The Role of Viral Infection in Acute Exacerbations of Non-cystic Fibrosis Bronchiectasis in Adults

Sponsor
The First Affiliated Hospital of Guangzhou Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01801657
Collaborator
(none)
100
1
13.9
7.2

Study Details

Study Description

Brief Summary

Bronchiectasis is clinically characterized by irreversible dilation of the bronchi and bronchioles leading to persistent cough, purulent sputum, and airway flow limitation, which may be accompanied by recurrent exacerbations.It has been increasingly recognized that respiratory viruses are mainly responsible for acute exacerbation of chronic pulmonary diseases, i.e. asthma, chronic obstructive pulmonary disease and cystic fibrosis. However,little is known about the roles of viral infection in driving exacerbations of bronchiectasis.This study aims to identify the frequency of common viral infections and determine the roles that viruses play in acute exacerbations of bronchiectasis.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Bronchiectasis is a chronic airway disease characterised by a vicious cycle of persistent bacterial colonization,inflammation and progressive tissue destruction.Patients with bronchiectasis frequently developed acute exacerbations characterised by acute worsening requiring changes in concomitant use of medication,with attendant adverse effects on their morbidity and health-related quality of life. The detailed pathogenesis of exacerbations of bronchiectasis, however, remains poorly understood.

    Recent data suggested that airway infection and inflammation are important drivers of exacerbations,therefore the imbalance between chronic bacterial infection and host immune response may result in bronchiectasis exacerbations. Viral infection may be an important factor that leads to this events.It has been established that respiratory viruses are mainly responsible for the exacerbations of other chronic respiratory diseases, i.e. asthma, COPD and cystic fibosis. However, the data regarding prospective studies that sought to investigate the roles of viruses in acute exacerbation of bronchiectasis are lacking. Furthermore,the associations between viruses and bacteria during exacerbation need to be assessed. This study targets at indentifying the frenquency of common viral infections in adults with non-cystic fibrosis bronchiectasis and may shed light on the effects they have on clinical parameters,i.e. the length of exacerbated symptom to recovery,lung function, pulmonary inflammation, bacterial load and quality of life.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    The Role of Viral Infection in Acute Exacerbations of Non-cystic Fibrosis Bronchiectasis in Adults
    Study Start Date :
    Feb 1, 2013
    Anticipated Primary Completion Date :
    Apr 1, 2014
    Anticipated Study Completion Date :
    Apr 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Bronchiectasis,stable

    A patient was defined as stable if there was no exacerbation for the previous 4 wk

    Bronchiectasis,exacerbations

    Bronchiectasis exacerbations were defined by subjective and persistent(>24 h) deterioration in at least three respiratory symptoms, including cough, dyspnea, hemoptysis, increased sputum purulence or volume, chest pain (with or without fever), radiographic deterioration, systemic disturbances, or changes in chest auscultation

    Outcome Measures

    Primary Outcome Measures

    1. The prevalence of respiratory virus infection in adults with bronchiectasis during a pulmonary exacerbation and when clinically stable. [1 year]

      Respiratory viruses in the nasal swab and sputum will be identified using the polymerase chain reaction(PCR)technique when clinically stable and during exacerbation.The following viruses will be tested for:influenza A,B(including influenza A H1N1),respiratory syncytial virus(RSV),Enterovirus,Parainfluenza 1-4,Rhinovirus,human Coronaviruses(subtypes OC43、229E、HKU1),human metapneumovirus,adenovirus, human bocavirus,chlamydia,mycoplasma.

    Secondary Outcome Measures

    1. The effect of respiratory virus infection on systemic and pulmonary inflammatory markers. [1 year]

      Systemic and airway inflammatory cytokines including IL-1β、IL-6、IL-8、TNF-a were measured using a commercial multiplex bead-based assay.

    2. The effect of respiratory virus on lung function [1 year]

      Spirometric indices in the present study is referred to as forced expiratory vilume in 1s(FEV1),forced vital capacity(FVC).Spirometry tests are carried out using a spirometer (COSMED, QUARK PFT, Italy). All operation procedures meet the joint recommendation by ATS and ERS. A total of at least 3 (not more than 8) spirometric maneuvers are performed, with the variation between the best two maneuvers of <5% or 200ml in FVC and FEV1. The maximal values of FVC and FEV1 are reported.

    3. The effect of respiratory virus infection on the bacterial load in bronchiectasis. [1 year]

      Type of bacterial infection, also referred to as potentially pathogenic organisms, and bacterial load, as expressed in cfu per mililiter

    4. Time to recovery of respective symptom [1 year]

      The time from exacerbation onset by which a 3-d moving average was equal to or exceeded the baseline value

    5. The effect of respiratory virus on quality of life in patients with bronchiectasis [1 year]

      Quality of life in patients with bronchiectasis were measured by St.George Respiratory Questionnaire、Leicester Cough Questionnaire and COPD assessment test during exacerbations,and then compared between virus-postive and virus-negative patients

    6. To investigate if upper respiratory tract symptoms are associated with viral infections. [1 year]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥ 18 years

    • HRCT-diagnosed Bronchiectasis

    • Capable of providing written informed consent

    Exclusion Criteria:
    • Patient judged to have poor compliance

    • Cystic fibrosis bronchiectasis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong China 510000

    Sponsors and Collaborators

    • The First Affiliated Hospital of Guangzhou Medical University

    Investigators

    • Principal Investigator: Rongchang Chen, MD, The First Affiliated Hospital of Guangzhou Medical University
    • Principal Investigator: Nanshan Zhong, MD, The First Affiliated Hospital of Guangzhou Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    yonghua gao, PHD, The First Affiliated Hospital of Guangzhou Medical University
    ClinicalTrials.gov Identifier:
    NCT01801657
    Other Study ID Numbers:
    • 2009CB522109
    First Posted:
    Mar 1, 2013
    Last Update Posted:
    Mar 12, 2014
    Last Verified:
    Mar 1, 2014
    Keywords provided by yonghua gao, PHD, The First Affiliated Hospital of Guangzhou Medical University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 12, 2014