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Clinical trial designs and models for analgesic medications for acute pain in neonates infants toddlers children and adolescents: ACTTION recommendations

机译:新生儿婴儿学步儿童儿童和青少年的急性疼痛止痛药的临床试验设计和模型:ACTTION建议

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摘要

Clinical trials to test the safety and efficacy of analgesics across all pediatric age cohorts are needed to avoid inappropriate extrapolation of adult data to children. However, the selection of acute pain models and trial design attributes to maximize assay sensitivity, by pediatric age cohort, remains problematic. Acute pain models used for drug treatment trials in adults are not directly applicable to the pediatric age cohorts – neonates, infants, toddlers, children, and adolescents. Developmental maturation of metabolic enzymes in infants and children must be taken into consideration when designing trials to test analgesic treatments for acute pain. Assessment tools based on levels of cognitive maturation and behavioral repertoire must be selected as outcome measures. Models and designs of clinical trials of analgesic medications used in the treatment of acute pain in neonates, infants, toddlers, children, and adolescents were reviewed and discussed at an Analgesic, Anesthetic, and Addiction Clinical Trial Translations, Innovations, Opportunities, and Networks (ACTTION) Pediatric Pain Research Consortium consensus meeting. Based on extensive reviews and continuing discussions, the authors recommend a number of acute pain clinical trial models and design attributes that have the potential to improve the study of analgesic medications in pediatric populations. Recommendations are also provided regarding additional research needed to support the use of other acute pain models across pediatric age cohorts.
机译:需要进行临床试验以测试所有儿科年龄组的镇痛药的安全性和有效性,以避免将成人数据不适当地推算给儿童。然而,按儿童年龄组选择急性疼痛模型和试验设计属性以最大化测定灵敏度仍然是有问题的。成人药物治疗试验中使用的急性疼痛模型不适用于婴儿,新生儿,婴儿,学步儿童,儿童和青少年。在设计试验镇痛药物治疗急性疼痛的试验时,必须考虑婴儿和儿童体内代谢酶的发育成熟。必须选择基于认知成熟度和行为能力水平的评估工具作为结果指标。在“止痛,麻醉和成瘾临床试验翻译,创新,机会和网络”中对用于新生儿,婴儿,学步车,儿童和青少年的急性疼痛的止痛药临床试验的模型和设计进行了回顾和讨论( ACTTION)儿童疼痛研究联盟共识会议。基于广泛的评论和持续的讨论,作者推荐了许多急性疼痛临床试验模型和设计属性,这些模型和设计属性可能会改善小儿人群镇痛药物的研究。还提供了一些建议,以支持需要在儿科年龄组中使用其他急性疼痛模型的其他研究。

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