Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario, Canada.
Department of Global Health and Development, London School of Hygiene & Tropical Medicine, London, UK.
BMJ Open. 2019 Apr 4;9(4):e025741. doi: 10.1136/bmjopen-2018-025741.
To systematically synthesise qualitative research that explores children's and caregivers' perceptions of mandatory reporting.
We conducted a meta-synthesis of qualitative studies.
Searches were conducted in Medline, Embase, PsycINFO, Cumulative Index to Nursing and Allied Health Literature, Criminal Justice Abstracts, Education Resources Information Center, Sociological Abstracts and Cochrane Libraries.
English-language, primary, qualitative studies that investigated children's or caregivers' perceptions of reporting child maltreatment were included. All healthcare and social service settings implicated by mandatory reporting laws were included.
Critical appraisal of included studies involved a modified checklist from the Critical Appraisal Skills Programme (CASP). Two independent reviewers extracted data, including direct quotations from children and caregivers (first-order constructs) and interpretations by study authors (second-order constructs). Third-order constructs (the findings of this meta-synthesis) involved synthesising second-order constructs that addressed strategies to improve the mandatory reporting processes for children or caregivers-especially when these themes addressed concerns raised by children or caregivers in relation to the reporting process.
Over 7935 citations were retrieved and 35 articles were included in this meta-synthesis. The studies represent the views of 821 caregivers, 50 adults with histories of child maltreatment and 28 children. Findings suggest that children and caregivers fear being reported, as well as the responses to reports. Children and caregivers identified a need for improvement in communication from healthcare providers about mandatory reporting, offering preliminary insight into child-driven and caregiver-driven strategies to mitigate potential harms associated with reporting processes.
Research on strategies to mitigate potential harms linked to mandatory reporting is urgently needed, as is research that explores children's experiences with this process.
系统综合定性研究,探索儿童和照顾者对强制报告的看法。
我们对定性研究进行了元综合。
在 Medline、Embase、PsycINFO、护理与联合健康文献累积索引、刑事司法摘要、教育资源信息中心、社会学摘要和 Cochrane 图书馆中进行了搜索。
包括调查儿童或照顾者对报告虐待儿童看法的英文、原始、定性研究。所有涉及强制报告法律的医疗保健和社会服务场所均包括在内。
对纳入研究的严格评估涉及来自关键评估技能计划(CASP)的修改检查表。两名独立审查员提取数据,包括儿童和照顾者的直接引语(一阶结构)和研究作者的解释(二阶结构)。第三级结构(本次元综合的结果)涉及综合解决改善儿童或照顾者强制报告流程的二级结构,特别是当这些主题涉及儿童或照顾者对报告过程提出的关切时。
检索到超过 7935 条引用,35 篇文章纳入本次元综合。这些研究代表了 821 名照顾者、50 名有虐待儿童史的成年人和 28 名儿童的观点。研究结果表明,儿童和照顾者担心被举报,以及对举报的反应。儿童和照顾者认为需要改善医疗保健提供者关于强制报告的沟通,初步了解儿童驱动和照顾者驱动的策略,以减轻与报告过程相关的潜在危害。
迫切需要研究减轻与强制报告相关的潜在危害的策略,也需要研究儿童对这一过程的体验。