Gastro-Nephro Flashcards

1
Q

What are the signs of shock in acute gastroenteritis?

A

Tachycardia, weak pulse volume, prolonged CRT >2s, cold peripheries, depressed mental state, with or without hypotension.

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2
Q

What are common viral causes of acute gastroenteritis?

A

Rotavirus (most common), norovirus.

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3
Q

What are common bacterial causes of acute gastroenteritis?

A

Campylobacter jejuni, E. coli, Salmonella, Vibrio cholera, Bacillus cereus.

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4
Q

What are common parasitic causes of acute gastroenteritis?

A

Entamoeba histolytica, Giardia lambdia, Cryptosporidium spp.

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5
Q

What laboratory findings suggest metabolic acidosis in gastroenteritis?

A

ABG: low pH, low bicarbonate.

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6
Q

How is oral rehydration solution (ORS) administered in gastroenteritis?

A

20-40 ml/kg over 4 hours, frequent small sips, continue giving extra fluid until diarrhea stops.

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7
Q

What are the complications of acute gastroenteritis?

A

Secondary lactose intolerance, hemolytic uremic syndrome (HUS), hypovolemic shock, electrolyte imbalance, metabolic acidosis.

Pathophysiology:

Diarrhea & vomiting → excessive fluid loss
Loss of Na⁺, K⁺, Cl⁻, HCO₃⁻ → hypovolemia, hypotension, and shock
Loss of K⁺ → hypokalemia → muscle weakness, arrhythmias
Loss of HCO₃⁻ → metabolic acidosis (from bicarbonate loss in diarrhea)
⏳ Complications:

Hypovolemic shock (low blood pressure, organ failure)
Electrolyte disturbances (arrhythmias, seizures)
Metabolic acidosis (rapid breathing, confusion)

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8
Q

What are the three categories of dehydration severity?

A

Mild (5%), moderate (5-10%), severe (>10%).

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9
Q

What is the first-line treatment for severe dehydration?

A

IV normal saline (NS) 10-20 ml/kg over 15-30 minutes.

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10
Q

What are primary causes of nephrotic syndrome?

A

Idiopathic nephrotic syndrome (most common), membranous nephropathy, membranoproliferative glomerulonephritis, IgA nephropathy.

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11
Q

What are secondary causes of nephrotic syndrome?

A

SLE, vasculitis (Henoch-Schönlein purpura), poststreptococcal glomerulonephritis, infective endocarditis.

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12
Q

What are the clinical features of nephrotic syndrome?

A

Edema (periorbital, lower extremities, sacral, scrotal), proteinuria (>50 mg/kg/day), hypoalbuminemia (<3 g/dL), hyperlipidemia.

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13
Q

What is the first-line treatment for idiopathic nephrotic syndrome?

A

Prednisolone 60 mg/m²/day for 4 weeks, then alternate-day 40 mg/m²/day for 4 weeks, then taper over 4 weeks.

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14
Q

What supportive management is needed for nephrotic syndrome?

A

Low-salt diet, strict I/O monitoring, ACE inhibitors (Captopril) for hypertension, prophylactic penicillin.

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15
Q

What defines steroid-resistant nephrotic syndrome?

A

Failure to respond to initial 4-week prednisolone therapy, or two consecutive relapses during tapering or within 14 days after stopping steroids.

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16
Q

What are complications of nephrotic syndrome?

A

Infection (due to immunosuppression), thromboembolism, growth suppression due to steroids.

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17
Q

What is the most common cause of postinfectious glomerulonephritis?

A

Group A beta-hemolytic Streptococcus (GAS).

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18
Q

What is the classic triad of poststreptococcal glomerulonephritis (PSGN)?

A

Hematuria (tea-colored urine), hypertension, edema.

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19
Q

How is PSGN diagnosed?

A

Evidence of recent GAS infection (ASO titer, positive throat culture), hematuria, proteinuria, reduced C3 levels.

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20
Q

What is the first-line treatment for PSGN?

A

Supportive care, loop diuretics (furosemide) for hypertension, low-salt diet, antibiotics if infection is still present.

