Department of Pharmacy, China-Japan Union Hospital of Jilin University, Changchun, China.
BMC Health Serv Res. 2022 Jul 19;22(1):925. doi: 10.1186/s12913-022-08320-8.
In China, 85.4% of adverse drug reactions (ADRs) are spontaneously reported by healthcare facilities. As a result, many ADRs are not reported due to lack of mandatory reporting requirements. As healthcare professionals, clinical pharmacists (CPhs) serve as a bridge between clinical work and medication and ensure rational drug use. In China, A team of CPhs implemented an intervention for ADRs reporting, with the goal of improving the number of ADRs reports, the number of unreported ADRs, and the standardized reporting rate.
On June 01, 2015, a team of CPhs implemented an intervention for ADRs reporting at a Grade A, Class 3 hospital in China. The drug review catalogue (DRC) was used to screen physician orders for having visible symptoms of ADRs across departments, pooled the ADRs, and submitted them to the Center for Advanced Drug Monitoring (CNCAM). We retrospectively analysed the effect of a CPhs ADRs reporting intervention on the number of clinical ADRs reports, the number of unreported ADRs, and the standardized reporting rate over a 9-year period by interrupted time series (ITS). The method was implemented at the hospital on June 1, 2015, and a segmented regression model was used to analyse the data from January 1, 2010, to December 31, 2019.
After the CPhs ADRs reporting intervention, the number of inpatient ADRs reports submitted to the CNCAM immediately increased by approximately 63 (62.658, P < 0.01) and then decreased by approximately 1 (0.701, P = 0.000151 < 0.01) per month afterward; the number of unreported ADRs was immediately reduced by approximately 44 (44.091, P < 0.01) and remained largely unchanged over time (P > 0.05); the standardized ADRs reporting rate per month immediately increased by 63.634% (P < 0.01) and remained largely unchanged over time (P > 0.05).
The CPhs ADRs reporting intervention had an immediate effect on improving ADRs reporting, which highlights the severity of ADRs underreporting in Chinese hospitals. The method is practical and should be used more widely in clinical practice. For example, the method can adjust and establish a DRC catalog that meets the actual situation of the implementing hospital based on the hospital's drug use habits and has the characteristics of good adaptability. However, it does have some limitations; for example, it may be difficult to detect early ADRs without visible symptoms.
在中国,85.4%的药品不良反应(ADR)是由医疗机构自发报告的。因此,由于缺乏强制性报告要求,许多 ADR 并未报告。作为医疗保健专业人员,临床药师(CPhs)充当临床工作与用药之间的桥梁,确保合理用药。在中国,一组 CPhs 实施了一项针对 ADR 报告的干预措施,目的是提高 ADR 报告数量、未报告 ADR 数量和标准化报告率。
2015 年 6 月 1 日,一组 CPhs 在一家中国三级甲等医院实施了一项针对 ADR 报告的干预措施。使用药物审查目录(DRC)筛查各科室具有 ADR 可见症状的医师医嘱,汇总 ADR 并提交给国家药品不良反应监测中心(CNCAM)。我们通过中断时间序列(ITS)回顾性分析了 9 年来 CPhs ADR 报告干预对临床 ADR 报告数量、未报告 ADR 数量和标准化报告率的影响。该方法于 2015 年 6 月 1 日在医院实施,并使用分段回归模型分析了 2010 年 1 月 1 日至 2019 年 12 月 31 日的数据。
实施 CPhs ADR 报告干预后,提交给 CNCAM 的住院患者 ADR 报告数量立即增加了约 63 份(62.658,P<0.01),此后每月减少约 1 份(0.701,P=0.000151<0.01);未报告的 ADR 数量立即减少了约 44 份(44.091,P<0.01),此后基本保持不变(P>0.05);每月的标准化 ADR 报告率立即增加了 63.634%(P<0.01),此后基本保持不变(P>0.05)。
CPhs ADR 报告干预措施对提高 ADR 报告具有立即影响,突出了中国医院 ADR 漏报的严重性。该方法实用,应在临床实践中更广泛地使用。例如,可以根据医院的用药习惯和具有良好适应性的特点,调整和建立符合实施医院实际情况的 DRC 目录。然而,它确实存在一些局限性;例如,对于没有明显症状的早期 ADR,可能难以检测到。