Evidence mapPaperPMID 39948563Full record

SynthesisCardiovascular diabetology2025

Impact of sodium‒glucose cotransporter-2 inhibitors in patients with recent versus previous myocardial infarction: a systematic review and meta-analysis.

Pedro Gabriel Scardini, Eric Shih Katsuyama, Alonzo Armani Prata, Julia Marques Fernandes, Christian Ken Fukunaga, Wilson Falco Neto, Ana Carolina Covre Coan, Naieli Machado de Andrade, Abraão Santana Silva, Rafael Petri Pinheiro and 2 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Cardiovascular diabetology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Pedro Gabriel ScardiniHigher School of Sciences of the Holy House of Mercy of Vitória, Av. Nossa Sra. da Penha, 2190 - Santa Luíza, Vitória, ES, 29045-402, Brazil. pgscardinims@gmail.com.ORCID 0009-0007-6323-5711
Eric Shih KatsuyamaDepartment of Medicine, FMABC University Centre, São Paulo, Brazil.
Alonzo Armani PrataFederal University of Espírito Santo, Vitória, Brazil.
Julia Marques FernandesFaculdade Israelita de Ciências da Saúde Albert Einstein, São Paulo, Brazil.
Christian Ken FukunagaDepartment of Medicine, FMABC University Centre, São Paulo, Brazil.
Wilson Falco NetoFAMECA University Center, Catanduva, São Paulo, Brazil.
Ana Carolina Covre CoanFederal University of Espírito Santo, Vitória, Brazil.
Naieli Machado de AndradeEBMSP, Bahiana School of Medicine and Public Health, Salvador, Brazil.
Abraão Santana SilvaUniversity of Rio Verde, Brasília, Brazil.
Rafael Petri PinheiroFederal University of Rio de Janeiro, UFRJ, Rio de Janeiro, Brazil.
Luciana Gioli PereiraFaculdade Israelita de Ciências da Saúde Albert Einstein, São Paulo, Brazil.
Remo H M FurtadoBrazilian Clinical Research Institute, Sao Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSodium‒glucose cotransporter 2 (SGLT2) inhibitors have been included in heart failure (HF) guidelines because of their benefits in reducing mortality and hospitalization rates. However, the timing and benefits of initiating SGLT2 inhibitors in patients after myocardial infarction (MI) remain controversial. Therefore, we aimed to perform a systematic review and meta-analysis comparing SGLT2 inhibitors with placebo in patients with MI.

methodsWe performed a systematic review and meta-analysis to determine the impact of SGLT2 inhibitors in patients with recent or previous MI. We systematically searched PubMed, Cochrane, and Embase for RCTs comparing SGLT2 inhibitors versus placebo in patients with MI. The primary outcome was (1) HF hospitalization. In this analysis, we also included the following secondary outcomes: (2) major adverse cardiovascular events (MACE) defined as a composite of cardiovascular (CV) death, MI or stroke; and (3) all-cause mortality. A subgroup analysis was conducted for the primary outcome, comparing patients who had experienced an MI more than 8 weeks prior to study enrolment (previous MI) versus those who had experienced an MI within the preceding 8 weeks (acute MI). Risk ratios (RRs) and 95% confidence intervals (CIs) were pooled with a random effects model.

resultsOur meta-analysis included 10 RCTs comprising 22,266 patients, of whom 11,339 (51.2%) had type 2 diabetes. The mean age was 62 years, and the median follow-up was 21 months. According to the pooled analysis, HF hospitalization rates were lower in patients on SGLT2 inhibitors compared with placebo (RR 0.77; 95% CI 0.69, 0.85; p < 0.001)). Differences in MACE were also observed in favor of SGLT2 inhibitors versus placebo (RR 0.88; 95% CI 0.79, 0.97; p = 0.012). There was no statistically significant difference in all-cause mortality between the groups (RR 0.88; 95% CI 0.78, 1.00; p = 0.058). Benefits of SGLT2 inhibitors for the primary outcome were consistent regardless of the timing of last MI, with no treatment by subgroup interaction (p for interaction = 0.56).

conclusionIn this meta-analysis of patients who experienced MI, the administration of SGLT2 inhibitors was associated with lower rates of hospitalization for HF. In addition, the treatment effect of SGLT2 inhibitors was consistent regardless of whether they were started in the recent versus previous MI setting.

Indexed as

Diabetes Mellitus, Type 2Heart FailureMyocardial InfarctionSodium-Glucose Transporter 2 InhibitorsAgedFemaleHospitalizationHumansMaleMiddle AgedRandomized Controlled Trials as TopicRecurrenceRisk AssessmentRisk FactorsTime FactorsTreatment OutcomeSodium-Glucose Transporter 2 InhibitorsCardiovascular riskMyocardial infarctionSodium‒glucose cotransporter 2 inhibitorsSystematic review and meta-analysis

Identifiers

PMID39948563
PMCPMC11827181

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.