{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T20:55:58Z","timestamp":1791406558265,"version":"4.3.3"},"reference-count":21,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2022,4,18]],"date-time":"2022-04-18T00:00:00Z","timestamp":1650240000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Journal of Genetic Counseling"],"published-print":{"date-parts":[[2022,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Prenatal and preconception genetic counselors are trained to take patient pedigrees to evaluate for potential risks for genetic conditions, including hereditary cancer syndromes. However, little research has been published on how often prenatal\/preconception genetic counselors provide recommendations for cancer genetic counseling solely based on a family history of cancer. Therefore, this study sought to (a) characterize the types of cancers recognized for a cancer genetic counseling recommendation, (b) analyze appointment indications associated with discussion documentation, and (c) investigate how often National Comprehensive Cancer Center (NCCN) genetic testing criteria for Hereditary Breast and Ovarian Cancer syndrome (HBOC) and Lynch syndrome were met and how often a recommendation for cancer genetic counseling was made. A retrospective chart review and pedigree analysis were performed for prenatal\/preconception genetic counseling patients with a family history of cancer seen at two academic institutions between August 10, 2019, and December 1, 2019. In the 170 charts included, a recommendation for cancer genetic counseling was documented in 40% of all genetic counseling summaries and in 59.2% of summaries when NCCN genetic testing criteria for HBOC and\/or Lynch syndrome was met. Using chi\u2010squared and logistic regression analysis, these data support that individuals were significantly more likely to receive a recommendation when NCCN genetic testing criteria were met (OR\u00a0=\u00a05.01, <jats:italic>p<\/jats:italic>\u00a0&lt;\u00a0.001) or when the family history contained two or more types of cancer (OR\u00a0=\u00a02.24, <jats:italic>p<\/jats:italic>\u00a0=\u00a0.02). Overall, this study identified the NCCN genetic testing criteria for HBOC and Lynch syndrome for which recommendations for cancer genetic counseling were commonly missed. This characterization suggests that continuing education for prenatal and preconception genetic counselors on updated NCCN guidelines may be helpful for improving rates of cancer genetic counseling referrals, uptake of genetic testing, and cancer screening recommendations.<\/jats:p>","DOI":"10.1002\/jgc4.1577","type":"journal-article","created":{"date-parts":[[2022,4,18]],"date-time":"2022-04-18T08:11:20Z","timestamp":1650269480000},"page":"1062-1070","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Prenatal genetic counseling practices regarding recommendations for cancer genetic counseling: A retrospective chart review from two academic institutions"],"prefix":"10.1002","volume":"31","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7411-0259","authenticated-orcid":false,"given":"Lisa F.","family":"Saba","sequence":"first","affiliation":[{"name":"School of Health Professions Baylor College of Medicine  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cathy M.","family":"Sullivan","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine Baylor College of Medicine  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tamara","family":"Solomon","sequence":"additional","affiliation":[{"name":"Department of Molecular and Human Genetics Baylor College of Medicine  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah","family":"Huguenard","sequence":"additional","affiliation":[{"name":"Department of Molecular and Human Genetics Baylor College of Medicine  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Salma A.","family":"Nassef","sequence":"additional","affiliation":[{"name":"School of Health Professions Baylor College of Medicine  Houston Texas USA"},{"name":"Department of Molecular and Human Genetics Baylor College of Medicine  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2022,4,18]]},"reference":[{"key":"e_1_2_10_2_1","doi-asserted-by":"publisher","DOI":"10.6004\/jnccn.2016.0018"},{"key":"e_1_2_10_3_1","doi-asserted-by":"publisher","DOI":"10.1053\/j.gastro.2019.11.297"},{"key":"e_1_2_10_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ygyno.2015.04.029"},{"key":"e_1_2_10_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jbi.2019.103208"},{"key":"e_1_2_10_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jbi.2008.08.010"},{"key":"e_1_2_10_7_1","doi-asserted-by":"crossref","unstructured":"Hereditary cancer syndromes and risk assessment: ACOG Committee opinion summary number 793. (2019).Obstetrics and Gynecology (New York. 1953) 134(6) 1366\u20131367.https:\/\/doi.org\/10.1097\/AOG.0000000000003563","DOI":"10.1097\/AOG.0000000000003563"},{"key":"e_1_2_10_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ygyno.2018.07.023"},{"key":"e_1_2_10_9_1","doi-asserted-by":"publisher","DOI":"10.1111\/cge.13654"},{"key":"e_1_2_10_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/pd.5048"},{"key":"e_1_2_10_11_1","unstructured":"National Comprehensive Cancer Network. (2019).Genetic\/Familial High\u2010Risk Assessment: Genetic\/Familial High\u2010Risk Assessment: Colorectal (Version 2.2019). Retrieved 03\/27\/2020 fromwww.nccn.org"},{"key":"e_1_2_10_12_1","unstructured":"National Comprehensive Cancer Network. (2019).Genetic\/Familial High\u2010Risk Assessment: Genetic\/Familial High\u2010Risk Assessment: Breast and Ovarian (Version 3.2019). Retrieved 03\/27\/2020 fromwww.nccn.org"},{"key":"e_1_2_10_13_1","unstructured":"National Comprehensive Cancer Network. (2021).Genetic\/Familial High\u2010Risk Assessment: Breast Ovarian and Pancreatic (Version 1.2021). Retrieved 03\/09\/2021 fromhttps:\/\/www.nccn.org\/professionals\/physician_gls\/pdf\/genetics_bop.pdf"},{"key":"e_1_2_10_14_1","unstructured":"NSGC Professional Status Survey: Executive Summary. (2020). p. 2. 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