T. Laperche et al., A STUDY OF BIOCHEMICAL MARKERS OF REPERFUSION EARLY AFTER THROMBOLYSIS FOR ACUTE MYOCARDIAL-INFARCTION, Circulation, 92(8), 1995, pp. 2079-2086
Background In acute myocardial infarction (AMI), early noninvasive ide
ntification of patients with occluded infarct-related arteries (IRAs)
after thrombolysis has important prognostic and therapeutic implicatio
ns. The aims of this study were to evaluate biochemical methods for th
e early diagnosis of patency after thrombolysis prospectively and to e
stablish the optimal diagnostic criteria retrospectively. Methods and
Results In 97 patients with AMI treated with thrombolytic agents less
than or equal to 6 hours after the onset of symptoms, myoglobin, tropo
nin T, creatine kinase, the MB isoenzyme and MM isoforms of creatine k
inase were measured just before thrombolysis began and 90 minutes late
r. IRA patency was assessed by means of 90-minute coronary angiography
. For each marker, compared with the expected sensitivity and specific
ity based on published thresholds for the diagnosis of patency, the ob
served values were consistently lower but were markedly improved in a
subset of patients treated >3 hours after the onset of symptoms. With
receiver-operator characteristic curve analysis of the slopes of incre
ase and relative increases in each marker over 90 minutes, the best di
agnostic performance was achieved by use of the relative increase in m
yoglobin, troponin T, and MM3/MM1 creatine kinase isoforms in patients
treated >3 hours after onset (areas under the curve of 0.84, 0.83, an
d 0.85, respectively).Conclusions Effective early noninvasive diagnosi
s of patency after thrombolysis is possible in patients treated >3 hou
rs after symptom onset by use of criteria derived from the relative in
crease over 90 minutes in plasma markers, particularly myoglobin, trop
onin T, and MM3/MM1 creatine kinase isoforms. The diagnostic performan
ce of the relative increase in myoglobin appears to be less susceptibl
e to small changes in the diagnostic threshold value.