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Full Ebook of Manual of Percutaneous Coronary Interventions A Step by Step Approach 1St Edition Emmanouil Brilakis Online PDF All Chapter
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Manual of Percutaneous Coronary Interventions
A Step-by-Step Approach
Copyright Elsevier 2020
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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 professional responsibility.
To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors, assume any liability 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.
3. Medications 15
Part A
3.1 Sedatives and analgesics 15
The steps 1 3.2 Vasodilators 16
3.3 Contrast media 20
1. Planning 3 3.4 Anticoagulants 21
1.1 Planning 3 3.5 Antiplatelet agents 24
1.2 Monitoring 7 3.6 Vasopressors and inotropes 29
1.3 Pharmacology 7 3.7 Antiarrhythmics 31
1.4 Access 7 References 32
1.5 Engagement 8
1.6 Angiography 9
1.7 Determine target lesion(s) 9 4. Access 35
1.8 Wiring 9
1.9 Lesion preparation 9 4.1 Choosing access site 35
1.10 Stenting 9 4.2 Femoral access 36
1.11 Access closure 9 4.3 Radial access 56
1.12 Physiology 9 4.4 Other access sites 67
1.13 Imaging 9 References 68
1.14 Hemodynamic support 10
References 10
5. Coronary and graft engagement 71
5.1 Step 1. Catheter selection 71
2. Monitoring 11
5.2 Step 2. Advance guidewire to aortic root 71
2.1 Patient 11 5.3 Step 3. Advance catheter to aortic root 77
2.2 Electrocardiogram 11 5.4 Step 4. Aspirate guide catheter 82
2.3 Pressure waveform 12 5.5 Step 5. Connect with manifold 84
2.4 Oxygen saturation 12 5.6 Step 6. Ensure there is good pressure
2.5 Radiation dose—X-ray system and waveform 85
shield positioning 13 5.7 Step 7. Manipulate catheter to engage
2.6 Contrast volume 13 coronary ostia 88
2.7 Access site 13 5.8 Step 8. Ensure there is good pressure
2.8 Medication administration waveform 94
(anticoagulation—ACT, sedation, other 5.9 Step 9. Proceed with contrast injection as
medications) 13 described in 6 95
2.9 Operator and team performance 13 References 95
vii
22. Other complex lesions 373 27.4 Microcatheter entrapment and fracture 456
References 457
22.1 Spontaneous coronary artery dissection 373
22.2 Stent failure 375
22.3 Small and large vessels 377
22.4 Long lesions 379
28. Other complications: hypotension,
References 380 radiation skin injury, contrast-induced
acute kidney injury 459
28.1 Hypotension 459
23. Balloon uncrossable and balloon 28.2 Radiation skin injury 462
undilatable lesions 381 28.3 Contrast-induced acute kidney injury 468
23.1 Balloon uncrossable lesions 381 References 470
23.2 Balloon undilatable lesions 389
References 394
29. Vascular access complications 471
29.1 Femoral access complications 471
24. Complex patient subgroups 397 29.2 Radial access complications 480
24.1 TAVR patients 397 References 484
24.2 Cardiogenic shock patients 402
References 405
Part D
Equipment 485
Part C 30. Equipment 487
Complications 407 Introduction 487
30.1 Sheaths 489
25. Acute vessel closure 409 30.2 Catheters 492
25.1 Maintain guidewire position 409 30.3 Guide catheter extensions 499
25.2 Determine the cause of acute vessel 30.4 Support catheters 511
closure and treat accordingly 409 30.5 Y-connectors with hemostatic valves 513
25.3 Hemodynamic support 419 30.6 Microcatheters 514
References 419 30.7 Guidewires 534
30.8 Embolic protection devices 541
30.9 Balloons 542
26. Perforation 421 30.10 Atherectomy 548
30.11 Laser 556
26.1 Perforation classification, causes, and 30.12 Thrombectomy devices 556
prevention 421 30.13 Aorto-ostial lesion equipment 558
26.2 General treatment of perforations 421 30.14 Stents 559
