Jensen L P, Lepäntalo M, Fossdal J E, Røder O C, Jensen B S, Madsen M S, Grenager O, Fasting H, Myhre H O, Baekgaard N, Nielsen O M, Helgstrand U, Schroeder T V
Department of Vascular Surgery B, Copenhagen University Gentofte Hospital, , Copenhagen, Denmark.
Eur J Vasc Endovasc Surg. 2007 Jul;34(1):44-9. doi: 10.1016/j.ejvs.2007.01.016. Epub 2007 Apr 2.
To compare polytetrafluorethylene (PTFE) and polyester grafts (Dacron) for above knee femoropopliteal bypass.
Multicenter randomised clinical trial.
427 patients were randomised between 6mm Dacron (Uni-Graft, B. Braun Melsungen AG, 34212 Melsungen, Germany) and PTFE (Goretex, W. L. Gore & Ass. Inc., Newark DE 19711, USA) above-knee femoropopliteal bypass grafts within 13 centres in Denmark (n=261), Norway (n=113) & Finland (n=53) between 1993 and 1998. Fourteen (3%) patients were excluded, leaving 413 patients with 208 Dacron and 205 PTFE grafts for analysis. Age, gender, indication (claudication: 65%), run-off (2 or 3 vessels: 76%), diabetes (17%) and hypertension (31%) as well as cerebrovascular (9%) and cardiac (33%) risks were evenly distributed. Patients were followed postoperatively at 1, 12 and 24 months. Patency assessment was based on ankle-brachial pressures or imaging in case of doubt.
The two-year primary patency rates for Dacron and PTFE were 70% and 57% (p=0.02), whereas the secondary patency rates were 76% and 65% (p=0.04), respectively. Primary patency at two years was significantly influenced by the number of patent crural vessels (two or three 67%, one 50%, p=0.01). Amputations at two years, major in 4% and minor in 3%, 30-days mortality and complications (wound infections: 3% and other wound complications: 13%) occurred equally frequent in both groups. At two years, patients treated for critical limb ischemia had a major amputation more often than patients operated on for intermittent claudication, 10 and 3 respectively (p=0.003), and had higher mortality rates, 20% and 8% respectively (p=0.001).
This trial confirms that Dacron is at least as durable as PTFE for above-knee bypass procedures, and might even be superior.
比较聚四氟乙烯(PTFE)和聚酯移植物(涤纶)用于膝上股腘动脉搭桥术的效果。
多中心随机临床试验。
1993年至1998年间,在丹麦(n = 261)、挪威(n = 113)和芬兰(n = 53)的13个中心,427例患者被随机分配接受6mm涤纶(Uni-Graft,贝朗医疗公司,德国梅尔松根34212)和PTFE(戈尔特斯,美国戈尔公司,特拉华州纽瓦克19711)膝上股腘动脉搭桥移植物治疗。14例(3%)患者被排除,剩余413例患者,其中208例使用涤纶移植物,205例使用PTFE移植物进行分析。年龄、性别、适应证(跛行:65%)、流出道(2或3支血管:76%)、糖尿病(17%)、高血压(31%)以及脑血管疾病风险(9%)和心脏疾病风险(33%)在两组中分布均匀。术后对患者进行1个月、12个月和24个月的随访。通畅性评估基于踝肱压力,如有疑问则采用影像学检查。
涤纶和PTFE的两年原发性通畅率分别为70%和57%(p = 0.02),而继发性通畅率分别为76%和65%(p = 0.04)。两年时的原发性通畅率受小腿通畅血管数量的显著影响(两支或三支血管通畅为67%,一支血管通畅为50%,p = 0.01)。两年时的截肢率,大截肢为4%,小截肢为3%,两组的30天死亡率和并发症(伤口感染:3%,其他伤口并发症:13%)发生率相同。两年时,因严重肢体缺血接受治疗的患者大截肢发生率高于因间歇性跛行接受手术的患者,分别为10%和3%(p = 0.003),且死亡率更高,分别为20%和8%(p = 0.001)。
该试验证实,在膝上搭桥手术中,涤纶至少与PTFE一样耐用,甚至可能更优。