囊性纤维化研究的变化:多中心微生物队列研究的挑战。

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM
Ieuan Es Evans, Christine M Duplancic, Timothy A Kidd, Emma L Ballard, Rachel M Thomson, Claire E Wainwright, Scott C Bell
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引用次数: 0

摘要

简介:感染是囊性纤维化(pwCF)患者进行性肺部疾病的主要原因。研究人员经常使用数据登记或基于中心的队列研究来研究CF中的感染。我们研究了在进行两项间隔十年的多中心非干涉性研究者主导的队列研究时遇到的挑战。方法:澳大利亚克隆假单胞菌研究(ACPinCF, 1294名参与者)和国家NTM在CF研究(1314名参与者)利用临床实践,数据由诊所和澳大利亚CF数据注册中心提供。诊断实验室根据当地规程进行了培养。结果:立地审批时间长;ACPinCF研究为16个月,National NTM在CF研究中为21-44个月。后者需要与每个临床站点进行单独的合同谈判,作为治理批准的要求。不断变化的临床需求和不可预见的挑战,如SARS-CoV-2大流行,严重影响了NTM研究。尽管存在这些挑战,参与者的保留率仍然很高,随访损失最小。CF中心领导层的变化和参与研究的成本回收卫生服务政策进一步加剧了维持纵向队列CF研究的挑战。结论:开展和维持纵向非介入性研究面临重大挑战。即使在赠款资金支付了中心参与、样本处理、数据管理、数据分析和结果输出的费用之后,这些研究仍将严重依赖没有大量资金的中心提供的大量支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The changing face of cystic fibrosis research: challenges of multi-centre microbiology cohort studies.

Introduction: Infection is a primary cause of progressive pulmonary disease in people with cystic fibrosis (pwCF). Researchers frequently utilize data registries or centre-based cohort studies to study infections in CF. We examine challenges encountered in conducting two multi-centre non-interventional investigator-led cohort studies undertaken a decade apart.

Methods: The Australian Clonal Pseudomonas Study (ACPinCF, 1294 participants) and the National NTM in CF study (1314 participants) leveraged clinical practice, with data was supplied by clinics and the Australian CF Data Registry. Diagnostic laboratories performed cultures according to local protocols.

Results: Site approval times were lengthy; 16 months for the ACPinCF study and between 21-44 months for the National NTM in CF study. The latter required individual contract negotiation with each clinical site as a requirement of governance approval. Changing clinical demands and unforeseen challenges such as the SARS-CoV-2 pandemic significantly impacted the NTM study. Despite these challenges, participant retention remained robust, with minimal loss to follow-up. Changes in CF centre leadership and health service policy on cost-recovery for research participation further exacerbates the challenges of maintaining longitudinal cohort CF studies.

Conclusions: Conducting and sustaining longitudinal non-interventional studies present significant challenges. Even after costs for centre participation, sample processing, data curation, data analysis and results output are covered by grant funding, these studies will still heavily depend on significant support provided by the centres without substantial funding.

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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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