Literature DB >> 21602723

Growing up with sickle cell disease: a pilot study of a transition program for adolescents with sickle cell disease.

Grant M Smith1, Vivian R Lewis, Elaine Whitworth, Deborah T Gold, Courtney D Thornburg.   

Abstract

We implemented the Duke Sickle Cell Disease (SCD) Transition Program for adolescents with SCD and investigated the knowledge about SCD; concerns and emotions about transitioning; and the initial impact of the Transition Program. Thirty-three adolescents participated in the initial study. Gaps in knowledge included ethnicities affected by SCD and inheritance of SCD. Adolescents were primarily concerned about transferring to a new medical team. There was a mix of both positive and negative emotions that varied over time. Overall, we have identified educational gaps and concerns and emotions about transitioning, which we will address through the Duke SCD Transition Program.

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Year:  2011        PMID: 21602723     DOI: 10.1097/MPH.0b013e318211bb2e

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  12 in total

1.  Exploring Adult Care Experiences and Barriers to Transition in Adult Patients with Sickle Cell Disease.

Authors:  C J Bemrich-Stolz; J H Halanych; T H Howard; L M Hilliard; J D Lebensburger
Journal:  Int J Hematol Ther       Date:  2015-09-06

2.  Assessing Disease Knowledge and Self-Management in Youth With Sickle Cell Disease Prior to Transition.

Authors:  Barbara Speller-Brown; Maureen Varty; Lisa Thaniel; Marni B Jacobs
Journal:  J Pediatr Oncol Nurs       Date:  2018-12-19       Impact factor: 1.636

3.  Pediatric to Adult Care Transition: Perspectives of Young Adults With Sickle Cell Disease.

Authors:  Jerlym S Porter; Kimberly M Wesley; Mimi S Zhao; Rebecca J Rupff; Jane S Hankins
Journal:  J Pediatr Psychol       Date:  2017-10-01

Review 4.  Measures of readiness to transition to adult health care for youth with chronic physical health conditions: a systematic review and recommendations for measurement testing and development.

Authors:  Lisa A Schwartz; Lauren C Daniel; Lauren D Brumley; Lamia P Barakat; Kimberly M Wesley; Lisa K Tuchman
Journal:  J Pediatr Psychol       Date:  2014-06-01

Review 5.  Adolescents with Hearing Loss and the International Classification of Functioning, Health, and Disability: Children & Youth Version.

Authors:  Kris English; Emily Pajevic
Journal:  Semin Hear       Date:  2016-08

6.  A program of transition to adult care for sickle cell disease.

Authors:  Anjelica C Saulsberry; Jerlym S Porter; Jane S Hankins
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

7.  Transitioning Adolescents and Young Adults With Sickle Cell Disease From Pediatric to Adult Health Care: Provider Perspectives.

Authors:  Natalie B Stollon; Christine W Paine; Matthew S Lucas; Lauren D Brumley; Erika S Poole; Tamara Peyton; Anne W Grant; Sophia Jan; Symme Trachtenberg; Miriam Zander; Christopher P Bonafide; Lisa A Schwartz
Journal:  J Pediatr Hematol Oncol       Date:  2015-11       Impact factor: 1.289

Review 8.  A scoping review of transition interventions for young adults with sickle cell disease.

Authors:  Adrienne Viola; Jerlym Porter; Jelaina Shipman; Ellen Brooks; Cecilia Valrie
Journal:  Pediatr Blood Cancer       Date:  2021-06-05       Impact factor: 3.167

9.  Feasibility of Medical Student Mentors to Improve Transition in Sickle Cell Disease.

Authors:  Adrienne S Viola; Richard Drachtman; Amanda Kaveney; Ashwin Sridharan; Beth Savage; Cristine D Delnevo; Elliot J Coups; Jerlym S Porter; Katie A Devine
Journal:  J Pediatr Psychol       Date:  2021-07-20

10.  Barriers in transition from pediatrics to adult medicine in sickle cell anemia.

Authors:  Jeffrey D Lebensburger; Christina J Bemrich-Stolz; Thomas H Howard
Journal:  J Blood Med       Date:  2012-09-19
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