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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.
Clin Chest Med ; 27(1): 17-28, v, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16543049

RESUMO

Asthma is one of the most common respiratory diseases, with immense social impact. Despite best efforts, asthma prevalence, morbidity, and mortality are increasing in the United States. This is especially the case in select communities which suffer an excess burden of asthma. Studying these groups and attempting to ameliorate the disease burden they suffer has an important moral and social imperative. It also may lend important insight into the complex factors that contribute to asthma outcomes. The factors that affect asthma interact in a complicated manner and require a comprehensive approach that addresses each of them. However, pursuing health disparities research is controversial, and important ethical and operative considerations need to be made by those to engage in health disparities research.


Assuntos
Asma/etnologia , População Negra , Efeitos Psicossociais da Doença , Acessibilidade aos Serviços de Saúde , Hispânico ou Latino , População Branca , Asma/etiologia , Asma/terapia , Comportamentos Relacionados com a Saúde/etnologia , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Fatores de Risco , Fatores Socioeconômicos , Estados Unidos/epidemiologia
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