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Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study

BACKGROUND AND AIM: Sickle cell disease (SCD) is an autosomal recessive disorder. Decisions following premarital screening results might be influenced by several factors. Thus, this study aims to assess the knowledge and beliefs toward SCD and reproductive decisions. MATERIAL AND METHODS: A cross-se...

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Autores principales: Alsalman, Mortadah, Alhamoud, Hassan, Alabdullah, Zainab, Alsleem, Raghad, Almarzooq, Zainab, Alsalem, Fatemah, Alsulaiman, Ahmed, Albeladi, Abdullah, Alsalman, Zaenb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039637/
https://www.ncbi.nlm.nih.gov/pubmed/36974077
http://dx.doi.org/10.2147/PPA.S404811
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author Alsalman, Mortadah
Alhamoud, Hassan
Alabdullah, Zainab
Alsleem, Raghad
Almarzooq, Zainab
Alsalem, Fatemah
Alsulaiman, Ahmed
Albeladi, Abdullah
Alsalman, Zaenb
author_facet Alsalman, Mortadah
Alhamoud, Hassan
Alabdullah, Zainab
Alsleem, Raghad
Almarzooq, Zainab
Alsalem, Fatemah
Alsulaiman, Ahmed
Albeladi, Abdullah
Alsalman, Zaenb
author_sort Alsalman, Mortadah
collection PubMed
description BACKGROUND AND AIM: Sickle cell disease (SCD) is an autosomal recessive disorder. Decisions following premarital screening results might be influenced by several factors. Thus, this study aims to assess the knowledge and beliefs toward SCD and reproductive decisions. MATERIAL AND METHODS: A cross-sectional study was conducted among adults in the eastern province of Saudi Arabia. Data was collected using a web-based questionnaire. Participants were divided into two groups based on their knowledge scores. RESULTS: A total of 390 participants were recruited with a mean age of 28.6 years. The majority (90.5%) of participants had general knowledge about the disease mode of inheritance however, 66.9% had poor knowledge about the disease overall. Regarding knowledge level, there was no statistically significant difference between the non-healthy group (diseased and carrier) and healthy participants (P=0.304). Moreover, the participants’ decisions about choosing future partners were more likely to be affected among those with prior knowledge about the disease (p=0.008). However, 152 (91.6%) male participants with prior knowledge would change their decision about selecting a future partner compared to 225 (92.4%) female participants. Regarding reproduction, only 38.5% of participants were aware of in vitro fertilization (IVF) as an assistive reproductive technology. Furthermore, female participants believed that IVF is a way to have healthy babies and would consider it despite the cost more than male participants (p=0.0001, p=0.007 respectively). CONCLUSION: SCD is an inherited disease with economic, physical, and psychological burdens. However, curative options are costly, and hence, prevention is key. Therefore, healthcare decision-makers should consider implementing policies to minimize the financial burden that may still affect society despite the availability of free medical care. This study warrants extensive community-based education programs that may contribute toward cost savings. It also highlights the importance of premarital counselling for disease and carrier people including alternative reproduction options.
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spelling pubmed-100396372023-03-26 Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study Alsalman, Mortadah Alhamoud, Hassan Alabdullah, Zainab Alsleem, Raghad Almarzooq, Zainab Alsalem, Fatemah Alsulaiman, Ahmed Albeladi, Abdullah Alsalman, Zaenb Patient Prefer Adherence Original Research BACKGROUND AND AIM: Sickle cell disease (SCD) is an autosomal recessive disorder. Decisions following premarital screening results might be influenced by several factors. Thus, this study aims to assess the knowledge and beliefs toward SCD and reproductive decisions. MATERIAL AND METHODS: A cross-sectional study was conducted among adults in the eastern province of Saudi Arabia. Data was collected using a web-based questionnaire. Participants were divided into two groups based on their knowledge scores. RESULTS: A total of 390 participants were recruited with a mean age of 28.6 years. The majority (90.5%) of participants had general knowledge about the disease mode of inheritance however, 66.9% had poor knowledge about the disease overall. Regarding knowledge level, there was no statistically significant difference between the non-healthy group (diseased and carrier) and healthy participants (P=0.304). Moreover, the participants’ decisions about choosing future partners were more likely to be affected among those with prior knowledge about the disease (p=0.008). However, 152 (91.6%) male participants with prior knowledge would change their decision about selecting a future partner compared to 225 (92.4%) female participants. Regarding reproduction, only 38.5% of participants were aware of in vitro fertilization (IVF) as an assistive reproductive technology. Furthermore, female participants believed that IVF is a way to have healthy babies and would consider it despite the cost more than male participants (p=0.0001, p=0.007 respectively). CONCLUSION: SCD is an inherited disease with economic, physical, and psychological burdens. However, curative options are costly, and hence, prevention is key. Therefore, healthcare decision-makers should consider implementing policies to minimize the financial burden that may still affect society despite the availability of free medical care. This study warrants extensive community-based education programs that may contribute toward cost savings. It also highlights the importance of premarital counselling for disease and carrier people including alternative reproduction options. Dove 2023-03-21 /pmc/articles/PMC10039637/ /pubmed/36974077 http://dx.doi.org/10.2147/PPA.S404811 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
Alhamoud, Hassan
Alabdullah, Zainab
Alsleem, Raghad
Almarzooq, Zainab
Alsalem, Fatemah
Alsulaiman, Ahmed
Albeladi, Abdullah
Alsalman, Zaenb
Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study
title Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study
title_full Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study
title_fullStr Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study
title_full_unstemmed Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study
title_short Sickle Cell Disease Knowledge and Reproductive Decisions: A Saudi Cross-Sectional Study
title_sort sickle cell disease knowledge and reproductive decisions: a saudi cross-sectional study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039637/
https://www.ncbi.nlm.nih.gov/pubmed/36974077
http://dx.doi.org/10.2147/PPA.S404811
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