Cardiometabolic & kidney

Effects of sodium-glucose co-transporter 2 inhibitors on heart failure events in chronic kidney disease: a systematic review and meta-analysis

Eur Heart J Cardiovasc PharmacotherPublished Systematic review and meta-analysis of randomised trials

Pooled result · HF events in CKDResult — go to the resultHazard ratio 0.68 95% CI 0.63–0.73

Authors' conclusion

Treatment with SGLT-2 inhibitors led to a significant reduction in HF events in patients with CKD.

Study context

Population
Patients with chronic kidney disease (CKD) at baseline or subgroups stratified by baseline estimated glomerular-filtration-rate (eGFR)
Participants
89,191 patients12 studies
Comparison
SGLT2 inhibitors vs placebo
Outcome
Time to hospitalisation or urgent visit for worsening HF

Pooled result

HF events in CKD

Hazard ratio

0.68

95% CI 0.63–0.73

SGLT-2 inhibitorsvs Placebo
HR 0.68 (95% CI 0.63–0.73)

As reported in the abstract

Further pooled results

OutcomeHR (95% CI)
HF events by baseline eGFR (subgroup)SGLT-2 inhibitorsvs PlaceboeGFR <60 ml/min/1.73 m²0.68 (0.62–0.74)
HF events by baseline eGFR (subgroup)SGLT-2 inhibitorsvs PlaceboeGFR ≥60 ml/min/1.73 m²0.76 (0.69–0.83)

Heart failure (HF) events by type of SGLT-2 inhibitor (subgroup)

Consistent treatment effect across all studied agents
p-subgroup-analysis = 0.44

HF events, eGFR <60 ml/min/1.73 m², studies of diabetic patients only (sensitivity analysis)

Even more pronounced effect in eGFR subgroup <60 ml/min/1.73 m²
HR 0.62; 95% CI 0.54-0.70
  • Sensitivity analysis

Original publication

Effects of sodium-glucose co-transporter 2 inhibitors on heart failure events in chronic kidney disease: a systematic review and meta-analysis. Eur Heart J Cardiovasc Pharmacother. Published 13 January 2024. doi:10.1093/ehjcvp/pvae003

Composed by AI from the published abstract and checked against it. How Briefs are made →

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