Nephro Flashcards

1
Q

Which medications worsen AKIs

A

-NSAIDs (except cardiac dose of arpsin at 75mg od)
-Aminoglycosides
-ACEi
-angiotensin II receptors
-Diuretics

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2
Q

Drugs which may have to be stopped in AKI as increased risk of toxicity

A

Metformin
Lithium
Digoxin

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3
Q

Berry aneurism site

A

Circle of Willis most commonly anterior communicating artery

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4
Q

Autosomal dominant polycystic kidney disease Sx + extra-renal manifestifations

A

-HTN
-Recurrent UTIs
-flank pain
-Haematuria

-Liver cysts (hepatomegaly)
-Berry aneurysms (SAH)
-mitral valve prolapse, mitral/tricuspid incompetence, aortic root dilation, aortic dissection

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5
Q

Haemolytic uraemic syndrome

A

young children usually: triad of
AKI,
microangiopathic haemolytic anaemia
thrombocytopenia
usually 2ndary to Shiga toxin-producing Escherichia coli

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6
Q

Acute interstitial nephritis causes + Sx

A

drugs: the most common cause, particularly antibiotics
penicillin
rifampicin
NSAIDs
allopurinol
furosemide
systemic disease: SLE, sarcoidosis, and Sjögren’s syndrome
infection: Hanta virus , staphylococci

Sx: fever, rash, arthralgia
eosinophilia
mild renal impairment
hypertension

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7
Q

Pre-renal uraemia vs acute tubular necrosis

A

Pre-renal(kidneys hold onto sodium to preserve voume): good response to fluid challenge, raised serum urea:creatinine ratio, brown granular casts in urine

Acute tubular necrosis: poor response, normal urea:creat ratio

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8
Q

Minimal change disease

A

Sx: nephrotic syndorme (proteinurea)
normal BP
Renal biopsy: normal glomeruli on light micro, electon micro shows podycyte fusion
mx: oral corticosteroids
2nd line: cyclophoaphamide

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9
Q

GBS causative agent

A

Campylobacter jejuni

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10
Q

membranoproliferative glomerulonephritis biopsy findings

A

Type 1: “tram-track”
Type 2: causes partial lipodystrophy “dense deposits”

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11
Q

Anti-glomerular basement membrane (GBM) disease/ Goodpasture’s syndrome
Path, Sx, Ix, Mx, RFs

A

*Path: small-vessel vasculitis caused by anti GBM antibodies against collagen
*RF: men, and bimodal prevalence 20-30 and 60-70
*Sx: Pulmonary haemorrhage (haemoptysis) and rapidly progressive glomerulonephritis (proteinuria and haematuria)
*Ix: renal biospy: linear IgG deposits in basement membrane
*Mx: Plasma exchange (plasmanephrisis)

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12
Q

Nephrotic syndrome

A

-Proteinuria >3g/24hr
-Hypoalbuminaemia <30g/L
-Oedema

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13
Q

Acute Tubular Necrosis

A

Most common cause of AKI, ischaemia or nephrotoxins e.g. gentamycin

Dx: Muddy brown casts on urinalysis

Epithelial cells regenerate so can reverse in 1-3 weeks

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14
Q

Acute interstitial Nephritis

A

inflammation of the interstitium by IMMUNE response to Drugs (e.g. NSAIDs or antibiotics), Infections (e.g., E. coli or HIV) or Autoimmune conditions (e.g., sarcoidosis or SLE)

Rash
Fever
Flank pain
Eosinophilia

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15
Q

Hypocalcaemia in CKD MOA

A

Chronic renal failure leads to impaired 25-hydroxyvit D conversion (needed for calcium absorption)

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16
Q

IgA nephropathy vs Post-strep glomerulonephritis

A

IgA: macroscopic haematuria 1-2 dyas after URTI
Post-Strep: proteinuria +/- haematuria 1-2 weeks after URTI

17
Q

ADPKD Features

A

Abdo pain
Early satiety
HTN
Flank masses
Systolic apical murmur (mitral valve prolapse)
Berry aneurysms
Liver cysts (hepatomegaly)

18
Q

Membranous glomerulonephritis

A

Can present with proteinuria or nephrotic syndrome

Renal biopsy: BM thickened with subepithelial electron dense deposits creating a ‘spike and dome’ appearance

19
Q

Fanconi syndrome

A

Underlying dysfunction in PCT resulting in impaired reabsorption

Sx: polydipsia, polyuria, failure to thrive, hypokalaemia

20
Q

Acute interstitial nephritis Ix

A

WBC/ white cell casts in urine

21
Q

IgA nephropathy pathophysiology

A

Mesangial deposition of IgA immune complexes
No tx required usually, follow up to check renal function

22
Q

Maintainence fluids regime

A

30ml/kg/24hours

23
Q

Anion gap calculation

A

(Na+Ka) - (Bicarb +Cl)

Normal is 8-14mmol/L

24
Q

Diabetes insipidus Ix

A

High plasma osmolality and low urine osmolality

Ix: Water deprivation test

Decreased ADH: cranial (desmopressin-vasopressin v2 agonist) nephrogenic (thiazides)

25
Q

Paediatric fluid requirements

A

100, 50, 20 rule
100 for first 10kg
50 for second 10kg
20 for everything above to a max of like 2L

25
Q

Osteomalacia secondary to CKD mx

A

1st line: reduce dietary phosphate intake
2nd line: phosphate binders

26
Q

Renal cell carcinoma sx

A

Haematuria, loin pain, abdo mass

Ongoing fevers, weight loss

27
Q

Acute graft failure

A

Few months post transplant

-leucocytes and protein in blood
-rising creatinine

Mx: IV steroids and T cell depletion