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Making Sense of Bioethics: Column 163: The Welcome Outreach of Perinatal Hospice

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During the course of preg­nancy, receiving an adverse prenatal diagnosis can be a tremendously jolting experience for parents. In severe cases, physicians may tell them that their unborn child has a condition that is “incompatible with life.”

While some children with this diagnosis may still receive helpful treatments and manage to live or even thrive for years, in other cases, no realistic treatment options exist and they may live only a matter of minutes or hours following their birth, particularly when they are born with severely damaged or missing vital organs. Sometimes it can be preferable to refer to the situation as one in which the un­born child is “affected by a lethal condition.”

Prior to the development of prenatal screening technologies and genetic testing, doctors who deliv­ered stillborn or terminally ill babies would often shuttle them away from their mothers to die, leaving the parents and family without a sense of closure or resolution. These losses were basically viewed and treated as “non-events” and the emotions and grief experienced by the family received little attention or notice. In recent years, there has fortunately been a growing aware­ness of the grief associated with all forms of perinatal loss, whether from miscarriage, stillbirth, new­born death, or direct abortion.

The prenatal diagnosis of a lethal anomaly creates a chal­lenging and unusual situation for many families when they are in­formed of their baby’s terminal condition weeks, or even months before their child’s death. What was once a surprise miscarriage or a surprise loss after birth becomes an anticipated and foreseen event.

In the wake of the diagnosis, medical professionals will some­times recommend and pressure parents to abort their unborn child. This unsatisfactory choice often relegates them to never reaching meaningful closure with respect to the difficult pregnancy they have traversed. It also tempts them to act contrary to every protective parental instinct they have, and deny the reality of their newest family member, as if he or she can simply disappear through the termination. 

Many hospitals and obstet­rics programs, however, are now offering an improved alternative known as “perinatal hospice.” This approach seeks to set up a particular supportive environ­ment within the hospital or an­other setting in which all the members of the family can re­ceive the child following delivery, hold and name the newborn, and fully acknowledge his or her brief but meaningful life. 

Perinatal hospice support staff will typically inquire as to what the parents and family would like to see happen, and try to tailor the experi­ence accordingly. Families can invite a religious leader into the room. They can make arrangements for baptism. They can take a mold of their infant’s footprints in clay. They can take photos of the child in the arms of other family members. If their baby will be born with a significant physi­cal defect, like a tiny skull from micro­cephaly, the staff can arrange for a small winter’s cap to cover the child’s head if the family prefers. They can sing lullabies and pray to­gether. Peri­natal hospice staff remain nearby and available to provide emo­tional sup­port or pain medication for a baby who appears uncomfortable, even as the child may shortly yield the breath of life and pass on.

In some cases, infants will have conditions that are not immediately fatal and they may be able to go home to be with family for a few days or weeks before passing on. Hospice care continues during this time, with ongoing input and support from the neonatal team.

Drs. Hoeldtke and Calhoun, two pioneers in the field of perinatal hos­pice, sum up this supportive and con­soling form of care this way: 

Perinatal hospice differs in em­phasis, though not necessarily in kind, from other modes of peri­natal health care. It focuses on the persons involved, rather than on the fetal pathology, and places the family in the central arena of care. It provides a con­tinuum of support for the family from the time of diagnosis until death and beyond. It is marked by a cognizance that “dying in­volves real people, even unborn fetuses; [and that] significant re­lationships are disrupted and familiar bonds are severed.” Hospice allows time — time for bonding, loving, and losing; time so that the entire course of liv­ing and dying is a gradual proc­ess that is not jarringly inter­rupted… We believe that a structured and compassionate approach, such as that embod­ied in perinatal hospice, can be woven into the mainstream of pregnancy care to best facilitate the challenging, yet rewarding, task of helping these families cope with the death of their youngest member, in comfort and with dignity.

Perinatal hospice offers an in­valuable model of medical and inter­personal outreach, one that hopefully will continue to expand in the context of modern neonatal care.

Copyright © 2020, The National Catholic Bioethics Center, Philadelphia, PA. All rights reserved. 

 


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