26.3 Large vessel perforation 424 30.15 Vascular closure devices 559
26.4 Distal vessel perforation 425 30.16 CTO PCI dissection/reentry
26.5 Collateral vessel perforation 436 equipment 561
26.6 Perforation in patients with prior 30.17 Intravascular imaging 562
coronary artery bypass graft surgery 30.18 Complication management 562
carries very high risk 436 30.19 Radiation protection 569
References 436 30.20 Hemodynamic support devices 571
30.21 Contrast management 571
30.22 Brachytherapy 571
27. Equipment loss and entrapment 439 30.23 The “CTOComplex PCI cart” 571
References 571
27.1 Stent loss or entrapment 439
27.2 Guidewire entrapment and fracture 445
Index 575
27.3 Balloon entrapment and fracture 450
J. Dawn Abbott Warren Alpert Medical School at Kenneth Baran Minneapolis Heart Institute,
Brown University, Providence, RI, United States Minneapolis, MN, United States
Nidal Abi Rafeh St. George Hospital University Medical Mir Babar Basir Henry Ford Health System, Detroit,
Center, Beirut, Lebanon MI, United States
Mazen Abu Fadel Oklahoma Heart Hospital North Nicolas Boudou Clinique Saint Augustin, Bordeaux, France
Campus, Oklahoma City, OK, United States; Konstantinos Dean Boudoulas The Ohio State
University of Oklahoma Cardiovascular Institute, University, Columbus, OH, United States
Oklahoma City, OK, United States Christos V. Bourantas Barts Heart Centre, Barts Health
Pierfrancesco Agostoni HartCentrum, Ziekenhuis Netwerk NHS Trust, London, United Kingdom; Institute of
Antwerpen (ZNA) Middelheim, Antwerp, Belgium Cardiovascular Sciences, University College London,
London, United Kingdom
Sukru Akyuz University of Health Sciences, Dr. Siyami
Ersek Thoracic and Cardiovascular Surgery Training and Nenad Ž. Božinović University Clinical Center Nis, Niš,
Research Hospital, Istanbul, Turkey Serbia
Leszek Bryniarski Department of Cardiology and
Khaldoon Alaswad Henry Ford Hospital, Detroit, MI,
Cardiovascular Interventions, University Hospital,
United States
Institute of Cardiology, Jagiellonian University
Dimitrios Alexopoulos National and Kapodistrian Medical College, Cracow, Poland
University of Athens Medical School, Athens, Greece; Alexander Bufe Heartcentre Niederrhein, Helios
Attikon University Hospital, Athens, Greece Clinic Krefeld, University Witten/Herdecke, Germany
Dominick J. Angiolillo University of Florida College of M. Nicholas Burke Minneapolis Heart Institute and
Medicine-Jacksonville, Jacksonville, FL, United States Minneapolis Heart Institute Foundation, Minneapolis
Herbert D. Aronow Alpert Medical School of Brown MN, United States
University, Providence, RI, United States; Lifespan Heinz Joachim Büttner Department of Cardiology and
Cardiovascular Institute, Providence, RI, United Angiology II University Heart Center Freiburg Bad
States; Rhode Island and The Miriam Hospitals, Krozingen, Bad Krozingen, Germany
Providence, RI, United States
Pedro Pinto Cardoso Cardiology Division, Heart and
Alexandre Avran Clinique Pasteur, Essey-lès-nancy, France Vessels Department, University Hospital, CHULN,
Lorenzo Azzalini Division of Cardiology, VCU Health Lisboa, Portugal; Faculty of Medicine, Universidade
Pauley Heart Center, Virginia Commonwealth de Lisboa, Centro Cardiovascular da Universidade de
University, Richmond, VA, United States Lisboa, Lisboa, Portugal
Avtandil M. Babunashvili Department of Mauro Carlino Interventional Cardiology Unit, Cardio-
Cardiovascular Surgery, Center for Endosurgery and Thoracic-Vascular Department, IRCCS San Raffaele
Lithotripsy, Moscow, Russian Federation Scientific Institute, Milan, Italy
