Evaluating the safety and efficacy of intravenous thrombolysis for acute ischemic stroke patients with a history of intracerebral hemorrhage: a systematic review and meta-analysis

Previous intracerebral hemorrhage (ICH) is labelled as a contraindication for the use of intravenous tissue plasminogen activator (IV-tPA) in acute ischemic stroke (AIS) based on expert opinion. However, there is a paucity of data available regarding the benefits and risks of IV-tPA in this populati...

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Veröffentlicht in:Journal of thrombosis and thrombolysis 2022-02, Vol.53 (2), p.485-494
Hauptverfasser: Goh, Sherill, Tan, Natalie H. W., Tan, Choon Han, Leow, Aloysius S. T., Sia, Ching-Hui, Ho, Andrew F. W., Lim, Mervyn J. R., Yeo, Leonard L. L., Tan, Benjamin Y. Q.
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Sprache:eng
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Zusammenfassung:Previous intracerebral hemorrhage (ICH) is labelled as a contraindication for the use of intravenous tissue plasminogen activator (IV-tPA) in acute ischemic stroke (AIS) based on expert opinion. However, there is a paucity of data available regarding the benefits and risks of IV-tPA in this population. Recent small retrospective cohort studies reporting its off-label use suggest it may be beneficial. This study aims to investigate the safety and efficacy of IV-tPA in AIS patients with previous ICH. We performed a systematic review and meta-analysis of studies reporting on IV-tPA use in AIS patients with and without previous ICH. We searched Embase, PubMed and Cochrane Library from inception to 20 April 2021. Outcomes measured included symptomatic ICH (sICH), 3-month modified Rankin Scale (mRS) score, and 3-month mortality. We included seven retrospective cohort studies comprising 5760 AIS patients who had received IV-tPA, of which 134 had previous ICH. There was no significant difference in the odds of sICH (OR 1.57, 95% CI 0.78–3.15, p = 0.21) and 3-month mRS (mRS 0–1: OR 0.78, 95% CI 0.37–1.65, p = 0.52; mRS 0–2: OR 1.07, 95% CI 0.36–3.15, p = 0.90) between patients with and without previous ICH. There was a trend towards higher 3-month mortality in patients with previous ICH (OR 1.69, 95% CI 0.98–2.91, p = 0.06), although this did not reach statistical significance. The use of IV-tPA in AIS patients with previous ICH was not associated with an increased risk of sICH or disability at 3 months. Further larger studies are needed to establish the safety and efficacy of IV-tPA use in this population.
ISSN:0929-5305
1573-742X
DOI:10.1007/s11239-021-02531-2