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    Development and validation of the Emergency Department assessment of chest pain score and 2 h accelerated diagnostic protocol

    Access Status
    Open access via publisher
    Authors
    Than, M.
    Flaws, D.
    Sanders, S.
    Doust, J.
    Glasziou, P.
    Kline, J.
    Aldous, S.
    Troughton, R.
    Reid, Christopher
    Parsonage, W.
    Frampton, C.
    Greenslade, J.
    Deely, J.
    Hess, E.
    Sadiq, A.
    Singleton, R.
    Shopland, R.
    Vercoe, L.
    Woolhouse-Williams, M.
    Ardagh, M.
    Bossuyt, P.
    Bannister, L.
    Cullen, L.
    Date
    2014
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Than, M. and Flaws, D. and Sanders, S. and Doust, J. and Glasziou, P. and Kline, J. and Aldous, S. et al. 2014. Development and validation of the Emergency Department assessment of chest pain score and 2 h accelerated diagnostic protocol. EMA: Emergency Medicine Australasia. 26 (1): pp. 34-44.
    Source Title
    EMA - Emergency Medicine Australasia
    DOI
    10.1111/1742-6723.12164
    ISSN
    1742-6731
    School
    Department of Health Policy and Management
    URI
    http://hdl.handle.net/20.500.11937/8248
    Collection
    • Curtin Research Publications
    Abstract

    Objective: Risk scores and accelerated diagnostic protocols can identify chest pain patients with low risk of major adverse cardiac event who could be discharged early from the ED, saving time and costs. We aimed to derive and validate a chest pain score and accelerated diagnostic protocol (ADP) that could safely increase the proportion of patients suitable for early discharge. Methods: Logistic regression identified statistical predictors for major adverse cardiac events in a derivation cohort. Statistical coefficients were converted to whole numbers to create a score. Clinician feedback was used to improve the clinical plausibility and the usability of the final score (Emergency Department Assessment of Chest pain Score [EDACS]). EDACS was combined with electrocardiogram results and troponin results at 0 and 2h to develop an ADP (EDACS-ADP). The score and EDACS-ADP were validated and tested for reproducibility in separate cohorts of patients. Results: In the derivation (n = 1974) and validation (n = 608) cohorts, the EDACS-ADP classified 42.2% (sensitivity 99.0%, specificity 49.9%) and 51.3% (sensitivity 100.0%, specificity 59.0%) as low risk of major adverse cardiac events, respectively. The intra-class correlation coefficient for categorisation of patients as low risk was 0.87. Conclusion: The EDACS-ADP identified approximately half of the patients presenting to the ED with possible cardiac chest pain as having low risk of short-term major adverse cardiac events, with high sensitivity. This is a significant improvement on similar, previously reported protocols. The EDACS-ADP is reproducible and has the potential to make considerable cost reductions to health systems.

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