Evidence map›Paper›PMID 41732576›Full record

ArticleCJC open2026

"I Am a Quarterback": A Mixed-Methods Study of Death Investigators' Communication with Family Members of Young Sudden Cardiac Death Victims.

Katherine L Mason, Katherine S Allan, June Carroll, Arnon Adler, Julie Rutberg, Sheldon Cheskes, Steve Lin, Erik K Mont, Joel A Kirsh, Lindsay J Denis and 8 more

Abstract read
In one paragraph

Article in CJC open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Katherine L MasonSchool of Nursing, Faculty of Health Sciences, University of Ottawa, Ottawa, Ontario, Canada.
Katherine S AllanDivision of Cardiology, Unity Health Toronto-St. Michael's Hospital, Toronto, Ontario, Canada.
June CarrollDepartment of Family & Community Medicine, Sinai Health, University of Toronto, Toronto, Ontario, Canada.
Arnon AdlerDepartment of Cardiology, Toronto General Hospital, Toronto, Ontario, Canada.
Julie RutbergChildren's Hospital of Eastern Ontario (CHEO), Ottawa, Ontario, Canada.
Sheldon CheskesDepartment of Family & Community Medicine, Sinai Health, University of Toronto, Toronto, Ontario, Canada.
Steve LinDivision of Cardiology, Unity Health Toronto-St. Michael's Hospital, Toronto, Ontario, Canada.
Erik K MontNova Scotia Medical Examiner Service, Dartmouth, Nova Scotia, Canada.
Joel A KirshOffice of the Chief Coroner for Ontario, Toronto, Ontario, Canada.
Lindsay J DenisNova Scotia Medical Examiner Service, Dartmouth, Nova Scotia, Canada.
Kris CunninghamOntario Forensic Pathology Service, Toronto, Ontario, Canada.
Jodi GarnerFamily Member of Sudden Cardiac Death Victim, Toronto, Ontario, Canada.
Liz SiydockOffice of the Chief Coroner for Ontario, Toronto, Ontario, Canada.
Katie N DaintyPatient Centred Outcomes, North York General Hospital, North York, Ontario, Canada.
Matthew BowesNova Scotia Medical Examiner Service, Dartmouth, Nova Scotia, Canada.
Karolyn YeeSchool of Nursing, Faculty of Health Sciences, University of Ottawa, Ottawa, Ontario, Canada.
Paul DorianDivision of Cardiology, Unity Health Toronto-St. Michael's Hospital, Toronto, Ontario, Canada.
Krystina B LewisSchool of Nursing, Faculty of Health Sciences, University of Ottawa, Ottawa, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sudden cardiac death (SCD) is a leading global cause of mortality and is often attributable to heritable cardiac conditions in the young (aged 2-45 years). Death investigators are responsible for determining the cause of death and communicating the risk of heritable conditions with the families of victims. Families often struggle to comprehend this information. This study explores how death investigators communicate with families of young SCD victims who die from suspected heritable causes about the cause of death and their risk for SCD. Methods: We conducted an explanatory sequential mixed-methods study, collecting quantitative data, via a web-based survey, and qualitative data, via telephone interviews, to investigate how death investigators in Ontario and Nova Scotia, Canada, communicate with family members of SCD victims. We used descriptive statistics to analyze quantitative data, and thematic analysis to analyze qualitative data. We triangulated the data at multiple levels. Results: Between October 2022 and July 2023, we surveyed 78 death investigators and interviewed a subset of these (n = 20). Participants (40%; n = 31) reported that SCDs due to heritable cardiac conditions were more difficult to investigate, requiring a higher frequency of communication with families. Participants (96.1%; n = 75) reported contacting family members via phone. Strategies to achieve their communication goals were influenced by family characteristics; involvement of other professionals; characteristics of the investigation, access to resources, and system-level barriers. Conclusions: SCD investigations in the young who die due to suspected heritable cardiac conditions are challenging and require a high frequency of communication. Further research should examine how systematic changes can improve communication among death investigators and families.

Indexed as

cause of deathcommunicationcoronerdeath investigatorheritable cardiac conditionmixed methodsSudden cardiac death

Identifiers

PMID41732576
PMCPMC12925756

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.