Key result
Thrombolysis resistance tracks with acute MI onset, peaking in early morning and late evening.
Why the study?
Does the time of symptom onset affect resistance to thrombolytic therapy in patients with acute myocardial infarction?
Observational (n=608)
Does the time of symptom onset affect resistance to thrombolytic therapy in patients with acute myocardial infarction?
p-value: p=<0.05
Resistance to thrombolytic therapy in acute myocardial infarction exhibits circadian variations with early morning and late evening peaks, similar to the onset of infarction.
OBJECTIVES The present study investigated whether the onset of acute myocardial infarction and resistance to thrombolysis have similar circadian variations. BACKGROUND Circadian variations of the onset of acute myocardial infarction and resistance to thrombolysis in the early morning have been reported. Some studies have also reported a secondary peak incidence in late evening; however, it is not known whether the resistance to thrombolysis has a similar circadian variation in these patients. METHODS Six hundred eight Japanese patients with an acute myocardial infarction were the subjects of the study. Two hundred forty-four of the 608 patients were treated with thrombolysis within 12 h of the onset of symptoms. One hundred thirteen patients received urokinase, and 131 patients received tissue-type plasminogen activator (t-PA) over 60 min. Patency of the infarct-related artery, the primary end point of the study, was evaluated at 60 min after the initiation of thrombolytic therapy, and Thrombolysis in Myocardial Infarction (TIMI) grade 0, 1 or 2 was defined as resistant to thrombolysis. RESULTS The onset of acute myocardial infarction and resistance to thrombolysis showed circadian variations with early morning and late evening peaks (p<0.001 and p<0.05, respectively). These circadian patterns showed similar distributions as evaluated with Spearman's method (r=0.70, p<0.05), although resistance to thrombolysis showed a phase difference of about 2 h earlier than the infarction incidence. The circadian variation of the resistance to thrombolysis was independent of the types of thrombolytic agents (urokinase or t-PA). CONCLUSIONS These findings suggest that adjustment of treatment based on the time of the onset of symptoms may be warranted for the patients with acute myocardial infarction.
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Kono et al. (1996) conducted an observational in acute myocardial infarction (n=608). Time of symptom onset (circadian variation) was evaluated on Patency of the infarct-related artery at 60 min after initiation of thrombolytic therapy (TIMI grade 0, 1 or 2 defined as resistant) (p=<0.05). The onset of acute myocardial infarction and resistance to thrombolysis showed similar circadian variations with early morning and late evening peaks (p<0.001 and p<0.05, respectively).
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