Abstract: A literature review is defined by Hart (2018) as an analysis, critical evaluation, and synthesis of existing knowledge relevant to a research problem. The aim of this chapter is to expand our understanding about disease knowledge and treatment adherence among adult patients with thalassemia. Previous studies on this topic were examined to identify gaps in the nursing literature and present what is already known about relevant issues from a nursing perspective. Data Search Strategy The strategy used to search the literature was designed to capture published theoretical and empirical articles related to disease..........
[1]. Alaithan, M. A., AbdulAzee, S., & Borgio, J. F. (2018). A comprehensive review of the prevalence of beta globin gene variations and the co-inheritance of related gene variants in Saudi Arabians with beta-thalassemia. Saudi Medical Journal, 39(4), 329.
[2]. Alenazi, S. A., Ali, H. W., Alharbi, M. G., Alenizi, A. F., & Wazir, F. (2015). Prevalence of thalassemia and sickle cell disease northern border region of Saudi Arabia. Kashmir Journal of Medical Sciences, 1(1), 3-6.
[3]. Al-Kloub, M.I., Abed, M.A., AlKhawaldeh, O.A., AlTawarah, Y.M., & Froelicher, E.S. (2014). Predictors of non-adherence to follow-up visits and deferasirox chelation therapy among Jordanian adolescents with thalassemia major. Pediatric Hematology and Oncology, 31(7), 624-637.
[4]. Al‐Kloub, M. I., Nayel Salameh , T., & Froelicher, E. S. (2014). Impact of psychosocial status and disease knowledge on deferoxamine adherence among thalassaemia major adolescents. International Journal of Nursing Practice, 20(3),265-274.
[5]. Alsaeed, E.S., Farhat, G.N., Assiri, A.M., Memish, Z., Ahmed, E. M., Saeedi, M. Y., . . . Bashawri, H. (2018). Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program , 2011 – 2015. Journal of Epidemiology and Global Health, 7(1): S41-S47.