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重组促红细胞生成素与医疗保险支付。

Recombinant erythropoietin and Medicare payment.

作者信息

Sisk J E, Gianfrancesco F D, Coster J M

机构信息

Office of Technology Assessment, US Congress, Washington, DC.

出版信息

JAMA. 1991 Jul 10;266(2):247-52.

PMID:2056627
Abstract

The biologic recombinant human erythropoietin provides a recent case study of the great influence federal policies, especially Medicare payment, exert over the use and cost of medical technologies. By covering most dialysis patients, Medicare has been the predominant payer for recombinant erythropoietin, which corrects anemia associated with chronic renal disease. Medicare's leverage seems to have produced a low US price for the product. Paying a fixed rate per treatment with the biologic agent gave dialysis facilities a financial incentive to use low doses, but Medicare did not routinely monitor patients' responses. By August 1990, average and modal doses were low, and fewer than 45% of patients who had been treated for 6 months or more had ever attained the target hematocrit. Medicare should recognize the financial incentives of its payment policies and routinely evaluate the quality of care for beneficiaries.

摘要

生物重组人促红细胞生成素提供了一个近期的案例研究,展现了联邦政策,尤其是医疗保险支付政策,对医疗技术的使用和成本产生的巨大影响。通过覆盖大多数透析患者,医疗保险一直是重组促红细胞生成素的主要支付方,该药物可纠正与慢性肾病相关的贫血。医疗保险的影响力似乎使得该产品在美国的价格较低。按每次使用生物制剂治疗支付固定费用,这给透析机构提供了使用低剂量药物的经济激励,但医疗保险并未定期监测患者的反应。到1990年8月,平均剂量和典型剂量都很低,接受治疗6个月或更长时间的患者中,只有不到45%的人达到了目标血细胞比容。医疗保险应该认识到其支付政策的经济激励因素,并定期评估受益人的护理质量。

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