(1)
Department of Emergency Medicine, Erasmus Medical Center, Rotterdam, The Netherlands
What is the other name for Berger’s disease ? | IgA nephropathy |
What seems to be the trigger for Berger’s disease? | A viral infection (mainly URIs with activation of mucosal defenses) |
What is the usual long-term outcome in Berger’s disease? | Spontaneously resolves |
Which post-infectious nephropathy has low complement levels? | Post-strep has low C3 |
What do you see in the kidney of a post-strep nephritis patient? | “Humps” on the basement membrane |
If a nephritis patient has sensorineural deafness and cataracts, what should you suspect is the cause? | Alport syndrome |
What is the long-term outcome for Alport nephritis? | Usually end-stage renal failure in teens or 20s |
If a patient has microscopic or gross hematuria and nephrolithiasis, what should you suspect? | Idiopathic hypercalciuria (although the blood could be due to a stone that formed for another reason) |
What medication should you avoid in a hypercalciuria patient? | Furosemide (Lasix ® ) – it increases calcium excretion further |
What medication is helpful for a hypercalciuria patient? | Thiazide diuretic (increases calcium retention) |
What dietary modifications are helpful in hypercalciuria? | Decrease oxalate-containing foods (chocolate, nuts, tea) – Do not decrease calcium-containing foods (Decreasing high-salt foods is also helpful, because increased Na intake promotes increased calcium excretion) |
Which kidney problem is associated with loss of “foot processes” on the glomerulus? | Minimal change disease |
What accounts for 80 % of the nephrotic syndrome cases seen in children? | Minimal change disease |
What is the triad of nephrotic syndrome? | Edema Proteinuria/low albumin Hyperlipidemia |
What is the description of the typical minimal change disease patient? | Male aged 2–8 years |
How is minimal change disease treated? | Steroids & cyclophosphamide, if needed |
How is nephrotic syndrome treated, if the patient’s condition requires it? | 25 % albumin fluids & furosemide & Often steroids (it may also be necessary to tap the ascites, but usually not) |
ACE inhibitors & angiotensin II receptor blockers are frequently used in patients with nephrotic syndrome. What are the two main purposes for using them? | To manage hypertension & Decrease proteinuria |
What is the classic presentation for children with renal dysfunction ? | Periorbital edema |
Alport nephritis, hypercalciuria, IgA nephropathy, and post-infectious glomerulonephritis all commonly present with what finding? | Gross or microscopic hematuria (post-infectious glomerulonephritis includes post-strep glomerulonephritis) |
Which type(s) of RTA produces acidosis and a urine anion gap? | Type 4 (also causes hyperkalemia) |
What is distal RTA ? | Failure to excrete hydrogen |
If there is metabolic acidosis, but no anion gap (normal anion gap, in other words), what are the likely causes? | Diarrhea or an RTA |
Which RTA is characterized by severe bicarb wasting? | Proximal (also known as RTA type 2) |
If the kidney is wasting a lot of bicarb, what other problems develop? | Wasting of glucose, phosphate, and amino acids |
Which type of RTA often accompanies congenital disorders and inborn errors of metabolism? | Proximal RTA (also known as RTA type 2) |
A low urine chloride (<10 mEq) suggests what possible underlying problems? | Gastric fluid losses Diarrhea Cystic fibrosis |
A high urine chloride (>10 mEq) in a patient with high blood pressure suggests what two diagnoses? | Cushing’s syndrome or Hyperaldosteronism |
If the urine chloride is high, and blood pressure is normal, what are the most likely causes? | Acute diuretic use Bartter’s syndrome |
Which psychiatric medication sometimes causes DI? | Lithium |
Normal urine output for an infant? | 1–2 cc/kg/day |
How can you calculate an approximate “ bladder capacity ?” (in ounces) | Child’s age + 2 For metric results use: 7 × weight in kg = mL in infants Age in years × 30 + 30 = mL in children |
How is proteinuria diagnosed? | Either a 24-h urine or A spot urine |
When can proteinuria be a normal finding? | Alkaline urine Concentrated urine (high specific gravity) |
How does the urine protein/creatinine ratio help you diagnose proteinuria in kids? | Urine protein/urine creatinine >0.2 diagnoses proteinuria (However, nephrotic range proteinuria is >2.0) |
How can you use the urine protein-creatinine ratio to diagnose proteinuria in an infant older than 6 months? | Same process, but >0.5 is considered proteinuria in infants (6–24 months) |
Which aspects of history are especially important to pay attention to in renal questions? | Edema UTI history Toxin exposure Hearing loss (Hearing loss is associated with certain causes like Alport syndrome, or drug side effects, and is also a tip-off to possible renal dysfunction in newly presenting patients, because renal patients have an unusually high rate of sensorineural hearing loss) |
If a question states that urine has both protein and bacteria in it, which is probably more important? | The bacteria |
What is a common presenting complaint for hypercalciuria – even if no kidney stones have formed? | Abdominal pain and dysuria |
What is the main underlying problem that leads to the nephrotic syndrome? | The glomerulus is too leaky (Podocyte dysfunction and loss of basement membrane negative charge are involved) |
Patients with nephrotic syndrome appear to be fluid overloaded, because they are edematous. What is their main fluid or electrolyte issue? | Intravascular fluid depletion (It’s all leaked out!) |
What are the immune consequences of nephrotic syndrome? | Poor immune function – IgG & complement are low (they leak out, also) |
What infection are nephrotic syndrome patients at special risk of developing? | Encapsulated organisms (such as Strep pneumo and H. flu ) < div class='tao-gold-member'>
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