Scope of this summary
Adults with suspected or established chronic kidney disease (CKD), from detection through risk-based longitudinal care. KDIGO is a global guideline commonly used in US nephrology; this page does not replace disease-specific glomerular, transplant, dialysis, pregnancy or acute-kidney-injury guidance.
sources for this section:KDIGO CKD 2024
The Bottom Line
- Confirm chronicity for at least three months when possible: CKD requires persistent reduced GFR or another marker of kidney damage, not a single creatinine or urine-albumin result obtained during acute illness.
- Classify CKD by cause, GFR category and albuminuria category, and interpret eGFR together with urine albumin-to-creatinine ratio because each contributes independent prognostic information.
- Use creatinine-based eGFR initially and add cystatin C in the situations identified by KDIGO when greater accuracy could alter diagnosis, drug dosing or another clinical decision.
- Estimate kidney-failure risk with a validated equation in appropriate CKD populations and combine the result with progression, complications and patient goals when planning nephrology referral or kidney-replacement preparation.
- Reduce kidney and cardiovascular risk through blood-pressure treatment, renin-angiotensin-system blockade for indicated albuminuria, an SGLT2 inhibitor when source criteria are met, lipid management, diabetes care, smoking treatment and avoidance of nephrotoxic exposure.
sources for this section:KDIGO CKD 2024
Practical clinical workflow
1
Repeat eGFR and urine albumin after an unexpected abnormality, review prior records for chronicity, and investigate hematuria, obstruction, systemic disease, family history and medicine or supplement exposure.
2
Assign cause, GFR and albuminuria categories; assess blood pressure, volume, diabetes, cardiovascular disease, anemia, potassium, bicarbonate and mineral-bone complications at a frequency matched to risk.
3
Calculate a validated kidney-failure risk where applicable, discuss prognosis without deterministic language, and use risk plus clinical features to determine follow-up and referral intensity.
4
Start or optimize kidney-protective treatment, checking contraindications and monitoring creatinine, potassium, volume and adverse effects after relevant changes.
5
Create a sick-day and medication-safety plan, reconcile every prescription and nonprescription product for kidney function, and prepare early for modality education when progression risk becomes substantial.
sources for this section:KDIGO CKD 2024
Safety boundaries and escalation
- A rapid fall in eGFR, new oliguria, severe hyperkalemia, pulmonary edema, uremic features, suspected obstruction or systemic inflammatory disease requires urgent evaluation rather than routine CKD follow-up.
- Do not stop renin-angiotensin-system or SGLT2 therapy solely because CKD is advanced; assess the specific acute change, hemodynamics, potassium, adverse effects and current source guidance.
- Drug doses based on kidney function may require a measure different from the laboratory eGFR; consult the current FDA label and pharmacy guidance, especially near a dosing threshold.
- Pregnancy, kidney transplantation, dialysis, nephrotic syndrome and suspected rapidly progressive glomerulonephritis follow specialist pathways with different treatment and safety rules.
sources for this section:KDIGO CKD 2024
Localization
KDIGO 2024 is international rather than a US federal guideline. Implement it with current FDA labeling, US laboratory reporting, local nephrology criteria and payer coverage.
sources for this section:KDIGO CKD 2024
Source documents
Use the linked source documents for complete recommendations, evidence grading, exclusions and implementation detail.
- Kidney Disease: Improving Global OutcomesKDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney DiseaseDOI 10.1016/j.kint.2023.10.018 路 published 2024-03-13 路 accessed 2026-08-20view source
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