CKD Flashcards

1
Q

what is the definition of CKD?

A

reduction in kidney function or structural damage (or both) present for more than 3months, with associated health implications.

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2
Q

what are the causes of CKD?

A

-conditions associated with intrinsic kidney damage (HTN, DM, glomerular disease, current/previous AKI, potentially nephrotoxic drugs)
-conditions associated with obstructive uropathy (structural renal tract disease, neurogenic bladder, BPH, recurrent kidney stones)
-multisystem disease with renal involvement (SLE, vasculitis, myeloma)

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3
Q

what are some of the common potentially nephrotoxic drugs that could cause CKD?

A

-aminoglycosides (vancomycin, gent)
-ACEis/ARBs
-bisphosphonates (alendronic acid)
-calcinuerin inhibitors (ciclosporin, tacrolimus)
-diuretics
-lithium
-mesalazine
-NSAIDs

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4
Q

what are the risk factors for CKD?

A

-having any of the conditions listed as causes
-FH of CKD stage 5 or hereditary kidney disease or familial glomerulonephritis
-cardiovascular disease
-obesity with metabolic syndrome (obesity itself not risk factor)
-gout

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5
Q

what is metabolic syndrome?

A

having a combination of diabetes, high blood pressure (hypertension) and obesity.

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6
Q

what are 2 examples of hereditary kidney disease?

A

autosomal dominant polycystic kidney disease
alport’s syndrome

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7
Q

what is alport’s syndrome?

A

sex linked recessive disease which typically causes haematuria as well as deafness and eye issues

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8
Q

what sort of monitoring do people on potentially nephrotoxic drugs need?

A

yearly monitoring of eGFR and urine ACR

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9
Q

what are the symptoms of CKD and why?

A

-anaemia cos kidney makes EPO: pallor, lethargy, breathlessness
-urea buildup: skin pigmentation and itchiness, bruising (platelet dysfunction), confusion, coma, fits, polyneuropathy, uraemic pericarditis
-toxin buildup: N+V, anorexia
-renal: nocturia, polyuria, oedema, bubbly urine
-renal bone disease: osteomalacia, bone pain, osteosclerosis, muscle weakness, cramps
-endocrine: amenorrhoea, erectile dysfunction, infertility
-CV: HTN, peripheral vascular disease

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10
Q

what are the signs/examinations you need to do for CKD?

A

-general examination: cachexia, signs of malnutitrion, uraemic odour
-CV exam: pallor, dehydration/hypovalaemia, tachypnoea, HTN, peripheral oedema, pulmonary oedema
-neurological exam: cognitive impairment, peripheral neuropathy, peripheral myopathy
-abdo exam: palpable bilateral flank masses with possible hepatomegaly suggests PCKD with possible liver cysts, palpable distended bladder suggests obstructive uropathy

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11
Q

when do you do initial investigations for CKD?

A

-someone with any risk factors for CKD
-incidental findings of: raised creatinine/eGFR <60, proteinuria (ACR>3), persistent haematuria, urine sediment abnormalities
-possible clinical features of CKD

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12
Q

what is persistent haematuria?

A

2/3 urine dipsticks showing 1+ or more of blood after exclusion of a UTI

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13
Q

what are the initial investigations for someone to do for CKD?

A

-serum creatinine and eGFR
-early morning urine sample to measure ACR
-urine dip for haematuria
-CV risk factors: BMI, BP, serum Hba1c, lipid profile
-renal tract USS if ?stones or ?PCKD

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14
Q

what’s a rule on what you can’t do before having your serum creatinine and eGFR measured?

A

can’t eat meat 12 hours before test

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15
Q

what do you do with the results of the initial serum creatinine/eGFR measurement?

A

if <60 repeat within 2 weeks. if remains <60 repeat within 3 months -obvi if reduced still and spanning 3 months indicates CKD

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16
Q

in which groups do you have to interpret eGFR with caution?

A

extremes of muscle mass
pregnant
oedema
malnourished
uses protein supplements
asian or chinese in origin

17
Q

what do you do with the initial ACR results?

A

<3: no action needed
3-70: repeat test in 3 months
70+ no repeat needed as significant proteinuria

18
Q

what do you do with the results of the urine dip for haematuria?

A

1+ or more -arrange MSU testing for ?UTI
isolated persistent haematuria -think about referral for ?urological cancer

19
Q

what are the diagnostic criteria for CKD?

A

1) markers of kidney damage: urine ACR >3, urine sediment abnormalities (eg RBCs, WBCs, casts, renal tubular epithelial cells), electrolyte abnormalities, histological abnormalities, structural abnormalities, history of kidney transplant
2) a persistent reduction in renal function (3 months or more) shown by an eGFR <60.

20
Q

what is accelerated progression of CKD?

A

decrease in eGFR or 25% or more AND change in CKD category within 12 months, or persistent decrease in eGFR of 15 within 12 months.

21
Q

what is the staging of CKD?

A

Gs are stage 1-stage 5 and based on GFR. stage 1=90+, stage 2=60-90, stage 3=45 up to <60, stage 4=15 up to <30, stage 5=<15 (kidney failure)
As are A1-A3 and and based on ACR. 1=<3, 2=3-30, 3=30+

22
Q

what is the management of CKD?

A

-proteinuria: if they have ACR>7- prescribe ACEi/ARB no matter what BP is-renoprotection
-manage HTN: 1st line =ACEi/ARB. targets =<130/80 if ACR 70+, <140/90 if ACR >70, <150/90 if 80+ with diabetes
-manage anaemia risk: measure FBC, check for other causes of anaemia, refer to nephrologist if renal anaemia suspected. iron tablets -> iron infusions -> EPO
-manage renal bone disease risks: arrange serum calcium, phosphate, vit D, and PTH tests for everyone with CKD. low phosphate diet, calcium supplements
-CVD prevention: atorvastatin 20mg for everyone with CKD, antiplatelet drug for everyone, consider dapagliflozin if optimised on ACEi/ARB and have DM or ACR>23
-flu and pneumococcal vaccines