Literature DB >> 17545930

Parental involvement in treatment decisions regarding their critically ill child: a comparative study of France and Quebec.

Franco A Carnevale1, Pierre Canoui, Robin Cremer, Catherine Farrell, Amélie Doussau, Marie-Josée Seguin, Philippe Hubert, Francis Leclerc, Jacques Lacroix.   

Abstract

OBJECTIVE: To examine whether physicians or parents assume responsibility for treatment decisions for critically ill children and how this relates to subsequent parental experience. A significant controversy has emerged regarding the role of parents, relative to physicians, in relation to treatment decisions for critically ill children. Anglo-American settings have adopted decision-making models where parents are regarded as responsible for such life-support decisions, while in France physicians are commonly considered the decision makers.
DESIGN: Grounded theory qualitative methodology.
SETTING: Four pediatric intensive care units (two in France and two in Quebec, Canada). PATIENTS: Thirty-one parents of critically ill children; nine physicians and 13 nurses who cared for their children.
INTERVENTIONS: None.
MEASUREMENTS AND MAIN RESULTS: Semistructured interviews were conducted. In France, physicians were predominantly the decision makers for treatment decisions. In Quebec, decisional authority practices were more varied; parents were the most common decision maker, but sometimes it was physicians, while for some decisional responsibility depended on the type of decision to be made. French parents appeared more satisfied with their communication and relationship experiences than Quebec parents. French parents referred primarily to the importance of the quality of communication rather than decisional authority. There was no relationship between parents' actual responsibility for decisions and their subsequent guilt experience.
CONCLUSIONS: It was remarkable that a certain degree of medical paternalism was unavoidable, regardless of the legal and ethical norms that were in place. This may not necessarily harm parents' moral experiences. Further research is required to examine parental decisional experience in other pediatric settings.

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Year:  2007        PMID: 17545930     DOI: 10.1097/01.PCC.0000269399.47060.6D

Source DB:  PubMed          Journal:  Pediatr Crit Care Med        ISSN: 1529-7535            Impact factor:   3.624


  18 in total

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2.  Ethically complex decisions in the neonatal intensive care unit: impact of the new French legislation on attitudes and practices of physicians and nurses.

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5.  Parental Moral Distress and Moral Schism in the Neonatal ICU.

Authors:  Gabriella Foe; Jonathan Hellmann; Rebecca A Greenberg
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6.  The acceptability among lay persons and health professionals of actively ending the lives of damaged newborns.

Authors:  Nathalie Teisseyre; Charles Vanraet; Paul C Sorum; Etienne Mullet
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7.  Elements of Family-Centered Care in the Pediatric Intensive Care Unit: An Integrative Review.

Authors:  Claire A Richards; Helene Starks; M Rebecca O'Connor; Ardith Z Doorenbos
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8.  Forgoing life support: how the decision is made in European pediatric intensive care units.

Authors:  Denis J Devictor; Jos M Latour
Journal:  Intensive Care Med       Date:  2011-10-01       Impact factor: 17.440

9.  End-of-life care decisions in the PICU: roles professionals play.

Authors:  Kelly Nicole Michelson; Rachna Patel; Natalie Haber-Barker; Linda Emanuel; Joel Frader
Journal:  Pediatr Crit Care Med       Date:  2013-01       Impact factor: 3.624

10.  Parental views on withdrawing life-sustaining therapies in critically ill children.

Authors:  Kelly Nicole Michelson; Tracy Koogler; Christine Sullivan; María del Pilar Ortega; Emily Hall; Joel Frader
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