Literature DB >> 33080299

Managing Mycobacterium avium Complex Lung Disease With a Little Help From My Friend.

David E Griffith1, Timothy R Aksamit2.   

Abstract

Management of Mycobacterium avium complex (MAC) lung disease is complicated, frequently unsuccessful, and frustrating to patients and clinicians. The initial treatment effort may not be directed solely at MAC infection, rather it is often initiating airway clearance measures for bronchiectasis. The next important steps are deciding who to treat and when to initiate therapy. Definitive or unambiguous guidance for these decisions is often elusive. The evidence supporting the current macrolide-based regimen for treating MAC lung disease is compelling. This regimen has been recommended in consensus nontuberculous mycobacterial treatment guidelines from 1997, 2007, and 2020, although clinician compliance with these recommendations is inconsistent. Understanding the idiosyncrasies of MAC antibiotic resistance is crucial for optimal antibiotic management. As a corollary, the importance of avoiding development of macrolide resistance due to inadequate therapy cannot be overstated. An inhaled liposome amikacin preparation is now approved for treating refractory MAC lung disease and holds promise for an even broader role in MAC therapy. Surgery is also an important therapeutic adjunct for selected patients. Microbiologic recurrences due either to new infection or treatment relapse/failure are common and require the same level of rigorous assessment and clinical judgment for determining their significance as initial MAC isolates. In summary, treatment of patients with MAC lung disease is rarely straight forward and requires familiarity with multiple factors directly and indirectly related to MAC lung disease. The many nuances of MAC lung disease therapy defy simple treatment algorithms; however, with patience, attention to detail, and perseverance, the outcome for most patients is favorable.
Copyright © 2020 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Mycobacterium avium complex; amikacin; bronchiectasis; macrolide; therapy

Mesh:

Substances:

Year:  2020        PMID: 33080299     DOI: 10.1016/j.chest.2020.10.031

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  5 in total

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

Authors:  Ganghee Chae; Yea Eun Park; Yong Pil Chong; Hyun Joo Lee; Tae Sun Shim; Kyung-Wook Jo
Journal:  Antimicrob Agents Chemother       Date:  2022-08-11       Impact factor: 5.938

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

Authors:  Jang Ho Lee; Yea Eun Park; Yong Pil Chong; Tae Sun Shim; Kyung-Wook Jo
Journal:  Antimicrob Agents Chemother       Date:  2021-12-20       Impact factor: 5.938

3.  Comparison of Rifamycins for Efficacy Against Mycobacterium avium Complex and Resistance Emergence in the Hollow Fiber Model System.

Authors:  Gunavanthi D Boorgula; Laxmi U M R Jakkula; Tawanda Gumbo; Bockgie Jung; Shashikant Srivastava
Journal:  Front Pharmacol       Date:  2021-04-15       Impact factor: 5.810

4.  Exacerbation of Mycobacterium avium pulmonary infection by comorbid allergic asthma is associated with diminished mycobacterium-specific Th17 responses.

Authors:  Yeeun Bak; Sang Chul Park; Dahee Shim; Yura Ha; Jumi Lee; Hongmin Kim; Kee Woong Kwon; Joo-Heon Yoon; Sung Jae Shin
Journal:  Virulence       Date:  2021-12       Impact factor: 5.882

Review 5.  Anti-Mycobacterial Drug Resistance in Japan: How to Approach This Problem?

Authors:  Keisuke Kamada; Satoshi Mitarai
Journal:  Antibiotics (Basel)       Date:  2021-12-24
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.