Bronchiectasis Clinical Trial
Nontuberculous mycobacteria (NTM) are ubiquitous organisms in the environment and are now
increasingly being recognized as significant causes of chronic pulmonary infection in
immunocompetent individuals (1). The most frequently encountered NTM lung disease worldwide
is caused by Mycobacterium avium-intracellular complex (MAC) (2-4).
In several studies with chest computed tomography (CT), researchers have demonstrated that
the presence of bilateral multifocal bronchiolitis (well-defined small nodules and branching
centrilobular nodules, or tree-in-bud pattern) and bronchiectasis distributed mainly in the
right middle lobe and lingular segment are indicative of NTM pulmonary infection (7-11).
Accordingly, it is believed that radiologic findings of bilateral bronchiolitis and
bronchiectasis on chest CT scans specifically suggest NTM pulmonary infection (1). These CT
findings, however, may not be specific for NTM pulmonary infection. CT patterns of
bronchiectasis and bronchiolitis in the pulmonary infections caused by various NTM organisms
have been reported, and these organisms include Mycobacterium kansasii, Mycobacterium
xenopi, and rapidly growing mycobacteria such as Mycobacterium abscessus, Mycobacterium
fortuitum, and Mycobacterium chelonae (12-14). In addition, not all patients with
bronchiectasis and bronchiolitis have NTM pulmonary infection. Two recent studies showed
that only about 50% of patients with such CT features have MAC pulmonary infection (9,15).
To the best of our knowledge, however, there is no report about the incidence of NTM in
patients with bronchiectasis or bronchiolitis in countries with low incidence of TB. Thus,
the purpose of our study was to determine the frequency of NTM pulmonary infection in
patients with bilateral bronchiectasis and bronchiolitis at chest CT and to investigate
whether these CT findings are specifically indicative of MAC infection or other specific
pathogen.
Study Population During the study period helical thin-section thoracic CT scans will
obtained in patients in whom a diagnosis of bronchiectasis was known or who were suspected
of having bronchiectasis on the basis of clinical symptoms and signs of a chronic cough and
sputum production.
One chest radiologist will review consecutive patients with bilateral multifocal
bronchiectasis and bronchiolitis (well-defined small nodules and branching centrilobular
nodules), regardless of the presence of cavitary lesions, who were suspected of having NTM
pulmonary infection on the basis of these chest CT findings. Those patients with unilateral
bronchiectasis, although the bronchiectasis was combined with bronchiolitis, will be
excluded from the study. Those with isolated findings of bilateral bronchiectasis or
bilateral bronchiolitis will also also be excluded.
The patients will undergo a diagnostic work-up for NTM pulmonary infection. For a diagnosis
of NTM infection, sputum AFB (Ziehl-Neelsen method) staining and culture examinations for
mycobacteria will be performed at least three times. Bronchoscopy also will be performed for
bronchial washing or transbronchial lung biopsy in patients with no sputum.
Isolation and Identification of Mycobacteria Expectorated sputum and samples that will be
obtained with bronchoscopy will be examined after AFB staining and will be cultured for
mycobacteria. Colony numbers will be counted after incubation for as long as 8 weeks.
Mycobacterium tuberculosis isolates will be identified (Gen-Probe Amplified Mycobacterium
Tuberculosis Direct Test; Gen-Probe, San Diego, Calif), and NTM species identification will
be confirmed by using a polymerase chain reaction-restriction fragment length polymorphism
method based on the rpoB gene (16). In all cases, sputum examinations and bronchoscopic
samples will be obtained within 6 months after CT.
Diagnostic Criteria The diagnosis of definite NTM pulmonary infection will be determined
when patients fulfilled the 1997 American Thoracic Society diagnostic criteria, which
include clinical, radiologic, and microbiologic criteria (1). Probable NTM pulmonary
infection will be diagnosed if the patients will be satisfied the clinical and radiologic
criteria of the 1997 American Thoracic Society diagnostic criteria but will not fully
satisfy the microbiologic criteria. Namely, the patients either will have only one or two
cultures positive for organisms specifically identified as NTM with smear results negative
for AFB or had more than three cultures positive for NTM without precise species
identification; in addition, the patients will have symptoms and radiologic evidence of
disease, which consisted of bilateral bronchiectasis and bronchiolitis. A diagnosis of
pulmonary tuberculosis will be made when patients will have a culture positive for M
tuberculosis.
The clinical diagnostic criteria for diffuse panbronchiolitis will be as follows (17): (a)
symptoms—chronic cough, sputum, and dyspnea on exertion; (b) physical signs—crackles and
rhonchi; (c) chest radiographs—diffusely disseminated fine nodular opacities, mainly in the
lower zones of the lung, with hyperinflation of the lungs; (d) lung function studies, with
at least three of the following four abnormalities—forced expiratory volume in 1 second of
less than 70%, vital capacity of less than 80% of the predicted value, residual volume of
more than 150% of the predicted value, and partial pressure of oxygen (arterial) of less
than 80 mm Hg. When no definite cause will be identified after evaluation of the causative
factors, patients will received a diagnosis of bronchiectasis or nonspecific bronchiolitis.
Chart Review The medical records of all patients will be reviewed by one of the authors for
the following information, if available: height, body weight, history of tobacco use,
history of previous antituberculous treatment, results of AFB staining, isolation and
identification of mycobacteria, and the number of NTM-positive isolates.
Imaging Evaluation Chest radiologists will retrospectively evaluate the chest CT scans. The
observer will be unaware of the microbiologic test results and final diagnoses;
A total of six lung lobes in each patient (the lingular segment will be considered a
separate lobe) will be assessed for the presence of lung lesions and other abnormal
findings. Each lobe in the lungs will be evaluated with regard to the presence or absence of
bronchiectasis, well-defined small nodules (<10 mm in diameter), and branching centrilobular
nodules (ie, tree-in-bud pattern). Bronchiolitis will be defined as the presence of
well-defined small nodules and branching centrilobular nodules on chest CT scans. The
extents of involvement of bronchiectasis and bronchiolitis will be estimated by counting the
number of involved lobes. The presence of other abnormalities, including nodules (10-30 mm
in diameter), lobular consolidation (consolidation of 10-20 mm in diameter with a polygonal
shape), segmental consolidation, cavities, and volume reduction, will be also recorded.
Comparison between Patients with NTM Disease and Patients with Non-NTM Disease After
classification of patients according to the previously mentioned diagnostic criteria, the
patients will be categorized into two groups: the NTM pulmonary infection group, including
the patients with definite or probable NTM pulmonary infection, and the non-NTM pulmonary
infection group. Comparisons of the clinical and chest CT findings in patients with NTM
diseases with those in patients with other airway diseases will be determined.
Statistical Analysis Values are expressed as the mean ± standard deviation. By stratifying
the age distribution of included patients according to birth sex and decades of patients'
ages, the investigators will be tested whether there will be statistically significant
differences between the distributions by using the χ2 test. All continuous variables will be
tested for normality with the Kolmogorov-Smirnov test, and all had a Gaussian distribution.
To statistically evaluate differences in continuous variables between the two groups, the
investigators will use the unpaired t test. Frequencies will be analyzed by using the χ2
test or the Fisher exact test, as appropriate. A difference with a P value of less than .05
will be considered statistically significant. Statistical software (SPSS 11.0; SPSS,
Chicago, Ill) will be used throughout.
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Observational Model: Cohort, Time Perspective: Prospective
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