Peds Nephrology (Exam 4) Flashcards

1
Q

What criteria must be met to diagnose pediatric CKD?

A

GFR <60 for > 3 months
or
GFR >60 + evidence for structural damage (albuminuria, proteinuria, pathologic abnormalities on histology or imaging)

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2
Q

Most common cause of pediatric CKD?

A

Congenital diseases (60% of cases)

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3
Q

Name 5 congenital diseases that can cause pediatric CKD.

A
Obstructive uropathy
Renal hypoplasia
Renal dysplasia
Reflux nephropathy
PKD
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4
Q

What is the second most common cause of pediatric CKD?

A

glomerular disorders

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5
Q

Name 3 causes of glomerular disorders?

A

FSGS
Membranoproliferative glomerulonephritis
Minimal change disease

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6
Q

Presenting signs and symptoms of non-glomerular pediatric CKD?

A

Polyuria
Elevation in serum Cr
Poor growth

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7
Q

Presenting signs and symptoms of pediatric glomerular CKD?

A

Tea or cola colored urine (hematuria, RBC casts)
Edema
Elevation of serum Cr
Elevated BP for age

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8
Q

What imaging study would you order for suspected pediatric CKD?

A

Ultrasound

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9
Q

When managing pediatric CKD, you want to treat reversible kidney dysfunction. What are some reversible causes of kidney dysfunction?

A
Decreased perfusion to kidneys (hypotension, volume depletion, some medications)
Nephrotoxic drugs (NSAIDs, contrast, aminoglycosides)
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10
Q

How do you slow progression of pediatric CKD?

A

Same as adults - ACEI/ARB for kids with HTN + proteinuria

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11
Q

Symptoms of pediatric CKD?

A

Anorexia, fatigue, N/V, pericarditis, bone and mineral disease, decreased neurocognitive function.

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12
Q

What are some examples of mineral bone disease that can occur secondary to pediatric CKD?

A

Growth failure, AVN, skeletal fractures/deformity/pain, vascular calcification

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13
Q

Treatment for mineral bone disease?

A

Diet, calcium binders, vitamin D2/D3, Vitamin D analogs

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14
Q

Renal replacement therapy should be considered at what GFR?

A

GFR <30

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15
Q

1st line renal replacement therapy?

A

Kidney transplantation

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16
Q

2nd and 3rd line renal replacement therapies?

A

2nd: Peritoneal dialysis
3rd: Hemodialysis

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17
Q

Examples of obstructive uropathy?

A

Stricture
Stones
Stenosis
Posterior ureteral valves

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18
Q

What is reflux nephropathy (vesicoureteral reflux)?

A

Retrograde passage of urine from the bladder to the upper urinary tract

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19
Q

What is renal dysplasia?

A

Malformed kidneys

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20
Q

T/F? Kidneys with renal dysplasia are usually normal in size

A

False - usually smaller than normal

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21
Q

Is renal dysplasia unilateral or bilateral?

A

Can be either

22
Q

What is multicystic dysplasia

A

Nonfunctioning dysplastic kidney with multiple cysts

23
Q

What is renal hypoplasia?

A

Low number of structurally normal nephrons

24
Q

What diagnosis must be excluded before diagnosing renal hypoplasia?
How do you rule this out?

A

Renal scarring

Ruled out by DMSA radionuclide scan

25
What is renal agenesis?
Congenital absence of renal parenchymal tissue.
26
Is renal agenesis more common in males or females?
males
27
T/F? patients with renal agenesis are more likely to have other nonrenal abnormalities.
True - malformations of heart, genitals, bones, gi tract, and respiratory tract are common
28
What does FSGS stand for?
Focal segmental glomerulosclerosis
29
What is FSGS?
Sclerosis in parts of at least 1 glomerulus in the entire kidney biopsy specimen
30
Causes of FSGS?
Genetics Injury to podocytes from drug toxicity or infection Secondary causes
31
Most common signs/symptoms of FSGS?
Acute onset of nephrotic syndrome
32
Symptoms of nephrotic syndrome?
Edema, hypoalbuminemia, proteinuria
33
Diagnosis of FSGS is made by?
Renal biopsy
34
Treatment of FSGS?
ACEI/ARB for HTN/proteinuria | Statin/niacin for HLD
35
2 major causes of membranoproliferative glomerulonephritis?
Immune-complex mediated | Complement mediated
36
In membranoproliferative glomerulonephritis, characteristic changes are seen on _____
light microscopy
37
Treatment for mild membranoproliferative glomerulonephritis?
ACEI/ARB
38
Treatment for severe membranoproliferative glomerulonephritis?
An immunosuppressant such as cyclophosphamide or MMF (Mycophenolate Mofetil) +steroids or rituximab
39
What is the most common cause of nephrotic syndrome in kids?
Minimal change disease
40
Why is it called minimal change disease?
No changes are seen on light microscopy | but there is effacement of podocyte foot processes on electron micriscopy
41
Causes of minimal change disease?
``` Idiopathic After viral URI neoplasms(Hodgkin) Meds (lithium) Hypersensitivity reactions ```
42
Signs/symptoms of MCD?
Tachycardia, peripheral vasoconstriction, oliguria, decreased GFR, elevation of plasma renin, aldosterone, and norepinephrine
43
MCD increases risk of
Infection Thromboembolic events severe hyperlipidemia
44
Diagnosis of MCD?
clinical
45
Treatment for MCD?
Prednisone for a good while or cyclophosphamide or rituximab
46
What is horseshoe kidney?
When one pole of each kidney fuses to the other
47
Horseshoe kidney is associated with
other congenital anomalies (up to half) | Turner syndrome, trisomy 13, 18 and 21
48
Patients with horseshoe kidney are at increase risk for what tumor?
Wilms tumor (a type of kidney tumor)
49
Prognosis for patients with horseshoe kidney?
Good, most don't need any intervention | Some get chronic UTIs
50
Imaging studies for horseshoe kidney?
Ultrasound | Voiding cystourethrogram