Jayant Bagai Vanderbilt University Medical Center, Jeff Chambers Metropolitan Heart and Vascular Institute,
Nashville, TN, United States Mercy Hospital, Minneapolis, MN, United States
Subhash Banerjee VA North Texas Health Care System Konstantinos Charitakis University of Texas Health
and UT Southwestern Medical School, Dallas, TX, Science Center at Houston, Houston, TX, United
United States States
xi
Anthony Doing University of Colorado Health, Medical Raja Hatem Hôpital du Sacré-Coeur de Montréal,
Université de Montréal, Montreal, QC, Canada
Center of the Rockies, Loveland, CO, United States
Jose P.S. Henriques Department of Cardiology,
Mohaned Egred Freeman Hospital, Newcastle
University of Amsterdam, Amsterdam UMC,
University, Newcastle upon Tyne, United Kingdom
Amsterdam, The Netherlands
Basem Elbarouni University of Manitoba, Winnipeg,
Yangsoo Jang Severance Hospital, Yonsei University
MB, Canada; St. Boniface Hospital, Winnipeg, MB,
College of Medicine, Seoul, Korea
Canada
Risto Jussila Helsinki Heart Hospital, Helsinki, Finland
Ahmed M. El Guindy Department of Cardiology,
Aswan Heart Centre, Magdi Yacoub Foundation, Artis Kalnins Clinic of Cardiovascular diseases, Riga
Cairo, Egypt East University hospital, Riga, Latvia
Abdallah El Sabbagh Mayo Clinic, Jacksonville, FL, Arun Kalyanasundaram Promed Hospital, Chennai,
United States India
Panayotis Fasseas Division of Cardiovascular Medicine, Paul Hsien-Li Kao Cardiovascular Center, Cardiology
Medical College of Wisconsin, Milwaukee, WI, Division, Department of Medicine, National Taiwan
United States University Hospital, Taipei City, Taiwan
xvii
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The goal of percutaneous coronary intervention (PCI) is to restore unimpeded blood flow in epicardial coronary arteries
without causing complications.
PCI is performed using the following 14 steps (Fig. 1).
2. Monitoring
3 Pharmacology
4. Access
5. Engagement
6. Angiography
8. Guidewire
Balloon angioplasty
Orbital atherectomy
Rotational atherectomy
9. Lesion Preparation
Laser
Intravascular lithotripsy
11. Closure
12. Physiology
13. Imaging
time
xxiii
G Stenting (sometimes balloon angioplasty, including drug-coated balloons, or thrombectomy only is performed)
(Chapter 10: Stenting).
G Physiology (Chapter 12: Coronary Physiology).
G Imaging (Chapter 13: Coronary Intravascular Imaging).
G Hemodynamic support (Chapter 14: Hemodynamic Support).
The Manual of PCI breaks down the PCI procedure into 14 sequential stages. The steps of each stage are then dis-
cussed, using the following template:
1. Goal (why?),
2. How?
3. Challenges, and
4. What can go wrong (complications)?
The same format (goal, how, challenges, what can go wrong) is used for the steps of each specialized technique,
such as atherectomy and thrombectomy. For each challenge and potential complication, we discuss: (1) potential
causes; (2) prevention; and (3) treatment strategies.
The first 14 chapters review in-depth each stage of PCI (part A). The subsequent 10 chapters review performance of
those steps in specific clinical and angiographic subgroups (part B). Chapters 2529, review complications (part C),
and Chapter 30 reviews equipment (part D).
Planning is the first stage of any procedure, including PCI, and is a key step. Plans can (and should) change depend-
ing on new information that becomes available during the procedure, but creating a plan before starting is invaluable.
The Manual of PCI aims to help each operator develop rich, accurate mental representations of what does or can
happen during PCI. Developing such mental representations is key to achieving expert performance [1].
