tests are used to monitor metabolic diseases such as diabetes.
Blood Bank
The blood bank or immunohematology department tests
red blood cells from donors for antigens and serum from
recipients for antibodies. Testing ensures that people receive
compatible units of blood during a transfusion. The blood
bank also transfuses other blood components such as plate­
lets, fresh frozen plasma, and specific clotting factors.
I m m unology and Serology
When invaded by microorganisms or other foreign bodies,
the human body produces antibodies to protect itself from
the threat. The immunology and serology department tests
blood for antibodies produced against pathogenic microor­
ganisms. Detection of antibodies against a particular patho­
gen affects the diagnosis and treatment of the disease, such
as hepatitis B virus and HIV infections. The department
also tests for abnormal configurations of antibodies.
Much testing is performed across laboratory departments.
For example, molecular diagnostics can be performed in a
microbiology laboratory to test for specific viruses and other
microorganisms. Serology and immunology testing may be
performed in the chemistry department. To increase labora­
tory efficiency, many large laboratories have a core labora­
tory. The composition of a core laboratory varies according
to the needs of the institution and its clients. One possible
configuration uses a menu of testing services for general
chemistries, hematology, coagulation, blood gases, thera­
peutic drugs, endocrine profiles, emergency toxicology, and
drugs of abuse. It usually includes automated analytic sys­
tems and specialized information management for critical
care testing on a 24-hour basis.
Technical Personnel
Laboratory workers include pathologists, laboratory manag­
ers, clinical laboratory scientists, clinical laboratory techni­
cians, medical laboratory assistants, and phlebotomists. The
educational requirements and duties of each type of worker
are discussed in the following sections.
Pathologist
A pathologist is a medical doctor who examines tissues and
oversees the quality of laboratory test results from a clini­
cal laboratory. Pathologists must complete medical school,
an accredited student resident program, and an approved
residency.
Pathologists are responsible for analyzing tissue samples
(e.g. , looking for cancer cells) and interpreting the mean­
ing of laboratory test results. They consult with treating
physicians to determine diagnostic and follow-up tests for
patients. They are also responsible for performing autopsies.
Anatomic pathologists assist surgeons by examining biop­
sies during surgery to produce an immediate diagnosis. This
helps the surgeon to determine whether additional tissue
must be removed from the patient's body to eradicate dis­
ease. Clinical pathologists oversee testing of body fluids and
confirm cellular identification in the hematology laboratory.
The clinical pathologist also consults with physicians about
blood transfusions and antibiotic treatment of bacterial and
other infections. Forensic pathologists examine evidence to
provide information for criminal and civil law cases.
Laboratory Manag er
A laboratory manager is responsible for the daily activities
of the laboratory. He or she has at least a bachelor's degree
and is a clinical laboratory scientist. The person is respon­
sible for the laboratory workers conducting tests and report­
ing test results.
Clinical Laboratory Scientists
Clinical laboratory scientists (CLSs) are also known as
medical laboratory scientists (MLSs) or medical technolo­
gists (MTs) . They perform routine and specialized labora­
tory tests. They also troubleshoot problems with specimens,
procedures, and instruments to ensure quality test results.
They examine blood and body fluids under the microscope
for microorganisms and possibly even cancer. These workers
communicate laboratory results to physicians and patholo­
gists. Clinical laboratory scientists train new employees,
perform quality control procedures on analytic test runs,
and evaluate instruments and new procedures. These indi­
viduals may also advance to department supervisors, techni­
cal supervisors, or the laboratory manager. They can also
choose to specialize in disciplines such as clinical chemis­
try, immunology, molecular pathology, microbiology, and
blood bank services.
CLSs possess a bachelor's degree in clinical or medical
laboratory science, 3 years of academic course work, and
6 months to 1 year of clinical experience. This is the most
common route to certification. Several other routes combine
education with experience that can be used to become certi­
fied. Most employers require CLSs to obtain a certification
from the ASCP Board of Certification (BOC) or the AMT.
Clinical Laboratory Technicians
Clinical laboratory technicians (CLTs) or medical labora­
tory technicians (MLTs) possess a 2-year associate degree,
 CHAPTER 1 Laboratory Essentials

and they perform all the routine testing in the laboratory.
CLTs who graduate from accredited programs are able to sit
for the national certification examination offered through
the BOC. CLTs use microscopes and all of the instrumenta-
tion in a clinical laboratory. CLTs also specialize in the same
disciplines as the CLSs.
Medical Laboratory Assistants
Medical laboratory assistants (MLAs) are trained to per-
form or assist in performing routine laboratory testing as
allowed by law and to perform administrative tasks. Some
MLAs also have duties involving patient contact. Most of
these professionals receive on-the-job training, but some
graduate from short-term educational programs accredited
by the Commission on Accreditation of Allied Health
Education Programs (CAAHEP) or the Accrediting
Bureau of Health Education Schools (ABHES).
Phlebotomists
Phlebotomists draw blood from patients. Usually, CLSs
and CLTs are also trained to draw blood as part of their
education. It is more cost effective to hire phlebotomists to
draw blood and have the CLSs and CLTs perform laboratory
tests . Phlebotomists are high school graduates with specific
training in phlebotomy. The ASCP BOC offers a certifica-
tion examination for phlebotomy technicians (Table 1-1 ).
~ ublic ea di laboratories are operated at a state level. The
Outpatient Clinics and Physicians' Office
Laboratories
An outpatient clinic or a doctor's office is a location
where patients receive medical care. Clinics usually ,Have
small laboratories that perform routine tests as allowed
by law. Physicians' office laboratories (POLs) range
from a small laboratory (for one to five physicians) that
performs a few tests to laboratories with a large volume
(500,000 tests per year) chat serve up to 200 physicians.
The large POL is usually the exception. POLs are defined
as a laboratory that performs tests in a physician office
setting, provides results to be used during the office visit,
and performs tests to be used for screening, diagnosis, and
monitoring.
Reference Laboratories
Reference laboratories are independent, commercial, large
laboratories chat perform routine and specialty testing.
POLs, nursing homes, and hospital laboratories send labo-
ratory testing to these facilities. Reference laboratories have
specialized equipment and perform low-volume specialized
tests. Reference laboratories usually have drawing stations
located in convenient locati0ns for patients.
State and Federal Laboratories
or isease Control and Prevention (CDC)
operates o , cl two biosafety level 4 laboratories in the
United States.it is an example of a federal laboratory. Many
tW.v0rk of public health laboratories plays a vital role in
kee2ing Americans healthy. Public health laboratories are
resp~ sible for performing public health reference tests; dis-
c.s:ase prevention, control, and surveillance; population-based
interventions; and emergency responses.

■ Laboratory Professionals' Profile

Laboratory Education
Professionals Where They Work Special Skills Required

Laboratory director Hospitals, reference Attention to detail, big PhD or MD

laboratories, pharma- picture; good communicator,
physicians ceutical companies planner, leader

Clinical laboratory Performs routine and Hospitals, reference Problem solver, troubleshooting Bachelor's degree
scientist (CLS) complex tests laboratories, clinics skills, attention to Licensure or
Performs quality control detail, organized, good certification
time management

Clinical laboratory Performs routine tests Hospitals, reference Good coordination, ability to Associate degree
technician (CLT) Performs quality control laboratories, clinics manipulate small objects, Licensure or
with supervision attention to detail, computer certification
literate

Clinical laboratory Performs or assists with Hospitals, reference Good coordination, ability to On-the-job training
assistant (CLA) routine laboratory tests laboratories, clinics manipulate small objects, or completion
as allowed by law attention to detail, computer of a short-term
literate program
Phlebotomist Collects blood specimens Hospitals, reference Good coordination, ability to On-the-job training
from patients laboratories, clinics manipulate small objects, or completion
attention to detail, computer of a short-term
literate program
8 PA R T 1 Laboratory Principles
M i l ita ry Laboratories
The Department of Defense operates many clinical labo­
ratories across the world. Military hospitals perform rou­
tine laboratory testing and are accredited by the College of
American Pathologists (CAP) . The very large military hospi­
tals perform routine tests for the physicians assigned to that
hospital and specialized tests for other military hospitals
around the world.
Military hospitals operate American hospitals to treat mili­
tary members and their dependents. Military hospitals have
laboratory officers and medical laboratory technicians staffing
the clinical laboratory. Laboratory officers have at least a bach­
elor's degree and CLS certification, and the enlisted members
serve as medical laboratory technicians and are graduates of
the service's medical laboratory technician school.
Regulation and Accreditation of Clinical
Laboratories
Federal regulations and accreditation agencies govern the
operation of clinical laboratories. Federal regulations that
affect clinical laboratories include the Clinical Laboratory
Improvement Act ( CLIA) of 1 967 and the Clinical Labo­
ratory Improvement Amendments of 1 988, the Needle­
stick Safety and Prevention Act of 2000, and those for
bloodborne pathogens, hazardous chemicals, and hazard
communications. The regulations concerning safety are
discussed in Chapter 2, and CLIA is discussed in the next
section. The Health Insurance Portability and Accountabil­
ity Act affects the laboratory as it relates to patient privacy.
Reg u lation
Congress first passed the CLIA in 1 967. The purpose of
this Act was to regulate clinical laboratories involved in
interstate commerce. Hospital and reference laboratories
were the only clinical laboratories affected by the Act. In
1 988, Congress passed regulatory amendments to the Act
in response to public concern about the quality of Pap
smears. The provisions of CLIA 1 988 govern the activities
of all laboratories. It was designed to enhance the quality
of laboratory services provided to all patients by mandating
quality control, quality assurance, and proficiency testing.
Trained personnel were required to perform particular levels
or complexities of tests. The more complex tests a labora­
tory performs, the higher the standards required for the per­
sonnel working in that laboratory. If a laboratory performs
only simple tests, the laboratory can obtain a certificate of
waiver. Laboratories performing "waived" tests are exempt
from proficiency testing requirements under CLIA.
Accred itation
Accreditation is a voluntary process by which laborato­
ries maintain certain standards of quality. Two accrediting
agencies have been given "deemed status" by the federal
government's Centers for Medicare and Medicaid Services
(CMS) . If laboratories are accredited by either agency, the
laboratory does not need to be inspected by the Department
of Health and Human Services. The two accrediting agen­
cies are The Joint Commission and the College of Ameri­
can Pathologists (CAP) .
The Joint Commission
The Joint Commission (formerly known as the Joint Com­
mission for the Accreditation of Healthcare Organizations
[JCAHO]) accredits hospitals and many other health care
organizations, such as ambulatory care facilities, stand­
alone surgery centers, long-term care facilities, behavioral
health centers, and laboratories. A team of individuals
from peer institutions that are accredited by The Joint
Commission visits an institution seeking accreditation or
reaccreditation. These site visitors examine each standard
and the evidence compiled by the institution for com­
pliance with the standard. Institutions must also collect
data on core measures (ORYX) and must comply with the
National Patient Safety Goals annually issued by The Joint
Commission. The Joint Commission accepts accreditation
by the CAP as evidence of compliance with a good portion
of laboratory standards.
College of American Pathologists
The CAP is an internationally known agency that accredits
clinical laboratories. Clinical laboratory professionals per­
form inspections at clinical laboratories using accreditation
checklists developed by CAP. CAP strives for excellence
well beyond regulatory compliance to assist physicians in
providing the best patient care possible. The foundation of
CAP accreditation is rigorous accreditation standards that
are molded into specific, comprehensive checklists. The
inspection team uses the checklists to analyze laboratory
operations.
Proficiency Testing
Proficiency testing is required by CAP, The Joint Commis­
sion, and the federal government through CLIA 1 988. Pro­
ficiency testing is a process in which a laboratory is provided
samples to analyze with a regular run. These samples are
provided for every department in the laboratory that per­
forms diagnostic tests. The laboratory analyzes the samples
and then sends the results back to the agency that provided
the samples. The agency analyzes the laboratory's results and
provides the analysis to the laboratory. This process tests the
accuracy of laboratory results being produced in that labora­
tory. Excellent clinical laboratories must produce accurate
and reliable laboratory test results.
Competency Testing
Competency testing involves testing the ability of the labo­
ratory professionals who perform the diagnostic tests. This
must occur yearly to ensure that individuals performing
diagnostic tests are well trained and competent.

