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1.
Am J Respir Crit Care Med ; 191(2): 219-27, 2015 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-25590155

RESUMO

RATIONALE: Intensive care unit (ICU) clinicians sometimes have a conscientious objection (CO) to providing or disclosing information about a legal, professionally accepted, and otherwise available medical service. There is little guidance about how to manage COs in ICUs. OBJECTIVES: To provide clinicians, hospital administrators, and policymakers with recommendations for managing COs in the critical care setting. METHODS: This policy statement was developed by a multidisciplinary expert committee using an iterative process with a diverse working group representing adult medicine, pediatrics, nursing, patient advocacy, bioethics, philosophy, and law. MAIN RESULTS: The policy recommendations are based on the dual goals of protecting patients' access to medical services and protecting the moral integrity of clinicians. Conceptually, accommodating COs should be considered a "shield" to protect individual clinicians' moral integrity rather than as a "sword" to impose clinicians' judgments on patients. The committee recommends that: (1) COs in ICUs be managed through institutional mechanisms, (2) institutions accommodate COs, provided doing so will not impede a patient's or surrogate's timely access to medical services or information or create excessive hardships for other clinicians or the institution, (3) a clinician's CO to providing potentially inappropriate or futile medical services should not be considered sufficient justification to forgo the treatment against the objections of the patient or surrogate, and (4) institutions promote open moral dialogue and foster a culture that respects diverse values in the critical care setting. CONCLUSIONS: This American Thoracic Society statement provides guidance for clinicians, hospital administrators, and policymakers to address clinicians' COs in the critical care setting.


Assuntos
Acesso à Informação/ética , Consciência , Acessibilidade aos Serviços de Saúde/ética , Unidades de Terapia Intensiva/ética , Direitos do Paciente/ética , Autonomia Profissional , Acesso à Informação/legislação & jurisprudência , Adolescente , Adulto , Idoso , Atitude do Pessoal de Saúde , Temas Bioéticos , Criança , Revelação/ética , Revelação/legislação & jurisprudência , Feminino , Guias como Assunto , Acessibilidade aos Serviços de Saúde/legislação & jurisprudência , Humanos , Lactente , Unidades de Terapia Intensiva/legislação & jurisprudência , Masculino , Pessoa de Meia-Idade , Política Organizacional , Direitos do Paciente/legislação & jurisprudência , Gravidez , Sociedades Médicas/ética , Estados Unidos , Recursos Humanos
2.
Crit Care Med ; 35(4): 1084-90, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17334245

RESUMO

OBJECTIVES: There is growing recognition of the importance of spiritual care as a quality domain for critically ill patients and their families, but there is a paucity of research to guide quality improvement in this area. Our goals were to: 1) determine whether intensive care unit (ICU) family members who rate an item about their spiritual care are different from family members who skip the item or rate the item as "not applicable" and 2) identify potential determinants of higher family satisfaction with spiritual care in the ICU. DESIGN: Cross-sectional study, using data from a cluster randomized trial aimed at improving end-of-life care in the ICU. SETTING: ICUs in ten Seattle-area hospitals. SUBJECTS: A total of 356 family members of patients dying during an ICU stay or within 24 hrs of ICU discharge. INTERVENTION: None. MEASUREMENTS AND MAIN RESULTS: Family members were surveyed about spiritual care in the ICU. Chart abstractors obtained clinical variables including end-of-life care processes and family conference data. The 259 of 356 family members (73%) who rated their spiritual care were slightly younger than family members who did not rate this aspect of care (p = .001). Multiple regression revealed family members were more satisfied with spiritual care if a pastor or spiritual advisor was involved in the last 24 hrs of the patient's life (p = .007). In addition, there was a strong association between satisfaction with spiritual care and satisfaction with the total ICU experience (p < .001). Ratings of spiritual care were not associated with any other demographic or clinical variables. CONCLUSIONS: These findings suggest that for patients dying in the ICU, clinicians should assess each family's spiritual needs and consult a spiritual advisor if desired by the family. Further research is needed to develop a comprehensive approach to ICU care that meets not only physical and psychosocial but also spiritual needs of patients and their families.


Assuntos
Família/psicologia , Unidades de Terapia Intensiva , Espiritualidade , Assistência Terminal/psicologia , Idoso , Comportamento do Consumidor , Estudos Transversais , Feminino , Humanos , Tempo de Internação , Masculino , Grupos Raciais , Ensaios Clínicos Controlados Aleatórios como Assunto , Fatores Socioeconômicos
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