Optimizing adolescent transition to adult care for sickle cell disease

MEDSURG Nursing

Volumn 22, Issue 4, 2013, Pages 255-257

  Cerns, Stephenie ^a   McCracken, Colleen ^a   Rich, Claire ^b  

^a FROEDTERT MEMORIAL LUTHERAN HOSPITAL   (United States)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANEMIA, SICKLE CELL; CHILD HEALTH CARE; HUMAN; ORGANIZATION AND MANAGEMENT; PATIENT CARE; TRANSITION TO ADULT CARE;

ADOLESCENT; ADOLESCENT HEALTH SERVICES; ADULT; ANEMIA, SICKLE CELL; HUMANS; PATIENT CARE TEAM; TRANSITION TO ADULT CARE;

EID: 84891598646     PISSN: 10920811     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

1. Anie, K.A., Egunjobi, F.E., & Akinyanju, O.O. (2010). Psychosocial impact of sickle cell disorder: Perspectives from a Nigerian setting. Globalization and Health, 6, 2. doi:10.1186/1744-8603-6-2
2. Baines, J.M. (2009). Promoting better care: Transition from child to adult services. Nursing Standard, 23(19), 35-40.
3. DeBaun, M., & Telfair, J. (2012). Transition and sickle cell disease. The American Academy of Pediatrics, 130(5), 926-935.
4. Kennedy, A., & Sawyer, S. (2008). Transition from pediatric to adult services: Are we getting it right? Current Opinion in Pediatrics, 20(4), 403-409. doi:10.1097/MOP.0b013e328305e128
5. Lee, L., Askew, R., Walker, J., Stephen, J., & Robertson-Artwork, A. (2012). Adults with sickle cell disease. Home Healthcare Nurse, 30(3), 173-183.
6. Newland, J. (2008). Factors influencing independence in adolescents with sickle cell disease. Journal of Child and Adolescent Psychiatric Nursing, 21(3), 177-185.
7. Pack-Mabien, A., & Haynes, J. (2009). A primary care provider’s guide to preventative and acute care management of adults and children with sickle cell disease. Journal of the American Academy of Nurse Practitioners, 21(5), 250-257. doi:10.1111/j.1745-7599.2009.00401.x.
8. Rapley, P., & Davidson, P.M. (2010). Enough of the problem: A review of time for health care transition solutions for young adults with a chronic illness. Journal of Clinical Nursing, 19(3-4), 313-323. doi: 10.1111/j. 1365-2702.2009.03027.x
9. Smith, G., Lewis, V., Whitworth, E., Gold, D., & Thornburg, C. (2011). Growing up with sickle cell disease: A pilot study of a transition program for adolescents with sickle cell disease. Journal of Pediatric Hematology Oncology, 33(5), 379-382. doi: 10.1097/MPH.0b013e318211bb2e.
10. Treadwell, M., Telfair, J., Gibson, R.W., Johnson, S., & Osunkwo, I. (2010). Transition from pediatric to adult care in sickle cell disease: Establishing evidence-based practice and directions for research. American Journal of Hematology, 86(1), 116-120.
11. Wright, K., & Adeosum, O. (2009). Barriers to effective pain management in sickle cell disease. British Journal of Nursing, 18(3), 158-161.