Omadacycline for management of Mycobacteriumabscessus infections: a review of its effectiveness, place in therapy, and considerations for use

The Mycobacteriumabscessus complex (MABC) is a group of acid-fast, rapidly dividing non-tuberculous mycobacteria (NTM) that include a number of clinically important subspecies, including M.abscessus,M.bolletii, and M.massiliense. These organisms are prevalent in the environment and are primarily associated with human pulmonary or skin and skin structure infections (SSSI) but may cause more deep-seeded disseminated infections and bacteremia in the immunocompromised. Importantly, these NTM are resistant to most first-line anti-tuberculous agents and, due to intrinsic or acquired resistance, exhibit exceedingly low, variable, and geographically distinct susceptibilities to commonly used antibacterial agents including older tetracyclines, macrolides, aminoglycosides, cephalosporins, carbapenems, and sulfamethoxazole-trimethoprim. Omadacycline is a novel third-generation member of the tetracycline family of antibacterials that has recently been demonstrated to have potent anti-NTM effects and clinical efficacy against MABC, including M.abscessus. The purpose of this review is to present a comprehensive and up-to-date assessment on the body of literature on the role of omadacycline for M.abscessus infections. Specifically, the in vitro and in vivo microbiology, mechanisms of action, mechanisms of resistance, clinical pharmacokinetics, clinical efficacy, adverse effects, dosage and administration, and place in therapy of omadacycline in management of M.abscessus infections will be detailed.

Automated summary

This review provides a comprehensive assessment on the role of omadacycline for M.abscessus infections. Omadacycline, a novel antibacterial agent, has been demonstrated to have potent anti-NTM effects and clinical efficacy against M.abscessus. However, due to the low susceptibility of M.abscessus to commonly used antibacterial agents, alternative treatment options need to be explored.