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Adolescents' experiences and views of the national school-based thalassaemia screening programme in Malaysia: a qualitative study.

Huey Yee TanNorita HusseinYew Kong LeeTun Firzara Abdul Malik
Published in: Journal of community genetics (2023)
In 2016, a national school-based thalassemia screening programme was implemented in Malaysia. This study aimed to explore the experiences and views of adolescents from an urban school who had undergone the screening programme. We carried out in-depth interviews with 18 participants aged between 18 and 19 years old, with 12 of them identified as carriers during the school screening. Interviews were transcribed verbatim and analysed using thematic analysis. Three main themes emerged from this study: (1) issues encountered at various levels of the school screening programme: appropriate age for screening, thalassaemia education in school, parental consent and follow-up visit and post-test counselling; (2) experiencing emotional rollercoaster: worry, anxiety, shame, stigma; (3) choosing future partners after carrier status was known-prepared or unprepared? Various issues and screening-related challenges were encountered before, during and after the screening test. Recommendations include improving thalassaemia screening education for both school-going adolescents and parents, and better follow-up care and support for those identified as carriers. These will help stakeholders to be well informed and supportive of thalassaemia screening in schools.
Keyphrases
  • physical activity
  • mental health
  • young adults
  • quality improvement
  • randomized controlled trial
  • hepatitis c virus
  • health insurance
  • chronic pain
  • smoking cessation
  • clinical practice
  • sickle cell disease