Panel 2: Five-step guide for the detection and assessment
of chronic kidney disease
1 Recognition of increased risk of CKD
• Increased susceptibility to CKD (ie, old age, family history,
history of acute kidney injury, member of ethnic or racial
minority in the USA, reduced nephron mass [history of
nephrectomy, low birthweight], genetic traits)
• Exposure to diseases or conditions that cause CKD—ie, risk
factors for CVD (hypertension, diabetes, obesity), CVD,
autoimmune disease (systemic lupus erythematosus,
vasculitis), infections (bacteria, HBV, HCV, HIV,
schistosomiasis, malaria), drugs or toxins (NSAID,
iodinated radiographic contrast, aristolochic acid)
2 Testing
for
CKD
• Measure serum creatinine to estimate GFR
• Measure
urinary
albumin
• Search for other markers of kidney damage that are
specifi c to the risk (urine sediment, imaging
abnormalities, or renal tubular syndromes)
• Confi rmatory tests (if indicated)
3 Detection
of
CKD
• GFR <60 mL/min per 1·73 m² (measured or estimated)
• Kidney damage (pathological abnormalities, markers, or
history of kidney transplantation)
• Duration >3 months (documented or inferred)
4 Evaluation of clinical diagnosis for implementation
of specifi c therapy
• Diabetic kidney disease (type 1 or type 2)
• Non-diabetic kidney disease (glomerular diseases other
than diabetic kidney disease, vascular diseases,
tubulointerstitial diseases, or cystic diseases)
• Kidney disease in recipients of kidney transplants
5 Assessment of stage for implementation
of stage-based non-specifi c therapy
• GFR
stages
• Albuminuria
stages
CKD=chronic kidney disease. CVD=cardiovascular disease. HBV=hepatitis B virus.
HCV=hepatitis C virus. NSAID=non-steroidal anti-infl ammatory drug. GFR=glomerular
fi ltration rate.
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