Heart failure with mildly reduced EF (HFmrEF, LVEF 41–49)
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Confirm chronic HFmrEF; if prior LVEF ≤40 → route cardio.hf-improved.core.v1; if decompensated → cardio.acute-hf.core.v1
EF in 41–49 band, no prior ≤40, hemodynamically stable
Patient inputs (19)
Age-adjusted NT-proBNP thresholds + drug tolerability
RAS/ARNi/MRA initiation requires SBP ≥100; monitor for hypotension
BB titration target; AF vs sinus changes BB indication (Cleland IPD 2018)
Weight diary for congestion; loop diuretic titration
eGFR gates SGLT2i (≥20), finerenone (≥25), ACEi/ARNi titration
Finerenone/spironolactone contraindicated K >5.0; baseline before RAS/MRA
HFmrEF gate (LVEF 41–49); migration in/out of band drives re-routing
If LVEF was ever ≤40 → HF-improved (continue HFrEF GDMT), NOT HFmrEF
NYHA II–IV drives visit cadence + advanced-HF thresholds
Ischemic etiology more common in HFmrEF — drives revascularization workup
AF abolishes BB mortality benefit; drives rate/rhythm + AC
CKD stage gates SGLT2i, finerenone, RAS titration
Dual cardiorenal indication — favors SGLT2i + finerenone
Detect existing HF therapy; flag NSAIDs / non-DHP CCB / glitazones
Diagnostic confirmation + monitoring; age-adjusted thresholds
IV iron in symptomatic HF + iron deficiency (AFFIRM-AHF)
Thyroid dysfunction as reversible HF cause/aggravator
DM co-prevalence drives SGLT2i + finerenone selection
AF vs sinus (BB indication), ischemic Q-waves, low-voltage (amyloid)
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (10)
- informationalsevereef_migration_down_to_hfrefSerial echo LVEF falls ≤40 — phenotype migration to HFrEF — Bozkurt 2021; ACC/AHA 2022Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverepregnancy_special_popPregnancy or planning — STOP ACEi/ARB/ARNi/SGLT2i/finerenone/spironolactone; use BB (metoprolol/bisoprolol/labetalol) + loop diuretic; cardio-obstetric team — ESC 2018 PregnancyTrigger could not be auto-evaluated — needs clinician judgement.
- informationalseverehyperkalemia_on_mra_or_rasK ≥5.5 on finerenone/spironolactone/RAS — pause offending agent, treat hyperK, recheck — FINEARTS-HF; ACC/AHA 2022Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateckd_special_popeGFR 20–60 — SGLT2i continue to 20, finerenone start at 10 mg if eGFR 25–60, intensify K monitoring — FINEARTS-HF; KDIGO 2024Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateaf_special_popConcurrent AF — beta-blocker mortality benefit is LOST; prioritise rate/rhythm control + anticoagulation by CHA₂DS₂-VASc; consider early rhythm control — Cleland IPD 2018; EAST-AFNET 4Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderategeriatric_frailty_special_popFrail elderly — simplify regimen, check orthostatic BP before RAS/BB up-titration, STOPP/START review, accept symptom-guided rather than target-dose titrationTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatehepatic_special_popHepatic impairment — sacubitril/valsartan caution Child-Pugh B, contraindicated C; finerenone avoid severe hepatic impairment; spironolactone caution (also used for ascites) — drug labelsTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateischemic_etiology_branchIschemic HFmrEF with angina or viable myocardium — Heart-team revascularization decision (STICH CABG benefit at 10 yr; REVIVED-BCIS2 PCI neutral) — individualiseTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmildef_migration_up_to_hfpefSerial echo LVEF rises ≥50 with no prior ≤40 — migration to HFpEF — Bozkurt 2021Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmilddm2_special_popConcurrent T2DM — SGLT2i + finerenone provide dual cardiorenal-metabolic benefit; add GLP-1 RA for obesity/ASCVD — ADA 2026Trigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
