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P100?A practical framework for the assessment of risks and benefits of off-label prescribing in paediatrics (ARBOP-P)

机译:P100-评估儿科处方外处方风险和益处的实用框架(ARBOP-P)

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Background Guidelines for off-label prescribing are emerging.sup1–6/sup However, these guidelines do not provide practical guidance to assess the risk benefit balance and select the right paediatric dose We, therefore, aimed to develop a practical framework to guide paediatric healthcare professionals to assess the risks and benefits of off-label use. Methods We have reviewed available literature on the suggested criteria for appropriate off-label use and evaluated these criteria for relevance in paediatrics. For guidance on dose-selection we searched for regulatory guidance on paediatric drug development. Next, the literature was searched for strategies that can be applied to assess the risks and benefits of off-label use. Based on literature findings a framework was proposed to provide practical guidance to physicians for off-label prescribing. Finally, the framework was applied to a case. Results The following conditions for appropriate off-label use were identified based on available literature: 1. Medical need for off-label use . 2. Off-label use is based on ‘high quality evidence’ . As ‘high quality evidence’ in paediatrics is often lacking-, we propose to replace the need for high quality evidence by a positive risk-benefit assessment based on available evidence. 3. Parents and patients are informed . This is not feasible for every single drug prescribed off-label, we propose a graded approach 4. The outcomes of off-label use are followed up . The PROACT-URL frameworksup7/sup for decision-making as well as the FDA paediatric decision treesup8/sup seem helpful tools to guide decisions in real-life practice. Conclusion We identified important aspects and tools to develop a framework (ARBOP-P) to guide healthcare professionals on how to systematically assess and balance the benefits and risks for off-label use, including dose selection, to ultimately optimize efficacy and safety of paediatric off-label prescribing. References Frattarelli DA, Galinkin JL, Green TP, et al. Off-label use of drugs in children. Pediatrics 2014;133:563–7Online. Dooms M, Killick J. Off-label use of medicines: The need for good practice guidelines. Int J Risk Saf Med . 2017;29:17–23Online. Gazarian M, Kelly M, McPhee JR, Graudins LV, Ward RL, Campbell TJ. Off-label use of medicines: consensus recommendations for evaluating appropriateness. Med J Aust 2006;185:544–8Online. Largent EA, Miller FG, Pearson SD. Going off-label without venturing off-course: evidence and ethical off-label prescribing. Arch Intern Med 2009;169:1745–7Online. Ansani N, Sirio C, Smitherman T, et al. Designing a strategy to promote safe, innovative off-label use of medications. Am J Med Qual 2006;21:255–61Online. Weda M, Hoebert J, Vervloet M, et al. Study on the off-label use of medicinal products in the European Union.: www.ec.europa.com 2017. Hammond J, Keeney R, Raiffa H. Smart Choices:A practical guide to making better decisions. Boston , MA.: Harvard Business School Press.; 2002. Dunne J, Rodriguez WJ, Murphy MD, et al. Extrapolation of adult data and other data in pediatric drug-development programs.
机译:1-6 然而,这些指南并未提供评估风险收益平衡和选择正确的儿科剂量的实用指南。因此,我们旨在开发一种实用的指南。框架,指导儿科医疗保健专业人员评估标签外使用的风险和益处。方法我们回顾了有关适当标签外使用的建议标准的现有文献,并评估了这些标准与儿科的相关性。对于剂量选择的指导,我们搜索了儿科药物开发的监管指导。接下来,在文献中搜索了可用于评估标签外使用风险和收益的策略。根据文献研究结果,提出了一个框架,为医生提供标签外处方的实用指导。最后,该框架适用于一个案例。结果根据现有文献,确定了适当使用非标签的以下条件:1.医疗上对非标签使用的需求。 2.标签外使用基于“高质量证据”。由于儿科常常缺乏“高质量证据”,因此,我们建议根据现有证据通过积极的风险效益评估来代替对高质量证据的需求。 3.告知父母和患者。对于处方药以外的每一种药物,这都是不可行的,我们提出了一种分级方法。4,对处方药的使用结果进行随访。用于决策的PROACT-URL框架 7 以及FDA儿科决策树 8 似乎是指导现实生活中决策的有用工具。结论我们确定了开发框架(ARBOP-P)的重要方面和工具,以指导医疗保健专业人员如何系统地评估和平衡非处方使用(包括剂量选择)的益处和风险,以最终优化小儿非处方药的疗效和安全性标签处方。参考文献Frattarelli DA,Galinkin JL,Green TP等。儿童不按规定使用药物。儿科2014; 133:563–7在线。 Dooms M,KilliickJ。药物的标签外使用:需要良好实践准则。国际风险管理科学。 2017; 29:17–23在线。 Gazarian M,Kelly M,McPhee JR,Graudins LV,Ward RL,Campbell TJ。标签外使用药物:评估适当性的共识性建议。 Med J Aust 2006; 185:544-8在线。大型EA,Miller FG,Pearson SD。不在标签范围内而不会偏离路线:证据和符合道德规范的处方。 Arch Intern Med 2009; 169:1745-7在线。 Ansani N,Sirio C,Smitherman T等。设计策略以促进安全,创新的非处方药物使用。 Am J Med Qual 2006; 21:255-61在线。 Weda M,Hoebert J,Vervloet M等。欧盟关于标签外使用药物的研究。:www.ec.europa.com2017。HammondJ,Keeney R和Raiffa H. Smart Choices:做出更好决策的实用指南。马萨诸塞州波士顿:哈佛商学院出版社。 2002。DunneJ,Rodriguez WJ,Murphy MD等。成人数据和小儿药物开发计划中的其他数据的推断。

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