Crossing the transition chasm: experiences and recommendations for improving transitional care of young adults, parents and providers

被引:197
作者
van Staa, A. L. [1 ,2 ]
Jedeloo, S. [2 ]
van Meeteren, J. [3 ]
Latour, J. M. [4 ]
机构
[1] Erasmus Univ, Inst Hlth Policy & Management, NL-3000 DR Rotterdam, Netherlands
[2] Rotterdam Univ, Expertise Ctr Transit Care, Rotterdam, Netherlands
[3] Erasmus MC Univ Med Ctr, Dept Rehabil Med & Physiotherapy, Rotterdam, Netherlands
[4] Erasmus MC Univ Med Ctr, Dept Paediat, Sophia Childrens Hosp, Rotterdam, Netherlands
关键词
adolescent; adult-oriented care; chronic illness; complex healthcare needs; transfer; transition; JUVENILE IDIOPATHIC ARTHRITIS; HEALTH-CARE; CEREBRAL-PALSY; POSITION PAPER; ADOLESCENTS; SERVICES; PERSPECTIVES; CHILD; LIFE; PATIENT;
D O I
10.1111/j.1365-2214.2011.01261.x
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Background Transition from paediatric to adult healthcare has received little attention in the Netherlands. This study aimed to: (i) map experiences with the transfer to adult care of young adults with chronic conditions; and (ii) identify recommendations for transitional care of young adults, their parents and healthcare providers. Methods Semi-structured interviews with 24 young adults after transfer (aged 15-22 years; diagnosed with haemophilia, diabetes mellitus, spina bifida, congenital heart disorders, cystic fibrosis, juvenile rheumatoid arthritis or sickle cell disease), 24 parents and 17 healthcare providers. Thematic analysis was performed. Results Only the haemophilia department offered a structured transition programme, most patients had not been prepared for transition. Experiences and views of patients, parents and professionals mainly overlapped and were condensed into four core themes. Two are related to moving to adult care: (1) 'leaving paediatric care is a logical step'. Leaving familiar surroundings was harder for parents than for young adults who displayed a positive 'wait-and-see' attitude; and (2) 'transition is complicated by cultural gaps between paediatric and adult services'. Young adults and parents felt lost after transfer and recommended their peers 'to be alert and involved'. Providers also recognized the cultural chasm between both services and worried about non-compliance, lost to follow-up and lack of independence. Two other themes indicated priorities for improvement: (3) 'better patient and parent preparation' for differences between healthcare settings and for new roles and responsibilities with respect to self-management; and (4) 'more collaboration and personal links' between paediatric and adult care providers. Conclusions Action is required to cross the chasm between paediatric and adult-oriented care. Preparation for transition should start early and focus on strengthening adolescents' independency without undermining parental involvement. Building bridges between services, gaining trust and investing in new personal relations is a challenge for all parties involved: transition is about responding and bonding.
引用
收藏
页码:821 / 832
页数:12
相关论文
共 41 条
[1]  
[Anonymous], EIGEN BENEN JONGEREN
[2]  
[Anonymous], ADOLESC MED STATE AR
[3]  
Anthony SJ, 2009, AM J TRANSPLANT, V9, P614, DOI 10.1111/j.1600-6143.2008.02515.x
[4]   What do we really know about the transition to adult-centered health care? A focus on cerebral palsy and spina bifida [J].
Binks, Jessie A. ;
Barden, Wendy S. ;
Burke, Tficia A. ;
Young, Nancy L. .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2007, 88 (08) :1064-1073
[5]   TRANSITION FROM CHILD-CENTERED TO ADULT HEALTH-CARE SYSTEMS FOR ADOLESCENTS WITH CHRONIC CONDITIONS - A POSITION PAPER OF THE SOCIETY FOR ADOLESCENT MEDICINE [J].
BLUM, RW ;
GARELL, D ;
HODGMAN, CH ;
JORISSEN, TW ;
OKINOW, NA ;
ORR, DP ;
SLAP, GB .
JOURNAL OF ADOLESCENT HEALTH, 1993, 14 (07) :570-576
[6]  
Blum RW, 2002, PEDIATRICS, V110, P1304
[7]  
Braun V., 2006, Qualitative Research in Psychology, V3, P77, DOI 10.1191/1478088706qp063oa
[8]  
Christie Deborah, 2009, Adolesc Med State Art Rev, V20, P981
[9]  
Clarizia NA, 2009, CAN J CARDIOL, V25, pE317
[10]   A pilot study on the effects of the transition of paediatric to adult health care in patients with haemophilia and in their parents: patient and parent worries, parental illness-related distress and health-related Quality of Life [J].
Geerts, E. ;
De Wiel, H. Van ;
Tamminga, R. .
HAEMOPHILIA, 2008, 14 (05) :1007-1013