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Review

Problems of Patients with Cystic Fibrosis during Transition to Adulthood

by
Violetta Opoka-Winiarska
1,
Szczepan Cofta
2,
Henryk Mazurek
3 and
Jerzy Kozielski
4,*
1
Department of Paediatric Pulmonology and Rheumatology, Medical University of Lublin, Lublin, Poland
2
Department of Pulmonology, Alergology and Respiratory Oncology, University of Medical Sciences, Poznan, Poland
3
Department of Bronchology and Cystic Fibrosis, National Institute for Tuberculosis and Lung Diseases, Pediatric Branch, Rabka, Poland
4
Department of Lung Diseases and Tuberculosis, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia, ul. Ks. Koziołka 1, Katowice, Poland
*
Author to whom correspondence should be addressed.
Adv. Respir. Med. 2015, 83(5), 394-400; https://doi.org/10.5603/PiAP.2015.0064
Submission received: 2 September 2014 / Revised: 8 September 2015 / Accepted: 8 September 2015 / Published: 8 September 2015

Abstract

The proper care of cystic fibrosis patients extends over their lifetime. More than half of the children with the disease die before adulthood. An important element in the patient’s care is a time of transition from a paediatric to the care of an internist and the patient’s acceptance of this necessity. Transition from paediatric care to an internist should be adequately prepared. It is not only a question of transfer of medical records, but also careful preparation of patients for such transition. The patients expect not only continuity of care but also the Introduction to the management with the disease. The creation of a base for specialist hospital treatment for exacerbation of the disease at the adulthood is an important element in the care of these patients. The problem has been solved in the children group, but is still waiting for solution in adults with cystic fibrosis. It has been proven that care in the centres carried out by a specialized team ensures longer life and better quality of life of these patients. The paper is an overview of these two important elements of care of adults with cystic fibrosis.
Keywords: cystic fibrosis; childhood to adulthood cystic fibrosis; childhood to adulthood

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MDPI and ACS Style

Opoka-Winiarska, V.; Cofta, S.; Mazurek, H.; Kozielski, J. Problems of Patients with Cystic Fibrosis during Transition to Adulthood. Adv. Respir. Med. 2015, 83, 394-400. https://doi.org/10.5603/PiAP.2015.0064

AMA Style

Opoka-Winiarska V, Cofta S, Mazurek H, Kozielski J. Problems of Patients with Cystic Fibrosis during Transition to Adulthood. Advances in Respiratory Medicine. 2015; 83(5):394-400. https://doi.org/10.5603/PiAP.2015.0064

Chicago/Turabian Style

Opoka-Winiarska, Violetta, Szczepan Cofta, Henryk Mazurek, and Jerzy Kozielski. 2015. "Problems of Patients with Cystic Fibrosis during Transition to Adulthood" Advances in Respiratory Medicine 83, no. 5: 394-400. https://doi.org/10.5603/PiAP.2015.0064

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