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一项病例对照试点研究,评估吻合器网片造口加强技术(SMART)在降低造口旁疝发生率方面的安全性和有效性。

A case-controlled pilot study assessing the safety and efficacy of the Stapled Mesh stomA Reinforcement Technique (SMART) in reducing the incidence of parastomal herniation.

作者信息

Williams N S, Hotouras A, Bhan C, Murphy J, Chan C L

机构信息

Academic Surgical Unit, Barts Health NHS Trust, National Centre for Bowel Research and Surgical Innovation, Queen Mary University London, 2 Newark street, London, UK.

出版信息

Hernia. 2015 Dec;19(6):949-54. doi: 10.1007/s10029-015-1346-9. Epub 2015 Feb 3.

Abstract

BACKGROUND

Parastomal hernias (PH) are frequent with a high morbidity. Three randomised controlled trials have shown that prophylactic mesh stoma reinforcement significantly reduces their incidence. Implantation and fixation of mesh can be time-consuming, difficult to perform laparoscopically and does not deal with the excessive stretching of the trephine and the creation of an oversized defect. The Stapled Mesh stomA Reinforcement Technique (SMART) obviates these technical problems. The aim of this study was to assess the safety and efficacy of a novel surgical technique called SMART in preventing parastomal herniation.

METHOD

SMART uses a purpose designed circular stapling gun (Compact™, Frankenman International Limited) of various diameters to create a precise trephine and simultaneously fixes a mesh sub-peritoneally and circumferentially to the trephine. Recruited patients were deemed to be high risk for parastomal herniation and randomisation in a controlled trial was contraindicated. Incidence of parastomal related symptoms and recurrences were documented at clinic visits and radiological confirmation of recurrences, when available, was used for final analysis. A control group of patients who underwent stoma resiting without mesh reinforcement for parastomal herniation was used for comparative purposes.

RESULTS

22 patients (16 F:6 M, mean age 49 ± 16 years, BMI 33.0 ± 7.0) underwent SMART (18 open, 4 laparoscopic). There were no intra-operative or early stoma complications. During a median FU of 21 months (range 12-24), four patients (19%) were diagnosed with recurrent parastomal herniation, one of which required re-operation. The parastomal herniation rate (73%) in the control group (6 F:5 M) was significantly higher (p = 0.003) although patients had similar age (59 ± 15 years, p = 0.1) and body-mass index (29.0 ± 3.0, p = 0.1).

CONCLUSION

SMART is a new and simple technique of precisely creating a reinforced stoma trephine at both open and laparoscopic surgery. It obviates the technical disadvantages of traditional stoma formation. This pilot study, in a selected group of patients at high risk for parastomal herniation, indicates that the procedure is clinically safe but randomised controlled trials are required to determine its efficacy in reducing parastomal herniation in all patients undergoing elective stoma formation.

摘要

背景

造口旁疝(PH)很常见,发病率很高。三项随机对照试验表明,预防性使用补片进行造口加固可显著降低其发生率。补片的植入和固定可能耗时较长,难以通过腹腔镜完成,且无法解决环形切口过度拉伸以及形成过大缺损的问题。吻合器补片造口加固技术(SMART)可避免这些技术问题。本研究的目的是评估一种名为SMART的新型手术技术在预防造口旁疝方面的安全性和有效性。

方法

SMART使用一种专门设计的不同直径的圆形吻合器(Compact™,弗兰肯曼国际有限公司)制作精确的环形切口,同时将补片在腹膜下环形固定于环形切口处。招募的患者被认为发生造口旁疝的风险较高,因此不适合进行对照试验随机分组。在门诊就诊时记录造口相关症状和复发的发生率,如有影像学确认的复发情况,则用于最终分析。为作比较,设立了一个对照组,该组患者因造口旁疝接受了不使用补片加固的造口重置手术。

结果

22例患者(16例女性:6例男性,平均年龄49±16岁,BMI 33.0±7.0)接受了SMART手术(18例开放手术,4例腹腔镜手术)。术中及早期造口均无并发症。在中位随访期21个月(范围12 - 24个月)内,4例患者(19%)被诊断为造口旁疝复发,其中1例需要再次手术。对照组(6例女性:5例男性)的造口旁疝发生率(73%)显著更高(p = 0.003),尽管两组患者年龄相似(59±15岁,p = 0.1),体重指数也相近(29.0±3.0,p = 0.1)。

结论

SMART是一种在开放手术和腹腔镜手术中精确制作加固造口环形切口的新的简单技术。它消除了传统造口形成的技术缺点。这项针对一组造口旁疝高风险患者的初步研究表明,该手术在临床上是安全的,但需要进行随机对照试验以确定其在所有接受择期造口形成手术的患者中减少造口旁疝的疗效。

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