Literature DB >> 27219336

Parental preparedness for late effects and long-term quality of life in survivors of childhood cancer.

Katie A Greenzang1,2, Angel M Cronin2, Jennifer W Mack1,2.   

Abstract

BACKGROUND: Parents of children with cancer desire information regarding the late effects of treatment. In the current study, the authors assessed parents' preparedness for late effects at least 5 years after their child's diagnosis.
METHODS: A cross-sectional survey was conducted of all eligible parents of children with cancer between April 2004 and September 2005 at Dana-Farber/Boston Children's Cancer and Blood Disorders Center within 1 year of diagnosis, and a follow-up questionnaire was administered at least 5 years later.
RESULTS: Approximately 66% of parents of children who were still living, and who were able to be contacted, completed the follow-up questionnaire (91 of 138 parents). Approximately 77% of respondents (70 of 91 respondents) were parents of disease-free survivors and 23% (21 of 91 respondents) were parents of children with recurrent disease. The majority of parents believed they were well prepared for their child's oncology treatment (87%), but fewer felt prepared for future limitations experienced by their children (70%; P = .003 using the McNemar test) or for life after cancer (62%; P<.001). On bivariable analysis among parents of disease-free survivors, parents were more likely to believe themselves to be prepared for future limitations when they also reported that communication with the oncologist helped to address worries regarding the future (odds ratio, 4.50; P = .01). At the time of diagnosis, both parents and physicians underestimated a child's risk of future limitations; 45% of parents and 39% of clinicians predicted future limitations in physical abilities, intelligence, or quality of life, but at the time of the follow-up questionnaire >5 years later, 72% of children experienced limitations in at least 1 domain.
CONCLUSIONS: Parents believe themselves to be less prepared for survivorship than for treatment. High-quality communication may help parents to feel more prepared for life after cancer therapy. Cancer 2016;122:2587-94.
© 2016 American Cancer Society. © 2016 American Cancer Society.

Entities:  

Keywords:  child; health communication; neoplasms; parents; prognosis; survivors

Mesh:

Year:  2016        PMID: 27219336      PMCID: PMC4974120          DOI: 10.1002/cncr.30092

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


  24 in total

1.  Information needs in parents of long-term childhood cancer survivors.

Authors:  Janine Vetsch; Corina S Rueegg; Micòl E Gianinazzi; Eva Bergsträsser; Nicolas X von der Weid; Gisela Michel
Journal:  Pediatr Blood Cancer       Date:  2015-02-07       Impact factor: 3.167

2.  Differences in parent-provider concordance regarding prognosis and goals of care among children with advanced cancer.

Authors:  Abby R Rosenberg; Liliana Orellana; Tammy I Kang; J Russell Geyer; Chris Feudtner; Veronica Dussel; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2014-09-20       Impact factor: 44.544

3.  An inventory for measuring clinical anxiety: psychometric properties.

Authors:  A T Beck; N Epstein; G Brown; R A Steer
Journal:  J Consult Clin Psychol       Date:  1988-12

4.  Childhood and adolescent cancer statistics, 2014.

Authors:  Elizabeth Ward; Carol DeSantis; Anthony Robbins; Betsy Kohler; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2014-01-31       Impact factor: 508.702

5.  Extent and determinants of error in doctors' prognoses in terminally ill patients: prospective cohort study.

Authors:  N A Christakis; E B Lamont
Journal:  BMJ       Date:  2000-02-19

6.  Diagnosis, disclosure, and informed consent: learning from parents of children with cancer.

Authors:  R B Levi; R Marsick; D Drotar; E D Kodish
Journal:  J Pediatr Hematol Oncol       Date:  2000 Jan-Feb       Impact factor: 1.289

7.  The influence of pediatric cancer diagnosis and illness complication factors on parental distress.

Authors:  Emma Hovén; Malin Anclair; Ulf Samuelsson; Per Kogner; Krister K Boman
Journal:  J Pediatr Hematol Oncol       Date:  2008-11       Impact factor: 1.289

8.  Parent perceptions of the quality of information received about a child's cancer.

Authors:  Erica Kaye; Jennifer W Mack
Journal:  Pediatr Blood Cancer       Date:  2013-06-18       Impact factor: 3.167

9.  Decision making during serious illness: what role do patients really want to play?

Authors:  L F Degner; J A Sloan
Journal:  J Clin Epidemiol       Date:  1992-09       Impact factor: 6.437

10.  Disease-related distress in parents of children with cancer at various stages after the time of diagnosis.

Authors:  Krister Boman; Annika Lindahl; Olle Björk
Journal:  Acta Oncol       Date:  2003       Impact factor: 4.089

View more
  12 in total

1.  Early information needs of adolescents and young adults about late effects of cancer treatment.

Authors:  Katie A Greenzang; Karen M Fasciano; Susan D Block; Jennifer W Mack
Journal:  Cancer       Date:  2020-05-04       Impact factor: 6.860

2.  Intended and unintended consequences: Ethics, communication, and prognostic disclosure in pediatric oncology.

Authors:  Jonathan M Marron; Angel M Cronin; Tammy I Kang; Jennifer W Mack
Journal:  Cancer       Date:  2017-12-26       Impact factor: 6.860

3.  Walking on Eggshells: Parents' First Year After Their Adolescent Completes Their Cancer Treatment [Formula: see text].

Authors:  Amy J Walker; Frances M Lewis; Abby R Rosenberg
Journal:  J Pediatr Oncol Nurs       Date:  2020-03-06       Impact factor: 1.636

4.  Perceptions of changes in clinical, informational, and supportive relationships after end of treatment among parents of young childhood cancer survivors.

Authors:  Justin G Wilford; Suellen Hopfer; Lari Wenzel
Journal:  Psychooncology       Date:  2019-03-14       Impact factor: 3.894

5.  Trying to Feel Normal Again: Early Survivorship for Adolescent Cancer Survivors.

Authors:  Amy J Walker; Frances M Lewis; Yuting Lin; Ellen Zahlis; Abby R Rosenberg
Journal:  Cancer Nurs       Date:  2019 Jul/Aug       Impact factor: 2.592

6.  Accurate understanding of infertility risk among families of adolescent males newly diagnosed with cancer.

Authors:  Vicky Lehmann; Jessica S Flynn; Rebecca H Foster; Kathryn M Russell; James L Klosky
Journal:  Psychooncology       Date:  2018-02-20       Impact factor: 3.894

7.  Thinking ahead: Parents' worries about late effects of childhood cancer treatment.

Authors:  Katie A Greenzang; Colleen A Kelly; Hasan Al-Sayegh; Clement Ma; Jennifer W Mack
Journal:  Pediatr Blood Cancer       Date:  2021-09-14       Impact factor: 3.167

8.  Parental distress and desire for information regarding long-term implications of pediatric cancer treatment.

Authors:  Katie A Greenzang; Angel M Cronin; Tammy I Kang; Jennifer W Mack
Journal:  Cancer       Date:  2018-10-01       Impact factor: 6.860

9.  Parent understanding of the risk of future limitations secondary to pediatric cancer treatment.

Authors:  Katie A Greenzang; Angel M Cronin; Tammy Kang; Jennifer W Mack
Journal:  Pediatr Blood Cancer       Date:  2018-03-30       Impact factor: 3.167

10.  Parent perspectives on information about late effects of childhood cancer treatment and their role in initial treatment decision making.

Authors:  Katie A Greenzang; Angela Dauti; Jennifer W Mack
Journal:  Pediatr Blood Cancer       Date:  2018-01-30       Impact factor: 3.838

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.