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As Americans become increasingly accustomed to learning more about their own health, it's becoming more common for research participants to expect to learn about their personal results during a study.
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For researchers and IRBs there is an ethical paradox in behavioral studies involving populations that are hard to engage.
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This is the second of a two-part series examining some of the regulatory and financial changes faced by hospices during recent years.
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The ideal time for a patient to learn about the potential need to deactivate the electrical shock feature of an implantable cardioverter-defibrillator (ICD) is when the decision to implant the device is made, says Chuck Wellman, MD, FAAHPM, chief medical officer at Hospice of the Western Reserve in Cleveland, OH.
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A 57-year-old nursing home resident with a history of dementia climbed out the open window in her room, falling 30feet to the ground below. The woman suffered severe injury as a result of the fall, and a jury awarded the plaintiff $276,164 in damages.
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A pregnant woman at full term presented to the hospital for the birth of her son. The baby was delivered via Caesarean section. Normal tests were conducted on the newborn, and all seemed to be in order.
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Gaining patient consent and provider adoption for health information exchanges (HIEs) is important for the success of the effort, and patients must be adequately educated about the HIE or they may not give their permission, says Jared Rhoads, senior research analyst with CSC, a technology consulting company based in Falls Church, VA.
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Resident elopement and wandering can be extremely dangerous for patients and costly to the facility if the patient is injured or dies, but many health care providers do not have a formal plan in place to prevent the problem or respond effectively once staff realize a patient is missing.
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A former University of California-Los Angeles (UCLA) Healthcare System employee who says he had no idea it was a crime to look at patient records will have four months in prison to think about it.