Laboratory M aterials
Laboratory professionals use many types of equipment and
chemicals in the laboratory. The following sections describe
common, nonautomated equipment and chemicals used in
the laboratory.
Glasswa re and Plasticwa re
All glassware is not made the same and has different char­
acteristics for different purposes. Characteristics of glass­
ware include thermal durability; alkali, zinc, or heavy metal
content; chemical stability; electrical conduction; optical
qualities; and color. Pyrex can be used in high-temperature
experiments, and it is heat shock resistant. Other qualities
of Pyrex include acid resistance and a low alkali content,
which is good for high-purity laboratory work. The name
probably looks familiar because Pyrex glassware is used for
home baking.
Many types of plasticware are sold for laboratory use.
Nalgene is a leader in providing high-quality plasticware
to laboratories. Plasticware can be made from polystyrene,
polypropylene, polycarbonate, Teflon, and nylon. Many
types of plasticware are biologically inert, chemically resis­
tant, break resistant, and durable. Because breakage is less
of an issue than when working with glassware, plasticware
makes good laboratory equipment.
Cleanliness of laboratory equipment is extremely critical
because contaminants residing in a piece of glass or plastic­
ware can severely disrupt the next analysis performed. All
glass and plasticware should be rinsed thoroughly after use
with water and a mild detergent solution. After using the
detergent, the item should be rinsed thoroughly with water.
If using a dishwasher to clean glass and plasticware, follow
manufacturer's guidelines for the best results.
Centrifuges
A centrifuge is a piece of motorized equipment that uses
centrifugal force to separate a mixture such as clotted blood.
There are four basic types of centrifuges: horizontal head
or swinging bucket, angle-head or fixed angle, axial, and
ultracentrifuge. Centrifuges can be small enough to set on a
bench top or large enough to stand alone on the floor. They
can be refrigerated or nonrefrigerated. They can have small
openings for placing test tubes or large openings for placing
a unit of blood.
Uses for Centrifuges
There are many uses for centrifuges in a clinical labora­
tory. Blood specimens are spun down in a centrifuge to
separate the red blood cells from the serum or plasma.
Urine specimens can be poured into a disposable plastic
tube and spun down in a centrifuge to concentrate the
nonliquid material that may be present in the urine speci­
men. Antibodies and antigens can be separated through
centrifugation.
CHAPTER 1 Laboratory Essentials
Periodic Maintenance
New centrifuges should be calibrated before they are put
into service in the laboratory and after repair. Centrifuges
should spin at the speed recommended by the manufacturer
because spinning too fast can lyse or break apart red blood
cells, and spinning too slowly can fail to adequately con­
centrate materials in a urine or other specimen. The speed
should be checked approximately every 3 to 6 months using
an external tachometer.
The timer should also be checked for accuracy periodi­
cally. If the centrifuge is refrigerated, the temperature should
be checked and recorded monthly. The temperature should
fall within the manufacturer's guidelines.
Bala nces
Types of Balances
Balances are devices used to accurately weigh substances.
There are two designs for balances: double pan and single
pan. The double pan balance has a single beam with two
arms of equal length. The single pan balance has arms of
unequal length. Both types of balances can be mechanical
or electronic. Balances should be placed in a vibration-free
and airflow-free area away from centrifuges.
Analytical balances are used in laboratories for preci­
sion measuring in weighing substances requiring 0 . 1 -mg to
1 0-).lg readability. Analytical balances can be electronic or
manual. Types of electronic balances are the electromagnetic
balancing or electrical resistance wire. Although they are
based on different principles, neither type of balance directly
measures mass. Instead, they measure the force that pushes
the pan downward. This force is converted to an electrical
signal, and the signal on the digital display is interpreted
as the mass of the object on the pan. The electromagnetic
balancing principle uses a magnet and a coil to generate an
electromagnetic force that is converted to an electronic sig­
nal and interpreted as mass. The electrical resistance wire
uses the change in resistance of a wire that is attached to a
piece of metal that bends when a force is applied. Balances
use reference weights to calibrate the output, which corre­
lates force to a particular number of grams.
Periodic Maintenance
Analytical standard weights are used to verifY the accuracy
of balances. The National Institute of Standards and Tech­
nology (NIST) recognizes five different classes of analytical
weights: M, S, S- 1 , P, and J. Class M weights are designated
as primary standard quality and are used to calibrate other
weights. Usually laboratories use class S weights to verifY the
accuracy of balances for weights between 1 00 g and 1 mg.
Pi pettes
Pipettes are devices used to transfer a specific amount
of a liquid to another container. Pipettes are classified as
manual, semiautomated, and automated. The two types
of manual pipettes are volumetric (i.e., transfer) and sero­
logic (i.e., measuring) . Semiautomated pipettes can have a
10 PA R T 1 Laboratory Principles
fixed volume or variable volume. These pipettes use plastic,
disposable pipette tips to draw up and dispense the liquid.
Semiautomatic pipettes are especially useful for transferring
extremely small volumes of liquids, such as 1 0 J..LL , 5 J..LL ,
1 00 J..LL , or 200 J..LL
Automated pipettes are usually electronic, computer­
ized pipettes that control the amount of liquid aspirated and
the amount of time allowed for aspirating and dispensing
liquids. All types of pipettes used in the laboratory must be
routinely calibrated to ensure accuracy. The manufacturer's
instructions provide details on calibration.
Volumetric Pipettes
The volumetric pipette is a long glass tube with a bubble in the
middle. The liquid being transferred is drawn up in the pipette
until it reaches an etched mark on the pipette. This mark indi­
cates the exact volume for the pipette. Volumetric pipettes
come in different sizes, and each pipette has only one volume.
Serologic Pipettes
The serologic glass pipette is etched with gradations so that
different amounts can be delivered with the same pipette.
There are two types of serologic pipettes: "to deliver" and "to
contain." "To deliver" pipettes retain some liquid in the tip
after the specified amount of liquid has been delivered. The
"to contain" pipettes require the liquid that remains in the
tip after delivery to be pushed out of the pipette for accurate
delivery.
Reagents
Reagents are chemical solutions that are used in diagnos­
tic tests. They are usually liquid, lyophilized, or frozen.
Reagents come in various purity states. Because there is no
agreement about the purity of a reagent, the standards put
forth by the American Chemical Society (ACS) are used to
determine reagent or analytical reagent grade. ACS chemi­
cals are considered to have very high purity and to be suit­
able for quantitative analyses.
Reagents must be monitored for reliability and reproduc­
ibility. The U.S. Food and Drug Administration Department
of Biologics enforces tough federal regulations to ensure
quality. Laboratories must be vigilant and verify the integ­
rity of purchased reagents. When changing lots of reagents,
the laboratory must perform parallel testing to ensure reli­
able results. Laboratories develop operating instructions for
performing this function.
Water
Water is a common substance with many laboratory uses.
Drinking water contains many impurities that can affect
laboratory test results. To ensure high-quality laboratory
results, high-quality chemicals and high-quality water must
be used.
Several methods are used to produce water that is free
of impurities and suitable for laboratory use. The methods
are discussed in great detail in the Clinical Laboratory Stan­
dards Institute (CLSI) guideline, Preparation and Testing of
Reagent \Vtzter in the Clinical Laboratory: Approved Guide­
line, 4th edition.
The most common purification processes used in clini­
cal laboratories include distillation, deionization, reverse
osmosis, and ultrafiltration. Distillation is a good pro­
cess for removing particulates and some dissolved con­
taminants. It is less effective at removing dissolved ions.
Deionization involves passing water through cation- and
anion-exchange resins. This is an excellent method for
removing ions, and when coupled with a carbon filter, most
dissolved organic compounds can be removed. This pro­
cess is less effective at removing particulate matter. Reverse
osmosis involves forcing water under pressure through a
semipermeable membrane. The semipermeable membrane
filters out dissolved organic, ionic, and particulate impu­
rities. This method is less effective at removing dissolved
gases. Ultrafiltration involves passing water through semi­
permeable membranes (i.e., pores less than 0.2 mm) to
remove most particulates from the water. It does not do
a good job of removing dissolved solids and gases. Most
laboratories choose water filtration systems that produce
the best water possible for its use.
There are three types of reagent-grade water. Type I
reagent-grade water is the highest quality water, and it is
used in test methods requiring minimal interference and
maximum sensitivity. Type II water is used for general lab­
oratory testing. Type III water is used for the initial rins­
ing and washing of glassware. The CLSI standard bases the
purity of reagent-grade water on microbiology content (col­
ony forming units per ml) , pH, resistivity, silicates, organ­
ics, and particulate matter. Water used for most routine
clinical laboratory testing is defined as clinical laboratory
reagent water by CLSI and has a resistivity of at least 1 0 mQ
· em at 25o C.
Chemistry Review
A clinical laboratory analyzes specimens from the human
body and other living animals. Clinical chemistry deals with
the concentrations of chemicals and ions in the body and
the changes that occur to these chemicals and ions in nor­
mal and disease states of the body. The following sections
review the chemical principles needed to understand clinical
chemistry.
Atomic Theory
Atomic theory states that all matter is made up of atoms.
Atoms have protons (i.e., positively charged particles [1 +])
and neutrons (i.e., neutral particles) in the center or nucleus
and electrons (i.e., negatively charged particles [ 1 - ] ) that
circle around the nucleus. Electrons are located in specific
areas around the nucleus called electron shells. The shells are
located a specific distance from the nucleus. Smaller shells
are located closer to the nucleus of the atom, and larger

shells are located farther away from the nucleus. Scientists
think there are up to seven electron shells surrounding the
nucleus. In most cases, electrons fill or partially fill the lower
energy level electron shells before filling the higher energy
level shells.
Various atoms have different numbers of protons, neu­
trons, and electrons. The outermost shell containing elec­
trons is called the valence shell. Electrons located in the
valence shell are usually involved in bonding with other
atoms to produce chemical compounds.
The valence of an atom is the number of electrons that
can be lost, gained, or shared by an atom when forming
a compound. If the atom gains electrons (- 1 charge), the
atom's valence is negative. If the atom loses electrons, the
atom's valence is positive. As a rule, when 2 atoms combine
to form a molecule, the sum of the valences of the atoms
is zero. The resulting molecule is considered to be neutral.
For example, hydrogen and oxygen combine to make water.
The valence of hydrogen is + 1 , and the valence of oxygen is
- 2. The result of combining 1 hydrogen atom and 1 oxygen
atom is a molecule with a valence of - 1. Another hydrogen
atom is needed to form the neutral molecule of water (H 2 0) .
When an atom loses or gains electrons, it becomes an ion.
Ions are charged atoms. If a hydrogen atom loses its elec­
tron, it becomes a positively charged ( + 1) ion, also known
as a cation. If the oxygen atom adds 2 electrons, it becomes a
negatively charged ( - 2) ion, also known as an anion. Oppo­
sitely charged atoms attract each other, and this force holds
the resulting molecule together. The force that holds atoms
together to form molecules is called a bond.
Chemica l Bonds
Atoms combine through ionic, covalent, coordinate cova­
lent, nonpolar covalent, and polar covalent bonds. In an
ionic bond, one atom transfers its electrons to another
atom. The atoms in this molecule each have their valence
shells completed. These atoms are held together with an
electrovalent bond. In a covalent bond, each atom donates
one or more electrons that are subsequently shared between
the two atoms. A coordinate covalent bond is a special case
of a covalent bond in which one atom donates all the elec­
trons to be shared. A nonpolar covalent bond occurs when
both atoms sharing electrons have similar characteristics. A
polar covalent bond occurs when one atom in a molecule is
more electronegative than the other atom. Chemical bonds
play a role in chemical reactions.
Factors Affecting Chemica l Reactions
Many factors affect chemical reactions. Some chemical reac­
tions are reversible, and others are irreversible. Some chemi­
cal reactions go much faster than other chemical reactions.
By understanding the factors that affect chemical reactions,
it is easier to predict the outcome or troubleshoot a prob­
lem. Factors affecting a chemical reaction include tempera­
ture, light, pressure, concentration, and catalysts.
CHAPTER 1 Laboratory Essentials
An increase in temperature causes an increase in the
rate of a chemical reaction. A higher temperature provides
energy for the molecules to move faster and collide more
frequently. Due to the increased collisions, the chemical
reaction rate increases. Conversely, lowering the tempera­
ture slows the chemical reaction rate and the collisions
between the molecules. Light is another form of energy
that can increase the rate of a chemical reaction. When
working with gases, increased pressure adds energy to the
chemical reaction and forces more molecular collisions,
resulting in an increased chemical reaction rate. The con­
centrations of the reactants may also influence the reac­
tion rate.
Important factors affecting a chemical reaction rate are
catalysts. Many biological reactions are extremely slow by
nature and require a catalyst to increase the reaction rate.
Some catalysts are organic and are called enzymes. Enzymes
are a clinically important group of compounds for diagnos­
ing diseases. Chemical reactions are also affected by the con­
centration of the reacting compounds.
Acid, Bases, and Sa lts
Acids, bases, and salts are important compounds in the
body. Acids and bases are produced and used in urine forma­
tion and respiration. Salt is the basis for the blood that runs
through our veins. Understanding the properties of these
substances helps to explain and troubleshoot test principles.
An acid is a substance that donates hydrogen atoms in
a water solution. Acids occur as liquids, solids, and gases.
When a strong acid is mixed with water, the acid completely
dissociates or ionizes. When a weak acid is mixed with water,
the acid partially dissociates or ionizes. Weak acids are used
as buffers to minimize large pH changes with the addition
of strong acids or bases to a system such as blood.
A base is a substance that donates hydroxide (OH - ) ions
in a water solution. Acids donate protons, and bases accept
the protons. Most bases have an -ide suffix: sodium hydrox­
ide (NaOH) , potassium hydroxide (KOH) , or lithium
hydroxide (LiOH) .
A neutralization reaction consists of combining an
acid and a base to produce a salt and water as products.
The hydrogen donated by the acid and the hydroxide ion
donated by the base combine to form water. The other
atoms in the acid and base compounds combine to form
the salt.
Orga nic Chemistry
Organic chemistry is the study of carbon-based compounds.
Carbon is a special compound that can have a valence of +4 or
- 4, meaning that it can donate all four of its electrons or take
on four electrons. Examples of other atoms that are found in
organic molecules include hydrogen, nitrogen, sulfur, chlorine,
bromine, and iodine. The versatility of the carbon atom's bond­
ing creates more than 5 million known organic compounds.
Most organic compounds are held together by covalent bonds.
12 PA R T 1 Laboratory Principles
Covalent bonds in organic compounds create lower melting
and boiling points than in inorganic compounds.
Hydrocarbons
Hydrocarbons are compounds made of hydrogen and car­
bon atoms. The atoms can be arranged as straight chains,
branched chains, or rings.
The two main types of hydrocarbons are aliphatic and
aromatic. Aromatic hydrocarbons contain one or more ben­
zene rings, and aliphatic hydrocarbons do not contain ben­
zene rings. Organic molecules can contain a special group
of atoms called a Junctional group. Five functional groups
are important in clinical chemistry: alcohols, aldehydes and
ketones, esters, sterols and phenols, and amines and amides.
Alcohols
Alcohols are compounds that contain a hydrocarbon chain
(R) and one or more hydroxyl (OH - ) groups. Alcohols are
extensively used in the clinical laboratory as preservatives
or solvents, and they may be a component of stains and
reagents. Examples of alcohols are ethyl alcohol, isopropyl
R-q_
alcohol, isopropanol, and glycerol.
H
Aldehydes and Ketones
The aldehyde functional group consists of an oxygen atom that
is double bonded to a carbon atom, which also has a hydrogen
atom attached. This group is attached to a hydrocarbon chain.
0
R),._ H
The ketone functional group consists of an oxygen atom
that is double bonded to a carbon atom that is bonded to
two other carbon atoms.
0I
C-C-C
Aldehydes usually have a detectable odor. Some smell
very bad, and others smell good. Examples of aldehydes
include formaldehyde and paraldehyde. An example of a
ketone is acetone.
Esters
An ester is an alcohol derivative of carboxylic acids. Carbox­
ylic acids are organic acids. Esters occur in plants and pro­
duce the fragrance in fruits. Esters may be found in reagents
used in chemical tests.
Sterols and Phenols
Sterols are high-molecular-weight cyclic alcohols produced
from fat metabolism. A cyclic structure has three or more
carbons joined together in a closed ring. If one of the carbons
is attached to an alcohol functional group, the cyclic struc­
ture is a cyclic alcohol. Examples of cyclic sterols are ben­
zene, toluene, and xylene. The benzene molecule (C 6 H 6) is
the smallest example of an aromatic ring. Benzene contains
six carbon atoms with alternating double bonds and single
bonds in the ring.
0
An aromatic ring that contains a hydroxyl group (OH - )
is a phenol. Phenol is a carbolic acid and is highly poison­
ous. Phenols are toxic to most organisms, especially micro­
organisms. Phenol is an ingredient in many antiseptics and
disinfectants. Examples of phenols include vanillin (i.e.,
found in vanilla beans) , eugenol (i.e., oil of cloves) , and thy­
mol (i.e., oil of thyme, a member of the mint family) .
6
Amines and Am ides
Amines are derivatives of ammonia (NH 3 ) , and amides
are compounds in which a nitrogen atom is attached to a
carbon chain. Amines and amides are found in alkaloids,
antihistamines, sulfa drugs, and barbiturates. A well-known
amine is amphetamine, which is a powerful stimulant. A
well-known amide is acetaminophen, which is a nonpre­
scription pain reliever.
�c
R,... ' N H 2
ami d e
Biochemistry
Biochemistry, also called physiologic chemistry, is the study of
the chemistry of living organisms. A sample of the biological
processes that are studied in biochemistry includes the study
of digestion, urine formation, reproduction, metabolism, and
respiration. The four classes of functional molecules in bio­
chemistry are carbohydrates, lipids, proteins, and nucleic acids.
Carbohydrates
Carbohydrates are polyhydroxy aldehydes or polyhydroxy
ketones. This means that the functional groups are alde­
hydes or ketones and that there are several hydroxyl groups
on each compound. When carbohydrates are hydrolyzed,
the resulting compounds are aldehydes or ketones.
Carbohydrates are the main food source for humans; the
body uses carbohydrates for energy. Carbohydrates are also
found in connective tissue and nucleic acids (i.e., ribose in
RNA and deoxyribose in DNA) .
Carbohydrates have a general molecular formula of
CH 2 0. They exist as sugars, starches, and cellulose. Simple
sugars are called saccharides and have names ending in -ose.
Examples include glucose, sucrose, fructose, and maltose.
Carbohydrates are classified by the number of saccharide
 CHAPTER 1 Laboratory Essentials

units in the molecule: monosaccharides, disaccharides, oli­ A trans fat has a double bond in a specific type of isomer (see
gosaccharide, and polysaccharides. Glucose is a monosaccha­ figure below) .
ride, sucrose is a disaccharide, and starch is a polysaccharide. Other classes of lipids include phospholipids, glycolipids,
and steroids. Phospholipids are found in the brain, spinal

