Comparison of two clinical scoring systems for emergency department risk stratification of suspected acute coronary syndrome
Access Status
Authors
Date
2011Type
Metadata
Show full item recordCitation
Source Title
ISSN
Faculty
Collection
Abstract
Objective: To compare two methods of risk stratification for suspected acute coronary syndrome (ACS) in the ED. Methods: A prospective observational multicentre study was undertaken of patients undergoing evaluation in the ED for possible ACS. We compared the National Heart Foundation of Australia/Cardiac Society of Australia and New Zealand (NHF/CSANZ) guideline and the Thrombolysis in Myocardial Infarction (TIMI) risk score for differentiating high- and low-risk patients. Composite outcome was all cause death, myocardial infarction or coronary revascularisation within 30 days. Results: Of 1758 enrolments, 223 (13%) reached the study outcome. Area under the receiver operator characteristic (ROC) curve was 0.79 (95% CI 0.76-0.81) for the NHF/CSANZ group and 0.71 (0.68-0.75) for TIMI score based on initial troponin result (P<0.001), and 0.82 (95% CI 0.80-0.84) and 0.76 (0.73-0.79) respectively when the 8-12h troponin result is included (P=0.001). Thirty day event rates were 33% for NHF/CSANZ high-risk vs 1.5% for combined low/intermediate risk (P<0.001). For TIMI score, 30 day event rates were 23% for a score =2 and 4.8% for TIMI<2 (P<0.001). The NHF/CSANZ guideline identified more patients as low risk compared with the TIMI risk score (61% vs 48%, P<0.001). Conclusions: The NHF/CSANZ guideline is superior to the TIMI risk score for risk stratification of suspected ACS in the ED. © 2011 The Authors. EMA © 2011 Australasian College for Emergency Medicine and Australasian Society for Emergency Medicine.
Related items
Showing items related by title, author, creator and subject.
-
Cullen, L.; Mueller, C.; Parsonage, W.; Wildi, K.; Greenslade, J.; Twerenbold, R.; Aldous, S.; Meller, B.; Tate, J.; Reichlin, T.; Hammett, C.; Zellweger, C.; Ungerer, J.; Rubini Gimenez, M.; Troughton, R.; Murray, K.; Brown, A.; Mueller, M.; George, P.; Mosimann, T.; Flaws, D.; Reiter, M.; Lamanna, A.; Haaf, P.; Pemberton, C.; Richards, A.; Chu, K.; Reid, Christopher; Peacock, W.; Jaffe, A.; Florkowski, C.; Deely, J.; Than, M. (2013)Objectives The study objective was to validate a new high-sensitivity troponin I (hs-TnI) assay in a clinical protocol for assessing patients who present to the emergency department with chest pain. Background Protocols ...
-
Aldous, S.; Mark Richards, A.; George, P.; Cullen, L.; Parsonage, W.; Flaws, D.; Florkowski, C.; Troughton, R.; O'Sullivan, J.; Reid, Christopher; Bannister, L.; Than, M. (2014)Objectives: The aim of this study is to compare a new improved point of care cardiac troponin assay (new POC-cTnI) with 1. its predecessor (old POC-cTnI) and 2. a high sensitivity assay (hs-cTnI) for the diagnosis of acute ...
-
Meller, B.; Cullen, L.; Parsonage, W.; Greenslade, J.; Aldous, S.; Reichlin, T.; Wildi, K.; Twerenbold, R.; Jaeger, C.; Hillinger, P.; Haaf, P.; Puelacher, C.; Kern, V.; Rentsch, K.; Stallone, F.; Gimenez, M.; Ballarino, P.; Bassetti, S.; Walukiewicz, A.; Troughton, R.; Pemberton, C.; Richards, M.; Chu, Chuan-Wei; Reid, Christopher; Than, M.; Mueller, C. (2015)Background: We aimed to evaluate the efficacy and safety of using high-sensitivity cardiac troponin T (hs-cTnT) within an accelerated diagnostic protocol (ADP) in patients presenting with symptoms suggestive of acute ...