Nephrotic/nephritic syndromes Flashcards

1
Q

Clinical consequences of glomerulonephritis

A
  • Dependent on where the inflammation is
  • Will then cause presence of protein, blood, wbc, casts in urine
  • Failure of the filtration membrane –> AKI
  • May or may not lead to scarring - CKD
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2
Q

Features of nephrotic syndrome

A
  • Preserved renal function
  • Proteinuria > 3g/day
  • Spot UPCR or ACR
  • > 300mg/mmol or >180mg/mmol
  • decreased serum albumin normal 40
  • Decreased total protein normal 65
  • Oedema
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3
Q

Features of nephritic syndrome

A
  • Impaired renal function (rapid or chronic)

- Proteinuria, haematuria, leucosuria

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4
Q

GN - presentation symptoms

A
  • Systemic, flu like symptoms
  • Rash
  • Arthralgia
  • Swelling
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5
Q

GN - Examination

A
  • Skin
  • CVS, oedema
  • Chest
  • Abdomen
  • Urine analysis
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6
Q

Urine dip - nephrotic vs nephritic

A
Nephrotic Nephritic 
Blood       -/+            ++
Protein   +++++         ++
Leucocytes -/+         ++
Nitrites        -              -
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7
Q

GN diagnosis - blood tests

A
  • Serum albumin, protein
  • Renal function
  • Autoimmune screen
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8
Q

GN diagnosis - analysis of a renal biopsy

A
  • Light microscopy
  • Immuno-histology
  • Electron microscopy
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9
Q

Minimal change nephrotic syndrome - Associations

A
  • NSAIDS
  • Lithium/gold
  • Allergy
  • Hodgkins
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10
Q

What to look for on slides - minimal change nephrotic syndrome

A
  • Epithelial foot processes
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11
Q

Minimal change nephrotic syndrome - presentation

A
  • Frothy urine, oedema
  • Low albumin
  • Preserved function
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12
Q

Minimal change nephrotic syndrome - treatment

A
  • Steroids, calcineurin inhibitors (tacrolimus)

- 50% relapse

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13
Q

Membranous nephrotic causes

A

Autoimmune disease
- Lupus, sjorgrens, Rh Arthritis, ank spond, post transplant

Infection
- Hep B, Hep C

Drugs
- Mercury, Captopril, Gold, penicillamine

  • Paraneoplastic
  • Idopathic
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14
Q

Membranous presentation

A
  • Nephrotic syndrome

- AKI/CKD

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15
Q

Membranous treatment

A
  • Underlying cause

- Steroids, CNIs, BP

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16
Q

Mesangial proliferative GN

A

Ig A deposition

  • Malaria
  • Typhoid
  • IgA nephropathy

Presentation variable

  • Haematuria
  • AKI, CKD, hypertensive crisis
17
Q

Diffuse proliferative GN

A
IgG, IgM, C3 deposition 
Causes 
- Endocarditis 
- Post-streptococcal GN 
AKI, haematuria 
Treat underlying infection
18
Q

Focal segmental glomerulosclerosis causes

A

Primary - idiopathic

Secondary
Familial - reoccurs after transplantation
Virus - HIV
Drugs - heroin, pamidronate
Obesity, hypertension, atheroemboli, sickle cell anaemia

19
Q

Focal segmental glomerulosclerosis treatment

A

Primary and familial

  • Immunosuppression and BP
  • Secondary underlying cause
20
Q

Crescentic GN

A

ANCA–associated is related to small vessel vasculitis

  • granulomatosis with polyangiitis (GPA), Wegener granulomatosis
  • microscopic polyangitis (MPA) Churg Strauss
GBM Disease ( Goodpasteurs)
Aggressive IgA nephropathy
21
Q

Treatment options for proliferative crescentic GN

A
Strict BP control
ACE inhibitors for proteinuria >1g/day
Immunosuppression
- steroids
- cyclophosphamide
- Azathioprine
- mycophenolate mofetil, 
- Rituximab
22
Q

Membranoproliferative/mesangial capillary GN

A

Primary

Secondary – Hep C, endocarditis, viral infections, malaria, sickle cell disease

23
Q

Treatment options for non-mesangial proliferative GN

A

Strict BP control
ACE inhibitors for proteinuria >1g/day

Immunosuppression

  • steroids
  • CNI
  • mycophenolate mofetil,
  • Rituximab
24
Q

What is glomerulonephritis

A

Inflammation/proliferation, immune deposits, scarring
BM, Mesangial cells, Podocytes
Infiltration of cells into, Bowmans space,