Relationship between activated clotting time and ischemic or hemorrhagic complications: analysis of 4 recent randomized clinical trials of percutaneous coronary intervention
Meta-analysis published in Circulation (2004)
Abstract
BACKGROUND: Unfractionated heparin (UFH) is the most widely used antithrombin during percutaneous coronary intervention (PCI). Despite significant pharmacological and mechanical advancements in PCI, uncertainty remains about the optimal activated clotting time (ACT) for prevention of ischemic or hemorrhagic complications. METHODS AND RESULTS: We analyzed the outcome of all UFH-treated patients enrolled in 4 large, contemporary PCI trials with independent adjudication of ischemic and bleeding events. Of 9974 eligible patients, maximum ACT was available in 8369 (84%). The median ACT was 297 seconds (interquartile range 256 to 348 seconds). The incidence of death, myocardial infarction, or revascularization at 48 hours, by ACT quartile, was 6.2%, 6.8%, 6.0%, and 5.7%, respectively (P=0.40 for trend). Covariate-adjusted rate of ischemic complications was not correlated with maximal procedural ACT (continuous value, P=0.29). Higher doses of UFH (>5000 U, or up to 90 U/kg) were independently associated with higher rates of events. The incidence of major or minor bleeding at 48 hours, by ACT quartile, was 2.9%, 3.5%, 3.8%, and 4.0%, respectively (P=0.04 for trend). In a multivariable logistic model with a spline transformation for ACT, there was a linear increase in risk of bleeding as the ACT approached 365 seconds (P=0.01), which leveled off beyond that value. Increasing UFH weight-indexed dose was independently associated with higher bleeding rates (OR 1.04 [1.02 to 1.07] for each 10 U/kg, P=0.001). CONCLUSIONS: In patients undergoing PCI with frequent stent and potent platelet inhibition use, ACT does not correlate with ischemic complications and has a modest association with bleeding complications, driven mainly by minor bleeding. Lower values do not appear to compromise efficacy while increasing safety.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Unfractionated heparin (UFH) is the most widely used antithrombin during percutaneous coronary intervention (PCI).
Warum dies für die Hirudotherapie relevant ist
Diese Studie analysierte die Ergebnisse von 8.369 auswertbaren Patienten, die mit unfraktioniertem Heparin (UFH) in vier perkutanen Koronarinterventions-(PCI-)Studien behandelt wurden, um den Zusammenhang zwischen der aktivierten Gerinnungszeit (ACT) und ischämischen oder hämorrhagischen Komplikationen zu untersuchen. Die Analyse ergab keine Korrelation zwischen der maximalen prozeduralen ACT und ischämischen Komplikationen (P=0,29) und nur eine modeste Assoziation mit Blutungen – vor allem minoren –, die bis 365 Sekunden linear zunahm. Höhere UFH-Dosen waren unabhängig sowohl mit höheren Ereignis- als auch mit höheren Blutungsraten assoziiert. Die Studie erwähnt weder Hirudin, Blutegel, Hirudotherapie noch irgendwelche aus Blutegeln stammenden Verbindungen in der Zusammenfassung. Folglich hat dieser Artikel keine direkte Relevanz für das ASH-Gebiet der Hirudotherapie oder das Blutegelsekretom; er betrifft ausschließlich die Heparindosierung und das ACT-Monitoring während PCI.
Zitation
Relationship between activated clotting time and ischemic or hemorrhagic complications: analysis of 4 recent randomized clinical trials of percutaneous coronary intervention
Brener SJ · Circulation, 2004
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