Renal Flashcards

1
Q

What can cause false positive protein in UA?

A

Alkaline urine >7.5
Chlorhexidine antiseptic
Radiocontrast

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2
Q

Coca Cola urine without clots means disease is where?

A

Upper tract disease (kidney)

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3
Q

Bright red urine with clots means disease is where?

A

Lower tract disease (ureters, bladder, urethra)

Can have localizing symptoms such as flank pain, freq, or dyslexia

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4
Q

HUS triad

A

Hemolytic anemia
Thrombocytopenia
Acute renal failure

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5
Q

If suspect HUS, what lab work should you get?

A

Peripheral smear most helpful to look for schistocytes and burr cells (also minimal platelets)

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6
Q

HSP pts can develop proteinuria how far out?

A

12 weeks, but commonly do within 4 weeks if they will

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7
Q

Gross painless hematuria with (or days after) an URI

A

IgA nephropathy : check renal function

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8
Q

Alport syndrome

A

X-linked disorder
Can present with microscopic hematuria in young boys progressing to hematuria with proteinuria by 10 years and eventually ESRD by AYA
80% develop bilateral deafness

Carriers can have microscopic hematuria

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9
Q

Ketogenic diet can do what to renal system

A

Predisposes patients to hypercalciuria and stones

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10
Q

Daytime symptoms of overactive bladder with bedwetting over night

A

Anticholinergic best choice : oxybutynin

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11
Q

most common etiology of abdomen masses in new born period

A

Multicystic dysplastic kidney
Hydronephrosis due to UPJ obstruction
Renal vein thrombosis, ARPKD, nephroma

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12
Q

When do you do VCUG?

A
Children >/= 2 febrile UTI
Children with 1 febrile UTI and one of the following:
- physical abnormalities on US
- abnormal pathogen
- HTN, poor growth
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13
Q

If has glomerulonephritis what two tests do you need to get?

A

Check BP and renal function

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14
Q

Fanconi syndrome

A

Proximal collecting tubule issue: metabolites aren’t reabsorbed
Can result in RTA type 2, rickets
Glycosuria, proteinuria, hypophos, hypoK, non gap MA

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15
Q

POTTER Syndrome

A
Pulmonary hypoplasia
Oligohydramnios
Twisted skin (wrinkly)
Twisted face (Abel fancies)
Extremities defects
Renal Agenesis
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16
Q

Ureterocele

A

Cystic dilation of distal ureter at bladder insertion
5x more common in girls
More likely assoc with duplex collecting system
(In bladder)

17
Q

If child has urinary stone, what other study should you get?

A

24 hour urine collection to assess for metabolic disorder

18
Q

Posterior urethral valves

A

Only occurs in males
Obstructive uropathy leading to bilateral hydronephrosis

Will have renal dysplasia and tubular damage, making them more susceptible to dehydration

19
Q

Poststrep glomerulonephritis

A

Low C3 on labs
Illness a few weeks prior
Most follow C3 to ensure it returns to normal

20
Q

Flank mass + low platelets + hematuria =

In neonate

A

Renal vein thrombosis

Can be associated with perinatal asphyxia

Cr >1.5 usually indicates AKI in neonate

Get US

21
Q

Low C3 Glomerulonephritis

A
Post infectious/poststrep
Membranoproliferative GN
Lupus nephritis
Shunt nephritis
Subacute bacterial endocarditis
22
Q

Normal C3 Glomerulonephritis

A
Immunoglobulin A GN
HSP
ANCA- associated GN
Alport syndrome
less commonly membranoproliferative