TY - JOUR
T1 - Shared decision making and the pathways approach in the prenatal and postnatal management of the trisomy 13 and trisomy 18 syndromes
AU - Andrews, Sasha E.
AU - Downey, Ann G.
AU - Showalter, David Scott
AU - Fitzgerald, Heather
AU - Showalter, Vivian P.
AU - Carey, John C.
AU - Hulac, Peter
N1 - Funding Information:
The authors appreciate the support from the Support Organization for Trisomy 18, 13 and Related Disorders, the Trisomy 18 Foundation, and the American Journal of Medical Genetics. In addition, administrative support was provided by the University of Colorado, Division of Neonatology, the University of Colorado Center for Bioethics and Humanities, and Feliz Martinez of the Department of Pediatrics, University of Utah. The authors acknowledge the input from the entire working group.
Publisher Copyright:
© 2016 Wiley Periodicals, Inc.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - The medical management of infants with the trisomy 13 and trisomy 18 syndromes is challenging and controversial. Both conditions have high neonatal and infant mortality, and surviving children display significant cognitive and motor disabilities. Currently, there exists a tension in the neonatal and perinatal communities regarding care. One view holds that management should consist solely of comfort care, while another opinion recommends offering medical and surgical intervention in appropriate situations. The purpose of this manuscript is to present a model for the care of fetuses and infants with trisomy 13 and 18 during the prenatal, perinatal, and postnatal periods. Adopting the pathways approach as a framework, we have identified several pertinent decision points, characterizing the goals of care and the resources needed for the decision points at various times. Additionally, we identified themes surrounding parental and professional experiences. The authors propose a care model for trisomy 13 and 18 that uses shared decision making as its foundational principle and the pathways approach as the method. Our model requires further investigation as a strategy for care in order to render it useful in other complex medical situations.
AB - The medical management of infants with the trisomy 13 and trisomy 18 syndromes is challenging and controversial. Both conditions have high neonatal and infant mortality, and surviving children display significant cognitive and motor disabilities. Currently, there exists a tension in the neonatal and perinatal communities regarding care. One view holds that management should consist solely of comfort care, while another opinion recommends offering medical and surgical intervention in appropriate situations. The purpose of this manuscript is to present a model for the care of fetuses and infants with trisomy 13 and 18 during the prenatal, perinatal, and postnatal periods. Adopting the pathways approach as a framework, we have identified several pertinent decision points, characterizing the goals of care and the resources needed for the decision points at various times. Additionally, we identified themes surrounding parental and professional experiences. The authors propose a care model for trisomy 13 and 18 that uses shared decision making as its foundational principle and the pathways approach as the method. Our model requires further investigation as a strategy for care in order to render it useful in other complex medical situations.
KW - pathways
KW - shared decision making
KW - trisomy 13
KW - trisomy 18
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U2 - 10.1002/ajmg.c.31524
DO - 10.1002/ajmg.c.31524
M3 - Comment/debate
C2 - 27557275
AN - SCOPUS:84988411261
SN - 1552-4868
VL - 172
SP - 257
EP - 263
JO - American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
JF - American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
IS - 3
ER -