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Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis.

Karin Schölin BywallJorien VeldwijkMats G HanssonUlrik Kihlbom
Published in: The patient (2020)
Patients thought PPI could be valuable to consider in regulatory decisions. It is essential for patients to be well-informed when asked for their preferences. Research on information materials to inform patients in preference studies is needed to increase the value of PPI in regulatory decision making.
Keyphrases
  • end stage renal disease
  • decision making
  • newly diagnosed
  • ejection fraction
  • chronic kidney disease
  • peritoneal dialysis
  • prognostic factors
  • small molecule
  • patient reported outcomes
  • patient reported