Does using the Lung Clearance Index (LCI) inform clinical decisions in children with cystic fibrosis?

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM Journal of Cystic Fibrosis Pub Date : 2025-01-11 DOI:10.1016/j.jcf.2024.12.001
Lucy Perrem, Stephanie Jeanneret-Manning, Stephanie D Davis, Margaret Rosenfeld, Todd Edwards, Sanja Stanojevic, Felix Ratjen
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Abstract

Introduction: The Lung Clearance Index (LCI) is an established research test, but its role in clinical decision-making is not well defined. This study estimated the proportion of treatment decisions that are changed or supported by the added information provided by LCI.

Methods: A mixed methods prospective observational study was conducted in North America. Providers were invited to participate in a clinical vignette survey consisting of 10 hypothetical scenarios involving pediatric cystic fibrosis (CF) management. First, they made a clinical decision based on information captured in routine clinical visits. Then, the LCI value was made available, and providers were asked whether the LCI changed or supported their decision. A prospective study was also conducted at three CF centres to determine how often physicians make pulmonary treatment decisions at CF clinic visits and how often they perceive additional lung function data would be helpful for these decisions.

Results: We received 522 vignette responses from 62 participants. LCI changed the decision in 18.4 % of cases, supported the decision in 57.1 % and did not impact the decision in 24.5 %. Data from patient encounters in the prospective study demonstrated that changes to pulmonary treatments were considered in 98/322 (30.4 %) visits; additional lung function information could potentially have helped in 64.3 % of the treatment decisions.

Conclusion: LCI changes or supports a significant proportion of treatment decisions. Providers perceive that additional information about lung function could be helpful at the majority of encounters where changes in treatment are considered.

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使用肺清除率指数(LCI)对囊性纤维化儿童的临床决策有帮助吗?
简介:肺清除率指数(LCI)是一项成熟的研究测试,但其在临床决策中的作用尚未明确。本研究估计了由LCI提供的附加信息改变或支持治疗决策的比例。方法:在北美进行了一项混合方法的前瞻性观察研究。提供者被邀请参加一项临床小插曲调查,包括10个涉及儿科囊性纤维化(CF)管理的假设场景。首先,他们根据在常规临床访问中获得的信息做出临床决策。然后,提供LCI值,并询问提供者LCI是否改变或支持他们的决定。在三个CF中心进行了一项前瞻性研究,以确定医生在CF门诊就诊时做出肺部治疗决定的频率,以及他们认为额外的肺功能数据对这些决定有帮助的频率。结果:我们收到了来自62名参与者的522份小问卷。LCI在18.4%的病例中改变了决定,在57.1%的病例中支持决定,在24.5%的病例中不影响决定。前瞻性研究中患者就诊的数据显示,98/322(30.4%)的患者考虑改变肺部治疗;额外的肺功能信息可能有助于64.3%的治疗决策。结论:LCI改变或支持很大比例的治疗决策。提供者认为,在大多数考虑改变治疗方案的情况下,关于肺功能的额外信息可能会有所帮助。
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
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.
期刊最新文献
From the editor's desk. Corrigendum to "Evaluation of the response to elexacaftor-tezacaftor-ivacaftor of the rare CFTR variants L383S, I507del, L1065P and R1066H in intestinal organoid-derived epithelial monolayers" [Journal of Cystic Fibrosis xxx (2025) 1-10]. Mental health and adherence in CF: Self-efficacy and perceived barriers as mediators. Strategies used to access CFTR modulators in countries without reimbursement agreements. The impact of pregnancy on mortality and lung function in cystic fibrosis patients.
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