Other Clin Med_hematuria, nephrotic syndrome, etc Flashcards

1
Q

for hematuria - when do we refer to UROLOGY?

A

kidney stones, mass cysts

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2
Q

for hematuria - when do we refer to NEPHROLOGY?

A

glomerular bleeding
elevated Creatinine
new or worsening HTN or edema

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3
Q

CASTS

muddy brown casts

A

acute tubular necrosis

(PPP)

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4
Q

CASTS

white blood cell casts

A

pyelonephritis

acute interstitial nephritis
PPP

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5
Q

CASTS

red blood cell casts

A

acute glomerulonephritis

vasculitis
PPP

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6
Q

four disorders classified as Critical Intrinsic Renal Disorders

A

vascular disorders
glomerular disorders
tubular disease
interstitial disorders

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7
Q

name one Intrinsic Renal Disorder / Vascular Disorder

A

renal atheroembolism

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8
Q

name two Intrinsic Renal Disorder / Glomerular Disorders

A

RPGN = Rapidly Progressive Glomerulonephritis

Thrombotic Microangiopathy

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9
Q

name two Intrinsic Renal Disorder / Tubular Diseases

A

ATN = Acute Tubular Necrosis

Pigment Nephropathy/Rhabdomyolysis

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10
Q

name one Intrinsic Renal Disorder / Interstitial Disorders

A

acute allergic interstitial nephritis

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11
Q

iatrogenic damage from catheterization - usually free plaque/cholesterol crystals

A

renal atheroembolism

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12
Q

blue toes

A

renal atheroembolism

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13
Q

loss of 50% of GFR w/in 3 months

A

Rapidly Progressive Glomerulonephritis (RPGN)

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14
Q

“crescent formation” in glomeruli

A

Rapidly Progressive Glomerulonephritis (RPGN)

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15
Q

diagnosis of Rapidly Progressive Glomerulonephritis (RPGN)

A

biopsy

serological workup

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16
Q

associated with Rapidly Progressive Glomerulonephritis (RPGN)

A

lupus (SLE)

Goodpasture syndrome

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17
Q

treatment of Rapidly Progressive Glomerulonephritis (RPGN)

A

immunosuppressants, corticosteroids

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18
Q

schistocytes

A

Thrombotic Microangiopathy

19
Q

inner surface of endothelial cells injured

or

prothrombotic agents disrupt smooth inner layer

A

Thrombotic Microangiopathy

20
Q

name six common causes for Acute Tubular Necrosis

A
aminoglycosides
vancomycin
acyclovir
HIV drugs
iodine contrast
rhabdo
21
Q

muddy brown casts

A

Acute Tubular Necrosis

22
Q

two main causes of Acute Tubular Necrosis

A

50% - ischemic

50% = toxic

23
Q

treatment of Pigment Nephropathy/Rhabdo

A

very aggressive ISOTONIC fluid for forced diuresis

24
Q

leukocyturia

A

Acute Allergic Interstitial Nephritis

25
WBC casts in urine
Acute Allergic Interstitial Nephritis
26
definitive imaging for post-renal acute kidney injury
bladder u/s
27
two distinct findings for diagnosis of pre-renal acute kidney injury
BUN/Cr ratio >20/1 (nml ~15/1) FENa (Fractional Excretion of Na) <1%
28
edema/hypoalbuminemia hyperlipidemia proteinuria
Nephrotic Syndrome
29
three main findings/presentations for nephrotic syndrome
edema/hypoalbuminemia hyperlipidemia proteinuria
30
blood clots in urine/easy bruising
nephrotic syndrome
31
three main etiologies for nephrotic syndrome
minimal change disease focal segmental glomerular sclerosis membranous nephropathy
32
three important indicators of kidney disease that should not be overlooked
hematuria proteinuria Cr
33
Can renal tubules heal? Can nephrons regenerate?
Renal tubules can heal but NEPHRONS DO NOT REGENERATE.
34
what is most common cause of CKD? second most common cause?
DM 2nd - HTN
35
S/S of CKD (four)
proteinuria (best predictor of disease progression) urine: albumin/Cr ratio or protein/Cr ratio U/A: metabolic acidosis renal US: get one early to establish baseline (have at least one US)
36
Trtmt of CKD
lifestyle: reduce salt, eat nml amts of protein get bp <140/90, ACE-Is or ARBs (renal protective) for the HTN/Proteinuria A1C < 7.0% for the DM met acidosis - fix it w/ diet
37
stages of CKD
Stage 1 - nml GFR (120-130) but other signs are present) Stage 2 - GFR 60-90 Stage 3 - GFR 30-60 Stage 4 - GFR 15-30 Stage 5 GFR <15
38
when is dialysis considered for CKD?
hyperkalemia fluid overload uremia (Cr/urea in blood)
39
PKD presentation
dilute urine/nocturnal/polyipsia (100%) hematuria proteinuria (mild, might have frothy urine) nephrolithiasis/UTIs HTN large palpable kidney
40
two types of PKD
type 1 - - most common (75%) - younger/earlier onset - more severe - larger cysts type 2 - - less common - older onset - less severe
41
life-threatening concerns for PKD pts
aneurysms subarachnoid hemorrhages mitral valve prolapses
42
common comorbidities for PKD
hepatic cysts | colonic diverticula
43
PKD U/A presentation
hematuria proteinuria low osmolarity low specific gravity
44
PKD management (6 things)
U/S: get at least one renal US suppress ADH with high fluid consumption (ADH drives cyst growth) Tolvaptan (ADH V2 receptor antagonist) ``` HTN management (target bp is lower than usual) - maybe add ACE-I or ARBs ``` manage pain watch for aneurysms