Hypertensive Nephrosclerosis (HTN-CKD)
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Hypertensive nephrosclerosis = chronic HTN + progressive CKD; KDIGO heat-map stage + APOL1 substrate + RAS exclusion (KDIGO 2012 CKD)
KDIGO stage + HTN-CKD pivot suspected
Patient inputs (14)
Age + ancestry stratify APOL1 + FMD vs atherosclerotic RAS probability
FMD predominantly young women; atherosclerotic RAS older male smokers
eGFR core input — KDIGO staging G1-G5 (KDIGO 2012 CKD)
A1/A2/A3 sub-staging — HTN-CKD typically A1-A2; A3 (>300) suggests overlap with diabetic / glomerular / APOL1-FSGS (KDIGO 2012 CKD)
ACEi/ARB + finerenone + spironolactone tolerability monitoring (KDIGO 2024 CKD)
BP target <120/80 SPRINT-driven for CKD-non-DM; <130/80 for DKD overlap (SPRINT NEJM 2015; KDIGO 2024)
DBP component; malignant HTN if DBP >120
DM substrate amplifies risk + changes phenotype to diabetic nephropathy primary; renal.diabetic-nephropathy.v1 if predominant
Tier ladder review — ACEi/ARB, CCB, thiazide, spironolactone, finerenone, SGLT2i (KDIGO 2024 CKD)
Bland sediment expected in pure HTN-CKD; active sediment → biopsy for GN overlap (KDIGO 2012 CKD)
CV disease drives target BP intensification + statin + antiplatelet (AHA 2017)
Familial APOL1, PKD, hereditary nephritis differentials (KDIGO 2012 CKD)
APOL1 high-risk G1/G2 genotype 13% of African-ancestry patients — amplifies HTN-CKD progression
Symmetric small kidneys = chronic HTN-CKD; asymmetric = RAS; cyst burden = PKD (KDIGO 2012 CKD)
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (9)
- informationallife_threateningmalignant_HTN_TMABP >180/120 + AKI + MAHA + thrombocytopenia + grade III/IV retinopathy → STAT IV BP reduction + plasmapheresis if TMA (AHA 2017; KDIGO 2012 AKI)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverebenign_HN_AA_predominant_APOL1African-ancestry adult with HTN-CKD + APOL1 high-risk G1/G2 genotype — 7-10× progression amplificationTrigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereischemic_atherosclerotic_RASAsymmetric kidneys + refractory HTN + flash pulm edema + atherosclerotic burden — atherosclerotic RAS (ASTRAL; CORAL)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverefibromuscular_dysplasiaYoung woman + refractory HTN + asymmetric kidneys / string-of-beads on angio — FMD (Olin-Sealove Mayo Clin 2010)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereAPOL1_FSGS_overlapAfrican-ancestry + nephrotic-range UACR + APOL1+ — collapsing FSGS variant overlap (KDIGO GN 2021)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereSCD_HTN_CKDSickle cell disease + HTN + progressive CKD — sickle nephropathy overlay (KDIGO 2012 CKD; ASH 2014)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatepregnancy_to_chronicPregnancy-induced HTN (preeclampsia, eclampsia, HELLP) → chronic HTN-CKD postpartum (ACOG 2020; KDIGO 2012 CKD)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateCKD_secondary_HTNCKD causes secondary HTN — volume + RAS activation + sympathetic; bidirectional (KDIGO 2012 CKD)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatepost_radiation_renovascularPost-radiation renovascular HTN — flank radiation history + new HTN + asymmetric kidneys (Cassady IJROBP 1995)Trigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
Hypertensive nephrosclerosis — BP control + renoprotection tier ladder + malignant HTN STAT pathway (KDIGO 2012 CKD; SPRINT NEJM 2015; DAPA-CKD; EMPA-KIDNEY)- lisinoprilfirst lineACEi10 mg PO daily; titrate to max 40 mg • PO • dailytriggers: htn_ckd_egfr_gt_20, no_history_aceiarb_intoleranceKDIGO 2012 CKD — RAS blockade slows progression; titrate to max-tolerated dose; recheck Cr+K at 1-2 wkrxcui 29046
