Utility of cardiac troponin I, creatine kinase-MBmass, myosin light chain 1, and myoglobin in the early in-hospital triage of "high risk" patients with chest pain

Citation
Gs. Hillis et al., Utility of cardiac troponin I, creatine kinase-MBmass, myosin light chain 1, and myoglobin in the early in-hospital triage of "high risk" patients with chest pain, HEART, 82(5), 1999, pp. 614-620
Citations number
36
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
HEART
ISSN journal
13556037 → ACNP
Volume
82
Issue
5
Year of publication
1999
Pages
614 - 620
Database
ISI
SICI code
1355-6037(199911)82:5<614:UOCTIC>2.0.ZU;2-4
Abstract
Objective-To evaluate the use of cardiac troponin I (cTnI), creatine kinase -MBmass (CK-MBmass), myosin light chain 1 (MLC 1), and myoglobin in identif ying "high risk" patients with chest pain who will experience serious cardi ac events (SCEs) in hospital. Design-Prospective study. Setting-University affiliated medical centre in Philadelphia, USA. Patients-208 patients with chest pain, at > 7% risk of acute myocardial inf arction (MI), but without new ST segment elevation on their presenting EGG. Interventions-cTnI, CK-MBmass, MLC 1, and myoglobin concentrations were obt ained on admission (0 hour) and at 4, 8, 16, and 24 hours. Main outcome measures-The sensitivity, specificity, positive and negative p redictive value, and pre- and post-test probabilities of patients suffering an SCE in hospital were determined. SCEs included cardiac death, acute MI, cardiac arrest, Life threatening cardiac arrhythmia, cardiogenic shock, an d urgent coronary revascularisation. Results-Admission concentrations of all markers were poor predictors of SCE s in hospital but improved substantially at subsequent timepoints. cTnI and CK-MBmass were consistently the most useful prognostic indicators. If both were negative at 0, 4, and 8 hours, then 99% (95% confidence interval 96% to 100%) of patients remained free from SCEs. The only SCEs not thus predic ted were revascularisation procedures and associated complications. Additio nal tests after 8 hours, or the inclusion of additional markers, did not im prove predictive accuracy further. Conclusions-Patients with high risk clinical features on admission who have negative cTnI and CK-MBmass concentrations at 0, 4, and 8 hours later have a favourable in-hospital prognosis and could be considered for early triag e out of coronary care units.