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21
Q

What is the most common cause of urinary tract infections (UTIs)?

A

Escherichia coli.

22
Q

What factors predispose to UTIs?

A

Female sex, vesicoureteral reflux (VUR), urinary stasis, constipation, catheterization.

23
Q

What is the recommended initial investigation for UTI in children?

A

Urine dipstick (leukocyte esterase, nitrites), urine microscopy & culture.

24
Q

What imaging is indicated for recurrent UTIs or structural abnormalities?

A

Renal ultrasound (RUS), micturating cystourethrogram (MCUG), nuclear renal scan.

25
Q

What is the first-line treatment for lower UTI (cystitis)?

A

Oral antibiotics (trimethoprim or nitrofurantoin) for 5 days.

26
Q

What are the indications for IV antibiotics in UTI?

A

Infants <3 months, signs of sepsis, upper UTI (pyelonephritis).

27
Q

What is vesicoureteral reflux (VUR)?

A

Retrograde flow of urine from the bladder into the ureters.

28
Q

How is VUR classified?

A

Grade 1 (reflux into non-dilated ureter) to Grade 5 (gross dilation, loss of papillary impressions).

29
Q

What is the management of VUR?

A

Antibiotic prophylaxis, periodic urine cultures, surgical reimplantation in severe cases.

30
Q

What is the classic triad of hemolytic uremic syndrome (HUS)?

A

Microangiopathic hemolytic anemia, thrombocytopenia, acute kidney injury (AKI).

31
Q

What infections are associated with HUS?

A

E. coli O157:H7, Shigella, Salmonella.

32
Q

What are the clinical features of HUS?

A

Bloody diarrhea (prodromal phase), pallor, jaundice, oliguria, neurological symptoms (seizures, confusion).

33
Q

How is HUS diagnosed?

A

FBC (hemolytic anemia, schistocytes), stool culture (Shiga toxin), renal function tests.

34
Q

What is the management of HUS?

A

Supportive care, dialysis if needed, blood transfusions, plasmapheresis in severe cases.

35
Q

What are the three types of acute kidney injury (AKI)?

A

Pre-renal (hypovolemia, sepsis), intrinsic (glomerulonephritis, ATN), post-renal (obstruction).

36
Q

What are the signs of pre-renal AKI?

A

Hypotension, tachycardia, dry mucous membranes, oliguria.

37
Q

What are common causes of intrinsic AKI?

A

Acute tubular necrosis (ischemia, nephrotoxins), glomerulonephritis, interstitial nephritis.

38
Q

What are the electrolyte abnormalities in AKI?

A

Hyperkalemia, metabolic acidosis, hypocalcemia, hyperphosphatemia.

39
Q

What are the indications for dialysis in AKI?

A

Severe hyperkalemia, refractory acidosis, uremic symptoms, fluid overload.

40
Q

What are the causes of generalized edema in children?

A

Increased hydrostatic pressure (heart failure, nephrotic syndrome), decreased oncotic pressure (hypoalbuminemia), increased capillary permeability (burns, sepsis).

41
Q

What is the most common cause of intussusception?

A

Idiopathic, triggered by viral infections (rotavirus, adenovirus).

42
Q

What is the classic triad of intussusception?

A

Intermittent abdominal pain, palpable ‘sausage-shaped’ mass, red currant jelly stool.

43
Q

What is the first-line imaging modality for intussusception?

A

Ultrasound (target sign, pseudokidney sign).

44
Q

What is the treatment for intussusception?

A

Nonoperative reduction (air or saline enema), surgical reduction if unsuccessful.

45
Q

What is the major complication of untreated intussusception?

A

Bowel ischemia, perforation, peritonitis.

46
Q

What is the hallmark sign of acute gastroenteritis on ABG?

A

Metabolic acidosis.

47
Q

What is the role of sodium bicarbonate in AKI management?

A

Corrects metabolic acidosis if pH <7.2 or symptomatic acidosis.

48
Q

What is the risk of giving excessive IV fluids in dengue or nephrotic syndrome?

A

Fluid overload leading to pulmonary edema.