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接受聚乙二醇非格司亭治疗患者的病历摘要中的处方模式:欧洲一项试点研究

Prescribing patterns from medical chart abstraction of patients administered lipegfilgrastim: a pilot study in Europe.

作者信息

Kaplan Sigal, Lang Nicole, Gasparic Maja, Rainville Carolyn, Haralabopoulos George, Borroni Emanuele

机构信息

Teva Pharmaceutical Industries Ltd, Netanya, Israel.

Ratiopharm GmbH (an affiliate of Teva Pharmaceuticals Europe BV), Ulm, Germany.

出版信息

J Drug Assess. 2019 May 3;8(1):70-76. doi: 10.1080/21556660.2019.1604376. eCollection 2019.

Abstract

The objective of this pilot study was to explore the feasibility of conducting a drug utilization study of lipegfilgrastim in Europe using medical records and to examine the pattern of lipegfilgrastim on-label and off-label use. Data on lipegfilgrastim use between September 2014 and April 2017 were abstracted from medical records by two independent medical abstractors. Lipegfilgrastim indication was categorized either as on-label or as one of four types of off-label (I-IV) according to pre-defined criteria. An inter-rater reliability analysis was conducted to measure the degree of abstractor agreement for on-label and off-label use. Information from 46 medical records was abstracted. Lipegfilgrastim use during the first chemotherapy treatment cycle was mostly indicated for prevention of neutropenia (82.6% of patients). On-label use was documented in 42 patients (91.3%), while off-label use was documented in two patients (4.3%); all events of off-label use were attributed to use with non-cytotoxic drugs. The remaining two patients (4.3%) had missing data. Overall agreement between the abstractors was high (91.6%). For three types (Types I-III) of off-label use, the kappa values suggested a perfect agreement ( = 1). For Type IV off-label use (use in patients treated with non-cytotoxic drugs),  = 0, suggesting a poor agreement. While recruitment was challenging, the results of this pilot study confirm the feasibility and availability of medical records and the use of pharmacists as abstractors to assess on- and off-label use of lipegfilgrastim. Lipegfilgrastim was mainly prescribed according to the approved indications.Key pointsFindings from this pilot study confirm the feasibility and availability of medical records and the use of pharmacists as abstractors to assess on-label and off-label use of lipegfilgrastim in routine clinical practice.Lipegfilgrastim was mainly prescribed according to the approved indications, and the proportion of off-label use was low.The high inter-rater agreement between the two abstractors suggests that one abstractor is sufficient for conducting chart abstraction of on- and off-label use.Additional data abstraction sources other than pharmacists will need to be identified to improve response rate and center recruitment.Findings from this pilot study are important for the successful planning and execution of subsequent drug utilization studies.

摘要

这项初步研究的目的是探讨利用医疗记录在欧洲开展聚乙二醇化重组人粒细胞刺激因子药物利用研究的可行性,并研究聚乙二醇化重组人粒细胞刺激因子的标签内和标签外使用模式。2014年9月至2017年4月期间聚乙二醇化重组人粒细胞刺激因子的使用数据由两名独立的医学摘要提取员从医疗记录中提取。根据预定义标准,聚乙二醇化重组人粒细胞刺激因子的适应症被分类为标签内或四种标签外类型(I-IV)之一。进行了评分者间可靠性分析,以衡量摘要提取员在标签内和标签外使用方面的一致程度。提取了46份医疗记录的信息。首次化疗治疗周期中聚乙二醇化重组人粒细胞刺激因子的使用主要用于预防中性粒细胞减少(82.6%的患者)。42例患者(91.3%)有标签内使用记录,2例患者(4.3%)有标签外使用记录;所有标签外使用事件均归因于与非细胞毒性药物联合使用。其余2例患者(4.3%)数据缺失。摘要提取员之间的总体一致性较高(91.6%)。对于三种类型(I-III型)的标签外使用,kappa值表明完全一致(κ=1)。对于IV型标签外使用(在接受非细胞毒性药物治疗的患者中使用),κ=0,表明一致性较差。虽然招募具有挑战性,但这项初步研究的结果证实了医疗记录的可行性和可用性,以及利用药剂师作为摘要提取员来评估聚乙二醇化重组人粒细胞刺激因子的标签内和标签外使用情况。聚乙二醇化重组人粒细胞刺激因子主要根据批准的适应症开具处方。要点这项初步研究的结果证实了医疗记录的可行性和可用性,以及利用药剂师作为摘要提取员在常规临床实践中评估聚乙二醇化重组人粒细胞刺激因子标签内和标签外使用情况的可行性。聚乙二醇化重组人粒细胞刺激因子主要根据批准的适应症开具处方,标签外使用比例较低。两名摘要提取员之间较高的评分者间一致性表明,一名摘要提取员足以进行标签内和标签外使用的图表摘要。需要确定药剂师以外的其他数据提取来源,以提高回复率和中心招募率。这项初步研究的结果对于后续药物利用研究的成功规划和实施具有重要意义。

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