Literature DB >> 27547816

School Performance and Disease Interference in Adolescents with Sickle Cell Disease.

Lori E Crosby1, Naomi E Joffe1, Mary Kay Irwin2, Heather Strong1, James Peugh1, Lisa Shook1, Karen A Kalinyak1, Monica J Mitchell1.   

Abstract

Sickle cell disease (SCD) results in neuropsychological complications that place adolescents at higher risk for limited educational achievement. A first step to developing effective educational interventions is to understand the impact of SCD on school performance. The current study assessed perceptions of school performance, SCD interference and acceptability of educational support strategies in adolescents with SCD. To identify potential risk factors, the relationship between school performance, SCD interference and demographics were also examined. Thirty adolescents aged 12 to 20 completed demographics and SCD school performance questionnaires. Approximately 37% of participants reported receiving special education services, but more than 60% reported that SCD interfered with their school performance. Females reported that SCD impacted their schooling more than males (X2 (1, N = 30) = 5.00, p < .05). Study findings provide important insights into demographic risk factors and support the need for individualized health and educational plans for adolescents with SCD.

Entities:  

Keywords:  adolescent health; chronic disease; health disabilities; school performance

Year:  2015        PMID: 27547816      PMCID: PMC4991639          DOI: 10.14434/pders.v34i1.13918

Source DB:  PubMed          Journal:  Phys Disabil        ISSN: 2372-451X


  32 in total

1.  A randomized, controlled pilot trial of a school intervention for children with sickle cell anemia.

Authors:  Kristine Koontz; Amy D Short; Karen Kalinyak; Robert B Noll
Journal:  J Pediatr Psychol       Date:  2004 Jan-Feb

Review 2.  Chronic health conditions and student performance at school.

Authors:  Howard Taras; William Potts-Datema
Journal:  J Sch Health       Date:  2005-09       Impact factor: 2.118

Review 3.  Neurocognitive sequelae of pediatric sickle cell disease: a review of the literature.

Authors:  Leslie D Berkelhammer; Adrienne L Williamson; Stacy D Sanford; Courtney L Dirksen; William G Sharp; Allison S Margulies; Rebecca A Prengler
Journal:  Child Neuropsychol       Date:  2007-03       Impact factor: 2.500

Review 4.  Transition from pediatric to adult services: are we getting it right?

Authors:  Andrew Kennedy; Susan Sawyer
Journal:  Curr Opin Pediatr       Date:  2008-08       Impact factor: 2.856

5.  Height and weight reference curves for homozygous sickle cell disease.

Authors:  P W Thomas; A Singhal; M Hemmings-Kelly; G R Serjeant
Journal:  Arch Dis Child       Date:  2000-03       Impact factor: 3.791

6.  The 9th grade shock and the high school dropout crisis.

Authors:  Nikolas Pharris-Ciurej; Charles Hirschman; Joseph Willhoft
Journal:  Soc Sci Res       Date:  2011-12-06

7.  White matter integrity and core cognitive function in children diagnosed with sickle cell disease.

Authors:  Nadia Scantlebury; Donald Mabbott; Laura Janzen; Conrad Rockel; Elysa Widjaja; Garland Jones; Melanie Kirby; Isaac Odame
Journal:  J Pediatr Hematol Oncol       Date:  2011-04       Impact factor: 1.289

8.  Acute silent cerebral ischemic events in children with sickle cell anemia.

Authors:  Charles T Quinn; Robert C McKinstry; Michael M Dowling; William S Ball; Michael A Kraut; James F Casella; Nomazulu Dlamini; Rebecca N Ichord; Lori C Jordan; Fenella J Kirkham; Michael J Noetzel; E Steve Roach; John J Strouse; Janet L Kwiatkowski; Deborah Hirtz; Michael R DeBaun
Journal:  JAMA Neurol       Date:  2013-01       Impact factor: 18.302

9.  Growth status in children and adolescents with sickle cell disease.

Authors:  Monica J Mitchell; Gloria J O Carpenter; Lori E Crosby; Chanelle T Bishop; Janelle Hines; Jennie Noll
Journal:  Pediatr Hematol Oncol       Date:  2009-06       Impact factor: 1.969

10.  Associates of school absenteeism in adolescents with sickle cell disease.

Authors:  Lisa A Schwartz; Jerilynn Radcliffe; Lamia P Barakat
Journal:  Pediatr Blood Cancer       Date:  2009-01       Impact factor: 3.167

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  10 in total

1.  The distinct longitudinal impact of pain catastrophizing on pain interference among youth living with sickle cell disease and chronic pain.

