Using an electronic medical record patient portal for warfarin self-management: Empowering children and parents.

anticoagulants child electronic medical record patient portals self-management warfarin

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 13 03 2022
revised: 09 12 2022
accepted: 08 01 2023
entrez: 9 3 2023
pubmed: 10 3 2023
medline: 10 3 2023
Statut: epublish

Résumé

Many children taking warfarin perform their international normalized ratio (INR) at home, with results phoned to a clinician who instructs warfarin dosing. Data suggest that parents can be supported to make warfarin dosing decisions themselves, a process known as patient self-management (PSM). This study aimed to determine the suitability and acceptability of warfarin PSM in children using the Epic Patient Portal. Children currently performing INR patient self-testing were eligible. Participation involved an individualized education session, adherence to the PSM program, and participation in phone interviews. Clinical outcomes (INR time in therapeutic range and safety outcomes), patient portal functionality, and family experience were assessed. The hospital human research ethics committee approved the study and consent was obtained from parents/guardians. Twenty-four families undertook PSM. The median age of children was 11 years and all children had congenital heart disease. A median of 13 INRs was uploaded to the portal per family (range, 8-47) across a 10-month period. Before PSM, the mean time the INR was in therapeutic range was 71%; this increased to 79.9% during PSM (difference: This study demonstrates that communication via the Epic Patient Portal is satisfactory to families and offers a suitable option for PSM for children. Importantly, PSM empowers and builds confidence in families to facilitate management of their child's health.

Sections du résumé

Background UNASSIGNED
Many children taking warfarin perform their international normalized ratio (INR) at home, with results phoned to a clinician who instructs warfarin dosing. Data suggest that parents can be supported to make warfarin dosing decisions themselves, a process known as patient self-management (PSM).
Objectives UNASSIGNED
This study aimed to determine the suitability and acceptability of warfarin PSM in children using the Epic Patient Portal.
Methods UNASSIGNED
Children currently performing INR patient self-testing were eligible. Participation involved an individualized education session, adherence to the PSM program, and participation in phone interviews. Clinical outcomes (INR time in therapeutic range and safety outcomes), patient portal functionality, and family experience were assessed. The hospital human research ethics committee approved the study and consent was obtained from parents/guardians.
Results UNASSIGNED
Twenty-four families undertook PSM. The median age of children was 11 years and all children had congenital heart disease. A median of 13 INRs was uploaded to the portal per family (range, 8-47) across a 10-month period. Before PSM, the mean time the INR was in therapeutic range was 71%; this increased to 79.9% during PSM (difference:
Conclusion UNASSIGNED
This study demonstrates that communication via the Epic Patient Portal is satisfactory to families and offers a suitable option for PSM for children. Importantly, PSM empowers and builds confidence in families to facilitate management of their child's health.

Identifiants

pubmed: 36891277
doi: 10.1016/j.rpth.2023.100066
pii: S2475-0379(23)00032-8
pmc: PMC9986642
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100066

Informations de copyright

© 2023 The Author(s).

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Auteurs

Sophie Jones (S)

Department of Nursing, The University of Melbourne, Melbourne, Australia.
Haematology Research, Murdoch Children's Research of Institute, Melbourne, Australia.
Department of Clinical Haematology, Royal Children's Hospital, Melbourne, Australia.

Jodi L Hislop (JL)

Haematology Research, Murdoch Children's Research of Institute, Melbourne, Australia.

Hollie Gilmore (H)

Department of Clinical Haematology, Royal Children's Hospital, Melbourne, Australia.

Anthea Greenway (A)

Haematology Research, Murdoch Children's Research of Institute, Melbourne, Australia.
Department of Clinical Haematology, Royal Children's Hospital, Melbourne, Australia.

James Hibbard (J)

Peter MacCallum Cancer Centre, Melbourne, Australia.

Paul Monagle (P)

Haematology Research, Murdoch Children's Research of Institute, Melbourne, Australia.
Department of Clinical Haematology, Royal Children's Hospital, Melbourne, Australia.
Kids Cancer Centre, Sydney Children's Hospital, Randwick, Australia.
Department of Paediatrics, University of Melbourne, Melbourne, Australia.

Fiona Newall (F)

Department of Nursing, The University of Melbourne, Melbourne, Australia.
Haematology Research, Murdoch Children's Research of Institute, Melbourne, Australia.
Department of Clinical Haematology, Royal Children's Hospital, Melbourne, Australia.
Department of Paediatrics, University of Melbourne, Melbourne, Australia.
Nursing Research Department, Royal Children's Hospital, Melbourne, Australia.

Classifications MeSH