Renal Medicine Flashcards

(26 cards)

1
Q

3 stages of a kidney biopsy

A
  1. Hematoxylin- eosin stain for messangial expansion
    2- fluorescinn stain for igA deposition
    3- electron microscopy
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2
Q

IgA nephropathy

What type of disease is it, and what is its clinical presentation

A

Also known as bergers or synonaryngitic glomerulonephritis

Type of proliferative glomerulonephritis

Occurs 1-2 days after URTI

Presents with nephritic syndrome with mild proteinuria

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3
Q

Post streptococcal glomerulonephritis clinical presentation

A

Nephritic syndrome 1-3 weeks after streptococcal infection

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4
Q

Goodpastures disease aetiology and presentation

A

Anti glomerular basement membrane antibodies attack kidney and lungs

Causes glomerular nephritis ( nephritic syndrome haematuria) and haemoptysis

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5
Q

Most common cause of glomerulonephritis overall

Presentation

A

Membranous glomerulonephritis

Bimodal district in 20s and 60s

Presents with nephrotic syndrome

Spike and dome appearance on biopsy

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6
Q

Minimal change disease

Presentation

Aetiology

A

Most common cause of nephrotic syndrome in kids

Lack of histological change with pods yet effacement

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7
Q

Thin basement disease presentation and aetiology

A

Microscopic haematuria with no other loss of kidney function

Caused by thinning of basement membrane

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8
Q

Alports syndrome presentation

A

Glomerulonephritis causing haematuria

Sensorineural hearing loss

Eye disease

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9
Q

Most common cause of adult nephrotic syndrome

A

Focal segmental glomeruloscleoris

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10
Q

Criteria of nephrotic syndrome

A

24 hour urinary protein >3G

Serum albumin <25g/L

Hypercholestriaemia

Peripheral oedema

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11
Q

Most common cause of AKI

A

Acute tubular necrosis

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12
Q

What casts are seen in acute tubular necrosis

A

Muddy brown casts

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13
Q

Causes of acute tubular necrosis

A

Ischaemia - shock, sepsis and dehydration

Nephrotoxicity- gentamicin, radiology contrast, and NSAIDS

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14
Q

Presentation of acute intistitial nephritis

A

AKI and hypertension

Classic triad of rash, fever and arthralgia

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15
Q

Causes of acute interstitial nephritis

A

Hypersensitivity reaction to infection or drugs

NSAIDS, abx and rifampicin

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16
Q

Presentation of nephritic syndrome

A

Haematuria, hypertension, oliguria

17
Q

Treatment of nephrotic syndrome

A

Treat underlying cause

ACE I

LMWH

Pneumococcal vaccines and infection surveillance

Statins

High dose corticosteroids

18
Q

What is released in rhabdomyolysis

A

Myoglobin
Phosphate
Potassium
CK

19
Q

Causes of rhabdomyolsis

A

Prolonged immobility
Seizures
Crush injury
Vigorous excessive

20
Q

AKI stages

A

1- creatinine rise 1.5 -1.9 x, creatinine rise by 26.5 or oliguria of <0.5ml/kg/hr for 6 hours

2- rise in creatinine 2-3 times and oliguria 0.5 ml/kg/hr for 12 hours

3- 3x increase in creatinine or oliguria <0.3ml/kg/hr

21
Q

What drugs must be stopped in AKI

A

DAMN + opioids, lithium and LMWH

Diuretics
AceI/ARB/Aminoglycosides (gentamicin)
Metformin
NSAIDS

22
Q

Which drugs don’t worsen renal impairment but have increased risk of toxicity in AKI

A

Metformin
Lithium
Digoxin

23
Q

What cell casts are seen in AIN

A

White cell casts

24
Q

What renal tests should all diabetics have annually

A

Annual urinary albumin creatinine ratio

Should not be more than 2.5

Manage with dietary protein control, tight glycemic control and BP mx with potential ACEI

25
Indication for acute dialysis (AEIOU)
Acidosis Electrolyte annormality Intoxication Oedema Uraemia
26
which type of PKD is more common What are some complications How is it managed
Autosomal dominant is far more common and presents earlier Associated with sub arrack bleeds, chronic loin pain, stones and haematuria HTN and cvd Can use tolvaptan, which is a a vasopresser receptor 2 antagonist