Content analysis of identity challenges in patients with haemophilia: A qualitative study

Roya Dolatkhah1, Reza Shabanloei2, Hossein Ebrahimi3

  • 1Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Nursing Open
|January 6, 2021
PubMed

Insights

Patients with hemophilia face identity challenges due to social and physical constraints. Understanding these challenges is crucial for providing better support and improving their quality of life.

Area of Science:

  • Medical Sociology
  • Psychology

Background:

  • Inherited bleeding disorders like hemophilia significantly impact patients' education, employment, social engagement, and overall quality of life.
  • These conditions can lead to profound challenges in self-identity, affecting various life domains.

Purpose of the Study:

  • To explore and identify the specific sources of identity challenges experienced by patients with hemophilia.
  • To understand the lived experiences of individuals with hemophilia concerning their self-perception and social integration.

Main Methods:

  • A qualitative content analysis approach was employed for this research.
  • Data were gathered through semi-structured, in-depth interviews with purposively selected hemophilia patients over a one-year period.
  • Interviews were analyzed using the Granheme and Landman method to identify key themes.

Main Results:

  • Key challenges contributing to identity disturbances included fear of rejection, loss of social roles, discrimination, and stigma.
  • Marriage breakdown was also identified as a significant concern impacting patients' self-identity.
  • Physical and social constraints imposed by hemophilia were found to be central to these identity challenges.

Conclusions:

  • Healthcare providers, particularly nurses, should implement enhanced protective measures and support systems for hemophilia patients.
  • Addressing the psychosocial aspects of hemophilia is essential for mitigating identity disturbances and improving patient well-being.
  • Interventions should focus on reducing stigma and fostering social inclusion for individuals with inherited bleeding diseases.
Abstract

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