Lee Soojin, Yang Mi Hee, Kim Jung Sun, Cho Yoonsuk, Choi Nigh, Cho Eun Jung, Park June Dong, Choi Yu Hyeon, Choi Kyung Hee
Department of Pharmacy, Seoul National University Hospital, Seoul 03080, Korea.
College of Pharmacy, Seoul National University, Seoul 03080, Korea.
Saudi Pharm J. 2023 Sep;31(9):101704. doi: 10.1016/j.jsps.2023.101704. Epub 2023 Jul 17.
Safety and efficacy are essential in the process of disease treatment. However, off-label medication use is inevitable because various medications do not contain regulatory labels for pediatric use. We aimed to examine off-label medication use and analyze the risk factors correlated with adverse drug reactions (ADRs). This study was performed retrospectively using electronic medical data from a pediatric intensive care unit (PICU) of a tertiary hospital in Korea from July 2019 to June 2020. A total 6,183 prescribed medications from 502 PICU patients were examined in the present study. A total of 80% were infants or children, and 96.0% of them were treated with off-label medications. It was discovered that 4,778 off-label cases (77.2%) of the top 100 drugs had prescriptions with dosage (67.8%). Drugs prescribed to patients admitted to the cardiothoracic department (odds ratio [OR], 3.248; p = 0.019), total number of medications (OR, 1.116; p = 0.001), and length of PICU stay of ≥ 7 days (OR, 4.981; p = 0.008) were significantly associated with ADRs. ADRs were noted to be more severe in off-label use (p = 0.0426). For appropriate medication use, evidence regarding the safety of off-label medications is required and ultimately reflected in the official regulation.
安全性和有效性是疾病治疗过程中的关键要素。然而,由于各种药物未包含儿科用药的监管标签,所以超说明书用药难以避免。我们旨在调查超说明书用药情况,并分析与药物不良反应(ADR)相关的风险因素。本研究采用回顾性研究方法,使用了韩国一家三级医院儿科重症监护病房(PICU)2019年7月至2020年6月的电子医疗数据。本研究共检查了502名PICU患者的6183份处方药。其中80%为婴儿或儿童,且96.0%的患者接受了超说明书用药治疗。研究发现,在前100种药物的4778例超说明书用药案例中(77.2%),有剂量处方的占67.8%。心胸外科收治患者所使用的药物(优势比[OR],3.248;p = 0.019)、用药总数(OR,1.116;p = 0.001)以及PICU住院时间≥7天(OR,4.981;p = 0.008)与ADR显著相关。超说明书用药时的ADR更为严重(p = 0.0426)。为了合理用药,需要有关超说明书用药安全性的证据,并最终反映在官方规定中。