[Cystic fibrosis, what follow-up action for adults in 2019?]
1Hôpital Cochin, 27, rue du Faubourg- Saint-Jacques, 75014 Paris, France.
Insights
Cystic fibrosis (CF) now affects more adults than children in France, shifting its classification from a pediatric to an adult pathology. This demographic change necessitates evolving healthcare strategies to meet the emerging needs of adult CF patients.
Area of Science:
- Pulmonology
- Genetics
- Epidemiology
Background:
- Cystic fibrosis (CF) was historically viewed as a pediatric disease.
- Recent data indicates a demographic shift in France, with adult CF cases now exceeding pediatric cases since 2015.
- This epidemiological transition highlights evolving patient demographics in CF care.
Purpose of the Study:
- To analyze the implications of the increasing adult population with cystic fibrosis.
- To underscore the need for adapting healthcare organization for adult CF patients.
- To identify emerging healthcare needs in the adult CF population.
Main Methods:
- Demographic analysis of cystic fibrosis patient data in France.
- Review of healthcare organization models for chronic diseases.
- Identification of specific needs in adult patient care pathways.
Main Results:
- Since 2015, adults represent the majority of the cystic fibrosis population in France.
- The shift necessitates a re-evaluation of healthcare structures and resource allocation.
- New and specific healthcare needs are emerging within the adult CF population.
Conclusions:
- Cystic fibrosis is transitioning into a predominantly adult disease in France.
- Healthcare systems require significant adaptation to address the evolving needs of adults with CF.
- Proactive planning is crucial for optimizing adult CF care and improving patient outcomes.
Abstract:
Long considered as a paediatric pathology, cystic fibrosis concerns in France more adults than children since 2015. Considering this demographic shift, the way healthcare is organized requires constant adaptation, particularly in the care of adults where new needs are rapidly emerging.
More Related Videos
08:00Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
Published on: April 11, 2018
07:04Forskolin-induced Swelling in Intestinal Organoids: An In Vitro Assay for Assessing Drug Response in Cystic Fibrosis Patients
Published on: February 11, 2017
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Chronic Obstructive Pulmonary Disease-V: Management
Smoking Cessation
Chronic Obstructive Pulmonary Disease-V: Nursing Management
Assessment
Asthma-IV: Nursing Management
First, in...
Kidney Transplant III: Nursing Management
