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American journal of hospital pharmacy最新文献

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Pharmacists in California HMOs gain expanded role. 药剂师在加州hmo获得扩大的作用。
A S Wittenburg
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引用次数: 0
Overview of the New York State program for prescription drug benefits. 概述纽约州处方药福利计划。
E L Lennard, P E Feinberg

New York State's prescription drug benefits program is described. The Empire Plan, a part of the New York State Health Insurance Program, includes a prescription drug benefits program. The prescription drug program began in 1986 and covers more than 700,000 people. In 1988 the state started a therapeutic drug-use-evaluation (DUE) program in correct with the supplier, Health Information Designs, a subsidiary of ValueRx Pharmacy Program. In 1991 the partnership with ValueRx was expanded to include patient profilling and physician education. In 1993 the state implemented a prior-authorization program for certain high-technology drugs, also administered by ValueRx. New York's public work force is heavily unionized, and the unions have been deeply involved in program design and vendor selection. Program participants have access to a large network of community pharmacies. The program also provides mail-order service. Quality is at the center of the state's and the unions' prescription drug program philosophy. Saving money is also a major objective; savings totaling $19.5 million were realized from 1988 through 1993 under the partnership between the state and ValueRx. The Empire Plan's prescription drug benefits program is building quality and saving money by integrating DUE, prior authorization, education, community pharmacy, and mail-order service.

