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G. Moutel [9]Grégoire Moutel [2]
  1.  25
    Reporting of Ethical Requirements in Phase III Surgical Trials.Valérie Bridoux, Lilian Schwarz, Grégoire Moutel, Francis Michot, Christian Herve & Jean-Jacques Tuech - 2014 - Journal of Medical Ethics 40 (10):687-690.
    Background Disclosure of obtaining informed consent from patients (ICP) and research ethics committee (REC) approval in published reports is sometimes omitted. To date, no disclosure data are available on surgical research. Objective Our aim was to assess whether REC approval and ICP were documented in surgical trials. Study design Overall, 657 randomised trials, published between 2005 and 2010 in 10 international journals, were included. We collected the report rate of REC approval and ICP and contacted the corresponding author when ethical (...)
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  2.  8
    What Ethics for Case Managers? Literature Review and Discussion.A. Corvol, G. Moutel & D. Somme - 2016 - Nursing Ethics 23 (7):729-742.
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  3.  38
    Advance Directives and the Family: French and American Perspectives.D. Rodríguez-Arias, G. Moutel, M. P. Aulisio, A. Salfati, J. C. Coffin, J. L. Rodríguez-Arias, L. Calvo & C. Hervé - 2007 - Clinical Ethics 2 (3):139-145.
    Several studies have explored differences between North American and European doctor patient relationships. They have focused primarily on differences in philosophical traditions and historic and socioeconomic factors between these two regions that might lead to differences in behaviour, as well as divergent concepts in and justifications of medical practice. However, few empirical intercultural studies have been carried out to identify in practice these cultural differences. This lack of standard comparative empirical studies led us to compare differences between France and the (...)
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  4.  1
    Ethical Issues in the Introduction of Case Management for Elderly People.A. Corvol, G. Moutel, D. Gagnon, M. Nugue, O. Saint-Jean & D. Somme - 2013 - Nursing Ethics 20 (1):0969733012452685.
    As case management is under development in France for elderly people, this study sets out to identify and analyse key situations responsible for ethical dilemmas for French case managers. We based our study on the analyses of individual interviews made with case managers and focus-group discussions, bringing together all case managers working in local organisations running for at least a year. We identified three situations giving rise to ethical dilemmas: in the order of importance, the refusals of care, the practicalities (...)
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  5.  6
    Les informations génétiques, droits des patients et confidentialité depuis la loi du 4 mars 2002.A. M. Duguet, C. Fecteau, J. Biga, G. Moutel & C. Hervé - 2004 - Médecine et Droit 2004 (65):35-41.
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  6.  25
    Ethical Issues Related to Computerised Family Medical Histories in Sickle Cell Disease: Inforare.S. Franrenet, N. Duchange, F. Galacteros, C. Quantin, O. Cohen, R. Nzouakou, S. Sudraud, C. Herve & G. Moutel - 2010 - Journal of Medical Ethics 36 (10):604-607.
    The Inforare project aims to set up a system for the sharing of clinical and familial data, in order to study how genes are related to the severity of sickle cell disease. While the computerisation of clinical records represents a valuable research goal, an ethical framework is necessary to guarantee patients' protection and their rights in this developing field. Issues relating to patient information during the Inforare study were analysed by the steering committee. Several major concerns were discussed by the (...)
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  7.  26
    Ethical Issues Arising From the Requirement to Sign a Consent Form in Palliative Care.I. Plu, I. Purssell-Francois, G. Moutel, F. Ellien & C. Herve - 2008 - Journal of Medical Ethics 34 (4):279-280.
    French healthcare networks aim to help healthcare workers to take care of patients by improving cooperation, coordination and the continuity of care. When applied to palliative care in the home, they facilitate overall care including medical, social and psychological aspects. French legislation in 2002 required that an information document explaining the functioning of the network should be given to patients when they enter a healthcare network. The law requires that this document be signed. Ethical issues arise from this legislation with (...)
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  8.  8
    Autoconservation de Sperme Et Prise En Charge des Demandes d'Insémination Post Mortem.G. Moutel, K. Corviole, C. Ballouard, M. Alcaraz, M. DesurMont, M. Alnot & C. Herve - 1996 - Médecine et Droit 1996 (19):1-4.
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  9.  9
    Women’s Participation in Breast Cancer Screening in France – an Ethical Approach.Grégoire Moutel, Nathalie Duchange, Sylviane Darquy, Sandrine de Montgolfier, Frédérique Papin-Lefebvre, Odile Jullian, Jérôme Viguier, Hélène Sancho-Garnier & $authorfirstName $authorlastName - 2014 - BMC Medical Ethics 15 (1):64.
    Breast cancer is a major public health challenge. Organized mammography screening (OS) is considered one way to reduce breast cancer mortality. EU recommendations prone mass deployment of OS, and back in 2004, France introduced a national OS programme for women aged 50–74 years. However, in 2012, participation rate was still just 52.7%, well short of the targeted 70% objective. In an effort to re-address the (in) efficiency of the programme, the French National Cancer Institute has drafted an expert-group review of (...)
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  10.  25
    Are the GFRUP's Recommendations for Withholding or Withdrawing Treatments in Critically Ill Children Applicable? Results of a Two-Year Survey.R. Cremer, A. Binoche, O. Noizet, C. Fourier, S. Leteurtre, G. Moutel & F. Leclerc - 2007 - Journal of Medical Ethics 33 (3):128-133.
    Objective: To evaluate feasibility of the guidelines of the Groupe Francophone de Réanimation et Urgence Pédiatriques for limitation of treatments in the paediatric intensive care unit .Design: A 2-year prospective survey.Setting: A 12-bed PICU at the Hôpital Jeanne de Flandre, Lille, France.Patients: Were included when limitation of treatments was expected.Results: Of 967 children admitted, 55 were included with a 2-day median delay. They were younger than others , had a higher paediatric risk of mortality score , and a higher paediatric (...)
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  11.  22
    Post Mortem Scientific Sampling and the Search for Causes of Death in Intensive Care: What Information Should Be Given and What Consent Should Be Obtained?J. P. Rigaud, J. P. Quenot, M. Borel, I. Plu, C. Herve & G. Moutel - 2011 - Journal of Medical Ethics 37 (3):132-136.
    Purpose The search for cause of death is important to improve knowledge and provide answers for the relatives of the deceased. Medical autopsy following unexplained death in hospital is one way to identify cause of death but is difficult to carry out routinely. Post mortem sampling (PMS) of tissues via thin biopsy needle or ‘mini incisions’ in the skin may be a useful alternative. A study was undertaken to assess how this approach is perceived by intensive care doctors and also (...)
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