�A
OH

O�
cord, and liver. Glycolipids (i.e., cerebrosides) are mainly
Q
OH
HO
__... found in the brain and at nerve synapses. Fats are the build­
ing blocks of steroids. Cholesterol is the major steroid in
OH the body.
Lipids Proteins
Lipids, mainly fats and oils, are insoluble in water and found Protein is considered by many to be the most important
in living organisms. As a general rule, fats, which are solid at compound in the body. Proteins are found in every tissue of
room temperature, come from animals, and oils, which are liq­ the body. Proteins are responsible for structure; they are the
uid at room temperature, come from vegetable sources. Fats are main component in hair, skin, and nails. Proteins are respon­
part of messenger systems (e.g., hormones) , are structural com­ sible for movement; muscles are made of protein. Proteins
ponents of membranes, and provide energy storage in animals. are responsible for catalyzing chemical reactions in the body;
Fats and oils share a similar structure; each has three catalytic enzymes are proteins. Proteins are responsible for
ester functional groups. These compounds are esters of tri­ transport; proteins transport molecules across cell membranes
alcohol, or glycerol. The common name is triglycerides, and and carry oxygen and carbon dioxide in blood. Proteins are
the more scientific name is triacylglycerol. part of hormones that regulate many body processes, includ­
H 0 H H H H H ing growth. Proteins are responsible for protection; special­
I II I I I I I ized white blood cells (i.e., lymphocytes) produce antibodies
H - C - 0 - C - C - C - C - C - C- H (i.e., immunoglobulins) to destroy foreign invaders that enter
I I I I I the body. Proteins facilitate storage; specialty proteins store
H H H H H
materials, such as iron in the liver by ferritin.
Proteins are made oflinear chains of amino acids (Fig. 1 -3) .
0 H H H H H Twenty amino acids make up the proteins in the body. Pro­
II I I I I I tein synthesis plays a large part in producing proteins to replace
H - c - o - c - c - c - c - c - c- H
those that wear out. Protein synthesis is controlled by genes.
I I I I I
H H H H H
Nucleic Acids
There are two types of nucleic acids in the body: deoxyribo­
0 H H H H H
II I I I I I nucleic acid (DNA) and ribonucleic acid (RNA) (Fig. 1 -4) .
H - c - o - c - c - c - c - c - c- H Genes are composed o f chromosomes, which are composed
I I I I I I of nucleic acids and DNA-bound proteins. DNA controls
H H H H H H
the hereditary traits that are expressed in an individual, and
The popular media often discuss the good qualities of RNA plays an important role in protein synthesis. Many
polyunsaturated fats and the bad qualities of saturated fats. inherited conditions, such as hemophilia and sickle cell ane­
Polyunsaturated fats have double bonds in the ester chains, mia, are caused by the absence of a protein or presence of an
and saturated fats have single bonds in the ester chains. abnormal protein.

0
I I I I
H H H

I I I
H - 0 - C - C - C- C - H

Butyric acid-saturated fatty acid

H H H

I I I I
O H H H
I I I I
H H H H H
I I
H H
I I
H
I I I I
H H H H

I I I
H H H H H H
I I I I I
H H
I
H H H H H H
I I I I
H- o - c - c - c - c - c - c - c - c - c � c - c-c- c- c - c - c - c - c -H

H H H
I I I I
Ol e i c aci d -monounsaturated fatty aci d
I I I I
O H H H
I
H H
I H
I I I I
H H H
I I I I
H H H H

I I I H H H
I I I I I I I I I I
H- o - c - c - c - c - c - c = c - c - c = c - c - c - c - c - c - c - c- c -H

H H H H H H H H H H
I I I I
H H H H

Linoleic acid-polyunsaturated fatty acid

14 PA R T 1 Laboratory Principles
Pri mary structure
Secondary structure
• Figure 1-3 Primary, secondary, tertiary, and quaternary protein structures.
Laboratory M athematics
Everyone who works in the clinical laboratory needs to
know the basic concepts of mathematics for technical
procedures. Computers perform most of the calcula­
tions, but laboratory workers must verify the results . It is
important to understand how to do mathematical calcu­
lations and to understand the concepts behind a formula.
Understanding the basis of a formula allows a laboratory
worker to modify the formula to better suit a particular
situation.
When performing mathematical calculations, follow the
procedure below to efficiently solve problems and reduce
errors:
1 . Read the problem carefully.
2. Determine the principles and relationships involved.
3. Determine exactly what the problem is asking and the
results required.
4. Think about all possible methods to solve the problem.
5. Write the intermediate stages of the calculations clearly
in a sequential format. Avoid writing one number on top
of another as a method of correction. Make each digit
legible.
6. Recognize different forms of the same value, such as: Yz ,
0 . 5 , and 50%.
7. Position the decimal point carefully.
8 . Mentally estimate an answer before working the prob­
lem; compare the calculated result with the estimated
answer. If the two figures disagree drastically, determine
which is wrong.
Mola rity
Definition
Atoms and molecules combine or separate during chemi­
cal reactions. In other words, chemical reactions take place
at the level of the atoms and molecules of the reactants.
Because atoms and molecules are not visible in a solution,
Tertiary structure Quaternary structure
some way to know the relative number of reactant particles
involved in a chemical reaction would be useful. The mole
and molarity measurements are useful methods for this
purpose.
A mole of a substance is the number of grams equal to
the atomic or molecular weight of the substance. Labora­
tory professionals work mostly with compounds, and use
the molecular weight of a molecule more often than that of
a single element. An easier way to determine the molecular
weight of a compound is to add the atomic weights of the
atoms comprising the molecule.
Examine the periodic chart of the elements on the inside
back cover. In the center of each block, there is a capital let­
ter or a capital letter and a small letter. These letters are the
chemical symbols for the elements. Beneath the chemical
symbol is a number (e.g., 52.0 1 ) that represents the atomic
mass (mass and weight are used synonymously throughout
this chapter) . This number is the sum of the number of pro­
tons and neutrons in the nucleus of the element.
To find the molecular weight of NaCI, first find the
atomic weight of Na (23 g) . Next find the atomic weight
of Cl (35 . 5 g) . The total of 23 + 3 5 . 5 equals the molecu­
lar weight, or 5 8 . 5 g. All atomic weights for elements are
rounded to the nearest whole number, except for Cl. The
atomic weight for Cl is always 3 5 . 5 . The 5 8 . 5 g also rep­
resents 1 mole of NaCI. The term gram molecular weight is
often used as a definition of mole.
Find the molecular weight of H 2 S04. The atomic
weight for hydrogen (H) is 1 g. Because there are 2 hydro­
gen atoms, multiply the atomic weight by 2: 2 H = 1 g
x 2 = 2 g. The atomic weight of sulfur (S) is 32 g, and
because there is only 1 sulfur atom, there is no need to
multiply the atomic weight: S = 32 g. The last element
needed in this problem is oxygen (0) . Because there are
4 atoms of oxygen in the chemical formula, the atomic
weight of oxygen ( 1 6 g) must be multiplied by 4 to derive
the weight. 1 6 g/atom x 4 atoms = 64 g. To calculate the
 CHAPTER 1 Laboratory Essentials

Cytosine Cytosine

Guani n e Guani n e

[D
Base pai r H....._N,-H
Sugar N� N H
� N )L NI >-
phosphate
backbone
H
Adeni n e

Uracil Thymine

Nitrogenous
bases Ri bonuclRNAe i c acid Deoxyri bDNA
onucl e i c acid Nitrogenous
bases
• Figure 1-4 N itrogenous bases found in DNA and RNA.

molecular weight of H 2 S04, sum the molecular weights of Calculations

the individual atoms: One way to calculate the concentration of a solution is to use
molarity. Because one mole of a substance is equal to the

=
2 g (hydrogen) + 32 g (sulfur) + 64 g (oxygen) gram molecular weight of a compound, mixing 1 mole or
98 g (H2S04) gram molecular weight of a compound with 1 L of water pro­
duces a 1 molar solution. In the previous example, we found
that 1 gram molecular weight of H 2 S04 (i.e., sulfuric acid)
Practice Problems equals 1 mole of H 2 S04 or 98 g. If we measure 98 g of H 2 S04
1 . Review the process and then calculate the molecu­ (i.e., 1 mole of H 2 S04) and dissolve it in 1 L of water, the con­
lar weights of the following compounds: KBr, H 2 0, centration of the resulting solution is 1 molar. When 1 gram
AgN0 3 , Fe2 (S04)j. molecular weight (or mole) of a compound is dissolved in
16 PA R T 1 Laboratory Principles
1 L of water, the concentration of the resulting solution is
1 molar. The molar concentration is also called molarity.
If two times the molecular weight of a compound is
dissolved in 1 L of solution, the concentration is 2 molar
and molarity 2. Given this information, how is a 5 molar
= out how many gram molecular weights the 1 00 g repre­
(5 M) solution ofNaCl made? Unless the volume is specified,
always use the standard 1 L solution. To make a 5 M solution
of NaCl, first calculate the gram molecular weight of NaCl.
The atomic weight ofNa is 23, and the atomic weight ofCl is
3 5 . 5 . Add these two atomic weights together to find the gram
molecular weight of NaCl (5 8 . 5 g) . To make a 5 M solution,
5 x 58.5 g of NaCl must be dissolved in 1 L of solution.
Practice Problems
2. If 5 moles of NaCl are dissolved in 5 L of solution, what
is the molarity of the resulting solution?
Consider also how to make 1 L of 3 M sodium hydroxide
(NaOH) solution. The molecular weight of NaOH is 40
(23 + 1 6 + 1 ) . To make a 3 M solution of NaOH, dissolve
3 moles x 40 g/mole 1 20 g of NaOH in 1 L of water. This
=
is a 3 M solution.
Molarity (M) is a number that expresses the number of
moles of substance in 1 L of solution. This is stated in math­
ematical terms as
moles
molarity = --
liter
grams of compound
1 mole = -=-------=----
gram molecular weight
By substituting grams of compound/gram molecular
weight the formula becomes
. ( grams of compound/gram molecular weight )
molanty = __:_:::_
____ ___:___ ___:::_
_______ .:::___:__
liters of solution
Using algebra, the equation can be simplified:
molecular weight X molarity = grams/liter
This formula is based on the fact that molarity is equal
to the number of moles per liter. For example, a 2 M solu­
tion contains 2 moles/L, and a 0 . 5 M solution contains 0 .5
moles/L. Use the formula to make 1 000 m L of 0 . 5M NaCl
(molecular weight of NaCl is 5 8 . 5 g) :
molecular weight X molarity = grams/liter
5 8 . 5 X 0. 5 = 29.25 g/L
Weigh 29.25 g/L of NaCl, and make 1 000 mL (1 L) of
solution.
Practice Problems
3. How much CaC12 would you weigh out to make a liter
of a 2 M solution?
4. How much KOH would it take to make 3 . 5 L of a 1 . 5 M
solution?
If you know how a solution is made, you can calcu­
late the concentration. For example, an NaOH solution
was made by dissolving 1 00 g of NaOH in enough water
to make 1 L. To find out the molar concentration, find
sent. NaOH has a molecular weight of 23 + 1 6 + 1 40, =
and 40 g represents 1 gram molecular weight. Therefore,
1 00 g is 1 00/40 2 . 5 gram molecular weights. This makes
=
the solution 2 . 5 M.
When faced with a volume other than 1 L, the same pro­
cess applies. Suppose you have a solution made by dissolv­
ing 3 g of NaOH in 1 00 mL of solution. Because molarity
is based on grams per liter, the first step is to find out how
much NaOH was used to make a liter of the same concen­
tration. This is done with a simple proportion equation. If
there are 3 g in 1 00 mL, there would be x grams in 1 000 mL:
3g xg
1 00 mL 1 000 mL
1 00x = 3000 g/mL
x = 30 g/mL
The numerators and denominators must be in the same
units-grams to grams or milligrams to milligrams, not
grams to milligrams; and liters to liters or milliliters to mil­
liliters, not milliliters to liters. The 1 gram molecular weight
is 40, and there are 40 g in 1 L of water in a 1 M solution.
Because there are only 30 g in 1 L of water, the molar con­
centration is 30/40 0.75 M .
=
Practice Problems
5 . A solution of NaCl is made by dissolving 9 g in enough
water to make a liter. What is the molarity?
6. A solution of NaCl is made by dissolving 1 00 g in 2 L of
solution. What is the molarity?
7. How would you make (a) 1 L of 3 M NaOH, (b) 3 L of
1 M KCL, and (c) 2.5 L of 2 M CaC12 ?
8 . What is the concentration of a KCl solution made by
dissolving 200 g of KCL in 900 mL of water?
Molal ity
Definition
Molality is a system of expressing concentration and is simi­
lar to molarity. The molal concentration ofa solution is equal
to the number of moles of solute per I 000 g of solvent. It is
a more accurate method of measuring concentration than
molarity, but it is usually much less convenient than molar­
ity and is infrequently used in the clinical laboratory.
The molal solution volume varies with temperature, the
density of the materials used, and the pattern of the inter­
action of molecules of solutes and solvent. However, the
relative masses of the constituents of the solution remain
constant.
Calculations
A one molal solution could be made by placing 1 mole ( 1
gram molecular weight) i n 1 000 g o f solvent. Th e resulting

