Literature DB >> 23809876

Identifying information needs among children and teens living with haemophilia.

G M Simmons1, N Frick, A Wang, M E Miller, D Fragueiro.   

Abstract

Transitioning from one life stage to the next can be difficult, but for those living with a chronic condition, it can be even more challenging. Children and adolescents with haemophilia need help to manage transitions while dealing with the complications of their disorder. The National Haemophilia Foundation (NHF), headquartered in New York City, has an extensive information centre on bleeding disorders, but it was not clear how much material existed on the topic of transition. The objectives of this project were to (i) assess the availability of literature about transition for children and adolescents living with haemophilia, (ii) determine which transition issues were the most relevant and (iii) develop and test information products that would address those transition issues. An inventory of NHF's resources and an environmental scan over the Internet was performed. Focus groups were conducted to determine messaging. Video prototypes containing messages were created, tested by focus groups and revised. The literature search yielded limited information available on transition for children and adolescents with haemophilia. Results of the formative research indicated that adolescents wanted more information on sports participation and disclosure of their condition (e.g. to peers, teachers, coaches, health care providers). Video was found to be the preferred delivery format. Children and adolescents living with haemophilia need information to help them transition through life. As a result of this study, two educational products were produced, but several more are recommended to guide these individuals in making healthy transitions into adulthood. Published 2013. This article is a US Government work and is in the public domain in the USA.

Entities:  

Keywords:  adolescents; children; disclosure; haemophilia; sports; transition

Mesh:

Year:  2013        PMID: 23809876      PMCID: PMC4481862          DOI: 10.1111/hae.12223

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  9 in total

1.  Creating an adolescent health promotion Internet.site. A community partnership between university nursing students and an inner-city high school.

Authors:  K Huyhn; B Kosmyna; H Lea; K R Munch; H S Reynolds; C Specht; E C Tinker; A J Yee; L R French
Journal:  Nurs Health Care Perspect       Date:  2000 May-Jun

2.  Recruiting adolescents into qualitative tobacco research studies: experiences and lessons learned.

Authors:  L K McCormick; M Crawford; R H Anderson; J Gittelsohn; B Kingsley; D Upson
Journal:  J Sch Health       Date:  1999-03       Impact factor: 2.118

3.  Effectiveness of a first aid information video in reducing epilepsy-related stigma.

Authors:  Rachel M Roberts; H S Aida Farhana
Journal:  Epilepsy Behav       Date:  2010-07-15       Impact factor: 2.937

4.  Knowledge, attitudes, and behaviors of youths in the US hemophilia population: results of a national survey.

Authors:  Ann-Marie Nazzaro; Sally Owens; W Keith Hoots; Kelly L Larson
Journal:  Am J Public Health       Date:  2006-07-27       Impact factor: 9.308

5.  Formative research on MySpace: online methods to engage hard-to-reach populations.

Authors:  Deborah Levine; Allegra Madsen; Erin Wright; Rana E Barar; John Santelli; Sheana Bull
Journal:  J Health Commun       Date:  2011-04

6.  Asking mom: formative research for an HPV vaccine campaign targeting mothers of adolescent girls.

Authors:  Autumn Shafer; Joan R Cates; Sandra J Diehl; Miriam Hartmann
Journal:  J Health Commun       Date:  2011-07-05

Review 7.  Psychosocial aspects of haemophilia: a systematic review of methodologies and findings.

Authors:  F R M Y Cassis; F Querol; A Forsyth; A Iorio
Journal:  Haemophilia       Date:  2011-11-08       Impact factor: 4.287

Review 8.  Transition: a literature review.

Authors:  Debbie Kralik; Kate Visentin; Antonia van Loon
Journal:  J Adv Nurs       Date:  2006-08       Impact factor: 3.187

Review 9.  Quality of life and sports activities in patients with haemophilia.

Authors:  S VON Mackensen
Journal:  Haemophilia       Date:  2007-09       Impact factor: 4.287

  9 in total
  4 in total

1.  Treatment-related knowledge and skills of patients with haemophilia and their informal caregivers.

Authors:  Teddy Novais; Antoine Duclos; Remi Varin; Isabelle Lopez; Valérie Chamouard
Journal:  Int J Clin Pharm       Date:  2016-02

Review 2.  Use of Technology-Based Tools to Support Adolescents and Young Adults With Chronic Disease: Systematic Review and Meta-Analysis.

Authors:  Jac Kee Low; Elizabeth Manias
Journal:  JMIR Mhealth Uhealth       Date:  2019-07-18       Impact factor: 4.773

3.  Health-related quality of life, developmental milestones, and self-esteem in young adults with bleeding disorders.

Authors:  P F Limperg; L Haverman; H Maurice-Stam; M Coppens; C Valk; M J H A Kruip; J Eikenboom; M Peters; M A Grootenhuis
Journal:  Qual Life Res       Date:  2017-09-12       Impact factor: 4.147

4.  Hemophilia Patient Experience in a Physical Therapy-Guided Health Education Intervention: A Mixed-Method Design.

Authors:  Alicia López-Casaus; Carolina Jiménez-Sánchez; Paula Cordova-Alegre; Fani Alfaro-Gervon; Laura Esteban-Repiso; Raquel Lafuente-Ureta
Journal:  Healthcare (Basel)       Date:  2021-12-14
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.