Publication:
Identification of optimal thalassemia screening strategies for migrant populations in Thailand using a qualitative approach

dc.contributor.authorJulia Z. Xuen_US
dc.contributor.authorMeghan Foeen_US
dc.contributor.authorWilaslak Tanongsaksakulen_US
dc.contributor.authorThidarat Suksangplengen_US
dc.contributor.authorSupachai Ekwattanakiten_US
dc.contributor.authorSuchada Riolueangen_US
dc.contributor.authorMarilyn J. Telenen_US
dc.contributor.authorBonnie N. Kaiseren_US
dc.contributor.authorVip Viprakasiten_US
dc.contributor.otherSiriraj Hospitalen_US
dc.contributor.otherUniversity of California, San Diegoen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherDuke Universityen_US
dc.contributor.otherUCSF Benioff Children's Hospital Oaklanden_US
dc.contributor.otherNational Heart, Lung, and Blood Institute (NHLBI)en_US
dc.contributor.otherDuke University School of Medicineen_US
dc.contributor.otherLaem Chabang Hospitalen_US
dc.date.accessioned2022-08-04T09:01:23Z
dc.date.available2022-08-04T09:01:23Z
dc.date.issued2021-12-01en_US
dc.description.abstractBackground: Thalassemia is a common inherited hemoglobin disorder in Southeast Asia. Severe thalassemia can lead to significant morbidity for patients and economic strain for under-resourced health systems. Thailand’s thalassemia prevention and control program has successfully utilized prenatal screening and diagnosis to reduce the incidence of severe thalassemia in Thai populations, but migrant populations are excluded despite having high thalassemia prevalence. We sought to identify key barriers to and facilitators of thalassemia screening and to develop tailored recommendations for providing migrants with access to thalassemia prevention and control. Methods: We conducted 28 in-depth interviews and 4 focus group discussions (FGDs) in Chonburi, Thailand with Myanmar and Cambodian migrants, Thai healthcare providers, Thai parents of children affected by thalassemia, and migrant agents. Results: Participant narratives revealed that migrants’ lack of knowledge about the prevalence, manifestations, severity, and inherited nature of thalassemia led to misconceptions, fear, or indifference toward thalassemia and screening. Negative perceptions of pregnancy termination were based in religious beliefs but compounded by other sociocultural factors, presenting a key obstacle to migrant uptake of prenatal screening. Additionally, structural barriers included legal status, competing work demands, lack of health insurance, and language barriers. Participants recommended delivering public thalassemia education in migrants’ native languages, implementing carrier screening, and offering thalassemia screening in convenient settings. Conclusions: An effective thalassemia prevention and control program should offer migrants targeted thalassemia education and outreach, universal coverage for thalassemia screening and prenatal care, and options for carrier screening, providing a comprehensive strategy for reducing the incidence of severe thalassemia in Thailand and establishing an inclusive model for regional thalassemia prevention and control.en_US
dc.identifier.citationBMC Public Health. Vol.21, No.1 (2021)en_US
dc.identifier.doi10.1186/s12889-021-11831-4en_US
dc.identifier.issn14712458en_US
dc.identifier.other2-s2.0-85116438441en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/77512
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85116438441&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleIdentification of optimal thalassemia screening strategies for migrant populations in Thailand using a qualitative approachen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85116438441&origin=inwarden_US

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