Authors:  Mallory B Schneider; Alison Manikowski; Lindsey Cohen; Carlton Dampier; Soumitri Sil
Journal:  J Behav Med       Date:  2022-02-16

Review 2.  Chronic pediatric diseases and risk for reading difficulties: a narrative review with recommendations.

Authors:  Donna Perazzo; Ryan Moore; Nadine A Kasparian; Megan Rodts; Tzipi Horowitz-Kraus; Lori Crosby; Brian Turpin; Andrew F Beck; John Hutton
Journal:  Pediatr Res       Date:  2022-02-04       Impact factor: 3.953

3.  Academic Challenges and School Service Utilization in Children with Sickle Cell Disease.

Authors:  Kristine A Karkoska; Kenneth Haber; Megan Elam; Sarah Strong; Patrick T McGann
Journal:  J Pediatr       Date:  2020-12-01       Impact factor: 4.406

4.  Cognitive performance as a predictor of healthcare transition in sickle cell disease.

Authors:  Anjelica C Saulsberry-Abate; Marita Partanen; Jerlym S Porter; Pradeep S B Podila; Jason R Hodges; Allison A King; Winfred C Wang; Jane E Schreiber; Xiwen Zhao; Guolian Kang; Lisa M Jacola; Jane S Hankins
Journal:  Br J Haematol       Date:  2021-02-11       Impact factor: 6.998

5.  Academic Performance of Children With Sickle Cell Disease in the United States: A Meta-Analysis.

Authors:  Andrew M Heitzer; Latacha Hamilton; Claire Stafford; Jeffrey Gossett; Lara Ouellette; Ana Trpchevska; Allison A King; Guolian Kang; Jane S Hankins
Journal:  Front Neurol       Date:  2021-12-13       Impact factor: 4.003

6.  Transitions to Postsecondary Education in Young Adults with Hemoglobinopathies: Perceptions of Patients and Staff.

Authors:  Brooke A Allemang; James Bradley; Rosemary Leone; Megan Henze
Journal:  Pediatr Qual Saf       Date:  2020-09-25

7.  Burden of disease, treatment utilization, and the impact on education and employment in patients with sickle cell disease: A comparative analysis of high- and low- to middle-income countries for the international Sickle Cell World Assessment Survey.

Authors:  Ifeyinwa Osunkwo; John James; Fuad El-Rassi; Alecia Nero; Caterina P Minniti; Cassandra Trimnell; Jincy Paulose; Nicholas Ramscar; Tom Bailey; Olivera Rajkovic-Hooley; Biree Andemariam
Journal:  Am J Hematol       Date:  2022-06-20       Impact factor: 13.265

8.  Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation.

Authors:  Megan M Miller; Deanna D Rumble; Adam T Hirsh; Tine Vervoort; Lori E Crosby; Avi Madan-Swain; Jeffrey Lebensburger; Anna M Hood; Zina Trost
Journal:  Pain Med       Date:  2021-10-08       Impact factor: 3.750

9.  Nutritional and Hematological Status of Sudanese Women of Childbearing Age with Steady-state Sickle Cell Anemia.

Authors:  Eltigani Hassan Ali; Salam Alkindi; Mohamed A Osman; Wafa Hilali; Hind M Mirgani; Gareeba Adam; Magdi M Morsi; Izzeldin S Hussein; Kebreab Ghebremeskel
Journal:  Oman Med J       Date:  2021-05-31

10.  The Impact of Sickle Cell Disease on Academic Performance among Affected Students.

Authors:  Abdulaziz Alhazmi; Khalid Hakami; Faisal Abusageah; Essa Jaawna; Meshal Khawaji; Essam Alhazmi; Basem Zogel; Salman Qahl; Ghadeer Qumayri
Journal:  Children (Basel)       Date:  2021-12-27
  10 in total

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