Chronic Kidney Disease (KDIGO G/A staging + GDMT)
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Confirm CKD: eGFR <60 OR UACR ≥30 OR structural marker, sustained ≥3 months (KDIGO 2024)
KDIGO 2024 chronicity criteria met (not acute injury)
Patient inputs (13)
eGFR + KFRE risk (Tangri JAMA 2016) + statin eligibility ages 50–79 (SHARP, Baigent Lancet 2011)
CKD-EPI 2021 race-free eGFR — KDIGO 2024 staging foundation
KDIGO 2024 A1/A2/A3 albuminuria stage; gates SGLT2i + finerenone
KDIGO 2024 BP target SBP <120 if tolerated; gates RAS titration
RAS + finerenone + MRA gating; baseline before titration (KDIGO 2024)
DKD = primary indication for SGLT2i (DAPA-CKD, Heerspink NEJM 2020) + finerenone (FIDELIO-DKD, Bakris NEJM 2020) + GLP-1 (FLOW)
Detect existing RAS/SGLT2i; flag NSAIDs, contrast risk (KDIGO 2024)
Statin + ASCVD risk assessment (SHARP, Baigent Lancet 2011)
DM control gates GLP-1 (FLOW NEJM 2024) + SGLT2i benefit independent of glycemic effect (DAPA-CKD)
CKD-MBD assessment stage 4–5 (KDIGO 2017 CKD-MBD)
CKD-MBD; secondary hyperparathyroidism (KDIGO 2017 CKD-MBD)
Anemia of CKD; iron + ESA threshold (KDIGO 2012 Anemia)
Metabolic acidosis stage 3b–5; oral bicarb target HCO3 22–29 (KDIGO 2024)
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (6)
- informationallife_threateninguremic_emergencyUremic pericarditis / encephalopathy / bleeding diathesis (KDIGO 2012)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereeGFR_under_15_initiate_rrteGFR <15 OR uremic symptoms — encephalopathy, pericarditis, anorexia, pruritus (KDIGO 2012)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderaterapid_progressioneGFR decline >3 mL/min/yr OR doubling of UACR (KDIGO 2024)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatehyperK_on_rasK >5.5 on ACEi/ARB/MRA/finerenone (KDIGO 2024)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateeGFR_under_30_vascular_accesseGFR <30 — initiate vascular access education + nephrology referral (KDIGO 2024)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatesick_day_aki_patternAcute illness (vomiting / diarrhea / sepsis) with rising Cr on RAS+SGLT2i (KDIGO 2024)Trigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
KDIGO G1-G5 stage-driven management (KDIGO 2024)- lisinoprilfirst lineACEi10 mg PO • PO • daily, titrate to 40 mgtriggers: UACR>=30, no_acei_intoleranceKDIGO 2024 proteinuric-CKD foundation. UACR ↓ ~35–40% over wks; expect acute eGFR dip 10–20% then slope flattens. REIN (PMID 9217756): GFR decline 0.53 vs 0.88 mL/min/mo, p=0.03; doubling-Cr/ESRD 18 vs 40 events, p=0.04 (non-diabetic proteinuric CKD)rxcui 29046
- atorvastatinadd onstatin20 mg PO • PO • dailytriggers: age_50_79, no_dialysisKDIGO 2024 lipid — fixed-dose statin, no LDL target. No eGFR-slope effect; ΔLDL ~−40% in wks. SHARP (PMID 21663949): major atherosclerotic events RR 0.83 (0.74–0.94), p=0.0021 in CKDrxcui 83367
outpatient playbook — drug actions (7)
- 1. lisinopril/losartanLisinopril 10-40 mg PO daily; losartan 50-100 mg • PO • dailytrigger: UACR ≥30KDIGO 2024 foundation; REIN (Ruggenenti Lancet 1998); titrate to max tolerated
- 2. dapagliflozin/empagliflozin10 mg PO daily • PO • dailytrigger: eGFR ≥20DAPA-CKD (Heerspink NEJM 2020) / EMPA-KIDNEY (Herrington NEJM 2023)
