Key result
Cardiogenic shock in STEMI linked to ~274% greater risk of delayed thrombolysis.
Why the study?
Delayed thrombolytic treatment significantly increases mortality risk in STEMI, motivating the identification of factors associated with delayed administration.
What factors are associated with delayed thrombolytic medication administration in patients with STEMI?
Cross-Sectional (n=781)
Yes
What factors are associated with delayed thrombolytic medication administration in patients with STEMI?
Effect estimate: AOR 3.74 (95% CI 1.94-7.20)
Absolute Event Rate: 79.37% vs 57.41%
p-value: p=<0.001
Advanced Killip classification and nighttime presentation are significant risk factors for delayed thrombolytic administration in STEMI patients, highlighting areas for targeted quality improvement in emergency cardiovascular care.
Killip IV shock was associated with delayed thrombolysis in STEMI; hypothesis-generating for quality targets, prospective studies needed.
Background: ST-Segment Elevation Myocardial Infarction (STEMI) is among the most prevalent heart diseases worldwide and a leading cause of death. Delayed thrombolytic treatment significantly increases mortality risk in affected patients. This study aimed to identify factors associated with delayed administration of thrombolytic medication in STEMI patients. Methods: A cross-sectional analytical study was conducted in Narathiwat Province, involving 1,074 STEMI patients documented in the Acute Coronary Syndrome Registry between January 1, 2016, and December 31, 2021. Of these, 781 eligible patients were categorized into two groups: 464 with delayed thrombolytic medication and 317 without. Descriptive statistics and multiple logistic regression used for data analysis. Results: The proportion of patients experiencing delayed thrombolytic medication was 59.4% (95% CI: 55.8-62.9). Factors such as the total number of underlying diseases, Killip classification, and timing of accessing health services were associated with delayed thrombolytic medication. Patients with four underlying diseases had a reduced risk of delayed thrombolytic medication (AOR = 0.40, 95% CI: 0.24-0.63). Conversely, those diagnosed with cardiogenic shock (Class IV) (AOR = 3.74, 95% CI: 1.94-7.20) and those accessing services at night increased risk of delayed thrombolytic mediation (AOR = 2.16, 95% CI: 1.37-3.40). Conclusion: The number of underlying diseases, Killip classification, and timing of health service access were linked to delayed thrombolytic medication. STEMI patients with advanced Killip classification, particularly those seeking care at night, should receive intensified attention to ensure timely administration of thrombolytic, thereby mitigating disease progression and reducing mortality.
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Suemae et al. (2025) conducted a cross-sectional in ST-Segment Elevation Myocardial Infarction (STEMI) (n=781). Cardiogenic shock (Killip Class IV) vs. No congestive heart failure (Killip Class I) was evaluated on Delayed thrombolytic medication (>30 min) (AOR 3.74, 95% CI 1.94-7.20, p=<0.001). Cardiogenic shock (Killip Class IV) increased the risk of delayed thrombolytic medication (AOR 3.74) compared to no congestive heart failure in patients with ST-segment elevation myocardial infarction.
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