Karolus Wangi, Rinanda Shaleha, Eri Wijaya, Barbara Birriel
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引用次数: 0
Abstract
Background: Thalassemia is a genetic disease that is inherited in families and has been designated as a global burden. Individuals living with thalassemia may experience impacts on their psychosocial well-being. However, there is a gap of limited study at the systematic review level regarding the extent to which psychosocial aspects contribute to the overall problems and burdens experienced by people living with thalassemia.
Aim: This study aimed to synthesize the evidence on psychosocial problems in people living with thalassemia to provide comprehensive insight.
Methods: The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guideline was used to guide this systematic review. All relevant empirical studies in the English language that assessed the variety of psychosocial aspects were included. A total of 1,466 articles were identified from PubMed, CINAHL, ProQuest, PsycINFO, Scopus, Web of Science, and Cochrane databases from those inceptions to 6 March 2023. 1,443 articles were excluded due to duplication, not thalassemia- or psychosocial-related, availability of full-text, and not including patients. Finally, 13 studies were included and assessed using Mixed Methods Appraisal Tool (MMAT) appraisal tools. This study is already registered in International Prospective Register of Systematic Reviews (CRD42023431082).
Results: This review analyzed 13 full-text studies conducted between 1993 and 2022. The MMAT quality assessment rated all 13 studies as high quality. The included studies used various designs, with six non-randomized quantitative studies, five descriptive quantitative studies, and two qualitative studies. The review summarizes each study's main findings, highlighting psychosocial problems and related outcomes, such as adherence and psychosocial morbidity, anxiety, educational and social impairment, coping style, internalizing and externalizing behaviors, and adaptive behaviors and family relationships.
Discussion: The available literature globally highlights the psychosocial challenges of people living with thalassemia, particularly those who require regular blood transfusions across different timeframes. Despite inconsistent definitions across studies, it is notable that patients with thalassemia major facing physical changes associated with facial defects and experience significant psychosocial issues related to self-image, social interactions, and relationships that influence quality of life.
背景:地中海贫血是一种家族遗传的遗传性疾病,已被确定为全球负担。地中海贫血患者的心理社会健康可能受到影响。然而,关于心理社会方面在多大程度上导致地中海贫血患者所经历的总体问题和负担,在系统评价水平上的有限研究存在差距。目的:本研究旨在综合地中海贫血患者的社会心理问题的证据,提供全面的见解。方法:采用《系统评价和荟萃分析首选报告项目》指南指导本系统评价。所有评估心理社会方面多样性的英语相关实证研究都包括在内。共从PubMed, CINAHL, ProQuest, PsycINFO, Scopus, Web of Science和Cochrane数据库中筛选出1466篇文章,从这些数据库开始到2023年3月6日。1443篇文章因重复、非地中海贫血或心理社会相关、可获得全文以及不包括患者而被排除。最后,纳入13项研究,并使用混合方法评估工具(MMAT)评估工具进行评估。本研究已在国际前瞻性系统评论注册(CRD42023431082)中注册。结果:本综述分析了1993年至2022年间进行的13项全文研究。MMAT质量评估将所有13项研究评为高质量。纳入的研究采用各种设计,包括6项非随机定量研究、5项描述性定量研究和2项定性研究。这篇综述总结了每项研究的主要发现,强调了社会心理问题和相关结果,如依从性和社会心理发病率、焦虑、教育和社会障碍、应对方式、内化和外化行为、适应行为和家庭关系。讨论:全球现有文献强调了地中海贫血患者面临的社会心理挑战,特别是那些需要在不同时间段定期输血的人。尽管不同研究的定义不一致,但值得注意的是,地中海贫血患者面临与面部缺陷相关的身体变化,并经历与自我形象、社会互动和影响生活质量的关系相关的重大社会心理问题。