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1.
Am J Hosp Palliat Care ; 32(4): 401-6, 2015 Jun.
Article in English | MEDLINE | ID: mdl-24526764

ABSTRACT

CONTEXT: In spite of the existence of clinical guidelines and a legal framework in France, the withdrawal of artificial nutrition (AN) in palliative care remains a difficult situation for caregivers who are confronted with this reality. OBJECTIVES: To describe the perception of caregivers on the withdrawal of AN and to compare this perception between caregivers who have already been confronted with this situation and those who have not. METHODS: Cross-sectional survey questionnaire of nurses and nurses' aides (n = 274) working in medicine, surgery, and palliative care departments of a regional hospital. RESULTS: Of the caregivers, 59.5% declared having been confronted with the withdrawal of AN in their professional practice. This was associated with a better perception by these caregivers even if their knowledge on the criteria to be considered in the decision was not significantly modified. CONCLUSION: The coherence of the withdrawal of AN with the personal beliefs of the caregivers, already high in the absence of being confronted with this practice, is better among caregivers who have been confronted with this situation. The lack of information perceived by caregivers should prompt us to develop additional training on the withdrawal of AN, its objectives, and its clinical consequences.


Subject(s)
Caregivers/psychology , Euthanasia, Passive/psychology , Nutritional Support/psychology , Palliative Care/psychology , Cross-Sectional Studies , Euthanasia, Passive/ethics , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Nutritional Support/ethics , Palliative Care/ethics , Perception
2.
Am J Hosp Palliat Care ; 32(7): 732-7, 2015 Nov.
Article in English | MEDLINE | ID: mdl-24928836

ABSTRACT

BACKGROUND: Withdrawing artificial nutrition in palliative care is an issue that often leads to ethical dilemmas among health care providers, despite clinical guidelines. OBJECTIVES: To describe the experience of health care providers confronted with the withdrawing of artificial nutrition at the end of life and identifying the factors related to the level of ethical dilemmas. METHODS: Cross-sectional survey questionnaire of all the nurses and nurses' aides working in medicine, surgery, and palliative care departments of a regional hospital and who have already been confronted with the withdrawal of artificial nutrition. RESULTS: Of 818 questionnaires sent, 274 were returned (response rate 33.5%); 60% (163) of the care providers who responded were involved in withdrawing artificial nutrition at the end of life. Among these, 42 (25.8%) had always or often been affected with ethical dilemmas, and 97 (60%) responded that withdrawing artificial nutrition had always or often been preceded by a multidisciplinary discussion. Items significantly associated with a high level of ethical dilemmas were (1) existence of differences in opinion within the health care team, (2) lack of information regarding the indication of the withdrawal of artificial nutrition, (3) feeling uncomfortable with the patient and his or her relatives, (4) guilt, (5) feeling of abandonment of care, and (6) uneasiness. CONCLUSION: Health care providers seem to have a lack of information and consensus regarding the withdrawal of artificial nutrition at the end of life. The ethical dimension of withdrawing artificial nutrition in palliative care has a strong impact on care providers, regardless of the circumstances of the withdrawal.


Subject(s)
Attitude of Health Personnel , Caregivers/psychology , Health Knowledge, Attitudes, Practice , Nutritional Support/psychology , Terminal Care/ethics , Terminal Care/psychology , Cross-Sectional Studies , Female , Humans , Male , Morals , Nutritional Support/ethics , Patient Care Team/ethics , Surveys and Questionnaires
3.
Geriatr Psychol Neuropsychiatr Vieil ; 12(4): 347-53, 2014 Dec.
Article in French | MEDLINE | ID: mdl-25515898

ABSTRACT

BACKGROUND: Interventions of mobile palliative care teams in nursing homes have been the subject special consideration, however very little data are available on this subject. OBJECTIVES: To determine the proportion of patients followed and consultations conducted in nursing homes for the dependent elderly by a mobile palliative care team, to describe the patients followed and to analyze the various aspects of this intervention. METHOD: Retrospective study on the interventions carried out by a mobile palliative care team in nursing homes between January 1st and December 31st, 2012. RESULTS: The interventions in nursing homes targeted, 7.2% of the followed patients and represented 8.7% of the total activity of the mobile team. Intervention requests were made primarily by the family physician. The followed patients were mostly women (63%), with a mean age of 84 years, presenting non-cancerous diseases (78.2%), and had an average of 4.4 consultations. Half of the patients died during follow-up. Three quarters of the patients presented pain, neuro-psychological symptoms and verbal communication disorders. Four out of ten patients met with the occupational therapist and one of ten, the psychologist. DISCUSSION: The activity of mobile palliative care teams remains marginal, although steadily (on the rise. The collected data illustrate the specificity of geriatric palliative care, while certain characteristics inherent to nursing homes require establishing appropriate therapy proposals. CONCLUSION: Although quantitatively limited, the activity of mobile palliative care teams in nursing homes appears important as these interventions are likely meet the needs of both patients and staff in addition to enabling patients in palliative care to remain at their current place of residence.


Subject(s)
Mobile Health Units , Nursing Homes , Palliative Care/methods , Aged, 80 and over , Female , Humans , Male , Pain Management , Palliative Care/organization & administration , Retrospective Studies
4.
Presse Med ; 41(10): 927-32, 2012 Oct.
Article in French | MEDLINE | ID: mdl-22341946

ABSTRACT

The effect of sedation for intractable distress on survival in terminally ill patients is a debated question. For certain people, this would limit the physician's intervention to the detriment of symptom alleviation for patients. The principle of double effect is traditionally used to overcome this ethical conflict. Studies conducted between 1990 and 2009 fail to show that the death of patients undergoing sedation for intractable distress is hastened. Some authors conclude that sedation does not hasten death and claim that principle of double effect is unnecessary in this debate. In our view, caution is required in the interpretation of studies results and absence of evidence of sedation effects on survival cannot be considered as an evidence of absence of sedation effects on survival. Furthermore, we consider obtaining a definitive answer as impossible in the future, as the required cannot be conducted for ethical reasons. Caution, we think, is necessary, especially as sedation is sometimes used with explicit intention of hastening the end of life. Physician's intention, key point of the principle of double effect, comes back into the foreground of ethical debate on sedation for intractable distress. Far from limiting the physician's action, the principle of double effect, which requires us to clarify our intentions, should allow us to make the distinction between sedation for intractable distress and euthanasia.


Subject(s)
Double Effect Principle , Hypnotics and Sedatives/therapeutic use , Pain, Intractable/drug therapy , Pain, Intractable/mortality , Palliative Care/methods , Euthanasia/ethics , Humans , Intention , Survival Analysis , Terminal Care/ethics , Terminal Care/methods , Terminally Ill , Thinking
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