Evidence map›Paper›PMID 32640451›Full record

ArticlePublic health genomics2020

Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer: A Population-Based Study in Southern Sweden.

Annelie Augustinsson, Carolina Ellberg, Ulf Kristoffersson, Håkan Olsson, Hans Ehrencrona

Open access · hybridAbstract read
In one paragraph

Article in Public health genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

5 authors at 1 institution in 1 country.

Annelie AugustinssonDepartment of Clinical Sciences in Lund, Cancer Epidemiology, Lund University, Lund, Sweden, annelie.augustinsson@med.lu.se.
Carolina EllbergDepartment of Clinical Sciences in Lund, Cancer Epidemiology, Lund University, Lund, Sweden.
Ulf KristofferssonDepartment of Laboratory Medicine in Lund, Clinical Genetics, Lund University, Lund, Sweden.
Håkan OlssonDepartment of Clinical Sciences in Lund, Cancer Epidemiology, Lund University, Lund, Sweden.
Hans EhrencronaDepartment of Laboratory Medicine in Lund, Clinical Genetics, Lund University, Lund, Sweden.
Lund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Swedish national breast cancer guidelines recommend that all women diagnosed with breast cancer (BC) at the age of 35 years or younger should be referred to their regional oncogenetic clinic for genetic counseling and testing, regardless of family history of cancer. The main objective of this study was to evaluate whether place of residence at BC diagnosis and treating hospital were associated with the fact that not all BC patients diagnosed at ≤35 years in the southern part of Sweden have attended genetic counseling and testing. Between 2000 and 2013, 279 women in the South Swedish Health Care Region were diagnosed with BC at ≤35 years. Information regarding place of residence at BC diagnosis, treating hospital, time of registration and first meeting at the Oncogenetic Clinic in Lund, and genetic testing was collected. With a follow-up period until August 2018, 64% were registered at the clinic (60% underwent genetic testing) and 36% were not. BC patients from 2 counties and from rural settings with a population of <10,000 inhabitants were significantly less likely to be registered at the clinic. Our results suggest that place of residence at BC diagnosis and treating hospital were associated with the probability of referral for genetic counseling and testing for women diagnosed with BC at ≤35 years in the South Swedish Health Care Region. We propose, as a generalizable finding, that further educational and outreach activities within the health care system and the community may be needed to ensure that all women diagnosed with early-onset BC receive proper genetic counseling.

Indexed as

Breast NeoplasmsAdultAge of OnsetBRCA1 ProteinBRCA2 ProteinFemaleGenetic CounselingGenetic TestingHumansPractice Patterns, Physicians'Referral and ConsultationSwedenBRCA1 ProteinBRCA2 ProteinBRCA1BRCA2Breast cancerEarly-onsetGenetic counseling

Identifiers

PMID32640451
PMCPMC7592930
OpenAlexW3041831741

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.