Combined Intravenous Thrombolysis and Thrombectomy vs Thrombectomy Alone for Acute Ischemic Stroke: A Pooled Analysis of the SWIFT and STAR Studies.

Coutinho, Jonathan M; Liebeskind, David S; Slater, Lee-Anne; Nogueira, Raul G; Clark, Wayne; Dávalos, Antoni; Bonafé, Alain; Jahan, Reza; Fischer, Urs; Gralla, Jan; Saver, Jeffrey L; Pereira, Vitor M (2017). Combined Intravenous Thrombolysis and Thrombectomy vs Thrombectomy Alone for Acute Ischemic Stroke: A Pooled Analysis of the SWIFT and STAR Studies. JAMA neurology, 74(3), pp. 268-274. American Medical Association 10.1001/jamaneurol.2016.5374

[img]
Preview
Text
jamaneurology_Coutinho_2017_oi_160109.pdf - Published Version
Available under License Publisher holds Copyright.

Download (318kB) | Preview

Importance

Mechanical thrombectomy (MT) improves clinical outcomes in patients with acute ischemic stroke (AIS) caused by a large vessel occlusion. However, it is not known whether intravenous thrombolysis (IVT) is of added benefit in patients undergoing MT.

Objective

To examine whether treatment with IVT before MT with a stent retriever is beneficial in patients undergoing MT.

Design, Setting, and Participants

This post hoc analysis used data from 291 patients treated with MT included in 2 large, multicenter, prospective clinical trials that evaluated MT for AIS (Solitaire With the Intention for Thrombectomy performed from January 1, 2010, through December 31, 2011, and Solitaire Flow Restoration Thrombectomy for Acute Revascularization from January 1, 2010, through December 31, 2012). An independent core laboratory scored the radiologic outcomes in each trial.

Interventions

Patients were treated with IVT with tissue plasminogen activator followed by MT (IVT and MT group) with the use of a stent retriever or MT with a stent retriever alone (MT group).

Main Outcomes and Measures

Successful reperfusion, functional independence (modified Rankin Scale score of 0-2) and mortality at 90 days, symptomatic intracranial hemorrhage, emboli to new territory, and vasospasm were compared.

Results

Of 291 patients included in the analysis, 160 (55.0%) underwent IVT and MT (mean [SD] age, 67 [13] years; 97 female [60.6%]), and 131 (45.0%) underwent MT alone (mean [SD] age, 69 [12] years; 71 [55.7%] female). Median Alberta Stroke Program Early CT Score at baseline was lower in the IVT and MT group (8 vs 9, P = .04). There was no statistically significant difference in the duration from symptom onset to groin puncture (254 minutes for the IVT and MT group vs 262 minutes for the MT group, P = .10). The number of passes, rate of successful reperfusion, functional independence at 90 days, mortality at 90 days, and emboli to new territory were also similar among groups. Symptomatic intracranial hemorrhage (1% vs 4%) and parenchymal hemorrhages type 1 (1% vs 3%) or type 2 (1% vs 2%) did not differ significantly (P = .25). Vasospasm occurred more often in patients who received IVT and MT vs MT alone (27% vs 14%, P = .006). In multivariate analysis, no statistically significant association was observed between IVT and MT vs MT alone for any of the outcomes.

Conclusions and Relevance

The results indicate that treatment of patients experiencing AIS due to a large vessel occlusion with IVT before MT does not appear to provide a clinical benefit over MT alone. A randomized clinical trial seems warranted.

Trial Registration

clinicaltrials.gov Identifiers: NCT01054560 and NCT01327989.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Institute of Diagnostic and Interventional Neuroradiology
04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology

UniBE Contributor:

Fischer, Urs Martin, Gralla, Jan

Subjects:

600 Technology > 610 Medicine & health

ISSN:

2168-6157

Publisher:

American Medical Association

Language:

English

Submitter:

Martin Zbinden

Date Deposited:

28 Jul 2017 12:55

Last Modified:

02 Mar 2023 23:28

Publisher DOI:

10.1001/jamaneurol.2016.5374

PubMed ID:

28097310

BORIS DOI:

10.7892/boris.94537

URI:

https://boris.unibe.ch/id/eprint/94537

Actions (login required)

Edit item Edit item
Provide Feedback