Literature DB >> 16541445

Use of health care services by survivors of childhood and adolescent cancer in Canada.

Amanda K Shaw1, Lisa Pogany, Kathy N Speechley, Elizabeth Maunsell, Maru Barrera, Leslie S Mery.   

Abstract

BACKGROUND: The number of survivors of childhood cancer in Canada is growing. The large majority of survivors experience at least 1 adverse late effect of their cancer therapy, which often becomes more severe and clinically apparent with time. The extent of survivors' use of health services in Canada is unknown, although coordinated, continuous, long-term follow-up care has been recommended by numerous investigators.
METHODS: Information on reported consultations with healthcare practitioners in the past year was obtained from 2152 survivors of child and adolescent cancer (mean age at diagnosis, 7.3; range, 0-19) and 2432 age- and sex-matched population-based controls through a mailed questionnaire.
RESULTS: Similar proportions of survivors (71%) and controls (73%) reported consulting a general practitioner in the past year. Survivors were more likely than controls to consult with any specialist (68% vs. 46%), including an oncologist (29% vs. 0.3%). Survivors' consultations with oncologists increased with concurrent physical health problems (adjusted odds ratio [OR(adj)], 1.7, 95% confidence interval [CI], 1.4-2.1), history of high risk therapy (OR(adj), 2.4, 95% CI, 1.9-2.9), and multiple treatment series (OR(adj), 2.2, 95% CI, 1.7- 3.0), but decreased with time since diagnosis (OR(adj), 0.3, 95% CI, 0.2-0.4).
CONCLUSION: Although most survivors reported consulting with at least 1 healthcare practitioner in the past year, the large majority did not report consulting an oncologist and thus may not be receiving optimal follow-up care. Moreover, consultations decreased with time since diagnosis, exactly when risk of late effects increases. This limited preventive care could have major implications on survivors' long-term health. 2006 American Cancer Society

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Year:  2006        PMID: 16541445     DOI: 10.1002/cncr.21798

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  15 in total

1.  Health knowledge about symptoms of heart attack and stroke in adult survivors of childhood acute lymphoblastic leukemia.

Authors:  James G Gurney; Janet E Donohue; Kirsten K Ness; Maura O'Leary; Stephen P Glasser; K Scott Baker
Journal:  Ann Epidemiol       Date:  2007-07-27       Impact factor: 3.797

Review 2.  Transition of care for young adult survivors of childhood and adolescent cancer: rationale and approaches.

Authors:  David R Freyer
Journal:  J Clin Oncol       Date:  2010-03-29       Impact factor: 44.544

3.  Cohort Profile: the French childhood cancer survivor study for leukaemia (LEA Cohort).

Authors:  Julie Berbis; Gérard Michel; André Baruchel; Yves Bertrand; Pascal Chastagner; François Demeocq; Justyna Kanold; Guy Leverger; Dominique Plantaz; Marilyne Poirée; Jean-Louis Stephan; Pascal Auquier; Audrey Contet; Jean-Hugues Dalle; Stéphane Ducassou; Virginie Gandemer; Patrick Lutz; Nicolas Sirvent; Marie-Dominique Tabone; Sandrine Thouvenin-Doulet
Journal:  Int J Epidemiol       Date:  2014-03-17       Impact factor: 7.196

4.  Early Posttherapy Hospitalizations Among Survivors of Childhood Leukemia and Lymphoma.

Authors:  Andrew B Smitherman; Tania M Wilkins; Julie Blatt; Stacie B Dusetzina
Journal:  J Pediatr Hematol Oncol       Date:  2016-08       Impact factor: 1.289

5.  Non-oncology physician visits after diagnosis of cancer in adolescents and young adults.

Authors:  Marianne J Heins; Maria F Lorenzi; Joke C Korevaar; Mary L McBride
Journal:  J Cancer Surviv       Date:  2016-02-13       Impact factor: 4.442

6.  Late new morbidity in survivors of adolescent and young-adulthood brain tumors in Finland: a registry-based study.

Authors:  Mirja Erika Gunn; Nea Malila; Tuire Lähdesmäki; Mikko Arola; Marika Grönroos; Jaakko Matomäki; Päivi Maria Lähteenmäki
Journal:  Neuro Oncol       Date:  2015-07-01       Impact factor: 12.300

7.  Psychological factors impacting transition from paediatric to adult care by childhood cancer survivors.

Authors:  Leeat Granek; Paul C Nathan; Zahava R S Rosenberg-Yunger; Norma D'Agostino; Leila Amin; Ronald D Barr; Mark L Greenberg; David Hodgson; Katherine Boydell; Anne F Klassen
Journal:  J Cancer Surviv       Date:  2012-05-01       Impact factor: 4.442

8.  Patterns of physician follow-up among young cancer survivors: report of the Childhood, Adolescent, and Young Adult Cancer Survivors (CAYACS) research program.

Authors:  Mary L McBride; Maria F Lorenzi; Jacqueline Page; Anne-Marie Broemeling; John J Spinelli; Karen Goddard; Sheila Pritchard; Paul Rogers; Sam Sheps
Journal:  Can Fam Physician       Date:  2011-12       Impact factor: 3.275

9.  Promoting physical activity in childhood cancer survivors: results from the Childhood Cancer Survivor Study.

Authors:  Cheryl L Cox; Michele Montgomery; Kevin C Oeffinger; Wendy Leisenring; Lonnie Zeltzer; John A Whitton; Ann C Mertens; Melissa M Hudson; Leslie L Robison
Journal:  Cancer       Date:  2009-02-01       Impact factor: 6.860

10.  Mental health-care utilization in survivors of childhood cancer and siblings: the Swiss childhood cancer survivor study.

Authors:  Micol E Gianinazzi; Corina S Rueegg; Nicolas X von der Weid; Felix K Niggli; Claudia E Kuehni; Gisela Michel
Journal:  Support Care Cancer       Date:  2013-10-01       Impact factor: 3.603

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