Research Integrity in Guidelines and evIDence synthesis (RIGID): a framework for assessing research integrity in guideline development and evidence synthesis

被引:13
作者
Mousa, Aya [1 ]
Flanagan, Madeline [2 ]
Tay, Chau Thien [1 ]
Norman, Robert J. [3 ]
Costello, Michael [4 ]
Li, Wentao [2 ,5 ,6 ]
Wang, Rui [2 ]
Teede, Helena [1 ]
Mol, Ben W. [2 ,7 ]
机构
[1] Monash Univ, Fac Med Nursing & Hlth Sci, Monash Ctr Hlth Res & Implementat MCHRI, Melbourne, Vic, Australia
[2] Monash Univ, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[3] Univ Adelaide, Robinson Res Inst, Adelaide Med Sch, Adelaide, SA, Australia
[4] Univ New South Wales, Sydney, NSW, Australia
[5] Univ New South Wales, Ctr Big Data Res Hlth, Natl Perinatal Epidemiol & Stat Unit, Sydney, Australia
[6] Univ New South Wales, Sch Womens & Childrens Hlth, Sydney, Australia
[7] Univ Aberdeen, Aberdeen Ctr Womens Hlth Res, Aberdeen, Scotland
基金
英国医学研究理事会;
关键词
Research integrity; Retraction; Evidence-based guidelines; Evidence synthesis; Guideline development; Clinical practice recommendations; RANDOMIZED CONTROLLED-TRIALS; QUALITY; MISCONDUCT;
D O I
10.1016/j.eclinm.2024.102717
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Clinical guidelines rely on sound evidence to underpin recommendations for patient care. Compromised research integrity can erode public trust and the credibility of the scientific fi c enterprise, with potential harm to patients. Despite increased recognition of integrity concerns in scientific fi c literature, there are no processes or guidance for incorporating integrity assessments into evidence-based guideline development or evidence synthesis more broadly. Methods In response to this crucial gap, we developed the Research Integrity in Guidelines and evIDence synthesis (RIGID) framework. Co-developed with international input from 80 multidisciplinary experts, and consumers, the RIGID framework and accompanying checklist provide an innovative and transparent six-step approach to assess the integrity of studies during the synthesis of evidence, including in the development of clinical guidelines. Central to the framework is an integrity committee, responsible for objective assessments and allocations, with constructive author engagement. Findings The six key steps of the RIGID framework are described, as follows: (1) Review: standard systematic review processes are followed, in line with approved evidence synthesis methodologies; (2) Exclude: studies which have been retracted are excluded, and those with expressions of concern are fl agged for further evaluation; (3) Assess: remaining studies are assessed for integrity using an appropriate tool and allocated an initial integrity risk rating of low, moderate or high risk for integrity concerns; (4) Discuss: integrity assessment results are discussed among integrity committee members with votes to determine fi nal integrity risk rating allocations for each study; (5) Establish contact: low risk studies are included without author contact, whereas authors of studies ranked as moderate or high risk are contacted for clarification; fi cation; (6) Reassess: studies are reassessed for inclusion using the RIGID author response algorithm (reclassified fi ed as ' included ' where authors have provided a satisfactory response, ' awaiting classification' fi cation ' where authors have engaged but time is needed to address concerns, or ' not included' ' where authors have not responded to contact attempts). An illustrative case study is presented, where these six steps of the RIGID framework were successfully implemented in an influential fl uential international guideline endorsed by 39 societies across six continents. Following implementation of the framework, 45 of the 101 originally identified fi ed studies (45%) were not included in the guideline. Interpretation Based on the latest literature and international expertise, the RIGID framework represents an important advancement in best practice standards for guideline development and evidence synthesis. Using this resource, guideline developers, policy-makers, clinicians and scientists are better positioned to navigate the currently precarious research landscape to ensure evidence synthesis and subsequent clinical recommendations prioritize patient care and preserve the sanctity of scientific fi c endeavors. Funding This study received no specific fi c funding. The guideline in which it was piloted was supported by the Australian National Health and Medical Research Council (NHMRC) for guideline development through the Centre of Research Excellence (CRE) in Women's ' s Health in Reproductive Life (CRE-WHiRL) (APP1171592) and the CRE in Polycystic Ovary Syndrome (CRE-PCOS) (APP1078444) led by Monash University, Australia, and partner societies: the American Society for Reproductive Medicine (ASRM), the US Endocrine Society (ENDO), the European Society of Endocrinology (ESE) and the European Society of Human Reproduction and Embryology (ESHRE). Copyright (c) 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).
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页数:16
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