The algorithms contained in this book are not the only or necessarily the best algorithms for these procedures. These
are algorithms used by the authors, but there will always be room for improvement. Please send feedback on how these
algorithms (and the book) can be improved.
Reading this manual (or any book for that matter) will not make you an expert interventionalist. Developing exper-
tise in PCI requires practice—not naı̈ve practice, but deliberate practice (working to improve areas of deficiency with a
teacher) [1].
“Always improving” what we do, so that the best possible outcome can be achieved for each patient, is the ultimate
goal of this book. We envision a future where all algorithms for all PCI procedures will be freely available to all and
continually improved upon.
Reference
[1] Ericsson A, Pool R. Peak: secrets from the new science of expertise. Boston: Houghton Mifflin Harcout Publishing Company; 2016.
The steps
Planning
1.1 Planning
Consent obtained
G Consent needs to be obtained and documented prior to the procedure. Discussion about the risks and benefits of ad
hoc PCI is critical, in patients without a prior angiogram.
History:
G Clinical presentation (stable angina, acute coronary syndromes (ACS), other).
G If stable coronary artery disease, is indication for procedure appropriate? (Review appropriate use criteria [2]).
G Ongoing chest pain?
G Prior cardiac catheterization or other procedure requiring fluoroscopy? If yes, are the prior images and reports
available?
G Prior coronary artery bypass graft surgery (CABG)? If yes, is surgical report available?
G Current medications (see Section 1.3).
G Comorbidities
G Valvular heart disease
G Congestive heart failure
G Arrhythmias
G Peripheral arterial disease (PAD)
G Renal failure
G Significant lung disease
G Obstructive sleep apnea
G Bleeding disorders
G Back pain or other musculoskeletal disorders that can affect lying flat on the cardiac catheterization table
G Diabetes mellitus
G Advanced age
G Is the patient likely to be noncompliant with medications or require noncardiac surgery in the upcoming 612
months? If yes, PCI may be best avoided to minimize the risk of stent thrombosis (due to the surgery and the early
discontinuation of dual antiplatelet therapy). Medical therapy only or CABG may be preferred.
G In patients with renal failure or those who are anticoagulated, it may be best to stage non-emergent PCI; ultra low or
zero contrast PCI, if feasible, may be beneficial in patients with advanced kidney disease.
G Contrast or latex allergy?
1. History
Allergies
use
(Continued )
Informed Consent
2. Physical Examination
(Continued )
INR:____
Beta hCG:____
Was EKG
If available, echocardiogram
If available, coronary CTA
Diagnostic and guide catheters used [and whether these provided optimal support based on report and
angiographic images]: ______
Physical examination:
G Radiation skin injury on the back (Fig. 28.3)? If yes, may need to postpone or modify procedure to avoid repeat
radiation of the affected area.
G Cardiovascular examination that includes all pulses in upper and lower extremities.
G Signs of congestive heart failure (pulmonary rales, high jugular venous pressure, lower extremity edema).
Labs:
G Hemoglobin
G White blood cell count
G Platelet count
G International normalized ratio (INR)
G Potassium level
G Creatinine 1 estimated glomerular filtration rate (GFR) (limit contrast to # 3.7 3 GFR for patients at increased risk
for contrast nephropathy, such as patients with chronic kidney disease, Section 28.3)
G Pregnancy test (for women of childbearing potential).
Prior imaging:
G Review prior coronary angiograms and PCIs.
G Review noninvasive testing results (echocardiography, magnetic resonance imaging [MRI], stress testing).
G In patients with recent diagnostic angiography or coronary computed tomography angiography (CTA), the target
lesion(s) can be determined prior to the procedure.
1.2 Monitoring
G Assess baseline ECG and heart rate.
G Assess patient’s baseline vital signs and pulse oximetry.
1.3 Pharmacology
G Allergies?
G Has patient received aspirin?
G For patients with a well-documented aspirin allergy: have they been desensitized?
G For patients allergic to contrast: have they been premedicated (Section 3.3)?
