Follow up care of bereaved parents after treatment withdrawal from newborns

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Abstract

Objective - To explore parents' experiences of bereavement care after withdrawal of newborn intensive care. Design - Face to face interviews with 108 parents of 62 babies born over two calendar years in the East of Scotland. Results - Only 22% were seen by six weeks after the death, 10% were not recalled before 6-11 months, and 8% were not seen at all in the first year. All except one couple saw the neonatologist who had cared for their baby. Only 33% remembered a neonatal nurse being present. Most (88%) were seen in the study hospital. Parents highlighted a number of specific needs. Appointments should be: (a) scheduled soon after the death of the baby and certainly within two months of the death irrespective of whether or not autopsy results are available; (b) with the named neonatologist; (c) in a setting away from the hospital if possible. Parents value: (a) efforts to find out how they are coping; (b) full frank information given sensitively to enable them to build up a cohesive picture of what happened and assess their future risks; (c) reassurance where possible, but half truths, false reassurances, and broken promises are unacceptable. Conclusions - Follow up care is a crucial part of the management of families from whose babies treatment has been withdrawn. Resources devoted to it should be re-examined to provide a service more in tune with parental need. In choosing the place, timing, and conduct of the meeting, staff should be sensitive to the expressed wishes of the parents themselves.

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APA

McHaffie, H. E., Laing, I. A., & Lloyd, D. J. (2001). Follow up care of bereaved parents after treatment withdrawal from newborns. Archives of Disease in Childhood: Fetal and Neonatal Edition, 84(2). https://doi.org/10.1136/fn.84.2.f125

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