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开发全国代表性的前列腺消融技术协调注册网络。

Development of a Nationally Representative Coordinated Registry Network for Prostate Ablation Technologies.

机构信息

Department of Urology, New York Presbyterian-Weill Cornell Medical College, New York, New York.

Department of Healthcare Policy and Research, Weill Cornell Medical College, New York, New York.

出版信息

J Urol. 2018 Jun;199(6):1488-1493. doi: 10.1016/j.juro.2017.12.058. Epub 2018 Jan 4.

Abstract

PURPOSE

The accumulation of data through a prospective, multicenter coordinated registry network is a practical way to gather real world evidence on the performance of novel prostate ablation technologies. Urological oncologists, targeted biopsy experts, industry representatives and representatives of the FDA (Food and Drug Administration) convened to discuss the role, feasibility and important data elements of a coordinated registry network to assess new and existing prostate ablation technologies.

MATERIALS AND METHODS

A multiround Delphi consensus approach was performed which included the opinion of 15 expert urologists, representatives of the FDA and leadership from high intensity focused ultrasound device manufacturers. Stakeholders provided input in 3 consecutive rounds with conference calls following each round to obtain consensus on remaining items. Participants agreed that these elements initially developed for high intensity focused ultrasound are compatible with other prostate ablation technologies. Coordinated registry network elements were reviewed and supplemented with data elements from the FDA common study metrics.

RESULTS

The working group reached consensus on capturing specific patient demographics, treatment details, oncologic outcomes, functional outcomes and complications. Validated health related quality of life questionnaires were selected to capture patient reported outcomes, including the IIEF-5 (International Index of Erectile Function-5), the I-PSS (International Prostate Symptom Score), the EPIC-26 (Expanded Prostate Cancer Index Composite-26) and the MSHQ-EjD (Male Sexual Health Questionnaire for Ejaculatory Dysfunction). Group consensus was to obtain followup multiparametric magnetic resonance imaging and prostate biopsy approximately 12 months after ablation with additional imaging or biopsy performed as clinically indicated.

CONCLUSIONS

A national prostate ablation coordinated registry network brings forth vital practice pattern and outcomes data for this emerging treatment paradigm in the United States. Our multiple stakeholder consensus identifies critical elements to evaluate new and existing energy modalities and devices.

摘要

目的

通过前瞻性、多中心协调注册网络积累数据是收集新型前列腺消融技术实际性能的真实世界证据的一种实用方法。泌尿科肿瘤学家、靶向活检专家、行业代表以及食品和药物管理局(FDA)的代表齐聚一堂,讨论协调注册网络的作用、可行性和重要数据元素,以评估新的和现有的前列腺消融技术。

材料与方法

采用多轮 Delphi 共识方法,包括 15 名泌尿科专家、FDA 代表和高强度聚焦超声设备制造商的领导层的意见。利益相关者在 3 轮会议中提供意见,每轮会议后进行电话会议,以就剩余项目达成共识。参与者一致认为,这些最初为高强度聚焦超声开发的元素与其他前列腺消融技术兼容。审查了协调注册网络的元素,并补充了来自 FDA 通用研究指标的数据元素。

结果

工作组就捕获特定患者人口统计学、治疗细节、肿瘤学结果、功能结果和并发症达成共识。选择经过验证的健康相关生活质量问卷来捕获患者报告的结果,包括 IIEF-5(国际勃起功能指数-5)、I-PSS(国际前列腺症状评分)、EPIC-26(扩展前列腺癌指数综合评分-26)和 MSHQ-EjD(男性性健康问卷射精功能障碍)。专家组一致认为,大约在消融后 12 个月,需要进行多参数磁共振成像和前列腺活检随访,并根据临床需要进行额外的成像或活检。

结论

美国的全国前列腺消融协调注册网络提供了这种新兴治疗模式的重要实践模式和结果数据。我们的多利益相关者共识确定了评估新的和现有的能量模式和设备的关键要素。

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