Current State of Clinical Care of People With Cystic Fibrosis.

IF 4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2026-04-01 DOI:10.1002/phar.70138
Cameron J McKinzie, Charissa W Kam, Paul M Beringer, Brittany A Wright, Wendy M Bullington, Sabrina Garcia, Jonathan J Grant, Rebecca S Pettit, David C Young
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引用次数: 0

Abstract

The advent of cystic fibrosis transmembrane conductance regulator (CFTR) modulators has dramatically changed the landscape of the clinical care of people with cystic fibrosis (PwCF). In particular, highly effective modulator therapy (HEMT) availability for the majority of PwCF has led to changes in pharmacotherapy regimens and clinical outcomes but has also been associated with adverse effects and drug interactions. The role of CFTR modulator therapy perinatally continues to be of great interest, related to both the mother with CF as well as the infant in utero and after birth. As the median life expectancy for PwCF continues to increase, consideration must also be given for treatment of cardiovascular disease and other comorbidities as well as cancer screening and other preventative care measures.

囊性纤维化患者的临床护理现状
囊性纤维化跨膜传导调节剂(CFTR)的出现极大地改变了囊性纤维化(PwCF)患者的临床护理。特别是,大多数PwCF的高效调节疗法(HEMT)的可用性导致了药物治疗方案和临床结果的变化,但也与不良反应和药物相互作用有关。CFTR调节治疗在围产期的作用仍然是人们非常感兴趣的,这与CF母亲以及子宫内和出生后的婴儿有关。随着PwCF的中位预期寿命持续增加,还必须考虑心血管疾病和其他合并症的治疗,以及癌症筛查和其他预防性护理措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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