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作 者:唐慕菲[1] 张保国[2] 沈芸竹 汤翠菊[2] 陈晶[2] 石文娟 潘希丁 TANG Mufei;ZHANG Baoguo;SHEN Yunzhu;TANG Cuiju;CHEN Jing;SHI Wenjuan;PAN Xiding(Department of Pharmacy,Nanjing First Hospital,Nanjing Medical University,Nanjing,Jiangsu 210006,China;Department of Oncology,Nanjing First Hospital,Nanjing Medical University,Nanjing,Jiangsu 210006,China)
机构地区:[1]南京医科大学附属南京医院(南京市第一医院)药学部,江苏南京210006 [2]南京医科大学附属南京医院(南京市第一医院)肿瘤内科,江苏南京210006
出 处:《安徽医药》2025年第1期196-199,共4页Anhui Medical and Pharmaceutical Journal
基 金:江苏省药学会-正大天晴医院药学科研项目(Q202214)。
摘 要:目的针对替雷利珠单抗建立药物利用评价(drug use evaluation,DUE)标准,对南京医科大学附属南京医院替雷利珠单抗使用情况进行评价,为临床合理用药提供参考依据。方法根据替雷利单抗药品说明书、临床相关指导原则、诊疗指南和专家共识等,建立替雷利珠单抗DUE标准,依据标准回顾性分析评价2023年1—9月南京医科大学附属南京医院使用替雷利珠单抗的住院病人用药情况。结果替雷利珠单抗DUE标准包含14个指标。纳入96例病人,共使用替雷利珠单抗687次。体力评分、器官功能和实验室指标、给药剂量、给药途径、输注时间、给药频次和疗效评估合理率100%;禁忌证、溶媒种类和用量合理率98.96%;联合用药合理率97.92%;药物相互作用合理率96.88%;给药顺序和时间合理率84.38%;适应证合理率80.21%;不良反应监测与处理合理率39.58%。结论建立并应用替雷利珠单抗DUE标准可发现用药过程中的不合理现象,为临床安全用药提供参考依据。Objective To establish a drug use evaluation(DUE)standard for the use of tislelizumab in Nanjing First Hospital,Nanjing Medical University,and to evaluate the use of tislelizumab in order to provide a reference basis for rational clinical medication.Methods Based on the drug instructions,clinical guidelines for tumor diagnosis and treatment,and expert consensus,as well as the clinical application guidelines for new anti-tumor drugs,a DUE standard for tislelizumab was established.Based on the standard,a retrospective analysis was conducted to evaluate the medication use of tislelizumab in hospitalized patients from January 2023 to September 2023.Results The DUE standard for tislelizumab included 14 indicators.A total of 96 patients were included and a total of 687 doses of tislelizumab were used.The reasonable rate of physical fitness score,organ function and laboratory indicators,dosage,route of administration,infusion time,frequency of administration,and efficacy evaluation was 100%;The reasonable rate of contraindications,types of solvents,and dosage was 98.96%;The reasonable rate of combination therapy was 97.92%;The reasonable rate of drug interaction was 96.88%;The reasonable rate of administration sequence and time was 84.38%;The reasonable rate of indications was 80.21%;The reasonable rate of adverse reaction monitoring and treatment was 39.58%.Conclusion Establishing and applying the DUE standard for tislelizumab can detect unreasonable phenomena during the medication process and provide reference for safe clinical use.
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