Evidence map›Paper›PMID 35658635›Full record

ArticleCancer control : journal of the Moffitt Cancer Center

Healthcare Predictors of Information Dissemination About Genetic Risks.

Vida Henderson, Shaila M Strayhorn, Nyahne Q Bergeron, Desmona C Strahan, Pamela S Ganschow, Aditya S Khanna, Karriem Watson, Kent Hoskins, Yamile Molina

Open access · goldAbstract read
In one paragraph

Article in Cancer control : journal of the Moffitt Cancer Center. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 25% of its field
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, 4 citations in OpenAlex.

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

9 authors at 4 institutions in 1 country.

Vida HendersonFred Hutchinson Cancer Research Center, Public Health Sciences Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0001-5799-0664
Shaila M Strayhorn14621School of Health and Applied Human Sciences, University of North Carolina Wilmington, Wilmington, NC, USA.
Nyahne Q Bergeron14681Community Health Sciences Division, University of Illinois Chicago, Chicago, IL, USA.ORCID https://orcid.org/0000-0003-3264-6044
Desmona C Strahan14681Community Health Sciences Division, University of Illinois Chicago, Chicago, IL, USA.
Pamela S GanschowCollege of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Aditya S KhannaDepartment of Behavioral and Social Sciences, Brown University, Providence, RI, USA.ORCID https://orcid.org/0000-0003-1049-3374
Karriem WatsonAll of Us Program, National Institutes of Health, Bethesda, MD, USA.
Kent HoskinsCollege of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Yamile Molina14681Community Health Sciences Division, University of Illinois Chicago, Chicago, IL, USA.
University of Illinois Chicago · USBrown University · USNational Institutes of Health · USUniversity of North Carolina Wilmington · US

Funding

Promoting Genetic Counseling among African American Women with Hereditary Risk for Breast CancerK01CA248852 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HENDERSON, VIDA ANN · 2020 to 2024
$809k
Assessing and modeling network-level consequences of patient navigationR21CA215252 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KHANNA, ADITYA SUBHASH, MOLINA, YAMILE · 2018 to 2019
$401k
NCI NIH HHS K01 CA248852NCI NIH HHS L30 CA242802NCI NIH HHS R21 CA215252
6 · The paper itself

Abstract

objectivesDespite the benefits of genetic counseling and testing (GCT), utilization is particularly low among African American (AA) women who exhibit breast cancer features that are common in BRCA-associated cancer. Underutilization is especially problematic for AA women who are more likely to die from breast cancer than women from any other race or ethnicity. Due to medical mistrust, fear, and stigma that can be associated with genetic services among racial/ethnic minorities, reliance on trusted social networks may be an impactful strategy to increase dissemination of knowledge about hereditary cancer risk. Informed by the social cognitive theory, the purpose of this study is to determine: 1) which AA patients diagnosed with breast cancer and with identified hereditary risk are sharing information about hereditary risk with their networks; 2) the nature of the information dissemination; and 3) if personal GCT experiences is associated with dissemination of information about hereditary risk.

methodsAmong consented participants (n = 100) that completed an interview administered using a 202-item questionnaire consisting of open- and closed-ended questions, 62 patients were identified to be at higher risk for breast cancer. Descriptive statistics, bivariable chi-square, Pearson's exact tests, and regression analyses were conducted to examine differences in characteristics between high-risk participants who disseminated hereditary risk information and participants who did not.

resultsAmong high-risk participants, 25 (40%) indicated they had disseminated information about hereditary risk to at least one member in their family/friend network and 37 (60%) had not. Receipt of both provider recommendations and receipt of GCT services was associated with greater odds of disseminating information about hereditary risk with networks, OR = 4.53, 95%CI [1.33, 15.50], p = .02.

conclusionInterventions that increase self-efficacy gained through additional personalized knowledge and experience gained through provider recommendations and by undergoing GCT may facilitate information dissemination among social/familial networks.

Indexed as

Breast NeoplasmsTrustDelivery of Health CareFemaleGenetic CounselingGenetic TestingHumansInformation Disseminationafrican americanscascade testinggenetic counselinggenetic testingsocial networks

Identifiers

PMID35658635
PMCPMC9174561
OpenAlexW4282944952

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.