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Mortadah Alsalman,1 Hassan Alhamoud,2 Zainab Alabdullah,1 Raghad Alsleem,1 Zainab Almarzooq,1 Fatemah Alsalem,1 Ahmed Alsulaiman,3 Abdullah Albeladi,2 Zaenb Alsalman4 1Department of Medicine, College of Medicine, King Faisal University, Al Ahsa, Saudi Arabia; 2Department of Medicine, King Fahad Hospital, Al Hofuf, Saudi Arabia; 3College of Medicine, Vision Colleges, Riyadh, Saudi Arabia; 4Departments of Family and Community Medicine, College of Medicine, King Faisal University, Al Ahsa, Saudi ArabiaCorrespondence: Zaenb Alsalman, College of Medicine, King Faisal University, Po Box 3311, Al Ahsa, 36346, Saudi Arabia, Tel +966545611633, Email Alsalman.zainab@hotmail.comBackground 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.Keywords: sickle cell disease, in vitro fertilization, counselling |
