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British Lung Foundation
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Understanding antibiotic resistance in patients with cystic fibrosis.

A defective gene causes thick, sticky mucus to build up in the lungs of patients with cystic fibrosis (CF). There, it traps bacteria, causing patients to develop frequent lung infections that progressively damage these vital organs and impair patients' ability to breathe.

Most patients with this progressive genetic disorder die by the fourth decade of life. A key to helping patients live even that long—a vast improvement from an average lifespan of 10 years just decades ago—is judicious use of antibiotics, explains Andrea Hahn, M.D., a pediatric infectious diseases specialist at Children's National Health System.

medicalxpress.com/news/2018...

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Yes, a judicious use..thanks for that 2greys x

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