描述了纽约州的处方药福利计划。帝国计划是纽约州健康保险计划的一部分,包括处方药福利计划。处方药项目始于1986年,覆盖了70多万人。1988年,该州与供应商健康信息设计公司(ValueRx Pharmacy program的子公司)共同启动了一项治疗性药物使用评估(DUE)计划。1991年,与ValueRx的合作扩大到包括患者分析和医生教育。1993年,该州对某些高科技药物实施了预先授权计划,同样由ValueRx管理。纽约的公共部门工作人员是高度工会化的,工会一直深入参与项目设计和供应商选择。项目参与者可以使用一个庞大的社区药房网络。该项目还提供邮购服务。质量是州政府和工会处方药项目理念的核心。省钱也是一个主要目标;1988年至1993年,在州政府与ValueRx的合作下,共节省了1,950万美元。帝国计划的处方药福利项目通过整合DUE、事先授权、教育、社区药房和邮购服务来提高质量并节省资金。
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引用次数: 0
Stability of mesalamine in rectal suspension diluted with distilled water. 用蒸馏水稀释直肠悬浮液中美沙拉胺的稳定性。
Pub Date : 1994-12-01 DOI: 10.1093/AJHP/51.23.2955
L. M. Henderson, C. Johnson, R. Berardi
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引用次数: 0
Pharmacists in California HMOs gain expanded role. 药剂师在加州hmo获得扩大的作用。
Pub Date : 1994-12-01 DOI: 10.1093/AJHP/51.23.2890
A. S. Wittenburg
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引用次数: 0
National health care reform, Part 1: Why it fizzled. 国家医疗改革,第一部分:失败的原因。
Pub Date : 1994-12-01 DOI: 10.1093/AJHP/51.23.3008
W. A. Zellmer
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引用次数: 0
Delaware State Society helps mold law on nurse prescribing. 特拉华州协会帮助制定护士处方的法律。
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引用次数: 0
Information on drop size needs to be eyed closely. 有关液滴大小的信息需要密切关注。
M A Weiss, J R Hendrickson
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引用次数: 0
Criteria for use of hypolipidemic agents in adults. 成人降血脂药物使用标准。
Pub Date : 1994-11-15 DOI: 10.1093/AJHP/51.22.2837
E. Morales, S. Spinler, M. Wilson, M. Chin, E. Jozefiak
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引用次数: 7
Compatibility of paclitaxel injection vehicle with intravenous administration and extension sets. 紫杉醇注射载体与静脉给药和延长装置的相容性。
Pub Date : 1994-11-15 DOI: 10.1093/AJHP/51.22.2804
L. Trissel, Q. Xu, J. Kwan, J. F. Martínez
The compatibility of paclitaxel injection vehicle with a variety of i.v. administration and extension sets was studied in terms of the amount of diethylhexyl phthalate (DEHP) leached from the sets. Test solutions of paclitaxel injection vehicle corresponding to paclitaxel injection 0.3 and 1.2 mg/mL were prepared in polyolefin bags of 5% dextrose injection. The solutions were delivered in triplicate over 24 hours through 26 models of administration sets and 24 models of extension sets and collected in glass containers. Portions were removed after delivery and analyzed in duplicate for DEHP concentration by high-performance liquid chromatography. All the extension sets were compatible with paclitaxel injection vehicle. Most of the administration sets were also compatible. However, two administration sets were incompatible with paclitaxel vehicle corresponding to either drug concentration, and five sets were incompatible with the vehicle simulating the high (1.2-mg/mL) concentration. Some of the incompatible sets were labeled as not containing polyvinyl chloride (PVC). Solutions of paclitaxel vehicle leached DEHP from administration sets containing PVC and from some sets labeled as not containing PVC.
研究了紫杉醇注射载体与多种静脉给药和延伸套的相容性,考察了从套中浸出邻苯二甲酸二乙基己酯(DEHP)的量。将紫杉醇注射液0.3、1.2 mg/mL对应的紫杉醇注射载体试验溶液装在5%葡萄糖注射液的聚烯烃袋中。溶液在24小时内通过26个模型的管理组和24个模型的扩展组一式三份交付,并收集在玻璃容器中。送出后取出部分,用高效液相色谱法一式两份分析DEHP浓度。所有延伸装置均与紫杉醇注射载体兼容。大多数管理集也是兼容的。然而,两组给药组与紫杉醇载体对应的药物浓度不相容,5组给药组与模拟高浓度(1.2 mg/mL)的载体不相容。一些不相容的套装被标记为不含聚氯乙烯(PVC)。紫杉醇溶液从含有PVC的管理组和一些标记不含PVC的管理组中浸出DEHP。
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引用次数: 16
Preparation of dextran 70 injection labeled with technetium 99m for use as a cardiac blood-pool imaging agent. 锝99m标记葡聚糖70注射液用于心脏血池显像剂的制备。
Pub Date : 1994-11-15 DOI: 10.1093/AJHP/51.22.2797
R. N. Dansereau, B. Line
A means of compounding dextran 70 injection labeled with technetium Tc 99m by using readily available pharmaceutical components is described, and the compound's biological distribution is evaluated. The radiopharmaceutical was prepared by mixing 10 mg (0.17 mL) of dextran 70 in sodium chloride with 0.33 mL of 0.9% sodium chloride injection in a 1-mL syringe. This solution was added to a sterile, pyrogen-free vial containing stannous chloride, and the steps were repeated until five vials had been prepared. The contents of each vial were mixed by swirling until the solids were dissolved. The mixture was incubated for five minutes at 22 degrees C, then 1.48 gigabecquerels of sodium pertechnetate Tc 99m injection in a volume of 0.5 mL was added to each vial. The final mixture was incubated for 15 minutes at 22 degrees C and then stored at room temperature. Thin-layer chromatography was performed after zero, three, and six hours of storage to assess radiochemical purity. Five more vials were prepared as above, and five male volunteers were given 185 megabecquerels of the radiopharmaceutical by i.v. push, and scintigraphic images of the anterior chest were taken immediately and 1, 2, and 24 hours after injection. Immediately after preparation, a mean +/- S.D. of 99.0 +/- 1.0% of the 99mTc was bound to dextran 70. Mean +/- S.D. binding was 98.1 +/- 3.7% and 95.8 +/- 7.5% at three and six hours, respectively. Scintigraphy in the five volunteers yielded high-contrast images of the cardiac blood pool with little uptake of the radionuclide by the lungs. (ABSTRACT TRUNCATED AT 250 WORDS)
本文描述了一种利用现成的药物成分配制以锝Tc 99m标记的葡聚糖70注射液的方法,并评价了该化合物的生物分布。用1 mL注射器将含氯化钠的葡聚糖70 10 mg (0.17 mL)与0.9%氯化钠注射液0.33 mL混合制备放射性药物。该溶液被加入到一个无菌的,无热原的小瓶含有氯化亚锡,并重复的步骤,直到五个小瓶已准备好。每个小瓶的内容物通过旋转混合,直到固体溶解。将混合物在22℃下孵育5分钟,然后在每个小瓶中加入1.48 g / g高技术酸钠Tc 99m注射液,体积为0.5 mL。最终混合物在22℃下孵育15分钟,然后在室温下保存。储存0、3、6小时后进行薄层色谱,以评估放射化学纯度。再按上述方法制备5个小瓶,5名男性志愿者静脉推注185兆贝克勒放射性药物,注射后即刻及注射后1、2、24小时分别拍摄前胸显像。制备后,99mTc的平均+/- sd值为99.0 +/- 1.0%,与葡聚糖70结合。在3小时和6小时,平均+/- sd结合率分别为98.1 +/- 3.7%和95.8 +/- 7.5%。五名志愿者的闪烁成像显示,肺部对放射性核素的吸收很少,心脏血池的对比度很高。(摘要删节250字)
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引用次数: 7
期刊
American journal of hospital pharmacy
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