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Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study
PURPOSE: Sickle cell disease (SCD) is a multisystemic disease that results in diverse clinical manifestations in the form of acute and chronic complications. This study aims to assess the academic achievements of patients with SCD. METHODS AND MATERIALS: A cross-sectional study was a study conducted...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576454/ https://www.ncbi.nlm.nih.gov/pubmed/37841200 http://dx.doi.org/10.2147/PPA.S434750 |
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author | Alsalman, Mortadah AlHaddad, Sajjad Alibrahim, Ibrahim Alabdullah, Abdulhakim Ibrahim Almutawa, Mohammed Hussain Alhamam, Abdullah Khalid Albaqshi, Mohammed Abdullah |
author_facet | Alsalman, Mortadah AlHaddad, Sajjad Alibrahim, Ibrahim Alabdullah, Abdulhakim Ibrahim Almutawa, Mohammed Hussain Alhamam, Abdullah Khalid Albaqshi, Mohammed Abdullah |
author_sort | Alsalman, Mortadah |
collection | PubMed |
description | PURPOSE: Sickle cell disease (SCD) is a multisystemic disease that results in diverse clinical manifestations in the form of acute and chronic complications. This study aims to assess the academic achievements of patients with SCD. METHODS AND MATERIALS: A cross-sectional study was a study conducted among adult patients with SCD from the eastern province of Saudi Arabia, where SCD is more widespread than in other regions. RESULTS: A total of ninety patients with SCD, whose median age was 32.33 ± 11.84, were retrospectively evaluated. Of the total number, 32 (35.5%) did not obtain a secondary higher education certificate, and five (3.3%) were illiterate. Sixty-three (70%) of the patients were female, indicating no significant association between gender and education level (p-value > 0.05). The patients’ mean annual hospitalizations and emergency visits totaling 4.7 and 8.43, respectively, were not significantly associated with education (p-value > 0.05). Throughout the patients’ lives, mean blood transfusions and ICU admissions occurred 6.29 and 2.75 times, respectively, which were not significantly associated with education level (p-value > 0.05). However, education was inversely proportional to a history of splenectomy and cholecystectomy (p < 0.05). Laboratory parameters (hemoglobin level, WBC, platelets, and hemoglobin F) showed no significant associations with education level (p-value > 0.05). Patients with sickle-thalassemia exhibited a trend of being better-educated than those without the diseases, but the difference did not reach statistical significance (p-value > 0.05). A linear regression analysis revealed no significant associations among clinical and laboratory parameters. CONCLUSION: SCD is a multisystemic disease that impacts socioeconomic status, learning ability, and academic achievements. More research is needed to identify factors that predict poor performance. Additionally, intelligence quotient (IQ) and cognitive assessment should be incorporated into early screening programs for SCD in order to implement preventive measures and a thorough investigation of underlying causes. |
format | Online Article Text |
id | pubmed-10576454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-105764542023-10-15 Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study Alsalman, Mortadah AlHaddad, Sajjad Alibrahim, Ibrahim Alabdullah, Abdulhakim Ibrahim Almutawa, Mohammed Hussain Alhamam, Abdullah Khalid Albaqshi, Mohammed Abdullah Patient Prefer Adherence Original Research PURPOSE: Sickle cell disease (SCD) is a multisystemic disease that results in diverse clinical manifestations in the form of acute and chronic complications. This study aims to assess the academic achievements of patients with SCD. METHODS AND MATERIALS: A cross-sectional study was a study conducted among adult patients with SCD from the eastern province of Saudi Arabia, where SCD is more widespread than in other regions. RESULTS: A total of ninety patients with SCD, whose median age was 32.33 ± 11.84, were retrospectively evaluated. Of the total number, 32 (35.5%) did not obtain a secondary higher education certificate, and five (3.3%) were illiterate. Sixty-three (70%) of the patients were female, indicating no significant association between gender and education level (p-value > 0.05). The patients’ mean annual hospitalizations and emergency visits totaling 4.7 and 8.43, respectively, were not significantly associated with education (p-value > 0.05). Throughout the patients’ lives, mean blood transfusions and ICU admissions occurred 6.29 and 2.75 times, respectively, which were not significantly associated with education level (p-value > 0.05). However, education was inversely proportional to a history of splenectomy and cholecystectomy (p < 0.05). Laboratory parameters (hemoglobin level, WBC, platelets, and hemoglobin F) showed no significant associations with education level (p-value > 0.05). Patients with sickle-thalassemia exhibited a trend of being better-educated than those without the diseases, but the difference did not reach statistical significance (p-value > 0.05). A linear regression analysis revealed no significant associations among clinical and laboratory parameters. CONCLUSION: SCD is a multisystemic disease that impacts socioeconomic status, learning ability, and academic achievements. More research is needed to identify factors that predict poor performance. Additionally, intelligence quotient (IQ) and cognitive assessment should be incorporated into early screening programs for SCD in order to implement preventive measures and a thorough investigation of underlying causes. Dove 2023-10-10 /pmc/articles/PMC10576454/ /pubmed/37841200 http://dx.doi.org/10.2147/PPA.S434750 Text en © 2023 Alsalman et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Alsalman, Mortadah AlHaddad, Sajjad Alibrahim, Ibrahim Alabdullah, Abdulhakim Ibrahim Almutawa, Mohammed Hussain Alhamam, Abdullah Khalid Albaqshi, Mohammed Abdullah Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study |
title | Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study |
title_full | Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study |
title_fullStr | Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study |
title_full_unstemmed | Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study |
title_short | Impact of Sickle Cell Disease on Academic Performance: A Cross Sectional Study |
title_sort | impact of sickle cell disease on academic performance: a cross sectional study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576454/ https://www.ncbi.nlm.nih.gov/pubmed/37841200 http://dx.doi.org/10.2147/PPA.S434750 |
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