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Selection bias resulting from the requirement for prior consent in observational research: a community cohort of people with ischaemic heart disease
  1. Brian Buckley1,
  2. Andrew W Murphy1,
  3. Molly Byrne2,
  4. Liam Glynn1
  1. 1Department of General Practice, National University of Ireland, Galway, Ireland
  2. 2Department of Psychology, National University of Ireland, Galway, Ireland
  1. Correspondence to:
    B Buckley
    Department of General Practice, National University of Ireland, Galway, Ireland; bsbuckley{at}iol.ie

Abstract

Objective: To evaluate differences between adults who consent to participate in observational research and those who do not.

Design: Prospective, population-based cohort study.

Setting: 35 randomised Irish general practices.

Participants: 1609 adults with ischaemic heart disease identified in 2000–1.

Intervention: Medical records search, postal questionnaire and consent form in 2005–6.

Main outcome measures: Differences in demographic and prognostic risk factors between consenters and non-consenters.

Results: At follow-up, charts were located for 1592 patients (98.9%). Questionnaires were sent to 1269 patients and 876 were returned (69%). Of these, 574 (65.5%) gave consent for participation in further research. Logistic regression identified four characteristics as independently positively predictive of consent to participation in further research among questionnaire responders: having undergone percutaneous transluminal coronary angioplasty was associated with an increased odds of consent, with an odds ratio (OR) of 1.77 (95% CI 1.09 to 2.86), as was a last recorded blood pressure <140/90 mm Hg (OR = 1.45 (1.00 to 2.09)), a last recorded total cholesterol level <5 mmol/l (OR = 1.71 (1.16 to 2.54)) and being an ex-smoker rather than a current smoker or non-smoker (OR = 1.73 (1.17 to 2.57)).

Conclusions: This research demonstrates the potential impact of consent bias in observational research on ischaemic heart disease, a disease of everyday clinical importance in Europe. It demonstrates that clinically important prognostic variables may be associated with consent preferences. Future cohorts, dependent upon prior written consent, may contain disproportionate numbers of those who have made healthy lifestyle decisions, have previously benefited from treatment or whose clinical risk factors are already well managed. As a result, the generalisability of such research may be diminished and the effects of treatments over- or underestimated.

  • AMI, acute myocardial infarction
  • BMI, body mass index
  • CABG, cardiac artery bypass grafting
  • GMS, General Medical Services
  • GP, general practitioner
  • IHD, ischaemic heart disease
  • OR, odds ratio
  • PTCA, percutaneous transluminal coronary angioplasty
  • selection bias
  • consent
  • observational research
  • ischaemic heart disease

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Footnotes

  • Published Online First 13 May 2007

  • Funding: Baseline and follow-up studies were both funded by the Health Research Board, Dublin and the Health Services Executive (Western Area).

  • Conflict of interest: None.

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