Abstract
BACKGROUND AND PURPOSE: Endovascular therapy has become the standard of care for patients with disabling anterior circulation ischemic stroke due to proximal intracranial thrombi. Our aim was to determine whether the beneficial effect of endovascular treatment on functional outcome could be explained by a reduction in posttreatment infarct volume in the Endovascular Revascularization With Solitaire Device Versus Best Medical Therapy in Anterior Circulation Stroke Within 8 Hours (REVASCAT) trial.
MATERIALS AND METHODS: The REVASCAT trial was a multicenter randomized open-label trial with blinded outcome evaluation. Among 206 enrolled subjects (endovascular treatment, n = 103; control, n = 103), posttreatment infarct volume was measured in 204 subjects. Posttreatment infarct volumes were compared with treatment assignment and recanalization status. Appropriate statistical models were used to assess the relationship among baseline clinical and imaging variables, posttreatment infarct volume, the 24-hour NIHSS score, and functional status with the 90-day modified Rankin Scale score.
RESULTS: The median posttreatment infarct volume in all subjects was 23.7 mL (interquartile range = 68.9 mL) and 16.3 mL (interquartile range = 50.2 mL) in the endovascular treatment arm and 38.6 mL (interquartile range = 74.9 mL) in the control arm (P = .02 for endovascular treatment versus control subjects). Baseline NIHSS (P < .01), site of occlusion (P < .03), baseline NCCT ASPECTS (P < .01), and recanalization status (P = .02) were independently associated with posttreatment infarct volume. Baseline NIHSS (P < .01), time from symptom onset to randomization (P = .02), treatment type (P = .04), and recanalization status (P < .01) were independently associated with the 24-hour NIHSS scores. The 24-hour NIHSS score strongly mediated the relationship between treatment type and 90-day mRS (P < .01 for indirect effect when adjusted for age), while posttreatment infarct volume did not (P = .26).
CONCLUSIONS: Endovascular treatment saves brain and improves 90-day clinical outcomes primarily through a beneficial effect on the 24-hour stroke severity.
ABBREVIATIONS:
- EVT
- endovascular treatment
- IQR
- interquartile range
Footnotes
Disclosures: Maria A. de Miquel—UNRELATED: Board Membership: Fundació Ictus. Andrew M. Demchuk—RELATED: Consulting Fee or Honorarium: Medtronic, Comments: honorarium for Continuing Medical Education events. Tudor G. Jovin—RELATED: Support for Travel to Meetings for the Study or Other Purposes: Fundació Ictus; UNRELATED: Consultancy: Neuravi, Johnson & Johnson; Employment: Stryker; Stock/Stock Options: FreeOx Biotech, Blockade Medical, Anaconda, Silk Road; Travel/Accommodations/Meeting Expenses Unrelated to Activities Listed: Stryker Neurovascular. Antoni Dávalos—RELATED: Grant: Covidien-Medtronic, Comments: unrestricted grant for conducting the REVASCAT trial*; UNRELATED: Payment for Lectures Including Service on Speakers Bureaus: Medtronic, Comments: less than US $2000. Mayank Goyal—UNRELATED: Grant: Medtronic, Comments: part funding for the ESCAPE trial and funding for the HERMES collaboration*; Consulting Fee or Honorarium: Medtronic, Stryker, MicroVention, Comments: for education and advice related to acute stroke; Other: GE Healthcare, Comments: licensing agreement for systems of stroke diagnosis. *Money paid to the institution.
REVASCAT was funded by a local independent Catalan institution (Fundació Ictus Malaltia Vascular) through an unrestricted grant from the manufacturer of the device (Covidien). This project has been partially supported by a grant from the Spanish Ministry of Health cofinanced by FEDER (Instituto de Salud Carlos III, RETICS-INVICTUS PLUS, RD 16/0019).
Clinical Trial Registration: https://clinicaltrials.gov/ct2/show/NCT01692379.
- © 2018 by American Journal of Neuroradiology
Indicates open access to non-subscribers at www.ajnr.org