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首页> 外文期刊>Joint Commission Journal on Quality and Safety >Improving the Safety of Intravenous Admixtures: Lessons Learned from a Pentostam~® Overdose
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Improving the Safety of Intravenous Admixtures: Lessons Learned from a Pentostam~® Overdose

机译:改善静脉内混合物的安全性:过量使用Pentostam〜®的经验教训

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Case Study: Weaknesses in the multistep process of admixture preparation and administration resulted in a patient with cutaneous leishmaniasis (CL) receiving a 10-fold intravenous (TV) overdose of Pentostam~® (sodium stibogluconate), a rarely used drug. Lessons Learned: A review of this adverse event resulted in five recommendations: (1) Provide staffing continuity among pharmacists and pharmacy technicians preparing and nurses administering the admixture; (2) Take time to ensure thorough and deliberative consideration of questions or concerns about admixture preparation; (3) Use due diligence in performing double checks of admixture calculations; (4) Know the drug and seek clarification when appropriate; and (5) Examine label information carefully. Progress Update: Two changes were made to improve patient safety. First, a form was developed to accompany the preparation of complex IV drugs, including chemotherapy solutions and nonformulary IV admixtures; the form is consistently used. Second, the pharmacy service developed information sheets for 12 high-risk drugs frequently used in IV admixtures. Discussion: The medical center had processes in place to prevent medication errors, yet an error occurred nonetheless. Weaknesses were identified in staff communication, quality assurance checks, and product labeling. Also, nurses and pharmacists had less than adequate information about new or unusually dosed medications.
机译:案例研究:混合物制备和给药的多步骤过程中的缺陷导致皮肤利什曼病(CL)的患者接受了10倍于静脉(TV)过量使用的Pentostam〜(司他葡糖酸钠)的过量使用。经验教训:对该不良事件进行了回顾,提出了五项建议:(1)在药剂师和配药技术人员的配制以及护士使用外加剂之间提供人员配备的连续性; (2)花时间确保对掺混料制备的问题进行彻底的审议; (3)使用尽职调查对混合物的计算进行双重检查; (4)了解药物并在适当时寻求澄清; (5)仔细检查标签信息。进展更新:为提高患者安全性进行了两项更改。首先,开发了一种形式,以配合复杂的IV药物的制备,包括化疗溶液和非常规IV混合物;该表格被一贯使用。其次,药房为12种常用于静脉注射剂的高风险药物开发了信息表。讨论:医疗中心已经制定了预防用药错误的程序,但是仍然发生了错误。在员工沟通,质量保证检查和产品标签中发现了缺陷。而且,护士和药剂师对新药或异常剂量药物的了解不足。

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