Evidence map›Paper›PMID 27624814›Full record

ArticleFamilial cancer2017

Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling.

Patrick R Benusiglio, Marina Di Maria, Leila Dorling, Anne Jouinot, Antoine Poli, Sophie Villebasse, Marine Le Mentec, Béatrice Claret, Diane Boinon, Olivier Caron

Abstract read
PubMed Publisher
In one paragraph

Article in Familial cancer, 2017. 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
2.1field-weighted citation impact, top 12% 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, 21 citations in OpenAlex.

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  6. The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review.Genetics in medicine : official journal of the American College of Medical Genetics · 2020
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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

10 authors at 3 institutions in 2 countries.

Patrick R BenusiglioConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France. patrick.benusiglio@gustaveroussy.fr.ORCID 0000-0003-1003-1997
Marina Di MariaConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Leila DorlingDepartment of Public Health and Primary Care, Centre for Cancer Genetic Epidemiology, Strangeways Research Laboratory, Worts Causeway, Cambridge, CB1 8RN, UK.
Anne JouinotConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Antoine PoliConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Sophie VillebasseConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Marine Le MentecConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Béatrice ClaretUnité de Psycho-Oncologie, Département Interdisciplinaire de Soins de Support, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Diane BoinonUnité de Psycho-Oncologie, Département Interdisciplinaire de Soins de Support, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Olivier CaronConsultation d'Oncogénétique, Département de Médecine Oncologique, Gustave Roussy Cancer Campus Grand Paris, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Institut Gustave Roussy · FRDélégation Paris 5 · FRMRC Epidemiology Unit · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increase in referrals to cancer genetics clinics, partially associated with the "Angelina Jolie effect", presents a challenge to existing services, many are already running at full capacity. More efficient ways to deliver genetic counselling are therefore urgently needed. We now systematically offer group instead of standard individual counselling to patients with suspected Hereditary Breast and Ovarian Cancer. Group sessions last 30 min. The first twenty consist of a presentation by the genetic counsellor, the next ten of a discussion involving a cancer geneticist and a psychologist. A short individual consultation ensues, where personal and family issues are addressed and consent obtained. Blood is drawn afterwards. Satisfaction and knowledge are evaluated. We report data for the Oct-2014-Aug-2015 period. 210 patients attended group counselling, up to eight simultaneously. We always fitted them within a 4-h time frame. Mean satisfaction score was 41/43. Knowledge scores increased from 3.1/6 to 4.9/6 post-counselling (p value < 2.2 × 10

Indexed as

Genetic CounselingAdultAgedBreast NeoplasmsFemaleFranceGenetic Predisposition to DiseaseHumansMiddle AgedOvarian NeoplasmsBRCA1BRCA2Delivery of health careGenetic counsellingHereditary breast and ovarian cancer syndromePatient education

Identifiers

PMID27624814
OpenAlexW2520302607

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.