Augutis Marika, Levi Richard, Asplund Kenneth, Berg-Kelly Kristina
Department of Neurobiology, Health Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
J Spinal Cord Med. 2007;30 Suppl 1(Suppl 1):S55-64. doi: 10.1080/10790268.2007.11753970.
BACKGROUND/OBJECTIVE: Spinal cord injury (SCI) occurring during adolescence poses additional challenges because of the concurrent age-specific bio-psychosocial development. Full understanding of the psychosocial dimensions of rehabilitation requires exploration of the patient perspective. The objective of this study was to focus on psychosocial factors from the patient perspective in persons who had previously sustained a SCI during early and mid-adolescence (11-15 years of age).
Twenty-four of the 28 persons who had sustained a SCI in Sweden from 1985 to 1996 participated in the study. Semistructured interviews were made an average of 10 years after injury. Narratives were analyzed qualitatively according to content analysis.
Parents and peers were found to have formed a crucial network. Parents frequently acted as advocates in interactions with health care providers, as supporters, and as containers of sorrow, frustration, and anger. Peers acted as promoters of activity and identity development. However, health care providers were perceived as not making sufficient use of this network.
Rehabilitation professionals might be encouraged to increase their knowledge of adolescence medicine to better meet the specific needs and demands of persons in this age group. It is further suggested that parents and peers be considered important partners in the joint rehabilitation effort.
背景/目的:青春期发生的脊髓损伤(SCI)会带来额外的挑战,因为这一时期同时存在特定年龄阶段的生物-心理-社会发展情况。全面理解康复过程中的心理社会层面需要探索患者的观点。本研究的目的是从患者角度关注在青春期早期和中期(11至15岁)曾遭受脊髓损伤的人群的心理社会因素。
1985年至1996年在瑞典遭受脊髓损伤的28人中,有24人参与了该研究。在受伤平均10年后进行了半结构化访谈。根据内容分析法对访谈内容进行了定性分析。
发现父母和同龄人形成了一个关键的网络。父母在与医疗服务提供者的互动中经常充当倡导者、支持者,以及悲伤、沮丧和愤怒的承受者。同龄人则充当活动和身份发展的推动者。然而,医疗服务提供者被认为没有充分利用这个网络。
或许应鼓励康复专业人员增加对青春期医学的了解,以更好地满足该年龄组人群的特殊需求。进一步建议将父母和同龄人视为联合康复工作中的重要伙伴。