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  • Special Article

    Dementia, a chronic disease of aging characterized by progressive cognitive decline that interferes with independent functioning, affects a large and growing number of older adults in the United States. Citing the growing effect of dementia on patients, families, and the health care and long-term…

    • April 4, 2013
    • Hurd M.D.Martorell P.Delavande A.Mullen K.J.Langa K.M.
    • N Engl J Med 2013; 368:1326-1334
    • Free Full Text

    This analysis of data from the Health and Retirement Study estimated that the prevalence of dementia among people older than 70 years of age in the United States in 2010 was 14.7% and that the total costs attributable to dementia were between $157 billion and $215 billion.

  • Special Article

    Health care transitions, such as the hospitalization of nursing home residents, have the potential for fragmentation of care, changes in the management of chronic diseases, duplication of diagnostic workups, and medical errors.– Few previous reports have described health care transitions among…

    • September 29, 2011
    • Gozalo P., Teno J.M., Mitchell S.L., et al.
    • N Engl J Med 2011; 365:1212-1221
    • Free Full Text

    Among nursing home residents with cognitive impairment, burdensome transitions between the nursing home and the hospital or hospice during the last months of life were common, varied according to state, and were associated with a poor quality of care.

  • Special Article

    Despite tremendous interest in medical malpractice and its reform,– data are lacking on the proportion of physicians who face malpractice claims according to physician specialty, the size of payments according to specialty, and the cumulative incidence of being sued during the course of a…

    • August 18, 2011
    • Jena A.B.Seabury S.Lakdawalla D.Chandra A.
    • N Engl J Med 2011; 365:629-636
    • Free Full Text
    • CME

    Despite tremendous interest in medical malpractice and its reform,110 data are lacking on the proportion of physicians who face malpractice claims according to physician specialty, the size of payments according to specialty, and the cumulative incidence ...

  • Special Article

    The design of a clinical trial includes specification of primary and secondary outcomes. Although a change in the primary outcomes over the course of a trial can be legitimate, good research practice dictates that the decision-making procedure, the timing of the change, and the reason for the…

    • November 12, 2009
    • Vedula S.S.Bero L.Scherer R.W.Dickersin K.
    • N Engl J Med 2009; 361:1963-1971
    • Free Full Text

    This article compares outcomes specified in research protocols with those described in published reports for trials of off-label use of gabapentin that were sponsored by the manufacturer. The authors had access to internal company documents; the article details discrepancies between the published record and the research plans.

  • Special Article

    Epidemiologic studies based on data from clinical registries have contributed to tremendous advances in modern medicine by enhancing our understanding of the natural history of disease and the value of many medical and surgical interventions. Studies using these data bases have increased the use of…

    • April 1, 2004
    • Tu J.V., Willison D.J., Silver F.L., et al.
    • N Engl J Med 2004; 350:1414-1421
    • Free Full Text

    Governments and ethics boards increasingly require written informed consent from all subjects before enrollment in clinical registries. The authors of this article examine the effect of a comprehensive effort to obtain informed consent on the participation rate in the prospective Registry of the Canadian Stroke Network. The overall participation rate was 39.3 percent during phase 1 of the project and 50.6 percent during phase 2. Obtaining written consent was costly, leading to selection bias.

  • Special Article

    More than 6 million adults in the United States provide long-term, unpaid care to disabled elderly persons in their families. This service saves the health care system billions of dollars annually, but it comes at the price of high levels of distress among family caregivers, an increased risk for…

    • November 13, 2003
    • Schulz R., Mendelsohn A.B., Haley W.E., et al.
    • N Engl J Med 2003; 349:1936-1942
    • Free Full Text

    The authors describe the experience of family caregivers who provided end-of-life care to patients with dementia. During the year before the patient's death, many caregivers reported feeling that they were “on duty” 24 hours a day and had symptoms of depression. These symptoms often resolved after the death of the patient, and 72 percent of caregivers reported that the death was a relief for them. These findings highlight the demanding and stressful nature of end-of-life care provided by family members to patients with dementia.

  • Special Article

    The demand for transplantable organs continues to increase, while the organizations involved in the procurement of organs struggle with a stagnant or possibly diminishing pool of potential organ donors. As of July 7, 2003, a total of 82,117 patients were waiting for a solid-organ transplant. The…

    • August 14, 2003
    • Sheehy E., Conrad S.L., Brigham L.E., et al.
    • N Engl J Med 2003; 349:667-674
    • Free Full Text

    Waiting lists for organ transplantation are growing. This study examined numbers of potential organ donors and actual organ donations from 1997 through 1999 in areas of the United States that are served by 36 organ-procurement organizations. Hospitals with 150 or more beds had significantly higher proportions of potential donors and actual donors than smaller hospitals; 19 percent of hospitals accounted for 80 percent of all potential donors.

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