监管机构的药物不良反应分析表明,在开始使用囊性纤维化联合调节剂疗法后,精神反应会在一段时间内增加。

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM
Jacob O'Connor, Dilip Nazareth, Dennis Wat, Kevin W Southern, Freddy Frost
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引用次数: 0

摘要

导言:尽管许多囊性纤维化患者的治疗效果有所改善,但仍有关于调节剂治疗对神经精神产生不良影响的报道。本研究旨在确定现有 CFTR 调节剂药物不良反应(ADR)报告的时间关联:方法包括通过访问交互式药物分析档案(iDAPs)分析英国黄卡计划的药物不良反应数据,以确定绝对计数和比例计数的时间趋势:结果:自 ETI 实施以来,在 ETI 实施前和 ETI 实施后,报告的精神疾病 ADR 的绝对数量有所增加,精神疾病 ADR 的比例也有显著的统计学增长:结论:在 EETI 后,精神科 ADR 是通过黄卡计划报告的最常见 ADR。尽管机制尚不明确,但对 CFTR 调节剂治疗的精神影响进行咨询和监测具有重要的临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory adverse drug reaction analyses support a temporal increase in psychiatric reactions after initiation of cystic fibrosis combination modulator therapies.

Introduction: Despite improved outcomes for many people with cystic fibrosis, there have been reports of adverse neuropsychiatric effects of modulator therapy. The aim of this research is to define temporal associations in adverse drug reaction (ADR) reports for available CFTR modulators.

Methods: Methods include an analysis of the UK Yellow Card Scheme data for ADRs through accessing interactive Drug Analysis Profiles (iDAPs) to define temporal trends in absolute and proportional counts.

Results: Since the introduction of ETI, there has been an increase in the absolute number of psychiatric ADRs reported as well as a statistically significant increase in the proportion of psychiatric ADRs in the pre-ETI and post-ETI periods.

Conclusion: In the post-ETI period, psychiatric ADRs are the most prevalent ADR reported via the Yellow Card scheme. Despite an unclear mechanism, there is significant clinical relevance in counselling and monitoring regarding psychiatric effects of CFTR modulator therapy.

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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
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