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dc.creatorBuiting, Hilde Men
dc.creatorKarelse, Maartje A Cen
dc.creatorBrouwers, Hens A Aen
dc.creatorOnwuteaka-Philipsen, Bregje Den
dc.creatorvan der Heide, Agnesen
dc.creatorvan Delden, Johannes J Men
dc.date.accessioned2016-01-09T00:41:45Zen
dc.date.available2016-01-09T00:41:45Zen
dc.date.created2010-04en
dc.date.issued2010-04en
dc.identifierdoi:10.1136/jme.2009.034397en
dc.identifier.bibliographicCitationJournal of medical ethics 2010 Apr; 36(4): 234-7en
dc.identifier.urihttp://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=Dutch+experience+of+monitoring+active+ending+of+life+for+newborns.&title=Journal+of+medical+ethics+&volume=36&issue=4&date=2010-04&au=Buiting,+Hilde+M;+Karelse,+Maartje+A+C;+Brouwers,+Hens+A+A;+Onwuteaka-Philipsen,+Bregje+D;+van+der+Heide,+Agnes;+van+Delden,+Johannes+J+Men
dc.identifier.urihttp://dx.doi.org/10.1136/jme.2009.034397en
dc.identifier.urihttp://hdl.handle.net/10822/1023482en
dc.description.abstractINTRODUCTION: In 2007, a national review committee was instituted in The Netherlands to review cases of active ending of life for newborns. It was expected that 15-20 cases would be reported. To date, however, only one case has been reported to this committee. Reporting is essential to obtain societal control and transparency; the possible explanations for this lack of reporting were therefore explored. METHODS: Data on end-of-life decision-making were scrutinised from Dutch nation-wide studies (1995, 2001 and 2005), before institution of the committee. Physicians received a questionnaire about their medical decision-making for stratified samples of deceased infants up to 1 year, drawn from the central death registry. RESULTS: In 2005, 58% of all deaths were preceded by an end-of-life decision, compared with 68% in 2001 and 62% in 1995. The use of drugs with a possible life-shortening effect tended to be lower. In 2005, all four cases in the study in which an infants' life was actively ended were preceded by a decision to forego life-prolonging treatment. In three cases, the infant's life expectancy was short; one case involved a longer life expectancy. DISCUSSION: The expected number of cases is probably an overestimation due to changes in medical practice such as the tendency to attribute less life-shortening effects to opioids. The lack of reports is probably also associated with requirements in the regulation; it may be difficult to fulfil them due either to time constraints or the nature of the suffering that is addressed. If societal control of active ending of life is considered useful, changes in the regulation may be needed.en
dc.formatArticleen
dc.languageenen
dc.sourceeweb:331715en
dc.subjectDeathen
dc.subjectDrugsen
dc.subjectInfantsen
dc.subjectLifeen
dc.subjectMethodsen
dc.subjectNatureen
dc.subjectNewbornsen
dc.subjectPhysiciansen
dc.subjectRegulationen
dc.subjectReviewen
dc.subjectReportingen
dc.subjectSufferingen
dc.subject.classificationAllowing Minors to Dieen
dc.titleDutch Experience of Monitoring Active Ending of Life for Newbornsen
dc.provenanceCitation prepared by the Library and Information Services group of the Kennedy Institute of Ethics, Georgetown University for the ETHXWeb database.en
dc.provenanceCitation migrated from OpenText LiveLink Discovery Server database named EWEB hosted by the Bioethics Research Library to the DSpace collection EthxWeb hosted by DigitalGeorgetown.en


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