Care maps and care plans for children with medical complexity.
Adult
Attitude of Health Personnel
Canada
/ epidemiology
Child
Child Health Services
/ organization & administration
Delivery of Health Care
/ organization & administration
Female
Health Personnel
Health Services Research
Humans
Male
Multiple Chronic Conditions
/ epidemiology
Needs Assessment
Parents
/ education
Patient Care Planning
/ organization & administration
Patient-Centered Care
/ organization & administration
Professional-Family Relations
Qualitative Research
care maps
care plans
medical complexity
Journal
Child: care, health and development
ISSN: 1365-2214
Titre abrégé: Child Care Health Dev
Pays: England
ID NLM: 7602632
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
15
01
2018
revised:
15
08
2018
accepted:
15
11
2018
pubmed:
22
11
2018
medline:
19
12
2019
entrez:
22
11
2018
Statut:
ppublish
Résumé
The support of families in the care of children with medical complexity (CMC) requires the integration of health care providers' (HCPs') medical knowledge and family experience. Care plans largely represent HCP information, and care maps demonstrate the family experience. Understanding the intersection between a care plan and a care map is critical, as it may provide solutions to the widely recognized tension between HCP-directed care and patient- and family-centered care (PFCC). This study used qualitative methods to explore the experience and usefulness of care maps. Parents of CMC who already had a care plan, created care maps (n = 15). Subsequent interviews with parents (n = 15) and HCPs (n = 30) of CMC regarding both care maps and care plans were conducted and analyzed using thematic analysis. Data analysis exploring the relationship and utility of care plans and care maps revealed six primary themes related to using care plans and care maps that were grouped into two primary categories: (a) utility of care plans and maps; and (b) intersection of care plans and care maps. Care plans and care maps were identified as valuable complementary documents. Their integration offers context about family experience and respects the parents' experiential wisdom in a standard patient care document, thus promoting improved understanding and integration of the family experience into care decision making.
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
104-110Informations de copyright
© 2018 John Wiley & Sons Ltd.