solution's volume may be greater or less than the volume
of the separate parts of the mixture. Why? A molal solu­
tion does not use volume as a method of measure, only
mass.
Place 5 8 . 5 g of NaCl into 1 000 g of water. The volume
of the solution is 1 000 mL. Why? The salt dissolves into the
water and does not add a measurable amount of volume to
the solution.
Practice Problems
9 . Make a 3 molal solution of NaCl and water. NaCl is
the solute and water is the solvent.
1 0 . What is the molality of a solution of 35 g of LiOH
(solute) in 750 g of NaC2 H 3 0i
1 1 . How many grams of NH40H (solvent) must 44 g
of NaCl be dissolved in to make a 2.75 molal
solution?
1 2 . How many grams of CaC12 must be dissolved in 475 g
of H 2 S04 to produce a 1 .4 molal solution?
Normal ity
Definition
Laboratory testing requires an understanding of normality
and normal solutions. The concentration of solutions often
is expressed in normality, and many of the concepts learned
about molarity can be applied to normality. The main dif­
ference is equivalent weights are used rather than gram
molecular weights.
Equivalent weight is the gram molecular weight of a
compound divided by the total positive valence in the
compound. For example, the gram molecular weight of
NaCl is 5 8 . 5 , and the total positive valence is 1 . Therefore,
the equivalent weight of NaCl is 5 8 . 5 / 1 or 5 8 . 5 . When the
total positive valence is 1 , the equivalent weight is equal to
the gram molecular weight.
What if the total positive valence is different from 1 ? The
gram molecular weight of MgC12 is 9 5 . 3 , and the total posi­
tive valence is 2. The equivalent weight is 9 5 . 3/2 or 47.7.
The gram molecular weight of FeC13 is 1 62 . 5 , and the total
positive valence is 3. The equivalent weight is 1 62. 5/3 or
54.2. The molecular weight of Na2 C0 3 is 1 06. The total
positive valence is 2, and the equivalent weight is 1 06/2 or
53 (notice the radical (C0 3- 2).)
What is the equivalent weight of K, MgS04, and
Ca3 (P04h? The answers are 39 for K, 60.2 for MgS04, and
5 1 .7 for Ca3 (P04h, It is important to use a periodic table
to obtain the elemental gram weights.
When determining the total positive valence, some
basic chemistry is applied. An atom has a positive nucleus
that contains neutrons and protons. Surrounding this
positive nucleus are electrons arranged in specified and
ordered orbits. Because the number of electrons is equal
to the number of protons in the nucleus, an atom has no
net charge. When an atom reacts to form a compound, it
tries to give up or accept electrons to form a completed
outer orbit. The first orbit can only hold 2 electrons.
When it contains one electron (as in hydrogen) , it can
give up the electron, as it does in most instances, forming
CHAPTER 1 Laboratory Essentials
a hydrogen ion having a charge of + 1 . The valence is
equal to the charge on the ion and is therefore + 1 , mean­
ing that each atom can give up one electron. In special
cases, hydrogen can accept another electron, giving it a
valence of - 1 .
The second orbit can contain 8 electrons. The periodic
chart shows the 8 major families of elemental atoms, labeled
IA to VIllA. Each atom under IA contains one electron in
its outer orbit; and each atom under IIA contains 2 electrons
in the outer orbit, continuing in that pattern until group
VIllA, which has 8 electrons in the outer orbit. Atoms in
group IA can obtain a completed outer orbit by giving up
the 1 electron each atom has in its outer shell or accepting
7 electrons into the outer shell. These atoms give up the 1
electron, giving them a valence of + 1 .
Atoms in group IIA have 2 electrons in the outer orbit.
They could get to a completed outer orbit by giving up these
electrons or by accepting 6 electrons. Similar to the previous
example, the atom gives up the 2 electrons.
The atoms in group VIllA have 8 electrons in their
outer orbit, making it completely filled. These atoms are
inert. They neither give up nor accept additional elec­
trons because the outer orbit is already completed. Group
VIlA, which has 7 electrons in the outer orbit, can get a
completed outer orbit by accepting 1 additional electron,
producing a valence of - 1 . Atoms in group VIA accept 2
electrons into the outer orbit to make it complete, giving
them a valence of - 2. The other possibility is to give up
6 electrons. Groups IliA, IVA, and VA have 3, 4, and 5
electrons, respectively, in their outer orbits. Some of these
elements, especially C and Si, develop covalent bonds in
which they share electrons rather than give up or accept
electrons.
Practice Problems
1 3 . Indicate the number of electrons in the outer orbit of
the following elements and the most likely valence.
Element Electrons i n Outer Orbit Valence
K ---------- ---
Ca ---------- ---
Br ---------- ---
0
Fe ---------- ---
---------- ---
Calculations
If you can determine the equivalent weight, you can
determine normality. Normality is the gram equivalent
weight of a compound per liter. We need to know two
things: the equivalent weight and the actual number of
grams per liter. If you dissolve 1 gram equivalent weight
of a compound in a liter of water, the resulting solution is
1 normal ( 1 N) . If 2 times the gram equivalent weight of
a compound is dissolved in a liter of water, the normality
is 2 N .
Consider how t o prepare a 3 N solution o f a compound
with an equivalent weight of 3 5 . A 1 N solution by defini­
tion contains 35 g in a liter of water, and a 3 N solution
18 PA R T 1 Laboratory Principles
contains 3 x 35 or 1 05 g of the compound in a liter of water;
3 N is the normality of the solution.
To determine the normality of a solution of NaCl
containing 1 1 7 g of NaCI in 2 L of water, start with
the equivalent weight. The molecular weight of NaCI is
23 + 35.5 58.5, and the total positive valence is 1 ; the equiv­
= 600 mL of a 0.9 g/dL solution? By definition, a 0.9 g/dL
alent weight of NaCI is therefore 58.5/1 or 58.5. A simple
proportion problem shows how many grams there are per liter.
1 17 g X
2L 1L
x = 58.5 g
The solution contains 58.5 g/L, and the gram equivalent
weight is 58.5 g. The normality of the solution therefore
equals 5 8 . 5/58.5 (actual g/L per gram equivalent weight) 1 .
=
To determine the normality of a solution containing 20 g of
NaOH per 800 mL, we need to know the equivalent weight
and the grams per liter. The gram molecular weight is 23 + 1 6 +
1 40 g, and the total positive valence is 1 ; the gram equivalent
=
weight is also 40. Set up the proportion equation:
20 g X
0.8 L 1L
x = 25 g/L
The normality is equal to 25 g/40 g/equivalent weight
or 0.625 N.
Practice Problems
1 4 . Calculate the normal concentration of the following
solutions:
a. 10 g of NaOH dissolved in 500 mL water
b. 90 g of MgC12 dissolved in 1 500 mL of water
1 5 . How would you prepare the following?
a. 1 L of a 3 N solution of KOH
b. 5 L of a 1 N solution of CaC12
Concentrations often are expressed in milliequivalents
per liter (mEq/L) . This represents the equivalent weight in
milligrams per liter. A milliequivalent is Yiooo of an equiva­
lent weight. All calculations are identical to those used in
normality problems. The only difference is that you are
working with milligrams rather than grams.
D i l utions
WeightNolume Dilutions
The concepts of grams per deciliter (g/dL) and milligrams
per deciliter (mg/dL) are easy compared with normality and
molarity. The gram per deciliter concentration is defined
as the number of grams of a compound dissolved in 1 00 mL
of water. The prefix deci means one tenth, and a deciliter is
one tenth of a liter or 1 00 mL. The most common deter­
mination reported in g/dL units is that for serum protein.
A normal serum protein concentration is 6 to 8 g/dL, which
is 6 to 8 g of protein per 1 00 mL of serum.
In go/o solutions, the molecular or equivalent weight
does not enter into the calculations, and a 1 0 g/ dL solution
of any compound contains 1 0 g of that compound per
1 00 mL. For example, a 10 g/dL solution of glucose contains
1 0 g of glucose per 1 00 mL of water, and a 1 0 g/ dL solution
of NaCl contains 1 0 g of NaCl per 1 00 mL of water.
How many grams of NaCl do you need to prepare
solution contains 0.9 g per 1 00 mL, and a simple propor­
tion completes this problem:
0.9 g x (grams)
1 00 mL 600 mL
( 0.9 X 600 )
x=
1 00
x = 5 .4 g of NaCl per 1 00 mL
Prepare 1 L of a 1 g/dL solution of glucose. By definition,
a 1 g/dL solution contains 1 g per 1 00 mL, and
1g X
1 00 mL 1 000 mL
x = 1 0 g/L
Notice that the volume is expressed the same way on
both sides of the equation. The liter is expressed as 1 000
mL. It would also be correct to express the 1 00 mL as 0. 1 L.
Practice Problems
1 6 . How would you make the following solutions?
a. 3 L of 1 . 5 g/dL KOH
b. 600 mL of 4 g/dL MgC12
c. 50 mL of 1 0g/dL NaOH
The concentration of many clinically important com­
pounds such as glucose, blood urea nitrogen (BUN) , and
cholesterol is reported in units of mg/dL. MgldL is defined
as the number of milligrams per 1 00 mL. A blood glucose
level that is reported as 1 00 mg/dL contains 1 00 mg of glu­
cose per 1 00 mL of blood, and a BUN value reported as
20 mg/dL contains 20 mg of the solute per 1 00 mL of
solution. To make a liter of a glucose standard containing
200 mg/dL, the solution must contain 200 mg of the solute
per 1 00 mL of solution:
200 mg x
1 00 mL 1 000 mL
2g
x = 2000 mg = -
1L
The liter was converted to 1 000 mL so that both volumes
are in the same units (there are 1 000 mg in 1 g, and 2000
mg 2 g) . All calculations involving mg/dL units are done
=
exactly like the g/dL calculations.
Although g/dL and mg/dL are the scientifically preferred
terms, in many instances, go/o is used instead of g/dL and
mg% or mg/ 1 00 mL instead of mg/dL. Sometimes, a solu­
tion's concentration is indicated only as a percentage, such
as 1 0 % NaCI. This percent solution is a shorthand way of
writing g/dL or g% . A 1 0% NaCl solution contains 1 0 g of
NaCl per 1 00 mL of water.

Practice Problems
17. For these problems, recall the information on normal­
ity and molarity.
a. What is the molarity of 1 0% NaOH?
b. How would you prepare 20 L of 0.9% NaCI?
c. What is the concentration in mg/dL of a 0. 1 N
KOH solution?
VolumeNolume Dilutions
Being able to correctly dilute concentrated solutions to a
desired concentration is an important time-saving skill. It
is much easier to make a simple dilution than it is to weigh
out and dissolve the raw material. This topic can be con­
densed into one equation:
volume1 X concentration 1 = volume2 X concentration2
Use of this equation is necessary to become proficient in
making dilutions. For example, you have a 4 N solution of
NaOH, and you need 1 L of 1 N solution. Solution one has
a concentration of 4 N and a volume of x (i.e., the required
volume) . We want to make 1 L of 1 N, so solution 2 has a
concentration of 1 N and a volume of 1000 mL. The equa­
tion then reads as follows:
4x = ( 1 ) ( 1000)
1 000
x = -- = 250 mL
4 tions after the first one are the same. This type of dilution
The units of volume and concentration must be the same on
both sides ofthe equation. If the volume of the desired solution
is expressed as 1000 mL, the volume of the initial solution is
250 mL, and if the volume of the desired solution is expressed
as 1 L, the required volume of the initial solution is 0.25 L
(0.25 L 250 mL) . Because the initial and final concentra­
= series of five dilutions is made of this first dilution by dilut­
tions are expressed in normality, this is not an issue.
You want to make 500 mL of 1 N NaOH from the 10%
NaOH solution available. Because one concentration is
expressed in normality and the other in percent, the first
step is to convert both to the same units. Since it does not
make a difference which one you convert to the other, con­
vert the 10% to normality. By definition, the solution con­
tains 10 g per 100 mL:
10 g X to a total volume of 1 0,000 mL. However, this quantity of a
100 mL 1 000 g
1000 g
x= -- = 100 g
10
There are 100 g per liter. The equivalent weight of NaOH
is 40, so the normality is 100/40 or 2.5. That can be substi­
tuted into the dilution equation:
2.5x = 500 ( 1) mL
500
x = - = 200 mL
2.5
Solve the same problem by converting the concen­
tration of the desired solution to a percentage (%) .
CHAPTER 1 Laboratory Essentials
A 1 N solution contains 40 g/L. If there are 40 g/L, the
equation is
40 g X
1 000 mL 100 mL
4g
x= = 4%
100 mL
Substitute this information in the dilution equation:
l Ox = (500 mL ) ( 4)
2000
x = -- = 200 mL
10
Th e result shows that 200 m L o f 1 0% NaOH diluted to
500 mL produces a 1 N solution.
Practice Problems
18 . Concentrated sulfuric acid is 36 N. How much concen­
trated sulfuric acid is needed to prepare 5 L of2 N H2 S04?
19. You have a 1 M solution of NaCI. How much do you
need to dilute to make 10 L of isotonic saline (0 .9%)?
Remember that the units of volume and concentration
must be the same on both sides of the equation.
Serial Dilutions
Many procedures call for a dilution series in which all dilu­
series is referred to as a serial dilution. The methods and
calculations discussed for any type of dilution series apply to
serial dilutions. This procedure is used in producing a series
of solutions having equal increments of concentration.
For example, a serum sample is diluted 1 :2 with buffer. A
ing it 1 : 10 and then three times more, with each resulting
solution being a 1: 1 0 dilution of the previous one in the
series. The concentration of serum in each solution is as fol­
lows: 1:2, 1 :20, 1:200, 1:2000, 1:20,000, 1:200,000.
The instructions indicate that a 1: 1 0,000 dilution of a
substance is to be made. This means 1 part of solute in a
total volume of 1 0,000 parts. A 1 : 1 0,000 dilution of serum
in saline is made by taking 1 mL of serum and diluting it up
solution is rarely needed. If the approximate volume needed
is known, a dilution problem procedure may be used to
determine how to make a smaller quantity or volume of the
desired concentration. The preceding dilution of serum can
be made in several ways:
• Make a 1: 10 dilution of serum, redilute 1 : 10, redilute
1 : 10, and redilute 1 : 10.
1 1 1 1 1
-X-X-X-= ---
1 0 1 0 10 1 0 1 0,000
This produces 10 mL of a 1 : 1 0,000 dilution of serum in
saline.
• Make a 1 : 10 dilution of serum, redilute 1 : 1 0, and redi­
lute 1: 100.
20 PA R T 1 Laboratory Principles

1 1 1 1 500x = 1 0 ,000
- X - X - = ---
1 0 1 0 1 00 1 0,000 x = 20 oz
This yields 1 00 mL of a 1 : 1 0,000 dilution of serum in saline. In 20 oz of the stock 1 :200 solution diluted up to 50 oz,
• Make a 1 : 1 00 dilution of serum and redilute 1 : 1 00 . 50 oz of the desired 1 : 500 solution are present.
1 1 1
- X -- = --- Conversions
1 00 1 00 1 0,000 Unit Conversions
This procedure gives 1 00 mL of a 1 : 1 0,000 dilution of When converting a larger unit (g) to a smaller unit (mg) ,
serum in saline (Fig. 1 -5) . Any combination of dilutions multiply by the appropriate factor (in this case, 1 000) .
that yields a final concentration of 1 : 1 0,000 may be used. When converting a smaller unit to a larger unit, divide
The combination is determined in part by the glassware by the appropriate factor (Table 1 -2) .
available and the volume needed.
grams ___, milligrams, multiply by 1 000
Several factors affect the decision about what dilutions
decigrams ___, milligrams, multiply by 1 00
to use:
centigrams ___, milligrams, multiply by 1 0
• Original concentration of the substance being diluted
mm 3 ---> m L (cc), divide by 1 000
• Final volume desired
milligrams ___, grams, divide by 1 000
• Final concentration desired
• Number of dilutions to be made (sometimes)
For example, a 1 :200 stock solution of boric acid is on Practice Problems
hand. The patient requires 50 oz of a 1 : 500 solution. Follow 20. How many milliliters in 1 L?
the process to make the necessary amount without making 21. How many milliliters in 20 L?
an excess amount. 22. How many milligrams in 3 dg?
• Recall the general rule for determining the concentra­ 23. How many milliliters in 1 dL?
tion of a dilution series: 24. How many grams in 1 kg?
original concentration X dilution 1 25. How many kilograms in 1 g?
X dilution 2 · · · = final concentration
• Fill in the known parts: Prefixes for Unit Conversions

original concentration X dilution 1 = final concentration Prefix Prefix Sym bo l N u meric Equ ivalent

l /200 x ( unknown ) = 1 1500 kilo K 1 03

centi c 1 Q-2
• Recall that the volume of the last dilution in a dilution
deci d 1 Q-1
series is the volume of the final solution. Fifty ounces
of the 1 : 500 solution are needed. If 50 is inserted for milli m 1 Q-3
the total volume of the dilution to be made, it will micro fl 1 Q-6
leave the amount to be diluted as the unknown (x).
nano n 1 Q-9
1 1200 X x/50 oz = 1 /500
pi co p 1 Q-9
x/ 1 0,000 = 1 1500

