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One health care lawyer suggests that there will be a phased implementation of the health care reform bill, the Patient Protection and Affordable Care Act, which was passed in March.
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At the University of California, Davis, the legal counsel and the ethics consultation services are "completely separated," according to Alexander A. Kon, MD, CM, FAAP, FCCM, who, among other appointments, serves as the director, clinical bioethics consultation service and chair, bioethics consultation committee.
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In the days after a child has been diagnosed with leukemia, parents often must wrestle with decisions about participation in clinical trials. It's a busy and stressful period, as family members are still dealing with the trauma of the diagnosis.
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Although most patient care scenarios can be worked out through careful communication with all those involved, there are certain situations where even greater diplomacy may be required on the part of ethics consultants.
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While there are certain scenarios regarding patient care when what is written in the law may seem to counter what is ethically appropriate, in general, the law and ethics complement each other in the health care arena, according to those interviewed by Medical Ethics Advisor.
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Recent reports that a Texas woman had her son's sperm retrieved following his unexpected death made headlines, while the American Society of Reproductive Medicine (ASRM) is in the process of updating its ethics policy on "posthumous donation" of germ cells using either eggs or sperm.
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The American Society for Bioethics and Humanities voted in 2006 to create a task force to revise the core competencies expected for those who perform ethics consults and for ethics consult services.
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The latest in a series of papers published by researchers led by Angelo Volandes, MD, MPH, instructor in medicine at Harvard Medical School and documentary filmmaker, looked at the use of a video depicting real-life cardiopulmonary resuscitation, as well as other life-sustaining treatments often faced by patients at the end of life.
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Acknowledging, respecting, and accommodating the role of the patient caregiver in physician-patient relationships was the impetus for a position paper published earlier this year by the American College of Physicians (ACP) and developed by its Ethics, Professionalism and Human Rights Committee.
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The National Institutes of Health (NIH) announced on March 18 that it is creating a public database that researchers, consumers, health care providers, and others can search for information submitted voluntarily by genetic test providers.
