Diagnosis and treatment of ADHD in pediatric patients during the first year of elexacaftor/tezacaftor/ivacaftor.

IF 2.7 3区 医学 Q1 PEDIATRICS
Pediatric Pulmonology Pub Date : 2024-12-01 Epub Date: 2024-09-06 DOI:10.1002/ppul.27246
Kimberly Pasley, Mary Lynn Dell, Anne May
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引用次数: 0

Abstract

Background: With elexacaftor/tezacaftor/ivacaftor (ETI), children with cystic fibrosis (CwCF) are living healthier lives with a focus on typical developmental issues such as attention deficit/hyperactivity disorder (ADHD). This paper characterizes CwCF with ADHD within the first year of ETI treatment.

Methods: This retrospective, observational analysis examines a subgroup of CwCF participating in a longitudinal study obtaining prospective data regarding the impact of ETI on mental health. All participants started on ETI were offered enrollment, with rolling enrollment as younger children became eligible. Clinical data regarding CF symptoms, mental health diagnoses, medications, changes in mental health symptoms and BMI were collected via chart review.

Results: Before ETI, ADHD diagnoses were identified in 21 children; an additional 3 were diagnosed within the first year. Eleven children were treated with ADHD medication at ETI initiation; nine children did not use ADHD medication during the study period. In the 1-year follow-up, four children started ADHD medication. Of the 11 who started ETI on ADHD medication, five increased doses, three changed medications and/or decreased dose, and one discontinued medication. Two children experienced no changes to their treatment.

Conclusion: Most CwCF on ADHD medication underwent changes in dosing and/or medication after ETI initiation. Several children were diagnosed with ADHD after starting ETI. The role of ETI in these recent diagnoses and treatment plans is unclear. Given the prevalence of pediatric ADHD diagnoses and the medication changes that were needed by this population, additional research is warranted to clarify the relationship between ETI and ADHD in CwCF.

在使用 elexacaftor/tezacaftor/ivacaftor 的第一年,诊断和治疗儿童多动症。
背景:通过使用 elexacaftor/tezacaftor/ivacaftor (ETI),囊性纤维化(CwCF)患儿过上了更健康的生活,并关注典型的发育问题,如注意力缺陷/多动症(ADHD)。本文描述了接受 ETI 治疗第一年内患有多动症的囊性纤维化儿童的特征:这项回顾性观察分析研究的对象是参与纵向研究的 CwCF 亚群,该研究获得了有关 ETI 对心理健康影响的前瞻性数据。所有开始接受 ETI 治疗的参试者都获得了入学机会,随着年龄的降低,符合条件的参试者也会滚动入学。通过病历审查收集有关 CF 症状、精神健康诊断、药物、精神健康症状变化和体重指数的临床数据:在 ETI 之前,21 名儿童被诊断出患有多动症;另外 3 名儿童在第一年内被诊断出患有多动症。11 名儿童在 ETI 开始时接受了多动症药物治疗;9 名儿童在研究期间没有使用多动症药物。在为期 1 年的随访中,有 4 名儿童开始接受 ADHD 药物治疗。在开始 ETI 时接受 ADHD 药物治疗的 11 名儿童中,有 5 名儿童增加了药物剂量,3 名儿童更换了药物和/或减少了药物剂量,1 名儿童停止了药物治疗。两名儿童的治疗没有变化:结论:大多数患有多动症的儿童和青少年在开始接受 ETI 治疗后,剂量和/或药物都发生了变化。多名儿童在开始接受 ETI 治疗后被诊断为多动症。ETI 在这些最新诊断和治疗计划中的作用尚不清楚。考虑到小儿多动症诊断的普遍性以及该人群所需的药物变化,有必要开展更多研究,以阐明 ETI 与 CwCF 多动症之间的关系。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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