Literature DB >> 32415792

Low educational level of head of household, as a proxy for poverty, is associated with severe anaemia among children with sickle cell disease living in a low-resource setting: evidence from the SPRING trial.

Halima Bello-Manga1, Aisha A Galadanci2, Shehu Abdullahi3, Shehi Ali4, Binta Jibir5, Safiya Gambo6, Lawal Haliru7, Lori C Jordan8, Muktar H Aliyu9, Mark Rodeghier10, Adetola A Kassim11, Michael R DeBaun12, Najibah A Galadanci13.   

Abstract

Severe anaemia, defined as haemoglobin level < 6·0 g/dl, is an independent risk factor for death in individuals with sickle cell disease living in resource-limited settings. We conducted a cross-sectional study of 941 children with sickle cell anaemia, who had been defined as phenotype HbSS or HbSβ0 thalassaemia, aged five to 12 years, and were screened for enrollment into a large primary stroke prevention trial in Nigeria (SPRING; NCT02560935). The main aim of the study was to determine the prevalence and risk factors for severe anaemia. We found severe anaemia to be present in 3·9% (37 of 941) of the SPRING study participants. Severe anaemia was significantly associated with the lower educational level of the head of the household (P = 0·003), as a proxy for poverty, and a greater number of children per room in the household (P = 0·004). Body mass index was not associated with severe anaemia. The etiology of severe anaemia in children living with sickle cell anaemia in Nigeria is likely to be multifactorial with an interplay between an individual's disease severity and other socio-economic factors related to poverty.
© 2020 British Society for Haematology and John Wiley & Sons Ltd.

Entities:  

Keywords:  severe anaemia; sickle cell disease; sub-Saharan Africa

Mesh:

Year:  2020        PMID: 32415792      PMCID: PMC7669582          DOI: 10.1111/bjh.16746

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  28 in total

1.  Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
Journal:  J Biomed Inform       Date:  2008-09-30       Impact factor: 6.317

2.  A significant proportion of children of African descent with HbSβ0 thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.

Authors:  Melissa E Day; Mark Rodeghier; Jennifer Driggers; Christopher J Bean; Emmanuel J Volanakis; Michael R DeBaun
Journal:  Br J Haematol       Date:  2018-05-24       Impact factor: 6.998

Review 3.  Cardiovascular abnormalities in sickle cell disease.

Authors:  Mark T Gladwin; Vandana Sachdev
Journal:  J Am Coll Cardiol       Date:  2012-03-27       Impact factor: 24.094

4.  Prevalence of inherited blood disorders and associations with malaria and anemia in Malawian children.

Authors:  Patrick T McGann; Anne M Williams; Graham Ellis; Kathryn E McElhinney; Laurel Romano; Julia Woodall; Thad A Howard; Gerald Tegha; Robert Krysiak; R Murray Lark; E Louise Ander; Carine Mapango; Kenneth I Ataga; Satish Gopal; Nigel S Key; Russell E Ware; Parminder S Suchdev
Journal:  Blood Adv       Date:  2018-11-13

5.  Beta thalassaemia trait in western Nigeria.

Authors:  Taiwo R Kotila; Adebowale A Adeyemo; Olusoji O Mewoyeka; Wuraola A Shokunb
Journal:  Afr Health Sci       Date:  2009-03       Impact factor: 0.927

6.  Factors associated with sickle cell disease mortality among hospitalized Angolan children and adolescents.

Authors:  J C Carlos Van-Dunem; J G B Alves; Luis Bernardino; José Natal Figueiroa; Cynthia Braga; Maria de Lourdes Pires do Nascimento; Sérgio José da Silva
Journal:  West Afr J Med       Date:  2007 Oct-Dec

Review 7.  An update on anemia in less developed countries.

Authors:  Karine Tolentino; Jennifer F Friedman
Journal:  Am J Trop Med Hyg       Date:  2007-07       Impact factor: 2.345

8.  Effects of maternal education on diet, anemia, and iron deficiency in Korean school-aged children.

Authors:  Hyeon-Jeong Choi; Hye-Ja Lee; Han Byul Jang; Ju Yeon Park; Jae-Heon Kang; Kyung-Hee Park; Jihyun Song
Journal:  BMC Public Health       Date:  2011-11-16       Impact factor: 3.295

9.  Coinheritance of B-Thalassemia and Sickle Cell Anaemia in Southwestern Nigeria.

Authors:  Osunkalu Vincent; Bamisaye Oluwaseyi; Babatunde James; Lawal Saidat
Journal:  Ethiop J Health Sci       Date:  2016-11

10.  Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions.

Authors:  Frédéric B Piel; Simon I Hay; Sunetra Gupta; David J Weatherall; Thomas N Williams
Journal:  PLoS Med       Date:  2013-07-16       Impact factor: 11.069

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  3 in total

Review 1.  Hydroxyurea (hydroxycarbamide) for sickle cell disease.

Authors:  Angela E Rankine-Mullings; Sarah J Nevitt
Journal:  Cochrane Database Syst Rev       Date:  2022-09-01

2.  Capacity Building for Primary Stroke Prevention Teams in Children Living With Sickle Cell Anemia in Africa.

Authors:  Djamila L Ghafuri; Brittany Covert Greene; Bilya Musa; Awwal Gambo; Abdulrasheed Sani; Shehu Abdullahi; Binta J Wudil; Halima Bello-Manga; Safiya Gambo; Matin Ghafuri; Holly Cassell; Kathleen Neville; Fenella Kirkham; Adetola A Kassim; Muktar H Aliyu; Michael R DeBaun; Lori C Jordan
Journal:  Pediatr Neurol       Date:  2021-09-04       Impact factor: 3.372

Review 3.  Hydroxyurea and blood transfusion therapy for Sickle cell disease in South Asia: inconsistent treatment of a neglected disease.

Authors:  Thamal Darshana; David Rees; Anuja Premawardhena
Journal:  Orphanet J Rare Dis       Date:  2021-03-23       Impact factor: 4.123

  3 in total

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