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父母在新生儿病房接受心理治疗支持的经历:一项混合方法的系统评价,为多元文化人群的干预发展提供信息。

Parents' experiences of psychotherapeutic support on the neonatal unit: A mixed methods systematic review to inform intervention development for a multicultural population.

作者信息

Jane Kirsty, Wood Dean, Gallagher Katie, Livermore Polly, Shoemark Helen, Robert Glenn

机构信息

Methodologies Division, Florence Nightingale Faculty of Nursing, Midwifery & Palliative Care, King's College London, Strand, UK.

Hoslistic Family Services, Noah's Ark Children's Hospice, Barnet, UK.

出版信息

Nurs Crit Care. 2025 May;30(3):e13194. doi: 10.1111/nicc.13194. Epub 2024 Oct 28.

Abstract

BACKGROUND

Parents of infants admitted to neonatal intensive care require support to minimize the impact on their mental health and to encourage engagement with their infants to support infant neurodevelopment. Many interventions aim to address this need, but there is a lack of research considering the accessibility of these for a multicultural population.

AIM

To systematically identify sources of psychotherapeutic support available for parents with infants admitted to neonatal care (NNU, neonatal intensive care unit [NICU] and special care units), assess their accessibility and acceptability and identify challenges and facilitators.

STUDY DESIGN

Six electronic databases with no restrictions on language or date were used to identify relevant studies following Preferred Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines. Publications were included in the review if they reviewed parent experience of an intervention actively in place to support parent experience during the neonatal unit stay. Any studies where the intervention's primary aim was infant focused, such as developmental care, were excluded. All publications were quality-assessed using quality appraisal tools appropriate for their design type. Data were extracted line by line using Sekhon et al.'s theoretical acceptability framework and questionnaire.

RESULTS

A total of 3309 studies were found, of which 36 studies met the inclusion criteria. Included studies were published worldwide between 2000 and 2023 and explored 15 different interventions. Challenges for parental engagement were due to preconceived ideas about intervention requirements and parents' ability to participate in them. Timely information and providers' experience in delivering the intervention were reported to support engagement and as being valuable for enhancing participant knowledge. The emotional content of interventions was found to be challenging by parents across most studies. This was prominent in interventions designed to be carried out in a group format and where keepsakes were created. However, the value of these interventions was in reducing parents' feelings of isolation through increased social support and providing a starting point for conversations with wider family and friends about the family's neonatal experience. Participant demographics were poorly reported, with only two studies taking into consideration the ethicality of the intervention.

CONCLUSION

Poor reporting of participant demographics, and a focus on mothers as participants, means findings are not transferrable to the wider population of parents in neonatal units. Future studies should consider how to ensure that research and interventions are accessible to multicultural populations to improve the understanding of the acceptability of interventions. Better knowledge of neonates and the NNU setting amongst intervention providers could increase the accessibility of psychotherapeutic support for parents. Training for providers on how to manage sensitive conversations may also be beneficial to support parents during interventions.

RELEVANCE TO CLINICAL PRACTICE

The impact of neonatal admission on parental mental health is increasingly recognized and reported. Interventions have been developed to reduce the negative impact on the mental health of parents. There continue to be significant health inequalities as a result of many services not taking into account the acceptability and accessibility of interventions in this setting for their multicultural populations. This review highlights the need for better reporting of participant demographics in research and the inclusion of those seldom heard to ensure interventions are culturally, religiously and linguistically appropriate for multicultural populations.

摘要

背景

入住新生儿重症监护病房的婴儿的父母需要得到支持,以尽量减少对其心理健康的影响,并鼓励他们与婴儿互动,以支持婴儿的神经发育。许多干预措施旨在满足这一需求,但缺乏针对多元文化人群对这些干预措施可及性的研究。

目的

系统识别可为入住新生儿护理病房(新生儿重症监护病房 [NICU] 和特殊护理病房)的婴儿的父母提供的心理治疗支持来源,评估其可及性和可接受性,并识别挑战和促进因素。

研究设计

按照系统评价与Meta分析的首选报告项目(PRISMA)指南,使用六个对语言和日期无限制的电子数据库来识别相关研究。如果出版物对正在实施的旨在支持父母在新生儿病房住院期间体验的干预措施的父母体验进行了回顾,则纳入该综述。任何主要目标是关注婴儿的研究,如发育护理,均被排除。所有出版物均使用适合其设计类型的质量评估工具进行质量评估。使用塞鸿等人的理论可接受性框架和问卷逐行提取数据。

结果

共检索到3309项研究,其中36项研究符合纳入标准。纳入的研究于2000年至2023年在全球范围内发表,探讨了15种不同的干预措施。父母参与的挑战源于对干预要求的先入为主的观念以及父母参与其中的能力。据报告,及时的信息和提供者实施干预的经验有助于促进参与,并且对于增强参与者的知识很有价值。在大多数研究中,父母发现干预措施的情感内容具有挑战性。这在以小组形式开展的干预措施以及制作纪念品的干预措施中尤为突出。然而,这些干预措施的价值在于通过增加社会支持减少父母的孤立感,并为与更广泛的家人和朋友谈论家庭的新生儿经历提供一个切入点。参与者的人口统计学数据报告不佳,只有两项研究考虑了干预措施的伦理问题。

结论

参与者人口统计学数据报告不佳,且以母亲作为参与者为重点,这意味着研究结果无法推广到新生儿病房中更广泛的父母群体。未来的研究应考虑如何确保多元文化人群能够获得研究和干预措施,以增进对干预措施可接受性的理解。干预提供者对新生儿和新生儿重症监护病房环境有更好的了解,可能会增加为父母提供心理治疗支持的可及性。对提供者进行如何处理敏感对话的培训,也可能有助于在干预期间支持父母。

与临床实践的相关性

新生儿住院对父母心理健康的影响越来越受到认可和报道。已经开发了一些干预措施来减少对父母心理健康的负面影响。由于许多服务没有考虑到在这种情况下针对多元文化人群的干预措施的可接受性和可及性,健康不平等现象仍然严重。本综述强调了在研究中更好地报告参与者人口统计学数据的必要性,以及纳入那些很少被听到声音的人群,以确保干预措施在文化、宗教和语言上适合多元文化人群。

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