Hemoglobin status in children attending paediatric clinics in Lomé, 2022.

Author:

Konu Yao Rodion1,Lack Fiali Ayawa2,Adama Oumarou I.Wone1,Kouanfack Harold Régis1,Gounon Kokou Herbert1,Sogbo François3,Womey Kodzovi Mawulé Corcellar1,Takassi Elom Ounoo3,Kolou Maléwé2,Ekouevi Didier Koumavi1

Affiliation:

1. Centre Africain de Recherche en Epidémiologie et en Santé Publique (CARESP)

2. Laboratoire de biochimie, Centre hospitalier universitaire Sylvanus Olympio

3. Service de pédiatrie, Centre hospitalier universitaire Sylvanus Olympio

Abstract

Abstract

Aim: to estimate the prevalence of sickle cell disease among children and adolescents in the pediatric department of the Sylvanus Olympio University Hospital in 2022. Methods: in this cross-sectional study, all children and adolescents attending the study site were proposed to participate and included if: i) aged between 18 months and 19 years, ii) present in pediatric consultations or hospitalizations and iii) provided assent or parental informed consent. A 4-5 ml blood sample was collected for hemoglobin electrophoresis on a cellulose acetate plate at alkaline pH. Sickle cell disease was defined as having either SS, SC, SF or Sß hemoglobin phenotype. Results: A total of 317 children and adolescents aged 8 years (IQR: 4-12) in median were enrolled. Only in 7.3% of cases did both parents know their hemoglobin status. 68 children/adolescents had hemoglobin S (21.5%), 19 had sickle cell disease (6.0%). Approximately 15.6% of children and adolescents had sickle cell trait AS. Conclusion: This study revealed a high SCD prevalence in an a priori naïve children/adolescents’ population. We stress that policy makers should consider continued sensitization, genetic counseling and neonatal screening as prevention strategies in Togo.

Publisher

Research Square Platform LLC

Reference20 articles.

1. Organisation Mondiale de la Santé (OMS). Drépanocytose, rapport du sécrétariat. Genève: OMS; 2006. p. 6.

2. WHO Africa. Progress report on the implementation of AFRO Sickle-Cell Disease Strategy 2010–2020 [Internet]. [cité 23 avr 2024]. Disponible sur: https://www.afro.who.int/sites/default/files/2020-10/AFR-RC70-INF-DOC-3%20Progress%20report%20on%20the%20implementation%20of%20AFRO%20Sickle-Cell%20Disease%20Strategy%202010-2020.pdf.

3. [Hemoglobin anomalies at the university hospital center in Lome, Togo];Segbena AY;Med Trop Rev Corps Sante Colon,2002

4. Ministère de la Santé et de la Protection Sociale. Plan national de développement sanitaire 2017–2022. Genève: République Togolaise; 2017. p. 93.

5. Région Africaine de l’Organisation Mondiale de la Santé (OMS Afro). Progrès réalisés dans la mise en oeuvre de la stratégie de luette contre la drépanocytose dans la région africaine de l’OMS 2010–2020. Brazzaville: OMS Afro; 2020. p. 6.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3