Literature DB >> 34930036

Efficacy of Fluoroquinolones as Substitutes for Ethambutol or Rifampin in the Treatment of Mycobacterium avium Complex Pulmonary Disease According to Radiologic Types.

Jang Ho Lee1, Yea Eun Park1, Yong Pil Chong2, Tae Sun Shim1, Kyung-Wook Jo1.   

Abstract

During the treatment of Mycobacterium avium complex pulmonary disease (MAC-PD), ethambutol or rifampin is often discontinued because of adverse events. This study investigated the treatment outcomes when broader-spectrum fluoroquinolones replace ethambutol or rifampin in MAC-PD treatment based on the radiologic type. From 2006 to 2019, patients who initiated standard treatment and whose treatment duration was ≥1 year were retrospectively identified at a tertiary referral center in South Korea, including 178 patients with cavitary disease (fibrocavitary and cavitary nodular bronchiectatic types) and 256 patients with the noncavitary nodular bronchiectatic (NC-NB) type. We compared the microbiologic cure at 1 year between the patients who maintained the initial regimen and those who replaced ethambutol or rifampin with fluoroquinolones (moxifloxacin or levofloxacin). The overall microbiologic cure rate of the 178 patients with cavitary disease was 71.3%. Among these, the microbiologic cure rates of the 16 patients who substituted fluoroquinolones for ethambutol were lower than those of the 156 patients who maintained three-drug oral antibiotics with aminoglycoside (37.5% versus 74.4%, respectively; P = 0.007), which was statistically significant in multivariate analysis. The outcomes of the six patients receiving fluoroquinolones as an alternative to rifampin were similar to that of those continuing the initial regimen. The microbiologic cure rate of the patients with the NC-NB type receiving daily or intermittent oral three-drug therapy was similar regardless of maintaining the initial therapy or replacing ethambutol or rifampin with fluoroquinolones. In conclusion, in cavitary MAC-PD, replacing ethambutol with fluoroquinolones resulted in inferior patient outcomes.

Entities:  

Keywords:  Mycobacterium avium complex; ethambutol; fluoroquinolones; rifampin; substitute

Mesh:

Substances:

Year:  2021        PMID: 34930036      PMCID: PMC8846399          DOI: 10.1128/AAC.01522-21

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.938


  30 in total

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3.  Intermittent Treatment with Azithromycin and Ethambutol for Noncavitary Mycobacterium avium Complex Pulmonary Disease.

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4.  Macrolide resistant Mycobacterium avium complex pulmonary disease following clarithromycin and ethambutol combination therapy.

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5.  Tuberculosis, pulmonary cavitation, and matrix metalloproteinases.

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6.  Efficacy of clarithromycin and ethambutol for Mycobacterium avium complex pulmonary disease. A preliminary study.

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7.  Treatment of refractory Mycobacterium avium complex lung disease with a moxifloxacin-containing regimen.

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8.  Treatment of nontuberculous mycobacterial pulmonary disease: an official ATS/ERS/ESCMID/IDSA clinical practice guideline.

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Journal:  Eur Respir J       Date:  2020-07-07       Impact factor: 16.671

9.  Outcome of shorter treatment duration in non-cavitary nodular bronchiectatic Mycobacterium avium complex lung disease.

Authors:  Yea Eun Park; Yong Pil Chong; Ye-Jee Kim; Ock-Hwa Kim; Byoung Soo Kwon; Tae Sun Shim; Kyung-Wook Jo
Journal:  J Thorac Dis       Date:  2020-03       Impact factor: 2.895

10.  Role of ethambutol and rifampicin in the treatment of Mycobacterium avium complex pulmonary disease.

Authors:  Hyung-Jun Kim; Jong Sik Lee; Nakwon Kwak; Jaeyoung Cho; Chang-Hoon Lee; Sung Koo Han; Jae-Joon Yim
Journal:  BMC Pulm Med       Date:  2019-11-11       Impact factor: 3.317

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  2 in total

1.  Treatment Outcomes of Cavitary Nodular Bronchiectatic-Type Mycobacterium avium Complex Pulmonary Disease.

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Journal:  Antimicrob Agents Chemother       Date:  2022-08-11       Impact factor: 5.938

2.  Antimicrobial susceptibility and minimum inhibitory concentration distribution of common clinically relevant non-tuberculous mycobacterial isolates from the respiratory tract.

Authors:  Guiqing He; Lianpeng Wu; Qingyong Zheng; Xiangao Jiang
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  2 in total

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