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      The current practice of handling and reporting missing outcome data in eight widely-used PROMS in RCT publications: are we doing well?

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      1 , 2 , , 3 , 4 , 1 , 5
      Trials
      BioMed Central
      3rd International Clinical Trials Methodology Conference
      16-17 November 2015

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          Abstract

          Purpose Patient reported outcome measures (PROMs) are designed to assess patients’ perceived health states or health-related quality of life. However, PROMs are susceptible to missing data, which can affect the validity of conclusions from randomised controlled trials (RCTs). This review aims to assess current practice in the handling, analysis and reporting of missing PROMs outcome data in RCTs in relation to contemporary methodology and guidance. Methods This structured review of the literature includes RCTs with a minimum of 50 participants per arm. Studies using the EQ-5D-3L, EORTC QLQ-C30, SF-12, and SF-36 were included if published in 2013, those using the less commonly implemented HUI, OHS, OKS, and PDQ were included if published between 2009 and 2013. Results The review included 209 papers (4 to 76 per relevant PROM). Complete case analysis and single imputation were commonly used in 33% and 15% of publications respectively. Multiple imputation was reported for 9% of the PROMs reviewed. The majority of publications (93%) failed to describe the assumed missing data mechanism, while low numbers of papers reported methods to minimise missing data (29%), performed sensitivity analyses (22%) or discussed the potential influence of missing data on results (16%). Conclusions Considerable discrepancy exists between approved methodology and current practice in handling, analysis and reporting of missing PROMs outcome data in RCTs. Greater awareness is needed of the potential bias introduced by inappropriate handling of missing data, the importance of sensitivity analysis and clear reporting to enable appropriate assessments of treatment effects and conclusions from RCTs.

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          Author and article information

          Conference
          Trials
          Trials
          Trials
          BioMed Central
          1745-6215
          2015
          16 November 2015
          : 16
          : Suppl 2
          : P67
          Affiliations
          [1 ]Health Economics Research Centre (HERC), Nuffield Department of Population Health, University of Oxford, Oxford, UK
          [2 ]RCS Surgical Intervention Trials Unit (SITU), Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK
          [3 ]National Perinatal Epidemiology Unit (NEPU), Nuffield Department of Population Health, University of Oxford, Oxford, UK
          [4 ]Health Services Research Unit (HSRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK
          [5 ]Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK
          Article
          1745-6215-16-S2-P67
          10.1186/1745-6215-16-S2-P67
          4660338
          4b9d2e71-46f7-4757-a998-cfe5ed3e07ce
          Copyright © 2015 Rombach et al.

          This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

          3rd International Clinical Trials Methodology Conference
          Glasgow, UK
          16-17 November 2015
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          Poster Presentation

          Medicine
          Medicine

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