HFmrEF tiered regimen (2023 ESC Focused Update; 2022 AHA/ACC/HFSA)- dapagliflozinfirst lineSGLT2i10 mg • PO • once dailytriggers: LVEF_41_49, eGFR>=20DELIVER NEJM 2022 (PMID 36027570) — worsening-HF/CV-death HR 0.82 (95% CI 0.73–0.92, p<0.001) across LVEF >40 incl. mid-range; consistent <60 vs ≥60% EF; benefit DM-independent; event-curve separation ~13–28 d. DEDICATED evidence. 2023 ESC Class I LOE A / 2022 AHA Class 2arxcui 1488564
- empagliflozinfirst lineSGLT2i10 mg • PO • once dailytriggers: LVEF_41_49, eGFR>=20EMPEROR-Preserved NEJM 2021 (PMID 34449189) — CV-death/HHF HR 0.79 (0.69–0.90, p<0.001) in LVEF >40; total HHF HR 0.73 (0.61–0.88); DM-independent. DEDICATED evidence. 2023 ESC Class I LOE A / 2022 AHA Class 2arxcui 1545653
outpatient playbook — drug actions (5)
- 1. dapagliflozin OR empagliflozin10 mg • PO • dailytrigger: LVEF 41–49, eGFR ≥20, no DKA (2023 ESC Class I)DELIVER NEJM 2022 / EMPEROR-Preserved NEJM 2021
- 2. finerenone10–40 mg • PO • dailytrigger: K ≤5.0, eGFR ≥25 (FINEARTS-HF)FINEARTS-HF NEJM 2024 — RR 0.84 total worsening HF + CV death
- 3. sacubitril/valsartan OR ARB OR ACEiARNi 24/26→97/103 BID • PO • BID/dailytrigger: SBP ≥100, residual symptoms (2022 ACC/AHA Class 2b)PARAGON-HF / CHARM-Preserved / PEP-CHF — stronger at lower EF
- 4. carvedilol OR metoprolol succinate OR bisoprololtitrate to max tolerated • PO • BID/dailytrigger: Sinus rhythm OR angina/AF rate (Cleland IPD 2018)Mortality benefit only in sinus rhythm; neutral in AF
- 5. furosemide / torsemidefurosemide 20–40 mg or torsemide 10–20 mg • PO • daily–BIDtrigger: Volume overload / weight gain >2 kg in 3 daysCongestion control (ACC/AHA 2022 HF)
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Echo LVEF 41–49 — HFmrEF phenotype; Dyspnea on exertion / orthopnea / PND; Lower-extremity edema.
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Heart failure with mildly reduced EF (HFmrEF, LVEF 41–49)** (cardio.hfmref.core.v1). Phenotype framing: HFmrEF vs HFpEF (EF ±5% band) vs HFrEF vs HF-improved vs high-output vs valvular vs infiltrative vs tachycardia-mediated Scope: Confirm chronic HFmrEF; if prior LVEF ≤40 → route cardio.hf-improved.core.v1; if decompensated → cardio.acute-hf.core.v1 No severity triggers fired against current inputs.
Plan
Regimen axis: **HFmrEF tiered regimen (2023 ESC Focused Update; 2022 AHA/ACC/HFSA)** — step "Tier 1 — SGLT2 inhibitor (Class I ESC 2023 / Class 2a AHA 2022 — first-line in ALL HFmrEF regardless of DM; the ONLY dedicated-RCT-grade therapy in the band)". 1. dapagliflozin 10 mg PO once daily (SGLT2i, first line) — DELIVER NEJM 2022 (PMID 36027570) — worsening-HF/CV-death HR 0.82 (95% CI 0.73–0.92, p<0.001) across LVEF >40 incl. mid-range; consistent <60 vs ≥60% EF; benefit DM-independent; event-curve separation ~13–28 d. DEDICATED evidence. 2023 ESC Class I LOE A / 2022 AHA Class 2a 2. empagliflozin 10 mg PO once daily (SGLT2i, first line) — EMPEROR-Preserved NEJM 2021 (PMID 34449189) — CV-death/HHF HR 0.79 (0.69–0.90, p<0.001) in LVEF >40; total HHF HR 0.73 (0.61–0.88); DM-independent. DEDICATED evidence. 