Argatroban as an Add-On to rtPA in Acute Ischemic Stroke: A Systematic Review and Meta-Analysis

Author:

Chlorogiannis David-Dimitris1ORCID,Mavridis Theodoros23ORCID,Adamou Anastasia4ORCID,Kyriakoulis Ioannis4ORCID,Stamatiou Iliana5ORCID,Botou Polyxeni6,Chen Hui-Sheng7ORCID,Ntaios George4ORCID

Affiliation:

1. Department of Radiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA

2. 1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, 11528 Athens, Greece

3. Department of Neurology, Tallaght University Hospital, D24 NR0A Dublin, Ireland

4. Department of Internal Medicine, School of Health Sciences, University of Thessaly, 41334 Larissa, Greece

5. Department of Internal Medicine, University Hospital of Alexandroupolis, 68100 Alexandroupolis, Greece

6. Department of Anaesthesiology, Hippocration General Hospital of Athens, 11527 Athens, Greece

7. Department of Neurology, General Hospital of Northern Theatre Command, Shenyang 110017, China

Abstract

Current treatment options for acute ischemic stroke, including intravenous thrombolysis (IVT) and mechanical thrombectomy, have undoubtedly revolutionized stroke care. The need for additional treatment options has brought into the light direct thrombin inhibitors (DTIs) and, specifically, argatroban as a promising candidate. However, there is uncertainty regarding the safety of adding argatroban to IVT, mainly due to the increased hemorrhagic risk. In this study, we performed a systematic review and meta-analysis examining the safety and efficacy of argatroban as an add-on treatment for IVT. The following databases were searched from inception until the 14th of May 2023: Pubmed/MEDLINE, ClinicalTrials.gov, the EU Clinical Trials Register, EMBASE/Scopus, and the Cochrane Library. Only randomized clinical trials (RCTs) enrolling patients with acute ischemic stroke who underwent IVT evaluating the add-on use of any DTIs were selected for the systematic review and further meta-analysis. The PRISMA guidelines were followed at all stages. Four studies with argatroban were included in the final analysis. Analysis of risk ratio and relative risk shows that the add-on therapy with argatroban seems to be effective and favors a good clinical outcome (mRS 0–2) at 90 days, similar to that of alteplase. All studies showed a low pooled incidence of symptomatic intracerebral hemorrhage (5%), parenchymal hematoma (3%), and other major bleeding (1%). Argatroban as an add-on treatment to IVT seems not to be associated with excessive bleeding risk; however, its efficacy remains unproven. According to this synopsis of the currently available evidence, it is premature to use argatroban as an add-on to IVT treatment outside the current clinical trial setting.

Publisher

MDPI AG

Subject

General Medicine

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