TY - JOUR
T1 - Macrolide-resistant mycobacterium avium complex lung disease
T2 - Analysis of 102 consecutive cases
AU - Nontuberculous Mycobacteriosis Japan Research Consortium
AU - Morimoto, Kozo
AU - Namkoong, Ho
AU - Hasegawa, Naoki
AU - Nakagawa, Taku
AU - Morino, Eriko
AU - Shiraishi, Yuji
AU - Ogawa, Kenji
AU - Izumi, Kiyohiko
AU - Takasaki, Jin
AU - Yoshiyama, Takashi
AU - Hoshino, Yoshihiko
AU - Matsuda, Shuichi
AU - Hayashi, Yuta
AU - Sasaki, Yuka
AU - Ishii, Makoto
AU - Kurashima, Atsuyuki
AU - Nishimura, Tomoyasu
AU - Betsuyaku, Tomoko
AU - Goto, Hajime
N1 - Publisher Copyright:
Copyright © 2016 by the American Thoracic Society.
PY - 2016/11
Y1 - 2016/11
N2 - Rationale: The management of macrolide-resistant Mycobacterium aviumcomplex (MR-MAC)pulmonary disease is difficult and is thought to be analogous to that of multidrug-resistant tuberculosis (MDR-TB). Objectives: This study aimed to clarify the cause of MR-MAC, to see how its management affected outcome, and to compare its prognosis with that of MDR-TB. Methods: The medical records of 102 consecutive cases with MR-MACpulmonary disease at three tertiary hospitals for mycobacteriosis in metropolitan Tokyo and one in Aichi prefecture from 2005 to 2014were reviewed.The data of 311 consecutive caseswith MDR-TB were extracted from the medical data at Fukujuji Hospital. Measurements and Main Results: Of the 90 patients who met the criteria, 53 (58.9%) received inappropriate first-line treatment, and 28 (31.1%) deviated from the standard treatment because of the adverse effects of ethambutol. The survival rates for MR-MAC disease and MDR-TB were not significantly different (P = 0.6). Multivariate analysis showed that the combination of aminoglycoside and surgery resulted in the best treatment outcome (P = 0.02), although neither of the two factors reached significance by themselves. The continuation of clarithromycin and the addition of fluoroquinolones did not improve the outcome for the treatment of disease caused by MR-MAC. Conclusions: Inappropriate prescription patterns and deviations from the standard treatment because of adverse drug reactions appeared to be the main causes of macrolide resistance in this patient series. Drug sensitivity testing should be performed at diagnosis to identify macrolide resistance and patients who may benefit from other therapy.
AB - Rationale: The management of macrolide-resistant Mycobacterium aviumcomplex (MR-MAC)pulmonary disease is difficult and is thought to be analogous to that of multidrug-resistant tuberculosis (MDR-TB). Objectives: This study aimed to clarify the cause of MR-MAC, to see how its management affected outcome, and to compare its prognosis with that of MDR-TB. Methods: The medical records of 102 consecutive cases with MR-MACpulmonary disease at three tertiary hospitals for mycobacteriosis in metropolitan Tokyo and one in Aichi prefecture from 2005 to 2014were reviewed.The data of 311 consecutive caseswith MDR-TB were extracted from the medical data at Fukujuji Hospital. Measurements and Main Results: Of the 90 patients who met the criteria, 53 (58.9%) received inappropriate first-line treatment, and 28 (31.1%) deviated from the standard treatment because of the adverse effects of ethambutol. The survival rates for MR-MAC disease and MDR-TB were not significantly different (P = 0.6). Multivariate analysis showed that the combination of aminoglycoside and surgery resulted in the best treatment outcome (P = 0.02), although neither of the two factors reached significance by themselves. The continuation of clarithromycin and the addition of fluoroquinolones did not improve the outcome for the treatment of disease caused by MR-MAC. Conclusions: Inappropriate prescription patterns and deviations from the standard treatment because of adverse drug reactions appeared to be the main causes of macrolide resistance in this patient series. Drug sensitivity testing should be performed at diagnosis to identify macrolide resistance and patients who may benefit from other therapy.
KW - Clarithromycin
KW - Multidrug-resistant tuberculosis
KW - Prognosis
KW - Side effect
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U2 - 10.1513/AnnalsATS.201604-246OC
DO - 10.1513/AnnalsATS.201604-246OC
M3 - Article
C2 - 27513168
AN - SCOPUS:84995538969
VL - 13
SP - 1904
EP - 1911
JO - Annals of the American Thoracic Society
JF - Annals of the American Thoracic Society
SN - 2325-6621
IS - 11
ER -