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Description of an Innovative Pediatric Individualized Therapeutics Clinic: Working toward Precision Drug Therapy

机译:创新的儿科个体化治疗诊所的描述:致力于精准药物治疗

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摘要

The GOLDILOKs® (Genomic and Ontogeny-Linked Dose Individualization and cLinical Optimization for KidS) Clinic aims to provide families and physicians with data to make more informed decisions with regard to pharmacological therapy by using innovative therapy and genomic technologies. The objectives are two-fold: (1) To describe the utility of the GOLDILOKs® Clinic to referring prescribers by evaluating the type of referrals made to the GOLDILOKs® Clinic and (2) to assess the most often utilized technologies (e.g., genotyping) completed to formulate therapy recommendations. Patient data from July 2010 to June 2016 was retrospectively reviewed following Institutional Review Board (IRB) approval. The GOLDILOKs® Clinic evaluated 306 patients and had increases in annual referrals from 14 in 2010–2011 to 84 in 2016–2017. The children that were referred were predominately Caucasian (82%) and male (59%) with an average age of 12.4 ± 5.9 years. Subspecialty versus primary care referrals accounted for 82% and 18% of referrals, respectively. Adverse drug reactions (n = 166) and poor medication response (n = 179) were the major reasons for referral. However, it must be noted that patients could have multiple reasons for referral. Pharmacogenetic results were extensively used to provide guidance for future therapy in patients with medication-related problems. Genotyping of drug metabolizing enzymes and drug target receptors was performed in 221 patients (72.2%). Recommendations were fully accepted by 63% and partially accepted by 22% of internal provider referrals.
机译:GOLDILOKs ®(KidS的基因组学和个体发育相关剂量个体化和临床优化)诊所旨在通过创新治疗和基因组技术为家庭和医生提供有关药物治疗方面更明智的决策的数据。目标有两个:(1)通过评估对GOLDILOKs ®诊所的转诊类型,来描述GOLDILOKs ®诊所对转诊处方者的效用,以及( 2)评估完成以制定治疗建议的最常用技术(例如基因分型)。在机构审查委员会(IRB)批准后,对2010年7月至2016年6月的患者数据进行了回顾性审查。 GOLDILOKs ®诊所对306例患者进行了评估,其每年转诊的人数从2010-2011年的14人增加到2016-2017年的84人。被推荐的孩子主要是白种人(82%)和男孩(59%),平均年龄为12.4±5.9岁。专科转诊与基层医疗转诊分别占转诊的82%和18%。药物不良反应(n = 166)和药物不良反应(n = 179)是转诊的主要原因。但是,必须注意,患者可能有多种转诊原因。药物遗传学结果被广泛用于为药物相关问题患者的未来治疗提供指导。 221例患者(72.2%)进行了药物代谢酶和药物靶受体的基因分型。内部提供者推荐中的63%完全接受了建议,22%的内部推荐中部分接受了建议。

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