1 mL 1 mL 1 mL 1 mL
+ 9 mL + 9 mL + 9 mL + 9 mL
Concentration .1 .01 .001 .0001

Actual
di l utistock
on Ful lstock
strength 1 /1 0 . 1 /1 0
( 1 /1 00)
. 0 1 /1 0
( 1 /1 000)
.001 /1 0
( 1 /1 0000)
• Figure 1-5 Serial d i l utio n .
 CHAPTER 1 Laboratory Essentials

26. How many liters in 1 mL? This formula is used to calculate the mass amount to
27. How many milligrams in 1 cg? amount of substance:
28. How many grams in 1 cg?
numeric value in mass units = amount of substance
Temperature Conversions molecular mass
It is often necessary to convert Fahrenheit temperatures to Use the formula to calculate urine albumin:
Celsius and Celsius temperatures to Fahrenheit. It may also 300 mmol/dL
be necessary to convert temperatures from Celsius to Kel­ 300 mg/dL = = 4.4 11mol/dL
vin. Three formulas are used for conversions: 69000
Celsius to Fahrenheit: C = 5/9 X (F - 32) Use the formula to calculate urine urate:
300
+
Fahrenheit to Celsius: F = (9/5 X C) 32 300 mg/dL = - = 1 .8 mmolldL
1 68
Celsius to Kelvin: K = C + 273 . pH
In the Kelvin system, zero represents absolute zero. Abso­ Many chemical reactions result from an interaction o f charged
lute zero is the point at which there is no heat in an element. particles. Ions are atoms or molecules in which the total num­
ber of protons does not equal the number of electrons. Ions
Practice Problems with more protons than electrons carry a net positive charge
29. Convert 39o F to C. and are called cations. Ions with more electrons than protons
30. Convert 50o C to F. carry a negative charge and are called anions. Cations are
31. Convert 67" F to C. attracted to anions by the electromagnetic forces associated
32. Convert 33o C to F. with atoms and molecules. Cations and anions are attracted to
33. Convert 98° F to C. one another and bond together to form a molecule. The bonds
34. Convert 45o C to F. between ions are called ionic bonds. If the positive charges
35. Convert 53o F to C. equal the negative charges, a neutral compound is formed.
36. Convert 53o F to K. When such compounds are not in solution, the molecules
37. Convert 1 00° C to K. remain intact. NaCI is an example of this type of a compound.
38. Convert - 50° F to K. When these compounds are added to an ionic solvent such as
water, the compound dissociates into its ionic molecules.
Conversion Between 51 Units and Conventional Acids are ionic compounds that dissociate when dissolved
Units in water. Dissociation releases H+ ions into the solution.
Results may be received from external laboratories with test The amount of dissociation that occurs and the number of
results in international units (Systeme International [SIJ ) . H+ ions in the solution correlate with the strength of the
Every laboratory may not report test results i n S I units, and acid and the pH of the solution. The pH is an expression of
hospital and clinic personnel may ask for assistance in con­ the acidity or alkalinity of a solution on a logarithmic scale
verting SI units to the units used for reporting. ( 1 to 1 0) on which 7 is neutral, values lower than 7 are more
This formula is used to change mass concentrations (mass acid, and values higher than 7 are more alkaline. This can be
units/dL to mass unit/L) : defined mathematically as pH = - log[H+] , with the hydro­
gen ion concentration given in moles per liter. More hydro­
numeric value in mass units
------- X 1 0 = mass units/L gen ions in solution indicate a strong acid. Fewer hydrogen
dL ions in solution indicate a weak acid. A strong acid may
Use the formula to change the protein value of 7.5 g/dL have a pH of 1 or 2, and a weak acid may have a pH of 5 or
to g/L: 6. Any pH value above 7 is basic (i.e., alkaline) .
7.5 g/dL X 1 0 = 75 g/L The acidity or alkalinity has a profound effect on the kinds
and speed of chemical reactions that occur in a solution.
This formula is used to change mass concentration to Because of this, it is important to know the relative concentra­
substance concentration: tions of the hydrogen and hydroxyl ions or pH in a solution.

(numeric value in mass concentration/dL X 1 0)

molecular mass Beer's Law
= substance units/L The optical density (00) or absorbance (A) of a substance
Use the formula to change the serum albumin value of is proportional to the amount of light of a wavelength that
7.5 g/dL to J..Lm ol/L: it absorbs. The greater the absorbance, the more light it
10 absorbs and the less it transmits. The relationship between
7.5 X-- = 1 087 J..Lm ol/L absorbance and percent transmission (o/o T) is
69000
A = 2 - log % T
22 PA R T 1 Laboratory Principles
If the o/o T of a solution is 1 00, the absorbance is 0 :
A = 2 - log % T
A = 2 - log 1 00
A =2-2=0
In the clinical laboratory, absorbance is used to calcu­
late concentration of an unknown component of serum or
plasma. When the test reaction follows Beer's law, absor­
bance is directly related to concentration. The law says that
the absorbance (A) of a colored solution is equal to the
product of the concentration of the color-producing sub­
stance (C) times the depth of the solution through which
the light must travel (L) times a constant (K) :
A =CXLXK
This one formula can refer to the standard and to the
unknown.
Standard: A, = C, X L, X K
Unknown: Au = C u X Lu X K
Using algebraic manipulations of these equations and
canceling out the K, the equation becomes
Aunknown/Astandard = Cunknown/Cstandard
Cunknown = Aunknown X Cstandard/Astandard
Practice Problems
39. Absorbance of the unknown = 0 . 1 6; absorbance of the
standard = 0 . 1 4; and concentration of the standard =
1 00 mgo/o . What is the concentration of the unknown?
S u m m a ry
Clinical laboratories were created in the early 20th century.
They were usually located in closet-sized rooms and staffed
with one pathologist. They progressed to larger rooms with
animal cages and laboratory assistants. As laboratories grew,
tests were logically grouped into sections or departments.
Modern departments commonly include clinical chemis­
try, hematology, microbiology, specimen collection, blood
bank, urinalysis, and immunology and serology. Clinical
laboratories evolved into one of the most important aspects
of medicine, employing physicians and a variety of academi­
cally credentialed professionals.
Clinical laboratories can be located in hospitals, physicians'
offices, and stand-alone reference laboratories. All laboratories
are governed by federal regulations and accrediting organiza­
tions, which include The Joint Commission and the CAP.
Laboratories are unique workplaces that use specialized
equipment. Specially prepared water is a mainstay of any
laboratory. Reagent-grade water, the purest water available,
is used for reagents prepared for analyses. Special types of
glassware and plasticware are routinely used in the labora­
tory. One specialized piece of equipment in every labora­
tory is a centrifuge. Centrifuges are used to spin down or
10
/
8
c
/
0
-�
6
c
Q)
(.)
u
/
c
4
0
2
0 +-------�--�--�
0.5 1 .5 2
Absorbance
-- Series 1
• Figure 1-6 Standard curve.
Sta ndard Cu rves
Constructing a standard curve involves running at least
three standards for a test procedure. The three points are
plotted on regular graph paper with concentration on the y
axis and absorbance on the x axis (Fig. 1 -6) . Treat the stan­
dards and controls as you treat a specimen.
Never draw the lines of the curve past the last point on
the curve. What happens to the relationship between the
readings and the concentration is not known beyond the
extremes of the curve.
separate blood cells and clots from the liquid portion of the
blood. Balances are also a basic piece of equipment found
in most laboratories. All laboratories make extensive use of
pipettes. Pipettes can be manual or serologic, volumetric,
semiautomatic, or automatic. Pipettes are used to transfer
chemicals and patient specimens.
Atomic theory states that chemicals are made of atoms
that contain protons (positively charged) and neutrons (no
charge) in the center or nucleus, with electrons (negatively
charged) revolving around the nucleus. Valence electrons
inhabit the outer electron shell of a chemical.
Organic chemistry focuses on the characteristics and com­
bining properties of hydrocarbons. Several functional groups
are important in clinical chemistry: aldehydes, ketones, amines,
alcohols, and esters. Biochemistry is often referred to as the
chemistry of life, and important biochemical compounds
include proteins, carbohydrates, lipids, and nucleic acids.
Laboratory math is important. Laboratory profes­
sionals must understand the processes for calculating
molarity, molality, normality, volume/volume dilutions,
weight/volume dilutions, serial dilutions, conversions,
pH, Beer's law, and standard curves (Table 1 -3) .
 CHAPTER 1 Laboratory Essentials

Usefu l Laboratory Formulas

Function Equations
Molarity M = (grams/molecular weight)/liters of solution

Molality m = (grams/molecular weight)/kg of solution

Normality N = [(grams/molecular weig ht)/(valence)]/liters of solution

Weight/volume dilutions g/d l (i . e . , g %) = grams of solute/deciliters of solution

Volume/volume dilutions

F to C conversion F = (9/5 X C) + 32

C to F conversion C = 5/9 x (F - 32)

C to K conversion K = C + 273

C, Celsius; F, Fahrenheit, K, Kelvin .

Rev i ew Q u e st i o n s
1 . A pathologist is c. Make 250 mL of a 0. 1 M solution of KBr.
a. A medical doctor specializing in pathology d. Make 700 mL of a 7.0 M solution of CaC0 3 .
b. A person with a bachelor's degree who is able to e. Make 500 mL of a 3.2 M solution of H 2 0 2 .
perform complex tests f. Make 3 L of 1 M NaBr.
c. A person with an associate degree who is able to g. Make 2 . 5 L of 2 M Na3 P04.
perform routine laboratory tests h. Make 450 mL of 3.33 M NaC 2 H 3 0 2 .
d. A medical doctor specializing in laboratory medi­ i. Make 200 mL of a 4 M solution of Ni2 (S 2 0 3 h.
cine 7 . What is the molarity of the following solutions?
2. The agency that accredits laboratories only and has a. 1 00 g of NaHS04 in 3 L of solution
"deemed status" from the Centers for Medicare and b. 250 g of KN0 3 in 250 mL of solution
Medicaid is c. 75 mg of NH40H in 1 00 mL of solution
a. The Joint Commission d. 99 g of NaB0 3 in 1 L of solution
b. The National Agency for Accreditation of Clinical e. 30 g of Na3 P04 in 1 L of solution
Laboratory Science f. 3.0 g of Na3 P04 dissolved in 1 00 mL of solution
c. The College of American Pathologists g. 44 g of Mg(OHh dissolved in 800 mL of solution
d. The National Certifying Agency h. 1 kg of KN0 3 dissolved in 2.75 L of solution
3. All of the following are departments in a clinical labo­ i. 55 dg of SnF 2 in 1 . 1 1 L of solution
ratory EXCEPT j. 75 g of Co 2 0 3 in 4.25 L of solution
a. Microbiology k. 44 g of Li2 Fe(CN) 6 in 3 . 5 L of solution
b. Hematology 8. Determine the normality of the following solutions:
c. Paleontology a . 1 00 g of NaHS04 in 3 L of solution

d. Urinalysis b. 250 g of KN0 3 in 250 mL of solution

4. One type of pipette used in the laboratory is c. 75 mg of NH40H in 1 00 mL of solution

a. Glass d. 99 g of NaB0 3 in 1 L of solution

b. Routine e. 30 g of Na3 P04 in 1 L of solution
c. Calibrated f. 3 g of Na3 P04 dissolved in 1 00 mL of solution
d. Volumetric g. 44 g of Mg(OHh dissolved in 800 mL of solution
5. The most common type of centrifuge used in the labo­ h. 1 kg of KN0 3 dissolved in 2.75 L of solution
ratory is the i. 55 dg of SnF 2 in 1 . 1 1 L of solution
a. Refrigerated j. 75 g of Co 2 0 3 in 4.25 L of solution
b. Bench top k. 44 g of Li2 Fe(CN) 6 in 3 . 5 L of solution
c. Fixed angle 9. Calculate the normality or the molarity of the follow­
d. Floor model ing solutions:
6. Determine how to make each solution: a. Normality of a 1 25 mgo/o solution of Na2 Cr2 0 7 .

a. Make 1 L of a 1 M solution of H 2 S04. b. Molarity of a 29.5 mgo/o solution of Cs2 C 2 04

b. Make 300 mL of a 0.45 M solution of Cu(N0 3 h. c. Normality of an 1 8 mgo/o solution of Ba3 (B0 3 h
24 P A R T 1 Laboratory Principles
d. Molarity of a 0.9go/o solution of NaCl
e. Normality of a 2 1 mgo/o solution of CaC0 3
f. Molarity of a 1 5 mgo/o solution of NH 3
g. Normality of a 24 mgo/o solution of HgC12
h. Molarity of a 1 7 . 5 mgo/o solution of HCl
i. Normality of a 30 mgo/o solution of FeC1 3
j. Molarity of a 4 1 mgo/o solution of ZnO
10. Determine the mgo/o concentration of the following
solutions:
a . 0.25 N solution of NaOH
b. 1 .2 M solution of Na2 Cr2 0 7
c. 1 . 8 N solution of Ba3 (B0 3 h
d. 0.9 M solution of NaCl
e. 2. 1 N solution of CaC0 3
f. 1 . 5 M solution of NH 3
g. 2.4 N solution of HgC12
h. 1 .75 M solution of HCl
i. 3.0 N solution of FeC1 3
j. 4. 1 M solution of ZnO
1 1 . Answer the following questions:
a . A solution of 1 00 mgo/o of ammonia nitrogen has
an A = 0 . 1 5 . The A of an unknown blood sample
is 0. 1 1 . What is the ammonia concentration of the
sample?
b. A solution of 50 mgo/o has an A = 0.2. The A of an
unknown blood sample is 0.48. What is the glucose
concentration of the blood sample?
c. A solution of 500 mg/dL glucose has an A = 0.63,
and the A of an unknown sample is 0.80. What is
the glucose concentration of the sample?
d. A solution of 350 mg/dL cholesterol has an
A = 0 .44, and the A of an unknown sample is 0.30.
What is the cholesterol concentration of the sam­
ple?
e. A solution of 9.0 mg/dL calcium has an A = 0 .5,
and the A of an unknown sample i s 0. 1 5 . What is
the calcium concentration of the sample?
f. A solution of 1 000 mg/dL triglyceride has an A =
0.968, and the A of an unknown sample is 0 . 5 5 0 .
What i s the triglyceride concentration o f the sam­
ple?
g. A solution of 6.0 mg/dL uric acid has an A 0.25,
=
and the A of an unknown sample is 0.70. What is
the uric acid concentration of the sample?
h. A solution of 4 . 5 g/dL albumin has an A 0.48,
= 20 1 2 .
and the A of an unknown sample is 0.32. What is
the albumin concentration of the sample?
Bibliography
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<http:/ /www.americanmedtech .org/ GetCertified/ CMLAEiigi bili t
y.aspx> Accessed 0 8 . 0 5 . 1 5 .
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botomy Technician, PET (ASCJ>i) Examination Content Guideline.
<http ://www.ascp.org/PDF/BOC-PDFs/Guidelines/Examination
ContentGuidelinePBT.aspx> Accessed 0 8 . 0 5 . 1 5 .
Austin A , Werle V. 7he United States Health Care System: Combining
Business, Health, and Delivery. Upper Saddle River, NJ : Pearson
Prentice Hall; 2008.
Burke MD. Laboratory medicine in the 2 1 st century. Am J Clin
Pathol. 2000; 1 1 4 : 8 4 1 -846. <http :/ /aj cp.ascpjournals.org/conten
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&
Carlson B. Physician office lab diagnostic market. Genetic
Engineering Biotechnology News. 20 1 0;30(2 1 ) .
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diagnostic-market/34931> Accessed 08.0 5 . 1 5 .
College of American Pathologists. About the CAP Accreditation Program.
Updated July 1, 20 1 4 . <http://www. cap.org/apps/cap.portal?_nfpb
=true&cntvwrPtlt_actionOverride=%2Fportlets%2FcontentViewe
r%2Fshow&_windowLabel=cntvwrPtlt&cntvwrPtlt{actionForm.c
ontentReference}=laboratory_accreditation%2Faboutlap.html&_st
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October 20 1 2 . <http:/ llabtestsonline.orgllabllabtypes/start/2>
Accessed 08.0 5 . 1 5 .
Lab Tests Online. Whos Who in the Lab: A Look at Laboratory Profossion­
als. <http://labtestsonline.org/lab/who/start/ 1 > Accessed 08.05 . 1 5 .
Lee J. Basic Biolumeniscence. Updated March 20 1 4 . <http ://www. phot
Moran LA, Horton RA, Scrimgeour G, Perry M. Principles of Bio­
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2

