Literature DB >> 16417861

Where do families of children with epilepsy obtain their information?

Cathy Lu1, Elaine Wirrell, Marlene Blackman.   

Abstract

A structured interview of 84 families of children with epilepsy followed through the neurology clinic of a tertiary care children's hospital was conducted to assess the epilepsy-specific information sources accessed and the perceived accuracy of these sources. Families accessed a mean of 3.5 sources from or specifically recommended by the clinic or family doctor and 4.1 sources outside these areas. Families of children with intractable epilepsy and higher-educated parents, but not those of higher socioeconomic status, consulted more extensively. The perceived accuracy of information rated highest for clinic-recommended Internet sites (100%), the clinic nurse (97%), and the neurologist (93%). Sources external to the clinic had variable ratings; those with the greatest perceived accuracy included other Internet sites or family members within the medical profession (85% for both) and lay organizations (84%). Friends within the medical profession, other families, and complementary health care providers also ranked highly. Recommendation of sites and books by epilepsy clinics is more helpful than general handouts.

Entities:  

Mesh:

Year:  2005        PMID: 16417861     DOI: 10.1177/08830738050200110801

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  11 in total

1.  Guiding parents in their search for high-quality health information on the Internet.

Authors: 
Journal:  Paediatr Child Health       Date:  2007-03       Impact factor: 2.253

2.  Health literacy and sources of health information for caregivers of urban children with asthma.

Authors:  Maria Fagnano; Jill S Halterman; Kelly M Conn; Laura P Shone
Journal:  Clin Pediatr (Phila)       Date:  2011-09-12       Impact factor: 1.168

3.  Health-related quality of life improvement via telemedicine for epilepsy: printed versus SMS-based education intervention.

Authors:  Pei Lin Lua; Widiasmoro Selamat Neni
Journal:  Qual Life Res       Date:  2013-01-18       Impact factor: 4.147

4.  Continuing psychosocial care needs in children with new-onset epilepsy and their parents.

Authors:  Cheryl P Shore; Janice M Buelow; Joan K Austin; Cynthia S Johnson
Journal:  J Neurosci Nurs       Date:  2009-10       Impact factor: 1.230

Review 5.  Disparities in epilepsy: report of a systematic review by the North American Commission of the International League Against Epilepsy.

Authors:  Jorge G Burneo; Nathalie Jette; William Theodore; Charles Begley; Karen Parko; David J Thurman; Samuel Wiebe
Journal:  Epilepsia       Date:  2009-09-03       Impact factor: 5.864

6.  Patterns of Internet and smartphone use by parents of children with chronic kidney disease.

Authors:  Deise Garrido; Andreia Watanabe; Ana Lídia Ciamponi; Taciana Mara Couto; Levy Anderson César Alves; Ana Estela Haddad
Journal:  PLoS One       Date:  2019-02-12       Impact factor: 3.240

7.  Family Interaction and Consensus with IT Support.

Authors:  Peter Karlsudd
Journal:  Int J Telemed Appl       Date:  2012-12-03

8.  Parental use of the Internet to seek health information and primary care utilisation for their child: a cross-sectional study.

Authors:  Gauthier Bouche; Virginie Migeot
Journal:  BMC Public Health       Date:  2008-08-28       Impact factor: 3.295

9.  Chinese Internet Searches Provide Inaccurate and Misleading Information to Epilepsy Patients.

Authors:  Jian-Ming Liu; Ru-Xiang Xu; Yong-Sheng Hu; Lian-Kun Ren; Hui Qiao; Hu Ding; Zhi-Liang Liu
Journal:  Chin Med J (Engl)       Date:  2015-12-20       Impact factor: 2.628

10.  Application of protection motivation theory to clinical trial enrolment for pediatric chronic conditions.

Authors:  Stephanie P Brooks; Tania Bubela
Journal:  BMC Pediatr       Date:  2020-03-16       Impact factor: 2.125

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.