Impact of Parental Presence at the Ethics Meeting in Neonatal Intensive Care

Обзор

In neonatal intensive care, physicians are sometimes confronted with decisions to withhold or withdraw life-sustaining treatment for a critically ill newborn. In France, these decisions are made by the medical team through a formal collegial ("ethics") meeting. Parents are not legally required to take part in this meeting, and their participation remains very rare at the national level. Since 2018, the neonatal intensive care unit of Hopital NOVO (Nord Ouest Val d'Oise) (Pontoise site) has systematically offered parents the possibility of attending the collegial ethics meeting concerning their child when withholding or withdrawal of treatment is being considered. This study aims to evaluate the value of parental presence at the ethics meeting in helping parents understand the medical decisions made for their newborn. This is a retrospective, single-centre, non-interventional, qualitative study based on a questionnaire developed specifically for this purpose, in the absence of any validated tool. Parents of newborns for whom an ethics meeting was held between 1 January 2018 and 31 December 2025 are invited to share their experience. Two questionnaire versions are used, one for parents who attended the meeting and one for parents who did not, allowing comparison between the two situations. The questionnaire explores parents' understanding of the decision, the emotional impact of the meeting, their sense of guilt and their acceptance of the decision. Main hypothesis: parental participation in the ethics meeting promotes a better understanding of the medical decision, reduces feelings of guilt, and improves parents' long-term emotional experience.

Подробное описание

End-of-life decisions account for a substantial proportion of deaths in neonatal intensive care units, exceeding 70% in some cohorts in Europe and North America. These decisions are most often made following a multidisciplinary collegial decision-making process.

In France, the legal framework (Loi Leonetti 2005, reinforced by Loi Claeys-Leonetti 2016) is based on the principles of non-obstination déraisonnable and proportionality of care. This framework does not require the formal presence of parents during collegial meetings.

International literature on shared decision-making is associated with improved parental outcomes. A French multicenter study (Caeymaex et al., 2013) reported that parental involvement in end-of-life decisions was associated with lower rates of complicated grief, including reduced feelings of guilt and exclusion.

Despite this, formal parental participation in collegial meetings remains uncommon in France, in the context of prevailing models of care and concerns regarding parental emotional burden.

Since 2018, the neonatal intensive care unit at Hôpital NOVO has offered parents the option to attend collegial meetings. This process includes prior preparation by the attending physician, who clarifies that final medical responsibility remains with the healthcare team, as well as optional psychological support before and/or after the meeting.

This model has been previously described (Boize et al., Arch Pédiatr, 2024), but parental subjective and emotional experiences have not been systematically evaluated. The PaReNCo study aims to assess these outcomes.

Первичные конечные точки

• Parents' understanding of the medical decision made for their child following the ethics meeting. [Срок оценки: Questionnaire completion (15 minutes per parent)]

Вторичные конечные точки (5)

• Overall emotional experience of the ethics meeting [Срок оценки: Questionnaire completion (15 minutes per parent)]
• Parental attendance rate at the ethics meeting [Срок оценки: Retrospective assessment for ethics meetings organized between 01/01/2018 and 31/12/2025]
• Mortality rate of newborns for whom an ethics meeting was organized. [Срок оценки: Retrospective assessment for ethics meetings organized between 01/01/2018 and 31/12/2025]
• Parental feeling of guilt regarding the decision [Срок оценки: Questionnaire completion (15 minutes per parent)]
• Parental acceptance of the decision made by the medical team. [Срок оценки: Questionnaire completion (15 minutes per parent)]

Критерии участия

Критерии включения

• Adult parent (≥18 years)
• Parent of a newborn for whom an ethics meeting was organized within the neonatal intensive care unit of Hôpital NOVO - Pontoise site
• Ethics meeting organized between 01/01/2018 and 31/12/2025

Критерии исключения

• Refusal to participate in the study (refusal to complete the questionnaire and refusal to allow use of the child's medical record data)
• Parent with a major inability to understand the study (severe cognitive impairment)
• Parent not understanding French and therefore unable to complete the questionnaire

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Когортное

Центры проведения

Франция · 1 центр

• Hôpital NOVO — Cergy-Pontoise

Идентификаторы

NCT: NCT07681518 · CHRD0624 · 2026-A00780-51

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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