The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.


Journal

Molecular genetics & genomic medicine
ISSN: 2324-9269
Titre abrégé: Mol Genet Genomic Med
Pays: United States
ID NLM: 101603758

Informations de publication

Date de publication:
11 2019
Historique:
received: 21 02 2019
revised: 15 07 2019
accepted: 17 07 2019
pubmed: 5 9 2019
medline: 1 7 2020
entrez: 5 9 2019
Statut: ppublish

Résumé

Individuals with hypertrophic cardiomyopathy (HCM), even when asymptomatic, are at-risk for sudden cardiac death and stroke from arrhythmias, making it imperative to identify individuals affected by this familial disorder. Consensus guidelines recommend that first-degree relatives (FDRs) of a person with HCM undergo serial cardiovascular evaluations. We determined the uptake of family screening in patients with HCM and developed an online video intervention to facilitate family communication and screening. Family screening and genetic testing data were collected through a prospective quality improvement initiative, a standardized clinical assessment and management plan (SCAMP), utilized in an established cardiovascular genetics clinic. Patients were prescribed an online video if screening of their FDRs was incomplete and a pilot study on video utilization and family communication was conducted. Two-hundred and sixteen probands with HCM were enrolled in SCAMP Phase I and 190 were enrolled in SCAMP Phase II. In both phases, probands reported that 51% of FDRs had been screened (382/749 in Phase I, 258/504 in Phase II). Twenty patients participated in a pilot study on video utilization and family communication. Nine participants reported watching the video and six participants reported sharing the video with relatives; however only one participant reported sharing the video with relatives who were not yet aware of the diagnosis of HCM in the family. Despite care in a specialized cardiovascular genetics clinic, approximately one half of FDRs of patients with HCM remained unscreened. Online interventions and videos may serve as supplemental tools for patients communicating genetic risk information to relatives.

Sections du résumé

BACKGROUND
Individuals with hypertrophic cardiomyopathy (HCM), even when asymptomatic, are at-risk for sudden cardiac death and stroke from arrhythmias, making it imperative to identify individuals affected by this familial disorder. Consensus guidelines recommend that first-degree relatives (FDRs) of a person with HCM undergo serial cardiovascular evaluations.
METHODS
We determined the uptake of family screening in patients with HCM and developed an online video intervention to facilitate family communication and screening. Family screening and genetic testing data were collected through a prospective quality improvement initiative, a standardized clinical assessment and management plan (SCAMP), utilized in an established cardiovascular genetics clinic. Patients were prescribed an online video if screening of their FDRs was incomplete and a pilot study on video utilization and family communication was conducted.
RESULTS
Two-hundred and sixteen probands with HCM were enrolled in SCAMP Phase I and 190 were enrolled in SCAMP Phase II. In both phases, probands reported that 51% of FDRs had been screened (382/749 in Phase I, 258/504 in Phase II). Twenty patients participated in a pilot study on video utilization and family communication. Nine participants reported watching the video and six participants reported sharing the video with relatives; however only one participant reported sharing the video with relatives who were not yet aware of the diagnosis of HCM in the family.
CONCLUSION
Despite care in a specialized cardiovascular genetics clinic, approximately one half of FDRs of patients with HCM remained unscreened. Online interventions and videos may serve as supplemental tools for patients communicating genetic risk information to relatives.

Identifiants

pubmed: 31482667
doi: 10.1002/mgg3.940
pmc: PMC6825857
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e940

Informations de copyright

© 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc.

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Auteurs

Stephanie Harris (S)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Allison L Cirino (AL)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Christina W Carr (CW)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Hiwot M Tafessu (HM)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Siddharth Parmar (S)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Jeffrey O Greenberg (JO)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Lara E Szent-Gyorgyi (LE)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Roya Ghazinouri (R)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Michelle G Glowny (MG)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Kara McNeil (K)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Efthalia F Kaynor (EF)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Catherine Neumann (C)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Christine E Seidman (CE)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Calum A MacRae (CA)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Carolyn Y Ho (CY)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

Neal K Lakdawala (NK)

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.

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