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1.
J Clin Ethics ; 27(2): 163-75, 2016.
Article in English | MEDLINE | ID: mdl-27333066

ABSTRACT

For all of the emphasis on quality improvement-as well as the acknowledged overlap between assessment of the quality of healthcare services and clinical ethics-the quality of clinical ethics consultation has received scant attention, especially in terms of empirical measurement. Recognizing this need, the second edition of Core Competencies for Health Care Ethics Consultation1 identified four domains of ethics quality: (1) ethicality, (2) stakeholders' satisfaction, (3) resolution of the presenting conflict/dilemma, and (4) education that translates into knowledge. This study is the first, to our knowledge, to directly measure all of these domains. Here we describe the quality improvement process undertaken at a tertiary care academic medical center, as well as the tools developed to measure the quality of ethics consultation, which include post-consultation satisfaction surveys and weekly case conferences. The information gained through these tools helps to improve not only the process of ethics consultation, but also the measurement and assurance of quality.


Subject(s)
Bioethics , Ethics Consultation/standards , Ethics, Clinical , Quality of Health Care , Ethicists/standards , Humans , Morals , Quality Improvement , Time Factors
2.
J Clin Ethics ; 26(3): 260-5, 2015.
Article in English | MEDLINE | ID: mdl-26399676

ABSTRACT

Typically, the determination of death by neurological criteria follows a very specific protocol. An apnea test is performed with further confirmation as necessary, and then mechanical ventilation is withdrawn with the consent of the family after they have had an opportunity to "say goodbye," and at such a time to permit organ retrieval (with authorization of the patient or consent of the next of kin). Such a process maximizes transparency and ensures generalizability. In exceptional circumstances, however, it may be necessary to deviate from this protocol in order to spare family members unnecessary suffering and to reduce moral distress felt by clinical staff. It may also be appropriate, we argue, to refrain from even inquiring about organ donation when the next-of-kin is not only certain to refuse, but lacks the decision-making capacity to potentially consent. The case described in this article calls into question generally reliable assumptions about determination of death by neurological criteria, where the best the clinical team could do for the patient and his family was "the least bad option."


Subject(s)
Adult Children , Airway Extubation/ethics , Brain Death/diagnosis , Decision Making/ethics , Denial, Psychological , Ethics Consultation , Respiration, Artificial , Stress, Psychological/etiology , Stroke/therapy , Third-Party Consent/ethics , Tissue and Organ Harvesting/ethics , Withholding Treatment/ethics , Adult Children/psychology , Aged , Apnea/diagnosis , Asian People , Death , Diagnosis, Differential , Dissent and Disputes , Grief , Health Personnel/psychology , Humans , Male , Tissue and Organ Procurement , United States , Waiting Lists
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