CHAPTER OUTLI N E
I ntrod uction The Laboratory Safety Prog ra m
Safety Reg u l ations C l i n ical Laboratories and Biosafety Levels
Occu pational Safety and Health Act Ma nagement of Risks
The Occu pational Exposu re to Haza rdous Chemicals i n La boratory Safety Equipment
Laboratories Sta ndard Employee Health
The Haza rd Com m u n ication Sta ndard Employee Safety
The Bloodborne Pathogens Sta ndard S u m ma ry
Needlestick Safety and Prevention Act

O BJ ECTIVES
At the completion of this chapter, the reader will be able to:
1 . Discuss the Occupational Expos u re to Haza rdous Chemica l s
i n Laboratories sta ndard, the Haza rdous Com m u n ication
sta ndard, the Blood borne Pathogens sta ndard, and the
Need lestick Safety and Prevention Act.
2. Compa re and contrast the fou r biosafety levels and their
mea n i ng for a clinical laboratory.
3. Describe the risks posed by sharp objects, centrifuges, refrig­
erators and freezers, fi res, electricity, compressed gases, and
biohaza rdous waste i n the laboratory.
4. Describe how each of the fol l owing can reduce hazards:
sta ndard operating proced u res, wa rning signs and labels, fi re
prevention, electrica l safety, and proced u re for disposa l of
haza rdous waste.
5. Compa re and contrast seven pieces of laboratory safety
eq uipment.
6. Describe how i m m u n izations can protect laboratory workers.
7. Describe six practices that ca n help keep laboratory workers
safe in the laboratory.
8. Describe the correct method for washing you r ha nds.

KEY TERMS
Biohaza rd Deconta m i nation Other potentially infectious materials
Biohazardous waste Dry chemical exti ngu isher (OPIM)

Biosafety level 1
Biological safety cabi net Eng i neering controls Occu pational Safety and Health

Biosafety level 2
Ergonomic haza rds Ad m i n istration (OSHA)

Biosafety level 3
Exposu re Control Plan Personal protective eq u i p ment (PPE)

Biosafety level 4
Flammable Safety Data Sheet (SDS)
Fume hood Sharps
Bloodborne pathogens Halotron Sta ndard operating proced u res (SOPs)
Centrifuge Haza rd com m u n ication Sta ndard preca utions
Chemical hazard National Fire Protection Association Steril ization
Chemical hygiene plan ( N F PA) la bel U n iversal preca utions

25
26 PA R T 1 Laboratory Principles
•• Case in Point
A laboratory worker drops a volumetric flask onto the floor,
breaking the flask and sending glass shards off in many
directions. The worker is embarrassed and begins picking
up the pieces of glass with her bare hands. What is the cor­
rect way for this worker to pick up the glass? Why should
the worker not use her hand to pick up the glass pieces of
the flask?
Points to Remember
• Four federal regulations address laboratory safety: the
Occupational Exposure to Hazardous Chemicals in
Laboratories standard, the Hazard Communication
standard, the Bloodborne Pathogens standard, and the
Needlestick Safety and Prevention Act.
• The federal agency that oversees interpretation and
enforces federal safety regulations is the Occupational
Safety and Health Administration (OSHA) .
• One way to increase needlestick safety is through engi­
neering controls and worker training.
• A laboratory safety program minimizes the risk of injury
by assuring that employees have training, information,
support, and equipment needed to work safely.
• There are four biosafety levels for clinical laboratories.
Level 1 , the lowest level, is for organisms that are not
known to cause human disease. Level 2 is the level
assigned to a regular laboratory in which human disease­
producing bacteria are handled. Level 3 is assigned to
a specialty laboratory in which organisms that cause
severe or potentially lethal diseases are handled. Level 4,
the highest level, is where organisms that are transmit­
ted through an aerosol route and cause fatal or incurable
diseases are housed.
• Risks in the laboratory include sharp objects, potential
infectious materials, centrifuges, refrigerators and freez­
ers, fires, electrical devices, compressed gases, and bio­
hazardous waste disposal.
• Laboratory safety equipment includes the biological
safety cabinet, fume hood, needlestick engineering con­
trols, fire suppression system, pipetting aids, eye wash
stations, and emergency showers.
• Other ways employers keep laboratory workers safe is
through immunizations, standard operating procedures,
biohazard signage, training, personal protective equip­
ment, dress codes, and hand washing procedures.
Introduction
This chapter covers laboratory safety from a practical view­
point. It begins with an overview of the federal regulations
that govern laboratory safety practices, continues with a
description of the typical laboratory safety program, bio­
hazards, chemical hazards, laboratory safety equipment, and
employee health and concludes with employee safety. Labo­
ratory safety is critical for a healthy workforce and workplace.
Safety Regulations
The major federal regulations affecting laboratory safety
are the Occupational Safety and Health Act of 1 970 ( OSH
Act) , the Occupational Exposure to Hazardous Chemicals
in Laboratories standard (29 CFR 1 9 1 0 . 1 450), the Hazard
Communication standard (29 CFR 1 9 1 0 . 1 200) , the
Bloodborne Pathogens standard (29 CFR 1 9 1 0 . 1 030) ,
and the Needlestick Safety and Prevention Act of 2000. A
short summary of each of these regulations follows.
Occupational Safety and H ea lth Act
In 1 970, the U.S. Congress passed the OSH Act, which cre­
ated the Occupational Safety and Health Administration
(OSHA) within the Department of Labor. Its mission is
to help employers and employees reduce on-the-job inju­
ries, illnesses, and deaths by maintaining a safe and healthy
workplace. This approach leads to lower workers' compen­
sation insurance costs and medical expenses for employers
and greater productivity from healthier workers. OSHA
focuses on enforcement of regulations, outreach and train­
ing for employers and employees, and partnerships through
voluntary programs (Box 2- 1 ) .
The Occu pational Exposu re t o Haza rdous
Chemica l s i n La boratories Sta ndard
In 1 990, OSHA issued the Occupational Exposure to Haz­
ardous Chemicals in Laboratories standard to protect labo­
ratory workers from small amounts of hazardous chemicals
used in laboratories. It was most recently updated in 20 1 2 .
This standard applies t o clinical laboratories; however,
because there is a low potential for exposure when a labo­
ratory uses a test kit, the chemicals in the kit are not cov­
ered by this standard. The provisions in the Occupational
Exposure to Hazardous Chemicals in Laboratories standard
cover the routes of exposure, chemical inventory, storage of
chemicals, chemical spills, and compressed gases.
1 . I mplement new or improved health and safety systems.
2 . Perform work site inspections.
4 . Establish rig hts a n d responsibilities o f both employers and
3 . Promote cooperative programs .
employees .
5. Support innovations in workplace safety.
6. I mplement record keeping and reporting req uirements for
employers .
7. Establish training programs for employers and employees.
8 . Partner with state occupational safety and health prog rams .
9 . Provide consultin g .
From Occupational Health and Safety Ad ministration.

Routes of Exposure
There are several ways that a hazardous chemical can enter the
body. Hazardous chemicals can enter through the mouth or
a cut on the hand, but also through the lungs or eyes. Some
hazardous chemicals can enter the body through intact skin.
Chemica/ Inventory
Laboratories keep an inventory of all chemicals used for testing
and other procedures. A chemical inventory is valuable and is
required by law for employers, but an inventory is also useful
in other ways. For example, laboratories share their chemical
inventory with the local fire department, so that fire department
personnel can come prepared to resolve a hazardous chemical
spill, an explosion, or another type of chemical emergency. The
local law enforcement or appropriate county officials may also
need to know the chemical inventory of a laboratory.
Storage of Chemicals
Storage of chemicals is important to ensure not only the
safety of the individuals working in a laboratory but also
the safety of others in the same building. Even if chemicals
are stored in proper containers, vapors may escape from the
storage vessel and interact with vapors from other chemi­
cals. This interaction could cause corrosion in the storage
cabinet, explosions when released from the storage cabi­
net, or hazardous conditions for employees working with
the chemicals. Two classes of chemicals that are notorious
for causing problems with off-gassing are acids and bases.
Specially developed cabinets are widely available for storing
acids and bases separately. Some storage cabinets for organic
materials contain a flame-retardant covering over the shelf.
Store similar chemicals together to minimize interactions
between chemicals-do not store chemicals alphabetically.
Keep flammable chemicals together in an approved, dedi­
cated, flammable-storage cabinet. Store hazardous chemicals
separately from nonhazardous chemicals. Store liquid chemi­
cals in unbreakable containers or in double packaging; the
containers, packaging, and cabinet for storing liquid chemi­
cals should be able to contain the chemical in case a container
breaks or spills. Do not store chemicals on the floor, on the
very top shelf of a cabinet, or higher than eye level. The shelves
on chemical storage cabinets should have anti-roll lips.
Always be alert when opening chemical storage cabinets.
Check for improperly stored chemicals, leaking contain­
ers, spilled chemicals, unusual temperature (too hot or too
cold) , poor lighting, open flames (cigarettes or matches) ,
absence of warning signs in area, and lack of security in the
chemical storage area. Correct the deficiencies or notifY the
appropriate individual so that the deficiencies can be cor­
rected. Keeping yourself and others safe in the laboratory is
everyone's responsibility.
Chemical Spills
Although most individuals are extremely careful when handling
chemicals, chemical spills are inevitable. The person spilling the
chemical should take responsibility for cleaning it up. NotifY
the supervisor and report the spilled chemical and location.
CHAPTER 2 Practica l Laboratory Safety
The nature of the spilled chemical will dictate the personal pro­
tective equipment (PPE) necessary for the person cleaning up
the spill and whether the area must be evacuated.
Chemical Hygiene Plan
OSHA mandates that each laboratory creates a chemical
hygiene plan (CHP) for good laboratory practices and stan­
dard operating procedures (SOPs) guiding chemical usage.
This plan must specifY procedures, equipment, personal
protective equipment (PPE) , and laboratory practices to
protect workers from chemical health hazards. Required ele­
ments of the CHP include:
• SOPs
• Criteria for exposure control measures
• Adequacy and proper functioning of fume hoods and
other protective equipment
• Information and training
• Requirement of prior approval of laboratory procedures
• Medical consultations and examinations
• Chemical hygiene officer designation
• Particularly hazardous substances
See Table 2-1 for a suggested CHP format.
The Haza rd Com m u n ication Sta ndard
Another federal regulation pertaining to protecting work­
ers from adverse health effects due to chemical exposure is
the Hazard Communication standard, which was issued in
1 983 and most recently updated in 20 1 2 . The purpose of
the Hazard Communication standard is to protect work­
ers from illnesses and injuries due to chemical exposure
through information and training about chemical hazards
and protective measures. This standard mandates employ­
ers to implement at least four steps to educate and train
employees (Box 2-2) .
Once the laboratory identifies all o f its hazardous chemi­
cals, the chemicals must be documented and a Safety Data
Sheet (SDS) must be obtained for each chemical. SDS is
provided by chemical suppliers and manufacturers. An SDS
will contain information about physical hazards; health haz­
ards; routes of entry; exposure limits; precautions for safe
handling and use; spill cleanup procedures; PPE to be worn
when handling the chemical; emergency first aid; and name,
address, and phone number of the manufacturer. The SDS
must be written in English and readily available to workers
close to the location of the chemical.
The Blood borne Pathogens Sta ndard
The Bloodborne Pathogens standard was issued in 1 99 1
and most recently updated in 20 1 2 . Its purpose is to pro­
tect workers from microbiological pathogens that are car­
ried in blood and body fluids. This standard covers workers
who are "reasonably anticipated" to become exposed to
blood and other potentially infectious materials (OPIM)
when performing job duties. OPIM include body fluids­
semen, vaginal secretions, cerebrospinal fluid, synovial
Another random document with
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to get the advice of a Captain Hudson, who had a young female
friend clever as a clairvoyant. We were both sceptical in the matter of
clairvoyance. At first Morton didn’t wish to meddle, he said, with ‘a
parcel of modern witchcraft,’ and that sort of thing; but he at last
yielded to his wife’s urgency and consented to go. There was first of
all a half-crown fee to Captain Hudson, and then the way was clear
for an interview with the young clairvoyant. I was present to ‘see fair.’
When the girl had been put into the clairvoyant state Morton was
instructed to take her right hand in his right hand and ask her any
questions he wished. The replies were in substance as follows:—
She went back mentally to the port whence the Theodore had sailed,
retracing with her hand as she in words also described the course of
the ship from Liverpool across the Atlantic, through the West Indian
group, etc., back to New Orleans. At length she said, ‘Yes, this is the
place where the cotton was lost; it’s put on board a big black ship
with a red mark round it.’ Then she began to trace with her hand and
describe the homeward course of the vessel, but after re-crossing
the Atlantic, instead of coming up the Irish Channel for Liverpool, she
turned along the English Channel as though bound for the coast of
France; and then stretching out her hand she exclaimed, ‘Oh, here’s
the cotton; but what funny people they are; they don’t talk English.’
Captain Morton said at once, ‘I see; it’s the Brunswick, Captain
Thomas,’ an American ship that lay alongside of him at New Orleans
and was taking in her cargo of cotton while the Theodore was
loading, and was bound for Havre de Grace. Captain Morton,
satisfied with his clairvoyant’s information, went home and wrote
immediately to Captain Thomas, inquiring for his lost cargo. In due
course he got an answer that the cotton was certainly there, that it
had been taken off the wharf in mistake, and that it was about to be
sold for whomsoever it might concern; but that if he (Captain Morton)
would remit a certain amount to cover freight and expenses the
bales should be forwarded to him at once. He did so, and in due time
received the cotton, subject only to the expenses of transit from
Havre to Liverpool. Such are the facts; I do not profess to offer any
explanation.”

CLAIRVOYANCE AN AID TO THE PHYSICIAN.

