...
首页> 外文期刊>The Journal of Thoracic and Cardiovascular Surgery >Femoral vein homograft for neoaortic reconstruction in the Norwood stage 1 operation: A follow-up study
【24h】

Femoral vein homograft for neoaortic reconstruction in the Norwood stage 1 operation: A follow-up study

机译:用于Norwood阶段的新动态重建的股静脉同质化1操作:随访研究

获取原文
获取原文并翻译 | 示例

摘要

Objective: The aim of this study was to analyze our experience with the cryopreserved femoral vein homograft in comparison with standard biomaterials for neoaortic reconstruction in the Norwood stage 1 operation. Methods: All patients who underwent the Norwood operation from September 2004 to April 2011 were analyzed retrospectively (n = 107). Patients were grouped into group A (cryopreserved femoral vein homograft; n = 72) or group B (other; n = 35). Intergroup comparisons and dimensional analyses of all available angiograms were performed. Two surgical techniques, "standard homograft cuff" and "homograft tube," were compared. Results: Multivariable Cox regression analysis revealed use of biomaterial other than femoral vein (P =.01; hazard ratio, 3.0; 95% confidence interval [CI], 1.4-6.4), weight less than 2.5 kg at the time of stage 1 (P =.01; hazard ratio, 3.7; 95% CI, 1.7-7.8), and need for extracorporeal membrane oxygenator support after stage 1 (P <.001; hazard ratio, 13.8; 95% CI, 5.9-31.9) as significant independent predictors of overall mortality. Improved late survival at 48 months was seen with the femoral vein homograft compared with other biomaterials when a "homograft tube with end-to-side ascending aortic reimplantation technique" was used (group A [75%] vs group B [44%]; P =.03). With the use of the "homograft cuff technique," survival was similar for femoral vein homografts and other biomaterials (group A [67%] vs group B [61%]; P =.85). Similar neoaortic coarctation rates were seen in both groups (A: 25/59 [42%] vs B: 12/26 [46%]; P =.81). A progressive increase in the diameter of the neoaorta was seen over time in both groups with both technical modifications (tube grafts pre-stage 2 vs pre-stage 3: group A [10.61 mm ± 1.93 vs 13.74 mm ± 3.16] [P <.001] and group B [13.93 mm ± 6.71 vs 17.38 mm ± 5.92] [P =.049]); cuff repair pre-stage 2 to pre-stage 3: group A [13.98 mm ± 2.13 vs 19.09 mm ± 4.18] [P =.002] and group B [16.06 mm ± 3.05 vs 19.73 mm ± 2.93] [P <.001]). The neoaortic Z-scores were generous with the use of homograft cuffs and modest when homograft tubes were used and maintained in range over the follow-up time. Conclusions: Survivals are improved with the use of femoral vein homograft for neoaortic reconstruction for Norwood stage 1 operation, especially when used as a homograft tube with end-to-side aortic reimplantation. Femoral vein homografts have similar recoarctation rates compared with standard biomaterials. Progressive growth/dilation of the neoaorta in proportion to somatic growth is seen with femoral vein tube grafts.
机译:目的:本研究的目的是分析我们对冷冻保存的股静脉同质移植物的经验,与Norwood第1阶段的新动脉重建标准生物材料相比。方法:回顾性地分析2004年9月至2011年4月至2011年4月的所有接受挪威行动的患者(n = 107)。将患者分为a组(冷冻保存股骨静脉同源疱疹; N = 72)或B组(其他; n = 35)。执行所有可用血管造影的互组比较和尺寸分析。比较了两种手术技术,“标准同性移植箍”和“同性移植管”。结果:多变量COX回归分析显示使用股骨静脉以外的生物材料(P = .01;危险比,3.0; 95%置信区间[CI],1.4-6.4),在第1阶段时重量小于2.5千克( p = .01;危险比,3.7; 95%CI,1.7-7.8),并需要第1阶段后体外膜氧吸附剂(P <.001;危险比,13.8; 95%CI,5.9-31.9)显着整体死亡率的独立预测因素。当使用“具有端到侧升高的主动脉再抑制技术”(A组[75%] VS组[44%])时,用股静脉同种植物与其他生物材料相比,与股静脉同质化相比,与股骨静脉同源物相比,与其他生物材料相比,与其他生物材料相比,改善了48个月p = .03)。随着“仿生套袖带技术”的使用类似于股静脉同种植物移植物等生物材料(A组[67%] Vs B组[61%]; p = .85)。在两组中可以看到类似的新旋转速率(A:25/59 [42%] Vs B:12/26 [46%]; p = .81)。在两组中随着技术修改的时间随着时间的推移,在两组中看到了Neoaorta直径的渐进增加(管移植前2 Vs Pre-阶段3:A组[10.61mm±1.93 Vs 13.74mm±3.16] [P <。 001]和B组[13.93mm±6.71 Vs 17.38mm±5.92] [p = .049]);袖带修复前阶段2至前阶段3:A组[13.98 mm±2.13 Vs 19.09 mm±4.18] [p = .002]和B组[16.06 mm±3.05 Vs 19.73mm±2.93] [P <.001 ])。当使用同种植物袖口和适度时,Neooortic Z分数慷慨,当使用同种植物管并在随访时间内保持范围内。结论:利用股骨静脉同源以诺伍德第1阶段的新动态重建的使用,改善了幸存者,特别是当用作具有端到侧主动脉造影的同种质移植管。与标准生物材料相比,股静脉同质移植物具有相似的再分辨率速率。与股静脉管移植物相比,对细胞生长成比例的渐进生长/扩张。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号