Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA.
Department of Anesthesiology and Pain Medicine, Seattle Children's Hospital, Seattle, WA, USA.
Pain. 2018 Feb;159(2):193-205. doi: 10.1097/j.pain.0000000000001104.
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 the 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.
需要进行临床试验,以测试各种儿科年龄组的镇痛药的安全性和疗效,从而避免将成人数据不适当地外推至儿童。然而,选择急性疼痛模型和试验设计属性,以最大限度地提高各儿科年龄组的检测灵敏度,仍然存在问题。用于成人药物治疗试验的急性疼痛模型不能直接应用于儿科年龄组-新生儿、婴儿、学步儿童、儿童和青少年。在设计用于测试急性疼痛的镇痛治疗的试验时,必须考虑婴儿和儿童代谢酶的发育成熟。必须选择基于认知成熟度和行为范围的评估工具作为疗效指标。在镇痛、麻醉、成瘾临床试验转化、创新、机遇和网络(ACTION)儿科疼痛研究联盟共识会议上,对用于治疗新生儿、婴儿、学步儿童、儿童和青少年急性疼痛的镇痛药物的临床试验模型和设计进行了审查和讨论。基于广泛的审查和持续的讨论,作者建议采用一些急性疼痛临床试验模型和设计属性,这些模型和属性有可能改善儿科人群中镇痛药的研究。还就支持在儿科各年龄组中使用其他急性疼痛模型所需的进一步研究提供了建议。