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Updated: Jul 31, 2025

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
Published on: April 11, 2018
Transition Care in Cystic Fibrosis
Nitin Dhochak1, Sushil K Kabra2
1Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Transitioning cystic fibrosis (CF) care requires careful coordination and patient self-management skills. Resource availability impacts successful transition, especially in resource-limited settings.
Area of Science:
- Pediatric Medicine
- Pulmonology
- Healthcare Management
Background:
- Cystic fibrosis (CF) is a chronic childhood illness with increasing adult survival.
- Adult CF patients face a significant disease burden.
- Transitioning care from pediatric to adult services is complex.
Purpose of the Study:
- To highlight the complexities of transitioning pediatric cystic fibrosis (CF) care to adult multidisciplinary teams.
- To emphasize the importance of patient self-reliance and readiness for managing CF.
- To discuss the challenges in resource-limited settings.
Main Methods:
- Literature review on CF care transition processes.
- Analysis of factors influencing successful patient self-management.
- Assessment of resource availability for CF transition.
Main Results:
- Successful transition necessitates a key worker for coordination.
- Patient readiness and self-management skills are crucial.
- Online resources exist but are insufficient in resource-limited areas.
Conclusions:
- Effective transition requires coordinated care and patient empowerment.
- Addressing resource limitations is vital for equitable CF care.
- Further development of transition support is needed globally.
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15:12Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein Expressed in Saccharomyces cerevisiae
Published on: May 10, 2014
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