Evidence map›Paper›PMID 40858368›Full record

Observational studyBMJ open2025

Guideline-directed medical therapy and in-hospital mortality in acute coronary syndrome patients with advanced renal dysfunction: analysis of two nationwide retrospective cohort studies.

Zhengyang Jin, Geru Aa, Yifan Guo, Hangkuan Liu, Haonan Sun, Zhi Li, Min Ma, Gregg Fonarow, Yuxia Gao, Dong Zhao and 3 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Zhengyang Jin *Department of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Geru Aa *Department of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Yifan Guo *Department of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Hangkuan LiuDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Haonan SunDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Zhi LiDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Min MaBay-max Technology Corporation, Beijing, China.
Gregg FonarowUniversity of California Los Angeles, Los Angeles, California, USA.
Yuxia GaoDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China.
Dong ZhaoBeijing Anzhen Hospital Affiliated to Capital Medical University Center for Clinical and Epidemiologic Research, Beijing, Beijing, China.ORCID http://orcid.org/0000-0002-3239-3449
Qing YangDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China xinzhou@tmu.edu.cn cardio-yq@tmu.edu.cn.
Xin ZhouDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, Tianjin, China xinzhou@tmu.edu.cn cardio-yq@tmu.edu.cn.ORCID http://orcid.org/0000-0001-5305-4975
CCC-AF investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe purpose of this study was to verify whether guideline-directed medical therapy (GDMT, ie, the combined use of β-blocker, ACE inhibitor/angiotensin receptor blocker, dual antiplatelet drugs and statin) could improve in-hospital mortality in acute coronary syndrome (ACS) patients with advanced renal dysfunction (estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m

designRetrospective cohort study.

settingThis study used data from two large, multicentre, observational cohorts: the Chinese National Electronic Disease Surveillance System Platform (CNEDSSP) and the Improving Care for Cardiovascular Disease in China-ACS (CCC-ACS) project. These cohorts consist of ACS patients admitted to 47 and 241 hospitals, respectively, across China from 2014 to 2019.

participantsA total of 6260 patients diagnosed with advanced renal dysfunction (eGFR <30 mL/min/1.73 m²) on admission were included in the analysis. Among these, 3013 patients were from the CNEDSSP cohort and 3247 from the CCC-ACS cohort. Patients were categorised based on receipt of GDMT within 24 hours of admission. MAIN EXPOSURE MEASURE: The main exposure measure was the early use of GDMT, defined as the administration of all four components of GDMT within 24 hours of hospital admission.

main outcome measureThe primary outcome was in-hospital mortality, assessed within the study cohort.

resultsIn a pooled analysis of the CNEDSSP and CCC-ACS cohorts, early GDMT was associated with a significant reduction in in-hospital mortality (relative risk (RR): 0.62, 95% CI: 0.47 to 0.81). More pronounced reductions were observed in myocardial infarction (MI) patients, with HRs of 0.31 (95% CI: 0.17 to 0.55) in the CNEDSSP cohort and 0.47 (95% CI: 0.28 to 0.77) in the CCC-ACS cohort. A random-effects pooled analysis of MI patients with advanced renal dysfunction at admission showed a 61% reduction in in-hospital mortality among GDMT users (RR: 0.39, 95% CI: 0.27 to 0.58).

conclusionsThis nationwide study highlights that early GDMT is associated with a reduced risk of in-hospital mortality in ACS patients (particularly in MI patients) with advanced renal dysfunction.

Indexed as

Acute Coronary SyndromeHospital MortalityAdrenergic beta-AntagonistsAgedAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsChinaFemaleGlomerular Filtration RateHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedPlatelet Aggregation InhibitorsPractice Guidelines as TopicRetrospective StudiesAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsHydroxymethylglutaryl-CoA Reductase InhibitorsPlatelet Aggregation InhibitorsCoronary heart diseaseKidney & urinary tract disordersMyocardial infarctionProtocols & guidelines

Identifiers

PMID40858368
PMCPMC12382570

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Registered trials

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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.