Literature DB >> 14681620

Prospective, randomized study of external jugular vein patch versus polytetrafluoroethylene patch during carotid endarterectomy: perioperative and long-term results.

Franco Grego1, Michelle Antonello, Sandro Lepidi, Stefano Bonvini, Giovanni P Deriu.   

Abstract

OBJECTIVES: The purpose of this study was to evaluate the relative risks and advantages of using external jugular vein (EJV) patch, compared with polytetrafluoroethylene (PTFE) patch, during carotid endarterectomy. The primary end point was the relevant neurologic complication rate (RNCR; fatal or disabling stroke) at any time during follow-up. Secondary end points included stroke-free survival, 30-day and long-term mortality, recurrent stenosis rate (> or =50%), occlusion, patch infection, aneurysm formation, and other local complications.
METHODS: The study, a prospective randomized clinical trial carried out at a single center, was divided into two 3-year phases: December 1996 to March 1999, when patients were enrolled, and March 1999 to March 2002, which was the follow-up period. Inclusion criteria included an external jugular vein suitable for patching, defined as vein diameter 3 mm or larger and absence of collateral vessels noted on preoperative color duplex ultrasound scans. Patients were prospectively randomized 1:1 to receive either the EJV (n = 80; group A) or synthetic (n = 80; group B) patch.
RESULTS: Carotid endarterectomy and patching was performed by one surgeon. At 30 months the RNCR-free rate, analyzed with the Kaplan-Meier method, was 98.7% for group A (1 ipsilateral lethal stroke) and 94.6% for group B (4 ipsilateral disabling strokes), and remained stable to 60 months. No statistical difference was observed with the log-rank test. Stroke-free survival rate was 100% for group A and 98.7% for group B at 1 year, 98.7% for group A and 93.6% for group B (1 ipsilateral minor stroke) at 30 months, and was unchanged at 60 months. Life table analysis demonstrated freedom from significant recurrent stenosis (> or =50%) of 97.5% for both groups at 6 months, 93.6% for group A and 92.2% for group B at 30 months, and 90.2% for group A and 86.7% for group B at 60 months. No statistical difference was observed with the log-rank test. In no patients was recurrent stenosis greater than 70%. No aneurysm formation was noted during follow-up.
CONCLUSIONS: We can conclude, with the power limitation of the study, that carotid endarterectomy can be safely performed with either the EJV or PTFE patch. Advantages of the EJV for carotid angioplasty include no cost for material, low risk for graft infection, and preservation of the saphenous vein.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14681620     DOI: 10.1016/s0741-5214(03)00912-1

Source DB:  PubMed          Journal:  J Vasc Surg        ISSN: 0741-5214            Impact factor:   4.268


  5 in total

Review 1.  Patches for carotid artery endarterectomy: current materials and prospects.

Authors:  Akihito Muto; Toshiya Nishibe; Herbert Dardik; Alan Dardik
Journal:  J Vasc Surg       Date:  2009-07       Impact factor: 4.268

2.  Prospective randomized trial of ACUSEAL versus Vascu-Guard patching in carotid endarterectomy.

Authors:  Patrick A Stone; Ali F AbuRahma; Albeir Y Mousa; David Phang; Stephen M Hass; Asmita Modak; David Dearing
Journal:  Ann Vasc Surg       Date:  2014-02-19       Impact factor: 1.466

Review 3.  Patches of different types for carotid patch angioplasty.

Authors:  Kittipan Rerkasem; Peter M Rothwell
Journal:  Cochrane Database Syst Rev       Date:  2010-03-17

4.  Patches of different types for carotid patch angioplasty.

Authors:  Saritphat Orrapin; Thoetphum Benyakorn; Dominic Pj Howard; Boonying Siribumrungwong; Kittipan Rerkasem
Journal:  Cochrane Database Syst Rev       Date:  2021-02-18

Review 5.  Systematic review of randomized controlled trials of different types of patch materials during carotid endarterectomy.

Authors:  Shiyan Ren; Xianlun Li; Jianyan Wen; Wenjian Zhang; Peng Liu
Journal:  PLoS One       Date:  2013-01-31       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.