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      Perinatal interventions to prevent Adverse Childhood Experiences (ACEs): A scoping review

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          Abstract

          Background

          Preventing Adverse Childhood Experiences (ACEs) is a public health priority, and the perinatal period is a sensitive life stage when preventive interventions could be particularly effective. Protecting and buffering pregnant persons and infants from exposure to adversity can optimize children’s development and health trajectories, reduce future morbidity and mortality, and even break intergenerational cycles of adversity, but no study has synthesized experimental evidence on effectiveness of interventions to address ACEs in the perinatal period.

          Objectives

          To (1) identify perinatal ACE prevention interventions, tested in high quality randomized control trials, with a dyadic perspective examining outcomes for mother and child; (2) describe their (a) place on the public health prevention continuum and (b) incorporation of life course characteristics that aim to optimize life health trajectories; and (3) determine which interventions show evidence of effectiveness.

          Methods

          We undertook a scoping review, using a modified PRISMA-Sc approach, of articles published in English between January 2000 and November 2023 identified through Psych info and PubMed using search terms for a broad range of adversities, with additional capture of articles from relevant reference lists. Interventions were included if they targeted an identified ACEs exposure or risk; were tested in randomized controlled trials (RCTs); reported outcome measures for both mother and child and were initiated during pregnancy. Interventions were further analyzed using the public health prevention continuum and Life Course Intervention Research (LCIR) characteristics frameworks. A two-tailed t test was used to ascertain the association between LCIR characteristics, and the outcomes achieved.

          Results

          Of 2148 articles identified, 57 were in scope for detailed analysis, yielding 53 unique interventions. Overall, 42 (74%) reported some positive impact; 37 (65%) for mothers; 37 (65%) for the child, and 32 (56%) for both. Interventions with the strongest evidence based on study quality and reported outcomes were co-parenting programs designed to improve the quality and function of the co-parenting relationship, home visiting interventions, and integrative health interventions incorporating baby massage and/or yoga. Half of effective interventions were secondary prevention focused. The mean number of life course characteristics was significantly higher in the studies that reported a positive impact on the mother and/or child (p = 0.003).

          Conclusions

          Few studies specifically addressed ACEs as a defined set of adversities, yet a range of perinatal interventions showed positive impacts on individual ACE risks or exposures. Intentional incorporation of life course characteristics and bundling of evidence-based components into comprehensive perinatal interventions hold promise for future ACEs prevention.

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          Most cited references56

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          PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation

          Scoping reviews, a type of knowledge synthesis, follow a systematic approach to map evidence on a topic and identify main concepts, theories, sources, and knowledge gaps. Although more scoping reviews are being done, their methodological and reporting quality need improvement. This document presents the PRISMA-ScR (Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews) checklist and explanation. The checklist was developed by a 24-member expert panel and 2 research leads following published guidance from the EQUATOR (Enhancing the QUAlity and Transparency Of health Research) Network. The final checklist contains 20 essential reporting items and 2 optional items. The authors provide a rationale and an example of good reporting for each item. The intent of the PRISMA-ScR is to help readers (including researchers, publishers, commissioners, policymakers, health care providers, guideline developers, and patients or consumers) develop a greater understanding of relevant terminology, core concepts, and key items to report for scoping reviews.
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            The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials

            Flaws in the design, conduct, analysis, and reporting of randomised trials can cause the effect of an intervention to be underestimated or overestimated. The Cochrane Collaboration’s tool for assessing risk of bias aims to make the process clearer and more accurate
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              Relationship of Childhood Abuse and Household Dysfunction to Many of the Leading Causes of Death in Adults

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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: VisualizationRole: Writing – original draft
                Role: Formal analysisRole: InvestigationRole: ResourcesRole: SoftwareRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: MethodologyRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS One
                plos
                PLOS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                24 October 2024
                2024
                : 19
                : 10
                : e0307441
                Affiliations
                [1 ] Center for Healthier Children, Families and Communities, University of California, Los Angeles (UCLA), Los Angeles, CA, United States of America
                [2 ] Department of Pediatrics, Geffen School of Medicine, UCLA, Los Angeles, CA, United States of America
                [3 ] Senior Harkness Fellow, The Commonwealth Fund, New York, NY, United States of America
                [4 ] Department of General Internal Medicine, University of California, Los Angeles, Los Angeles, CA, United States of America
                Caribbean Center for Child Neurodevelopment, GRENADA
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                https://orcid.org/0009-0003-0768-8434
                https://orcid.org/0000-0002-6496-7558
                https://orcid.org/0000-0002-6676-9889
                https://orcid.org/0000-0002-3182-1384
                Article
                PONE-D-24-14933
                10.1371/journal.pone.0307441
                11501017
                39446908
                241f4cc9-6f4f-4771-9524-8c43425c297a
                © 2024 Kinsey et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 19 April 2024
                : 4 July 2024
                Page count
                Figures: 2, Tables: 9, Pages: 22
                Funding
                Funded by: Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services
                Award ID: UA6MC32492
                Funded by: Life Course Intervention Research Network
                Award ID: U9DMC49250
                Funded by: Life Course Translational Research Network
                Funded by: National Clinician’s Scholar Program and Cedars Sinai Medical Center
                Funded by: funder-id http://dx.doi.org/10.13039/100009633, Eunice Kennedy Shriver National Institute of Child Health and Human Development;
                Award ID: K23HD099308
                Award Recipient :
                Funded by: Life Course Intervention Research Network
                Award ID: UA6MC32492
                Award Recipient :
                Funded by: Life Course Translational Research Network
                Award ID: U9DMC49250
                This project is/was supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) under award UA6MC32492, the Life Course Intervention Research Network; and award U9DMC49250, The Life Course Translational Research Network. The information, content and/or conclusions are those of the authors and should not be construed as the official position or policy of, nor should any endorsements be inferred by HRSA, HHS or the U.S. Government. JK was supported by The Commonwealth Fund, Harkness Fellowship as the Aotearoa | New Zealand Harkness Fellow. JLC received funding for her fellowship position from the National Clinician’s Scholar Program and Cedars Sinai Medical Center. AS was funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (K23HD099308). SR was supported UA6MC32492, the Life Course Intervention Research Network (UA6MC32492); and The Life Course Translational Research Network (U9DMC49250). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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