Title of article
Two Mechanistic Pathways for Thienopyridine-Associated Thrombotic Thrombocytopenic Purpura: A Report From the SERF-TTP Research Group and the RADAR Project Original Research Article
Author/Authors
Charles L. Bennett، نويسنده , , Benjamin Kim، نويسنده , , Anaadriana Zakarija، نويسنده , , Nicholas Bandarenko، نويسنده , , Dilip K. Pandey، نويسنده , , Charlie G. Buffie، نويسنده , , June M. McKoy، نويسنده , , Amul D. Tevar، نويسنده , , John F. Cursio، نويسنده , , Paul R. Yarnold، نويسنده , , Hau C. Kwaan، نويسنده , , Davide De Masi، نويسنده , , Ravindra Sarode، نويسنده , , Thomas J. Raife، نويسنده , , Joseph E. Kiss، نويسنده , , Dennis W. Raisch، نويسنده , , Charles Davidson، نويسنده , , J. Evan Sadler، نويسنده , , Thomas L. Ortel، نويسنده , , X. Long Zheng، نويسنده , , et al.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
6
From page
1138
To page
1143
Abstract
Objectives
We sought to describe clinical and laboratory findings for a large cohort of patients with thienopyridine-associated thrombotic thrombocytopenic purpura (TTP).
Background
The thienopyridine derivatives, ticlopidine and clopidogrel, are the 2 most common drugs associated with TTP in databases maintained by the U.S. Food and Drug Administration (FDA).
Methods
Clinical reports of TTP associated with clopidogrel and ticlopidine were identified from medical records, published case reports, and FDA case reports (n = 128). Duration of thienopyridine exposure, clinical and laboratory findings, and survival were recorded. ADAMTS13 activity (n = 39) and inhibitor (n = 30) were measured for a subset of individuals.
Results
Compared with clopidogrel-associated TTP cases (n = 35), ticlopidine-associated TTP cases (n = 93) were more likely to have received more than 2 weeks of drug (90% vs. 26%), to be severely thrombocytopenic (84% vs. 60%), and to have normal renal function (72% vs. 45%) (p < 0.01 for each). Compared with TTP patients with ADAMTS13 activity >15% (n = 13), TTP patients with severely deficient ADAMTS13 activity (n = 26) were more likely to have received ticlopidine (92.3% vs. 46.2%, p < 0.003). Among patients who developed TTP >2 weeks after thienopyridine, therapeutic plasma exchange (TPE) increased likelihood of survival (84% vs. 38%, p < 0.05). Among patients who developed TTP within 2 weeks of starting thienopyridines, survival was 77% with TPE and 78% without.
Conclusions
Thrombotic thrombocytopenic purpura is a rare complication of thienopyridine treatment. This drug toxicity appears to occur by 2 different mechanistic pathways, characterized primarily by time of onset before versus after 2 weeks of thienopyridine administration. If TTP occurs after 2 weeks of ticlopidine or clopidogrel therapy, therapeutic plasma exchange must be promptly instituted to enhance likelihood of survival.
Keywords
TPE , von Willebrand factor , Thrombotic thrombocytopenic purpura , TTP , VWF , therapeutic plasma exchange
Journal title
JACC (Journal of the American College of Cardiology)
Serial Year
2007
Journal title
JACC (Journal of the American College of Cardiology)
Record number
472787
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