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  • Oral presentation
  • Open Access

Impact of timing of follow-up upon outcome in the TOPKAT trial

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Trials201516 (Suppl 2) :O33

  • Published:


  • Confidence Interval
  • Osteoarthritis
  • Cost Effectiveness
  • Primary Outcome Measure
  • Mean Difference

Due to the practicalities of recruitment, randomisation of participants in surgical trials may need to take place prior to the day of surgery. However, substantial post-randomisation delays in receiving surgery due to limited capacity may then occur. This can create a tension between timing the follow-up from randomisation (scientifically most desirable) and surgery (clinically most relevant). It is unclear what impact alternative follow-up timings have upon the outcome.


TOPKAT compared the clinical and cost effectiveness of total or partial knee replacements for medial compartment osteoarthritis. An additional assessment at 1 year post surgery of the primary outcome measure, Oxford Knee Score (OKS) was administered to patients who had a waiting time following randomisation of greater than 12 weeks as well as baseline and post-randomisation follow-up. Mean difference (MD) between treatments (95% confidence interval (CI)) was calculated using 1 year post-surgery and post-randomisation data.


Waiting times for surgery (0-407 days) resulted in a number of participants (n=134 of 531 recruited) receiving their 1 year post randomisation follow up questionnaire at a time point much earlier than 1 year post surgery. However, the mean difference in OKS was very similar for post randomisation (1.8 95% CI (0.2,3.4)) and surgery (1.7 95% CI(0.0,3.3)) analyses.


Results of the 1 year post-randomisation and surgery follow-ups were very similar. Further assessment in other trials is required to explore the generalisability of this finding. Timing of follow up needs to be carefully chosen to ensure interpretable results.

Authors’ Affiliations

University of Oxford, Oxford, UK
University of Aberdeen, Aberdeen, UK


© Cook et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.


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