Evidence map›Paper›PMID 41527619›Full record

ArticleCureus2025

Impact of Sodium-Glucose Co-transporter 2 Inhibitors After Discharge in Patients With Heart Failure With Reduced Activities of Daily Living: A Single-Center Retrospective Cohort Study.

Masanori Suzuki, Shintaro Akiyama, Hiroshi Saito, Hiroki Matsui, Ryohkan Funakoshi

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Masanori SuzukiFaculty of Pharmaceutical Sciences, Teikyo Heisei University, Nakano, JPN.
Shintaro AkiyamaDepartment of Pharmacy, Kameda Medical Center, Kamogawa, JPN.
Hiroshi SaitoDepartment of Rehabilitation, Kameda Medical Center, Kamogawa, JPN.
Hiroki MatsuiClinical Research Support Division, Kameda Medical Center, Kamogawa, JPN.
Ryohkan FunakoshiDepartment of Pharmacy, Kameda Medical Center, Kamogawa, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSodium-glucose co-transporter 2 (SGLT2) inhibitors benefit patients with heart failure (HF) with reduced ejection fraction (HFrEF), as well as preserved EFs (HFpEF). Frailty increases the risk of treatment intolerance and adverse events. SGLT2 inhibitors have demonstrated cognitive and clinical benefits, even in cases of severe frailty. However, there is limited evidence regarding its effects post-hospitalization in patients with reduced activities of daily living (ADL). This study investigated whether declining ADL affects SGLT2 inhibitor efficacy in reducing one-year all-cause and HF-specific readmissions.

methodsThis single-center, retrospective cohort study analyzed patients with HF admitted to Kameda General Hospital from December 2020 to February 2022. Eligible patients were discharged without major interventions and were stratified into four groups based on frailty (Barthel Index (BI): < 85) and whether they were prescribed an SGLT2 inhibitor at discharge. Demographic data, comorbidities, laboratory results, medications, and echocardiographic findings were collected. The primary endpoint was one-year HF rehospitalization, while secondary endpoints included all-cause hospitalization and mortality. One-way analysis of variance and chi-square (χ²) tests were used to compare group differences, and logistic regression with inverse probability of treatment weighting (IPTW) was applied to adjust for confounders.

resultsWe analyzed 188 patients with HF after excluding 81 based on the eligibility criteria. Patients were stratified into frail (BI < 85, n = 78) and non-frail (BI ≥ 85, n = 110) groups, with the further subdivision based on SGLT2 inhibitor prescription. The frail group was older and had lower renal function, whereas the non-frail group had higher hemoglobin A1c levels and often lived alone. In unadjusted results, SGLT2 inhibitors increased the readmission rate in frail patients. After IPTW adjustment to reduce bias, the results aligned with the unadjusted findings, confirming that frailty and SGLT2 inhibitors significantly influenced outcomes, with a standardized mean difference imbalance in selected variables.

conclusionsThe findings of this study support the cautious use of SGLT2 inhibitors in patients with HF with a BI < 85 at discharge. While these drugs reduced HF rehospitalization in patients with frailty, they also increased the overall rehospitalization rate, likely due to their side effects.

Indexed as

barthel indexfrailtyheart failurereadmissionsglt2 inhibitors

Identifiers

PMID41527619
PMCPMC12790576

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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 OpenQuestion graph.