Literature DB >> 26122692

Transition Needs of Adolescents With Sickle Cell Disease.

Regina A Abel1, Esther Cho2, Kelley R Chadwick-Mansker3, Natalia D'Souza4, Ashley J Housten5, Allison A King6.   

Abstract

OBJECTIVE: This article describes how adolescents with sickle cell disease (SCD) perceive their ability to perform everyday tasks required for transition to adult health care and independent living.
METHOD: The Adolescent Autonomy Checklist (AAC) was adapted to include skills associated with managing SCD (AAC-SCD) and was administered to adolescents during clinic visits. Participants indicated "can do already" or "needs practice" for 100 activities in 12 categories.
RESULTS: Of 122 patients, the percentage of adolescents who needed practice was greatest in living arrangements (38.7%), money management (35.8%), vocational skills (29.6%), and health care skills (25.5%). We found a significant effect of age and of cerebrovascular injury on the percentage of those who reported "needs practice" in multiple categories. We found no effect of gender and limited effect of hemoglobin phenotype on any skill category.
CONCLUSION: Findings support the need for educational intervention to improve transition skills in adolescents with SCD.
Copyright © 2015 by the American Occupational Therapy Association, Inc.

Entities:  

Mesh:

Year:  2015        PMID: 26122692      PMCID: PMC4480057          DOI: 10.5014/ajot.2015.013730

Source DB:  PubMed          Journal:  Am J Occup Ther        ISSN: 0272-9490


  21 in total

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Authors:  Janet S Hess; Diane M Straub
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2.  Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease.

Authors:  J Schatz; R T Brown; J M Pascual; L Hsu; M R DeBaun
Journal:  Neurology       Date:  2001-04-24       Impact factor: 9.910

3.  Preliminary evidence suggesting caution in the use of psychiatric self-report measures with adolescents with high-functioning autism spectrum disorders.

Authors:  C A Mazefsky; J Kao; D P Oswald
Journal:  Res Autism Spectr Disord       Date:  2011-01

4.  Parent education and biologic factors influence on cognition in sickle cell anemia.

Authors:  Allison A King; John J Strouse; Mark J Rodeghier; Bruce E Compas; James F Casella; Robert C McKinstry; Michael J Noetzel; Charles T Quinn; Rebecca Ichord; Michael M Dowling; J Philip Miller; Michael R Debaun
Journal:  Am J Hematol       Date:  2014-02       Impact factor: 10.047

5.  Health-related quality of life (HRQoL) of children with type 1 diabetes mellitus (T1DM): self and parental perceptions.

Authors:  Efrosini Kalyva; Evlampia Malakonaki; Christine Eiser; Dimitrios Mamoulakis
Journal:  Pediatr Diabetes       Date:  2011-02       Impact factor: 4.866

6.  Cerebrovascular accidents in sickle cell disease: rates and risk factors.

Authors:  K Ohene-Frempong; S J Weiner; L A Sleeper; S T Miller; S Embury; J W Moohr; D L Wethers; C H Pegelow; F M Gill
Journal:  Blood       Date:  1998-01-01       Impact factor: 22.113

7.  Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia.

Authors:  Elliott P Vichinsky; Lynne D Neumayr; Jeffrey I Gold; Michael W Weiner; Randall R Rule; Diana Truran; Jeffrey Kasten; Barry Eggleston; Karen Kesler; Lillian McMahon; Eugene P Orringer; Thomas Harrington; Karen Kalinyak; Laura M De Castro; Abdullah Kutlar; Cynthia J Rutherford; Cage Johnson; Joel David Bessman; Lanetta B Jordan; F Daniel Armstrong
Journal:  JAMA       Date:  2010-05-12       Impact factor: 56.272

8.  Prevalence and treatment of depression in children and adolescents with sickle cell disease: a retrospective cohort study.

Authors:  Jeanette M Jerrell; Avnish Tripathi; Roger S McIntyre
Journal:  Prim Care Companion CNS Disord       Date:  2011

9.  Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.

Authors:  Marsha Treadwell; Joseph Telfair; Robert W Gibson; Shirley Johnson; Ifeyinwa Osunkwo
Journal:  Am J Hematol       Date:  2011-01       Impact factor: 10.047

10.  An observational study of patient versus parental perceptions of health-related quality of life in children and adolescents with a chronic pain condition: who should the clinician believe?

Authors:  Thomas R Vetter; Cynthia L Bridgewater; Gerald McGwin
Journal:  Health Qual Life Outcomes       Date:  2012-07-23       Impact factor: 3.186

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  7 in total

1.  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

2.  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

3.  Genetic counselling in sickle cell disease: views of single young adults in Ghana.

Authors:  Stella Appiah; Kwadwo Ameyaw Korsah; Charles AmpongAdjei; Osei Evans Appiah
Journal:  J Community Genet       Date:  2020-07-01

4.  Transition for Adolescents and Young Adults With Sickle Cell Disease in a US Midwest Urban Center: A Multilevel Perspective on Barriers, Facilitators, and Future Directions.

Authors:  Cecelia Calhoun; Lingzi Luo; Ana A Baumann; Anna Bauer; Evelyn Shen; Virginia McKay; Cole Hooley; Aimee James; Allison A King
Journal:  J Pediatr Hematol Oncol       Date:  2021-09-22       Impact factor: 1.170

5.  Improving self-management in adolescents with sickle cell disease.

Authors:  Lori E Crosby; Anna Hood; Katherine Kidwell; Cara Nwankwo; James Peugh; Heather Strong; Charles Quinn; Maria T Britto
Journal:  Pediatr Blood Cancer       Date:  2020-07-22       Impact factor: 3.167

6.  Transition in Sickle Cell Disease (SCD): A German Consensus Recommendation.

Authors:  Ferras Alashkar; Carmen Aramayo-Singelmann; Janine Böll; Annette Hoferer; Andrea Jarisch; Haytham Kamal; Lena Oevermann; Michaela Schwarz; Holger Cario
Journal:  J Pers Med       Date:  2022-07-17

7.  Patient-reported neurocognitive symptoms influence instrumental activities of daily living in sickle cell disease.

Authors:  Jennifer N Longoria; Norma L Pugh; Victor Gordeuk; Lewis L Hsu; Marsha Treadwell; Allison A King; Robert Gibson; Mariam Kayle; Nancy Crego; Jeffrey Glassberg; Cathy L Melvin; Jane S Hankins; Jerlym Porter
Journal:  Am J Hematol       Date:  2021-08-24       Impact factor: 10.047

  7 in total

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