Given the efficacy and need for effective therapies such as amikacin liposome inhalation suspension for MAC lung disease, what clinical strategies do you recommend for optimizing adherence, patient satisfaction, and tolerability for this formulation?
Given the efficacy and need for effective therapies such as amikacin liposome inhalation suspension for MAC lung disease, what clinical strategies do you recommend for optimizing adherence, patient satisfaction, and tolerability for this formulation?
Presenter
Professor of Medicine and Pediatrics
Medical University of South Carolina
Powers-Huggins Endowed Chair for Cystic Fibrosis
University of South Carolina
Charleston, South Carolina