Glomerular DO Flashcards

(40 cards)

1
Q

what is glomerular disease

A

any process that causes damage to glomerulus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is tubulointertititial disease

A

any process that casues damage to the interstitital tissues or tubules
(everything but glomerulus and capillaries)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is AIN

A

acute interstitial nephritis (aka acute tubulointertitial nephritis or ATIN)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is the presentation of chronic tubulointerstitial nephritis

A

obstructive, vesicoureteral reflux, analgesic nephropathy, heavy metals, myeloma kidney

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the causes of ATIN

A

medications #1 cause
RSVP: rifampin, sulfa, and 5 Ps
(PPI, Pain killers (nsaids), Pee pills (diuretics), penicillin and phenytoin)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the classic triad of ATIN

A

fever, rash, arthralgia
often with oliguira

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is seen on labs with ATIN

A

often with eosinophilia
pyuria
proteinuria
microscopic hematuria
renal tubular epithelial cell casts or granular casts
WBC casts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is the definitive diagnostic test for ATIN

A

kidney biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what patients get biopsy with ATIN

A

no improvement when agent discontinued
diagnosis is unclear
progressive kidney dysfunction
im considering steroids
its early disease and thus unclear

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is the treatment of ATIN

A

stop offending drug
supportive (BP control, tx anemiiuas, fluids)
Maybe steroid if persistent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the prognosis of ATIN

A

recovery of kidney function in 6-8 weeks, but not always to baseline
risk of progression to CKD
prognosis worst with NSAID induced AIN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the hallmark of glomerular diseases

A

proteinuria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what are the classifications of glomerular disease

A

nephritic or nephrotic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is nephritic

A

‘less severe’
proteinuria < 3g/day
hematuria
RBC casts
edema, hypertension, oliguira
labs: elevated Scr, decreased GFR, increased BUN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is nephrotic

A

‘more severe’
proteinuria >3g/day
edema
hypoalbuminemia
hyperlipidemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is the primary presenting sign on physical exam for glomerular disease

A

edema
acute GFR reduction - hypernatremia - edema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what is the workup for glomerular disease

A

CBC (eosinophilia)
albumin level
BMP (kidney and sodium)
urinalysis
proteinuria (24 hour collection or spot urine protein:creatinine ratio)

18
Q

What is the definitive test for glomerular disease

A

kidney biopsy

19
Q

what is post-infectious glomerulonephritis, nephritic or nephrotic

20
Q

what is Henoch Schonlein Purpura (HSP)

A

acute, immune-mediated (IgA), small vessel vasculitis
90% of cases in kids < 10 years old

21
Q

if a patient with post-infectious GN presents with palpable purpura on LEs/buttocks what are you thinking

A

Henoch Schonlein Purpura (HSP)

22
Q

what is the most common nephritic syndrome

Kids and yonger adults (20-30s)

A

IgA Nephropathy

23
Q

What is thetreatment of post-infectious GN

A

Self-limiting, treat infection

24
Q

What is the treatment of Anti-GBM GN

A

plasma exchange + steroids + cyclophosphamide

25
what is the diagnosis of choice for Anti=GBM GN
biopsy: crescent formation and linear IgG deposition inthe basement membrane
26
what is the patho of idiopathic membranoproliferative GN
thickening and splitting onf the BM (tram track appearance)
27
what is the pathophysiology of diffuse proliferative GN
increased glomerular cellularity, thickening of MG capillaries, IgG and C3 deposits most common SLE manifestation
28
what is the classic presentation of HSP
**palpable purpura** arthritis abdominal pain **renal disease (GN)**
29
What is the treatment of HSP
supportive treatment, usually resolves on its own can use steroids
30
what is the treatment of NST
supportive treatments diuresis if necessary pts without AKI - ACEI/ARB for anti-proteinuric and HTN tx if AKI - dialysis if inflam - steroids
31
what are the nephrotic syndromes | there are three
Minimal change disease focal and segmental Glomerulosclerosis membranous nephropathy
32
what is the most common nephrotic syndrome in kids
minimal change disease
33
what is the most common nephrotic syndrome in adults
focal or segmental glomerulosclerosis
34
what is the treatment on minimal change disease
steroids until proteinuria resolves should resolve in 4-8 weeks
35
What is the treatment of focal and segemental glomerulosclerosis
corticosteroids (more likely to fail tx) if fail - immunosuppressant or ACEI/ARB
36
what is the treatment of membranous nephropathy
ACEI/ARB and corticosteroids if fail, add immunosuppressant
37
what is the general treatment for nephrotic syndromes
sodium restriction fluid restriction diuresis
38
when are complications more likely
Nephrotic syndrome (more severe)
39
what is the most ocommon complication of nephrotic syndrome
VTE
40