Wagner Janelle L, Modi Avani C, Johnson Erica K, Shegog Ross, Escoffery Cam, Bamps Yvan, Austin Joan K, Schultz Rebecca J, MapelLentz Sarah, Smith Gigi
Department of Pediatrics, College of Nursing, Medical University of South Carolina, Charleston, South Carolina, U.S.A.
Center for Treatment Adherence and Self-Management, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, U.S.A.
Epilepsia. 2017 May;58(5):743-754. doi: 10.1111/epi.13711. Epub 2017 Feb 24.
To respond to recommendations put forth by the Institute of Medicine to improve self-management resources for youth with epilepsy by conducting a systematic review of the self-management literature in pediatric epilepsy.
Inclusion criteria: youth birth to 18 years with a seizure disorder or an epilepsy diagnosis and/or their caregivers, published 1985-2014 in English, and conducted in countries with a very high human development index. Abstract and keywords had to explicitly refer to "self-care" (pre-1996) and/or self-management (post-1996). The review was conducted in seven phases: (1) identification of bibliographical search criteria and databases; (2) abstract assessment; (3) full article review; (4) organization of final citations into instrument development, intervention, factors associated with self-management categories; (5) American Academy of Neurology level of evidence (LOE) assessment for intervention studies; (6) CONsolidated Standards of Reporting Trials (CONSORT) evaluation of LOE level III articles utilizing a control group; and (7) categorization of intervention outcomes across four self-management domains.
Of the 87 articles that met eligibility criteria, 24 were interventions and received LOE scores of level III or IV. Most studies (n = 20, 80%) were scored at level III; however, only eight had a control group and adhered to CONSORT guidelines. They largely neglected information on intervention components (e.g., implementation, treatment fidelity), randomization, participant flow, missing data, and effect size or confidence intervals. The 24 intervention studies reported significant impact in four domains: individual (n = 13), family (n = 6), health care system (n = 3), and community (n = 2).
There are no level I or II studies. No study met full CONSORT guidelines. Outcomes were well described; however, the nature of self-management interventions (e.g., multiple foci, skills targeted) and the observed heterogeneity in outcomes complicates comparisons across studies. Randomized controlled trials (RCTs) that include large sample sizes, impact of the intervention, treatment fidelity, and power analyses are necessary to further this evidence base.
通过对儿科癫痫自我管理文献进行系统综述,回应医学研究所提出的改善癫痫青少年自我管理资源的建议。
纳入标准:年龄在18岁以下患有癫痫发作障碍或被诊断为癫痫的青少年及/或其照料者;1985年至2014年以英文发表;在人类发展指数非常高的国家开展。摘要和关键词必须明确提及“自我护理”(1996年前)和/或自我管理(1996年后)。综述分七个阶段进行:(1)确定文献检索标准和数据库;(2)摘要评估;(3)全文审查;(4)将最终引用文献整理到工具开发、干预、与自我管理类别相关的因素中;(5)对干预研究进行美国神经病学学会证据水平(LOE)评估;(6)利用对照组对LOE III级文章进行试验报告的统一标准(CONSORT)评估;(7)将干预结果归类到四个自我管理领域。
在符合纳入标准的87篇文章中,24篇为干预研究,证据水平得分为III级或IV级。大多数研究(n = 20,80%)得分为III级;然而,只有8篇有对照组并遵循CONSORT指南。这些研究很大程度上忽略了关于干预组成部分(如实施、治疗保真度)、随机化、参与者流程、缺失数据以及效应大小或置信区间的信息。24项干预研究在四个领域报告了显著影响:个体(n = 13)、家庭(n = 6)、医疗保健系统(n = 3)和社区(n = 2)。
没有I级或II级研究。没有研究完全符合CONSORT指南。结果描述得很充分;然而,自我管理干预的性质(如多个重点、针对的技能)以及观察到的结果异质性使跨研究比较变得复杂。需要进行包括大样本量、干预影响、治疗保真度和效能分析的随机对照试验(RCT)来进一步充实这一证据基础。