Literature DB >> 34209506

Care Coordination Needs of Families of Children with Down Syndrome: A Scoping Review to Inform Development of mHealth Applications for Families.

Beth Skelton1, Kathleen Knafl1, Marcia Van Riper1, Louise Fleming1, Veronica Swallow2.   

Abstract

Care coordination is a critical component of health management aimed at linking care providers and health-information-involved care management. Our intent in this scoping review was to identify care coordination needs of families of children with Down syndrome (DS) and the strategies they used to meet those needs, with the goal of contributing to the evidence base for developing interventions by using an mHealth application (mHealth apps) for these families. Using established guidelines for scoping reviews, we searched five databases, yielding 2149 articles. Following abstract and full-text review, we identified 38 articles meeting our inclusion criteria. Studies incorporated varied in regard to research designs, samples, measures, and analytic approaches, with only one testing an intervention by using mHealth apps. Across studies, data came from 4882 families. Common aspects of families' care coordination needs included communication and information needs and utilization of healthcare resources. Additional themes were identified related to individual, family, and healthcare contextual factors. Authors also reported families' recommendations for desirable characteristics of an mHealth apps that addressed the design of a personal health record, meeting age-specific information needs, and ensuring access to up-to-date information. These results will further the development of mHealth apps that are tailored to the needs of families with a child with DS.

Entities:  

Keywords:  care coordination; child/children; chronic/long-term condition; down syndrome; family; health; health information; health management; intervention; mHealth

Year:  2021        PMID: 34209506     DOI: 10.3390/children8070558

Source DB:  PubMed          Journal:  Children (Basel)        ISSN: 2227-9067


  47 in total

1.  Uncertainty management and communication preferences related to genetic relativism among families affected by down syndrome, Marfan syndrome, and neurofibromatosis.

Authors:  Roxanne Parrott; Kathryn F Peters; Tara Traeder
Journal:  Health Commun       Date:  2011-12-14

2.  Mothers' perceptions concerning oral health of children and adolescents with Down syndrome: a qualitative approach.

Authors:  A C Oliveira; I A Pordeus; C L Luz; S M Paiva
Journal:  Eur J Paediatr Dent       Date:  2010-03       Impact factor: 2.231

3.  Pediatric Care Coordination.

Authors:  Megan A Moreno
Journal:  JAMA Pediatr       Date:  2019-01-01       Impact factor: 16.193

4.  Breastfeeding Experiences of Mothers of Children with Down Syndrome.

Authors:  Rebeca Barros da Silva; Maria do Céu Barbieri-Figueiredo; Marcia Van Riper
Journal:  Compr Child Adolesc Nurs       Date:  2018-08-10

5.  NAPNAP Position Statement. Position Statement on Pediatric Health Care/Medical Home: Key Issues on Care Coordination, Transitions, and Leadership.

Authors: 
Journal:  J Pediatr Health Care       Date:  2016 Mar-Apr       Impact factor: 1.812

6.  Disparities in Access to Healthcare Transition Services for Adolescents with Down Syndrome.

Authors:  James Nugent; Gregory Gorman; Christine R Erdie-Lalena
Journal:  J Pediatr       Date:  2018-03-20       Impact factor: 4.406

7.  A population-based assessment of the health, functional status, and consequent family impact among children with Down syndrome.

Authors:  Laura A Schieve; Sheree L Boulet; Michael D Kogan; Kim Van Naarden-Braun; Coleen A Boyle
Journal:  Disabil Health J       Date:  2010-08-21       Impact factor: 2.554

8.  Services and supports for young children with Down syndrome: parent and provider perspectives.

Authors:  J Marshall; J P Tanner; Y A Kozyr; R S Kirby
Journal:  Child Care Health Dev       Date:  2014-06-10       Impact factor: 2.508

9.  User-Centered Design Groups to Engage Patients and Caregivers with a Personalized Health Information Technology Tool.

Authors:  Molly Maher; Elizabeth Kaziunas; Mark Ackerman; Holly Derry; Rachel Forringer; Kristen Miller; Dennis O'Reilly; Larry C An; Muneesh Tewari; David A Hanauer; Sung Won Choi
Journal:  Biol Blood Marrow Transplant       Date:  2015-09-05       Impact factor: 5.742

10.  A qualitative analysis of information sharing for children with medical complexity within and across health care organizations.

Authors:  Laura Quigley; Ashley Lacombe-Duncan; Sherri Adams; Charlotte Moore Hepburn; Eyal Cohen
Journal:  BMC Health Serv Res       Date:  2014-06-30       Impact factor: 2.655

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  2 in total

1.  Dental health care for children with Down syndrome: Parents' description of their children's needs in dental health care settings.

Authors:  Malin Stensson; Johanna Norderyd; Marcia Van Riper; Luc Marks; Maria Björk
Journal:  Eur J Oral Sci       Date:  2022-02-26       Impact factor: 2.160

Review 2.  Digital Technologies for Children and Parents Sharing Self-Management in Childhood Chronic or Long-Term Conditions: A Scoping Review.

Authors:  Jill Edwards; Jenny Waite-Jones; Toni Schwarz; Veronica Swallow
Journal:  Children (Basel)       Date:  2021-12-18
  2 in total

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