G For planned PCI or for patients with ST-segment elevation acute myocardial infarction (STEMI): have they received
a P2Y12 inhibitor?
G On metformin: in patients with chronic kidney disease hold metformin the day of the procedure and do not restart
until at least 48 hours after the procedure. In patients without chronic kidney disease metformin does not necessarily
need to be discontinued; instead renal function can be checked after the procedure and metformin withheld if renal
function deteriorates.
G On insulin: reduce insulin to adjust for fasting status before the procedure.
G On warfarin: discontinue 5 days prior to elective procedures and check the INR on the day of the procedure. Radial
access is preferred in anticoagulated patients.
G On direct oral anticoagulants (DOAC): discontinue prior to elective procedures, as outlined in Table 1.2.
1.4 Access
History:
G Prior radial artery harvesting for CABG?
G Arteriovenous (AV) fistula for dialysis? Avoid using this arm for cardiac catheterization.
G Access site(s) used for any prior procedures? Has a closure device been used? Consider using contralateral femoral
or radial access if an Angioseal was used within 90 days.
G Prior access site complications? If yes, what was the complication and how was it managed? If yes, avoid using the
same access site.
TABLE 1.2 How long to stop a DOAC before a cardiac catheterization procedure.
G History of PAD? Access through severely diseased or occluded iliofemoral or subclavian arteries should be avoided.
G Clinical presentation: radial access is especially favored in STEMI patients.
G On warfarin or DOAC: radial access is preferred.
G High risk of bleeding: radial access is preferred.
G Patient preference (patients who work extensively with their hands/arms or use them for support may prefer femoral
approach).
Physical examination:
G Good distal pulses?
G Morbid obesity? (Favors radial access)
Labs: high INR and low platelet count favor radial access.
Prior imaging:
G Review prior cardiac and/or peripheral catheterization films: disease or tortuosity in aortoiliac and upper extremity
vessels?
G Computed tomography (CT) of the chest:
G Anomalous aortic arch anatomy?
G Size of iliac/subclavian vessels and presence of disease.
G Arteria lusoria? (Anomalous origin of right subclavian from the aortic arch.) Arteria lusoria favors use of left
radial or femoral access.
G CT of the abdomen/pelvis: location of common femoral artery bifurcation and disease in iliofemoral vessels.
G Ultrasound of peripheral arteries.
Desired outcome: Decide on access site and size/length of the sheath.
1.5 Engagement
G Prior CABG: what is the anatomy (surgical report, prior coronary angiograms)?
G Catheters used in prior coronary angiograms/PCIs? If significant difficulty or inability to engage the coronary arter-
ies well from one access site was encountered, you should switch to a different access site (such as femoral).
G Aortic CT angiography: aortic dilation? Anomalous coronary arteries?
G Aortic stenosis or regurgitation (associated with dilated ascending aorta that may require larger catheters for coro-
nary engagement)?
1.6 Angiography
G Renal failure? If yes:
G Limit contrast volume, by using biplane angiography if available, limiting cine angiographic projections, using
intravascular ultrasound (IVUS), and potentially using contrast savings systems, such as the DyeVert Plus
(Osprey Medical) (Section 29.3).
G Consider using isoosmolar contrast agents (Section 29.3).
G Administer preprocedural and postprocedural hydration (13 mL /kg/h of normal saline).
G Prior radiation skin injury? If yes: Limit number of cineangiography runs and avoid including the previously
affected area within the radiation beam.
1.8 Wiring
History:
G Prior challenges wiring the target lesion(s)?
1.10 Stenting
History:
G Able to take dual antiplatelet therapy (DAPT)? (History of bleeding or high risk of bleeding, compliance with medications)
1.12 Physiology
History: If symptoms are equivocal and there is no preprocedural noninvasive testing showing ischemia, physiologic
coronary assessment can be useful.
G Prior adverse reaction or contraindication to intracoronary vasodilators such as adenosine?
1.13 Imaging
History:
G Prior PCI of the target lesion(s) strongly favors performing intravascular imaging.
