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21.
R. D. Harris J. P. Chalmers P. J. Henschke A. Tonkin P. Y. Popplewell A. M. Stewart A. J. Radford K. P. O'Brien M. J. Bond M. G. Harris R. J. Turnbull G. Champion E. R. Hobbin G. R. Andrews 《Internal medicine journal》1991,21(2):230-234
The aim of this study was to identify differences in the medical management and clinical outcome in a group of elderly patients admitted to a designated geriatric assessment unit (GAU) or to two general medical units (GMUs). A prospective randomised controlled trial was undertaken in 267 patients aged 70 years and over (mean age = 78.3 years). Following discharge from hospital, patients were followed up at three monthly intervals for a total of 12 months. At the time of discharge, no significant differences were found in inpatient management, length of stay, mortality rates, discharge rates to institutional care or utilisation of community services in patients admitted to the GAU and the GMUs. Similarly, no significant differences were found at three, six, nine, and 12 month follow up in case fatality, activities of daily living indices, mental health status, rates of institutional referral and the level of community service support in patients admitted to the GAU and the GMUs studied. These findings do not show any advantage for the unselected 70 + acutely ill elderly patient who is admitted to a designated geriatric assessment unit rather than to a general medical unit. Therefore, an admission policy to GAU, based solely on age 70 + is medically inappropriate and cost-inefficient. Evidence from other sources suggests that an age cohort of acutely admitted patients beyond 80 years may well have returned more optimistic findings for the GAU. In future, GAUs will require a more selective admission policy to maximise the benefits of their rehabilitative and interdisciplinary approach. (Aust NZ J Med 1991; 21: 230–234.) 相似文献
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P. N. Sambrook MD FRACP J. A. Eisman MB BS PhD FRACP G. D. Champion MB BS FRACP N. A. Pocock MB BS FRACP 《Arthritis \u0026amp; Rheumatology》1988,31(8):973-978
Sex hormones have important effects on bone, especially in postmenopausal women. These hormones may be of particular significance in patients with rheumatoid arthritis (RA), who have a high frequency of osteoporosis. To examine this, we measured estrogen and androgen concentrations and bone mineral density (BMD) in 49 postmenopausal women with RA and 49 normal postmenopausal women. Compared with the controls, postmenopausal RA patients had significantly reduced levels of estrone (median 18 pmoles/liter versus 49; P < 0.001), dehydroepiandosterone sulfate (DHEAS) (median 0.3 μmoles/liter versus 2.0; P < 0.001), testosterone (median 0.6 nmoles/liter versus 0.95; P < 0.001), and femoral BMD (mean 0.72 gm/cm2 versus 0.80; P < 0.002). Prednisolone therapy in 22 patients (mean dosage 8 mg/day) was associated with reductions in estrone and testosterone levels; however, DHEAS and femoral BMD were also decreased in RA patients who were not receiving corticosteroids. Reduced DHEAS levels in postmenopausal women with RA may increase their risk of osteoporosis. 相似文献
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Targeted sequencing using a 47 gene multiple myeloma mutation panel (M3P) in ‐17p high risk disease 下载免费PDF全文
Klaus M. Kortüm Christian Langer Jorge Monge Laura Bruins Jan B. Egan Yuan X. Zhu Chang Xin Shi Patrick Jedlowski Jessica Schmidt Juhi Ojha Lars Bullinger Peter Liebisch Miriam Kull Mia D. Champion Scott Van Wier Gregory Ahmann Leo Rasche Stefan Knop Rafael Fonseca Hermann Einsele A Keith Stewart Esteban Braggio 《British journal of haematology》2015,168(4):507-510
We constructed a multiple myeloma (MM)‐specific gene panel for targeted sequencing and investigated 72 untreated high‐risk (del17p) MM patients. Mutations were identified in 78% of the patients. While the majority of studied genes were mutated at similar frequency to published literature, the prevalence of TP53 mutation was increased (28%) and no mutations were found in FAM46C. This study provides a comprehensive insight into the mutational landscape of del17p high‐risk MM. Additionally, our work demonstrates the practical use of a customized sequencing panel, as an easy, cheap and fast approach to characterize the mutational profile of MM. 相似文献
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