Abstract

BackgroundThe “Patients’ Rights and End of Life Care” Act came into force in France in 2005. It allows withholding/withdrawal of life-support treatment, and intensified use of medications that may hasten death through a double effect, as long as hastening death is not the purpose of the decision. It also specifies the requirements of the decision-making process. This study assesses the situation by examining the frequency of end-of-life decisions by patients’ and physicians’ characteristics, and describes the decision-making processes.MethodsWe conducted a nationwide retrospective study of a random sample of adult patients who died in December 2009. Questionnaires were mailed to the physicians who certified/attended these deaths. Cases were weighted to adjust for response rate bias. Bivariate analyses and logistic regressions were performed for each decision.ResultsOf all deaths, 16.9% were sudden deaths with no information about end of life, 12.2% followed a decision to do everything possible to prolong life, and 47.7% followed at least one medical decision that may certainly or probably hasten death: withholding (14.6%) or withdrawal (4.2%) of treatments, intensified use of opioids and/or benzodiazepines (28.1%), use of medications to deliberately hasten death (i.e. not legally authorized) (0.8%), at the patient’s request (0.2%) or not (0.6%). All other variables held constant, cause of death, patient's age, doctor’s age and specialty, and place of death, influenced the frequencies of decisions. When a decision was made, 20% of the persons concerned were considered to be competent. The decision was discussed with the patient if competent in 40% (everything done) to 86% (intensification of alleviation of symptoms) of cases. Legal requirements regarding decision-making for incompetent patients were frequently not complied with.ConclusionsThis study shows that end-of-life medical decisions are common in France. Most are in compliance with the 2005 law (similar to some other European countries). Nonetheless, the study revealed cases where not all legal obligations were met or where the decision was totally illegal. There is still a lot to be done through medical education and population awareness-raising to ensure that the decision-making process is compatible with current legislation, the physician's duty of care and the patient’s rights.

Highlights

  • The “Patients’ Rights and End of Life Care” Act came into force in France in 2005

  • This paper focuses on the medical decisions relating to end-of-life care in France

  • End-of-life medical decisions We had to exclude 168 cases owing to missing data

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Summary

Methods

Retrospective survey of physicians As in previous European surveys [10], we conducted a retrospective survey on a sample of deaths where the respondents were the certifying physicians. We conducted a telephone survey on a sample of 620 non-responding physicians to ensure that the results were representative. We recorded their socio-demographic profiles and their reasons for non-response. Questions and variables The questionnaire was based on the Eureld survey questionnaire [10] but was adapted to take account of the French legal context and of the results of preliminary tests. Logistic regressions were performed for each medical decision with more than 150 observed cases, taking into account both patients' and physicians' characteristics. Ethics This survey was approved by the Comité Consultatif sur le Traitement de l’Information en Matière de Recherche dans le Domaine de la Santé (CCTIRS) in January 2010 and authorized by the Commission Nationale de l’Informatique et des Libertés data protection committee (CNIL, - authorization No 1410166 at sitting 2010–107 of 15 April 2010)

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13. Observatoire national de la fin de vie
15. Bilsen J
21. Kompanje EJO
29. Seale C
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