Literature DB >> 26717957

Applicability of the SMART Model of Transition Readiness for Sickle-Cell Disease.

Siddika S Mulchan1, Jessica M Valenzuela2, Lori E Crosby3, Claudia Diaz Pow Sang4.   

Abstract

OBJECTIVES: This study aimed to examine the applicability of the Social-ecological Model of Adolescent and Young Adult Readiness to Transition (SMART) model for adolescents and young adults (AYA) with sickle-cell disease (SCD).
METHODS: 14 AYA with SCD (14-24 years old) and 10 clinical experts (6-20 years of experience) completed semi-structured interviews. AYA completed brief questionnaires. Interviews were coded for themes, which were reviewed to determine their fit within the SMART model.
RESULTS: Overall, most themes were consistent with the model (e.g., sociodemographics/culture, neurocognition/IQ, etc.). Factors related to race/culture, pain management, health-care navigation skills, societal stigma, and lack of awareness about SCD were salient for AYA with SCD.
CONCLUSIONS: Findings suggest the SMART model may be appropriate in SCD with the consideration of disease-related stigma. This study is a step toward developing a disease-specific model of transition readiness for SCD. Future directions include the development of a measure of transition readiness for this population.
© The Author 2015. Published by Oxford University Press on behalf of the Society of Pediatric Psychology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  adolescents; qualitative methods; sickle-cell disease

Mesh:

Year:  2015        PMID: 26717957      PMCID: PMC4888114          DOI: 10.1093/jpepsy/jsv120

Source DB:  PubMed          Journal:  J Pediatr Psychol        ISSN: 0146-8693


  37 in total

Review 1.  Cognitive functioning in children with sickle cell disease: a meta-analysis.

Authors:  Jeffrey Schatz; Robert L Finke; Julie M Kellett; Joel H Kramer
Journal:  J Pediatr Psychol       Date:  2002-12

2.  Reducing racial disparities in pain treatment: the role of empathy and perspective-taking.

Authors:  Brian B Drwecki; Colleen F Moore; Sandra E Ward; Kenneth M Prkachin
Journal:  Pain       Date:  2011-01-28       Impact factor: 6.961

Review 3.  Managing sickle cell disease.

Authors:  Susan Claster; Elliott P Vichinsky
Journal:  BMJ       Date:  2003-11-15

4.  Introduction to commentary: exploiting opportunities created by the patient-reported measurement information system in pediatric psychology.

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Journal:  J Pediatr Psychol       Date:  2012-03-15

5.  Evaluation of a disease-specific self-efficacy instrument in adolescents with sickle cell disease and its relationship to adjustment.

Authors:  Olivio J Clay; Joseph Telfair
Journal:  Child Neuropsychol       Date:  2007-03       Impact factor: 2.500

6.  Commentary: the patient-reported outcome measurement information system (PROMIS®) for children and youth: application to pediatric psychology.

Authors:  Christopher B Forrest; Katherine B Bevans; Carole Tucker; Anne W Riley; Ulrike Ravens-Sieberer; William Gardner; Kathleen Pajer
Journal:  J Pediatr Psychol       Date:  2012-02-23

7.  Supporting the health care transition from adolescence to adulthood in the medical home.

Authors:  W Carl Cooley; Paul J Sagerman
Journal:  Pediatrics       Date:  2011-06-27       Impact factor: 7.124

8.  Health care transition: youth, family, and provider perspectives.

Authors:  John G Reiss; Robert W Gibson; Leslie R Walker
Journal:  Pediatrics       Date:  2005-01       Impact factor: 7.124

9.  Pain management and symptoms of substance dependence among patients with sickle cell disease.

Authors:  James Elander; Joanne Lusher; David Bevan; Paul Telfer
Journal:  Soc Sci Med       Date:  2003-11       Impact factor: 4.634

10.  Transfer as a component of the transition of adolescents with sickle cell disease to adult care: adolescent, adult, and parent perspectives.

Authors:  J Telfair; J Myers; S Drezner
Journal:  J Adolesc Health       Date:  1994-11       Impact factor: 5.012

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  15 in total

1.  Stigma of Sickle Cell Disease: A Systematic Review.

Authors:  Dominique Bulgin; Paula Tanabe; Coretta Jenerette
Journal:  Issues Ment Health Nurs       Date:  2018-04-13       Impact factor: 1.835

2.  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

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

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Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

Review 4.  Development and Content Validation of the Transition Readiness Inventory Item Pool for Adolescent and Young Adult Survivors of Childhood Cancer.

Authors:  Lisa A Schwartz; Jessica L Hamilton; Lauren D Brumley; Lamia P Barakat; Janet A Deatrick; Dava E Szalda; Katherine B Bevans; Carole A Tucker; Lauren C Daniel; Eliana Butler; Anne E Kazak; Wendy L Hobbie; Jill P Ginsberg; Alexandra M Psihogios; Elizabeth Ver Hoeve; Lisa K Tuchman
Journal:  J Pediatr Psychol       Date:  2017-10-01

5.  Preferences for cancer survivorship care among adolescents and young adults who experienced healthcare transitions and their parents.

Authors:  Alexandra M Psihogios; Lisa A Schwartz; Janet A Deatrick; Elizabeth S Ver Hoeve; Lindsay M Anderson; Elicia C Wartman; Dava Szalda
Journal:  J Cancer Surviv       Date:  2019-07-04       Impact factor: 4.442

6.  Moving up: Healthcare transition experiences of adolescents and young adults with cystic fibrosis.

Authors:  Katherine South; Maureen George; Hossein Sadeghi; Victoria Piane; Arlene Smaldone
Journal:  J Pediatr Nurs       Date:  2022-03-30       Impact factor: 2.523

7.  Opioid Prescription Filling Trends Among Children with Sickle Cell Disease After the Release of State-Issued Guidelines on Pain Management.

Authors:  Susan E Creary; Deena J Chisolm; Sharon K Wrona; Jennifer N Cooper
Journal:  Pain Med       Date:  2020-10-01       Impact factor: 3.750

8.  High health satisfaction among emerging adults with diabetes: Factors predicting resilience.

Authors:  Sarah D Corathers; Jessica C Kichler; Nora F Fino; Wei Lang; Jean M Lawrence; Jennifer K Raymond; Joyce P Yi-Frazier; Dana Dabelea; Angela D Liese; Sharon H Saydah; Michael Seid; Lawrence M Dolan
Journal:  Health Psychol       Date:  2016-10-13       Impact factor: 4.267

9.  Disease Self-Efficacy and Health-Related Quality of Life in Adolescents With Sickle Cell Disease.

Authors:  Alana Goldstein-Leever; James L Peugh; Charles T Quinn; Lori E Crosby
Journal:  J Pediatr Hematol Oncol       Date:  2020-03       Impact factor: 1.170

10.  Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project.

Authors:  Donna K McClish; Wally R Smith; James L Levenson; Imoigele P Aisiku; John D Roberts; Susan D Roseff; Viktor E Bovbjerg
Journal:  Biomed Res Int       Date:  2017-03-28       Impact factor: 3.411

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