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一项关于药剂师干预对昂丹司琼止吐治疗费用影响的随机试验。

A randomized trial of the effects of pharmacist intervention on the cost of antiemetic therapy with ondansetron.

作者信息

Dranitsaris G, Warr D, Puodziunas A

机构信息

Department of Pharmaceutical Services, Ontario Cancer Institute/Princess Margaret Hospital, Toronto, Canada.

出版信息

Support Care Cancer. 1995 May;3(3):183-9. doi: 10.1007/BF00368888.

Abstract

Ondansetron has had a major impact on the prevention of emesis in patients receiving chemotherapy. However, the high cost and potential for inappropriate prescribing of this agent warranted a closer examination of its utilization. Hospital guidelines regarding the use of ondansetron were prepared by the Pharmacy and Therapeutics Committee and approved by the Medical Advisory Committee. The guidelines were then distributed to all physicians. Physicians were randomized into an intervention or non-intervention group. A prospective drug use evaluation was then conducted for a 10-week period where pharmacists monitored ondansetron prescribing and compared each order against hospital guidelines. For orders deemed inappropriate, only the intervention-group physicians were contacted for therapy modification. The control of nausea and vomiting was then assessed for all patients 24 h and 72 h after chemotherapy via a simple patient questionnaire. There were no significant differences with respect to the control of nausea and vomiting between patients who received ondansetron according to guidelines and those who did not. A total of 76% (48/63) of the prescriptions met hospital guidelines in the intervention group compared to 51.6% (33/64) in the control (P = 0.007). During the study period, physicians in the intervention group prescribed $Can 757 worth of ondansetron inappropriately compared to $1814 in the control. Drug use evaluation with pharmacist intervention was an effective method of controlling unnecessary hospital costs and contributed towards the appropriate use of ondansetron without compromising patient care.

摘要

昂丹司琼对预防接受化疗患者的呕吐产生了重大影响。然而,该药物的高成本以及不当处方的可能性促使对其使用情况进行更深入的审查。关于昂丹司琼使用的医院指南由药学与治疗学委员会制定,并经医学咨询委员会批准。然后将这些指南分发给所有医生。医生被随机分为干预组或非干预组。随后进行了为期10周的前瞻性药物使用评估,在此期间药剂师监测昂丹司琼的处方情况,并将每份医嘱与医院指南进行对照。对于被认为不适当的医嘱,仅联系干预组医生以修改治疗方案。然后通过一份简单的患者问卷对所有患者化疗后24小时和72小时的恶心和呕吐控制情况进行评估。按照指南使用昂丹司琼的患者与未按指南使用的患者在恶心和呕吐控制方面没有显著差异。干预组共有76%(48/63)的处方符合医院指南,而对照组为51.6%(33/64)(P = 0.007)。在研究期间,干预组医生不当开具了价值757加元的昂丹司琼,而对照组为1814加元。药剂师干预下的药物使用评估是控制不必要医院费用的有效方法,有助于在不影响患者护理的情况下合理使用昂丹司琼。

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