Impact of Walgreens Connected Care® Cystic Fibrosis program on adherence and quality of life for enrolled CF patients
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چکیده
presents a considerable management challenge to healthcare providers. In patients with CF, a defective gene causes a loss of cystic fibrosis transmembrane conductance regulator (CFTR) protein activity, which leads to a buildup of thick, sticky mucus. CF primarily affects the respiratory and digestive systems. Patients often experience progressive lung damage, which results in increased rates of morbidity and mortality. Lung transplantation remains an option for some of these patients.
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