Literature DB >> 14679482

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

Patrick A Flume1, Lloyd A Taylor, Deborah L Anderson, Sue Gray, David Turner.   

Abstract

We previously surveyed cystic fibrosis (CF) center directors and adult patients with CF to assess their perceptions regarding transition from a pediatric to an adult setting. An important finding in those studies was a lack of standard programs for transfer of young adults with CF from pediatric to adult care settings. Patients with CF typically receive care from clinics utilizing a multidisciplinary approach, suggesting that every member of the CF team can impact the transition process. Our purpose in this study was to gain an appreciation for various team members' perspectives on transition. An Internet survey was offered to all CF centers across the country to be completed by team members, excluding physicians. We received 291 completed surveys, nearly half completed by nurses, but our respondents included social workers, nutritionists, respiratory therapists, and a few team members with other training. Nearly half of the respondents work for both pediatric and adult teams. The majority of respondents (71.8%) reported that their adult patients receive care from an internist in a separate adult program, but nearly 20% reported that a pediatrician follows their adult patients. A minority thought that age (37.4% of respondents), marriage (16.2%), and pregnancy (27.1%) were criteria for transfer, though most (86.2%) suggested that patients should be transferred by age 21 years. Criteria precluding transfer included patient/family resistance (45%), disease severity (34%), and developmental delay (31.3%). It was uncommon (11.4%) for an introduction to the concept of transition at the time of diagnosis. Over one-half of patients did not meet the adult team until time of transfer. Team members' perceptions of patients' concerns were similar to what we had previously measured in physicians, again far greater than what we have measured in patients themselves. In many ways, what we have measured here in team members reflects what we have reported by physicians, demonstrating slow development of standard transition programs and an overestimate of patients' concerns regarding transition. These differences may impede the successful transition of patients into an adult program. It is clear from this study that team members have an interest in and opinions on transition, and are likely play a vital role in the transition process. Standard programs of transition should be developed, and team members should be engaged in that process. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2004        PMID: 14679482     DOI: 10.1002/ppul.10391

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  13 in total

Review 1.  Health care transitions among youth with disabilities or special health care needs: an ecological approach.

Authors:  Grace Wang; Barbara Burns McGrath; Carolyn Watts
Journal:  J Pediatr Nurs       Date:  2009-08-22       Impact factor: 2.145

2.  Transition of care in children with chronic disease.

Authors:  Colin Wallis
Journal:  BMJ       Date:  2007-06-16

3.  Cystic fibrosis adolescent transition care in Canada: A snapshot of current practice.

Authors:  Anna Gravelle; George Davidson; Mark Chilvers
Journal:  Paediatr Child Health       Date:  2012-12       Impact factor: 2.253

4.  Measuring the transition readiness of youth with special healthcare needs: validation of the TRAQ--Transition Readiness Assessment Questionnaire.

Authors:  Gregory S Sawicki; Katryne Lukens-Bull; Xiaoping Yin; Nathan Demars; I-Chan Huang; William Livingood; John Reiss; David Wood
Journal:  J Pediatr Psychol       Date:  2009-12-29

5.  Improving transition from paediatric to adult cystic fibrosis care: programme implementation and evaluation.

Authors:  Megumi J Okumura; Thida Ong; Diana Dawson; Dennis Nielson; Nancy Lewis; Martha Richards; Claire D Brindis; Mary Ellen Kleinhenz
Journal:  BMJ Qual Saf       Date:  2014-01-10       Impact factor: 7.035

Review 6.  Transition care: future directions in education, health policy, and outcomes research.

Authors:  Niraj Sharma; Kitty O'Hare; Richard C Antonelli; Gregory S Sawicki
Journal:  Acad Pediatr       Date:  2014 Mar-Apr       Impact factor: 3.107

7.  Transitioning adolescents and young adults with a chronic health condition to adult healthcare - an exemplar program.

Authors:  Karen Kaufmann Rauen; Kathleen J Sawin; Tera Bartelt; William P Waring; Merle Orr; R Corey O'Connor
Journal:  Rehabil Nurs       Date:  2013 Mar-Apr       Impact factor: 1.625

Review 8.  [Cystic fibrosis care in transition from adolescence to adult age].

Authors:  R Fischer; S Nährig; M Kappler; M Griese
Journal:  Internist (Berl)       Date:  2009-10       Impact factor: 0.743

Review 9.  [Cystic fibrosis : A new disease pattern in adult medicine].

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

10.  A new tool for the paediatric HIV research: general data from the Cohort of the Spanish Paediatric HIV Network (CoRISpe).

Authors:  Ma Isabel de Jose; Santiago Jiménez de Ory; Maria Espiau; Claudia Fortuny; Ma Luisa Navarro; Pere Soler-Palacín; Ma Angeles Muñoz-Fernandez
Journal:  BMC Infect Dis       Date:  2013-01-02       Impact factor: 3.090

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.