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[Intracoronary dipyridamole reduces the incidence of acute coronary vessel occlusion in percutaneous transluminal coronary angioplasty--a prospective randomized study].
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- Author(s): Heintzen MP;Heintzen MP; Heidland UE; Klimek WJ; Michel CJ; Kelm M; Leschke M; Schwartzkopff B; Vester EG; Strauer BE
- Source:
Zeitschrift fur Kardiologie [Z Kardiol] 1997 Dec; Vol. 86 (12), pp. 961-7.- Publication Type:
Clinical Trial; Comparative Study; English Abstract; Journal Article; Randomized Controlled Trial- Language:
German - Source:
- Additional Information
- Transliterated Title: Dipyridamol intrakoronar reduziert die Inzidenz des akuten Koronargefässverschlusses bei der perkutanen transluminalen Koronarangioplastie--Eine prospektiv randomisierte Untersuchung.
- Source: Publisher: Steinkopff Country of Publication: Germany NLM ID: 0360430 Publication Model: Print Cited Medium: Print ISSN: 0300-5860 (Print) Linking ISSN: 03005860 NLM ISO Abbreviation: Z Kardiol Subsets: MEDLINE
- Publication Information: Original Publication: Darmstadt, Steinkopff.
- Subject Terms: Angioplasty, Balloon, Coronary*; Coronary Circulation/*drug effects ; Coronary Thrombosis/*prevention & control ; Coronary Vessels/*drug effects ; Dipyridamole/*administration & dosage ; Myocardial Infarction/*prevention & control ; Vasodilation/*drug effects ; Vasodilator Agents/*administration & dosage; Adult ; Aged ; Angina, Unstable/therapy ; Aspirin/administration & dosage ; Coronary Artery Bypass ; Coronary Disease/therapy ; Coronary Thrombosis/therapy ; Female ; Heparin/administration & dosage ; Humans ; Injections, Intra-Articular ; Male ; Middle Aged ; Myocardial Infarction/therapy ; Premedication ; Prospective Studies ; Recurrence
- Abstract: Even in the era of coronary stenting, acute coronary artery occlusion continues to represent a significant limitation of percutaneous transluminal coronary angioplasty (PTCA). Despite application of heparin and aspirin, abrupt vessel closure still occurs in 2-8%, depending on the definition applied. Especially patients receiving PTCA for acute coronary syndromes are at high risk for abrupt vessel closure. The formation of an intracoronary thrombus plays a central role in the pathogenesis of abrupt vessel closure. Dipyridamole induces dilatation of coronary arteries and prevents platelet aggregation by a mechanism that differs from that of aspirin. The primary purpose of the study was to evaluate whether adjunctive local intracoronary therapy with dipyridamole could reduce the incidence of coronary artery occlusion following PTCA. Secondary endpoints were defined as myocardial infarction, necessity for bypass grafting, and death. In 939 PTCA procedures performed for stable angina and in 155 angioplasty procedures for acute coronary syndromes (unstable angina, acute myocardial infarction), patients were randomized to receive conventional pretreatment consisting of heparin 15,000 I.E. and aspirin 500 mg i.v. or additional intracoronary infusion of dipyridamole (0.5 mg/kg body weight). Dipyridamole was applied in 550 interventions (455 interventions in men, 95 interventions in women, age = 59.2 +/- 8.4; 74 emergency procedures); conventional pretreatment was performed in 544 interventions (444 interventions in men, 100 interventions in women, age 58.3 +/- 7.9; 81 emergency procedures). Intracoronary application of dipyridamole resulted in a significant reduction in the incidence of abrupt vessel closure following PTCA. This significant reduction was observed in patients presenting with stable ischemia as well as in patients receiving PTCA for acute coronary syndromes. Concerning secondary end points, intracoronary application of dipyridamole did not affect the need for bypass grafting or the incidence of death following PTCA. Intracoronary application of dipyridamole was associated with a reduction in the incidence of myocardial infarction following PTCA which, however, failed to reach significance.
- Accession Number: 0 (Vasodilator Agents)
64ALC7F90C (Dipyridamole)
9005-49-6 (Heparin)
R16CO5Y76E (Aspirin) - Publication Date: Date Created: 19980321 Date Completed: 19980422 Latest Revision: 20191024
- Publication Date: 20240628
- Accession Number: 10.1007/s003920050137
- Accession Number: 9499493
- Transliterated Title:
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