The prevalence of sickle cell anemia in Saudi children and adolescents. A community-based survey.
نویسنده
چکیده
I read the interesting article by Al-Qurashi et al1 on the prevalence of sickle cell anemia in Saudi children and adolescents: a community-based survey. The World Health Organization (WHO) has recognized sickle cell anemia (SCA) as a problem of major public-health threat with a significant morbidity and mortality, particularly in developing countries. Saudi Arabia is located within the geographical distribution of SCA genotype that extends throughout sub-Saharan Africa, the Middle East, and parts of the Indian sub-continent, where carrier frequencies range from 5-40% or more of the population.2 The true prevalence of SCA is variable among these countries. Such variation might disclose variations in the study design, methodology applied during estimation, and ethnicity. Despite that, SCA remains a significant health burden in these countries. Therefore, collaboration among regional countries is needed to focus research and interventions on items that will lead to the maximum benefits with the objective of encircling the magnitude of SCA and jeopardizing its sequelae. A neonatal screening program for SCA has proven to be effective in early detection of potential cases.3 The authors stated a regional variation of SCA in Saudi Arabia, and advocated selective installation of a neonatal screening program for SCA in regions with higher SCA prevalence. Indeed, I contradict with their advocacy, as consanguineous marriages are common in many Middle Eastern countries, including Saudi Arabia. In a recent survey of a representative sample of Saudi families defined by a multistage random sampling procedure representing both urban and rural settlements, the prevalence of consanguinity was 56% with the first cousin type being the most common (33.6%).4 Therefore, screening for SCA should form part of basic health services in these countries situated within the geographical basin of SCA genotype, despite regional variation in the prevalence of SCA within the same country. Such an option will detect early breeding cases.
منابع مشابه
The prevalence of sickle cell disease in Saudi children and adolescents. A community-based survey.
OBJECTIVE To determine the prevalence and regional distribution of sickle cell disease in Saudi children. METHODS A sample size of 45,682 children and adolescents from newborn to 19 years of age was selected by multistage random probability sampling of the Saudi households from each of the 13 regions of the country. The study is cross-sectional, community based, and conducted over 2 years fro...
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عنوان ژورنال:
- Saudi medical journal
دوره 30 3 شماره
صفحات -
تاریخ انتشار 2009