Literature DB >> 33688790

Parental Cancer-related Information Seeking, Health Communication and Satisfaction with Medical Providers of Childhood Cancer Survivors: Differences by Race/Ethnicity and Language Preference.

Carol Y Ochoa1, Kimberly A Miller1,2, Lourdes Baezconde-Garbanati1, Rhona I Slaughter1, Ann S Hamilton1, Joel E Milam1.   

Abstract

For childhood cancer survivors (CCS), parents play an important role in communicating with providers and conveying patient's needs. This exploratory study examined the prevalence of cancer-related information-seeking among parents of CCS and investigated the association between parents' race/ethnicity and language preference with health communication and satisfaction with child's medical providers. One hundred and sixty CCS and their parents from two hospitals in Los Angeles County were recruited from the SEER registry. Multivariable logistic regression analyses assessed associations between parents' race/ethnicity and language preference and their health communication with their child and with their child's medical care providers. Among the parents, 29% were Spanish-speaking Hispanics, 27% English-speaking Hispanics, and 43% English-speaking non-Hispanics. Regardless of language preference, Hispanic parents were more likely than non-Hispanic parents to receive health information about their CCS's cancer from hospital sources versus the internet. There was no difference by ethnicity/language in parent satisfaction with their CCS's medical provider. Spanish-speaking Hispanic parents were more likely to report talking to their CCS about the need for cancer-related follow-up care compared to non-Hispanic English-speaking parents. These findings point to the potential importance of parents' ethnicity and language for sources of health information and frequency of communication with their CCS about their cancer care.

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Mesh:

Year:  2021        PMID: 33688790      PMCID: PMC8547415          DOI: 10.1080/10810730.2021.1895919

Source DB:  PubMed          Journal:  J Health Commun        ISSN: 1081-0730


  33 in total

1.  Predictors of Self and Surrogate Online Health Information Seeking in Family Caregivers to Cancer Survivors.

Authors:  Young Sam Oh
Journal:  Soc Work Health Care       Date:  2015

2.  Patient- and Family-Centered Care: It's Not Just for Pediatrics Anymore.

Authors:  Aaron M Clay; Bridget Parsh
Journal:  AMA J Ethics       Date:  2016-01-01

Review 3.  Hospital and Health System-Level Interventions to Improve Care for Limited English Proficiency Patients: A Systematic Review.

Authors:  Breena R Taira; Kenneth Kim; Nisha Mody
Journal:  Jt Comm J Qual Patient Saf       Date:  2019-03-23

4.  "Forewarned and forearmed": Long-term childhood cancer survivors' and parents' information needs and implications for survivorship models of care.

Authors:  Janine Vetsch; Joanna E Fardell; Claire E Wakefield; Christina Signorelli; Gisela Michel; Jordana K McLoone; Thomas Walwyn; Heather Tapp; Jo Truscott; Richard J Cohn
Journal:  Patient Educ Couns       Date:  2016-09-22

5.  The impact of language barriers and immigration status on the care experience for Spanish-speaking caregivers of patients with pediatric cancer.

Authors:  Eduardo R Zamora; Sapna Kaul; Anne C Kirchhoff; Vannina Gwilliam; Ornella A Jimenez; Deborah K Morreall; Roberto E Montenegro; Anita Y Kinney; Mark N Fluchel
Journal:  Pediatr Blood Cancer       Date:  2016-07-21       Impact factor: 3.167

Review 6.  The challenge of quality care for family caregivers in pediatric cancer care.

Authors:  Barbara L Jones
Journal:  Semin Oncol Nurs       Date:  2012-11       Impact factor: 2.315

7.  Classifying the intensity of pediatric cancer treatment protocols: the intensity of treatment rating scale 2.0 (ITR-2).

Authors:  Branlyn E Werba; Wendy Hobbie; Anne E Kazak; Richard F Ittenbach; Anne F Reilly; Anna T Meadows
Journal:  Pediatr Blood Cancer       Date:  2007-06-15       Impact factor: 3.167

8.  Youth and parent perceptions of parenting in childhood cancer survivors and healthy peers.

Authors:  Sasja A Schepers; Alanna M Long; Kathryn Russell; Sean Phipps
Journal:  Support Care Cancer       Date:  2018-06-03       Impact factor: 3.603

9.  Medical care in long-term survivors of childhood cancer: a report from the childhood cancer survivor study.

Authors:  Paul C Nathan; Mark L Greenberg; Kirsten K Ness; Melissa M Hudson; Ann C Mertens; Martin C Mahoney; James G Gurney; Sarah S Donaldson; Wendy M Leisenring; Leslie L Robison; Kevin C Oeffinger
Journal:  J Clin Oncol       Date:  2008-09-20       Impact factor: 50.717

10.  Population-Based Survey Methods for Reaching Adolescent and Young Adult Survivors of Pediatric Cancer and Their Parents.

Authors:  Ann S Hamilton; Xueyan Zhuang; Denise Modjeski; Rhona Slaughter; Anamara Ritt-Olson; Joel Milam
Journal:  J Adolesc Young Adult Oncol       Date:  2018-09-15       Impact factor: 1.757

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