- losartanfirst lineARB50 mg PO daily; titrate to 100 mg • PO • dailytriggers: acei_intolerant_cough_angioedemaKDIGO 2012 CKD — ARB if ACEi intolerant; same renoprotective effectrxcui 52175
outpatient playbook — drug actions (7)
- 1. lisinopril titrationStart 10 mg, titrate to max 40 mg • PO • dailytrigger: HTN-CKD foundationalKDIGO 2012 CKD
- 2. dapagliflozin add10 mg PO daily • PO • dailytrigger: eGFR ≥20 + progressiveDAPA-CKD
- 3. chlorthalidone add12.5-25 mg PO daily • PO • dailytrigger: BP unmet on RAS+SGLT2iAHA 2017
- 4. amlodipine add5-10 mg PO daily • PO • dailytrigger: BP unmet on 3-drugAHA 2017
- 5. spironolactone if resistant12.5-25 mg PO daily • PO • dailytrigger: Resistant HTN + K+ <5PATHWAY-2; route cardio.htn.resistant.v1
- 6. finerenone if DM albuminuric10-20 mg PO daily • PO • dailytrigger: DM + UACR ≥30 + K+ <5FIDELIO-DKD
- 7. atorvastatin40-80 mg PO daily • PO • dailytrigger: ASCVD risk + CKDAHA 2018 + KDIGO lipid 2014
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Declining eGFR in long-standing HTN patient ± modest albuminuria (KDIGO 2012 CKD); Persistent UACR 30-300 + chronic HTN (no diabetes) — hypertensive CKD phenotype (KDIGO 2012 CKD); Long-standing uncontrolled HTN ≥10 yrs (KDIGO 2012 CKD; AHA 2017).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Hypertensive Nephrosclerosis (HTN-CKD)** (renal.hypertensive-nephrosclerosis.v1). Phenotype framing: Sub-phenotypes: benign_HN_AA_predominant_APOL1 / malignant_HTN_TMA / ischemic_atherosclerotic_RAS / fibromuscular_dysplasia / APOL1_FSGS_overlap / SCD_HTN_CKD / pregnancy_to_chronic / CKD_secondary_HTN / post_radiation_renovascular (KDIGO 2012 CKD) Scope: Hypertensive nephrosclerosis = chronic HTN + progressive CKD; KDIGO heat-map stage + APOL1 substrate + RAS exclusion (KDIGO 2012 CKD) No severity triggers fired against current inputs.
Plan
Regimen axis: **Hypertensive nephrosclerosis — BP control + renoprotection tier ladder + malignant HTN STAT pathway (KDIGO 2012 CKD; SPRINT NEJM 2015; DAPA-CKD; EMPA-KIDNEY)** — step "Step 1 — RAS blockade foundational". 1. lisinopril 10 mg PO daily; titrate to max 40 mg PO daily (ACEi, first line) — KDIGO 2012 CKD — RAS blockade slows progression; titrate to max-tolerated dose; recheck Cr+K at 1-2 wk 2. losartan 50 mg PO daily; titrate to 100 mg PO daily (ARB, first line) — KDIGO 2012 CKD — ARB if ACEi intolerant; same renoprotective effect Setting playbook (outpatient) — Tier-ladder BP + renoprotection + APOL1 / RAS / FMD differentiation + CV risk reduction (KDIGO 2012 CKD; AHA 2017; SPRINT NEJM 2015) 3. lisinopril titration Start 10 mg, titrate to max 40 mg PO daily — HTN-CKD foundational (KDIGO 2012 CKD) 4. dapagliflozin add 10 mg PO daily PO daily — eGFR ≥20 + progressive (DAPA-CKD) 5. chlorthalidone add 12.5-25 mg PO daily PO daily — BP unmet on RAS+SGLT2i (AHA 2017) 6. amlodipine add 5-10 mg PO daily PO daily — BP unmet on 3-drug (AHA 2017) 7. spironolactone if resistant 12.5-25 mg PO daily PO daily — Resistant HTN + K+ <5 (PATHWAY-2; route cardio.htn.resistant.v1) 8. finerenone if DM albuminuric 10-20 mg PO daily PO daily — DM + UACR ≥30 + K+ <5 (FIDELIO-DKD) 9. atorvastatin 40-80 mg PO daily PO daily — ASCVD risk + CKD (AHA 2018 + KDIGO lipid 2014) Non-pharmacologic actions: - DASH diet + sodium <2 g/day (AHA 2017) - BP target <120/80 SPRINT-style for non-DM CKD (SPRINT NEJM 2015) - BP