- 3. finerenone10 mg PO daily, up to 20 mg • PO • dailytrigger: DKD + UACR ≥30 + K <5.0 + eGFR ≥25FIDELIO-DKD (Bakris NEJM 2020) / FIGARO-DKD (Pitt NEJM 2021)
- 4. semaglutide0.25 mg SC weekly, titrate to 1-2 mg • SC • weeklytrigger: DM2 + CKD + not at glycemic target on metformin/SGLT2iFLOW (Perkovic NEJM 2024); ADA 2026 §11
- 5. atorvastatin20-80 mg PO daily • PO • dailytrigger: Age 50-79 + no dialysisSHARP (Baigent Lancet 2011); KDIGO 2013 Lipid
- 6. sodium bicarbonate650 mg PO BID-TID • PO • BID-TIDtrigger: HCO3 <22KDIGO 2024 alkali therapy
- 7. erythropoiesis-stimulating agentEpoetin 50-100 U/kg SC 3x/week OR darbepoetin 0.45 mcg/kg q2w • SC • 1-3x/weektrigger: Hb <10 + iron-replete + no contraindicationKDIGO 2012 Anemia; target Hb 10-11.5
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: eGFR <60 sustained ≥3 months (KDIGO 2024); UACR ≥30 mg/g sustained ≥3 months (KDIGO 2024); Existing CKD on problem list — titration visit (KDIGO 2024).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Chronic Kidney Disease (KDIGO G/A staging + GDMT)** (neph.ckd.core.v1). Phenotype framing: KDIGO 2024 G/A stage assignment via ckd-staging.service.ts; subtype: DKD / HTN / GN / cystic / ischemic Scope: Confirm CKD: eGFR <60 OR UACR ≥30 OR structural marker, sustained ≥3 months (KDIGO 2024) No severity triggers fired against current inputs.
Plan
Regimen axis: **KDIGO G1-G5 stage-driven management (KDIGO 2024)** — step "G1 — eGFR ≥90 with markers of damage — UACR ≥30 or structural (KDIGO 2024)". 1. lisinopril 10 mg PO PO daily, titrate to 40 mg (ACEi, first line) — KDIGO 2024 proteinuric-CKD foundation. UACR ↓ ~35–40% over wks; expect acute eGFR dip 10–20% then slope flattens. REIN (PMID 9217756): GFR decline 0.53 vs 0.88 mL/min/mo, p=0.03; doubling-Cr/ESRD 18 vs 40 events, p=0.04 (non-diabetic proteinuric CKD) 2. atorvastatin 20 mg PO PO daily (statin, add on) — KDIGO 2024 lipid — fixed-dose statin, no LDL target. No eGFR-slope effect; ΔLDL ~−40% in wks. SHARP (PMID 21663949): major atherosclerotic events RR 0.83 (0.74–0.94), p=0.0021 in CKD Setting playbook (outpatient) — Slow progression with KDIGO 2024 4-pillar (RAS + SGLT2i + finerenone + statin), prevent CV events, prepare for RRT only when needed 3. lisinopril/losartan Lisinopril 10-40 mg PO daily; losartan 50-100 mg PO daily — UACR ≥30 (KDIGO 2024 foundation; REIN (Ruggenenti Lancet 1998); titrate to max tolerated) 4. dapagliflozin/empagliflozin 10 mg PO daily PO daily — eGFR ≥20 (DAPA-CKD (Heerspink NEJM 2020) / EMPA-KIDNEY (Herrington NEJM 2023)) 5. finerenone 10 mg PO daily, up to 20 mg PO daily — DKD + UACR ≥30 + K <5.0 + eGFR ≥25 (FIDELIO-DKD (Bakris NEJM 2020) / FIGARO-DKD (Pitt NEJM 2021)) 6. semaglutide 0.25 mg SC weekly, titrate to 1-2 mg SC weekly — DM2 + CKD + not at glycemic target on metformin/SGLT2i (FLOW (Perkovic NEJM 2024); ADA 2026 §11) 7. atorvastatin 20-80 mg PO daily PO daily — Age 50-79 + no dialysis (SHARP (Baigent Lancet 2011); KDIGO 2013 Lipid) 8. sodium bicarbonate 650 mg PO BID-TID PO BID-TID — HCO3 <22 (KDIGO 2024 alkali therapy) 9. erythropoiesis-stimulating agent Epoetin 50-100 U/kg SC 3x/week OR