Family Interviews Improve Health Service Recommendations in Mortality Review Process: A Mixed-Methods Assessment

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Catherine Kothari, Fernando Ospina, Nia Evans, Cynthia Bane, Joi Presberry Dixon, Vaishali Patil, Ruth Butters, Rosemary Fournier, Susanna C. Joy, Brenda O'Rourke, Josephine Woods, Debra Lenz, Aaron L. Davies
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引用次数: 0

Abstract

Background

Within the United States, although there is strong motivation for incorporating family interviews into Fetal Infant Mortality Reviews (FIMR) and important potential for expanding it to other types of reviews, there is limited evidence that family interviews make a difference in review team outcomes.

Objective

This study aims to assess the impact of FIMR family interviews identifying health service gaps and generating actionable improvements.

Design

Mixed methods design with quantitative case-control analysis and qualitative semi-structured interviews. Quantitative data collection was secondary analysis of FIMR administrative records, comparing outcomes with and without family interviews using Generalized Estimating Equation (GEE) and descriptive analysis of annual FIMR team evaluation responses. Qualitative data collection included audio-taping, transcribing and consensus coding of semi-structured interviews.

Setting and Participants

The quantitative setting was Kalamazoo County, Michigan, FIMR reviews from 2015 to 2023, whereas the qualitative setting was virtual. Quantitative sample was the full population of completed FIMR case reviews (N = 158), and the 15 FIMR team case reviewers completing the 2023 annual evaluation. The qualitative sample was a purposive sample of 28 FIMR administrators across the United States.

Main Outcome Measures

Quantitative outcomes were review-identified contributing stressors and subsequent recommendations generated in the case review process. Qualitative outcomes were thematic experiences of family interview implementation and impact within mortality review process.

Results

The 53 cases (34%) with family interviews were similar to the 105 (66%) non-interview cases regarding multipleperinatal characteristics and were different regarding death type and manner. Controlling for these differences, GEE analysis found that family interviews were associated with increased identification of stressors, especially medical and socioeconomic, with a 2.6 increase in the number of stressors identified (aOR = 2.6, 95% CI: 1.5–4.7, p < 0.001). Family interviews were associated with a 40% increase in recommendations generated (aOR = 1.4, 95% CI: 1.0–2.0, p = 0.05), especially regarding patient-provider communication. Two-thirds of the FIMR team reported that family interviews were ‘Very Impactful’ in making meaningful system changes. Qualitatively, three primary themes emerged: Hurdles to Getting Interviews, Completing the Picture and Bringing the Human Connection.

Conclusions

This study drew upon multiple types of data, documenting the challenges obtaining interviews, while emphasizing their value identifying root causes, producing actionable healthcare service recommendations and motivating action.

Patient or Public Contribution

Locally, members of community advocate organizations representing birthing and parenting individuals and those representing people identifying as Black race contributed by actively refining the implementation of FIMR family interviews, including how interview information was utilized in FIMR case review meetings (study interventions). Mock FIMR case review meetings conducted as part of United Way public ‘bus tours’ and with undergraduate/graduate university students further refined recommendations coding and dissemination strategies. Leadership from public and private health service organizations shared the facilitators and barriers for applying FIMR recommendations to institutional policy and practice (shaping the development of recommendations coding as well as dissemination and interpretation of study findings). Nationally, a network of mortality review funders and administrators, in a 4-year learning series convened by the National Center for Fatality Prevention and Review, provided input in centreing family interviews within different types of mortality review processes (influencing study objectives, qualitative interview structure and results interpretation). Additionally, US policy leaders in maternal child health and health equity provided historical and current context for FIMR family interview funding and enabling legislation (informing the interpretation of study results and specifically referenced within the manuscript).

Abstract Image

家庭访谈改善死亡率审查过程中的卫生服务建议:一种混合方法评估
背景在美国,虽然有强烈的动机将家庭访谈纳入胎儿死亡率评估(FIMR),并且有将其扩展到其他类型的评估的重要潜力,但很少有证据表明家庭访谈对评估小组的结果有影响。目的本研究旨在评估FIMR家庭访谈的影响,确定卫生服务差距并产生可操作的改进。设计采用定量病例对照分析和定性半结构化访谈的混合方法设计。定量数据收集是对FIMR管理记录的二次分析,使用广义估计方程(GEE)比较有和没有家庭访谈的结果,并对年度FIMR团队评估反应进行描述性分析。定性数据收集包括半结构化访谈的录音、转录和共识编码。定量环境为密歇根州卡拉马祖县,2015年至2023年的FIMR评估,而定性环境为虚拟环境。定量样本为完成FIMR病例综述的全人群(N = 158),以及完成2023年年度评价的15名FIMR团队病例综述者。定性样本是美国28名FIMR管理人员的有目的样本。主要结果测量定量结果是审查确定的贡献压力源和随后在病例审查过程中产生的建议。定性结果是家庭访谈实施的专题经验和死亡率审查过程中的影响。结果53例(34%)家庭访谈与105例(66%)非访谈多胎围产儿特征相似,死亡类型和死亡方式不同。在控制了这些差异后,GEE分析发现,家庭访谈与压力源识别的增加有关,特别是医疗和社会经济压力源的识别增加了2.6 (aOR = 2.6, 95% CI: 1.5-4.7, p < 0.001)。家庭访谈与推荐率增加40%相关(aOR = 1.4, 95% CI: 1.0-2.0, p = 0.05),尤其是在医患沟通方面。三分之二的FIMR团队报告说,家庭访谈在进行有意义的制度变革方面“非常有影响力”。从质量上讲,出现了三个主要主题:获得面试的障碍,完成图片和带来人际关系。本研究利用了多种类型的数据,记录了获得访谈的挑战,同时强调了访谈的价值,确定了根本原因,提出了可操作的医疗保健服务建议,并激励了行动。在当地,代表生育和养育个体的社区倡导组织成员以及代表黑人种族的组织成员通过积极改进FIMR家庭访谈的实施,包括如何在FIMR病例审查会议(研究干预)中利用访谈信息,做出了贡献。作为联合劝募会公共“巴士之旅”的一部分,与本科生/研究生一起进行了模拟FIMR案例审查会议,进一步完善了建议编码和传播策略。来自公共和私营卫生服务组织的领导分享了将FIMR建议应用于机构政策和实践的促进因素和障碍(影响建议编码的发展以及研究结果的传播和解释)。在全国范围内,死亡率审查资助者和管理人员网络在由国家死亡率预防和审查中心召集的为期4年的学习系列中,为在不同类型的死亡率审查过程中集中家庭访谈提供了投入(影响研究目标、定性访谈结构和结果解释)。此外,美国在妇幼保健和卫生公平方面的政策领导人为FIMR家庭访谈资助和授权立法提供了历史和当前背景(告知研究结果的解释,并在手稿中具体引用)。
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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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