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Randomized Controlled Trial
. 2012 Sep;11(9):755-63.
doi: 10.1016/S1474-4422(12)70159-X. Epub 2012 Aug 2.

Restenosis after carotid artery stenting and endarterectomy: a secondary analysis of CREST, a randomised controlled trial

Collaborators, Affiliations
Randomized Controlled Trial

Restenosis after carotid artery stenting and endarterectomy: a secondary analysis of CREST, a randomised controlled trial

Brajesh K Lal et al. Lancet Neurol. 2012 Sep.

Abstract

Background: In the Carotid Revascularization Endarterectomy versus Stenting Trial (CREST), the composite primary endpoint of stroke, myocardial infarction, or death during the periprocedural period or ipsilateral stroke thereafter did not differ between carotid artery stenting and carotid endarterectomy for symptomatic or asymptomatic carotid stenosis. A secondary aim of this randomised trial was to compare the composite endpoint of restenosis or occlusion.

Methods: Patients with stenosis of the carotid artery who were asymptomatic or had had a transient ischaemic attack, amaurosis fugax, or a minor stroke were eligible for CREST and were enrolled at 117 clinical centres in the USA and Canada between Dec 21, 2000, and July 18, 2008. In this secondary analysis, the main endpoint was a composite of restenosis or occlusion at 2 years. Restenosis and occlusion were assessed by duplex ultrasonography at 1, 6, 12, 24, and 48 months and were defined as a reduction in diameter of the target artery of at least 70%, diagnosed by a peak systolic velocity of at least 3·0 m/s. Studies were done in CREST-certified laboratories and interpreted at the Ultrasound Core Laboratory (University of Washington). The frequency of restenosis was calculated by Kaplan-Meier survival estimates and was compared during a 2-year follow-up period. We used proportional hazards models to assess the association between baseline characteristics and risk of restenosis. Analyses were per protocol. CREST is registered with ClinicalTrials.gov, number NCT00004732.

Findings: 2191 patients received their assigned treatment within 30 days of randomisation and had eligible ultrasonography (1086 who had carotid artery stenting, 1105 who had carotid endarterectomy). In 2 years, 58 patients who underwent carotid artery stenting (Kaplan-Meier rate 6·0%) and 62 who had carotid endarterectomy (6·3%) had restenosis or occlusion (hazard ratio [HR] 0·90, 95% CI 0·63-1·29; p=0·58). Female sex (1·79, 1·25-2·56), diabetes (2·31, 1·61-3·31), and dyslipidaemia (2·07, 1·01-4·26) were independent predictors of restenosis or occlusion after the two procedures. Smoking predicted an increased rate of restenosis after carotid endarterectomy (2·26, 1·34-3·77) but not after carotid artery stenting (0·77, 0·41-1·42).

Interpretation: Restenosis and occlusion were infrequent and rates were similar up to 2 years after carotid endarterectomy and carotid artery stenting. Subsets of patients could benefit from early and frequent monitoring after revascularisation.

Funding: National Institute of Neurological Disorders and Stroke and Abbott Vascular Solutions.

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Conflict of interest statement

Author conflicts of interest information: B.K. Lal: None. K.W. Beach: None. G.S. Roubin: Royalties, Abbott Vascular and Cook, Inc. H.L. Lutsep: Consultant/Advisory Board, Gore. W.S. Moore: Consultant/Advisory Board, WL Gore. M.B. Malas: None. D. Chiu: None. N.R. Gonzales: None. J.L. Burke: None. M. Rinaldi: Consultant/Advisory Board, Abbott, Cordis, and Boston Scientific. J.R. Elmore: None. F.A. Weaver: None. C.R. Narins: None. M. Foster: Honoraria, Abbott Vascular. K. Hodgson: None. A.D. Shepard: None. J.F. Meschia: None. R.O. Bergelin: None. J.H. Voeks: None. G. Howard: Support from Abbott Vascular for preparation of FDA materials. T.G. Brott: None.

Figures

Figure 1
Figure 1
Four-year Kaplan-Meier graph demonstrating restenosis or occlusion in patients randomized to undergo carotid artery stenting versus carotid endarterectomy. There are more subjects included in this analysis and in the Figure than are listed in Table 1 (i.e. some subjects had only 36 or 48 month US but not 24 month US, and so could be included in this analysis which extends past 2 years). CAS=Carotid artery stenting, CEA=Carotid endarterectomy, n=number of patients assessed at each time point, day 0 is defined as the date for the CAS or CEA procedure.
Figure 2
Figure 2
Frequency of restenosis after carotid artery stenting or endarterectomy with different PSV thresholds Bars indicate SE. PSV=peak systolic velocity.

Comment in

References

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