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Lived Experiences of Mothers Caring for Children with Thalassemia Major in Thailand

Overview
Publisher Wiley
Specialties Nursing
Pediatrics
Date 2007 Jan 20
PMID 17233664
Citations 14
Authors
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Abstract

Issues And Purpose: Thalassemic patients must be given continuous treatment throughout their lives due to the physical and psychological effects of their disorder; their families also are impacted. This qualitative study explored the lived experiences of 15 mothers of children with thalassemia major by conducting semistructured interviews; the data were analyzed utilizing content analysis.

Conclusion: Six themes were identified: lack of knowledge about thalassemia, psychosocial problems, concerns for the future, social support systems, financial difficulty, and the effectiveness of healthcare services.

Practice Implications: These findings suggest that a holistic, culturally sensitive nursing approach should be considered when caring for children with thalassemia.

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A cross-sectional study: caregiver burden and related determinants of adult patients with β-thalassemia major in mainland China.

Zhang R, Zhang S, Ming J, Xie J, Liu B, Jiang W BMC Nurs. 2024; 23(1):151.

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Thalassemia: A Review of the Challenges to the Families and Caregivers.

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A Qualitative Study Exploring the Experiences of Mothers Caring for Their Children with Thalassemia in Iran.

Nabavian M, Cheraghi F, Shamsaei F, Tapak L, Tamadoni A Ethiop J Health Sci. 2022; 31(6):1287-1294.

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The psychosocial challenges of mothers of children with thalassemia: A qualitative study.

Nabavian M, Cheraghi F, Shamsaei F, Tapak L, Tamaddoni A J Educ Health Promot. 2022; 11:37.

PMID: 35281396 PMC: 8893092. DOI: 10.4103/jehp.jehp_163_21.