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Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine
IntroductionIn order to provide baseline data on genetic testing as a key element of personalised medicine (PM), Canadian physicians were surveyed to determine roles, perceptions and experiences in this area. The survey measured attitudes, practice, observed benefits and impacts, and barriers to ado...
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description | IntroductionIn order to provide baseline data on genetic testing as a key element of personalised medicine (PM), Canadian physicians were surveyed to determine roles, perceptions and experiences in this area. The survey measured attitudes, practice, observed benefits and impacts, and barriers to adoption.MethodsA self-administered survey was provided to Canadian oncologists, cardiologists and family physicians and responses were obtained online, by mail or by fax. The survey was designed to be exploratory. Data were compared across specialties and geography.ResultsThe overall response rate was 8.3%. Of the respondents, 43%, 30% and 27% were family physicians, cardiologists and oncologists, respectively. A strong majority of respondents agreed that genetic testing and PM can have a positive impact on their practice; however, only 51% agreed that there is sufficient evidence to order such tests. A low percentage of respondents felt that they were sufficiently informed and confident practicing in this area, although many reported that genetic tests they have ordered have benefited their patients. Half of the respondents agreed that genetic tests that would be useful in their practice are not readily available. A lack of practice guidelines, limited provider knowledge and lack of evidence-based clinical information were cited as the main barriers to practice. Differences across provinces were observed for measures relating to access to testing and the state of practice. Differences across specialties were observed for the state of practice, reported benefits and access to testing.ConclusionsCanadian physicians recognise the benefits of genetic testing and PM; however, they lack the education, information and support needed to practice effectively in this area. Variability in practice and access to testing across specialties and across Canada was observed. These results support a need for national strategies and resources to facilitate physician knowledge, training and practice in PM. |
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The survey measured attitudes, practice, observed benefits and impacts, and barriers to adoption.MethodsA self-administered survey was provided to Canadian oncologists, cardiologists and family physicians and responses were obtained online, by mail or by fax. The survey was designed to be exploratory. Data were compared across specialties and geography.ResultsThe overall response rate was 8.3%. Of the respondents, 43%, 30% and 27% were family physicians, cardiologists and oncologists, respectively. A strong majority of respondents agreed that genetic testing and PM can have a positive impact on their practice; however, only 51% agreed that there is sufficient evidence to order such tests. A low percentage of respondents felt that they were sufficiently informed and confident practicing in this area, although many reported that genetic tests they have ordered have benefited their patients. Half of the respondents agreed that genetic tests that would be useful in their practice are not readily available. A lack of practice guidelines, limited provider knowledge and lack of evidence-based clinical information were cited as the main barriers to practice. Differences across provinces were observed for measures relating to access to testing and the state of practice. Differences across specialties were observed for the state of practice, reported benefits and access to testing.ConclusionsCanadian physicians recognise the benefits of genetic testing and PM; however, they lack the education, information and support needed to practice effectively in this area. Variability in practice and access to testing across specialties and across Canada was observed. These results support a need for national strategies and resources to facilitate physician knowledge, training and practice in PM.