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深部子宫内膜异位症手术记录共识:CORDES声明

Consensus on Recording Deep Endometriosis Surgery: the CORDES statement.

作者信息

Vanhie A, Meuleman C, Tomassetti C, Timmerman D, D'Hoore A, Wolthuis A, Van Cleynenbreugel B, Dancet E, Van den Broeck U, Tsaltas J, Renner S P, Ebert A D, Carmona F, Abbott J, Stepniewska A, Taylor H, Saridogan E, Mueller M, Keckstein J, Pluchino N, Janik G, Zupi E, Minelli L, Cooper M, Dunselman G, Koh C, Abrao M S, Chapron C, D'Hooghe T

机构信息

Department of Obstetrics and Gynecology, University Hospital Leuven, Leuven, Belgium.

Department of Abdominal Surgery, University Hospital Leuven, Leuven, Belgium.

出版信息

Hum Reprod. 2016 Jun;31(6):1219-23. doi: 10.1093/humrep/dew067. Epub 2016 Apr 19.

Abstract

STUDY QUESTION

Which essential items should be recorded before, during and after endometriosis surgery and in clinical outcome based surgical trials in patients with deep endometriosis (DE)?

SUMMARY ANSWER

A DE surgical sheet (DESS) was developed for standardized reporting of the surgical treatment of DE and an international expert consensus proposal on relevant items that should be recorded in surgical outcome trials in women with DE.

WHAT IS KNOWN ALREADY

Surgery is an important treatment for symptomatic DE. So far, data have been reported in such a way that comparison of different surgical techniques is impossible. Therefore, we present an international expert proposal for standardized reporting of surgical treatment and surgical outcome trials in women with DE.

STUDY DESIGN, SIZE, DURATION: International expert consensus based on a systematic review of literature.

PARTICIPANTS/MATERIALS, SETTING, METHODS: Taking into account recommendations from Consolidated Standards of Reporting Trials (CONSORT), the Innovation Development Exploration Assessment and Long-term Study (IDEAL), the Initiative on Methods, Measurement and Pain Assessment in Clinical trials (IMMPACT) and the World Endometriosis Research Foundation Phenome and Biobanking Harmonisation Project (WERF EPHect), a systematic literature review on surgical treatment of DE was performed and resulted in a proposal for standardized reporting, adapted by contributions from eight members of the multidisciplinary Leuven University Hospitals Endometriosis Care Program, from 18 international experts and from audience feedback during three international meetings.

MAIN RESULTS AND THE ROLE OF CHANCE

We have developed the DESS to record in detail the surgical procedures for DE, and an international consensus on pre-, intra- and post-operative data that should be recorded in surgical outcome trials on DE.

LIMITATIONS, REASONS FOR CAUTION: The recommendations in this paper represent a consensus among international experts based on a systematic review of the literature. For several items and recommendations, high-quality RCTs were not available. Further research is needed to validate and evaluate the recommendations presented here.

WIDER IMPLICATIONS OF THE FINDINGS

This international expert consensus for standardized reporting of surgical treatment in women with DE, based on a systematic literature review and international consensus, can be used as a guideline to record and report surgical management of patients with DE and as a guideline to design, execute, interpret and compare clinical trials in this patient population.

STUDY FUNDING/COMPETING INTERESTS: None of the authors received funding for the development of this paper. M.A. reports personal fees and non-financial support from Bayer Pharma outside the submitted work; H.T. reports a grant from Pfizer and personal fees for being on the advisory board of Perrigo, Abbvie, Allergan and SPD.

TRIAL REGISTRATION NUMBER

N/A.

摘要

研究问题

对于深部子宫内膜异位症(DE)患者,在子宫内膜异位症手术前、手术期间和手术后以及基于临床结局的手术试验中,应记录哪些基本项目?

总结答案

制定了一份DE手术记录表(DESS),用于对DE的手术治疗进行标准化报告,并就DE女性手术结局试验中应记录的相关项目提出了一项国际专家共识提案。

已知信息

手术是有症状的DE的重要治疗方法。到目前为止,所报告的数据方式使得不同手术技术之间无法进行比较。因此,我们提出一项国际专家提案,用于对DE女性的手术治疗和手术结局试验进行标准化报告。

研究设计、规模、持续时间:基于对文献的系统评价达成国际专家共识。

参与者/材料、设置、方法:考虑到《试验报告统一标准》(CONSORT)、创新发展探索评估与长期研究(IDEAL)、临床试验方法、测量与疼痛评估倡议(IMMPACT)以及世界子宫内膜异位症研究基金会表型与生物样本库协调项目(WERF EPHect)的建议,对DE的手术治疗进行了系统的文献综述,并得出了一份标准化报告提案,该提案由鲁汶大学医院多学科子宫内膜异位症护理项目的八名成员、18名国际专家以及三次国际会议期间的听众反馈做出贡献后进行了调整。

主要结果及机遇的作用

我们开发了DESS来详细记录DE的手术过程,并就DE手术结局试验中应记录的术前、术中和术后数据达成了国际共识。

局限性、谨慎原因:本文中的建议代表了国际专家基于对文献的系统评价达成的共识。对于几个项目和建议,缺乏高质量的随机对照试验。需要进一步研究来验证和评估此处提出的建议。

研究结果的更广泛影响

基于系统的文献综述和国际共识,这份关于DE女性手术治疗标准化报告的国际专家共识可作为记录和报告DE患者手术管理的指南,也可作为设计、执行、解释和比较该患者群体临床试验的指南。

研究资金/利益冲突:本文的撰写未获得任何作者的资金支持。M.A.报告在提交的工作之外从拜耳制药获得个人费用和非财务支持;H.T.报告获得辉瑞公司的资助,以及因担任佩里戈、艾伯维、艾尔建和SPD咨询委员会成员而获得的个人费用。

试验注册号

无。

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