Evidence map›Paper›PMID 39271992›Full record

SynthesisBMC cardiovascular disorders2024

Comparative effectiveness and safety of eplerenone and spironolactone in patients with heart failure: a systematic review and meta-analysis.

Ahmed Elshahat, Ahmed Mansour, Mohamed Ellabban, Ahmed Diaa, Atef Hassan, Ahmed Fawzy, Omar Abdulrahman Saad, Moaz Abouelmagd, Mahmoud Eid, Ahmed Elaraby and 2 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC cardiovascular disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  12. Cardiac fibrosis: from mechanisms and models to medicines.Trends in pharmacological sciences · 2025
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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.

Ahmed ElshahatMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA. Ahmedeshahat98@gmail.com.ORCID 0009-0009-0042-6101
Ahmed MansourMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Mohamed EllabbanMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Ahmed DiaaMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Atef HassanMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Ahmed FawzyMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Omar Abdulrahman SaadMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Moaz AbouelmagdMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Mahmoud EidMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Ahmed ElarabyMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Mohamed Hamouda ElkasabyMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.
Ahmed AbdelazizMedical Research Group of Egypt (MRGE), Negida Academy, Arlington, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEplerenone and spironolactone, recognized as mineralocorticoid receptor antagonists (MRAs), have been reported to improve clinical prognosis among individuals diagnosed with heart failure (HF). However, the difference in the clinical effects between eplerenone and spironolactone in individuals with HF remains uncertain. We aimed to assess the impact of eplerenone compared to spironolactone on clinical outcomes within the HF population.

methodsAn extensive search was executed in several databases (PubMed, Web of Science, Scopus, Cochrane Library). All relevant studies evaluating eplerenone compared to spironolactone in patients with HF were included. Dichotomous data were pooled as Hazard ratio (HR) or Risk ratio (RR) with a 95% confidence interval (CI). Our main outcome was all-cause mortality. Secondary outcomes included death from cardiovascular causes, treatment withdrawal, and gynecomastia.

resultsTen studies, comprising 21,930 HF individuals, were included in our investigation. Eplerenone showed a lower risk of all-cause mortality (HR = 0.78, 95%CI [0.64 to 0.94], P = 0.009) and cardiovascular mortality (HR = 0.54, 95%CI [0.39, 0.74], P = 0.0001) compared to spironolactone. Furthermore, eplerenone exhibited a reduced risk of treatment withdrawal (RR = 0.69, 95% CI [0.62, 0.78], P = 0.0001) and gynecomastia (RR = 0.07, 95% CI [0.02 to 0.31], P = 0.0001) than spironolactone.

conclusionEplerenone revealed lower all-cause and cardiovascular mortality events in comparison to spironolactone. Moreover, eplerenone was associated with lower gynecomastia and treatment withdrawal events compared to spironolactone. Further well-designed randomized controlled trials are still warranted better to identify the clinical differences between eplerenone and spironolactone.

trial registrationProtocol registration: https://doi.org/10.17605/OSF.IO/VNMGK.

Indexed as

EplerenoneGynecomastiaHeart FailureMineralocorticoid Receptor AntagonistsSpironolactoneAdultAgedAged, 80 and overCause of DeathFemaleHumansMaleMiddle AgedRecovery of FunctionRisk AssessmentRisk FactorsEplerenoneMineralocorticoid Receptor AntagonistsSpironolactoneEplerenoneHeart failureMineralocorticoid receptor antagonistMRASpironolactone

Identifiers

PMID39271992
PMCPMC11395778

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.