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16 - The role of quality of life assessments in neonatal care

from Section 2 - Ethical issues at the beginning of life: perinatology and neonatology

Published online by Cambridge University Press:  07 October 2011

Douglas S. Diekema
Affiliation:
Seattle Children's Research Institute
Mark R. Mercurio
Affiliation:
Yale University School of Medicine
Mary B. Adam
Affiliation:
Department of Pediatrics, University of Arizona School of Medicine, Tucson
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Summary

Case narrative

A female baby is delivered unexpectedly at 25 weeks’ gestation following acute placental abruption. She is in poor condition at delivery and requires active resuscitation with endotracheal intubation. Mechanical ventilation is provided over the first 4 days of life. Routine cranial ultrasonography on day 4 indicates a large unilateral intraventricular hemorrhage with evidence of parenchymal infarction.

The findings are communicated to the parents and they are warned that there is a high possibility that the child may develop some form of cerebral palsy. The parents are distressed and horrified by this information. It appears that they have had a lifelong fear of having a disabled child. They state that they are deeply concerned that their child will have a poor quality of life, leading to lifelong distress and suffering. They are also concerned about the likely effect of the child’s disability on the family, and on their marriage. The parents argue that it is morally wrong for aggressive medical interventions to be continued to ensure the survival of a child who will have such a poor quality of life, creating burdens for herself, her family, and to society.

Type
Chapter
Information
Clinical Ethics in Pediatrics
A Case-Based Textbook
, pp. 89 - 93
Publisher: Cambridge University Press
Print publication year: 2011

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References

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