Complications of Intravenous Tenecteplase Versus Alteplase for the Treatment of Acute Ischemic Stroke: A Systematic Review and Meta-Analysis.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
05 2023
Historique:
pmc-release: 01 05 2024
medline: 26 4 2023
pubmed: 24 3 2023
entrez: 23 3 2023
Statut: ppublish

Résumé

Prior systematic reviews have compared the efficacy of intravenous tenecteplase and alteplase in acute ischemic stroke, assigning their relative complications as a secondary objective. The objective of the present study is to determine whether the risk of treatment complications differs between patients treated with either agent. We performed a systematic review including interventional studies and prospective and retrospective, observational studies enrolling adult patients treated with intravenous tenecteplase for ischemic stroke (both comparative and noncomparative with alteplase). We searched MEDLINE, Embase, the Cochrane Library, Web of Science, and the www. gov registry from inception through June 3, 2022. The primary outcome was symptomatic intracranial hemorrhage, and secondary outcomes included any intracranial hemorrhage, angioedema, gastrointestinal hemorrhage, other extracranial hemorrhage, and mortality. We performed random effects meta-analyses where appropriate. Evidence was synthesized as relative risks, comparing risks in patients exposed to tenecteplase versus alteplase and absolute risks in patients treated with tenecteplase. Of 2226 records identified, 25 full-text articles (reporting 26 studies of 7913 patients) were included. Sixteen studies included alteplase as a comparator, and 10 were noncomparative. The relative risk of symptomatic intracranial hemorrhage in patients treated with tenecteplase compared with alteplase in the 16 comparative studies was 0.89 ([95% CI, 0.65-1.23]; I Across medium- and low-dose tiers, the risks of complications were generally comparable between those treated with tenecteplase versus alteplase for acute ischemic stroke.

Sections du résumé

BACKGROUND
Prior systematic reviews have compared the efficacy of intravenous tenecteplase and alteplase in acute ischemic stroke, assigning their relative complications as a secondary objective. The objective of the present study is to determine whether the risk of treatment complications differs between patients treated with either agent.
METHODS
We performed a systematic review including interventional studies and prospective and retrospective, observational studies enrolling adult patients treated with intravenous tenecteplase for ischemic stroke (both comparative and noncomparative with alteplase). We searched MEDLINE, Embase, the Cochrane Library, Web of Science, and the www.
CLINICALTRIALS
gov registry from inception through June 3, 2022. The primary outcome was symptomatic intracranial hemorrhage, and secondary outcomes included any intracranial hemorrhage, angioedema, gastrointestinal hemorrhage, other extracranial hemorrhage, and mortality. We performed random effects meta-analyses where appropriate. Evidence was synthesized as relative risks, comparing risks in patients exposed to tenecteplase versus alteplase and absolute risks in patients treated with tenecteplase.
RESULTS
Of 2226 records identified, 25 full-text articles (reporting 26 studies of 7913 patients) were included. Sixteen studies included alteplase as a comparator, and 10 were noncomparative. The relative risk of symptomatic intracranial hemorrhage in patients treated with tenecteplase compared with alteplase in the 16 comparative studies was 0.89 ([95% CI, 0.65-1.23]; I
CONCLUSIONS
Across medium- and low-dose tiers, the risks of complications were generally comparable between those treated with tenecteplase versus alteplase for acute ischemic stroke.

Identifiants

pubmed: 36951049
doi: 10.1161/STROKEAHA.122.042335
pmc: PMC10133185
mid: NIHMS1881280
doi:

Substances chimiques

Tissue Plasminogen Activator EC 3.4.21.68
Tenecteplase WGD229O42W
Fibrinolytic Agents 0

Types de publication

Meta-Analysis Systematic Review Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1192-1204

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL161426
Pays : United States
Organisme : NIA NIH HHS
ID : R56 AG074279
Pays : United States
Organisme : NIA NIH HHS
ID : K76 AG060001
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG078803
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG070859
Pays : United States

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Auteurs

Deborah Rose (D)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).

Annie Cavalier (A)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).

Wayneho Kam (W)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).

Sarah Cantrell (S)

Duke University Medical Center Library & Archives, Durham, NC (S.C.).
Duke University School of Medicine, Durham, NC (S.C., J.L.).

Jay Lusk (J)

Duke University School of Medicine, Durham, NC (S.C., J.L.).

Matthew Schrag (M)

Department of Neurology, Vanderbilt University School of Medicine, Nashville, TN (M.S.).

Shadi Yaghi (S)

Department of Neurology, Alpert Medical School of Brown University, Providence, RI (S.Y., C.S.).

Christoph Stretz (C)

Department of Neurology, Alpert Medical School of Brown University, Providence, RI (S.Y., C.S.).

Adam de Havenon (A)

Department of Neurology, Yale University School of Medicine, New Haven, CT (A.d.H.).

Ian J Saldanha (IJ)

Center for Evidence Synthesis in Health, Departments of Health Services, Policy, and Practice and of Epidemiology, Brown School of Public Health, Providence, RI (I.J.S.).

Teddy Y Wu (TY)

Department of Neurology, Christchurch Hospital, New Zealand (T.Y.W.).

Anna Ranta (A)

Department of Medicine, University of Otago, Wellington, New Zealand (A.R.).

P Alan Barber (PA)

Department of Medicine, University of Auckland, New Zealand (P.A.B.).

Elizabeth Marriott (E)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).

Wayne Feng (W)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).

Andrzej S Kosinski (AS)

Department of Biostatistics & Bioinformatics, Duke University, Durham, NC (A.S.K.).
Duke Clinical Research Institute, Durham, NC (A.S.K., D.L.).

Daniel Laskowitz (D)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).
Duke Clinical Research Institute, Durham, NC (A.S.K., D.L.).

Sven Poli (S)

Department of Neurology and Stroke (S.P.), University of Tübingen, Germany.
Hertie Institute for Clinical Brain Research (S.P.), University of Tübingen, Germany.

Brian Mac Grory (B)

Department of Neurology, Duke University School of Medicine, Durham, NC (D.R., A.C., W.K., E.M., W.F., D.L., B.M.G.).

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