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Clinician Article

Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Heart Failure : A Systematic Review and Meta-analysis.



  • Zou X
  • Shi Q
  • Vandvik PO
  • Guyatt G
  • Lang CC
  • Parpia S, et al.
Ann Intern Med. 2022 Jun;175(6):851-861. doi: 10.7326/M21-4284. Epub 2022 Apr 12. (Review)
PMID: 35404670
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Disciplines
  • Internal Medicine
    Relevance - 7/7
    Newsworthiness - 5/7
  • Family Medicine (FM)/General Practice (GP)
    Relevance - 6/7
    Newsworthiness - 6/7
  • General Internal Medicine-Primary Care(US)
    Relevance - 6/7
    Newsworthiness - 6/7
  • Cardiology
    Relevance - 6/7
    Newsworthiness - 5/7

Abstract

BACKGROUND: Randomized controlled trials established the cardiac protection of sodium-glucose cotransporter-2 (SGLT2) inhibitors among adults with type 2 diabetes. New evidence suggests that these results could extend to people without diabetes.

PURPOSE: To evaluate the effect of SGLT2 inhibitors in patients with heart failure, regardless of the presence of type 2 diabetes.

DATA SOURCES: PubMed, Web of Science, Cochrane Library, and Embase (OVID interface).

STUDY SELECTION: Eligible trials randomly assigned adults with heart failure to SGLT2 inhibitors or control.

DATA EXTRACTION: Time-to-event individual patient data were reconstructed from published Kaplan-Meier plots; time-varying risk ratios (RRs) were calculated in half-, 1-, and 2-year time frames; and anticipated absolute benefits were calculated using simple models applying relative effects to baseline risks.

DATA SYNTHESIS: Sodium-glucose cotransporter-2 inhibitors reduce hospitalization for heart failure by 37% (95% CI, 25% to 47%) at 6 months, 32% (CI, 20% to 42%) at 1 year, and 26% (CI, 10% to 40%) at 2 years (all high certainty) and reduce cardiovascular death by 14% (CI, 1% to 25%) at 1 year (high certainty). Nevertheless, low-certainty evidence did not indicate protection against all-cause death, kidney disease progression, or kidney failure. Anticipated absolute benefits are greater for patients treated in the first year and for those with poorer prognoses, such as those newly diagnosed with heart failure in the hospital. In addition, SGLT2 inhibitors doubled the risk for genital infections (RR, 2.69 [CI, 1.61 to 4.52]; high certainty).

LIMITATION: Covariates were unavailable in meta-analyses with reconstructed individual patient data.

CONCLUSION: Among people with heart failure, SGLT2 inhibitors reduce hospitalizations for heart failure regardless of the presence of diabetes; absolute benefits are most pronounced in first-year treatment and vary with prognostic factors. Clinicians should note the increased risk for genital infection in patients receiving SGLT2 inhibitors.

PRIMARY FUNDING SOURCE: 1.3.5 Project for Disciplines of Excellence, West China Hospital of Sichuan University. (PROSPERO: CRD42021255544).


Clinical Comments

Family Medicine (FM)/General Practice (GP)

This was a systematic review done by the highest standards and includes RCTs of adults with diagnosed heart failure who were treated with SGLT2 inhibitors. The SGLT2 inhibitors reduced many important outcomes, but also caused an increase in genital infections. As a primary care physician, I wish the absolute benefits and harms were emphasized in the study over the relative benefits and harms.

General Internal Medicine-Primary Care(US)

This is highly relevant and practice-changing evidence on a new treatment for a prevalent condition that is currently under-treated with this class of agents.

Internal Medicine

The only outcome that is clearly much better is symptoms / hospitalizations. It is unclear to me that there are not other less expensive ways to improve this outcome, which is probably due to improved diuresis.

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