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Neonatal and Pediatric Medicine
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  • Neonat Pediatr Med 10: 464,

Cystic Fibrosis Management Comprehensive Care for Patients

Paul Lomas*
Department of Pediatrics, University of Cincinnati College of Medicine, California, U.S.A
*Corresponding Author : Paul Lomas, Department of Pediatrics, University of Cincinnati College of Medicine, California, U.S.A, Email: paul@gmail.com

Received Date: Oct 02, 2024 / Published Date: Oct 30, 2024

Abstract

Cystic fibrosis (CF) is a life-threatening genetic disorder that primarily affects the lungs and digestive system, characterized by the production of thick, sticky mucus. Effective management of CF requires a multidisciplinary approach to improve patient outcomes and quality of life. This article explores the pathophysiology of cystic fibrosis, its clinical manifestations, and current management strategies, including respiratory care, nutritional support, and innovative therapies. Additionally, the role of psychological support and the importance of patient education and family involvement in managing this complex condition will be emphasized. By integrating various management strategies, healthcare providers can significantly enhance the lives of those affected by cystic fibrosis.

Citation: Paul L ( 2024) Cystic Fibrosis Management: Comprehensive Care for Patients. Neonat Pediatr Med 10: 464.

Copyright: © 2024 Paul L. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

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