darbepoetin 0.45 mcg/kg q2w SC 1-3x/week — Hb <10 + iron-replete + no contraindication (KDIGO 2012 Anemia; target Hb 10-11.5) Non-pharmacologic actions: - Sodium restriction <2 g/day (KDIGO 2024) - Protein 0.8 g/kg/day in G3b-G5; 0.6-0.8 with low protein supplemented in G4-G5 (KDIGO 2024) - Smoking cessation (KDIGO 2024) - Vaccinations — flu, PCV20, HBV, COVID (KDIGO 2024) - Avoid NSAIDs, IV contrast unless essential (KDIGO 2024) - Patient education on sick day rules — hold RAS+SGLT2i+diuretic during AKI/dehydration (KDIGO 2024) AVOID / contraindication checks: - RAS block if K >5.0 (KDIGO 2024) - RAS pause if AKI (KDIGO 2024) - SGLT2i block if eGFR <20 or active DKA (KDIGO 2024) - finerenone block if K >5.0 or eGFR <25 (KDIGO 2024) - GLP 1 caution if gastroparesis or pancreatitis (ADA 2026) - metformin hold if eGFR <30 (KDIGO 2024) - NSAID avoid in CKD (KDIGO 2024)
Monitoring
Regimen monitoring: - BMP 2 weeks after initiation or titration (KDIGO 2024) - BMP q3m at steady state (KDIGO 2024) - UACR q3-6m (KDIGO 2024) - A1c q3m if DM (ADA 2026) - Phos PTH Ca q6-12m in G3b-G5 (KDIGO 2017) - Hb iron q3m in G3b-G5 (KDIGO 2012) Setting (outpatient) monitoring: - BMP 1-2 weeks after RAS / finerenone / SGLT2i titration (KDIGO 2024) - BMP, UACR, eGFR q3-6m at steady state (KDIGO 2024) - BP q visit (KDIGO 2024) - Hb, iron q3-6m in G3b-G5 (KDIGO 2012 Anemia) - Phos, PTH, Ca q6-12m in G3b-G5 (KDIGO 2017 CKD-MBD) Follow-up plan: Cadence by KDIGO 2024 stage; vaccinations (flu/pneumo/HBV/COVID); patient education; CKM review (Ndumele Circulation 2023) - Close-out criterion: Follow-up scheduled Monitoring phase: BMP within 1–2 weeks of titration; UACR + eGFR q3–6m; K trend on RAS + finerenone; A1c q3m if DM (KDIGO 2024)
Disposition
Current setting: outpatient — Slow progression with KDIGO 2024 4-pillar (RAS + SGLT2i + finerenone + statin), prevent CV events, prepare for RRT only when needed Disposition criteria: - Continue current stage management if stable (KDIGO 2024) - Advance to vascular access prep when eGFR <30 (KDIGO 2024) - RRT initiation when eGFR <10 or uremic symptoms (KDIGO 2012) Escalation triggers (move to higher acuity): - eGFR decline >3 mL/min/yr → nephrology referral (KDIGO 2024) - eGFR <30 → vascular access education + nephrology referral (KDIGO 2024) - eGFR <20 → AV fistula creation; transplant referral (KDIGO 2024) - K >5.5 on RAS → pause RAS / add patiromer; reassess (KDIGO 2024) - AKI on CKD → ED / inpatient (KDIGO 2012)
Patient Action Plan
**CKD Sick Day & Self-Monitoring Action Plan (KDIGO 2024)** Personalised values: baseline_creatinine, baseline_eGFR, current_RAS, current_SGLT2i, current_diuretic, home_BP_target. **Stable — feeling well** (green): Triggers: - Eating and drinking normally (KDIGO 2024) - No vomiting / diarrhea / fever (KDIGO 2024) - Home BP at goal SBP <120-130 (KDIGO 2024) - No new medications (KDIGO 2024) Actions: - Continue all CKD medications as prescribed — RAS, SGLT2i, finerenone, statin (KDIGO 2024) - Stay well hydrated — water; avoid dehydration (KDIGO 2024) - Avoid NSAIDs — ibuprofen, naproxen, diclofenac (KDIGO 2024) - Keep all labs and follow-ups (KDIGO 2024) **Caution — mild illness** (yellow): Triggers: - Vomiting or diarrhea more than 1-2 episodes (KDIGO 2024) - Decreased oral intake or dehydration (KDIGO 2024) - Fever (KDIGO 2024) - Unable to keep down medications (KDIGO 2024) - Home BP much higher or lower than usual (KDIGO 2024) Actions: - HOLD: ACEi/ARB, SGLT2i, diuretic, NSAIDs, metformin — sick day rules (KDIGO 2024) - Drink small frequent sips of water/electrolyte solution (KDIGO 2024) - Continue blood pressure monitoring (KDIGO 2024) - Call CKD clinic / primary care within 24 hours for guidance (KDIGO 2024) - Resume medications when eating/drinking normally — confirm with provider (KDIGO 2024) Contact provider when: - Symptoms persist >24 hours (KDIGO 2024) - Unable to drink fluids (KDIGO 2024) - Decreased urination (KDIGO 2024) - New leg swelling or shortness of breath (KDIGO 2024) **Medical alert — severe illness** (red): Triggers: - No urine output for ≥6-8 hours (KDIGO 2012) - Severe shortness of breath / chest pain (KDIGO 2012) - Confusion, severe weakness, fainting (KDIGO 2012) - Severe vomiting/diarrhea unable to keep fluids down (KDIGO 2012) - Black/tarry stools or vomiting blood (KDIGO 2012) - Severe leg swelling with shortness of breath — volume overload (KDIGO 2012) Actions: - Go to ED immediately (KDIGO 2012) - Bring complete medication list (KDIGO 2024) - Tell ED you have CKD and your baseline creatinine (KDIGO 2024) - Do not take any new NSAIDs or contrast-requiring imaging until stable (KDIGO 2024) Contact provider when: - Any red zone symptom — go to ED now (KDIGO 2012)
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] Uremic pericarditis / encephalopathy / bleeding diathesis (KDIGO 2012) - [SEVERE] eGFR <15 OR uremic symptoms — encephalopathy, pericarditis, anorexia, pruritus (KDIGO 2012) - [MODERATE] eGFR decline >3 mL/min/yr OR doubling of UACR (KDIGO 2024)
Citations
- KDIGO 2024 CKD Guideline (Kidney Int Mar 2024) + KDIGO 2024 Diabetes-in-CKD update + 2025 AHA/ACC HTN Guideline + ADA Standards of Care 2026 + 2022 AHA/ACC/HFSA HF Guideline (cardiorenal protective Rx) + 2023 ACC/AHA/HFSA HF Focused Update (finerenone in HFmrEF/HFpEF) + KDIGO 2013 Lipid + KDIGO 2017 CKD-MBD + KDIGO 2012 Anemia [PMID:38490803](https://pubmed.ncbi.nlm.nih.gov/38490803/) - Cited evidence (PMID 32970396) [PMID:32970396](https://pubmed.ncbi.nlm.nih.gov/32970396/) - Cited evidence (PMID 33338413) [PMID:33338413](https://pubmed.ncbi.nlm.nih.gov/33338413/) - Cited evidence (PMID 36331190) [PMID:36331190](https://pubmed.ncbi.nlm.nih.gov/36331190/) - Cited evidence (PMID 30990260) [PMID:30990260](https://pubmed.ncbi.nlm.nih.gov/30990260/) Last reconciled with current guidelines: 2026-05-22.
- KDIGO 2024 CKD Guideline (Kidney Int Mar 2024) + KDIGO 2024 Diabetes-in-CKD update + 2025 AHA/ACC HTN Guideline + ADA Standards of Care 2026 + 2022 AHA/ACC/HFSA HF Guideline (cardiorenal protective Rx) + 2023 ACC/AHA/HFSA HF Focused Update (finerenone in HFmrEF/HFpEF) + KDIGO 2013 Lipid + KDIGO 2017 CKD-MBD + KDIGO 2012 Anemia — PMID:38490803
- Cited evidence (PMID 32970396) — PMID:32970396
- Cited evidence (PMID 33338413) — PMID:33338413
- Cited evidence (PMID 36331190) — PMID:36331190
- Cited evidence (PMID 30990260) — PMID:30990260