Skip to search boxSkip to navigationSkip to main content

Safety and efficacy of thrombectomy in acute ischaemic stroke (REVASCAT): 1-year follow-up of a randomised open-label trial

  • Antoni Dávalos
    ,
  • Erik Cobo
    ,
  • Carlos A. Molina
    ,
  • Angel Chamorro
    ,
  • M. Angeles de Miquel
    ,
  • Luis San Román
*Corresponding author for this work
  • Generalitat de Catalunya
    ,
  • Polytechnic University of Catalonia
    ,
  • Hospital Vail d'Hebron
    ,
  • Hospital Clinico Villaroel
    ,
  • Oncobell Program. L'Hospitalet de Llobregat
    ,
  • Hospital Josep Trueta
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Background The REVASCAT trial and other studies have shown that the neurovascular thrombectomy improves outcomes at 90 days post stroke. However, whether the observed benefit is sustained in the long term remains unknown. We report the results of the prespecified 12-month analysis of the REVASCAT trial. Methods Patients with acute ischaemic stroke who could be treated within 8 h of symptom onset were randomly assigned to medical therapy (including intravenous alteplase when eligible) and neurovascular thrombectomy with Solitaire FR or medical therapy alone. The main secondary outcome measure at 1 year follow-up was disability, measured using the modified Rankin Scale (mRS), ranging from 0 (no symptoms) to 6 (death) with categories 5 (severe disability) and 6 (death) collapsed into one category (severe disability or death), analysed as the distribution of the mRS. Additional prespecified secondary outcome measures included health-related quality of life measured with the EuroQol five dimensions questionnaire (EQ-5D) utility index (ranging from −0·3 to 1, higher values indicate better quality of life), the rate of functional independence (mRS 0–2), and cognitive function measured with the Trail Making Test (reported elsewhere). Treatment allocation was open label but endpoints at 12 months were assessed by masked investigators. The trial was registered at ClinicalTrials.gov, number NCT01692379. Findings From Nov 24, 2012, to Dec 12, 2014, 206 patients were randomly assigned to medical therapy plus endovascular treatment (n=103) or medical treatment alone (n=103), at four centres in Catalonia, Spain. At 12 months post randomisation, based on 205 of 206 outcomes available at 12 months, thrombectomy reduced disability over the range of the mRS (common adjusted odds ratio [aOR] 1·80, 95% CI 1·09–2·99), and improved functional independence (mRS=0–2; 45 [44%] of 103 patients vs 31 [30%] of 103 patients; aOR 1·86, 95% CI 1·01–3·44). Health-related quality of life was superior in the thrombectomy group (mean EQ-5D utility index score, 0·46 [SD 0·38] in the thrombectomy group vs 0·33 [0·33] in the control group, difference 0·12 [95% CI 0·03–0·22]; p=0·01). 1-year mortality was 23% (24 of 103 patients) in the thrombectomy group versus 24% (25 of 103 patients) in the control group. Interpretation At 12 months follow-up, neurovascular thrombectomy reduced post-stroke disability and improved health-related quality of life, indicating sustained benefit. These findings have important clinical and public health implications for evaluating the cost-effectiveness of the intervention in the long term. Funding Fundació Ictus Malaltia Vascular through an unrestricted grant from Medtronic.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 369-376 (8 pages)

Journal (Volume, Issue Number)

The Lancet Neurology (Volume 16, Issue 5)

Publication milestones

  • Published - 05/01/2017

Publication status

Published - 05/01/2017

ISSN

1474-4422

Publication IDs

  • Scopus: 85015367759
  • PubMed: 28318984

Publication metrics

Metrics

Scopus
citations
Fractional count
1
Fractional count
0.01
Fractional count
85
Fractional count
0.99
Fractional count
1
Fractional count
1
SciVal
citations
36
SciVal
FWCI
3.36
SciVal
Author count
85
SciVal
Paper percentile
95
SciVal
Top percentile
5

PlumX, opens in new tab

Mentions
2
Captures
217
Citation count
91

Funding Details

AD reports grants from Medtronic, during the conduct of the study, personal fees from Boehringer Ingelheim, and non-financial support from the Fundació Ictus Malaltia Vascular (Barcelona, Spain). EC reports grants and personal fees from Barcelona-Tech University, during the conduct of the study. CC reports personal fees from Medtronic. TGJ reports study-related travel expenses for REVASCAT from Fundació Ictus Malaltia Vascular, Anaconda, and Silk Road, non-financial support and study related travel expenses for DAWN from Stryker Neurovascular, and personal fees from Codman Neurovascular and Neuravi. CAM, AC, MAdM, LSR, JS, EL-C, MRi, MM, XU, PC, AT, JB, LA, MRu, MG, AR, BL, JM-F, BJ, and NC declare no competing interests. REVASCAT was funded by the Fundació Ictus Malaltia Vascular (Barcelona, Spain) through an unrestricted grant from the manufacturer of the device (Medtronic). This project has been partial supported by a grant from the Spanish Ministry of Health co-financed by FEDER (Instituto de Salud Carlos III, RETICS-INVICTUS, RD 12/0014/008) and a grant from the Generalitat de Catalunya (SGR 464/2014). We thank Bruce Stouch for expert statistical review.
FundersFunding numbers
Fundació Ictus Malaltia Vascular
-
Medtronic
-
Generalitat de Catalunya
SGR 464/2014
ISCIII
RD 12/0014/008
ERDF
-
Consejería de Salud y Familias, Junta de Andalucía
-