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2011-000110</identifier><identifier>PMID: 22021765</identifier><language>eng</language><publisher>England: British Medical Journal Publishing Group</publisher><subject>Attitudes ; Cancer ; Cancer therapies ; Cardiology ; Costs ; Drug therapy ; Genetic testing ; Genetics and Genomics ; Knowledge ; Medical practices ; Medicine ; Oncology ; Perceptions ; Physicians ; Polls & surveys ; Precision medicine ; Professional education ; Provinces ; Response rates ; Studies</subject><ispartof>BMJ open, 2011-01, Vol.1 (1), p.e000110-e000110</ispartof><rights>2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>2011 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b585t-bb0efc0eb59cf09c3d1da7b2982aa78f89c5b928297435f511e7e1096e0cd8fa3</citedby><cites>FETCH-LOGICAL-b585t-bb0efc0eb59cf09c3d1da7b2982aa78f89c5b928297435f511e7e1096e0cd8fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1783499175/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1783499175?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>112,113,230,314,727,780,784,885,3194,25753,27549,27550,27924,27925,37012,37013,44590,53791,53793,55341,55350,75126,77594,77595,77596,77597,77601,77632,77660,77686</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22021765$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonter, Katherine</creatorcontrib><creatorcontrib>Desjardins, Clarissa</creatorcontrib><creatorcontrib>Currier, Nathan</creatorcontrib><creatorcontrib>Pun, Jason</creatorcontrib><creatorcontrib>Ashbury, Fredrick D</creatorcontrib><title>Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine</title><title>BMJ open</title><addtitle>BMJ Open</addtitle><addtitle>BMJ Open</addtitle><description>IntroductionIn order to provide baseline data on genetic testing as a key element of personalised medicine (PM), Canadian physicians were surveyed to determine roles, perceptions and experiences in this area. The survey measured attitudes, practice, observed benefits and impacts, and barriers to adoption.MethodsA self-administered survey was provided to Canadian oncologists, cardiologists and family physicians and responses were obtained online, by mail or by fax. The survey was designed to be exploratory. Data were compared across specialties and geography.ResultsThe overall response rate was 8.3%. Of the respondents, 43%, 30% and 27% were family physicians, cardiologists and oncologists, respectively. A strong majority of respondents agreed that genetic testing and PM can have a positive impact on their practice; however, only 51% agreed that there is sufficient evidence to order such tests. A low percentage of respondents felt that they were sufficiently informed and confident practicing in this area, although many reported that genetic tests they have ordered have benefited their patients. Half of the respondents agreed that genetic tests that would be useful in their practice are not readily available. A lack of practice guidelines, limited provider knowledge and lack of evidence-based clinical information were cited as the main barriers to practice. Differences across provinces were observed for measures relating to access to testing and the state of practice. Differences across specialties were observed for the state of practice, reported benefits and access to testing.ConclusionsCanadian physicians recognise the benefits of genetic testing and PM; however, they lack the education, information and support needed to practice effectively in this area. Variability in practice and access to testing across specialties and across Canada was observed. These results support a need for national strategies and resources to facilitate physician knowledge, training and practice in PM.</description><subject>Attitudes</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cardiology</subject><subject>Costs</subject><subject>Drug therapy</subject><subject>Genetic testing</subject><subject>Genetics and Genomics</subject><subject>Knowledge</subject><subject>Medical practices</subject><subject>Medicine</subject><subject>Oncology</subject><subject>Perceptions</subject><subject>Physicians</subject><subject>Polls & surveys</subject><subject>Precision medicine</subject><subject>Professional education</subject><subject>Provinces</subject><subject>Response rates</subject><subject>Studies</subject><issn>2044-6055</issn><issn>2044-6055</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNks1q3DAURk1paUKaJygUQxfd1Mm9lmVbXRTC0J9AoF20a3EtS1MNtuRK48C8fZXxdJJ0EbqxhXS-wxX6suw1wgUiqy-7ceMn7YoSEAuA9IVn2WkJVVXUwPnzB-uT7DzGTWKg4oLz8mV2UpZQYlPz08x91yF6R4ONus9H3Vtlnc6ty1fkqKcPOeVxDrd6l3uTU--nrfUuJ9fnUyC1tWoPe6f84Ne797mi0Nv9eg8ZGu2wO4pfZS8MDVGfH_5n2c_Pn36svhY3375cr65uio63fFt0HWijQHdcKANCsR57arpStCVR05pWKN6Jsi1FUzFuOKJuNIKoNai-NcTOsuvF23vayCnYkcJOerJyv-HDWlJIww9aAjQcWxKcYZVkvK2RCcNMA2hq4l1yfVxc09yleyjttoGGR9LHJ87-kmt_KxkKrBCS4N1BEPzvWcetHG1UehjIaT9HKQBqVgsuEvn2H3Lj55BeJyYZ1AIY1s1TFDYtq4TAhieKLZQKPsagzXFiBHnXIXnokLzrkFw6lFJvHl72mPnbmARcLEBK_6fx8j5wP-gTiT9pjuCS</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Bonter, Katherine</creator><creator>Desjardins, Clarissa</creator><creator>Currier, Nathan</creator><creator>Pun, Jason</creator><creator>Ashbury, Fredrick