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将温度控制要求融入药学实践。

Integration of temperature-controlled requirements into pharmacy practice.

作者信息

Ziance Ronald, Chandler Chris, Bishara Rafik H

机构信息

College of Pharmacy, University of Southern Nevada, Henderson, USA.

出版信息

J Am Pharm Assoc (2003). 2009 May-Jun;49(3):e61-7; quiz e68-9. doi: 10.1331/JAPhA.2009.08140.

Abstract

OBJECTIVES

To describe (a) Food and Drug Administration (FDA) regulations and guidelines issued by several professional organizations to ensure appropriate storage, handling, and distribution of temperature-controlled prescription drugs from manufacturer to wholesaler to pharmacy to patients; (b) pharmacy business practices that ensure the dispensing of high-quality temperature-controlled drug products; and (c) education that facilitates patients' important role in maintaining product quality.

DATA SOURCES

PubMed from 1950 to 2007 using the search terms drug stability in transit, drug stability storage tablet, drug stability testing, drug stability transportation, drug stability relative humidity, and drug storage high temperature. Nonprimary sources included the FDA website (www.fda.gov), presentations from meetings or workshops, and websites of professional organizations. Additional resources were identified from bibliographies collected by the authors.

DATA EXTRACTION

Relevant data were extracted independently by the authors.

DATA SYNTHESIS

The important role of pharmacists in ensuring the quality of drugs dispensed to and handled/stored by patients is supported by business practices that (a) promote purchase of quality temperature-controlled drugs (including quality agreements with providers), (b) ensure appropriate handling and storage upon receipt, (c) ensure proper packaging for receipt by patients, (d) provide relevant information to patients, and (e) evaluate issues associated with possible compromised transit, handling, and storage of temperature-controlled drug products.

CONCLUSION

The transit, handling, and storage of temperature-controlled drug products within complex supply chains provide opportunities for exposure of such drugs to temperatures above or below those recommended by the manufacturer. Pharmacists have opportunities to integrate business practices that facilitate the proper receipt, handling, and storage of temperature-controlled drug products. These practices will enhance the dispensing of high-quality, efficacious drug products to patients and proper handling and storage by patients.

摘要

目的

描述(a)美国食品药品监督管理局(FDA)的相关规定以及几个专业组织发布的指南,以确保温控处方药从制造商到批发商、再到药房直至患者的妥善储存、处理和分发;(b)确保高质量温控药品配药的药房业务操作;以及(c)有助于患者在维持产品质量方面发挥重要作用的教育。

数据来源

1950年至2007年的PubMed,使用搜索词“运输过程中的药物稳定性”“片剂储存药物稳定性”“药物稳定性测试”“药物稳定性运输”“药物稳定性相对湿度”以及“高温药物储存”。非主要来源包括FDA网站(www.fda.gov)、会议或研讨会的报告以及专业组织的网站。作者从收集的参考文献中确定了其他资源。

数据提取

作者独立提取相关数据。

数据综合

药剂师在确保分发给患者以及由患者处理/储存的药品质量方面的重要作用得到以下业务操作的支持:(a)促进购买高质量的温控药品(包括与供应商签订质量协议);(b)确保收到药品后的妥善处理和储存;(c)确保患者接收时的适当包装;(d)向患者提供相关信息;以及(e)评估与温控药品可能在运输、处理和储存过程中受到影响相关的问题。

结论

复杂供应链中温控药品的运输、处理和储存为这些药品暴露于制造商推荐温度之上或之下提供了机会。药剂师有机会整合业务操作,以促进温控药品的正确接收、处理和储存。这些操作将提高向患者分发高质量、有效药品的水平,并促进患者的妥善处理和储存。

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