Evidence map›Paper›PMID 22892900›Full record

ArticleJournal of genetic counseling2013

Life events may contribute to family communication about cancer risk following BRCA1/2 testing.

Julie Lapointe, Claudia Côté, Karine Bouchard, Béatrice Godard, Jacques Simard, Michel Dorval

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of genetic counseling, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Canadian oncology nursing journal = Revue canadienne de nursing oncologique · 2022
    Article
  3. Issues associated with a hereditary risk of cancer: Knowledge, attitudes and practices of nurses in oncology settings.Canadian oncology nursing journal = Revue canadienne de nursing oncologique · 2022
    Article
  4. The Role of Palliative Medicine in Assessing Hereditary Cancer Risk.The American journal of hospice & palliative care · 2018
    Observational
  5. Article
  6. Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families.Genetics in medicine : official journal of the American College of Medical Genetics · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

6 authors at 5 institutions in 1 country.

Julie LapointeFaculté de pharmacie, Université Laval, Québec, Canada.
Claudia Côté
Karine Bouchard
Béatrice Godard
Jacques Simard
Michel Dorval
Hôpital du Saint-Sacrement · CACentre hospitalier de l'Université Laval · CACentre hospitalier universitaire de Québec · CAUniversité de Montréal · CAUniversité Laval · CA

Funding

Canadian Institutes of Health Research MOP 82917Canadian Institutes of Health Research TGF- 63285
6 · The paper itself

Abstract

We assessed whether certain life events contributed to the communication about cancer risk within families who have undergone BRCA1/2 testing. We also explored what type of resources participants would have valued to help in supporting family communication about genetic information. Two hundred and forty-six individuals (218 women, 28 men) who received a BRCA1/2 genetic test result 3 to 10 years earlier (mean of 6.4 years) participated in a telephone interview. Participants were asked about the occurrence of a number of life events (cancer diagnosis, death, uptake of prophylactic surgery, and providing care to a family member with cancer) in their family since their BRCA1/2 test result disclosure and, for each occurrence, whether it fostered family communication about cancer risk. A total of 182 participants (74 %) reported that they or one of their relatives received a cancer diagnosis, 176 (72 %) reported that someone died in their family, and 73 (30 %) stated that they or one of their relatives undertook a prophylactic surgery. During this period, 109 participants (44 %) also provided care for a family member who had cancer. Among participants who reported these life events, family communication was fostered by these events in proportions varying from 50 % (death) to 69 % (cancer diagnosis). Our results indicate that life events may contribute to family communication about cancer risk. Further research is needed to determine whether these events provide a "window of opportunity" to reach family members, address their needs and concerns about cancer, update family cancer history, and introduce genetic counseling and risk assessment.

Indexed as

FamilyGenes, BRCA1Genes, BRCA2Genetic Predisposition to DiseaseGenetic TestingLife Change EventsAdolescentAdultAgedFemaleHumansMaleMiddle AgedYoung Adult

Identifiers

PMID22892900
OpenAlexW2056460299

What OpenQuestion holds

Textmetadata
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.