Nephrology Flashcards
Define Stage 1, 2 and 3 AKI per 2022 KDIGO staging.
Stage I: Cr 1.5-1.9x baseline in 7 d OR increase >/=0.3mg/dl in 48hr, U/O <0.5ml/kg/h for 6-12hr
Stage II: Cr 2-2.9xbaseline, <0.5ml/kgh for >/=12hrs
Stage III: Cr >/=3x baseline or >4mg/dl or initiation of RRT or eGFR<35ml/min/1.73m2, U/O <0.3 for >/=24hr or anuria for >/=12hrs
DDx for pre-renal AKI?
GI losses, hemorrhage, decreased cardiac output, decreased vascular resistance (sepsis), nephrotic syndrome, liver failure, impaired renal autoregulation (hyperCa+, ACEi, NSAIDs, tacrolimus, cyclosporine)
DDx for renal AKI?
Tubules/interstitium: ischemic tubular injury, nephrotoxic AKI, acute interstitial nephritis
Glomerulus: PIGN, HUS
Blood vessels: renal vein thrombosis
DDx for post-renal AKI?
UPJ obstruction, ureteric obstruction, bladder obstruction, urethral obstruction
*Both kidneys need to be obstructed!
Name 5 medications known to be nephrotoxic.
Acyclovir, AmphoB, Captopril, Cisplatin, Cyclosporine, Enalapril, Gentamicin, Ibuprofen, Ketorolac, Lisinopril, Tacrolimus, Tobramycin, Vancomycin
Name the ECG changes associated with hyperkalemia
Tall peaked T waves, flattened/absent P waves, sine wave, prolonged PR, widened QRS, bradycardia/Vtach/VFib
What are the indications for dialysis?
AEIOU
A: acidosis
E: electrolyte abnormalities (hyperK, hyperNa, hyperPO4)
I: ingestions (methanol, ethylene glycol, ASA, lithium)
O: fluid overload
U: symptoms of uremia (pericarditis, encephalopathy, seizures, bleeding)
What is the criteria for CKD?
Either of the following present for >3 months:
Markers of kidney damage (1 or more): albuminuria, ACR >30mg/g or 3mg/mmol, urine sediment abN, abN ‘lytes due to tubular d/o, abN histology, structural anomaly, hx transplant
Decreased GFR: < 60ml/min per 1.73M2
What is the most common cause of childhood CKD?
Renal dysplasia: hypodysplasia, solitary kidney, VUR, posterior urethral valves
- Dx on U/S: sm kidneys, echogenic parenchyma, cortical cysts
2nd most common: glomerulopathy
3rd most common: cystic kidney disease
What is oligohydramnios sequence (Potter’s phenotype)?
Deep set eyes, beaked nose, micrognathia, low set ears, extremity contractures, pulmonary hypoplasia (about 1/2 die soon after birth of pulmonary insuff)
What are the features of a distal RTA (Type 1)?
Impaired hydrogen ion excretion Urine pH >5.5 HypoK Renal stones, hypercalciuria ALL RTAs = hyperchloremic metabolic acidosis w/ normal serum AG
What are the features of a proximal RTA (Type 2)?
Impaired bicarbonate reabsorption
High urine pH initially, later <5.5
HypoK
ALL RTAs = hyperchloremic metabolic acidosis w/ normal serum AG
What are the features of a Type IV RTA?
Decreased aldosterone secretion or aldosterone resistance
Urine pH <5.5
HyperK
ALL RTAs = hyperchloremic metabolic acidosis w/ normal serum AG
What findings do you expect in SIADH for the following parameters:
- Serum Na
- Urine Na
- Serum osm
- Urine osm
- HypoNa
- Urine Na >20meq/L
- Low serum osm
- Elevated urine osm (>100)
- Fun fact: uric acid does the same as sodium; SIADH will have low serum uric acid and high urine excretion of uric acid
What is the most common pathogen associated with infection in patients with nephrotic syndrome?
S. pneumoniae (patients with nephrotic syndrome are at risk for SBP)