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Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels
BACKGROUND: Identification and adequate management of individuals at risk for hereditary nonpolyposis colorectal cancer (HNPCC) is crucial since surveillance programmes reduce morbidity and mortality. We investigated knowledge about key features of HNPCC in at risk individuals and physicians in surg...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671498/ https://www.ncbi.nlm.nih.gov/pubmed/19323816 http://dx.doi.org/10.1186/1471-2350-10-30 |
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author | Domanska, Katarina Carlsson, Christina Bendahl, Pär-Ola Nilbert, Mef |
author_facet | Domanska, Katarina Carlsson, Christina Bendahl, Pär-Ola Nilbert, Mef |
author_sort | Domanska, Katarina |
collection | PubMed |
description | BACKGROUND: Identification and adequate management of individuals at risk for hereditary nonpolyposis colorectal cancer (HNPCC) is crucial since surveillance programmes reduce morbidity and mortality. We investigated knowledge about key features of HNPCC in at risk individuals and physicians in surgery, gynecology and oncology. METHODS: Data were collected using a questionnaire which was answered by 67 mutation carriers and 102 physicians from the southern Swedish health care region. The statements were related to colorectal cancer, heredity and surveillance and the physicians were also asked questions about cancer risks and surveillance strategies. RESULTS: Both groups answered questions on colorectal cancer risk, surveillance and genetic testing well, whereas answers about inheritance and risks for HNPCC associated cancer were less accurate. Only half of the family members and one third of the physicians correctly estimated the risk to inherit an HNPCC predisposing mutation. Among family members, young age (<57 years), female sex and recent genetic counseling significantly correlated with better results. Physicians generally underestimated the risk of HNPCC associated cancers and three out of four suggested a later starting age for surveillance than recommended. CONCLUSION: The finding of similar levels of knowledge about key features of HNPCC in at risk individuals and physicians reflect the challenge physicians face in keeping up to date on hereditary cancer and may have implications for the clinical management and professional relations with HNPCC family members. |
format | Text |
id | pubmed-2671498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26714982009-04-22 Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels Domanska, Katarina Carlsson, Christina Bendahl, Pär-Ola Nilbert, Mef BMC Med Genet Research Article BACKGROUND: Identification and adequate management of individuals at risk for hereditary nonpolyposis colorectal cancer (HNPCC) is crucial since surveillance programmes reduce morbidity and mortality. We investigated knowledge about key features of HNPCC in at risk individuals and physicians in surgery, gynecology and oncology. METHODS: Data were collected using a questionnaire which was answered by 67 mutation carriers and 102 physicians from the southern Swedish health care region. The statements were related to colorectal cancer, heredity and surveillance and the physicians were also asked questions about cancer risks and surveillance strategies. RESULTS: Both groups answered questions on colorectal cancer risk, surveillance and genetic testing well, whereas answers about inheritance and risks for HNPCC associated cancer were less accurate. Only half of the family members and one third of the physicians correctly estimated the risk to inherit an HNPCC predisposing mutation. Among family members, young age (<57 years), female sex and recent genetic counseling significantly correlated with better results. Physicians generally underestimated the risk of HNPCC associated cancers and three out of four suggested a later starting age for surveillance than recommended. CONCLUSION: The finding of similar levels of knowledge about key features of HNPCC in at risk individuals and physicians reflect the challenge physicians face in keeping up to date on hereditary cancer and may have implications for the clinical management and professional relations with HNPCC family members. BioMed Central 2009-03-26 /pmc/articles/PMC2671498/ /pubmed/19323816 http://dx.doi.org/10.1186/1471-2350-10-30 Text en Copyright © 2009 Domanska et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Domanska, Katarina Carlsson, Christina Bendahl, Pär-Ola Nilbert, Mef Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
title | Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
title_full | Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
title_fullStr | Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
title_full_unstemmed | Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
title_short | Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
title_sort | knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671498/ https://www.ncbi.nlm.nih.gov/pubmed/19323816 http://dx.doi.org/10.1186/1471-2350-10-30 |
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