Quiz 1 - Nephritic/Nephrotic Flashcards
(43 cards)
3 major causes of Nephritic syndrome
Auto-immune (SLE, Wegener’s)
Post-infectious (strep PSGN)
IgA nephropathy (Berger’s)
DDX PHAROH
nephritic cirrhosis/liver failure severe HTN AIN RCHF DM Hemolytic-uremic syndrome
Glomerular bleeding characteristics
coca cola proteinuria HTN hx of URI fever, rash
Post-Infectious GN pathophys
HSN III
Ag-Ab complexes lodged in GBM podcytes leads to complement activation
Post-Infectious GN serology and light microscopy
Streptozymes (5)
Decreased complement
neutrophuils in glomerulus
Treatment of PSGN
1) Treat infection if present (penicillin, erythromycin) (tho won’t nec prevent PSGN)
2) Treat any edema or HTN (conventional: loop diuretics/ furosemide)
3) Limit (but adequate) protein and sodium
4) Bed rest
5) Botanicals– AI: Curcuma and boswelia; Antimicrobials: Echinacea
6) Anti–inflammatories: Quercitin, bromelain
7) Antioxidants; Vit C to bowel tolerance Vit E 800 IU
8) Constitutional hydrotherapy or wet sheet wrap
DDX/Variant of Post-Infectious GN
Rapidly Progressing Glomerulonephritis
can –> ARF
“crescentic GN” (Bowman’s capsule compressed)
Auto-Immune GN
Wegener’s
Churg-Strauss
Goodpasture’s
Berger’s dz/ IgA nephropathy etiology
?
assoc with Celiac, Hep B, alcoholic cirrhosis, sarcoidosis, HIV, SLE, RA, Sjogren’s
Berger’s dz/ IgA nephropathy sxs
PHAROH
Berger’s dz/ IgA nephropathy dz
kidnex bx= IgA
Berger’s dz/ IgA nephropathy Tx
monitor GF diet Artemesia (wormwood) fish oil S. boulardii Cordyceps Rheum palmatum
Nephritic Syndrome Tx
1) Avoid sodium, avoid high-potassium foods, low protein diet, low antigen diet (gluten, meat, dairy)
2) Immune amphoterics (Ganoderma, Grifola, Withania, Tinospora)
3) Diuretics may be needed for edema (use with caution)
4) Fish oil (4-12 g/d in divided doses) Donadio NEJM 1994 Nov 3;331(18) 1194-9
5) Treat HTN: goal BP is <125/75 mm Hg in presence of proteinuria >1g/d
Pharmacologic: ACEi
6) Probiotics: decrease uremic toxic production in gut
7) Remove other allergens (environmental, etc)
8) quit smoking, limit/no alcohol
9) maintain healthy weight
10) Conventional approach: corticosteroids, alkyating agents (cyclophosphamide),
calcineurin inhibitors, biologics: rituximab and ocrelizumab
Acute GN can progress to…
Chronic
Nephrotic Syndrome etiology
damage to podocytes–> lipid and protein wasting
Poorly controlled DM, IgA nephropathy and nephritic conditions,
SLE, amyloidosis, HIV, pre-eclampsia, drugs (penicillamine, NSAIDs, lithium, heroin, gold compounds), Snake bite, cancer (lymphomas and leukemias), FHx of congenital kidney dz (Alport dz, Fabry dz)
Nephrotic syndrome presentation
HTN, oliguria, edema, ascites, foamy urine, cough, DOE
> 3.5 g protein/d
Minimal change dz
90% kids
Focal segmental glomerulosclerosis
young adults, MC in AA
Secondary causes of nephrotic syndrome
SLE, diabetic nephropahty, amyloidosis, HIV, HBV, HCV, multiple myeloma
DDX Edema states
CHF liver failure Pyelo ATN multiple myeloma
Acute Interstitial Nephritis causes
Drug HSN (abx, NSAIDs), infections
Acute Interstitial Nephritis ssxs
Rash
fever, hematuria, oliguria, nausea, vomiting, malaise, flank pain, arthralgia
AIN labs
Eosinophiluria
FENa > 1%
WBCs, WBC casts
BX if persisting sx:
infiltration of inflammatory cells into interstitium, glomeruli usually spared (except SLE)
AIN Tx
discontinue case
Renafood
anti-inflammatories
‘roids