J. Hung et al., DIPYRIDAMOLE TL-201 SCINTIGRAPHY FOR EARLY RISK STRATIFICATION OF PATIENTS AFTER UNCOMPLICATED MYOCARDIAL-INFARCTION, HEART, 78(4), 1997, pp. 346-352
Objective-To determine the safety and prognostic value of dipyridamole
thallium-201 scintigraphy performed in patients within three to five
days of acute myocardial infarction, including those receiving thrombo
lytic treatment. Design-A prospective study of dipyridamole thallium-2
01 scintigraphy in patients early after acute myocardial infarction. S
etting-University hospital. Patients-200 patients who were clinically
uncomplicated at day 3 after infarction, 92 (46%) of whom had received
thrombolysis. Main outcome measures-Incidence of cardiac death, non-f
atal reinfarction, readmission to hospital for unstable angina, or non
-elective revascularisation procedure within six months' follow up. Re
sults-No patient had a serious complication from the dipyridamole stud
y. At six month follow up, 55 patients (28%) had suffered a defined ca
rdiac event. Patients who received thrombolysis had the same extent of
thallium-201 redistribution and the same occurrence of subsequent car
diac events as those not receiving thrombolysis. Patients who subseque
ntly had an event had more myocardial segments showing thallium-201 re
distribution than event free patients: 2.7 (SD 1.9) v 1.2 (1.4), respe
ctively (p < 0.001). Among all clinical and scintigraphic variables, m
ultivariate analysis identified the extent of thallium-201 redistribut
ion as the only independent predictor of outcome (p < 0.001). Among 63
patients (32%) of the study cohort who showed more than two myocardia
l segments with thallium-201 redistribution, the adjusted risk ratio f
or a cardiac event was 7.5 (95% confidence interval 2.9 to 19.1) compa
red with patients without any redistribution. Conclusions-Dipyridamole
thallium-201 scintigraphy can be performed safely within a few days o
f the event in patients with uncomplicated myocardial infarction, incl
uding those who received thrombolysis, and can identify a subgroup of
patients at high risk of future ischaemic events.