Evidence map›Paper›PMID 30385886›Full record

Trial reportGenetics in medicine : official journal of the American College of Medical Genetics2019

Disparities in genetic services utilization in a random sample of young breast cancer survivors.

Christos Nikolaidis, Debra Duquette, Kari E Mendelsohn-Victor, Beth Anderson, Glenn Copeland, Kara J Milliron, Sofia D Merajver, Nancy K Janz, Laurel L Northouse, Sonia A Duffy and 1 more

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Genetics in medicine : official journal of the American College of Medical Genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01612338 (Interventions to Increase Screening Utilization by Breast Cancer Survivors and Their High Risk Female Relatives), which is not on this map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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.

NCT01612338 nacompletednot on this map

Interventions to Increase Screening Utilization by Breast Cancer Survivors and Their High Risk Female Relatives: Using Cancer Surveillance and the Michigan Genomics Academic-Practice Partnership

TypeinterventionalSponsorUniversity of MichiganRan2012 to 2014Enrolled1,290ConditionsBreast Cancer, Breast Cancer in Young Women, Breast Cancer in Women With a Strong Family HistoryArmsTargeted, Enhanced Tailored
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Gynecologic Care of Black Breast Cancer Survivors.Current breast cancer reports · 2024
    Article
  17. Article
  18. Review
  19. Article
  20. Article
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

11 authors at 5 institutions in 2 countries.

Christos NikolaidisNursing Science, Faculty of Medicine, University of Basel, Basel, Switzerland.
Debra DuquetteFeinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Kari E Mendelsohn-VictorUniversity of Michigan School of Nursing, Ann Arbor, MI, USA.
Beth AndersonMichigan Department of Health and Human Services, Lansing, MI, USA.
Glenn CopelandMichigan Department of Health and Human Services, Lansing, MI, USA.
Kara J MillironComprehensive Cancer Center, University of Michigan, Ann Arbor, MI, USA.
Sofia D MerajverUniversity of Michigan School of Public Health, Ann Arbor, MI, USA.
Nancy K JanzUniversity of Michigan School of Public Health, Ann Arbor, MI, USA.
Laurel L NorthouseUniversity of Michigan School of Nursing, Ann Arbor, MI, USA.
Sonia A DuffyOhio State University College of Nursing, Columbus, OH, USA.
Maria C KatapodiNursing Science, Faculty of Medicine, University of Basel, Basel, Switzerland. maria.katapodi@unibas.ch.
University of Michigan · USMichigan Department of Health and Human Services · USUniversity of Basel · CHNorthwestern University · USThe Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
PREVENTION RESEARCH CENTER OF MICHIGANU48DP001901 · DP · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZIMMERMAN, MARC A · 2009 to 2013
$5.9M
NCCDPHP CDC HHS U48 DP001901
6 · The paper itself

Abstract

purposeIncreasing use of genetic services (counseling/testing) among young breast cancer survivors (YBCS) can help decrease breast cancer incidence and mortality. The study examined use of genetic services between Black and White/Other YBCS, attitudes and knowledge of breast cancer risk factors, and reasons for disparities in using genetic services.

methodsWe used baseline data from a randomized control trial including a population-based, stratified random sample of 3000 potentially eligible YBCS, with oversampling of Black YBCS.

resultsAmong 883 YBCS (353 Black, 530 White/Other) were significant disparities between the two racial groups. More White/Other YBCS had received genetic counseling and had genetic testing than Blacks. Although White/Other YBCS resided farther away from board-certified genetic counseling centers, they had fewer barriers to access these services. Black race, high out-of-pocket costs, older age, and more years since diagnosis were negatively associated with use of genetic services. Black YBCS had lower knowledge of breast cancer risk factors. Higher education and genetic counseling were associated with higher genetic knowledge.

conclusionRacial inequalities of cost-related access to care and education create disparities in genetic services utilization. System-based interventions that reduce socioeconomic disparities and empower YBCS with genetic knowledge, as well as physician referrals, can increase access to genetic services.

Indexed as

AdultBlack PeopleBreast NeoplasmsCancer SurvivorsEthnicityFacilities and Services UtilizationFemaleGenetic CounselingGenetic ServicesGenetic TestingHealth Knowledge, Attitudes, PracticeHumansRace FactorsSocioeconomic FactorsWhite Peoplecancer registrydistance as a barrier to access genetic servicesequity in using cancer genetic servicesgeocodingyoung breast cancer survivors

Identifiers

PMID30385886
OpenAlexW2898968898

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.