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佛罗伦萨机器人体内新膀胱术(FloRIN):一种遵循IDEAL指南制定的新重构策略。

Florence robotic intracorporeal neobladder (FloRIN): a new reconfiguration strategy developed following the IDEAL guidelines.

作者信息

Minervini Andrea, Vanacore Davide, Vittori Gianni, Milanesi Martina, Tuccio Agostino, Siena Giampaolo, Campi Riccardo, Mari Andrea, Gavazzi Andrea, Carini Marco

机构信息

Department of Urology, University of Florence, Florence, Italy.

Azienda Sanitaria di Firenze (ASF), Florence, Italy.

出版信息

BJU Int. 2018 Feb;121(2):313-317. doi: 10.1111/bju.14077. Epub 2017 Dec 11.

Abstract

OBJECTIVE

To describe our step-by-step technique for robotic intracorporeal neobladder configuration, including the stages of conception, development and exploration of this surgical innovation, according to the Idea, Development, Exploration, Assessment, Long-term follow-up (IDEAL) Collaboration guidelines.

PATIENTS AND METHODS

The Florence robotic intracorporeal neobladder (FloRIN) was performed employing the following main surgical steps: isolation of 50 cm of ileum; bowel anastomosis; urethro-ileal anastomosis creating an asymmetrical 'U'-shape (30 cm distally and 20 cm proximally to anastomosis), ileum detubularisation; posterior wall reconfiguration as an 'L'; bladder neck reconstruction; anterior folding of the posterior plate to reach the 12 o'clock position; uretero-enteral 'orthotopic' bilateral anastomosis. The conception and development of the FloRIN followed the IDEAL guidelines recommended stages: Phase 1 (simulation) involved the neobladder robotic configuration using silicone models. Phase 2a (development) aimed to reproduce the configuration in an open fashion in one patient, and then in the first three robotic procedures. Phase 2b (exploration) consisted of the technique standardisation in 15 consecutive robotic approaches. Phase 2a and 2b included urodynamics and imaging assessment of the patients treated.

RESULTS

From February 2016 to September 2017 FloRIN was performed in 18 patients. Comparing the first three (Phase 2a) with the subsequent 15 patients (Phase 2b), the median (interquartile range [IQR]) reconstruction operating time was 260 (220-340) vs 160 (150-210) min, respectively. Postoperative surgical complications occurred in four of the 18 patients (22.1%), including one surgical Clavien-Dindo Grade III and three Grade I, postoperative medical Clavien-Dindo Grade II complications occurred in three (16.7%) patients. On urodynamic examination (available in nine [50%] patients) the median (IQR) reservoir cystometric capacity, compliance, and post-void residual were 240 (220-267) mL, 18 (12.5-19.8) mL/cmH O, and 0 (0-50) mL, respectively. Ultrasonography showed no Grade ≥2 vesico-ureteric reflux.

CONCLUSION

We describe the FloRIN configuration, showing its technical feasibility with acceptable time efficiency. The first cases studied had good reservoir capacity, low pressure with no reflux, and complete voiding.

摘要

目的

根据“理念、开发、探索、评估、长期随访(IDEAL)协作组”指南,描述我们机器人体内新膀胱构建的分步技术,包括该手术创新的构思、开发和探索阶段。

患者与方法

采用以下主要手术步骤实施佛罗伦萨机器人体内新膀胱术(FloRIN):游离50cm回肠;肠吻合;尿道-回肠吻合形成不对称的“U”形(吻合口远端30cm、近端20cm),回肠去管化;后壁重建为“L”形;膀胱颈重建;后板向前折叠至12点位置;输尿管-肠“原位”双侧吻合。FloRIN的构思和开发遵循IDEAL指南推荐的阶段:第1阶段(模拟)使用硅胶模型进行新膀胱机器人构建。第2a阶段(开发)旨在以开放方式在1例患者中重现该构建,然后在最初的3例机器人手术中进行。第2b阶段(探索)包括在连续15例机器人手术中进行技术标准化。第2a阶段和第2b阶段包括对接受治疗患者的尿动力学和影像学评估。

结果

2016年2月至2017年9月,对18例患者实施了FloRIN。将前3例(第2a阶段)与随后的15例患者(第2b阶段)进行比较,重建手术的中位(四分位间距[IQR])时间分别为260(220 - 340)分钟和160(150 - 210)分钟。18例患者中有4例(22.1%)发生术后手术并发症,包括1例手术Clavien-DindoⅢ级和3例Ⅰ级,3例(16.7%)患者发生术后内科Clavien-DindoⅡ级并发症。在尿动力学检查中(9例[50%]患者可进行),储尿囊测压容量、顺应性和排尿后残余尿量的中位(IQR)值分别为[240(220 - 267)mL、18(12.5 - 19.8)mL/cmH₂O和0(0 - 50)mL]。超声检查未显示≥2级膀胱输尿管反流。

结论

我们描述了FloRIN构建方法,显示了其技术可行性及可接受的时间效率。首批研究病例具有良好的储尿囊容量、低压且无反流以及完全排空情况。

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