 I am indebted to Dr. George Wyld for this case, which also exhibits
the value of clairvoyance. Dr. Wyld had the good fortune to make the
acquaintance of a Mrs. D——, a lady in private life who was
endowed with the gift of natural clairvoyance. Dr. Wyld told this lady
of “a friend who had for years suffered intense agony for hours every
night in his back and chest, and that latterly he had been obliged to
sit up all night in a chair, and his legs began to swell.”
“This gentleman had regularly for three years been under many of
the leading physicians of London. Some said that there must be
some obscure heart affection, others said it was neuralgia, one said
it was gout, and the last consulted said it was malignant caries of the
spine.”
Dr. Wyld’s friend called upon him by appointment, and met Mrs. D
——. This lady merely looked at him. When he had retired from the
room Mrs. D—— made the following statement of his case to the
doctor:—“I have seen what the disease is; I saw it as distinctly as if
the body were transparent. There is a tumour behind the heart,
about the size of a walnut; it is of a dirty colour; and it jumps and
looks as if it would burst. Nothing can do him any good but entire
rest.”
“I at once saw,” says Dr. Wyld, what she meant, and sat down to
write to my friend’s medical attendant as follows:—
“I believe I have discovered the nature of Mr.——’s disease. He
has an aneurism on the descending aorta, about the size of a
walnut. It is this which causes the slight displacement which has
been observed in the heart, and the pressure of the tumour against
the intercostal nerves is the cause of the agony in the back, and the
peripheral pains in the front of the chest. You are going to-morrow to
see Sir —— in consultation; show him this diagnosis, and let me
know what he says.”
“Next the patient had the consultation, and Mrs. D——’s diagnosis
was confirmed; and the doctors agreed with Mrs. D—— the only
thing to be done was to take entire rest. The treatment was duly
followed up, with successful results.” Dr. Wyld thoughtfully adds—“It
is true that the diagnosis cannot be absolutely confirmed during life,
but as the profession unanimously pronounce the disease to be
aneurism, the diagnosis may be accepted as correct. This diagnosis
has probably saved the gentleman’s life, as before Mrs. D—— saw
him he was allowed to shoot over Scotch moors, and to ride, drive,
and play billiards.”
The use of clairvoyance in the diagnosis of disease is by no
means as rare as the majority of physicians and the general public
would naturally assume. I have had many opportunities of witnessing
the accuracy of diagnosis and the excellence of the methods of
treatment advised by clairvoyants. In my own personal experience I
have had much evidence of correctness of clairvoyance in diagnosis,
and subsequent success in treatment. It is a phase most desirable to
cultivate if possible, and all allied conditions connected therewith.

TRAVELLING CLAIRVOYANCE.

As a public entertainer at one time, giving demonstrations of

mesmeric phenomena, I have had naturally many opportunities of
seeing different types of clairvoyance. During a course of
entertainments given by me in Rothesay, 1881, I was able to
introduce clairvoyance to public notice by the most difficult method,
that of public experiments.
M. C., the clairvoyante, was a native of Newcastle-on-Tyne. All her
clairvoyant experiments were satisfactory. Her husband was also a
clairvoyant, but not so striking for public exhibition. M. C. seemed to
possess all phases. One or two experiments out of many will be
interesting not only as illustrative of clairvoyance, but because what I
relate can be easily ratified.
M. C. arrived in Rothesay for the first time about four hours
previously to taking her seat upon the platform, in the New Public
Halls. It was neither possible nor probable she could have obtained
the information she possessed by other than psychic means. The
clairvoyant was mesmerised and blindfolded before the audience.
After some experiments in objective clairvoyance were given, such
as describing a watch, telling the time, and the number, by having
the watch held silently over her forehead, she gave several
experiments in travelling clairvoyance. Many visitors in the hall—for
Rothesay is a well known and fashionable seaside resort—sent up
requests to the platform, and desired the clairvoyante should visit
their homes in Kent, Cornwall, Island of Jersey, in the Isle of Man,
Glasgow, and other places. Her visits and descriptions were in all
instances extremely satisfactory. How far thought-transference and
objective clairvoyance commingled and entered into her descriptions
it would be difficult to say, but the results were simply marvellous.
Test case, by the late Dr. Maddever, M.D., M.R.C.S., and Dr. John
Maddever, his son. These medical gentlemen resided in Rothesay,
and were present in the hall. Dr. Maddever desired me to send the
clairvoyante into a certain room in his house and that she should
describe it.
All the directions the clairvoyante obtained were, “to go out of the
hall, down the front steps; when out turn to the right and proceed
onward till she came to an iron-railed gate, on which was a small
brass plate, bearing the name of ‘Dr. Maddever,’ she was to open the
gate, go up to the hall-door, enter, pass the first door to the left, and
turn round a passage to the left and enter the first door to which she
came, and describe what she saw.”
Sitting still upon the platform in silence for a minute or two, she
suddenly exclaimed:—“I am at the gate—at the door—now in the hall
—I have found the room, and I am now inside, and stand with my
back to the door.” She then proceeded to describe the room, the
book-cases which surrounded it, their peculiar structure; the mantel-
piece, the form of the clock, the time, and the appearance of the
ornaments. The table in the centre of the room, its form, the colour
and style of the cloth upon it, books, albums, and papers thereon,
the flower vase support in the window, and a number of other
particulars.
At the conclusion Dr. Maddever arose in the audience and said:
—“Ladies and gentlemen, Professor Coates is a stranger to me, I
only know of him by report. The young lady on the platform I do not
know. I have not seen either till this evening, and they have never
been in my house. The experiment we have had is most remarkable,
and should be of deep and profound interest to all. The young lady
has described the room, as far as I can remember, most correctly—
in fact very much better than I could have done myself.” This
statement was received with applause.
After one or two instances of travelling clairvoyance, a young
gentleman rose in the body of the hall and desired I should send the
sensitive to a house or villa not far from the juncture of Marine Place
and Ardbeg Road.
The directions given to the clairvoyante were briefly to the effect,
she was to leave the place, on reaching the front street she was to
turn to her left and keep on past the Post Office, Esplanade, past the
Skeoch Woods, etc., till she came to the house. She nodded her
head in compliance, and presently announced she “had found the
house.” Then she shivered and appeared to draw back, and said “I
won’t go in.”
Some persons in the audience laughed, and one (I think it was the
young gentleman who asked that she might be sent) said: “The
whole thing is a swindle.” Now, considering there was not a single
flaw in the experiments that night, surprise after surprise being given,
and the audience had risen in enthusiasm, this opinion was not
favourably received.
I asked the gentleman “to have patience.” I had no doubt but we
would know soon enough the reasons. “Whatever they were I would
try and ascertain them.”
With much hesitancy she declared that “the house was not one
any respectable female would enter, and she would not.” When I
repeated this statement to the audience, there was what the
newspapers call “sensation.” The sensation was intensified when
one of the Rothesay Magistrates, Bailie Molloy, the then senior Bailie
of the Royal Burgh, declared “the young woman was right, perfectly
right, this was a house which had been inadvertently let to persons
of ill-fame, and he, for one, had recently had the facts of the case
placed before him, and he was most anxious that these people
should be put out, and they would be, as soon as the proper steps
could be taken.”
 The young gentleman retired somewhat discomfited, and the
excitement produced by these and other experiments brought
crowded houses during my professional stay.
When my “mesmeric exposition” was concluded, the two medical
gentlemen referred to, were good enough to introduce themselves,
and invited me to call next day to see the room. I accepted the
invitation during the following day and saw how truly correct and
vivid her description had been. In the first experiment the sensitive
described the state of the doctor’s library, pointing out what had not
been recollected by either of the medical men, and I believe the
other case comes under the heading of direct and objective
clairvoyance. Dr. Maddever’s house was about a quarter of a mile,
and the other house about a mile and a half from the hall.
The persistent and reliable clairvoyance evinced by this sensitive
was induced. She was a mesmeric subject, and when such subjects
are properly treated they make the very best clairvoyants.

PSYCHIC VISION POSSESSED BY THE PHYSICALLY BLIND.

Mrs. Croad resided at Redland, Bristol. My attention was called to

her case about fifteen years ago by Dr. J. G. Davey, of Bristol.
Unfortunately circumstances at the time prevented a personal visit
and report. Her psychic gifts and wonderful supersensitivity have
been amply testified to, by most reliable witnesses, such as Dr.
Davey, Hy. G. Atkinson, F.G.S., and others.
Clairvoyance in Mrs. Croad’s case was and is (for I believe the
lady is still living) a singular admixture of subtle sense transference
so well known to mesmerists of the old school, and spontaneous
psychic vision. Thought-transference and indirect clairvoyance, more
or less induced, by intense voluntary concentration.
Mrs. Croad is deaf, dumb, and paralysed, and stone blind. She
can see and hear, read with powers “denied to ordinary mortals,” and
discern pictures and writings in the dark. She is aware of her
daughter’s thoughts when the latter touches her, and becomes at
once acquainted with what her daughter wishes to communicate.
She possesses supersensitivity of touch, and discerns colour by their
degrees of heat, roughness or smoothness. She can also identify
photographs and pictures in the same way. From time to time she
has exhibited the highest phases of clairvoyance. Reports have been
made in this case by medical experts in the Journal of Psychological
Medicine, and other magazines and journals several years ago. The
most recent was contributed by the Rev. Taliesin Dans, The Cottage,
Claptons, to The Review of Reviews in January, 1891.

THE SPIRITUALISTIC AND PRACTICAL CHARACTER OF CLAIRVOYANCE

might be further illustrated by the well known case of Miss Eliza

Hamilton, who became paralysed in her limbs and right arm, through
severe injury to the spine. She had been in hospital for four months,
on her return home frequently passed into the trance state, and on
awakening described various people and places she had visited, and
objects seen. These descriptions have been invariably verified
subsequently. “She also at times,” says her physician, “speaks of
having been in the company of persons with whom she was
acquainted in this world, but who have passed away; and she tells
her friends that they have become more beautiful, and have cut off
their infirmities with which they were afflicted while here. She often
describes events which are about to happen, and these are always
fulfilled exactly as she predicts.”
“Her father,” says Mr. Hudson Tuttle, “read in her presence a letter
he had received from a friend in Leeds, speaking of the loss of his
daughter, about whose fate he was very unhappy, as she had
disappeared nearly a month before, and left no trace. Eliza went into
the trance state, and cried out, ‘Rejoice! I have found the lost girl!
She is happy in the angel world.’ She said the girl had fallen into the
dark water where dyers washed their cloths; that her friends could
not have found her had they sought her there, but now the body had
floated a few miles, and would be found in the River Aire. The body
was found as described.
“Now, knowing that her eyes were closed, that she could not hear,
that her bodily senses were in profound lethargy, how are we to
account for the intensity and keenness of sight? Her mental powers
were exceedingly exalted, and scarcely a question could be asked
her but she correctly answered.
“In this case the independence of the mind of the physical body
are shown in every instance of clairvoyance, is proven beyond cavil
or doubt. If it is demonstrated that the mind sees without the aid of
eyes, hears when the ears are deaf, feels when the nerves of
sensation are at rest, it follows that it is independent of these
outward avenues, and has other channels of communication with the
external world essentially its own.”

CLAIRVOYANCE FROM DISEASE.

Miss Mollie Fancher, of Brooklyn Heights, fell off a tramway car

when eighteen years of age, experienced very severe injuries to
head and spine, her body being dragged a distance, through her
dress catching on the step of the car. She became paralysed, lost all
her senses, except touch. She gradually recovered hearing, taste,
and ability to talk in time. She was also blind for nine years. Drs.
Speir and Ormiston were her physicians, men of skill and marked
probity. These, with a veritable host of medical men—ministers of the
Gospel, educationists and specialists—have borne testimony to her
remarkable endowments, from which we take two extracts. Mr.
Charles Ewart, Principal of the Brooklyn Heights Seminary, where
she was under special care, writes:—
“For many days together she has been to all appearances dead.
The slightest pulse could not be detected; there was no evidence of
respiration. Her limbs were as cold as ice, and had there not been
some warmth about her heart, she would have been buried. When I
first saw her she had but one sense—that of touch. By running her
fingers over the printed page, she could read with equal facility in
light or darkness. The most delicate work is done by her in the
night.... Her power of clairvoyance, or second sight, is marvellously
developed. Distance imposes no barriers, without the slightest error
she dictates the contents of sealed letters which have never been in
her hands. She discriminates in darkness the most delicate shades
of colour. She writes with extraordinary rapidity.”
Mr. Henry M. Parkhurst, the astronomer (residing at 173 Gates
Avenue, Brooklyn, N.Y.), writes:—
“From the waste-basket of a New York gentleman acquaintance he
fished an unimportant business letter, without reading it, tore it into
ribbons, and tore the ribbons into squares. He shook the pieces well
together, put them into an envelope, and sealed it. This he
subsequently handed to Miss Fancher. The blind girl took the
envelope in her hand, and passed her hand over it several times,
called for paper and pencil, and wrote it verbatim. The seal of the
letter had not been broken. Mr. Parkhurst himself opened it, pasted
the contents together, and compared the two. Miss Fancher’s was a
literal copy of the original.”

MESMERIC CLAIRVOYANCE AND SPIRITUALISM.

“A few evenings ago I called upon Mr. and Mrs. Loomis, 2 Vernon
Place, Bloomsbury, and after we had chatted for a short time in the
drawing-room with the door closed and nobody else present, I asked
if they would try a mesmeric experiment for me. They willingly
agreed, and Mr. Loomis, by passes, threw his wife into a mesmeric
state, as he often does, and an intelligence, which claimed to be the
spirit of her mother, spoke through her lips. Until this moment I had
said nothing to any living soul about the nature of my contemplated
experiment, but I then asked the unseen intelligence if it could then
and there go to the house of Mrs. Macdougall Gregory, 21 Green
Street, Grosvenor Square, London, and move a heavy physical
object in her presence. The reply was, I do not know, I will try. About
three minutes afterwards, at 8.40 p.m., the intelligence said that Mrs.
Gregory was in her drawing-room with a friend, and added, ‘I have
made Mrs. Gregory feel a prickly sensation in her arm from the
elbow down to the hand, as if some person had squeezed the arm,
and she has spoken about it to her friend.’
“I took a note in writing of this statement at the time it was made. A
few minutes later I left Mr. and Mrs. Loomis, and without telling them
my intention to do so, went straight to the house of Mrs. Gregory
about a mile and a half off. I had selected Mrs. Gregory for this
experiment because she is not afraid to publish her name in
connection with psychic truths, and her word carries weight,
especially in Scotland, where she and her family are well-known.
She is the widow of Professor Gregory, of Edinburgh University, and
is a lineal descendant of the Lord of the Isles. I then for the first time
told Mrs. Gregory of the experiment. She replied that between half-
past eight and nine o’clock that evening she was playing the piano,
and suddenly turned round to her friend, Miss Yauewicz, of Upper
Norwood, saying, ‘I don’t know what is the matter with me, I feel
quite stupid, and have such a pain in my right arm that I cannot go
on playing.’ Miss Yauewicz, who was no believer in spiritualism or
any of the marvels of psychology, felt a lively interest when she was
informed of the experiment. She told me that she clearly
remembered Mrs. Gregory’s statement that she could not go on
playing because of the pain in her right arm.”[C]
Mrs. Loomis was a remarkable clairvoyante, whom I accidently
became acquainted with in Liverpool many years ago, shortly after
her arrival from America. I introduced the lady and her husband, Mr.
Daniel Loomis, to Mr. Harrison, then editor of The Spiritualist. The
Guion steamer, Idaho, in which they came from New York, was
wrecked off the Irish Coast, and all they possessed in this world was
lost with the vessel. Mrs. Loomis predicted the disaster, where it was
likely to take place; that all hands would be saved, but all they had
lost. Upon the arrival of the officers of the vessel in Liverpool, they
presented Mrs. Loomis, at the Bee Hotel, John Street, Liverpool, with
a basket of flowers, purse, and testimonial, in recognition of her gift,
and heroic conduct during and after the disaster. I may add I knew
Mr. Harrison as a most careful investigator and a man of scientific
tastes and ability.
I select the following case of a mesmeric sensitive controlled by a
disembodied spirit, from the writings of Mr. Epes Sargent, author of
“Planchette on the Despair of Science,” etc., as appropriately
illustrative of this form of clairvoyance:—
 “One of the daughters of my valued correspondent, the late
William Howett, was a mesmeric sensitive. Howett told Professor W.
D. Gunning, whose words (slightly abridged) I here use, that, on one
occasion his daughter, being entranced, wrote a communication
signed with the name of her brother, supposed to be in Australia.
The import was, that he had been drowned a few days before in a
lake. Dates and details were given. The parents could only wait, as
there was no trans-oceanic telegraph. Months passed, and at last a
letter came from a nephew in Melbourne, bearing the tidings that
their son had been drowned on such a day, in such a lake, under
such and such circumstances. Date, place, and all the essential
details were the same as those given months before through the
daughter. Mr. Howett believed that the freed spirit of his son
influenced the sister to write; and I know of no explanation more
rational that this.”

