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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.
RapidHFmrEFHFpEFdiastolic dysfunctionSGLT2 inhibitorMRA

Heart failure with mildly reduced or preserved ejection fraction

Essential points for quick revision.

Synopsis

Confirm HFmrEF or HFpEF rather than diagnosing by EF alone, relieve congestion and apply the NICE 2025 phenotype-specific medicine combinations.

  • NICE defines HFmrEF as symptomatic HF with LVEF 41–49%; HFpEF requires symptomatic HF with LVEF at least 50% plus structural/functional evidence, not a normal EF alone.
  • For HFmrEF, consider an ACE inhibitor, beta-blocker, MRA and SGLT2 inhibitor; use an ARB instead of ACE inhibitor when ACE intolerance applies.
  • For HFpEF, consider an MRA plus an SGLT2 inhibitor under the NICE 2025 update.

Key red flags

Acute decompensation

Rest dyspnoea, hypoxaemia, rapid oedema/weight change or hypoperfusion needs urgent acute-HF assessment despite preserved EF.

Investigation priorities

01
NT-proBNPFirst step

Triage suspected HF using the NICE chronic-HF route.

Management branches

First-lineConfirm phenotype

Suspected HF with LVEF above 40%

  1. Use NT-proBNP to triage and obtain expert echo; assess structural/filling criteria rather than using EF alone.
  2. Exclude mimics and identify congestion, AF, BP, valve/coronary disease, renal disease, diabetes, obesity and pulmonary contributors.

Key medicines

Dapagliflozin10 mg orally once daily.
SpironolactoneA typical HF start is 25 mg orally once daily; use lower/alternate-day dosing or cautious titration according to renal function, potassium, BP and frailty.
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Sources and review status6 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom