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Renal Disorders NCM 112
Renal Disorders NCM 112
Renal Disorders NCM 112
GLOMERULONEPHRITIS
CHRONIC GLOMERULONEPHRITIS
PATHO CLINICAL ASSESSMENT / MED. MGT NSG. MGT
MANIFESTATIONS DIAGNOSTIC FINDINGS
• Kidneys reduced to Discovered: • Urinalysis • Reduce BP: sodium & • observe for fluid &
1/5 of their normal • hypertension, fixed specific gravity water restriction, electrolyte imbalance
Due to repeated episodes size elevated BUN & 1.010, variable hypertensive meds • report cardiac &
of acute nephritic • Cortex layer shrinks creatinine proteinuria, urinary • monitor weight daily neurologic status
syndrome, hypertensive 1-2 mm • loss of weight & casts (proteins • prescribed with • provide emotional
nephrosclerosis, • Glomeruli & tubules strength secreted by damaged diuretic meds to treat support, explore
hyperlipidemia & etc. • Become scarred • increasing irritability kidney tubules) fluid overload options, have their
• Branches of renal • increased need to • high biologic protein questions answered
artery thickened urinate at night GFR below 50 ml/min: (dairy products, eggs, • Educate on self-care:
• Severe damage (nocturia) - Hyperkalemia meats) • Follow up: labs, BP,
(stage 5) • headaches - Metabolic acidosis • Treat UTIs promptly casts for protein &
• dizziness - Anemia secondary to Dialysis initiated in casts
• Requiring renal
decreased eryhropoieis early course of the •
replacement therapy • digestive Access site (dialysis)
- Hypoalbunemia disease to keep
disturbances • dietary restriction
-decreased s. phosphorus patient in optimal • lifestyle modification
-decreased s. calcium physical condition &
Progresses to:
-mental changes minimize
• periorbital &
-impaired nerve complications
peripheral edema
conduction due to
• Anemia
electrolyte imbalance &
• cardiomegaly (gallop
uremia
rhythm) to distended
neck veins (HF signs)
• Chest x-rays
• peripheral
cardiac enlargement &
neuropathy with
pulmonary edema
diminished deep
tendon reflexes
• CT & MRI
(confused & limited
decrease renal cortex size
attention span)
3 | 10
N 1 RENAL DISORDERS
C 1 Lecturer: DOLLIMAR YOGORE, RN, MAN
M2 By: kaye
NEPHROTIC SYNDROME
Clinical Assessment / Med. Mgt. Nsg. mgt
PATHO manifestations Diagnostic findings
Type of kidney disease • GLOMERULAR Major manifestation: • Protein exceeding 3.5 Address underlying • Early: similar to AGN
characterized by DAMAGE • EDEMA (soft, pitting) g/day-hallmark of disease causing mgt.
increased glomerular • Increased around eyes, diagnosis proteinuria, slowing • Later: ESKD
permeability marked by permeability to dependent in sacrum, • protein progression of CKD, Medication & dietary
massive increase in protein (proteinuria ankles, & hands), electrophoresis relieving symptoms changes
protein, decrease >3.5 g/24H) abdomen (ascites) • Immunoelectro • Diuretic
albumin, diffuse edema, • HYPOPROTEINEMIA • Irritability phoresis • ACE inhibitors
high s,. Cholesterol, low • 1-Decreased plasma • Headache • Increased WBCs • reduce proteinuria
density lipoprotein oncotic pp. to EDEMA • malaise (granular & epithelial • lipid-lowering agents
(hyperlipidemia) • 2-Compensatory casts) for hyperlipidemia
synthesis of proteins • needle biopsy
by liver to
HPERLIPIDEMIA
WATCH VIDEO:
https://www.youtube.com/watch?v=ZGPa_4FN9M4
5 | 10
POLYCYSTIC KIDNEY DISEASE (PKD)
Genetic disorder PATHO CLINICAL MANIFESTATIONS Assessment / Med. Mgt.
Characterized by growth of Diagnostic findings
numerous fluid-flied cysts in the
kidneys (destroys nephrons PKD cysts enlarged kidneys • Kidney damage result in • Check family history NO CURE
(replacing normal structure) HEMATURIA, polyuria, • palpation of abdomen: Supportive treatment:
hypertension, development enlarged cystic kidneys • BP control
FAILURE of renal calculi, associated • UTZ-preferred • pain control
UTIs, proteinuria • antibiotic agents
2 major forms inherited: • abdominal fullness • renal replacement therapy-
1. Autosomal dominant • flank pain once kidneys fail
(30-40 y.0), can beigin • Genetic linkage studies &
early in childhood, counseling (screening
about 90% family members for
potential kidney donation)
2. Autosomal recessive
(rare)
TREATMENT OPTIONS: ESRD 1. When is the best time to administer calcium acetate to a
patient with ESKD?
a. With food
b. 2 hours before meals
c. 2 hours after meals
d. At bedtime with 8 ounces of fluid
WATCH VIDEO
https://www.youtube.com/watch?v=4Q2qQTWTaYc