Literature DB >> 19714300

[Cystic fibrosis care in transition from adolescence to adult age].

R Fischer1, S Nährig, M Kappler, M Griese.   

Abstract

During the last 30 years, life expectancy in patients with cystic fibrosis has significantly improved. In Germany, almost half of the 8500 patients are 18 years or older. Older patients have increased rates of cystic fibrosis typical complications, In addition the characteristic complications of adulthood, including arterial hypertension, hyperlipidemia, and cardiovascular diseases, occur. Also crisis of marriage or loss of work place, as well as family planning measures including in-vitro-fertilization are problems merely of the adult cystic fibrosis patient. Therefore adult patients should be treated in a centre specialized on adults. At the moment, in Germany only one third of all adult patients are followed up in an adult center, many patients are treated in age-independent centers, and also a significant number is treated in small clinics. In this article models for transition currently established in Germany are described and occurring problems with their implementation are discussed.

Entities:  

Mesh:

Year:  2009        PMID: 19714300     DOI: 10.1007/s00108-009-2399-6

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  11 in total

1.  Transition programs in cystic fibrosis centers.

Authors:  Steven P Conway
Journal:  Pediatr Pulmonol       Date:  2004-01

Review 2.  Life beyond pediatrics. Transition of chronically ill adolescents from pediatric to adult health care systems.

Authors:  D V Schidlow; S B Fiel
Journal:  Med Clin North Am       Date:  1990-09       Impact factor: 5.456

3.  Improving transition from pediatric to adult cystic fibrosis care: lessons from a national survey of current practices.

Authors:  Suzanne Elizabeth McLaughlin; Marie Diener-West; Alka Indurkhya; Haya Rubin; Rebekah Heckmann; Michael Patrick Boyle
Journal:  Pediatrics       Date:  2008-05       Impact factor: 7.124

4.  Transition from paediatric to adult care for persons with cystic fibrosis: patient and parent perspectives.

Authors:  A Westwood; L Henley; P Willcox
Journal:  J Paediatr Child Health       Date:  1999-10       Impact factor: 1.954

5.  Strategies for improving transition to adult cystic fibrosis care, based on patient and parent views.

Authors:  M P Boyle; Z Farukhi; M L Nosky
Journal:  Pediatr Pulmonol       Date:  2001-12

6.  Transition programs in cystic fibrosis centers: perceptions of patients.

Authors:  Deborah L Anderson; Patrick A Flume; Kristina K Hardy; Sue Gray
Journal:  Pediatr Pulmonol       Date:  2002-05

7.  Transition programs in cystic fibrosis centers: perceptions of team members.

Authors:  Patrick A Flume; Lloyd A Taylor; Deborah L Anderson; Sue Gray; David Turner
Journal:  Pediatr Pulmonol       Date:  2004-01

8.  Clinical changes of patients with cystic fibrosis during transition from pediatric to adult care.

Authors:  Ingrid Duguépéroux; Aline Tamalet; Isabelle Sermet-Gaudelus; Muriel Le Bourgeois; Michèle Gérardin; Nadine Desmazes-Dufeu; Dominique Hubert
Journal:  J Adolesc Health       Date:  2008-06-16       Impact factor: 5.012

9.  A model for transition from pediatric to adult care in cystic fibrosis.

Authors:  Susan Madge; Mandy Bryon
Journal:  J Pediatr Nurs       Date:  2002-08       Impact factor: 2.145

10.  Transition of transplant patients with cystic fibrosis to adult care: today's challenges.

Authors:  Louise Taylor; Anna Tsang; Alison Drabble
Journal:  Prog Transplant       Date:  2006-12       Impact factor: 1.065

View more
  1 in total

Review 1.  [Cystic fibrosis : A new disease pattern in adult medicine].

Authors:  D Staab; C Schwarz
Journal:  Internist (Berl)       Date:  2018-11       Impact factor: 0.743

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.