Cost-Effectiveness of Sodium-Glucose Cotransporter-2 Inhibitors and Angiotensin Receptor-Neprilysin Inhibitors in Addition to Standard Treatment of Chronic Heart Failure: A Systematic Review and Meta-Analysis.

Value HealthApr 8, 2026 (epub)
Clinical ResearchCardiology

Nattakrit Tongpoonsakdi, Amarit Tansawet, Teerapat Yingchoncharoen et al.

✦ AI-curated · Sources linked

In 30 seconds

This systematic review and random-effects meta-analysis assessed the cost-effectiveness of adding SGLT2 inhibitors and/or angiotensin receptor-neprilysin inhibitors to traditional guideline-directed therapy for chronic heart failure. It included 70 economic evaluations identified through October 2024 and compared results by heart failure phenotype, country income level, and analytic perspective. For HFrEF in high-income countries, adding an SGLT2 inhibitor was cost-effective from the healthcare perspective, with a pooled incremental net benefit of US $13 114.52 (95% CI: 4257.40-21 971.63). Findings for other phenotypes and income settings were often inconclusive.

Key findings

  • For HFrEF in high-income countries, adding an SGLT2 inhibitor had a pooled healthcare-perspective INB of US $13 114.52 (95% CI: 4257.40-21 971.63).
  • The SGLT2 inhibitor plus ARNI quadruple regimen appeared cost-effective in high- and upper-middle-income countries, but evidence was limited.
  • Replacing other renin-angiotensin-aldosterone system blockers with ARNI was cost-effective only for HFrEF from a societal perspective in high-income countries (INB = US $14 843.66; 95% CI: 566.36-29 120.96).
  • Evidence for SGLT2 inhibitors in upper-middle- or lower-income countries and for other heart failure phenotypes was inconclusive.

Why it matters

Economic value of newer heart failure therapies may differ by phenotype, country income level, and analytic perspective. These findings suggest that cost-effectiveness evidence is most supportive for HFrEF in high-income settings, while uncertainty remains elsewhere. This distinction is relevant when interpreting economic evaluations and considering how well their conclusions apply across health systems.

What to keep in mind

Evidence was limited for the quadruple regimen and inconclusive for several phenotypes and income settings. Some variances were imputed when not available in the included evaluations.

Source

Published in Value Health. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Cardiology

Clinical ResearchOncology (Medical)

Zamtocabtagene autoleucel, a tandem CD20-CD19-directed CAR T-cell therapy, for second line treatment of large B-cell lymphoma in patients ineligible for transplantation (DALY 2-EU): primary analysis of an open-label, multicentre, randomised phase 2 study.

DALY 2-EU was an open-label, multicentre, randomised phase 2 trial comparing tandem CD20-CD19-directed zamtocabtagene autoleucel (zamto-cel) with R-GemOx in adults with second-line relapsed or refractory large B-cell…

Lancet OncolOct 27, 2026Read summary
Clinical ResearchOncology (Medical)

Neoadjuvant short-course radiotherapy followed by camrelizumab and chemotherapy versus standard of care for locally advanced rectal cancer (UNION): a prespecified interim analysis of a multicentre, open-label, randomised, phase 3 trial.

UNION was a multicentre, open-label, randomised phase 3 trial at nine hospitals in China comparing neoadjuvant short-course radiotherapy followed by camrelizumab plus CAPOX with long-course chemoradiotherapy followed by…

Lancet OncolOct 25, 2026Read summary
Clinical ResearchHematology

Efficacy and safety of mitapivat in patients with sickle cell disease (RISE UP): a phase 3, double-blind, global, randomised, placebo-controlled trial.

RISE UP was a phase 3, double-blind, global, randomised, placebo-controlled trial conducted at 69 sites in 15 countries. It evaluated twice-daily mitapivat in patients older than 16 years with sickle cell disease…

LancetOct 24, 2026Read summary

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.