DeWitt Esi M, Sherry David D, Cron Randy Q
Children's Hospital of Philadelphia, and the University of Pennsylvania School of Medicine, 3615 Civic Center Boulevard, Philadelphia, PA 19104-4318, USA.
J Clin Rheumatol. 2005 Feb;11(1):21-33. doi: 10.1097/01.rhu.0000152151.12999.76.
Treatment of children with rheumatic diseases has advanced with novel therapeutics and the use of early aggressive treatment to achieve better long-term functional outcome. Many of the current treatments in pediatric rheumatology are based on studies in adults on medications without U.S. Food and Drug Administration labeling for pediatric use. This is not ideal because the pharmacokinetics (absorption, distribution, metabolism, and elimination) of many medications when used in children vary according to age, somatic growth, sexual maturity, and ontogeny of drug-metabolizing enzymes. Special dosing, administration considerations, and toxicity screening are reviewed for the more commonly used medications. Vaccinations for children on antirheumatic drugs are also discussed. Continued study of the long-term impact of medications and biologic treatments on children is necessary, but given the paucity of children with rheumatic diseases, this will require multicentered trials and collaborations. Lastly, this article reviews recent regulatory and legislative action on pediatric drug testing. Passage of the Pediatric Research Equity Act of 2003, which requires testing of pharmaceuticals in children, will facilitate more rational use of drugs in pediatric rheumatic diseases in the future.
随着新型疗法的出现以及早期积极治疗的应用,风湿性疾病患儿的治疗取得了进展,以实现更好的长期功能预后。儿科风湿病学目前的许多治疗方法都是基于针对成人药物的研究,这些药物未获得美国食品药品监督管理局的儿科用药标签。这并不理想,因为许多药物在儿童中使用时的药代动力学(吸收、分布、代谢和排泄)会因年龄、身体生长、性成熟度以及药物代谢酶的个体发育而有所不同。本文对更常用药物的特殊给药方法、用药注意事项及毒性筛查进行了综述。还讨论了抗风湿药物治疗患儿的疫苗接种问题。有必要继续研究药物和生物治疗对儿童的长期影响,但鉴于患风湿性疾病的儿童数量较少,这将需要多中心试验与合作。最后,本文回顾了近期儿科药物测试的监管和立法行动。2003年《儿科研究公平法案》的通过要求对儿童进行药物测试,这将有助于未来更合理地使用儿科风湿性疾病药物。