AI Article Synopsis

  • The study aimed to evaluate how the duration of chest pain affects the sensitivity and specificity of early cardiac marker tests (CK-MB and myoglobin) in emergency department patients with nondiagnostic ECGs.
  • It involved 5005 patients over 25 years old, stratified by pain duration, and found that sensitivity of the markers increased with longer chest pain duration, but never exceeded 73% for CK-MB and 73% for myoglobin.
  • The results indicate that using single assays at early time points is insufficient to rule out acute myocardial infarction (AMI), highlighting the need for serial testing and longer observation periods to accurately assess AMI risk.

Article Abstract

Objective: Cardiac marker sensitivity depends on chest pain duration at the time of sampling. Our objective was to estimate the sensitivity, specificity, and likelihood ratios of early CK-MB and myoglobin assays in patients presenting to the emergency department (ED) with nondiagnostic ECGs, stratified by the duration of ongoing chest pain at the time of ED assessment.

Methods: This was a prospective observational study carried out in 10 US and 2 Canadian EDs. Patients >25 years of age with ongoing chest pain and nondiagnostic ECGs were stratified by pain duration (0-4 h, 4-8 h, 8-12 h, >12 h). CK-MB and myoglobin assays were drawn at T = 0 (ED assessment) and T = 1 hr. Patients were followed for 7-14 days to identify all cases of acute myocardial infarction (AMI). ED test results were correlated with patient outcomes.

Results: Of 5005 eligible patients, 565 had AMI. Pain duration was 0-4 h in 3014 patients, 4-8 h in 961, 8-12 h in 487, and >12 h in 543. Marker sensitivity increased with pain duration, ranging from 28%-77% for CK-MB and 39%-73% for myoglobin. The maximal sensitivity achieved by a T = 0 assay was 73%, and this was in patients with 8-12 or >12 h of ongoing pain. No combination of tests achieved 90% sensitivity in any pain duration strata.

Conclusions: Regardless of chest pain duration, single assays and early serial markers (0+1 hr) do not rule out AMI; therefore, serial assays over longer observation periods are required. Likelihood ratios derived in this study will help physicians who use Bayesian analysis to determine post-test AMI likelihood in patients with chest pain.

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Source
http://dx.doi.org/10.1017/s1481803500007715DOI Listing

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