Nephrology Flashcards

1
Q

what is the most common nephrological affliction in ageing?

A

membranous nephropathy which is when glomeruli become damaged and thickened and allow proteins to pass through

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2
Q

what is ageing?

A

a slow inflammatory process

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3
Q

give examples of drugs given post-renal transplant and their effects

A
basiliximab - anti CD25
anti-lymphocyte ab - against T cells
campath/alemtuzumab - anti-CD52
Rituximab - anti CD20
ecilizumab - anti C5
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4
Q

what drugs are given as maintenance therapy for post-renal transplant

A

tacrolimus (cyclosporin)
antiproliferative: mycophenolate
prednisolone
mTOR inhibitors

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5
Q

what are the signs of acute renal rejection?

A

abrupt rise in serum creatinine, fluid retention, fever, graft tenderness

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6
Q

what is the management for acute renal rejection

A

pulse steroids and increase immunosupression

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7
Q

what are absolute contraindications of renal transplantation patient

A
  • untreated current infection
  • maligancy with short lifespan
  • lifespan<1yr
  • active psychosis
  • active substance abuse
  • bilateral severe peripheral vascular occlusive disease
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8
Q

what are contraindications of transplant donation

A
<18yrs
HTN with end organ damage
diabetes
active malignancies
evidence of donor coercion
low GFR by age
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9
Q

what is gold standard treatment of CMV

A

IV ganciclovir or oral vlganciclovir

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10
Q

when should one start dialysis

A
eGRF < 15ml/min per 1.73m2
intractable fluid overload, hyperkalemia
malnutrition due to uremia
uremic neurologic dysfunction
uremic sierostitis
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11
Q

during dialysis are we giving acid or alkali to the patients

A

alkali

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12
Q

where does the blood and dialysis fluid first meet

A

in the dialyser

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13
Q

what is disequilibrium syndrome

A

a set of systemic, neurologic symptoms occur during/after dialysis. nausea, vomiting, restlessness, seizures, headaches. It is thought to be due to an acute increase in brain water content

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14
Q

how is water purified?

A

treat with a water softener and carbon adsorption. Reverse osmosis and deionization. Distilation

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15
Q

what is ADPKD

A

It is an inherited disorder that presents as cyst developing on the kidney surface

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16
Q

what genes are associated with ADPKD and what proteins do they code for?

A

PKD1 (codes for PC1)

PKD2 (codes for PC2)

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17
Q

what is the function of PC1?

A

it acts as a mechanosensor on cilium of the kidney. They can sense urine flow rate and convey this information to intracellular calcium signalling. These changes in calcium affect gene transcription

18
Q

relate ADPKD and corresponding levels of intracellular calcium

A

in ADPKD the levels of intracellular calcium are decreased due to loss of function of PC complex.

19
Q

what is another role of PC1

A

it helps formation of desmosomal junctions, adherens junctions.

20
Q

relate cAMP levels to ADPKD. Name a drug used for treatment

A

cAMP levels are increased in ADPKD. Tolvaptan

21
Q

list some extrarenal manifestations of ADPKD

A

Hepatic cysts
diverticulosis
pancreatic cysts, abdominal hernia, cholangiocarcinoma, liver fibrosis, cardiac valve abnormalities, aortic aneurysm, intracranial aneurysm

22
Q

what are vaptans

A

are vasopressin receptor 2 antagonists

23
Q

define hepatorenal syndrome type 1

A

acute, functional AKI developing close to deterioration of other organs.

24
Q

define hepatorenal syndrome type 2

A

renal imapairment that is less severe than that of type 1. Most common sign is ascites that is resistant to diuretics

25
Q

what do the kidneys look like in type 1 hepatorenal syndrome

A

normal. You must diagnose based on exclusion of other syndromes

26
Q

what are percipitating factors of type 1 HRS

A

severe alcoholic hepatitis, infection, large volume paracentesis w/out plasma expansion, GI bleed

27
Q

what are diagnosis criteria for HRS type1

A

cirrhosis with ascites, serum creatinine >133mmol/L, no shock, no parenchymal kidney disease

28
Q

signs of ANCA associated renal vasculitis

A

cutaneous purpura, nodules, ulceration, peripheral neuropathy, abdominal pain, blood in stool, hematuria, protienuria, necrotizing sinusitis, myalgia

29
Q

list histology findings of ANCA associated renal vasulitis

A

LM: necrotizing GN
IF: neccrotizing vasculitis
EM: diffuse foot process effacement

30
Q

what is the target of ANCA’s

A

myeloperoxidase or proteinase 3

31
Q

how do you treat vasculitis

A

corticosteroids

32
Q

pathogenesis of lupus glomerulonephritis

A
autoantibodies against self DNA
weird clearance of cellular debris
loss of immune tolerance
increase in cell death
inflammation
fibrosis and proliferation of endothelial and mesangial cells
33
Q

treatments of SLE nephritis

A

plasmapheresis, cyclophosphamide (rituximab), corticosteroids

34
Q

hypoalbuminema levels

A

less than 3.5g/dL

35
Q

presentation of Nephrotic syndrome

A

edema in legs, xanthelasma, periorbital edema in morning

36
Q

what are the 2 causes of nephrotic syndrome

A

glomerulonephritis, and systemic diseases

37
Q

what med do you give for alports

A

ACEi

38
Q

name the 3 benign renal tumors

A

renal papillary adenoma, angiomyolipoma, oncocytoma

39
Q

renal cell carcinoma is due to mutation in what gene

A

VHL

40
Q

prostate tumors are most often in the

A

peripheral zone