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Update on the practice of premarital screening for sickle cell traits in Africa: a systematic review and meta-analysis.
Dilli, Priscilla Peter; Obeagu, Emmanuel; Tamale, Andrew; Ajugwo, Anselm; Pius, Theophilus; Makeri, Danladi.
Afiliación
  • Dilli PP; Department of Public Health, Kampala International University-Western Campus, Ishaka, Uganda.
  • Obeagu E; Department of Medical Laboratory Science, Kampala International University-Western Campus, Ishaka, Uganda.
  • Tamale A; Department of Public Health, Kampala International University-Western Campus, Ishaka, Uganda.
  • Ajugwo A; Department of Medical Laboratory Science, Kampala International University-Western Campus, Ishaka, Uganda.
  • Pius T; Department of Medical Laboratory Science, Kampala International University-Western Campus, Ishaka, Uganda.
  • Makeri D; Department of Microbiology and Immunology, Kampala International University-Western Campus, Ishaka, Ishaka, Uganda. makeri@kiu.ac.ug.
BMC Public Health ; 24(1): 1467, 2024 May 31.
Article en En | MEDLINE | ID: mdl-38822327
ABSTRACT

BACKGROUND:

Screening for sickle cell traits before marriage or producing children is one of the outstanding preventive measures for sickle cell disease (SCD).The disease is a collection of inherited blood disorders that impact millions globally, with a predominant 75% occurrence in the sub-Saharan region. With increasing burden of SCD on the continent amidst a cost effective prevention method, no study has systematically reviewed or presented meta-analytic uptake or practice of premarital sickle cell trait screening.

METHODS:

This review systematically explored the uptake or practice of premarital genotype screening in Africa. We searched PubMed and Scopus databases for African studies on premarital screening for sickle cell traits.

RESULTS:

Our results indicate that the pooled uptake of premarital sickle cell trait screening in Africa is 47.82% (95% CI [46.53-49.11]; I2 98.95% [98.74-99.13]). Our review observed, a significant relationship between the awareness of sickle cell disease and the uptake of genotype screening; F(1, 13) = 12.04, p = 0.004). The model explained approximately 48.08% of the variation in genotype screening (R² = 0.4808) and predicted a 0.729 increase in the likelihood of genotype screening uptake for every unit rise in sickle cell disease awareness (ß = 0.729, p = 0.004). Additionally, Pearson correlation (r = 0.6934) indicated a moderately strong positive correlation between the two variables.

CONCLUSION:

With over 75% of the global burden of sickle cell disease domiciled in Africa, the continent cannot overlook the cost of hemoglobinopathies. The uptake of sickle cell traits screening is suboptimal across the continent. To achieve the mandate of sustainable development goal number (3); to end preventable deaths of newborns and children under 5 years of age by 2030, there is need to intensify campaigns on premarital genetic screening through education and other health promotion tools.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Exámenes Prenupciales / Rasgo Drepanocítico / Anemia de Células Falciformes Límite: Humans País/Región como asunto: Africa Idioma: En Revista: BMC Public Health Asunto de la revista: SAUDE PUBLICA Año: 2024 Tipo del documento: Article País de afiliación: Uganda

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Exámenes Prenupciales / Rasgo Drepanocítico / Anemia de Células Falciformes Límite: Humans País/Región como asunto: Africa Idioma: En Revista: BMC Public Health Asunto de la revista: SAUDE PUBLICA Año: 2024 Tipo del documento: Article País de afiliación: Uganda