Key result
Early SGLT2i plus MRA initiation in suspected HF linked to avoiding ~84 events per 1000 patients.
Why the study?
Does the early initiation of an SGLT2i and/or MRA reduce the risk of HF hospitalization or death in community-based patients with suspected HF and elevated NT-proBNP?
Cohort (n=74,945)
Does the early initiation of an SGLT2i and/or MRA reduce the risk of HF hospitalization or death in community-based patients with suspected HF and elevated NT-proBNP?
Answers are grounded in this paper and cite their sources.
Early initiation of SGLT2i and MRA in patients with suspected HF and elevated NT-proBNP who have non-HF indications for these drugs may substantially reduce early adverse outcomes while awaiting diagnostic echocardiography.
The initiation of heart failure (HF) therapies at the time of detection of an elevated N-terminal pro-B-type natriuretic peptide (NT-proBNP) level in community-based patients with suspected HF may reduce the risk of early adverse outcomes. The aim of this analysis was to estimate the potential benefit of the early initiation of a sodium-glucose cotransporter 2 inhibitor (SGLT2i) and/or mineralocorticoid receptor antagonist (MRA) in patients with suspected HF and a preexisting non-HF-related indication for treatment. A cohort study was performed from 01/01/2015 to 31/03/2023 using linked primary and secondary care data from the Clinical Practice Research Datalink (CPRD). Patients without a history of HF and who were not prescribed an SGLT2i or MRA, were followed up for 12 months following a community-measured NT-proBNP ≥400 pg/mL. The primary outcome was a composite of a HF hospitalization as the first recorded HF diagnostic event, or death from any cause in patients without a documented HF diagnosis during follow-up and who did not undergo echocardiography. The effect of the initiation of treatment with an SGLT2i, MRA, or both (effective treatments for HF regardless of ejection fraction) was modelled at the time of NT-proBNP measurement in patients with a preexisting non-HF-related indication for these drugs (type 2 diabetes, chronic kidney disease, or resistant hypertension) using treatment effect estimates from meta-analyses of randomised placebo-controlled trials in patients with established HF. An NT-proBNP ≥400 pg/mL was recorded in 74945, 24082 (32%) of whom had a HF diagnosis recorded within 12 months; 15398 (67%) as an outpatient and 8684 (33%) during a HF hospitalization. If both an SGLT2i and MRA were commenced at the measurement of an elevated NT-proBNP in those with a preexisting non-HF-related indication, we estimated that for every 1000 patients treated, 84 would avoid either a HF hospitalization or death at 12 months, equating to a number needed to treat of 12 (95% confidence interval 11-14). In community-based patients with suspected HF and elevated NT-proBNP, the early initiation of an SGLT2i and an MRA in patients with a pre-existing non-HF-related indication for treatment may reduce the risk of early adverse outcomes whilst awaiting diagnostic echocardiography. These findings suggest a simple clinical strategy with potentially large public health benefits.
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Docherty et al. (2025) conducted a cohort in suspected heart failure (n=74,945). Early initiation of SGLT2i and MRA vs. No early initiation was evaluated on Composite of HF hospitalization as the first recorded HF diagnostic event, or death from any cause in patients without a documented HF diagnosis during follow-up and who did not undergo echocardiography (NNT 12, 95% CI 11-14). Modeling early initiation of an SGLT2i and MRA in patients with suspected heart failure and elevated NT-proBNP estimated an avoidance of 84 events per 1000 patients treated (NNT 12; 95% CI 11-14).
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