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Abstract
The combination of rifamycin (RFP), ethambutol (EB), and macrolides is currently the standard regimen for treatment of Mycobacterium avium complex pulmonary disease (MAC-PD). However, poor adherence to the standardized regimens recommended by current guidelines have been reported. We undertook a single-centred retrospective cohort study to evaluate the long-term outcomes in 295 patients with MAC-PD following first line treatment with standard (RFP, EB, clarithromycin [CAM]) or alternative (EB and CAM with or without fluoroquinolones (FQs) or RFP, CAM, and FQs) regimens. In this cohort, 80.7% were treated with standard regimens and 19.3% were treated with alternative regimens. After heterogeneity was statistically corrected using propensity scores, outcomes were superior in patients treated with standard regimens. Furthermore, alternative regimens were significantly and independently associated with sputum non-conversion, treatment failure and emergence of CAM resistance. Multivariate cox regression analysis revealed that older age, male, old tuberculosis, diabetes mellitus, higher C-reactive protein, and cavity were positively associated with mortality, while higher body mass index and M. avium infection were negatively associated with mortality. These data suggest that, although different combination regimens are not associated with mortality, first line administration of a standard RFP + EB + macrolide regimen offers the best chance of preventing disease progression in MAC-PD patients.
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1 National Hospital Organization, Osaka Toneyama Medical Centre, Department of Respiratory Medicine, Toyonaka, Japan (GRID:grid.416698.4); Osaka University Graduate School of Medicine, Department of Respiratory Medicine and Clinical Immunology, Suita, Japan (GRID:grid.136593.b) (ISNI:0000 0004 0373 3971)
2 Yao Tokushukai General Hospital, Department of Respiratory Medicine, Yao, Japan (GRID:grid.417339.b)
3 Osaka University, Department of Biomedical Statistics, Graduate School of Medicine, Osaka, Japan (GRID:grid.136593.b) (ISNI:0000 0004 0373 3971); Osaka University, Institute for Open and Transdisciplinary Research Initiatives, Osaka, Japan (GRID:grid.136593.b) (ISNI:0000 0004 0373 3971)
4 National Hospital Organization, Osaka Toneyama Medical Centre, Department of Respiratory Medicine, Toyonaka, Japan (GRID:grid.416698.4)