References
[1] Practice Guidelines for Preoperative Fasting and the Use of Pharmacologic Agents to Reduce the Risk of Pulmonary Aspiration: Application to
Healthy Patients Undergoing Elective Procedures: An Updated Report by the American Society of Anesthesiologists Task Force on Preoperative
Fasting and the Use of Pharmacologic Agents to Reduce the Risk of Pulmonary Aspiration. Anesthesiology 2017;126:37693.
[2] Patel MR, Calhoon JH, Dehmer GJ, et al. ACC/AATS/AHA/ASE/ASNC/SCAI/SCCT/STS 2017 appropriate use criteria for coronary revasculari-
zation in patients with stable ischemic heart disease: a report of the American College of Cardiology Appropriate Use Criteria Task Force,
American Association for Thoracic Surgery, American Heart Association, American Society of Echocardiography, American Society of Nuclear
Cardiology, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, and Society of
Thoracic Surgeons. J Am Coll Cardiol 2017;69:221241.
Monitoring
Monitoring the patient should be continually performed from the beginning to the end of the case, so that potential com-
plications are promptly identified and corrected. The following parameters are assessed (Fig. 2.1).
2.1 Patient
1. Patient comfort level: patient discomfort can lead to movement, potentially leading to complications. It can also
lead to tachycardia and tachypnea, which may in turn worsen ischemia.
2. Chest pain, abdominal pain, groin pain? Is the pain anticipated based on the procedure or is it unexpected? The pain
could be due to ischemia, perforation, or other complications.
3. Level of consciousness and breathing. Is breathing assistance needed (BiPAP or intubation)?
4. Ability to move all extremities (no stroke) or conversely excessive movements that may hinder performance of the
procedure.
5. Signs of allergic reactions: skin rash; itching and hives; swelling of the lips, tongue, or throat; hypotension.
2.2 Electrocardiogram
The ECG morphology and heart rate should be evaluated at the beginning of the case, so that subsequent ECG changes
can be promptly identified.
Electrocardiographic changes of concern include:
1. New ST segment depression.
2. New ST segment elevation (Fig. 2.2).
1. Patient
9. Operators
12. Equipment
position within body
8. Anticoagulation
–ACT 7. Access
Sedation site
Medication 11. Sterile field
6.Contrast
volume
3mmHg
(A) (B)
FIGURE 2.2 Electrocardiographic and pressure waveform changes during CTO PCI. (A) Baseline. (B) ST-segment elevation (arrows) and develop-
ment of 35 mmHg pulsus paradoxus after a distal vessel perforation in a patient with prior coronary artery bypass graft surgery. Reproduced with per-
mission from the Manual of CTO Interventions, 2nd ed. (Figure 3.35). Copyright Elsevier.
3. Bradycardia.
4. Tachycardia.
5. QRS widening.
6. Ventricular premature beats during wire manipulations.
7. Ventricular fibrillation.
Medications
In this chapter we discuss the following classes of medications that are commonly used in the cardiac catheterization
laboratory:
1. Sedatives and analgesics
2. Vasodilators
3. Contrast media
4. Anticoagulants
5. Antiplatelet agents
6. Vasopressors and inotropes
7. Antiarrhythmics
3.1.2 How?
G Midazolam (Versed): 0.51 mg intravenous (IV)—can be repeated. Duration of action: 1580 minutes.
G Fentanyl: 25100 mcg IV—can be repeated. Duration of action: 3060 minutes. Other opioids, such as morphine
can also be used.
3.1.3.2 Delayed response to oral P2Y12 inhibitors which may lead to thrombotic complications
Causes:
G Opioids delay gastric empting and slow-down drug adsorption, such as P2Y12 inhibitor absorption.
Prevention:
G Avoid opioids use in STEMI if not deemed necessary.
Treatment:
G Use intravenous antiplatelet agents (e.g., cangrelor or GP IIb/IIIa inhibitors).
