Randomized, Multicenter Trial of ARTSS-2 (Argatroban With Recombinant Tissue Plasminogen Activator for Acute Stroke)
Author:
Barreto Andrew D.1, Ford Gary A.1, Shen Loren1, Pedroza Claudia1, Tyson Jon1, Cai Chunyan1, Rahbar Mohammad H.1, Grotta James C.1, Ajani Zahra, Alexandrov Andrei V., Cherches Igor, Coull Bruce, Dawson Jesse, del Junco Debra, Demchuk Andrew, Devine Joseph, Dickerson Aisha S., Dixit Anand, Frey James L., James Martin, Khan Usman, Levine Steven, MacDonald Claire, Malkoff Marc, McColl Elaine, Misra Vivek, Mullen Michael, Perry Richard, Piechowski-Jozwiak Bartlomiej, Roffe Christine, Sangha Navi, Sisson April, Tsivgoulis Georgios, Volpi John J.,
Affiliation:
1. From the Department of Neurology (A.D.B., L.S.), Center for Clinical Research and Evidence-Based Medicine (A.D.B., C.P., J.T.), and Division of Clinical and Translational Sciences (DCTS), Department of Internal Medicine (C.C., M.H.R.), McGovern Medical School at The University of Texas Health Science Center at Houston; Newcastle Clinical Trials Unit (NCTU), Newcastle University, United Kingdom (G.A.F.); Division of Medical Sciences, Oxford University, and Oxford University Hospitals NHS Foundation...
Abstract
Background and Purpose—
We conducted a randomized exploratory study to assess safety and the probability of a favorable outcome with adjunctive argatroban, a direct thrombin-inhibitor, administered to recombinant tissue-type plasminogen activator (r-tPA)–treated ischemic stroke patients.
Methods—
Patients treated with standard-dose r-tPA, not receiving endovascular therapy, were randomized to receive no argatroban or argatroban (100 μg/kg bolus) followed by infusion of either 1 (low dose) or 3 μg/kg per minute (high dose) for 48 hours. Safety was incidence of symptomatic intracerebral hemorrhage. Probability of clinical benefit (modified Rankin Scale score 0–1 at 90 days) was estimated using a conservative Bayesian Poisson model (neutral prior probability centered at relative risk, 1.0 and 95% prior intervals, 0.33–3.0).
Results—
Ninety patients were randomized: 29 to r-tPA alone, 30 to r-tPA+low-dose argatroban, and 31 to r-tPA+high-dose argatroban. Rates of symptomatic intracerebral hemorrhage were similar among control, low-dose, and high-dose arms: 3/29 (10%), 4/30 (13%), and 2/31 (7%), respectively. At 90 days, 6 (21%) r-tPA alone, 9 (30%) low-dose, and 10 (32%) high-dose patients were with modified Rankin Scale score 0 to 1. The relative risks (95% credible interval) for modified Rankin Scale score 0 to 1 with low, high, and either low or high dose argatroban were 1.17 (0.57–2.37), 1.27 (0.63–2.53), and 1.34 (0.68–2.76), respectively. The probability that adjunctive argatroban was superior to r-tPA alone was 67%, 74%, and 79% for low, high, and low or high dose, respectively.
Conclusions—
In patients treated with r-tPA, adjunctive argatroban was not associated with increased risk of symptomatic intracerebral hemorrhage and provides evidence that a definitive effectiveness trial is indicated.
Clinical Trial Registration—
URL:
http://www.clinicaltrials.gov
. Unique Identifier: NCT01464788.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Advanced and Specialised Nursing,Cardiology and Cardiovascular Medicine,Clinical Neurology
Cited by
81 articles.
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