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首页> 外文期刊>Drug safety: An international journal of medical toxicology and drug experience >The impact of unlicensed and off-label drug use on adverse drug reactions in paediatric patients.
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The impact of unlicensed and off-label drug use on adverse drug reactions in paediatric patients.

机译:小儿患者中未经许可和标签外使用药物对药物不良反应的影响。

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BACKGROUND AND OBJECTIVE: Many drugs that are used to treat children are either not licensed for use in paediatric patients (unlicensed) or prescribed outside the terms of the product licence (off label). The incidence of adverse drug reactions (ADRs) associated with the use of such drugs is yet to be established. This study investigates, for the first time in a German patient population, the impact of unlicensed and off-label drug use on ADRs in paediatric patients. PATIENTS AND METHODS: An 8-month prospective pharmacoepidemiological cohort-based survey was conducted on a ten-bed paediatric isolation ward at the University Hospital Erlangen-Nuremberg, Germany. All patients were intensively monitored for ADRs by a pharmacoepidemiological team. ADRs were characterised according to international classification methods. All drug prescriptions were evaluated retrospectively as to unlicensed or off-label use on the basis of the product information. RESULTS: A total of 178 patients were included in the studyand 740 drug prescriptions were given to 156 patients (median three prescriptions per patient). In 198 cases (27.7% of all prescriptions) drugs were used in either an unlicensed (n = 3) or off-label (n = 195) manner. A total of 46 ADRs were observed in 31 patients (17.4%). Patients receiving at least one unlicensed or off-label drug prescription during hospitalisation (n = 92) experienced an ADR significantly more frequently (n = 26 patients) than patients receiving only licensed drugs (n = 64 vs 5 patients). ADRs were associated with 29 (5.6%) of the 517 licensed drug prescriptions and with 12 (6.1%) of the 198 unlicensed or off-label drug prescriptions. The majority of ADRs caused by unlicensed and off-label drug use were recognised by the attending physician. However, statistical analysis revealed no significant difference in the number of licensed and unlicensed/off-label drug prescriptions causing ADRs. CONCLUSION: This study demonstrated that at a paediatric isolation ward the incidence of ADRs caused by unlicensed or off-label drug use was not significantly more than that caused by the licensed drug use. However, patients treated with unlicensed or off-label drugs were shown to possess a significantly increased risk for developing ADRs.
机译:背景与目的:许多用于治疗儿童的药物要么未获得许可用于儿科患者(未经许可),要么在产品许可的条款范围外(未标注标签)开出了处方。与使用此类药物相关的药物不良反应(ADR)的发生率尚未确定。这项研究首次在德国患者人群中调查了无证和标签外药物使用对儿科患者ADR的影响。患者和方法:在德国埃尔兰根-纽伦堡大学医院的十张病床隔离病房进行了为期8个月的前瞻性药物流行病学队列研究。药物流行病学小组对所有患者进行了ADR严格监测。根据国际分类方法对ADR进行了表征。根据产品信息,对所有药物处方进行了回顾性评估,以评估其是否未经许可或在标签外使用。结果:共纳入178例患者,对156例患者给予740剂药物处方(每位患者中位数为3剂)。在198例病例中(占所有处方的27.7%),以无执照(n = 3)或标签外(n = 195)的方式使用药物。在31例患者中共观察到46种ADR(占17.4%)。与仅接受许可药物的患者相比,住院期间接受至少一种未经许可或标签外药物处方的患者(n = 92)比接受仅许可药物的患者(n = 64 vs 5)的发生频率高得多。 ADR与517个许可药品处方中的29个(5.6%)以及198个非许可或标签外药品处方中的12个(6.1%)相关。主治医生认可了大多数由无牌和非标签使用药物引起的ADR。但是,统计分析表明,引起ADR的许可和非许可/标签外药物处方的数量没有显着差异。结论:这项研究表明,在儿科隔离病房,由无执照或标签外药物使用引起的ADR发生率并不明显高于由执照使用药物引起的ADR发生率。但是,使用未经许可或标签外药物治疗的患者显示出发生ADR的风险显着增加。

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