Impact of Pharmacogenomics on Pediatric Psychotropic Medication Prescribing in an Ambulatory Care Setting.

IF 1.5 4区 医学 Q2 PEDIATRICS
Erica Tonti, Yee Ming Lee, Nathan Gruenke, Janie Ferren, Danielle L Stutzman
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引用次数: 0

Abstract

Objective: Evidence for pharmacogenomic (PGx) guided treatment in child and adolescent psychiatry is growing. This study evaluated the impact of PGx testing on psychotropic medication prescribing in an ambulatory child and adolescent psychiatry and a developmental pediatrics clinic. Methods: This was a single-center, retrospective, descriptive analysis of patients who underwent PGx testing between January 2015 and October 2022 at a child and adolescent psychiatry clinic or developmental pediatrics clinic. The primary outcome was the proportion of patients with at least one psychotropic medication modification made 6-month posttesting that could be attributed to CYP2C19, CYP2D6, HLA-B*15:02, or HLA-A*31:01. Secondary outcomes included reason for testing, types of therapeutic modifications made, and whether the therapeutic modifications concorded with PGx guidelines. Results: A total of 193 patients were analyzed. The average age was 10 ± 4 years old, 60% were male, 78% were Caucasian. Sixty-eight percent had a primary diagnosis of a neurodevelopmental disorder, namely autism spectrum disorder (51%), and attention-deficit/hyperactivity disorder (14%). The reasons for PGx testing included medication inefficacy (34%), medication intolerance (20%), and family request (19%). At the time of PGx testing, 37% of patients were taking ≥1 psychotropic medication with PGx annotation. Overall, 35 PGx-related therapeutic modifications were made in 32 (17%) patients. These included continuing current PGx medication (6.2%) and starting PGx medication (5.2%). These modifications mainly involved antidepressants. Out of these 35 PGx-related therapeutic modifications, 94% were concordant with PGx guidelines. Among 29 patients who were prescribed at least one CYP2D6 inhibitor, 25 (86%) underwent CYP2D6 phenoconversion. Conclusions: It is critical to apply pediatric age-specific considerations when utilizing PGx testing in child and adolescent psychiatry. PGx testing stewardship could provide a framework to guide the clinical utility of PGx in a pediatric population with mental health conditions, including neurodevelopmental disorders.

药物基因组学对非住院医疗机构儿科精神药物处方的影响。
目的:在儿童和青少年精神病学中,药物基因组学(PGx)指导治疗的证据越来越多。本研究评估了 PGx 检测对门诊儿童与青少年精神病学诊所和发育儿科诊所精神药物处方的影响。研究方法这是一项单中心、回顾性、描述性分析,对象是2015年1月至2022年10月期间在儿童与青少年精神病学诊所或发育儿科诊所接受PGx检测的患者。主要结果是检测后6个月内至少有一项精神药物调整可归因于CYP2C19、CYP2D6、HLA-B*15:02或HLA-A*31:01的患者比例。次要结果包括检测原因、治疗调整类型以及治疗调整是否符合 PGx 指南。结果:共分析了 193 名患者。平均年龄为 10 ± 4 岁,60% 为男性,78% 为白种人。68%的患者主要诊断为神经发育障碍,即自闭症谱系障碍(51%)和注意力缺陷/多动障碍(14%)。进行 PGx 检测的原因包括药物治疗无效(34%)、药物不耐受(20%)和家人要求(19%)。在进行 PGx 检测时,37% 的患者正在服用≥1 种带有 PGx 注释的精神药物。总体而言,32 名患者(17%)进行了 35 次与 PGx 相关的治疗调整。其中包括继续服用目前的 PGx 药物(6.2%)和开始服用 PGx 药物(5.2%)。这些调整主要涉及抗抑郁药物。在这 35 项与 PGx 相关的治疗调整中,94% 符合 PGx 指南。在处方至少一种 CYP2D6 抑制剂的 29 名患者中,25 人(86%)进行了 CYP2D6 表观转换。结论:在儿童和青少年精神病学中使用 PGx 检测时,应用儿科特定年龄的考虑因素至关重要。PGx检测管理可提供一个框架,指导PGx在患有精神疾病(包括神经发育障碍)的儿科人群中的临床应用。
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来源期刊
CiteScore
3.60
自引率
5.30%
发文量
61
审稿时长
>12 weeks
期刊介绍: Journal of Child and Adolescent Psychopharmacology (JCAP) is the premier peer-reviewed journal covering the clinical aspects of treating this patient population with psychotropic medications including side effects and interactions, standard doses, and research on new and existing medications. The Journal includes information on related areas of medical sciences such as advances in developmental pharmacokinetics, developmental neuroscience, metabolism, nutrition, molecular genetics, and more. Journal of Child and Adolescent Psychopharmacology coverage includes: New drugs and treatment strategies including the use of psycho-stimulants, selective serotonin reuptake inhibitors, mood stabilizers, and atypical antipsychotics New developments in the diagnosis and treatment of ADHD, anxiety disorders, schizophrenia, autism spectrum disorders, bipolar disorder, eating disorders, along with other disorders Reports of common and rare Treatment Emergent Adverse Events (TEAEs) including: hyperprolactinemia, galactorrhea, weight gain/loss, metabolic syndrome, dyslipidemia, switching phenomena, sudden death, and the potential increase of suicide. Outcomes research.
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