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一项关于减少化疗日间病房处方错误方法的初步研究——药师审核流程中需要考虑的方面。

A pilot study about methods to reduce prescription errors in a chemotherapy day unit - Aspects to consider in pharmacist verification process.

机构信息

HUS Pharmacy, University of Helsinki and Helsinki University Hospital, Uusimaa, Finland.

Clinical Pharmacy Group, Division of Pharmacology and Pharmacotherapy, Faculty of Pharmacy, University of Helsinki, Finland.

出版信息

J Oncol Pharm Pract. 2023 Mar;29(2):276-282. doi: 10.1177/10781552211066500. Epub 2021 Dec 22.

Abstract

INTRODUCTION

Prescribing errors can happen unintentionally during the prescribing process, or when choosing a treatment therapy. Prescribing errors have the highest prevalence amongst common error types related to chemotherapy medication in outpatient settings. According to the Joint Commission International (JCI), prescriptions should be reviewed for appropriateness by someone else than the prescriber or practitioner to prevent medication errors.

AIM

The study was aimed to map out the existing type and amount of occurring deviations in prescribing and to clarify the current chemotherapy prescribing practices at the Comprehensive Cancer Center at Helsinki University Hospital. Similar research has not been published in Finland before.

METHODS AND PATIENTS

The researcher selected patients randomly from the daily outpatient attendance list following a predetermined numerical order. Data was collected by conducting a medication verification review in line with the JCI guidance by a clinical pharmacist the day before the patient's clinic appointment using the available medical documentation. A clinical pharmacist evaluated findings from prescriptions and contacted an oncologist if the findings were considered clinically significant.

RESULTS

A clinical pharmacist verified prescriptions from 101 patients for appropriateness and found discrepancies in four percent of the prescriptions ( = 4/101). The oncologist approved 50 percent of the suggested amendments by the pharmacist as clinically significant ( = 2/4). The study revealed that patient's regular home medications were not always correctly recorded into the database, so verification of medicine interactions could not be trusted as completely accurate. It took on average 16 min per patient to perform a medication verification review. The process was slowed down by the lack of detailed enough protocols for this purpose and the current patient care record system not having structural formatting of data entry.

CONCLUSIONS

Verification of prescriptions provides a tool to identify prescribing discrepancies and to prevent unintended medication errors affecting patients. The development of detailed protocols and guidelines, as well as an appropriate training program, would support pharmacists in compiling clinical medication reviews for chemotherapy patients. More research is needed to further develop the operating model in Finland. Information gathered from this study can be used for identifying training requirements.

摘要

简介

在开处方过程中或选择治疗方案时,可能会无意中出现开处方错误。在门诊环境中,与化疗药物相关的常见错误类型中,开处方错误的发生率最高。根据国际联合委员会(JCI)的规定,应让开处方者以外的其他人审查处方的适宜性,以防止药物错误。

目的

本研究旨在阐明赫尔辛基大学医院综合癌症中心目前的化疗开处方实践,并阐明目前存在的开处方类型和数量的偏差。在芬兰,以前没有发表过类似的研究。

方法和患者

研究人员按照预定的数字顺序,从每日门诊就诊名单中随机选择患者。在患者预约就诊的前一天,临床药剂师按照 JCI 指南进行药物验证审查,收集数据,使用可用的医疗文件。临床药剂师评估处方结果,如果发现结果具有临床意义,将联系肿瘤医生。

结果

一名临床药剂师对 101 名患者的处方进行了适宜性验证,发现 4%的处方存在差异(=4/101)。药剂师建议的 50%的修改意见被肿瘤医生认为具有临床意义(=2/4)。研究表明,患者的常规家庭用药并未始终正确记录到数据库中,因此无法完全信任药物相互作用的验证结果。对每位患者进行药物验证审查平均需要 16 分钟。由于缺乏详细的目的协议以及当前的患者护理记录系统没有数据输入的结构化格式,该过程的速度减慢了。

结论

处方验证提供了一种工具,可以识别处方差异,防止影响患者的意外用药错误。详细的协议和指南的制定以及适当的培训计划将支持药剂师为化疗患者编写临床药物审查。需要进一步的研究来进一步发展芬兰的运作模式。本研究收集的信息可用于确定培训需求。

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