D</creator><general>British Medical Journal Publishing Group</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110101</creationdate><title>Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine</title><author>Bonter, Katherine ; Desjardins, Clarissa ; Currier, Nathan ; Pun, Jason ; Ashbury, Fredrick D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b585t-bb0efc0eb59cf09c3d1da7b2982aa78f89c5b928297435f511e7e1096e0cd8fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Attitudes</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Cardiology</topic><topic>Costs</topic><topic>Drug therapy</topic><topic>Genetic testing</topic><topic>Genetics and Genomics</topic><topic>Knowledge</topic><topic>Medical practices</topic><topic>Medicine</topic><topic>Oncology</topic><topic>Perceptions</topic><topic>Physicians</topic><topic>Polls & surveys</topic><topic>Precision medicine</topic><topic>Professional education</topic><topic>Provinces</topic><topic>Response rates</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonter, Katherine</creatorcontrib><creatorcontrib>Desjardins, Clarissa</creatorcontrib><creatorcontrib>Currier, Nathan</creatorcontrib><creatorcontrib>Pun, Jason</creatorcontrib><creatorcontrib>Ashbury, Fredrick D</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Complete (ProQuest Database)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMJ open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonter, Katherine</au><au>Desjardins, Clarissa</au><au>Currier, Nathan</au><au>Pun, Jason</au><au>Ashbury, Fredrick D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine</atitle><jtitle>BMJ open</jtitle><stitle>BMJ Open</stitle><addtitle>BMJ Open</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>1</volume><issue>1</issue><spage>e000110</spage><epage>e000110</epage><pages>e000110-e000110</pages><issn>2044-6055</issn><eissn>2044-6055</eissn><abstract>IntroductionIn order to provide baseline data on genetic testing as a key element of personalised medicine (PM), Canadian physicians were surveyed to determine roles, perceptions and experiences in this area. The survey measured attitudes, practice, observed benefits and impacts, and barriers to adoption.MethodsA self-administered survey was provided to Canadian oncologists, cardiologists and family physicians and responses were obtained online, by mail or by fax. The survey was designed to be exploratory. Data were compared across specialties and geography.ResultsThe overall response rate was 8.3%. Of the respondents, 43%, 30% and 27% were family physicians, cardiologists and oncologists, respectively. A strong majority of respondents agreed that genetic testing and PM can have a positive impact on their practice; however, only 51% agreed that there is sufficient evidence to order such tests. A low percentage of respondents felt that they were sufficiently informed and confident practicing in this area, although many reported that genetic tests they have ordered have benefited their patients. Half of the respondents agreed that genetic tests that would be useful in their practice are not readily available. A lack of practice guidelines, limited provider knowledge and lack of evidence-based clinical information were cited as the main barriers to practice. Differences across provinces were observed for measures relating to access to testing and the state of practice. Differences across specialties were observed for the state of practice, reported benefits and access to testing.ConclusionsCanadian physicians recognise the benefits of genetic testing and PM; however, they lack the education, information and support needed to practice effectively in this area. Variability in practice and access to testing across specialties and across Canada was observed. These results support a need for national strategies and resources to facilitate physician knowledge, training and practice in PM.</abstract><cop>England</cop><pub>British Medical Journal Publishing Group</pub><pmid>22021765</pmid><doi>10.1136/bmjopen-2011-000110</doi><oa>free_for_read</oa></addata></record> |
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subjects | Attitudes Cancer Cancer therapies Cardiology Costs Drug therapy Genetic testing Genetics and Genomics Knowledge Medical practices Medicine Oncology Perceptions Physicians Polls & surveys Precision medicine Professional education Provinces Response rates Studies |
title | Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine |
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