Key result
SGLT2 inhibitors fail to significantly reduce mortality in pediatric and adolescent heart failure.
Why the study?
SGLT2 inhibitors are increasingly prescribed off-label for pediatric heart failure, but pediatric outcomes have never been pooled.
Do SGLT2 inhibitors improve clinical outcomes and echocardiographic parameters in children and adolescents with heart failure?
Meta-Analysis (n=696)
Do SGLT2 inhibitors improve clinical outcomes and echocardiographic parameters in children and adolescents with heart failure?
Relative Risk: 0.8 (95% CI 0.11–6.07)
SGLT2 inhibitors in pediatric heart failure are associated with improvements in left ventricular ejection fraction and have a reassuring safety profile, though comparative data on hard clinical endpoints remains limited.
Supports cautious off-label SGLT2 inhibitor use in pediatric HF with low adverse events; first pooled evidence extends adult data but leaves efficacy open.
Sodium-glucose cotransporter-2 (SGLT2) inhibitors are a cornerstone of adult heart failure (HF) therapy and are increasingly prescribed off-label to children, yet pediatric outcomes have never been pooled. We searched PubMed/MEDLINE, Embase, Scopus, and Web of Science to 14 August 2026 for studies of any SGLT2 inhibitor in children or adolescents with HF and performed a single-arm meta-analysis of all exposed patients and a pairwise meta-analysis of the comparative studies with random-effects models. Nine studies contributed 599 exposed patients and 97 controls. Pooled rates were 3.8% (95% confidence interval [CI] 1.6–8.4) for mortality, 8.5% (6.2–11.5) for transplantation, 11.2% (8.2–15.1) for worsening HF, 0.2% (0.03–1.6) for ketoacidosis, 4.5% (1.2–14.9) for acute kidney injury, 3.7% (1.1–11.7) for urinary tract infection, and 4.1% (1.4–11.2) for discontinuation because of an adverse event. After initiation, left ventricular ejection fraction rose by 7.7 percentage points (3.6–11.8) and natriuretic peptide fell by 0.42 standard deviations (0.34–0.49). In the comparative synthesis (63 exposed, 97 unexposed), risk ratios were 0.80 (0.11–6.07) for mortality and 0.21 (0.03–1.68) for worsening HF; ejection fraction improved 3.34 percentage points more with SGLT2 inhibitors (0.22–6.46) whereas natriuretic peptide did not differ (standardized mean difference −0.09, −0.50 to 0.33).
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Aldossary et al. (2026) conducted a meta-analysis in Heart failure (n=696). Sodium-glucose cotransporter-2 (SGLT2) inhibitors vs. Controls was evaluated on Mortality (RR 0.80, 95% CI 0.11-6.07). SGLT2 inhibitors in children and adolescents with heart failure were associated with a risk ratio of 0.80 (95% CI 0.11-6.07) for mortality compared to unexposed controls.
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