Literature DB >> 21499990

How parents cope with their child's diagnosis and treatment of an embryonal tumor: results of a prospective and longitudinal study.

Shawna L Palmer1, Shawn Lesh, Dana Wallace, Melanie J Bonner, Michelle Swain, Lynn Chapieski, Laura Janzen, Donald Mabbott, Sarah Knight, Robyn Boyle, Carol L Armstrong, Amar Gajjar.   

Abstract

The current study reports longitudinal coping responses among parents of children diagnosed with an embryonal brain tumor. Patients (n = 219) were enrolled on a treatment protocol for a pediatric embryonal brain tumor. Their parents (n = 251) completed the Coping Response Inventory at time of their child's diagnosis and yearly thereafter, resulting in 502 observations. Outcomes were examined with patient and parent age at diagnosis, patient risk, parent gender and education as covariates. At the time of diagnosis, the highest observed coping method was seeking guidance with well above average scores (T = 61.6). Over time, younger parents were found to seek guidance at a significantly higher rate than older parents (P = .016) and the use of acceptance resignation and seeking alternative results by all parents significantly increased (P = .011 and P < .0001 respectively). The use of emotional discharge was also observed above average at time of diagnosis (T = 55.4) with younger fathers being more likely to exhibit emotional discharge than older fathers (P = .002). Differences in coping according to age of the patient and parent education level are also discussed. Results show a high need for guidance, and above average emotional discharge, especially among younger parents. It is imperative for the healthcare team to lead with accurate information so that these parents may make informed decisions about the care of their child. This need remains high years after diagnosis. Therefore it is critical to continue a consistent level of effective communication and support, even following treatment.

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Year:  2011        PMID: 21499990      PMCID: PMC3537225          DOI: 10.1007/s11060-011-0574-9

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  18 in total

1.  Neurocognitive consequences of risk-adapted therapy for childhood medulloblastoma.

Authors:  Raymond K Mulhern; Shawna L Palmer; Thomas E Merchant; Dana Wallace; Mehmet Kocak; Pim Brouwers; Kevin Krull; Murali Chintagumpala; Robyn Stargatt; David M Ashley; Vida L Tyc; Larry Kun; James Boyett; Amar Gajjar
Journal:  J Clin Oncol       Date:  2005-08-20       Impact factor: 44.544

2.  The coping experience of Chinese parents of children diagnosed with cancer.

Authors:  Maggie Yi-fung Wong; Sally Wai-chi Chan
Journal:  J Clin Nurs       Date:  2005-05       Impact factor: 3.036

3.  Predictors of distress in parents of children with cancer: a prospective study.

Authors:  P Sloper
Journal:  J Pediatr Psychol       Date:  2000-03

4.  Longitudinal data analysis for discrete and continuous outcomes.

Authors:  S L Zeger; K Y Liang
Journal:  Biometrics       Date:  1986-03       Impact factor: 2.571

5.  Using problem-solving skills training to reduce negative affectivity in mothers of children with newly diagnosed cancer: report of a multisite randomized trial.

Authors:  Olle Jane Z Sahler; Diane L Fairclough; Sean Phipps; Raymond K Mulhern; Michael J Dolgin; Robert B Noll; Ernest R Katz; James W Varni; Donna R Copeland; Robert W Butler
Journal:  J Consult Clin Psychol       Date:  2005-04

Review 6.  Coping theory and research: past, present, and future.

Authors:  R S Lazarus
Journal:  Psychosom Med       Date:  1993 May-Jun       Impact factor: 4.312

7.  Coping strategies in parents of children with cancer.

Authors:  Annika Lindahl Norberg; Frank Lindblad; Krister K Boman
Journal:  Soc Sci Med       Date:  2005-03       Impact factor: 4.634

8.  "You can only take so much, and it took everything out of me": coping strategies used by parents of children with cancer.

Authors:  Baukje Miedema; Ryan Hamilton; Pierrette Fortin; Julie Easley; Maria Matthews
Journal:  Palliat Support Care       Date:  2010-06

9.  Development and validation of the parent experience of child illness.

Authors:  Melanie J Bonner; Kristina K Hardy; Ann B Guill; Colleen McLaughlin; Holly Schweitzer; Karen Carter
Journal:  J Pediatr Psychol       Date:  2005-05-25

10.  Beacon in the storm: an exploration of the spirituality and faith of parents whose children have cancer.

Authors:  Margaret A Schneider; Roger C Mannell
Journal:  Issues Compr Pediatr Nurs       Date:  2006 Jan-Mar
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  3 in total

1.  Parent-reported social outcomes after treatment for pediatric embryonal tumors: a prospective longitudinal study.

Authors:  Tara M Brinkman; Shawna L Palmer; Si Chen; Hui Zhang; Karen Evankovich; Michelle A Swain; Melanie J Bonner; Laura Janzen; Sarah Knight; Carol L Armstrong; Robyn Boyle; Amar Gajjar
Journal:  J Clin Oncol       Date:  2012-10-15       Impact factor: 44.544

2.  The relationship between socio-demographic characteristics, family environment, and caregiver coping in families of children with cancer.

Authors:  Elizabeth A Gage-Bouchard; Katie A Devine; Charles E Heckler
Journal:  J Clin Psychol Med Settings       Date:  2013-12

3.  Feasibility and efficacy of a computer-based intervention aimed at preventing reading decoding deficits among children undergoing active treatment for medulloblastoma: results of a randomized trial.

Authors:  Shawna L Palmer; Laurie Leigh; Susan C Ellison; Arzu Onar-Thomas; Shengjie Wu; Ibrahim Qaddoumi; Gregory T Armstrong; Karen Wright; Cynthia Wetmore; Alberto Broniscer; Amar Gajjar
Journal:  J Pediatr Psychol       Date:  2013-12-25
  3 in total

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