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Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study

BACKGROUND: Sickle cell disease (SCD) is a chronic hematologic disease associated with increased morbidity and mortality. Hemoglobinopathies are the most prevalent genetic disease globally, and SCD is estimated to affect 0.7% of Ugandan. The disease may adversely impact on the quality of life of sic...

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Autores principales: Kambasu, David Muthahi, Rujumba, Joseph, Lekuya, Hervé Monka, Munube, Deogratias, Mupere, Ezekiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518788/
https://www.ncbi.nlm.nih.gov/pubmed/31114692
http://dx.doi.org/10.1186/s12878-019-0141-8
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author Kambasu, David Muthahi
Rujumba, Joseph
Lekuya, Hervé Monka
Munube, Deogratias
Mupere, Ezekiel
author_facet Kambasu, David Muthahi
Rujumba, Joseph
Lekuya, Hervé Monka
Munube, Deogratias
Mupere, Ezekiel
author_sort Kambasu, David Muthahi
collection PubMed
description BACKGROUND: Sickle cell disease (SCD) is a chronic hematologic disease associated with increased morbidity and mortality. Hemoglobinopathies are the most prevalent genetic disease globally, and SCD is estimated to affect 0.7% of Ugandan. The disease may adversely impact on the quality of life of sickle cell patients. This study aimed to evaluate the health related quality of life (HRoL) of adolescents with SCD. METHODS: This was a mixed-methods study of adolescents with sickle cell disease and their caretakers living in Kampala city, Uganda. All children aged 8–17 years with homozygous sickle cell disease attending the sickle cell clinic at Mulago Hospital during the study period were included in this study. Participants completed the PedsQL™ generic core scales parent-proxy and child self-report questionnaire during a routine clinic visit. HRQoL was the primary outcome measured. Socio-demographics and disease related data were obtained through personal interview with caretakers and reviewing patients’ medical records. Mean scores were used for HRQoL and linear regression for associated factors. RESULTS: Of the 140 adolescents with SCD included in the study, 40% were male. A total of 95 adolescents (68%) were between the age of 8–12 years with a mean age of 14.25 years. The physical function was assessed slightly higher by adolescents with a mean score of57.5 ± 20.3 compare to caretakers with 52.8 ± 22.1(p < 0.001). As assessed by caretakers, physical HRQoL scores were negatively associated with pain about-10.02 CI [− 19.22, − 0.81](p = 0.033), whereas it was positively associated with Pneumococcal vaccine with the score of 28.43 CI [16.78,40.09](p < 0.001) as assessed by adolescents and 31.37CI [22.22,40.51](p < 0.001) by caretakers. Pneumococcal vaccination impacted positively the psychosocial functioning with a score of 8.67CI [1.51,15.84] (p = 0.018) as assessed by children and 15.94 CI [5.50,26.38](p = 0.003) as assessed by the caretakers. CONCLUSIONS: This study highlighted that pain was negatively associated with both physical and psychosocial functioning; whereas getting Pneumococcal vaccine was positively associated with both physical and psychosocial functioning as reported by children and caretakers.
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spelling pubmed-65187882019-05-21 Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study Kambasu, David Muthahi Rujumba, Joseph Lekuya, Hervé Monka Munube, Deogratias Mupere, Ezekiel BMC Hematol Research Article BACKGROUND: Sickle cell disease (SCD) is a chronic hematologic disease associated with increased morbidity and mortality. Hemoglobinopathies are the most prevalent genetic disease globally, and SCD is estimated to affect 0.7% of Ugandan. The disease may adversely impact on the quality of life of sickle cell patients. This study aimed to evaluate the health related quality of life (HRoL) of adolescents with SCD. METHODS: This was a mixed-methods study of adolescents with sickle cell disease and their caretakers living in Kampala city, Uganda. All children aged 8–17 years with homozygous sickle cell disease attending the sickle cell clinic at Mulago Hospital during the study period were included in this study. Participants completed the PedsQL™ generic core scales parent-proxy and child self-report questionnaire during a routine clinic visit. HRQoL was the primary outcome measured. Socio-demographics and disease related data were obtained through personal interview with caretakers and reviewing patients’ medical records. Mean scores were used for HRQoL and linear regression for associated factors. RESULTS: Of the 140 adolescents with SCD included in the study, 40% were male. A total of 95 adolescents (68%) were between the age of 8–12 years with a mean age of 14.25 years. The physical function was assessed slightly higher by adolescents with a mean score of57.5 ± 20.3 compare to caretakers with 52.8 ± 22.1(p < 0.001). As assessed by caretakers, physical HRQoL scores were negatively associated with pain about-10.02 CI [− 19.22, − 0.81](p = 0.033), whereas it was positively associated with Pneumococcal vaccine with the score of 28.43 CI [16.78,40.09](p < 0.001) as assessed by adolescents and 31.37CI [22.22,40.51](p < 0.001) by caretakers. Pneumococcal vaccination impacted positively the psychosocial functioning with a score of 8.67CI [1.51,15.84] (p = 0.018) as assessed by children and 15.94 CI [5.50,26.38](p = 0.003) as assessed by the caretakers. CONCLUSIONS: This study highlighted that pain was negatively associated with both physical and psychosocial functioning; whereas getting Pneumococcal vaccine was positively associated with both physical and psychosocial functioning as reported by children and caretakers. BioMed Central 2019-05-14 /pmc/articles/PMC6518788/ /pubmed/31114692 http://dx.doi.org/10.1186/s12878-019-0141-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kambasu, David Muthahi
Rujumba, Joseph
Lekuya, Hervé Monka
Munube, Deogratias
Mupere, Ezekiel
Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study
title Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study
title_full Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study
title_fullStr Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study
title_full_unstemmed Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study
title_short Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study
title_sort health-related quality of life of adolescents with sickle cell disease in sub-saharan africa: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518788/
https://www.ncbi.nlm.nih.gov/pubmed/31114692
http://dx.doi.org/10.1186/s12878-019-0141-8
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