A 2-h diagnostic protocol to assess patients with chest pain symptoms in the Asia-Pacific region (ASPECT): A prospective observational validation study

Than, Martin, , Reid, Christopher, Lim, Swee Han, Aldous, Sally, Ardagh, Michael, Peacock, W. Frank, , Ho, Hiu Fai, Ko, Hiu Fai, Kasliwal, Ravi, Bansal, Manish, Soerianata, Sunarya, Hu, Dayi, Ding, Rongjing, Hua, Qi, Seok-Min, Kang, Sritara, Piyamitr, Sae-Lee, Ratchanee, Chiu, Te-Fa, Tsai, Kuang-Chau, Chu, Fang-Yeh, Chen, Wei-Kung, Chang, Wen-Han, Flaws, Dylan, George, Peter, & Richards, A. Mark (2011) A 2-h diagnostic protocol to assess patients with chest pain symptoms in the Asia-Pacific region (ASPECT): A prospective observational validation study. The Lancet, 377(9771), pp. 1077-1084.

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Description

Background: Patients with chest pain contribute substantially to emergency department attendances, lengthy hospital stay, and inpatient admissions. A reliable, reproducible, and fast process to identify patients presenting with chest pain who have a low short-term risk of a major adverse cardiac event is needed to facilitate early discharge. We aimed to prospectively validate the safety of a predefined 2-h accelerated diagnostic protocol (ADP) to assess patients presenting to the emergency department with chest pain symptoms suggestive of acute coronary syndrome. Methods: This observational study was undertaken in 14 emergency departments in nine countries in the Asia-Pacific region, in patients aged 18 years and older with at least 5 min of chest pain. The ADP included use of a structured pre-test probability scoring method (Thrombolysis in Myocardial Infarction [TIMI] score), electrocardiograph, and point-of-care biomarker panel of troponin, creatine kinase MB, and myoglobin. The primary endpoint was major adverse cardiac events within 30 days after initial presentation (including initial hospital attendance). This trial is registered with the Australia-New Zealand Clinical Trials Registry, number ACTRN12609000283279. Findings: 3582 consecutive patients were recruited and completed 30-day follow-up. 421 (11•8%) patients had a major adverse cardiac event. The ADP classified 352 (9•8%) patients as low risk and potentially suitable for early discharge. A major adverse cardiac event occurred in three (0•9%) of these patients, giving the ADP a sensitivity of 99•3% (95% CI 97•9–99•8), a negative predictive value of 99•1% (97•3–99•8), and a specificity of 11•0% (10•0–12•2). Interpretation: This novel ADP identifies patients at very low risk of a short-term major adverse cardiac event who might be suitable for early discharge. Such an approach could be used to decrease the overall observation periods and admissions for chest pain. The components needed for the implementation of this strategy are widely available. The ADP has the potential to affect health-service delivery worldwide.

Impact and interest:

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ID Code: 50728
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Parsonage, Williamorcid.org/0000-0002-0223-5378
Measurements or Duration: 8 pages
Keywords: Acute Coronary Syndrome, Chest Pain, Decision Making, Emergency Medicine
DOI: 10.1016/S0140-6736(11)60310-3
ISSN: 0140-6736
Pure ID: 32069833
Divisions: Past > QUT Faculties & Divisions > Faculty of Health
Past > Institutes > Institute of Health and Biomedical Innovation
Copyright Owner: Consult author(s) regarding copyright matters
Copyright Statement: This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au
Deposited On: 03 Jun 2012 22:44
Last Modified: 18 Jun 2024 11:42