School performance of children with sickle cell disease in Basra, Iraq

BACKGROUND: Children with sickle cell disease (SCD) have a greater likelihood of demonstrating many medical complications that may put them at risk for a variety of difficulties, including poor school performance and cognitive impairment. OBJECTIVES: This study was designed to assess the school perf...

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Main Authors: Falah Hassan Abid, Mea'ad Kadhum Hassan, Bahaa Abd Al Hussein Ahmed
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Iraqi Journal of Hematology
Subjects:
Online Access:http://www.ijhonline.org/article.asp?issn=2072-8069;year=2019;volume=8;issue=1;spage=29;epage=37;aulast=Abid
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spelling doaj-aefad827a2984e3d887a4bc75f6066b92020-11-24T20:51:28ZengWolters Kluwer Medknow PublicationsIraqi Journal of Hematology2072-80692019-01-0181293710.4103/ijh.ijh_21_18School performance of children with sickle cell disease in Basra, IraqFalah Hassan AbidMea'ad Kadhum HassanBahaa Abd Al Hussein AhmedBACKGROUND: Children with sickle cell disease (SCD) have a greater likelihood of demonstrating many medical complications that may put them at risk for a variety of difficulties, including poor school performance and cognitive impairment. OBJECTIVES: This study was designed to assess the school performance of primary school-aged patients with SCD compared to age- and gender-matched healthy students and to evaluate the factors that influence school performance in these patients. MATERIALS AND METHODS: A total of 68 patients with SCD from 48 primary schools and 68 healthy student classmates (control group), aged 7–12 years, were recruited. The average school examination scores were used as a school performance measure, while cognitive functioning was assessed by using the Draw-A-Person test. RESULTS: The average school examination scores and cognitive function scores of patients with SCD (82.46 ± 15.48 and 24.72 ± 7.48, respectively) were significantly lower than the corresponding scores of their classmate control group (93.42 ± 10.02 and 27.84 ± 7.46, respectively), P < 0.05. Students with SCD missed significantly more school days (12.37 ± 10.57) than healthy students (3.18 ± 3.62), P < 0.001, and high school absence was significantly associated with low school performance among SCD patients, P = 0.027. Among patients with SCD, Pearson correlation revealed a negative association between school performance and age and school absence days (r = −0.346 and r = −0.390, respectively, P < 0.01) and a positive association between school performance and maternal education (r = −0.388, P < 0.001). CONCLUSIONS: School performance and cognitive function were significantly lower among patients with SCD than among their classmates, and school absence and the age of patients had a negative impact on school performance.http://www.ijhonline.org/article.asp?issn=2072-8069;year=2019;volume=8;issue=1;spage=29;epage=37;aulast=AbidChildrencognitive functionschool absenceschool performancesickle cell disease
collection DOAJ
language English
format Article
sources DOAJ
author Falah Hassan Abid
Mea'ad Kadhum Hassan
Bahaa Abd Al Hussein Ahmed
spellingShingle Falah Hassan Abid
Mea'ad Kadhum Hassan
Bahaa Abd Al Hussein Ahmed
School performance of children with sickle cell disease in Basra, Iraq
Iraqi Journal of Hematology
Children
cognitive function
school absence
school performance
sickle cell disease
author_facet Falah Hassan Abid
Mea'ad Kadhum Hassan
Bahaa Abd Al Hussein Ahmed
author_sort Falah Hassan Abid
title School performance of children with sickle cell disease in Basra, Iraq
title_short School performance of children with sickle cell disease in Basra, Iraq
title_full School performance of children with sickle cell disease in Basra, Iraq
title_fullStr School performance of children with sickle cell disease in Basra, Iraq
title_full_unstemmed School performance of children with sickle cell disease in Basra, Iraq
title_sort school performance of children with sickle cell disease in basra, iraq
publisher Wolters Kluwer Medknow Publications
series Iraqi Journal of Hematology
issn 2072-8069
publishDate 2019-01-01
description BACKGROUND: Children with sickle cell disease (SCD) have a greater likelihood of demonstrating many medical complications that may put them at risk for a variety of difficulties, including poor school performance and cognitive impairment. OBJECTIVES: This study was designed to assess the school performance of primary school-aged patients with SCD compared to age- and gender-matched healthy students and to evaluate the factors that influence school performance in these patients. MATERIALS AND METHODS: A total of 68 patients with SCD from 48 primary schools and 68 healthy student classmates (control group), aged 7–12 years, were recruited. The average school examination scores were used as a school performance measure, while cognitive functioning was assessed by using the Draw-A-Person test. RESULTS: The average school examination scores and cognitive function scores of patients with SCD (82.46 ± 15.48 and 24.72 ± 7.48, respectively) were significantly lower than the corresponding scores of their classmate control group (93.42 ± 10.02 and 27.84 ± 7.46, respectively), P < 0.05. Students with SCD missed significantly more school days (12.37 ± 10.57) than healthy students (3.18 ± 3.62), P < 0.001, and high school absence was significantly associated with low school performance among SCD patients, P = 0.027. Among patients with SCD, Pearson correlation revealed a negative association between school performance and age and school absence days (r = −0.346 and r = −0.390, respectively, P < 0.01) and a positive association between school performance and maternal education (r = −0.388, P < 0.001). CONCLUSIONS: School performance and cognitive function were significantly lower among patients with SCD than among their classmates, and school absence and the age of patients had a negative impact on school performance.
topic Children
cognitive function
school absence
school performance
sickle cell disease
url http://www.ijhonline.org/article.asp?issn=2072-8069;year=2019;volume=8;issue=1;spage=29;epage=37;aulast=Abid
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