Chiu Aubrey S, Blanchette Victor S, Barrera Maru, Hilliard Pamela, Young Nancy L, Abad Audrey, Feldman Brian M
The Hospital for Sick Children Toronto Ontario Canada.
The University of Toronto Toronto Ontario Canada.
Res Pract Thromb Haemost. 2021 Nov 30;5(8):e12627. doi: 10.1002/rth2.12627. eCollection 2021 Dec.
Patients with hemophilia may experience joint damage, which can impair participation, yet few studies have examined the impact hemophilia may have on social participation and quality of life.
The aims of this study are to assess the relationship between patient social participation and self-perception, social support, and impact on the family.
PATIENTS/METHODS: A random representative sample of 50 boys with hemophilia from The Hospital for Sick Children, Toronto, Canada, completed measures of social participation (Participation Scale for kids), self-perception (Self-Perception Profile for children and adolescents), and social support (Social Support Scale for children). Participants' parents completed Family Impact Module of the Pediatric Quality of Life Inventory. Data were analyzed using Pearson product-moment correlations.
Social participation was strongly correlated with self-perception subscales Social Acceptance (= -0.5, = <0.001) and Global Self-Worth (= -0.6, = <0.001) for all participants. The Athletic Competence subscale was strongly correlated for adolescents only (= -0.6, = <0.01). There were strong correlations between social participation and social support from parents (= -0.6, = <0.001), teachers (= -0.5, = <0.001), and classmates (= -0.6, = <0.001) and moderate correlations for support from close friends (= -0.4, = <0.01). There were no significant correlations with family impact.
In the context of a country with unlimited access to safe clotting factor concentrates, boys with hemophilia have few social participation restrictions. Although correlational findings do not represent causality, they suggest that encouragement of social participation may be beneficial in boys with hemophilia to increase self-perception as well as strengthen their social support network.
血友病患者可能会出现关节损伤,这会影响其参与度,但很少有研究探讨血友病对社会参与和生活质量的影响。
本研究旨在评估患者社会参与与自我认知、社会支持以及对家庭影响之间的关系。
患者/方法:从加拿大多伦多病童医院随机抽取50名患血友病的男孩作为代表性样本,他们完成了社会参与量表(儿童参与量表)、自我认知量表(儿童及青少年自我认知量表)和社会支持量表(儿童社会支持量表)。参与者的父母完成了儿童生活质量量表的家庭影响模块。数据采用Pearson积差相关分析。
对于所有参与者,社会参与与自我认知子量表社会接纳(r = -0.5,p < 0.001)和总体自我价值(r = -0.6,p < 0.001)密切相关。运动能力子量表仅与青少年密切相关(r = -0.6,p < 0.01)。社会参与与来自父母的社会支持(r = -0.6,p < 0.001)、教师的社会支持(r = -0.5,p < 0.001)和同学的社会支持(r = -0.6,p < 0.001)密切相关,与亲密朋友的支持中度相关(r = -0.4,p < 0.01)。与家庭影响无显著相关性。
在一个能够无限制获取安全凝血因子浓缩剂的国家,患血友病的男孩几乎没有社会参与限制。尽管相关研究结果并不代表因果关系,但它们表明鼓励社会参与可能有助于提高患血友病男孩的自我认知,并加强他们的社会支持网络。