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Landets første klinisk etisk komite for pædiatri

Behandling af børn kan rejse særlige klinisk-etiske spørgsmål
Forfatter(e)
Peter Uldall1, Mette Andersen2, Gorm Greisen2, Birte Hagelund Hansen3, Ester Holte Kofoed4, Jeanette Bresson Ladegaard Knox5, Henning Nabe-Nielsen6, Gitte Petersen1, Thomas Ploug7 & Astrid Sehested1 1) BørneUngeKlinikken, Rigshospitalet 2) Neonatalafdelingen, Rigshospitalet 3) Spastikerforeningen, Tåstrup 4) Institut for Kommunikation, Aalborg Universitet 5) Institut for Folke-sundhedsvidenskab, Københavns Universitet 6) Juliane Marie Centret, Rigshospitalet 7) Center for Anvendt Etik og Videnskabsteori, Aalborg Universitet Ugeskr Læger 2015;177:V10140579
Reference: 
Ugeskr Læger 2015;177:V10140579
Blad nummer: 
Sidetal: 
1993-1995
The first Danish paediatric ethical committee
We report the experiences from the first two years of a paedi­atric ethical committee at Rigshospitalet. The committee consists of five clinicians (nurses and doctors) and five non-clinicians. Themes of the sixteen reported case were: genetic testing, life-sustaining treatment (“when is enough enough?”), non-consen­sus between the parents and health personal and between different health personal, controversies to different religious wishes and to optimizing resources of the department versus individual care of a critically ill child. Within paediatrics a need for ethical reflection seems obvious.
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