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What are the characteristics and timing of ischemic cerebral infarction in patients treated with rt-PA and heparin for acute myocardial infarction?
What are the characteristics and timing of ischemic cerebral infarction in patients treated with rt-PA and heparin for acute myocardial infarction?
Ischemic cerebral infarction is a rare (0.7%) complication of rt-PA and heparin therapy for acute MI, with characteristics and timing similar to those seen before the use of thrombolytics.
Answers are grounded in this paper and cite their sources.
Stroke risk after rt-PA for MI remains low with unchanged timing and sites; supports prethrombolytic estimates in the thrombolytic era.
BACKGROUND AND PURPOSE: Ischemic cerebral infarction (CI) is a serious complication of acute myocardial infarction (MI). Little information exists on CI after thrombolytic therapy for MI. METHODS: Of 3924 MI patients treated with recombinant tissue plasminogen activator (rt-PA) and heparin, 29 (0.7%) developed CI after treatment. All CI patients had detailed neurological evaluations, and 27 (93%) had CT scans centrally reviewed. RESULTS: Age range was 40 to 74 years (mean, 60 years); 25 patients (86%) were men, and 22 (76%) were white. The electrocardiographic location of MI was anterior in 22 (76%) and nonanterior in 7 (24%). Five CIs occurred within 6 hours, 4 between 6 to 24 hours, 8 during the remainder of the first week, 10 during the second week, and 2 others distributed over the 4 weeks after study entry. Six of 29 CIs did not involve the cerebral cortex; 9 patients (31%) had multiple CIs. Of 28 CIs thought to be embolic in origin, 17 showed strong evidence for at least one cardiac abnormality (mural clot, wall-motion abnormality, aneurysm, or atrial fibrillation) known to be associated more specifically with embolism than MI. Eight of 27 CIs (30%) with CT scans had hemorrhagic transformation of varying degrees; 5 were symptomatic. CONCLUSIONS: The time of occurrence and sites of CI after rt-PA and heparin therapy for acute MI are similar to those reported during the prethrombolytic era.
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Sloan et al. (1997) studied this question.
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