Māori patients' experiences and perspectives of chronic kidney disease: a New Zealand qualitative interview study

BMJ Open. 2017 Jan 19;7(1):e013829. doi: 10.1136/bmjopen-2016-013829.

Abstract

Objectives: To explore and describe Māori (the indigenous people of New Zealand) patients' experiences and perspectives of chronic kidney disease (CKD), as these are largely unknown for indigenous groups with CKD.

Design: Face-to-face, semistructured interviews with purposive sampling and thematic analysis.

Setting: 3 dialysis centres in New Zealand (NZ), all of which offered all forms of dialysis modalities.

Participants: 13 Māori patients with CKD and who were either nearing the need for dialysis or had started dialysis within the previous 12 months.

Results: The Māori concepts of whakamā (disempowerment and embarrassment) and whakamana (sense of self-esteem and self-determination) provided an overarching framework for interpreting the themes identified: disempowered by delayed CKD diagnosis (resentment of late diagnosis; missed opportunities for preventive care; regret and self-blame); confronting the stigma of kidney disease (multigenerational trepidation; shame and embarrassment; fear and denial); developing and sustaining relationships to support treatment decision-making (importance of family/whānau; valuing peer support; building clinician-patient trust); and maintaining cultural identity (spiritual connection to land; and upholding inner strength/mana).

Conclusions: Māori patients with CKD experienced marginalisation within the NZ healthcare system due to delayed diagnosis, a focus on individuals rather than family, multigenerational fear of dialysis, and an awareness that clinicians are not aware of cultural considerations and values during decision-making. Prompt diagnosis to facilitate self-management and foster trust between patients and clinicians, involvement of family and peers in dialysis care, and acknowledging patient values could strengthen patient engagement and align decision-making with patient priorities.

Keywords: NEPHROLOGY; QUALITATIVE RESEARCH.

Publication types

  • Multicenter Study

MeSH terms

  • Adult
  • Aged
  • Culture
  • Decision Making
  • Delayed Diagnosis / psychology
  • Denial, Psychological
  • Emotions
  • Fear
  • Female
  • Health Status Disparities
  • Healthcare Disparities / ethnology
  • Humans
  • Interpersonal Relations
  • Kidney Failure, Chronic / ethnology*
  • Kidney Failure, Chronic / psychology
  • Kidney Failure, Chronic / therapy
  • Male
  • Middle Aged
  • Native Hawaiian or Other Pacific Islander / ethnology*
  • Native Hawaiian or Other Pacific Islander / psychology
  • New Zealand / ethnology
  • Patient Satisfaction / ethnology
  • Renal Dialysis
  • Self Concept
  • Shame
  • Social Stigma
  • Young Adult