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. 2020 Jul 12;23(5):1028–1036. doi: 10.1111/hex.13099

TABLE 2.

Determinants of identifying, incorporating and reporting patient preferences in guidelines

Study Barriers Facilitators
Armstrong 38
Li 39
  • Adding patient and caregiver stakeholders to the institutional review board protocol

  • Involving them in large conference calls (vs. more personal meetings)

  • Training in research methods

  • Combination of in‐person and virtual meetings

Goodman 41
Pinheiro 42
Zhang 43
  • Difficult to identify relevant studies that described preferences

  • Information about values and preferences from panel members could be biased and was sometimes difficult to use

den Breejen 44
Fraenkel 45
  • Hämeen‐Anttila 46

  • Difficult to find appropriate persons from the target group who would be capable of representing the larger patient population and not just their own personal experiences and views

  • Training in clinical practice guidelines

Utens 47
  • Understanding of what constitutes a preference

  • Difficult to identify relevant studies that described preferences

  • The weight to give patient preferences

Pittens 48
Serrano‐Agu 49
  • Patients holding their own when facing a team of professionals

  • Becoming easily overruled by professionals resulting in tokenism

Garcia‐Toyos 50
Den Breejen 51
  • Users found it difficult to find and use the website (questionnaire to rank guideline questions)

  • They did not fully understand the purpose of the website (to rank recommendations based on preferences)

Tong 52
  • Difficult to achieve an adequate attendance rate as some participants were unable to attend at the last minute

  • Medical jargon

Musila 53