Qualitative research: consumer preferences


Patients’ priorities for health research: focus group study of patients with chronic kidney disease
Tong A, Sainsbury P, Carter SM, Hall, B, Harris DC, Walker RG, Hawley CM, Chadban S, Craig JC Nephrology Dialysis and Transplantation 2008; 23:3206-3214
[PubMed abstract]

Patients’ experiences and perspectives of living with CKD
Tong A, Sainsbury P, Chadban S, Walker RG, Harris DC, Carter SM, Hall, B, Hawley CM, Craig JC. American Journal of Kidney Disease 2009; 53:689-700
[PubMed abstract]


The inclusion of consumer preferences in prioritizing research topics is widely advocated, but prioritization is driven largely by professional agendas. Patients with chronic kidney disease (CKD) were purposively sampled from four kidney dialysis and transplant centres in Australia to participate in nine focus groups (three each for pre-dialysis, dialysis and transplant patients), which were conducted from July 2006 to September 2006.

Each involved 6-8 participants. Transcripts were coded and thematically analysed to identify recurrent research topics and the participants' reasons for their choices. Participants suggested 8 research priorities:

  • prevention of kidney disease;
  • better access to and improvement in kidney transplantation;
  • reduction of symptoms of CKD and complications associated with treatment;
  • new technological therapies;
  • psychosocial aspects of living with CKD;
  • whole body not organ-specialized care;
  • improvement in dialysis and caregiver support

Five major reasons for the selections were identified:

  • normalization of life (developing therapies and regimens that fit into daily living);
  • altruism (considering the welfare of others before personal needs);
  • economic efficiency (channelling resources for maximum economic gain);
  • personal needs (preferences based on feelings, values, personal needs);
  • clinical outcomes (improving health states and the physiological condition of patients with CKD)

A patient-focused research agenda is possible to elicit for CKD, and by inference for other healthcare issues. Unlike researchers who focus on specific interventions and questions, consumers think in terms of broad themes and quality of life outcomes. Effective methods for translating a patient-focused agenda into research priority setting and resource allocation are now needed.