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加拿大重度A型血友病患儿的临床和费用问题的研究
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作者 Kern M. blanchettev. +1 位作者 Stain A.M. 张振 《世界核心医学期刊文摘(儿科学分册)》 2005年第9期19-20,共2页
To compare target joint-associated costs incurred by boys with severe hemophilia A 1 year before and 1 year after development of a target joint (pre-TJ, post-TJ). Resource utilization data were extracted retrospective... To compare target joint-associated costs incurred by boys with severe hemophilia A 1 year before and 1 year after development of a target joint (pre-TJ, post-TJ). Resource utilization data were extracted retrospectively from medical and hemophilia clinic charts and patient diaries for 16 boys attending the Hospitalfor Sick Children (HSC)’s comprehensive care hemophilia program. Resources examined included drugs, medical care, hospitalization, laboratory tests, therapies, and transfusions received. All costs were figured using standard price lists and were discounted using an annual rate of 3% . Fifteen of the 16 boys developed at least one target joint, defined as three bleeds into any single joint within a consecutive 3-month period, at an average age of 54 months (range, 15-94 months), with ankles being most often affected, followed by elbows and knees (46% vs 28% and 23% , respectively). The total cost of treating a boy with on-demand Factor VIII (FVIII) increased by 119% after development of a target joint, from $ 20,091 (in 2002 Canadian dollars $ CDN ) in the year before to $ 43,890 in the year after target joint development. Factor VIII use accounted for 87% of the total cost in the year before target joint development and 93% in the year after. This study identified substantial increased costs of care associated with target joint development. This finding provides further support for more aggressive treatmentaimed at reducing target joints -either more aggressive treatment of joint bleeds or institution of primary prophylactic therapy at an early age. 展开更多
关键词 费用问题 关节受累 医疗记录 男性患儿 加拿大元 医疗花费 费用总额 初级预防 儿童医院 综合医疗
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