High-sensitivity troponin assays facilitate the rapid exclusion of acute myocardial infarction (AMI). However, elevated results are also seen in other conditions causing myocardial injury. Serial measurements increase the specificity for AMI, helping to rapidly identify patients for whom revascularisation may be appropriate. In this study, we explore a strategy for rapidly excluding AMI in symptomatic patients using serial high-sensitivity troponin measurements. Main findings: (1) all patients presenting more than 3 h after symptom onset with a negative result had a second negative result; (2) AMI was excluded in all patients with two results falling below the lower limit of detection of a standard troponin assay by 8 h post-symptom onset.
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Competing interests None.
Ethics approval We retrospectively examined routine clinical practice. The study was deemed to be clinical audit and service evaluation, and did not require ethics committee approval. Data were recorded anonymously and in line with NHS Caldicott Guardian principles.
Provenance and peer review Not commissioned; externally peer reviewed.
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