Krezel Aniela K, Hogg Ruth E, Azuara-Blanco Augusto
Centre for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Br J Ophthalmol. 2015 Nov;99(11):1560-4. doi: 10.1136/bjophthalmol-2014-306544. Epub 2015 Apr 30.
BACKGROUND/AIMS: The purpose of this systematic review was to identify the frequency and type of patient-reported outcome measures (PROMs) used in recent randomised controlled trials (RCTs) for age-related macular degeneration (AMD).
The authors conducted a systematic search between January 2010 and November 2013 in MEDLINE, EMBASE, Scopus, Cochrane Library (Central) and the clinical trials registries (http://www.controlled-trials.com and http://www.ClinicalTrials.gov) according to defined inclusion criteria (RCTs on AMD in English). Two independent reviewers evaluated studies for inclusion. One reviewer extracted data of included studies, and a second masked reviewer assessed 10% to confirm accuracy in data collection. Reference lists of included papers and appendices of relevant Cochrane systematic reviews were scanned to identify other relevant RCTs. Information collected on extracted outcomes was analysed using descriptive statistics.
Literature and registry search yielded 3816 abstracts of journal articles and 493 records from trial registries. A total of 177 RCTs were deemed to have met inclusion criteria. Of the 858 outcomes reported, 38 outcomes were identified as PROMs (4.4%). Of the 177 RCTs examined, PROMs were used in 25 trials (14.1%). The National Eye Institute Visual Function Questionnaire-25 was the most frequently used PROM instrument (64% of RCTs with PROMs included).
This review highlights that a small proportion of AMD RCTs included PROMs as outcome measures and that there was a variety in the instruments used.
The systematic review was registered in the PROSPERO database for systematic reviews, registration number CRD42014010040.
背景/目的:本系统评价旨在确定近期年龄相关性黄斑变性(AMD)随机对照试验(RCT)中使用的患者报告结局指标(PROMs)的频率和类型。
作者于2010年1月至2013年11月期间,根据既定纳入标准(英文撰写的AMD的RCT),在MEDLINE、EMBASE、Scopus、Cochrane图书馆(CENTRAL)和临床试验注册库(http://www.controlled-trials.com和http://www.ClinicalTrials.gov)中进行了系统检索。两名独立评审员评估纳入研究。一名评审员提取纳入研究的数据,另一名盲态评审员评估10%以确认数据收集的准确性。扫描纳入论文的参考文献列表和相关Cochrane系统评价的附录,以识别其他相关RCT。使用描述性统计分析提取结局的收集信息。
文献和注册库检索得到3816篇期刊文章摘要和493条试验注册记录。共有177项RCT被认为符合纳入标准。在报告的858项结局中,38项结局被确定为PROMs(4.4%)。在177项纳入研究的RCT中,25项试验(14.1%)使用了PROMs。美国国立眼科研究所视觉功能问卷-25是最常用的PROM工具(纳入PROMs的RCT中有64%使用)。
本评价强调,一小部分AMD的RCT将PROMs作为结局指标,且使用的工具存在差异。
本系统评价已在PROSPERO系统评价数据库中注册,注册号为CRD42014旦场测渡爻盗诧醛超互010040。