Lundell A, Lindblad B, Bergqvist D, Hansen F
Department of Surgery, Malmö General Hospital, Sweden.
J Vasc Surg. 1995 Jan;21(1):26-33; discussion 33-4. doi: 10.1016/s0741-5214(95)70241-5.
The purpose of this study was to evaluate whether intensive surveillance compared with routine follow-up examinations improves femoropopliteal/crural graft patency.
After operation the patients were randomized to intensive (n = 79) or routine surveillance (n = 77). The groups were matched with regard to sex, diabetes, indication for surgical procedure, surgical procedure, and graft material. Intensive surveillance was clinical examination, ankle/brachial index measurements, and duplex scans 1, 3, 6, 9, 12, 15, 18, 21, 24, and 36 months after operation. Routine surveillance was clinical examination and ankle/brachial index measurements without duplex scanning 1, 12, 24, and 36 months after operation. Grafts with a decrease in ankle/brachial index of more than 0.15 compared with the initial postoperative ankle/brachial index or a duplex scan showing a graft or anastomotic stenosis of more than 50% underwent angiography and if necessary, a revision or repeat procedure. Occluded grafts were reopened with thrombectomy or thrombolysis or were replaced with a new graft.
Assisted primary cumulative vein graft patency in the intensive group (n = 56) compared with that in the routine surveillance group (n = 50) after 3 years was 78% versus 53% (chi square analysis, 4.51; one degree of freedom; p < 0.05). Secondary patency was 82% versus 56% (chi square analysis, 5.62; one degree of freedom; p < 0.05). Assisted primary cumulative e-polytetrafluoroethylene and composite graft patency after 1 year in the intensive group (n = 23) compared with that of the routine surveillance group (n = 20) was 57% vs 50% (chi square analysis, 2.17; one degree of freedom; p > 0.1). Secondary patency was 67% vs 54% (chi square analysis, 1.85; one degree of freedom; p > 0.1). Revisions were made on 14 patent and 10 thrombosed grafts in the intensive group and on four patent and 15 thrombosed grafts in the routine surveillance group. All except eight were made during the first postoperative year.
Intensive surveillance identified failing vein grafts leading to a significantly higher cumulative assisted primary and secondary patency compared with cumulative assisted primary and secondary patency after routine follow-up examination. The patency of e-polytetrafluoroethylene and composite grafts was not influenced by intensive surveillance.
本研究旨在评估与常规随访检查相比,强化监测是否能提高股腘/小腿移植血管的通畅率。
术后患者被随机分为强化监测组(n = 79)和常规监测组(n = 77)。两组在性别、糖尿病、手术指征、手术方式和移植材料方面进行了匹配。强化监测包括术后1、3、6、9、12、15、18、21、24和36个月的临床检查、踝肱指数测量和双功超声扫描。常规监测包括术后1、12、24和36个月的临床检查和踝肱指数测量,不进行双功超声扫描。与术后初始踝肱指数相比,踝肱指数下降超过0.15或双功超声扫描显示移植血管或吻合口狭窄超过50%的移植血管进行血管造影,必要时进行修复或重复手术。闭塞的移植血管通过血栓切除术或溶栓术重新开通,或用新的移植血管替换。
3年后,强化监测组(n = 56)与常规监测组(n = 50)相比,辅助原发性累积静脉移植血管通畅率分别为78%和53%(卡方分析,4.51;自由度为1;p < 0.05)。继发性通畅率分别为82%和56%(卡方分析,5.62;自由度为1;p < 0.05)。强化监测组(n = 23)与常规监测组(n = 20)相比,术后1年辅助原发性累积e-聚四氟乙烯和复合移植血管通畅率分别为57%和50%(卡方分析,2.17;自由度为1;p > 0.1)。继发性通畅率分别为67%和54%(卡方分析,1.85;自由度为1;p > 0.1)。强化监测组对14条通畅和10条血栓形成的移植血管进行了修复,常规监测组对4条通畅和15条血栓形成的移植血管进行了修复。除8例外,所有修复均在术后第一年进行。
与常规随访检查后的累积辅助原发性和继发性通畅率相比,强化监测可识别出功能不良的静脉移植血管,从而使累积辅助原发性和继发性通畅率显著提高。强化监测对e-聚四氟乙烯和复合移植血管的通畅率没有影响。