Τόμος 12 (1998) – Τεύχος 1 & 2 – Άρθρο 6 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 12 (1998) – Issue 1 & 2 – Article 6 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title Ultra rapid infusion of rt-PA in acute myocardial infarction
Authors I. Kanonidis¹, C. Papadopoulos¹, G. Koukoulekidis¹, L. Papayannis¹, N. Nikolaidis¹, B. Pavlidis¹, G. Sakadamis¹, B. Kokkas² and C.Th. Gitsios¹

1. 2nd Cardiology Department and 2. Laboratory of Pharmacology, Aristotle University of Thessaloniki, Greece

Citation Kanonidis, I.E., Papadopoulos, C.L., Koukoulekidis, G., Papayannis, L., Nikolaidis, N. et al.: Ultra rapid infusion of rt-PA in acute myocardial infarction, Epitheorese Klin. Farmakol. Farmakokinet. 12(3): 39-46 (1998)
Publication Date Received for publication: 15 October 1997

Accepted for publication. 20 October 1997

Full Text Language English
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Keywords Thrombolysis, myocardial infarction, recombinant tissue-type plasminogen activator, front loaded regimens.
Other Terms Statistical study
Summary Clinical evidence supports the point that the earlier the reperfusion the better the prognosis. In that view we studied an ultra-rapid infusion scheme of rt-PA in 73 patients presented within 4 hours from onset of symptoms for Acute Myocardial Infarction (AMI). Included patients had no previous history of AMI, hypertension or any other cardiovascular disease. Thirty-five of these patients were given rt-PA 50 mg IV bolus followed by 50 mg iv infusion in 30 min. The remaining 38 were assigned to the standard regimen that is 100 mg rt-PA given as 10 mg IV bolus followed by IV infusion of 90 mg in 90 min. Heparin was given concomitantly. Reperfusion was evaluated 1 hour after treatment by noninvasive criteria that are: a) relief of pain, b) resolution of ST segment elevation. The latter was evaluated quantitatively (ST index) as the percentage of reduction of the sum of ST elevations in all affected leads from basal (pre-treatment) values. If ST index was <50% reperfusion was considered to have taken place. Coronary angiography carried out at discharge (7-10 days) and 30 day mortality was also evaluated. The rapid infusion did not cause any changes in blood pressure or cardiac rhythm. Signs of reperfusion were noticed in 32 patients in the ultra-rapid group (91%) and in 27 patients (71%) in the standard group. ST reduction correlated well with time from onset of symptoms to onset of treatment in the ultra-rapid infusion group. Four cases of reocclusion were noticed. Mortality was excellent in both groups. Coronary angiography did not reveal any differences in coronary artery patency between the two groups. Ultra rapid infusion of rt-PA is a safe and very effective means of promptly restoring a long lasting coronary patency in the setting of AMI.
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