CLAIRVOYANCE DUE TO SPIRITUAL CONTROL.

Such cases as the above are the most difficult of all to prove.
What I contend for is, if it is demonstrated we can control a fellow-
being, throw him or her into a trance state—in which the phenomena
of the psychic state are evolved—and seeing such state is induced
largely by the control of spirit over spirit in the body, why may not a
disembodied spirit control, direct, or influence a suitable sensitive or
medium in the body? If not, why not? There is abundant evidence of
such controls.
Seeing objects concealed in boxes and letters, or reading books
and mottoes, etc., appears to some clairvoyants to be more difficult
than diagnosing disease, or seeing objects at a distance. The why
and wherefore seems at first difficult to explain.
The deliberate concealment of objects for the purpose of testing
clairvoyance is often the result of a spirit of virulent suspicion,
disbelief, and what is worse, an earnest desire for failure, so that the
parties may rejoice on the discomfiture of the clairvoyants. With such
people failure is a source of pleasure. Nevertheless, seeming
impossibilities have been triumphed over. Long lost wills have been
found, and places of the accidental or intentional hiding discovered.
In more than one case deliberate fraud has been exposed, and the
guilty parties brought to acknowledge the truth of the sensitive’s
revelations.

THE FUGITIVE NATURE OF CLAIRVOYANCE.

“The chief feature,” said Alexis Didier, “of the somnambulistic

lucidity is its variability. While the conjurer or juggler, at all moments
in the day and before all spectators, will invariably succeed, the
somnambulist, endowed with the marvellous power of clairvoyance,
will not be lucid with all interviewers and at all moments of the day;
for the faculty of lucidity being a crisis painful and abnormal, there
may be atmospheric influences or invincible antipathies at work
opposing its production, and which seem to paralyse all
supersensual manifestation. Intuition, clairvoyance, lucidity, are
faculties which the somnambulist gets from the nature of his
temperament, and which are rarely developed in force.” Further, he
adds, “the somnambulistic lucidity varies in a way to make one
despair; success is continually followed by failure; in a word, error
succeeds a truth; but when one analyses the causes of this no right-
minded person will bring up the charge of Charlatanism, since the
faculty is subject to influences independent of the will and the
consciousness of the clairvoyant.”
Alexis Didier, like his brother Adolphe, was a natural clairvoyant,
and excelled in direct and objective clairvoyance, phases of the most
striking and convincing character.
Clairvoyance can be cultivated by the aid of mesmerism and by
the introspection process. By the first, the sensitive can be materially
assisted by the experience and help of the operator. By the second,
something like natural clairvoyance can be induced. Either
processes are more or less suitable to subdue the activity of the
senses, and give greater range to the psychic powers. General
instructions are of little use. Personal advice is best. The operator
then knows with whom he has to do, their special temperament and
character, what are the best processes to adopt to cultivate their gift,
and how far such sensitives and students are themselves likely to be
suitable for clairvoyant experiments. I have found the “Mirror Disc”
useful in inducing favourable conditions in the normal state for the
development of clairvoyance, and recommend its use.
 CHAPTER IV.

Psychometry.

J. RHODES BUCHANAN, M.D.

What is psychometry? Dr. George Wyld esteems psychometry a
phase of clairvoyance—“the knowledge the psychic obtains by a
clue, such as a lock of the hair of some absent person, or some
portion of a distant object.” Mr. Stead calls it (Review of Reviews, p.
221, September, 1892) “the strange new science of psychometry.” In
this he pardonably errs. Psychometry may be strange, but it is not
new. We may not recognise the name as old, but the class of
phenomena it specialises is as old as clairvoyance and mind-
reading.
“The word psychometry,” says Dr. Buchanan, “coined in 1842, to
express the character of a new science and art, is the most pregnant
and important word that has been added to the English language.
Coined from the Greek (psyche, soul; and metron, measure), it
literally signifies soul-measuring.”... “The psychometer measures the
soul.”
In the case of psychometry, the measuring assumes a new
character, as the object measured and the measuring instrument are
the same psychic element, and its measuring power is not limited to
the psychic, as it was developed in the first experiments, but has
appeared by successive investigations to manifest a wider and wider
area of power, until it became apparent that this psychic capacity
was really the measure of all things in the universe. Hence,
psychometry signifies not merely the measuring of souls and soul
capacities, or qualities by our own psychic capacities, but the
measurement and judgment of all things conceivable by the human
mind; and psychometry means practically measuring by the soul, or
grasping and estimating all things which are within the range of
human intelligence. Psychometry, therefore, is not merely an
instrumentality for measuring soul powers, but a comprehensive
agency like mathematics for the solution of many departments of
science.
“Prophecy,” says Buchanan, “is the noblest aspect of psychometry,
and there is no reason why it should not become the guiding power
to each individual life, and the guiding power of the destiny of
nations.” For instance, while all Europe feared for Boulanger, Metz
was getting stored with food; Lord Wolseley declared war imminent,
and the French themselves prepared for revanche. Psychometers
declared for peace in 1889, and said there was no prospect of war
for five years. Subsequent events have proved Boulanger lacking in
both generalship and statesmanship—a veritable Bombastes
Furioso; and peace up to the time of writing is as yet unbroken.
 Dr. Buchanan claims—“In physiology, pathology, and hygiene,
psychometry is as wise and parental as in matters of character and
ethics. A competent psychometer appreciates the vital forces, the
temperament, the peculiarities, and every departure from the normal
state, realising the diseased condition with an accuracy in which
external diagnosis often fails. In fact, the natural psychometer is born
with a genius for the healing art, and if the practice of medicine were
limited to those who possess this power in an eminent degree, its
progress would be rapid, and its disgraceful failures in diagnosis and
blunders in treatment and prognosis would be less frequently heard
of.” Many happy tests in diagnosis and in the successful treatment of
disease—out of the ordinary routine—are due, in my opinion, not so
much to elaborate medical training as to the fact of the practitioner—
perhaps unconscious to himself—being possessed of more or less of
the psychometric faculty.
Dr. Buchanan,[D] in his “Original Sketch,” gives us the history and
some details of his discovery, based upon certain investigations of
the nervous system. Already he was well versed in the phenomena
of hypnotism, which is at this late day becoming a fashionable study
and recreation of medical men. He had demonstrated the responsive
action of cerebral organs to mesmeric touch and influence, and he
was already acquainted with the curious psychological phenomena
of sense and thought transference, of double consciousness, and all
the nervous and pathological phases peculiar to natural and artificial
somnambulism. His investigation for years of the nervous system
had clearly shown him that its capacities were far more extensive,
varied, and interesting than physiologists and philosophers either
knew or were prepared to admit. He found in the nervous system a
vast aggregate of powers which constitute the vitality of man,
existing in intimate connection with the vast and wonderful powers of
his mind. Was it possible or rational to suppose that this nerve-
matter, so intimately co-related with mind, and upon which the mind
depends for the manifestation of its powers, could be entirely limited
to the narrow materialistic sphere assigned by physiologists? He
thought not.
 In a conversation with Bishop Polk (who afterwards became the
celebrated General Polk of Confederate fame), Dr. Buchanan
ascertained that Bishop Polk’s nervous sensibility was so acute that,
if by accident he touched a piece of brass in the night, when he
could not see what he had touched, he immediately felt the influence
through his system, and recognised an offensive metallic taste.
The discovery of such sensitiveness in one of the most vigorous
men, in mind and body, of his day, led Dr. Buchanan to believe it
might be found in many others. It is needless to say his conjecture
was correct. Accordingly, in the numerous neurological experiments
which he afterwards commenced, he was accustomed to place
metals of different kinds in the hands of persons of acute sensibility,
for the purpose of ascertaining whether they could feel any peculiar
influence, recognise any peculiar taste, or appreciate the difference
of metals, by any impression upon their own sensitive nerves. It soon
appeared that the power was quite common, and there were a large
number of persons who could determine by touching a piece of
metal, or by holding it in their hands, what the metal was, as they
recognised a peculiar influence proceeding from it, which in a few
moments gave them a distinct taste in the mouth. But this
sensitiveness was not confined to metallic substances. Every
substance possessing a decided taste—sugar, salt, nutmeg, pepper,
acid, etc.—appeared to be capable of transferring its influence. The
influence appeared to affect the hand, and then travel upwards. He
afterwards demonstrated when a galvanic or electric current passed
through a medicinal substance, the influence of the substance was
transmitted with the current, detected and described by the person
operated upon. Medicinal substances, enclosed in paper, were
readily recognised and described by their effects. In due time,
stranger still, a geological specimen, an article worn, a letter written
upon, a photograph which had been handled, a coin, etc.,
transmitted their influence, and the psychometrist was enabled to
read off the history concerning the particular object.
Nearly fifty years have elapsed since the discovery of this “strange
new science” and art. “To-day it is widely known, has its respected
and competent practitioners, who are able to describe the mental
and vital peculiarities of those who visit or write them, and who
create astonishment and delight by the fidelity and fulness of the
descriptions which they send to persons unknown, and at vast
distances. They give minute analysis of character and revelations of
particulars known only to the one described, pointing out with
parental delicacy and tenderness the defects which need correction,
or in the perverse and depraved they explain what egotism would
deny, but what society, family, and friends recognise to be too true.”

PSYCHOMETRIC REFLECTIONS.

Professor J. W. Draper says:—“A shadow never falls upon a wall

without leaving thereupon a permanent trace—a trace made visible
by resorting to proper processes. Upon the walls of private
apartments, where we think the eye of intrusion is altogether shut
out, and our retirement can never be profaned, there exists the
vestiges of our acts, silhouettes of whatever we have done. It is a
crushing thought to whoever has committed secret crime, that the
picture of his deed, and the very echo of his words, may be seen and
heard countless years after he has gone the way of all flesh, and left
a reputation for ‘respectability’ to his children.”
Detectives have received impressions from a scene of crime, a
clue to the unravelment of the mystery and the detection of the
criminal. Yet they could not trace the impressions to anything they
saw or heard during their preliminary investigations. No detective will
throw aside such impressions. Indeed, those most successful are
those who, while paying attention to all outward and so-called
tangible clues, do not neglect for one moment the impressions
received, and the thoughts felt, when gathering information likely to
lead to the detection of the law-breakers. Hugh Miller was right when
he said, “I suspect that there are provinces in the mind that
physicians have not entered into.”
Thoughts are things—living, real and tangible, images, visions,
deep and pungent sensations—which exist after their creation
distinct and apart from ourselves—“Footprints on the sands of time,”
in more senses than one. We all leave our mark in a thousand subtle
ways. No material microscope or telescope can detect, nevertheless
our mark can be discovered by the powers of the human soul. From
our cradle to the grave—does it stop there?—every thought,
emotion, movement, and action have left their subtle traces, so that
our whole life can be traced out by the psychometric expert. We
verily give hostages to fortune all through life.

PSYCHOMETRIC SENSITIVES.

Professor Denton was very fortunate in having in his wife, children,

and in his sister, Mrs. Cridge, gifted psychometers. His sister
possessed this psychic, intuitive faculty in a high degree. Dr.
Buchanan was equally fortunate; not only was his wife a first-class
sensitive, but he discovered the faculty in several university
professors, and in students innumerable. Denton in his travels over
America, Europe, and Australia found several hundred good
sensitives, some of whom have since made a reputation both in
Europe and America for their powers.
One important fact we learn from these pioneers in psychometric
research is that not one of these persons knew they were endowed
with the psychometric gift prior to taking part in classes or
experiments.
The possession of the faculty is not confined to any age, or to the
gentle sex; and Denton concludes, as an average, that one female in
four and one man in ten are psychometric sensitives. The possibility
is all healthy, sensitive, refined, intuitive, and impressionable persons
possess the soul-measuring faculty, and this faculty, like all other
innate human powers, can be cultivated and brought to a high stage
of perfection.
The psychometer, unlike the induced clairvoyant or entranced
medium, is in general, or outwardly at least, a mere spectator, as
one who beholds a drama or witnesses a panorama, and tells in his
own way to someone else what he sees and what he thinks about it.
The sensitive can dwell on what is seen, examine it closely, and
record individual opinions of the impressions of the persons,
incidents, and scenes of the long hidden thus brought to light. The
sensitive has merely to hold the object in hand—as Mrs. Coates is
represented doing in frontispiece—or hold it to the forehead
(temple), when he or she is enabled to come in contact with the soul
of the person or thing with which the object has been in relation.
There is no loss of external consciousness, no “up rush” of the
subliminal, obliterating and overlapping that of common life. The
sensitive appears to be in a perfectly normal condition during the
whole time of examination, can lay the article down, noticing what
takes place, and entering into conversation with those in the room, or
drawing subjects, seen or not, as they think best.

WHAT PSYCHOMETRY CAN DO.

We can do little more than give a few general illustrations.

Professor Denton, having thoroughly satisfied himself of the reality of
psychometry, wondered if letters had photographed upon them the
impressions of the life and the image of the writer. Why not fossils?
“He gave his sister a specimen from the carboniferous formation;
closing her eyes, she described those swamps and trees, with their
tufted heads and scaly trunks, with the great frog-like animals that
existed in that age. To his inexpressible delight the key to the ages
was in his hands. He concluded that nature had been photographing
from the very first. The black islands that floated upon the fiery sea,
the gelatinous dots, the first life on our planet, up through everything
that flew or swam, had been photographed by Nature, and ten
thousand experiments had confirmed the theory. He got a specimen
of the lava that flowed from Kilava, in Hawaii, in 1848. His sister by
its means described the boiling ocean, the cataract of molten lava
that almost equalled Niagara in size. A small fragment of a meteorite
that fell in Painesville, O., was given to his wife’s mother, a sensitive
who did not then believe in psychometry. This is what she said: ‘I
seem to be travelling away, away, through nothing, right forward. I
see what look like stars and mist. I seem to be taken right up; the
other specimens took me down.’ His wife, independently, gave a
similar description, but saw it revolving, and its tail of sparks. He took
steps to prove that this was not mind reading by wrapping the
specimens in paper, shaking them up in a hat, and allowing the