Management of Cystic Fibrosis: Integrating Nursing, Radiology, Laboratory Science, Health Administration, Surgical Nursing, Physical Therapy, and General Medicine

Abstract

The management of cystic fibrosis (CF) requires a collaborative, multidisciplinary approach that integrates various fields of healthcare to address the complex needs of patients with this genetic disorder. Nursing plays a pivotal role by providing patient education on disease management and administering therapies that include nebulized treatments, antibiotics, and nutrition plans. Additionally, nurses monitor lung function, manage symptoms, and support psychosocial needs. Radiologists contribute by performing imaging studies, such as chest X-rays and CT scans, which are crucial for assessing lung health and guiding treatment decisions. Laboratory scientists play an essential role by conducting tests to monitor respiratory function and screen for potential complications, ensuring that timely interventions can be made based on lab results. Furthermore, health administration ensures that a cohesive team approach is maintained, facilitating communication between disciplines and optimizing resource allocation to enhance patient care. Surgical nursing may become essential for patients requiring lung transplants or other surgical interventions, where pre-operative and post-operative care is critical for recovery. Physical therapy also has a vital role in managing CF, focusing on airway clearance techniques and exercise regimens that enhance pulmonary function and overall well-being. By integrating these diverse areas—nursing, radiology, laboratory science, health administration, surgical nursing, physical therapy, and general medicine—healthcare teams can provide comprehensive, individualized care that improves the quality of life and health outcomes for individuals living with cystic fibrosis.