Diabetic Nephropathy/ Glomerular Diseases Flashcards

1
Q

What are the two major types of Renal Disease

A

Glomerular and Interstitial

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2
Q

Proteinuria in Glomerular and Interstitial renal disease

A

Glomerular: >2.0 gm/day
Interstitial: <2.0 gm/day

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3
Q

Urine sediment in Glomerular and Interstitial renal disease

A

Glomerular: Hematuria, RBC casts
Interstitial: Pyuria, WBC casts

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4
Q

Hypertension in Glomerular and Interstitial renal disease

A
  • Common in glomerular and less common in interstitial
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5
Q

Edema in Glomerular and Interstitial renal disease

A

Usual in glomerular, rare in interstitial

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6
Q

Quantitation of proteinuria on spot urine

A

Protein (mg/dL)/ Creatinine (mg/dL)= g protein/24 hour

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7
Q

Nephrotic syndrome

A
  • Proteinuria
  • Hypoalbuminemia
  • Edema
  • Hyperlipidemia
  • Lipiduria
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8
Q

Most common glomerular disease in the US

A

Diabetic nephropathy- most common cause of end-stage renal disease in US.

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9
Q

Microalbuminuria value

A

30-300mg/24 hrs

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10
Q

Macroalbuminuria value

A

> 300 mg/24 hrs

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11
Q

General history of glomerular nephropathy

A

Elevated glomerulofiltration rate and increased kidney size —–> Microalbuminuria—-> Proteinuria—-> Decreased GFR, ESRD

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12
Q

With elevated GFR and increased renal size, what do you control and how would you treat

A

BP control (<130/80). ACE Inhibitor?

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13
Q

With microalbuminuria, what do you control and how would you treat?

A

BP Control: ACE inhibitor, Glycemic control? (Statin)

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14
Q

With proteinuria, what do you control and how?

A

BP control (<125/75): ACE inhibitor. Statin?

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15
Q

Lab evaluation of glomerulonephritis

A

1) UA
2) Spot urine for protein and creatinine
3) Serum chemistries
4) Hgb A1c
5) ANA
6) C3, C4
7) ANCA
8) Blood culture

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16
Q

Minimal change disease: Most common in what population? Presents how?

A

-most common in kids, presents with acute onset edema and nephrotic syndrome. Cell mediated immunity may play role in primary disease.

17
Q

How to treat minimal change disease

A

Steroids

18
Q

Most common primary glomerular disease in US blacks. Presentation from nephrotic syndrome to progressive kidney dysfunction. Can recur quickly following kidney transplant.

A

Focal and Segmental Glomerulosclerosis (FSGS)

19
Q

Treatment in Focal and Segmental Glomerulosclerosis (FSGS)

A

General: Blood pressure control, block Renin angiotensin system, Diuretics for edema, statin therapy
-Idiopathic: Immune modulation with steroids and/or cyclosporine

20
Q

Clinical presentation of what: Progressive edema related to gradual worsening proteinuria. Overt nephrotic syndrome (80%). Microscopic hematuria (

A

Membranous Nephropathy

21
Q

Etiology of Membranous Nephrology

A
  • Idiopathic- most common
  • Autoimmune disease (SLE)
  • Drugs (Gold, NSAIDS)
  • Infections (Hepatitis, syphilus)
22
Q

Membranous nephropathy treatment:

A

General: Blood pressure control, block Renin angiotensin system, Diuretics for edema, statin therapy
-Idiopathic: Immune modulation with steroids and/or cyclosporine

23
Q

Most common glomerular disease worldwide

A

IgA Nephropathy- Most primary but can be secondary

24
Q

IgA Presentation

A

Microscopic hematuria, gross hematuria (SYNpharyngenitic), proteinuria, progressive renal dysfunction

25
Q

MPGN Type I Presentation

A

Microscopic hematuria and non-nephrotic proteinuria, LOW SERUM COMPLEMENT LEVELS, Hypertension

26
Q

Serum Complement levels: Low complement causes

A
  • Lupus nephritis
  • MPGN
  • Post infectious glomerulonephritis (Strep, endocarditis)
27
Q

Serum Complement Levels: Anti-Neutrophil Cytoplasmic Antibodies

A

Wegener, microscopic polyangiitis, churg straus

28
Q

40 yo male who has noticed a little swelling in legs and urine is weird colored: How would you approach it?

A

1) Detailed History
2) PE: Skin rashes, tenderness, BP
3) Labs: UA, Creatinine, Serum Chemistries, Complements, blood culture, ANCA, ANA

29
Q

Anti-glomerular basement membrane disease clinical presentation

A

Hematuria and proteinuria. Progressive loss of kidney function.

  • Goodpasture’s Disease-when combined with lung involvement
  • Autoantibody to type IV collagen
30
Q

Treatment for Anti-GBM

A

Treated with plasmapheresis, steroids, cyclophosphamide

31
Q

Glomerulonephritis and ANCA

A

Renal limited ANCA disease: Hematuria and proteinuria. Progressive renal dysfunction.
-As part of systemic disease (Wegener, MPA, Churg-Straus): Night sweats, wt. loss, fatigue (esp. elderly), pulmonary and Upper airway disease

32
Q

ANCA treatment

A

Steroids, cyclophosphamide. Plasmapheresis for severe renal disease or pulmonary hemmorrhage

33
Q

A systemic disease characterized by autoimmunity with antinuclear antibodies (ANA) and low serum complements

A

Systemic Lupus Erythematosis

34
Q

T/F: Lupus nephritis can present with multiple type of kidney lesions

A

True- immune complex glomerular disease

35
Q

Treatment of lupus nephritis

A

Steroids, cyclophosphamide, mycophenolate mofetil