Queen's University, Centre for Health Services and Policy Research, Abramsky Hall, Kingston, ON K7L 3N6.
Can Fam Physician. 2012 Nov;58(11):1207-16, e626-35.
To perform a scoping review of the empirical evidence between 1980 and 2009 regarding primary care for adults with spinal cord injury (SCI).
Peer-reviewed journals were searched from 1980 to 2009 using CINAHL, PubMed-MEDLINE, EMBASE, PsycINFO, Social Sciences Abstracts, and Social Work Abstracts.
The key word-driven electronic search identified 42 articles on primary care and SCI. Inclusion criteria narrowed the set to 21 articles that were published in English, that had a sample size of greater than 3, and that offered empirical analysis.
Approximately 90% of people with SCI identify family physicians as their regular doctors; 63% have SCI specialists. People with long-term SCI develop complex rubrics for navigating their personal health care systems. There is conflicting evidence about the effectiveness of outreach programs for maintaining health and preventing complications following SCI. Regular follow-up by specialized teams and annual comprehensive health examination are supported by the evidence. The research shows a high level of consistency in identifying the most common issues raised by people with SCI in primary care, most of which are related to disability-specifically, secondary complications such as bowel or bladder dysfunction and pain. There is also good evidence that many general health issues require attention in this population, such as bone density problems, depression, and sexual and reproductive health issues. There is level 4 and 5 evidence for unmet health needs among individuals living with SCI in the community. Despite patients with SCI being high users of primary care and health services in general, the evidence suggests that the information needs of these patients in particular are poorly met.
A robust system of primary care is the best assurance of good health outcomes and reasonable health service use for people with SCI, including annual comprehensive examination, appropriate specialist use, and attention to accessibility and unmet needs.
对 1980 年至 2009 年期间有关成人脊髓损伤(SCI)初级保健的实证证据进行范围界定综述。
使用 CINAHL、PubMed-MEDLINE、EMBASE、PsycINFO、Social Sciences Abstracts 和 Social Work Abstracts,从 1980 年至 2009 年对同行评审期刊进行了检索。
关键词驱动的电子检索确定了 42 篇关于初级保健和 SCI 的文章。纳入标准将该组缩小到 21 篇,这些文章以英文发表,样本量大于 3 ,并且提供了实证分析。
大约 90%的 SCI 患者将家庭医生视为他们的常规医生;63%的人有 SCI 专科医生。长期患有 SCI 的人在驾驭个人医疗保健系统方面会出现复杂的问题。关于外展计划在维持 SCI 后的健康和预防并发症方面的有效性存在相互矛盾的证据。有证据表明,专门团队的定期随访和年度综合健康检查是有效的。研究表明,在初级保健中,大多数人(约 90%)会提出最常见的问题,这些问题与残疾有关,特别是继发性并发症,如肠或膀胱功能障碍和疼痛。也有很好的证据表明,许多一般健康问题在这一人群中需要关注,如骨密度问题、抑郁和性健康和生殖健康问题。有证据表明,生活在社区中的 SCI 患者存在未满足的健康需求,水平为 4 和 5。尽管 SCI 患者是初级保健和一般医疗服务的高使用者,但证据表明,这些患者的信息需求尤其得不到满足。
一个强大的初级保健系统是确保 SCI 患者获得良好健康结果和合理医疗服务使用的最佳保障,包括年度综合检查、适当的专家使用以及关注可达性和未满足的需求。