Literature DB >> 22006640

What effect does a cancer diagnosis have on the educational engagement and school life of teenagers? A systematic review.

Simon Pini1, Siobhan Hugh-Jones, Peter H Gardner.   

Abstract

OBJECTIVES: A diagnosis of cancer during the teenage years arrives at an important stage of development, where issues of normality, identity and independence are crucial. Education provides opportunity for peer contact, achievement and development for teenagers. This systematic review examined the impact of a diagnosis of cancer on the educational engagement and school life of teenagers.
METHOD: Five electronic databases were searched, returning a total of 3209 articles. Inclusion criteria were broad to allow for the range of literature within this area. Following screening, 22 articles (inclusive of both quantitative and qualitative methodologies) were retained and subjected to independent review and quality assessment.
RESULTS: Key areas involved in the impact of a cancer diagnosis on teenagers' educational engagement include school attendance, reintegration, peer relationships and long-term effects on education and employment.
CONCLUSION: School absences are a concern for teenagers, but do not necessarily lead to a reduction in educational and vocational attainment. It is important to involve health care and education professionals, as well as parents and teenagers themselves, in school reintegration if it is to be successful. Peer groups and body image are two areas that could mediate education engagement for teenagers. Further research needs to be undertaken to determine the overall impact of successfully maintaining education engagement specifically for teenagers, the role that peer groups play in this process and how education engagement contributes to the overall coping and well-being of teenage cancer patients.
Copyright © 2011 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2011        PMID: 22006640     DOI: 10.1002/pon.2082

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  5 in total

Review 1.  Provision of integrated psychosocial services for cancer survivors post-treatment.

Authors:  Christopher J Recklitis; Karen L Syrjala
Journal:  Lancet Oncol       Date:  2017-01       Impact factor: 41.316

2.  Health-related quality of life of adolescent and young adult patients with cancer in the United States: the Adolescent and Young Adult Health Outcomes and Patient Experience study.

Authors:  Ashley Wilder Smith; Keith M Bellizzi; Theresa H M Keegan; Brad Zebrack; Vivien W Chen; Anne Victoria Neale; Ann S Hamilton; Margarett Shnorhavorian; Charles F Lynch
Journal:  J Clin Oncol       Date:  2013-05-06       Impact factor: 44.544

3.  Impact of cancer on school, work, and financial independence among adolescents and young adults.

Authors:  Bryan A Sisk; Karen Fasciano; Susan D Block; Jennifer W Mack
Journal:  Cancer       Date:  2020-07-13       Impact factor: 6.860

4.  Patient-reported neurocognitive function in adult survivors of childhood and adolescent osteosarcoma and Ewing sarcoma.

Authors:  Nina S Kadan-Lottick; Daniel J Zheng; Mingjuan Wang; Michael W Bishop; Deo Kumar Srivastava; Wilhelmenia L Ross; Rozalyn L Rodwin; Kirsten K Ness; Todd M Gibson; Sheri L Spunt; Mehmet Fatih Okcu; Wendy M Leisenring; Leslie L Robison; Gregory T Armstrong; Kevin R Krull
Journal:  J Cancer Surviv       Date:  2022-01-21       Impact factor: 4.062

5.  Quality assessment with diverse studies (QuADS): an appraisal tool for methodological and reporting quality in systematic reviews of mixed- or multi-method studies.

Authors:  Reema Harrison; Benjamin Jones; Peter Gardner; Rebecca Lawton
Journal:  BMC Health Serv Res       Date:  2021-02-15       Impact factor: 2.655

  5 in total

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