target <130/80 for DM-CKD overlap (KDIGO 2024) - Weight loss + exercise (AHA 2017) - Smoking cessation (AHA 2017) - Annual ophthalmology for HTN retinopathy + DM if applicable AVOID / contraindication checks: - No_combined_acei_arb_ras_blockade (KDIGO 2012 CKD; ONTARGET) - Hold_ras_blockade_during_severe_AKI (KDIGO 2012 AKI) - Avoid_NSAIDs_in_HTN_CKD (KDIGO 2012 CKD) - MAP_reduction_no_more_than_25_percent_first_hour_malignant_HTN (AHA 2017) - RAS_stent_NOT_routine_per_ASTRAL_CORAL (ASTRAL 2009; CORAL 2014) - Balloon_angioplasty_NOT_stent_for_FMD - Monitor_K_within_1_2_wk_after_RAS_or_MRA_initiation (KDIGO 2024)
Monitoring
Regimen monitoring: - Cr K at 1 2 wk post RAS initiation (KDIGO 2024) - BP self monitoring logs at each visit (AHA 2017) - eGFR UACR q3 6 mo (KDIGO 2012 CKD) - K at 1 4 wk after finerenone or spironolactone (FIDELIO-DKD) - MAP continuous during malignant HTN titration (AHA 2017) Setting (outpatient) monitoring: - BP at every visit + home log (AHA 2017) - eGFR + UACR q3-6 mo (KDIGO 2012 CKD) - K+ at 1-2 wk after each RAS / MRA change (KDIGO 2024) - CKD-MBD labs if eGFR <60 (KDIGO CKD-MBD 2017) Follow-up plan: q3-6 mo nephrology; transplant + RRT planning at G4 (eGFR <30); cardiology co-management for CV; ophtho for retinopathy; patient education on BP self-monitoring + lifestyle (KDIGO 2012 CKD; AHA 2017) - Close-out criterion: Long-term plan documented Monitoring phase: eGFR + UACR + BP + K+ q3-6 mo; lipid + CKD-MBD if eGFR <60; eGFR slope quarterly; APOL1+ patients more frequent (KDIGO 2012 CKD)
Disposition
Current setting: outpatient — Tier-ladder BP + renoprotection + APOL1 / RAS / FMD differentiation + CV risk reduction (KDIGO 2012 CKD; AHA 2017; SPRINT NEJM 2015) Disposition criteria: - Continue nephrology q3-6 mo if eGFR <60 (KDIGO 2012 CKD) - Refer cardiology if refractory HTN or CV disease (AHA 2017) Escalation triggers (move to higher acuity): - Sustained BP >150/95 despite max tier → resistant HTN workup → cardio.htn.resistant.v1 - Rapid eGFR decline (>5 ml/min/year) → biopsy consideration (KDIGO 2012 CKD) - New nephrotic UACR → renal.fsgs.v1 or biopsy for APOL1-FSGS overlap
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] BP >180/120 + AKI + MAHA + thrombocytopenia + grade III/IV retinopathy → STAT IV BP reduction + plasmapheresis if TMA (AHA 2017; KDIGO 2012 AKI) - [SEVERE] African-ancestry adult with HTN-CKD + APOL1 high-risk G1/G2 genotype — 7-10× progression amplification - [SEVERE] Asymmetric kidneys + refractory HTN + flash pulm edema + atherosclerotic burden — atherosclerotic RAS (ASTRAL; CORAL)
Citations
- KDIGO 2021 BP in CKD + KDIGO 2024 CKD + AASK (JAMA 2002) + SPRINT (NEJM 2015) + SGLT2i renal protection (EMPA-KIDNEY 2023) [PMID:12435255](https://pubmed.ncbi.nlm.nih.gov/12435255/) - Cited evidence (PMID 26551272) [PMID:26551272](https://pubmed.ncbi.nlm.nih.gov/26551272/) - Cited evidence (PMID 33637192) [PMID:33637192](https://pubmed.ncbi.nlm.nih.gov/33637192/) - Cited evidence (PMID 38490803) [PMID:38490803](https://pubmed.ncbi.nlm.nih.gov/38490803/) - Cited evidence (PMID 36331190) [PMID:36331190](https://pubmed.ncbi.nlm.nih.gov/36331190/) Last reconciled with current guidelines: 2026-05-22.
- KDIGO 2021 BP in CKD + KDIGO 2024 CKD + AASK (JAMA 2002) + SPRINT (NEJM 2015) + SGLT2i renal protection (EMPA-KIDNEY 2023) — PMID:12435255
- Cited evidence (PMID 26551272) — PMID:26551272
- Cited evidence (PMID 33637192) — PMID:33637192
- Cited evidence (PMID 38490803) — PMID:38490803
- Cited evidence (PMID 36331190) — PMID:36331190