Room for improvement in capturing cancer family history in a gynecologic oncology outpatient setting.

Cancer family history Genetic testing Medical history taking Medical records Pedigree

Journal

Gynecologic oncology reports
ISSN: 2352-5789
Titre abrégé: Gynecol Oncol Rep
Pays: Netherlands
ID NLM: 101652231

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 01 12 2021
revised: 07 02 2022
accepted: 09 02 2022
entrez: 4 3 2022
pubmed: 5 3 2022
medline: 5 3 2022
Statut: epublish

Résumé

The literature demonstrates that the quality of cancer family history (CFH) as currently collected in the outpatient setting is inadequate to assess disease risk. Prior to implementation of a web-based application for cancer family history collection, we aimed to review the quality of collected CFH in a gynecologic oncology outpatient clinic and determine contributing patient factors. Medical records were reviewed for 200 new patients presenting between 4/2019-7/2019. CFH was collected during the patient interview and evaluated for inclusion of eight elements based on standards set by the genetics community. Univariate and multivariable linear regression analyses were utilized to evaluate the effect of patient characteristics on the number of relatives included in the CFH. Among our cohort of 200 patients, CFH was documented for 185 patients (92.5%). On univariate analysis, patients with a family history of cancer and prior genetic testing had significantly greater median number of relatives included in the CFH. On multivariable analysis, patients with family members with cancer had significantly more relatives included. Our data are consistent with the literature, suggesting that the current collection methods may not adequately capture all measures of a high quality CFH. Patients reporting no family history of cancer and those without prior genetic testing were least likely to have CFH that included key quality elements and these patients might benefit from health information technology CFH collection tools.

Identifiants

pubmed: 35242980
doi: 10.1016/j.gore.2022.100941
pii: S2352-5789(22)00021-2
pmc: PMC8861387
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100941

Subventions

Organisme : NCI NIH HHS
ID : K07 CA216326
Pays : United States

Informations de copyright

© 2022 The Authors. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Jenny Lin (J)

Weill Cornell Medicine, United States.

Isabel Wolfe (I)

Weill Cornell Medicine, United States.

Muhammad Danyal Ahsan (MD)

Weill Cornell Medicine, United States.

Hannah Krinsky (H)

Weill Cornell Medicine, United States.

Andreas I Lackner (AI)

Weill Cornell Medicine, United States.

Joe Pelt (J)

Weill Cornell Medicine, United States.

Karen Bolouvi (K)

Weill Cornell Medicine, United States.

Charlotte Gamble (C)

Weill Cornell Medicine, United States.

Charlene Thomas (C)

Weill Cornell Medicine, United States.

Paul J Christos (PJ)

Weill Cornell Medicine, United States.

Evelyn Cantillo (E)

Weill Cornell Medicine, United States.

Kevin Holcomb (K)

Weill Cornell Medicine, United States.

Eloise Chapman-Davis (E)

Weill Cornell Medicine, United States.

Ravi Sharaf (R)

Weill Cornell Medicine, United States.

Steven M Lipkin (SM)

Weill Cornell Medicine, United States.

Stephanie V Blank (SV)

Icahn School of Medicine at Mount Sinai, Blavatnik Family Women's Health Research Institute, United States.

Melissa K Frey (MK)

Weill Cornell Medicine, United States.

Classifications MeSH