Evidence map›Paper›PMID 34547796›Full record

ArticleRevista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia2021

Hereditary Breast and Ovarian Cancer Screening Syndrome Profile in Women Diagnosed with Breast Cancer from Paraná State Southwest.

Juliana Batista de Moura, Carla Camila Ghedin, Érika Tomie Takakura, Thalita Basso Scandolara, Daniel Rech, Carolina Panis

Open access · diamondAbstract read
In one paragraph

Article in Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia, 2021. 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
0.3field-weighted citation impact, top 33% 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, 2 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

6 authors at 3 institutions in 1 country.

Juliana Batista de MouraLaboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.ORCID 0000-0001-8512-2856
Carla Camila GhedinLaboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.ORCID 0000-0003-2228-836X
Érika Tomie TakakuraLaboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.ORCID 0000-0001-8739-9058
Thalita Basso ScandolaraLaboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.ORCID 0000-0003-4709-9207
Daniel RechCenter of Health Sciences, Francisco Beltrão Cancer Hospital, Francisco Beltrão, PR, Brazil.ORCID 0000-0002-2654-4562
Carolina PanisLaboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.ORCID 0000-0002-0104-4369
Universidade do Estado do Pará · BRAC Camargo Hospital · BRUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study evaluated the risk of the hereditary breast and ovarian cancer (HBOC) syndrome in patients with breast cancer by using the Family History Screening 7 (FHS-7) tool, a validated low-cost questionnaire with high sensitivity able to screen the HBOC risk in the population.

methodsWomen diagnosed with breast cancer (

resultsThe risk of HBOC was 19.80% (

conclusionOur findings suggest a possible family inheritance associated with worse clinical features in women with breast cancer in this population, indicating that HBOC investigation can be initially performed with low-cost instruments such as FHS-7.

Indexed as

Breast NeoplasmsHereditary Breast and Ovarian Cancer SyndromeOvarian NeoplasmsEarly Detection of CancerFemaleGenetic Predisposition to DiseaseHumansMass Screening

Identifiers

PMID34547796
PMCPMC10183857
OpenAlexW3201107012

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.