Lobar distribution in non-cystic fibrosis bronchiectasis predicts bacteriologic pathogen treatment
Non-cystic fibrosis bronchiectasis (NCFBr) is a major cause of morbidity due to frequent infectious exacerbations. We analyzed the influence of patient age and bronchiectasis location on the bacterial profile of patients with NCFBr. This retrospective cohort study included 339 subjects diagnosed wit...
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Veröffentlicht in: | European journal of clinical microbiology & infectious diseases 2016-05, Vol.35 (5), p.791-796 |
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Sprache: | eng |
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Zusammenfassung: | Non-cystic fibrosis bronchiectasis (NCFBr) is a major cause of morbidity due to frequent infectious exacerbations. We analyzed the influence of patient age and bronchiectasis location on the bacterial profile of patients with NCFBr. This retrospective cohort study included 339 subjects diagnosed with an infectious exacerbation of NCFBr during the 9-year period between January 2006 and December 2014. Bronchoalveolar lavage (BAL) cultures and high-resolution computed tomography scans (HRCT) were utilized to characterize the location of the bronchiectasis and bacteriologic pathogenic profile. In univariate logistic regression, the frequency of
Haemophilus influenza
e was higher in patients aged ≤64 years (OR = 0.969, p 64 years. The lobar distribution of bronchiectasis in the subjects was 25.9 % in the right middle lobe (RML), 20.7 % in the right lower lobe (RLL), 20.4 % in the left lower lobe (LLL), 13.8 % in the lingula, 13 % in the right upper lobe (RUL), and 6.2 % in the left upper lobe (LUL). In the lower lobes,
H. influenzae
was the dominant species isolated, whereas in the RUL it was
P. aeruginosa
and in the LUL it was non- tuberculous mycobacterium (NTM).
H. influenza
e was more prevalent in younger patients, whereas
P. aeruginosa
, Enterobacteriaceae and NTM predominated in older patients. Different pathogens were associated with different lobar distributions. The RML, RLL and LLL showed a greater tendency to develop bronchiectasis than other lobes. |
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ISSN: | 0934-9723 1435-4373 |
DOI: | 10.1007/s10096-016-2599-7 |