The CONSORT Patient-Reported Outcome (PRO) extension: implications for clinical trials and practice

被引:90
|
作者
Calvert, Melanie [1 ]
Brundage, Michael [2 ]
Jacobsen, Paul B. [3 ]
Schuenemann, Holger J. [4 ,5 ]
Efficace, Fabio [6 ]
机构
[1] Univ Birmingham, Sch Hlth & Populat Sci, MRC Midland Hub Trials Methodol Res, Birmingham, W Midlands, England
[2] Queens Univ, Dept Med Oncol, Kingston, ON, Canada
[3] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Dept Hlth Outcomes & Behav, Tampa, FL 33612 USA
[4] McMaster Univ, Hlth Sci Ctr, Dept Clin Epidemiol, Hamilton, ON L8S 4L8, Canada
[5] McMaster Univ, Hlth Sci Ctr, Dept Biostat & Med, Hamilton, ON L8S 4L8, Canada
[6] GIMEMA Data Ctr, Italian Grp Adult Hematol Dis GIMEMA, Head Hlth Outcomes Res Unit, I-00161 Rome, Italy
来源
基金
加拿大健康研究院; 英国医学研究理事会;
关键词
Quality of life; CONSORT PRO; Reporting; Clinical trials; QUALITY-OF-LIFE; MEDICAL JOURNALS; GUIDELINES; EDITORS; GRADE; TIME;
D O I
10.1186/1477-7525-11-184
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
To inform clinical guidelines and patient care we need high quality evidence on the relative benefits and harms of intervention. Patient reported outcome (PRO) data from clinical trials can "empower patients to make decisions based on their values" and "level the playing field between physician and patient". While clinicians have a good understanding of the concept of health-related quality of life and other PROs, evidence suggests that many do not feel comfortable in using the data from trials to inform discussions with patients and clinical practice. This may in part reflect concerns over the integrity of the data and difficulties in interpreting the results arising from poor reporting. The new CONSORT PRO extension aims to improve the reporting of PROs in trials to facilitate the use of results to inform clinical practice and health policy. While the CONSORT PRO extension is an important first step in the process, we need broader engagement with the guidance to facilitate optimal reporting and maximize use of PRO data in a clinical setting. Endorsement by journal editors, authors and peer reviewers are crucial steps. Improved design, implementation and transparent reporting of PROs in clinical trials are necessary to provide high quality evidence to inform evidence synthesis and clinical practice guidelines.
引用
收藏
页数:7
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