Cavity formation and its predictors in noncavitary nodular bronchiectatic Mycobacterium avium complex pulmonary disease

被引:5
作者
Han, Dong-Woo [1 ]
Jo, Kyung-Wook [1 ]
Kim, Ock-Hwa [1 ]
Shim, Tae Sun [1 ]
机构
[1] Univ Ulsan, Asan Med Ctr, Dept Internal Med, Div Pulmonol & Crit Care Med,Coll Med, Seoul, South Korea
关键词
Mycobacterium avium complex; Noncavitary nodular bronchiectatic; Cavity formation; NONTUBERCULOUS MYCOBACTERIA; LUNG-DISEASE; RISK-FACTORS; TUBERCULOSIS; IDENTIFICATION; DIAGNOSIS;
D O I
10.1016/j.rmed.2021.106340
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The temporal dynamics of cavity formation in patients with the noncavitary nodular bronchiectatic (NC-NB) form of Mycobacterium avium complex pulmonary disease (MAC-PD) have not yet been well described. We aimed to investigate the development of new cavities in the NC-NB form of MAC-PD. Methods: Of the patients diagnosed with NC-NB-type MAC-PD between 2002 and 2013 and followed-up until July 2018 at a tertiary referral center in South Korea, we identified 589 patients who underwent follow-up chest computed tomography at least once after the diagnosis and retrospectively analysed their medical records. Results: The patients' mean age was 62.0 years, 64.7% were women. During the median follow-up of 3.8 years (interquartile range [IQR] 1.7-5.9), new cavity formation was noted in 51 (8.7%) patients. The median interval between the diagnosis of NC-NB MAC-PD and cavity formation was 3.7 years (IQR 1.8-5.4), with a constant occurrence over time. The Cox regression analysis showed that a history of pulmonary tuberculosis (adjusted hazard ratio [HR] 1.85; 95% confidence interval [CI] 1.06-3.23; P = 0.030) and M. intracellulare as the causative organism (adjusted HR 2.03; 95% CI 1.15-3.59; P = 0.014) were independently associated with new cavity formation. Conclusions: New cavity formation was noted in 8.7% of the patients with NC-NB MAC-PD in approximately 4 years after diagnosis, particular in those infected with M. intracellulare and those with a previous history of tuberculosis.
引用
收藏
页数:6
相关论文
共 28 条
[21]   Species identification of mycobacteria by PCR-restriction fragment length polymorphism of the rpoB gene [J].
Lee, H ;
Park, HJ ;
Cho, SN ;
Bai, GH ;
Kim, SJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (08) :2966-2971
[22]   Long-term natural history of non-cavitary nodular bronchiectatic nontuberculous mycobacterial pulmonary disease [J].
Moon, Seong Mi ;
Jhun, Byung Woo ;
Baek, Sun-Young ;
Kim, Seonwoo ;
Jeon, Kyeongman ;
Ko, Ryoung-Eun ;
Shin, Sun Hye ;
Lee, Hyun ;
Kwon, O. Jung ;
Huh, Hee Jae ;
Ki, Chang-Seok ;
Lee, Nam Yong ;
Chung, Myung Jin ;
Lee, Kyung Soo ;
Shin, Sung Jae ;
Daley, Charles L. ;
Koh, Won-Jung .
RESPIRATORY MEDICINE, 2019, 151 :1-7
[23]  
Narvaiz de Kantor I, 1998, LAB SERVICES TUBERCU
[24]   Tuberculosis, Pulmonary Cavitation, and Matrix Metalloproteinases [J].
Ong, Catherine W. M. ;
Elkington, Paul T. ;
Friedland, Jon S. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 190 (01) :9-18
[25]   Treatment for Mycobacterium avium complex lung disease [J].
Pan, Sheng-Wei ;
Shu, Chin-Chung ;
Feng, Jia-Yih ;
Su, Wei-Juin .
JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2020, 119 :S67-S75
[26]   Routine use of PCR reverse cross-blot hybridization assay for rapid identification of Mycobacterium species growing in liquid media [J].
Sanguinetti, M ;
Posteraro, B ;
Ardito, F ;
Zanetti, S ;
Cingolani, A ;
Sechi, L ;
De Luca, A ;
Ortona, L ;
Fadda, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (06) :1530-1533
[27]   Risk factors for pulmonary disease due to culture-positive M-tuberculosis or nontuberculous mycobacteria in South African gold miners [J].
Sonnenberg, P ;
Murray, J ;
Glynn, JR ;
Thomas, RG ;
Godfrey-Faussett, P ;
Shearer, S .
EUROPEAN RESPIRATORY JOURNAL, 2000, 15 (02) :291-296
[28]   Update on pulmonary disease due to non-tuberculous mycobacteria [J].
Stout, Jason E. ;
Koh, Won-Jung ;
Yew, Wing Wai .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2016, 45 :123-134