Why do people choose not to have screening for hemochromatosis?
Hemochromatosis is a common disorder of iron overload most commonly due to homozogosity for the HFE C282Y substitution. A workplace-screening program was conducted in which over 11,000 individuals were screened for this mutation. A substudy of this project was to ascertain why people chose not to at...
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Veröffentlicht in: | Genetic testing and molecular biomarkers 2013-01, Vol.17 (1), p.21-24 |
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creator | Wolthuizen, Michelle Nisselle, Amy Halliday, Jane Metcalfe, Sylvia A Aitken, MaryAnne Allen, Katie J Delatycki, Martin B |
description | Hemochromatosis is a common disorder of iron overload most commonly due to homozogosity for the HFE C282Y substitution. A workplace-screening program was conducted in which over 11,000 individuals were screened for this mutation. A substudy of this project was to ascertain why people chose not to attend information and screening sessions offered in their workplace.
Staff were recruited by email, questionnaires in common areas, and direct approach. A purpose-designed questionnaire sought the reasons for not attending information and screening sessions.
The nonattender questionnaire was distributed at 24 workplaces and completed by 872 individuals. The most common reason for not attending sessions, accounting for 70.1%, was practical (e.g., unaware of session, too busy, or unavailable). Other relatively common reasons were that the individual had low iron levels or were a blood donor (14.9%), or that hemochromatosis was considered unimportant (12.2%). Insurance concerns were very rarely cited as the reason for nonattendance (1.0%).
The nonattender data presented here indicate that concerns about insurance, anxiety, and use of genetic information are not major factors for why people did not attend workplace information and screening sessions for hereditary hemochromatosis. Practical barriers were the major reasons identified. This highlights that when implementing screening programs, as many practical barriers as possible need to be overcome, so that a maximum number of people who would like to be informed about screening are given the opportunity to do so. |
doi_str_mv | 10.1089/gtmb.2012.0247 |
format | Article |
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Staff were recruited by email, questionnaires in common areas, and direct approach. A purpose-designed questionnaire sought the reasons for not attending information and screening sessions.
The nonattender questionnaire was distributed at 24 workplaces and completed by 872 individuals. The most common reason for not attending sessions, accounting for 70.1%, was practical (e.g., unaware of session, too busy, or unavailable). Other relatively common reasons were that the individual had low iron levels or were a blood donor (14.9%), or that hemochromatosis was considered unimportant (12.2%). Insurance concerns were very rarely cited as the reason for nonattendance (1.0%).
The nonattender data presented here indicate that concerns about insurance, anxiety, and use of genetic information are not major factors for why people did not attend workplace information and screening sessions for hereditary hemochromatosis. Practical barriers were the major reasons identified. This highlights that when implementing screening programs, as many practical barriers as possible need to be overcome, so that a maximum number of people who would like to be informed about screening are given the opportunity to do so.</description><identifier>ISSN: 1945-0265</identifier><identifier>EISSN: 1945-0257</identifier><identifier>DOI: 10.1089/gtmb.2012.0247</identifier><identifier>PMID: 23098241</identifier><language>eng</language><publisher>United States</publisher><subject>Anxiety ; Blood Donors ; Data processing ; Early Diagnosis ; Female ; Genetic screening ; Genetic Testing ; Hemochromatosis ; Hemochromatosis - diagnosis ; Hemochromatosis - epidemiology ; Hemochromatosis - genetics ; Hemochromatosis - prevention & control ; Humans ; Inventories ; Iron ; Iron - blood ; Iron - metabolism ; Male ; Mass Screening - organization & administration ; Mass Screening - psychology ; Mutation ; Surveys and Questionnaires ; Workplace</subject><ispartof>Genetic testing and molecular biomarkers, 2013-01, Vol.17 (1), p.21-24</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-62fe8f43c269a8ada1b915f435b84293056db95a90c41bef6aca853b22fa87403</citedby><cites>FETCH-LOGICAL-c328t-62fe8f43c269a8ada1b915f435b84293056db95a90c41bef6aca853b22fa87403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23098241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wolthuizen, Michelle</creatorcontrib><creatorcontrib>Nisselle, Amy</creatorcontrib><creatorcontrib>Halliday, Jane</creatorcontrib><creatorcontrib>Metcalfe, Sylvia A</creatorcontrib><creatorcontrib>Aitken, MaryAnne</creatorcontrib><creatorcontrib>Allen, Katie J</creatorcontrib><creatorcontrib>Delatycki, Martin B</creatorcontrib><title>Why do people choose not to have screening for hemochromatosis?</title><title>Genetic testing and molecular biomarkers</title><addtitle>Genet Test Mol Biomarkers</addtitle><description>Hemochromatosis is a common disorder of iron overload most commonly due to homozogosity for the HFE C282Y substitution. A workplace-screening program was conducted in which over 11,000 individuals were screened for this mutation. A substudy of this project was to ascertain why people chose not to attend information and screening sessions offered in their workplace.
Staff were recruited by email, questionnaires in common areas, and direct approach. A purpose-designed questionnaire sought the reasons for not attending information and screening sessions.
The nonattender questionnaire was distributed at 24 workplaces and completed by 872 individuals. The most common reason for not attending sessions, accounting for 70.1%, was practical (e.g., unaware of session, too busy, or unavailable). Other relatively common reasons were that the individual had low iron levels or were a blood donor (14.9%), or that hemochromatosis was considered unimportant (12.2%). Insurance concerns were very rarely cited as the reason for nonattendance (1.0%).
