Estimated Impact of Fungal Colonization in Cystic Fibrosis From Secondary Exploitation of MucoFong Database.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 57
- 试验地点
- 1
- 主要终点
- Describe the micromycetes find in lung in patients with cystic fibrosis
研究概览
简要总结
The main objective of the project "MucoFong" (19021906 national french program n which Vaincre La Mucoviscidose participated: N82006/ 351) was to determine the fungi present the respiratory tract of CF patients responsible for either colonization or authentic infectious diseases. The Mucofong data allowed the team to provide for the 1st time national French guidelines for the management of CF sputum mycological analysis (MucoMicrobes work group coordinated by Prof. Plésiat published in 2015 in the REMIC book). Nevertheless, the team has a comprehensive database that it still has to analyze beyond these initial results. The main goal today is to clarify the role of fungi in the lung function degradation of these patients by studying the overall risk and estimated impact of fungal colonization in our cohort.
详细描述
The material includes data from the followup of the 300 patients (3 visits per patient for which the team collected and verified the biological radiological and clinical data).
Relations between Aspergillus fumigatus or Candida albicans and lung function or clinical outcome of patients will be longitudinally analyzed taking as output variable FEV1, according to bibliography data available.
To assess the attributed fungal risk, the team will focus on the 57 patients de novo colonized by fungi at the second visit. Three physician experts will determine the impact of such fungal colonization on the patient clinical and respiratory parameters.
The expert conclusion concordance and statistical significance will be evaluated using the kappa score.
This project will be realized in collaboration with the groups of Prof. R. Thiebaut (Methodology and Epidemiology Service Bordeaux University Hospital, INSERM U1219 / INRIA SISTM) and Prof. M. Fayon (Department of Pediatrics, Pediatric reference centre) University Hospital of Bordeaux.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 6 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •All patients included in the database meet the following criteria:
- •Patient whose diagnosis of cystic fibrosis has been validated on the criteria in force,
- •Patient usually followed in one of the 7 centers involved in the PHRC,
- •Patient aged at least 6 years without an upper age limit,
- •Patient benefiting from a mycological assessment carried out in the context of the usual microbiological monitoring (good clinical practice),
- •Cystic fibrosis Patient benefiting from a mycological assessment carried out in front of a clinical episode of aggravation requiring biological exploration,
- •Patient who has signed informed consent at the time of inclusion,-patient affiliated with a social security scheme.
排除标准
- •Patients meeting the following criteria were not included in the database:
- •Pulmonary transplant Patient,
- •Patient or their parents (if the patient is a minor) refusing any participation in the study,
- •Major incapable subject, under guardianship or under the protection of Justice,
- •Refusal or inability to give informed consent.
结局指标
主要结局
Describe the micromycetes find in lung in patients with cystic fibrosis
时间窗: Day 1
Relation between the micromycetes and the pathologic lung in patients with cystic fibrosis
次要结局
- Number of patient with a. fumigatus, c. albicans or other micromycete(Day 1)
- Detect, from data of high-throughput sequencing, combinations of bacteria or fungi are present and clear profile of affinity between genres, in patients with cystic fibrosis.(Day 1)