2023 ESC Class I LOE A / 2022 AHA Class 2a Setting playbook (outpatient) — Start SGLT2i, layer finerenone/RAS/BB by EF-band evidence weight, treat comorbidities, and serially re-phenotype (2023 ESC Focused Update; 2022 AHA/ACC/HFSA) 3. dapagliflozin OR empagliflozin 10 mg PO daily — LVEF 41–49, eGFR ≥20, no DKA (2023 ESC Class I) (DELIVER NEJM 2022 / EMPEROR-Preserved NEJM 2021) 4. finerenone 10–40 mg PO daily — K ≤5.0, eGFR ≥25 (FINEARTS-HF) (FINEARTS-HF NEJM 2024 — RR 0.84 total worsening HF + CV death) 5. sacubitril/valsartan OR ARB OR ACEi ARNi 24/26→97/103 BID PO BID/daily — SBP ≥100, residual symptoms (2022 ACC/AHA Class 2b) (PARAGON-HF / CHARM-Preserved / PEP-CHF — stronger at lower EF) 6. carvedilol OR metoprolol succinate OR bisoprolol titrate to max tolerated PO BID/daily — Sinus rhythm OR angina/AF rate (Cleland IPD 2018) (Mortality benefit only in sinus rhythm; neutral in AF) 7. furosemide / torsemide furosemide 20–40 mg or torsemide 10–20 mg PO daily–BID — Volume overload / weight gain >2 kg in 3 days (Congestion control (ACC/AHA 2022 HF)) Non-pharmacologic actions: - Sodium <2 g/day; fluid restriction if hyponatraemia/congestion — ACC/AHA 2022 - Cardiac rehab referral — ACC/AHA 2022 - Revascularization decision in ischemic HFmrEF (Heart-team; STICH vs REVIVED context) - Vaccinations (flu, pneumococcal, COVID, RSV) — ACC/AHA 2022 - AF rhythm-control / catheter ablation discussion (EAST-AFNET 4 early rhythm control) AVOID / contraindication checks: - Finerenone block if K gt 5.0 or eGFR lt 25 — FINEARTS HF Solomon NEJM 2024 - Spironolactone block if K gt 5.0 — TOPCAT Pitt NEJM 2014 - Sglt2i block if egfr lt 20 or active DKA — DELIVER Solomon NEJM 2022 - Arni acei arb block in pregnancy — fetotoxic RAS blockade - Sglt2i finerenone spironolactone block in pregnancy — inadequate safety data - Bb no mortality benefit in AF — Cleland IPD Eur Heart J 2018 - Angioedema arni history block — PARAGON HF Solomon NEJM 2019 - Aki rasi pause if Cr rise gt 30pct — ACC/AHA 2022 HF
Monitoring
Regimen monitoring: - BMP 1-2wk after RAS or MRA change — ACC/AHA 2022 - K within 4w of finerenone start and after each titration — FINEARTS-HF Solomon NEJM 2024 - serial echo 3-6mo for phenotype migration — Universal Definition Bozkurt 2021 - NT-proBNP q3-6m or after decompensation — ACC/AHA 2022 - weight daily at home — ACC/AHA 2022 - iron panel q6m until repleted — AFFIRM-AHF Ponikowski Lancet 2020 - BP HR rhythm at each visit BB indication depends on sinus vs AF — Cleland IPD 2018 Setting (outpatient) monitoring: - BMP 1–2 wk after RAS/MRA change, then q3m steady state — ACC/AHA 2022 - Serial echo at 3–6 mo — re-phenotype to HFrEF (≤40) or HFpEF (≥50) — Bozkurt 2021 - NT-proBNP q3–6 mo — ACC/AHA 2022 - Daily home weight; alert if >2 kg in 3 days — ACC/AHA 2022 Follow-up plan: Cardiac rehab, vaccinations, re-phenotype: re-route to HFrEF if EF ≤40 or HFpEF if EF ≥50 - Close-out criterion: follow-up scheduled with re-phenotype trigger documented Monitoring phase: BMP within 1–2 wk of RAS/MRA change; weight diary; serial echo 3–6 mo for phenotype migration; NT-proBNP q3–6 mo
Disposition
Current setting: outpatient — Start SGLT2i, layer finerenone/RAS/BB by EF-band evidence weight, treat comorbidities, and serially re-phenotype (2023 ESC Focused Update; 2022 AHA/ACC/HFSA) Disposition criteria: - Stable NYHA I–II on tolerated regimen → q6–12 mo visits with annual echo - Symptomatic / recently titrated → q1–3 mo visits - Phenotype migration out of 41–49 band → re-route dossier Escalation triggers (move to higher acuity): - Echo LVEF falls ≤40 → route cardio.hfref.core.v1 + start 4-pillar GDMT — ACC/AHA 2022 - NYHA IV / refractory congestion → advanced HF referral — ACC/AHA 2022 - SBP <90 + hypoperfusion → ED + cardio.cardiogenic-shock.core.v1 — ACC/AHA 2022
