Assessment of the Attitude, Knowledge, and Complications Related to Sickle Cell Disease in Al-Ahsa Region, Saudi Arabia
Abstract
Sickle-cell disease (SCD) is one of the well-known hematological disorders that affects many people around the world. The risk of disease transmission increases with consanguineous marriage. SCD is considered a life-threatening condition, with mortality rates increasing annually because of the large number of comorbidities associated with this disease. The Al-Ahsa region carries the highest rate of SCD in Saudi Arabia. The aim of the study is to evaluate the attitude, knowledge, perceptions, and misunderstandings regarding SCD and its complications. An analytical cross-sectional study was conducted among 387 participants of the Al-Ahsa population. Data was collected using a structured, self-administered questionnaire. The questionnaire contains four important domains: socio-demographical information, knowledge, attitude, and complications of SCD. Of the 387 people sampled, 80% of the participants had heard about SCD, and the major source of information were their friends and families. More than half of the population knew that SCD is inherited, although 40% did not know about the treatment for SCD. Most of the participants showed a positive attitude, being sympathetic toward people with SCD, while half of the participants preferred not to have a child rather than have one with SCD. A high proportion of the population did not know that SCD is a leading cause of life-threatening infections, kidney failure, and stroke. The study indicates that there is a need for awareness programs to address some misconceptions and expand information regarding SCD, which could contribute to improving knowledge about SCD.
Keywords: sickle cell disease, knowledge, attitude, Saudi Arabia.
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WARE R. E., DE MONTALEMBERT M., TSHILOLO L., and ABBOUD M. R. Sickle cell disease. Lancet, 2017, 390(10091): 311-323. https://doi.org/10.1016/s0140-6736(17)30193-9
ZAINI R. G. Sickle-cell Anemia and Consanguinity among the Saudi Arabian Population. Archives of Medicine, 2016, 8(3): 3-15. https://www.itmedicalteam.pl/articles/sicklecell-anemia-and-consanguinity-among-the-saudi-arabian-population-103872.html
LANZKRON S., CARROLL C. P., and HAYWOOD JR. C. Mortality rates and age at death from sickle cell disease: U.S., 1979-2005. Public Health Reports, 2013, 128(2): 110-116. https://doi.org/10.1177/003335491312800206
MODELL B., & DARLISON M. Global epidemiology of haemoglobin disorders and derived service indicators. Bulletin of the World Health Organization, 2008, 86(6): 480-487. https://doi.org/10.2471/blt.06.036673
ALOTAIBI M. M. Sickle cell disease in Saudi Arabia: A challenge or not. Journal of Epidemiology and Global Health, 2017, 7(2): 99-101. https://doi.org/10.1016/j.jegh.2016.12.006
AL-QURASHI M. M., EL-MOUZAN M. I., AL-HERBISH A. S., AL-SALLOUM A. A., and AL-OMAR A. A. The prevalence of sickle cell disease in Saudi children and adolescents. A community-based survey. Saudi Medical Journal, 2008, 29(10): 1480-1483. https://smj.org.sa/content/29/10/1480
ALHAMDAN N. A., ALMAZROU Y. Y., ALSWAIDI F. M., and CHOUDHRY A. J. Premarital screening for thalassemia and sickle cell disease in Saudi Arabia. Genetics in Medicine, 2007, 9(6): 372-377. https://doi.org/10.1097/gim.0b013e318065a9e8
ALHOSAIN A. Premarital Screening Programs in the Middle East, from a Human Right’s Perspective. Diversity and Equality in Health and Care, 2018, 15(2): 41-45. https://doi.org/10.21767/2049-5471.1000154
Awad LA. A study to assess knowledge and misconceptions on sickle cell disease among university students in eastern province of Saudi Arabia. International Journal of Education and Research, 2018, 6(3): 147-158. https://ijern.com/journal/2018/March-2018/16.pdf
ALTURAIFI A. H., ALSHARIF N. M., ABULOLA W. K., MAIMANI Y. T., AHMAD R. S., ALSULAMI E. F., and ALOTAIBI A. A. An Assessment of Knowledge towards Complications of Sickle Cell Disease among General Population in Jeddah City. Egyptian Journal of Hospital Medicine, 2018, 70(11): 1880-1886. https://doi.org/10.12816/0044836
POURHOSEINGHOLI M. A., VAHEDI M., and RAHIMZADEH M. Sample size calculation in medical studies. Gastroenterology and Hepatology from Bed to Bench, 2013, 6(1): 14-17. https://doi.org/10.22037/ghfbb.v6i1.332
BOADU I., & ADDOAH T. Knowledge, Beliefs and Attitude towards Sickle Cell Disease among University Students. Journal of Community Medicine & Health Education, 2018, 8(1): 593. https://doi.org/10.4172/2161-0711.1000593
TUSUUBIRA S. K., NAKAYINGA R., MWAMBI B., ODDA J., KICONCO S., and KOMUHANGI A. Knowledge, perception and practices towards sickle cell disease: a community survey among adults in Lubaga division, Kampala Uganda. BMC Public Health, 2018, 18(1): 561. https://doi.org/10.1186/s12889-018-5496-4
AL-SUWAID H., DARWISH M., and SABRA A. Knowledge and misconceptions about sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency among adult sickle cell anemia patients in al Qatif Area (eastern KSA). International Journal of Medicine and Public Health, 2015, 5(1): 86-92. https://dx.doi.org/10.4103/2230-8598.151269
AL-QATTAN H. M., AMLIH D. F., SIRAJUDDIN F. S., ALHUZAIMI D. I., ALAGEEL M. S., BIN TUWAIM R. M., and AL QAHTANI F. H. Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults. Advances in Hematology, 2019, 2019: 3961201. https://doi.org/10.1155/2019/3961201
ALGHAMDI A., ALAMRI A., and ALGHAMDI A. Perceptions about Sickle Cell Disease among Adults in Albaha Region: A Cross-Sectional Study. The Egyptian Journal of Hospital Medicine, 2018, 70(2): 357-363. https://doi.org/10.12816/0043105
OBEED H. A.-H., AMEEN Z. H., FADHEL M. A., and ALZUBAIDI L. Automated Real-Time Sickle Cell Anemia Diagnosis Based on a Field Programmable Gate Array Accelerator. Journal of Southwest Jiaotong University, 2019, 54(6). https://doi.org/10.35741/issn.0258-2724.54.6.58
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