3. Chronic Lung Infections
CLF is the primary cause of death in patients suffering from cystic fibrosis. The thickened mucus provides an ideal Petri dish for the development of bacteria and other pathogens. As a result, it’s common for people suffering from the condition to experience frequent bouts of sinusitis, bronchitis or pneumonia.
Studies in life expectancy for individuals suffering from CS has decreased over the years as medical practitioners introduce new treatment methods to extend longevity. A few decades ago, it was common for CS patients to reach a life expectancy of 30-years.
Recent advances in treatment now allow some patients to enjoy a full life, with some adults reaching the ages of 75-years old before succumbing to the condition. Recent statistics show annual mortality rates for individuals between the ages of 26 and 30-years at 50 per 1,000.
Despite the advancement of treatment methods, chronic lung infections remain the leading cause of death for people suffering from cystic fibrosis.