Evidence map›Paper›PMID 39147798›Full record

ArticleScientific reports2024

The impact of admission modes on the treatment outcome and in-hospital mortality rate of STEMI patients undergoing PPCI.

Qing Wang, Chun Zan, Fangshi Li, Yuanbin Li, Feiyu Wang, Taiyu Wang, Xueming Zhao, Yue Du

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In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Qing Wang *Tianjin Medical University, Tianjin, China.
Chun Zan *Tianjin Medical University, Tianjin, China.
Fangshi Li *Tianjin Medical University, Tianjin, China.
Yuanbin LiTianjin Medical University, Tianjin, China.
Feiyu WangTianjin Medical University, Tianjin, China.
Taiyu WangTianjin Medical University, Tianjin, China.
Xueming ZhaoTianjin Medical University, Tianjin, China. xmzhao@tmu.edu.cn.
Yue DuTianjin Medical University, Tianjin, China. duyue@tmu.edu.cn.

Funding

The Ministry of education of Humanities and Social Science project 22YJC630216
6 · The paper itself

Abstract

The current research on ST elevation myocardial infarction (STEMI) patients has been mostly limited to Door-to-Balloon (D-to-B) time. This study aimed to compare the effects of different hospital admission modes to on the time metrics of patients undergoing primary percutaneous coronary intervention (PPCI). It also examined the effects of these modes on in-hospital mortality and other influencing factors. The goal was to prompt healthcare facilities at all levels, including chest hospitals, the Centers for Disease Control and Prevention (CDC), and communities to take measures to enhance the treatment outcomes for patients with STEMI. A total of 1053 cases of STEMI patients admitted to Tianjin Chest Hospital from December 2016 to December 2023 and successfully underwent PPCI were selected for this study. They were divided into three groups based on the admission modes: the ambulances group (363 cases), the self-presentation group (305 cases), and the transferred group (385 cases). Multivariate logistic regression was used to explore the impact of different modes of hospital admission on the standard-reaching rate of key treatment time metrics. The results showed that the S-to-FMC time of transferred patients (OR = 0.434, 95% CI 0.316-0.596, P < 0.001) and self-presentation patients (OR = 0.489, 95% CI 0.363-0.659, P < 0.001) were more likely to exceed the standard than that of ambulance patients; The cath lab pre-activation time of self-presented patients was also less likely to meet the standard than that of ambulance patients (OR = 0.695, 95% CI 0.499-0.967, P = 0.031); D-to-W time of self-presentation patients was less likely to reach the standard than that of ambulance patients (OR = 0.323, 95% CI 0.234-0.446, P < 0.001);However, the FMC-to-ECG time of self-presentation patients was more likely to reach the standard than that of ambulance patients (OR = 2.601, 95% CI 1.326-5.100, P = 0.005). The Cox proportional hazards model analysis revealed that for ambulance patients, the time spent at each key treatment time point is shorter, leading to lower in-hospital mortality rate (HR0.512, 95% CI 0.302-0.868, P = 0.013) compared to patients admitted by other means. We found that direct arrival of STEMI patients to the PCI hospital via ambulance at the onset of the disease significantly reduces the S-to-FMC time, FMC-to-ECG time, D-to-W time, and catheterization room activation time compared to patients who self-present. This admission mode enhances the likelihood of meeting the benchmark standards for each time metric, consequently enhancing patient outcomes.

Indexed as

Hospital MortalityPercutaneous Coronary InterventionST Elevation Myocardial InfarctionAgedAmbulancesFemaleHumansMaleMiddle AgedPatient AdmissionTime FactorsTime-to-TreatmentTreatment OutcomeAmbulancePPCISelf-presentationSTEMITransferred

Identifiers

PMID39147798
PMCPMC11327245

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