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  • Poster presentation
  • Open Access

Measuring impact of systematic reviews using individual participant data: evidence from clinical guidelines

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Trials201314 (Suppl 1) :P123

  • Published:


  • Public Health
  • Gold
  • Clinical Practice
  • Cardiovascular Disease
  • Systematic Review


Systematic reviews (SRs) using individual participant data (IPD) are often referred to as the gold standard due to improved precision and reliability. Furthermore, they may identify treatment by participant subgroup interactions, enabling better targeting of treatments. IPD SRs have enormous potential to influence clinical guidelines, however their uptake by guideline developers, as Level 1 evidence, is unclear.


We aimed to assess the impact of IPD SRs of interventions on clinical guidelines across a variety of healthcare areas.


30 eligible IPD SRs published from 2008 to 2010 spanning clinical areas including cancer, cardiovascular disease, and epilepsy were identified from records of the Cochrane IPD Meta-analysis Methods Group. Clinical guidelines across corresponding healthcare areas, published or revised since 2010, were searched for references to these IPD SRs. Details of recommendations based on the results of these reviews and citations of other relevant SRs were collected.


Searches identified 227 potentially relevant clinical guidelines. Preliminary results are based on four IPD SRs in cancer and 34 relevant guidelines. Each of the four IPD SRs was cited in 2 to 5 guidelines, however citations were only identified in 11/34 guidelines (32%). Three of the 14 guidelines also cited aggregate data SRs, with little distinction between results of IPD or aggregate data SRs.

Further results for all 30 IPD SRs and 227 guidelines will be presented.


Results of this study will help develop guidance regarding how best to use IPD SRs to inform guidelines and thus impact on clinical practice.

Authors’ Affiliations

MRC Clinical Trials Unit Hub for Trials Methodology Research, London, UK
Centre for Research and Dissemination, University of York, York, UK
The Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
UMR5558, CNRC, University of Lyon, Lyon, France
Clinical Trial Service Unit and Epidemiological Studies Unit, Oxford, UK


© Vale et al; licensee BioMed Central Ltd. 2013

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.


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