Increased transparency was required when reporting imputation of primary outcome data in clinical trials

Anna Kearney *, Anna Rosala-Hallas , Naomi Rainford , Jane Blazeby, Mike Clarke , J. Athene Lane, Carrol Gamble

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

1 Citation (Scopus)
31 Downloads (Pure)

Abstract

Objectives
The aim of this study is to explore the transparency of reporting primary outcome data within randomized controlled trials in the presence of missing data.
Study Design and Setting
A cohort examination of randomized controlled trials published in the four major medical journals (NEJM, JAMA, BMJ, Lancet) in 2013 and the first quarter of 2018. Data were extracted on reporting quality, the number of randomized participants, and the number of participants included within the primary outcome analysis with observed or imputed data.
Results
Ninety-one of 159 (57%) studies analyzed from 2013 and 19 of 46 (41%) from 2018 included imputed data within the primary outcome analysis. Of these, only 13 of 91 (14%) studies from 2013 and 1 of 19 (5%) studies from 2018 explicitly reported the number of imputed values in the CONSORT diagram. Results’ tables included levels of imputed data in 12 of 91 (13%) studies in 2013 and 4 of 19 (21%) in 2018. Consequently, identification of imputed data was a time-consuming task requiring extensive cross-referencing of all manuscript elements.
Conclusion
Imputed primary outcome data are poorly reported. Participant flow diagrams frequently reported participant status which does not necessarily correlate to availability of data. We recommended that the number of imputed values are explicitly reported within CONSORT flow diagrams to increase transparency.
Original languageEnglish
Pages (from-to)60-67
Number of pages8
JournalJournal of Clinical Epidemiology
Volume146
Early online date23 Feb 2022
DOIs
Publication statusPublished - 1 Jun 2022

Bibliographical note

Funding Information:
Funding Statement: Medical Research Council Methodology Research Program (Grant MR/K024310/1 ).

Publisher Copyright:
© 2022 The Author(s)

Keywords

  • Missing data
  • Retention
  • Imputation
  • Reporting transparency
  • CONSORT

Fingerprint

Dive into the research topics of 'Increased transparency was required when reporting imputation of primary outcome data in clinical trials'. Together they form a unique fingerprint.

Cite this