Lecture 2: CKD & Nephrotic Syndrome Flashcards
(21 cards)
Diagnostic Criteria for Nephrotic Syndrome
- Spot urine showing a protein-to-creatinine ratio of > 3 to 3.5 mg protein/mg creatinine, or 24-hour urine collection showing > 3 to 3.5 g protein
- Serum albumin < 3 g/dL
- Clinical evidence of peripheral edema (d/t loss of oncotic pressure)
Common causes of Nephrotic Syndrome
Type II DM Systemic Lupus Erythematosus Membranous Nephropathy Amyloidosis Preeclampsia
Other lab findings/features in Nephrotic Syndrome
- Severe hyperlipidemia (decreased plasma oncotic pressure stimulate hepatic lipoprotein synthesis
- Oval fat bodies (pathognomonic)
- Hypercoagulable (Loss of protein C & S, antithrombin II through damaged basement membrane)
- Prone to infection (Loss of immunoglobulin through damaged basement membrane)
Management of nephrotic syndrome
- Fluid restrictions (<1500 ml/day)
- Loop Diuretics
- Ace-Inhibitor
- Monitor for s/s PE, DVT, renal vein thrombosis (flank pain)
- Treat underlying cause
Definition of chronic kidney disease
CKD is defined as abnormalities of kidney structure or function, present for >3 months, with implications for
health.
Criteria of CKD
Markers of kidney damage & GFR
Markers of kidney damage:
1. Albuminuria (AER 30 mg/24 hours; ACR 30 mg/g)
2. Urine sediment abnormalities
3. Electrolyte and other abnormalities due to tubular disorders
4. Abnormalities detected by histology
5. Structural abnormalities detected by imaging
6. History of kidney transplantation
OR
GFR <60 ml/min/1.73 m2
Staging: What are the GFR categories of CKD?
G1 >90 Normal or high
G2 60–89 Mildly decreased
G3a 45–59 Mildly to moderately decreased
G3b 30–44 Moderately to severely decreased
G4 15–29 Severely decreased
G5 <15 Kidney Failure
Staging: What are the albuminuria categories of CKD?
(AER or ACR)
A1 <30 Normal to mildly increased
A2 30-300 Moderately increased
A3 >300 Severely increased
Which GFR equation is most accurate in GFR >60 & subgroups (DM, transplant status, elderly, & at higher BMIs)?
CKD-EPI creatinine equation
Increased protein in the urine correlate with what complications of CKD?
- Faster progression to ESRD
- Increase risk of CV events
- Increased risk of mortality
What are other proteinuria etiologies?
- Fever
- Vigorous exercise
- Dehydration
- Acute illness
- Glomerulonephritis
- Congestive Heart Failure
- Seizures
- Drugs
- Interstitial nephritis
Orthostatic Proteinuria epidemiology & etiology
Epidemiology
• 60% of all childhood cases & 75% of adolescent cases
• Rare in those > 30 years of age
• Does not appear to be a predictor of CKD
Etiology
• Exaggerated hemodynamic response to upright position
• Normal variant; Not well understood
• Subtle glomerular abnormalities
American Society of Nephrology recommends screening in which 2 populations?
- Family history of CKD
2. Person history of Diabetes Mellitus, HTN, or CV Disease
Presentation of patient with GFR <30
o Fatigue
o Worsening edema
o Increased blood pressure
o Pruritus
Presentation of patient with GFR <15
o Uremia: Nausea, vomiting o Fatigue o Seizures o Altered mental status: Confusion o Uremic pericarditis, cardiac tamponade
What are the predictors of progression of CKD?
- Level of GFR & Albuminuria
- Elevated BP
- Hyperglycemia
- Age/Sex/Race/ethnicity
- Dyslipidemia
- Smoking
- Obesity
- H/o CV Disease
- Ongoing exposure to nephrotoxins
What are some recommendations for disease prevention?
- Exercise
- Weight loss
- Smoking cessation
- Managing CV Dz
- ASA, Statins
- Optimize glucose & BP control
- D/c nephrotoxins when possible
What are the 7 main complications associated with CKD?
- Diabetes
- Hypertension —> B/P Goal: <130/80, Avoid hypotension (AKI), ACE/ARB
- Dyslipidemia —> Statin
- Coronary Artery Disease —> CV MC cause of death in CKD; treat ALL CKD patients with statin
- Mineral & Bone Disorders —> Osteoporosis & Osteopenia
- Uremia & Acidosis —> Excess build up of urea & H+
- Anemia —> Decrease erythropoietin, decreased erythrocyte life span and blood loss
How does CKD cause mineral and bone disorders?
o Decreased GFR causes ↑ in phosphorus in the blood
o Hyperphosphatemia causes ↓ Ca absorption in the gut
o Hypocalcemia causes ↑ in PTH
o Hyperparathyroidism causes Ca released from bone & reabsorbed in proximal tubules
o Tubular damage causes ↓ Vitamin D activation causing ↓ reabsorption of Ca in tubules
o ↑ H+ (metabolic acidosis) cause move into bone cells which causes ↑ Ca++ release
How do you monitor & manage bone disease in eGFR < 30ml/min/1.73m2?
Monitor labs:
• Ca, Ph, PTH, Alkaline phosphatase
Manage with:
o Calcium 1200 mg/day & 800 IU Vitamin D daily
o Bisphosphonates: Denosomab or bisphosphonates (Not on dialysis & by specialist)
What are the 6 CKD management components?
• Optimize management of glucose, blood pressure, dyslipidemia, bone health
o ACE-I or ARB
o Statin & ASA when indicated
o Meds to be renally dosed
o Avoid NSAIDS, nephrotoxins
• Nutrition consult
o Low protein, phosphate, potassium, +/-supplementation
• Vaccines
o Flu, hep B, PCV
• Monitor disease progression & complications
o Electrolyte abnormalities (potassium, calcium, phosphorus)
o Anemia, PTH, uremia
• Refer to specialist for co-management when indicated
o Nephrologist & cardiologist
• Extensive patient education & empowerment
o Exercise, smoking cessation, limit EtOH, dietary health, avoid obesity