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英国使用SphinKeeper™ 括约肌间植入物治疗大便失禁的初步经验:一项双中心回顾性临床审计

Initial experience with SphinKeeper™ intersphincteric implants for faecal incontinence in the UK: a two-centre retrospective clinical audit.

作者信息

Leo C A, Leeuwenburgh M, Orlando A, Corr A, Scott S M, Murphy J, Knowles C H, Vaizey C J, Giordano P

机构信息

Imperial College London, London, UK.

Sir Alan Park's Physiology Unit, St Mark's Hospital Academic Institute, Harrow, UK.

出版信息

Colorectal Dis. 2020 Dec;22(12):2161-2169. doi: 10.1111/codi.15277. Epub 2020 Sep 22.

Abstract

AIM

The SphinKeeper™ artificial bowel sphincter implant is a relatively new surgical technique for the treatment of refractory faecal incontinence. This study presents the first experience in two UK tertiary centres.

METHOD

This is a retrospective audit of prospectively collected clinical data in relation to technique, safety, feasibility and short-term effectiveness from patients undergoing surgery from January 2016 to April 2019. Baseline data, intra-operative and postoperative complications, symptoms [using St Mark's incontinence score (SMIS)] and radiological outcomes were analysed.

RESULTS

Twenty-seven patients [18 women, median age 57 years (range 27-87)] underwent SphinKeeper. In 30% of the patients, the firing device jammed and not all prostheses were delivered. There were no intra-operative complications and all patients were discharged the same or the following day. SMIS significantly improved from baseline [median -6 points (range -12 to +3); P < 0.00016] with 14/27 (51.9%) patients achieving a 50% reduction in the SMIS score. On postoperative imaging, a median of seven prostheses (range 0-10) were identified with a median of five (range 0-10) optimally placed. There was no relationship between number of well-sited prostheses on postoperative imaging and categorical success based on 50% reduction in SMIS (χ test, P = 0.79).

CONCLUSION

SphinKeeper appears to be a safe procedure for faecal incontinence. Overall, about 50% patients achieved a meaningful improvement in symptoms. However, clinical benefit was unrelated to the rate of misplaced/migrated implants. This has implications for confidence in proof of mechanism and also the need for technical refinement.

摘要

目的

SphinKeeper™人工肛门括约肌植入术是一种治疗难治性大便失禁的相对较新的外科技术。本研究展示了英国两个三级医疗中心的首例经验。

方法

这是一项对2016年1月至2019年4月接受手术患者的前瞻性收集的临床数据进行的回顾性审计,涉及技术、安全性、可行性和短期有效性。分析了基线数据、术中及术后并发症、症状[使用圣马克失禁评分(SMIS)]和影像学结果。

结果

27例患者[18名女性,中位年龄57岁(范围27 - 87岁)]接受了SphinKeeper手术。30%的患者发射装置发生故障,并非所有假体都成功植入。无术中并发症,所有患者均在手术当天或次日出院。SMIS较基线显著改善[中位改善 -6分(范围 -12至 +3);P < 0.00016],14/27(51.9%)的患者SMIS评分降低了50%。术后影像学检查显示,中位发现7个假体(范围0 - 10个),其中位有5个(范围0 - 10个)放置理想。术后影像学检查中放置良好的假体数量与基于SMIS降低50%的分类成功之间无相关性(χ检验,P = 0.79)。

结论

SphinKeeper手术对于大便失禁似乎是一种安全的手术方法。总体而言,约50%的患者症状得到了有意义的改善。然而,临床获益与植入物位置不当/移位的发生率无关。这对机制验证的可信度以及技术改进的必要性都有影响。

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