Ns. Kleiman et al., Death and nonfatal reinfarction within the first 24 hours after presentation with an acute coronary syndrome: Experience from GUSTO-IIb, AM HEART J, 137(1), 1999, pp. 12-23
Citations number
39
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Background A large proportion of deaths among patients with myocardial infa
rction occurs within the first 24 hours after presentation. It is not clear
whether this phenomenon is also true of patients without ST-segment elevat
ion who may or may not have infarction at the time of presentation. Thrombi
n activity may also be greatest during the first 24 hours after plaque rupt
ure. Accordingly, this study was designed to examine the pattern of early i
schemic events among patients with acute coronary syndromes and to determin
e whether the direct thrombin inhibitor desirudin (r-hirudin) would be most
effective during this period.
Methods and Results Among the 11,142 patients enrolled in GUSTO-II, death o
r (re)infarction occurred within 24 hours in 210 patients (1.7%), represent
ing 19% of the 1135 deaths that had occurred by 30 days. Death or (re)infar
ction occurred within 24 hours in 113 patients (2.7%) with ST-segment eleva
tion and in 97 patients without ST-segment elevation (1.2%, P < .001), repr
esenting 26% and 14% of the 30-day event rates, respectively, for the 2 enr
ollment strata. Among patients with ST-segment elevation, most of these eve
nts were deaths, whereas among patients without ST-segment elevation, most
events were (re)infarctions. Death or (re)infarction by 24 hours occurred i
n 80 (1.3%) patients treated with desirudin and 130 (2.1%) patients treated
with heparin (P = .01). This finding predominantly consisted of prevention
of death among patients with ST-segment elevation and of (re)infarction am
ong patients without ST-segment elevation.
Conclusions These findings have important implications for early triage of
patients with acute coronary syndromes and for the development of new thera
pies directed at stabilizing the unstable atherosclerotic plaque.