3.2 Vasodilators
Medications that cause vasodilation can be categorized into those causing mainly large vessel vasodilation (nitroglyc-
erin) and those causing mainly small vessel vasodilation (nicardipine, nitroprusside, adenosine).
3.2.1 Nitroglycerin
3.2.1.1 Goals
G Dilate coronary arteries (intracoronary nitroglycerin should be routinely administered before coronary angiography,
to prevent coronary spasm and allow accurate interpretation of coronary anatomy).
G Treat hypertension.
G Treat pulmonary edema.
3.2.1.2 How?
G Intracoronary/intragraft: 100300 mcg.
G Intravenous: nitroglycerin drip is usually started at 10 mcg/min and increased by 10 mcg/min at 5-minute intervals
until the desired effect is achieved and systolic blood pressure remains above 100 mmHg. Maximum dose is
200 mcg/min.
G Sublingual: 0.4 mg.
hypotension persists, also assess for other potential causes, such as bleeding.
3.2.1.3.3 Tachycardia
Reflex tachycardia may result from the hypotensive effect of nitroglycerin.
3.2.2 Nicardipine
3.2.2.1 Goals
G Prevent and treat no reflow. Nicardipine is a calcium channel blocker that can be used intracoronary to achieve vasodila-
tion of small arteries. Nicardipine is the preferred agent for treating or preventing no reflow (Section 25.2.3.2), for
example, during atherectomy (Section 19.3) and during saphenous vein graft PCI (Section 18.9.2), as it has less hypo-
tensive effect compared with nitroprusside and verapamil and also has shorter duration of action.
3.2.2.2 How?
G Intracoronary: 100300 mcg.
3.2.3 Nitroprusside
3.2.3.1 Goals
G Prevent and treat no reflow.
3.2.3.2 How?
G Intracoronary: 100300 mcg.
3.2.4 Verapamil
3.2.4.1 Goals
G Prevent radial spasm.
G Prevent and treat no reflow.
3.2.4.2 How?
G Radial artery: 23 mg.
G Intracoronary: 1 mg intracoronary over 2 minutes.
3.2.5 Adenosine
3.2.5.1 Goals
G Prevent and treat no reflow.
G Cause vasodilation during physiologic testing (Section 12.2.6).
3.2.5.2 How?
G Intracoronary: RCA: 50100 mcg.
G Intracoronary left main: 100200 mcg—several thousand mcg could be administered (slowly) in case of no reflow.
G Intragraft: 100200 mcg.
G Intravenous: 140 mcg/kg/min, administered through a central vein or a large peripheral vein.
G Regadenoson or papaverine (papaverine is not available in the United States) can also be administered for inducing
vasodilation. Regadenoson is costly and papaverine may cause ventricular fibrillation.
Causes:
G Premature ventricular beats occurring during adenosine administration, sometimes during periods of AV block
(Figs. 3.1 and 3.2) [4].
FIGURE 3.1 Atrial fibrillation occurring after adenosine administration. Adenosine caused ST-segment depression (arrowheads). A premature ven-
tricular beat (arrow) subsequently triggered atrial fibrillation.
(A) (B)
Adenosine administration
(C) (D)
Atrial fibrillation
FIGURE 3.2 Coronary angiography demonstrating an in-stent restenotic lesion of the mid right coronary artery (A). Intracoronary adenosine admin-
istration through the right coronary artery (40 mcg) resulted in complete heart block (B), followed by development of atrial fibrillation (C). After stent-
ing the right coronary artery lesion resolved. Sinus rhythm was restored with cardioversion at the end of the procedure. Reproduced with permission
from Mahmood A, Papayannis AC, Brilakis ES. Pro-arrhythmic effects of intracoronary adenosine administration. Hellenic J Cardiol 2011;52:3523
(Figure 2). Copyright Elsevier.
Prevention:
G Same as for heart block above.
Treatment:
G DC cardioversion. If cardioversion is not desired, antiarrhythmics, such as amiodarone, and AV nodal blocking
agents, such as beta blockers or calcium channel blockers could be used.