Patient Action Plan
**HFmrEF action plan (weight + dyspnea zones) — ACC/AHA 2022** Personalised values: dry_weight_kg, home_diuretic, home_diuretic_rescue_dose, NYHA_baseline. **All clear — at dry weight, baseline activity — ACC/AHA 2022** (green): Triggers: - Weight within 1 kg of dry weight — ACC/AHA 2022 - No new dyspnea, orthopnea, PND, or edema — ACC/AHA 2022 - Usual activity tolerance — ACC/AHA 2022 Actions: - Take all HF meds (SGLT2i, finerenone/MRA, RAS, BB) every day — ACC/AHA 2022 - Sodium <2 g/day; daily weight same time after voiding — ACC/AHA 2022 - Keep clinic + lab + echo appointments (re-phenotype echo) — Bozkurt 2021 **Caution — early congestion or symptom drift — ACC/AHA 2022** (yellow): Triggers: - Weight up 2 kg in 3 days OR 2.5 kg in a week — ACC/AHA 2022 - New ankle/leg swelling — ACC/AHA 2022 - Extra pillow to sleep or waking short of breath — ACC/AHA 2022 - Reduced exercise tolerance — ACC/AHA 2022 Actions: - Take prescribed rescue diuretic dose per action plan — ACC/AHA 2022 - Recheck weight + symptoms in 24 h — ACC/AHA 2022 - Tighten sodium and fluid intake — ACC/AHA 2022 - Call HF clinic / PCP within 24–48 h — ACC/AHA 2022 Contact provider when: - No return to dry-weight range after 48 h rescue diuretic — ACC/AHA 2022 - Any worsening symptoms despite rescue diuretic — ACC/AHA 2022 **Medical alert — severe decompensation — ACC/AHA 2022** (red): Triggers: - Severe shortness of breath at rest — ACC/AHA 2022 - Cannot lie flat / cannot sleep due to breathlessness — ACC/AHA 2022 - New chest pain or pressure — ACC/AHA 2022 - Confusion, fainting, or near-fainting — ACC/AHA 2022 Actions: - Call 911 / emergency services immediately — ACC/AHA 2022 - Sit upright; do not drive yourself — ACC/AHA 2022 - Bring medication list + weight diary — ACC/AHA 2022 Contact provider when: - Any red-zone symptom — go to ED now — ACC/AHA 2022
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [SEVERE] Serial echo LVEF falls ≤40 — phenotype migration to HFrEF — Bozkurt 2021; ACC/AHA 2022 - [SEVERE] Pregnancy or planning — STOP ACEi/ARB/ARNi/SGLT2i/finerenone/spironolactone; use BB (metoprolol/bisoprolol/labetalol) + loop diuretic; cardio-obstetric team — ESC 2018 Pregnancy - [SEVERE] K ≥5.5 on finerenone/spironolactone/RAS — pause offending agent, treat hyperK, recheck — FINEARTS-HF; ACC/AHA 2022
Citations
- 2022 AHA/ACC/HFSA HF Guideline + 2023 ESC Focused Update on HF + 2021 Universal Definition of HF (Bozkurt) [PMID:35363499](https://pubmed.ncbi.nlm.nih.gov/35363499/) - Cited evidence (PMID 35379503) [PMID:35379503](https://pubmed.ncbi.nlm.nih.gov/35379503/) - Cited evidence (PMID 37622666) [PMID:37622666](https://pubmed.ncbi.nlm.nih.gov/37622666/) - Cited evidence (PMID 33605000) [PMID:33605000](https://pubmed.ncbi.nlm.nih.gov/33605000/) - Cited evidence (PMID 36027570) [PMID:36027570](https://pubmed.ncbi.nlm.nih.gov/36027570/) Last reconciled with current guidelines: 2026-05-26.
- 2022 AHA/ACC/HFSA HF Guideline + 2023 ESC Focused Update on HF + 2021 Universal Definition of HF (Bozkurt) — PMID:35363499
- Cited evidence (PMID 35379503) — PMID:35379503
- Cited evidence (PMID 37622666) — PMID:37622666
- Cited evidence (PMID 33605000) — PMID:33605000
- Cited evidence (PMID 36027570) — PMID:36027570