The nonattender data presented here indicate that concerns about insurance, anxiety, and use of genetic information are not major factors for why people did not attend workplace information and screening sessions for hereditary hemochromatosis. Practical barriers were the major reasons identified. This highlights that when implementing screening programs, as many practical barriers as possible need to be overcome, so that a maximum number of people who would like to be informed about screening are given the opportunity to do so.</description><subject>Anxiety</subject><subject>Blood Donors</subject><subject>Data processing</subject><subject>Early Diagnosis</subject><subject>Female</subject><subject>Genetic screening</subject><subject>Genetic Testing</subject><subject>Hemochromatosis</subject><subject>Hemochromatosis - diagnosis</subject><subject>Hemochromatosis - epidemiology</subject><subject>Hemochromatosis - genetics</subject><subject>Hemochromatosis - prevention & control</subject><subject>Humans</subject><subject>Inventories</subject><subject>Iron</subject><subject>Iron - blood</subject><subject>Iron - metabolism</subject><subject>Male</subject><subject>Mass Screening - organization & administration</subject><subject>Mass Screening - psychology</subject><subject>Mutation</subject><subject>Surveys and Questionnaires</subject><subject>Workplace</subject><issn>1945-0265</issn><issn>1945-0257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkDtPwzAUhS0EolBYGZFHlgS_Y08VqnhJlVhAjJbtOE1QEgc7Req_p1FLV6ZzdfTdM3wA3GCUYyTV_XrsbE4QJjkirDgBF1gxniHCi9PjLfgMXKb0hZBgVIpzMCMUKUkYvgCLz3oLywAHH4bWQ1eHkDzswwjHAGvz42Fy0fu-6dewChHWvguujqEzY0hNWlyBs8q0yV8fcg4-nh7fly_Z6u35dfmwyhwlcswEqbysGHVEKCNNabBVmO8KbiUjiiIuSqu4UcgxbH0ljDOSU0tIZWTBEJ2Du_3uEMP3xqdRd01yvm1N78MmaUwxF4RSUfyPEqqQwIizHZrvURdDStFXeohNZ-JWY6Qnv3ryqye_evK7e7g9bG9s58sj_ieU_gJgDnVT</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Wolthuizen, Michelle</creator><creator>Nisselle, Amy</creator><creator>Halliday, Jane</creator><creator>Metcalfe, Sylvia A</creator><creator>Aitken, MaryAnne</creator><creator>Allen, Katie J</creator><creator>Delatycki, Martin B</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201301</creationdate><title>Why do people choose not to have screening for hemochromatosis?</title><author>Wolthuizen, Michelle ; Nisselle, Amy ; Halliday, Jane ; Metcalfe, Sylvia A ; Aitken, MaryAnne ; Allen, Katie J ; Delatycki, Martin B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-62fe8f43c269a8ada1b915f435b84293056db95a90c41bef6aca853b22fa87403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anxiety</topic><topic>Blood Donors</topic><topic>Data processing</topic><topic>Early Diagnosis</topic><topic>Female</topic><topic>Genetic screening</topic><topic>Genetic Testing</topic><topic>Hemochromatosis</topic><topic>Hemochromatosis - diagnosis</topic><topic>Hemochromatosis - epidemiology</topic><topic>Hemochromatosis - genetics</topic><topic>Hemochromatosis - prevention & control</topic><topic>Humans</topic><topic>Inventories</topic><topic>Iron</topic><topic>Iron - blood</topic><topic>Iron - metabolism</topic><topic>Male</topic><topic>Mass Screening - organization & administration</topic><topic>Mass Screening - psychology</topic><topic>Mutation</topic><topic>Surveys and Questionnaires</topic><topic>Workplace</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wolthuizen, Michelle</creatorcontrib><creatorcontrib>Nisselle, Amy</creatorcontrib><creatorcontrib>Halliday, Jane</creatorcontrib><creatorcontrib>Metcalfe, Sylvia A</creatorcontrib><creatorcontrib>Aitken, MaryAnne</creatorcontrib><creatorcontrib>Allen, Katie J</creatorcontrib><creatorcontrib>Delatycki, Martin B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genetic testing and molecular biomarkers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wolthuizen, Michelle</au><au>Nisselle, Amy</au><au>Halliday, Jane</au><au>Metcalfe, Sylvia A</au><au>Aitken, MaryAnne</au><au>Allen, Katie J</au><au>Delatycki, Martin B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Why do people choose not to have screening for hemochromatosis?</atitle><jtitle>Genetic testing and molecular biomarkers</jtitle><addtitle>Genet Test Mol Biomarkers</addtitle><date>2013-01</date><risdate>2013</risdate><volume>17</volume><issue>1</issue><spage>21</spage><epage>24</epage><pages>21-24</pages><issn>1945-0265</issn><eissn>1945-0257</eissn><abstract>Hemochromatosis is a common disorder of iron overload most commonly due to homozogosity for the HFE C282Y substitution. A workplace-screening program was conducted in which over 11,000 individuals were screened for this mutation. A substudy of this project was to ascertain why people chose not to attend information and screening sessions offered in their workplace.
Staff were recruited by email, questionnaires in common areas, and direct approach. A purpose-designed questionnaire sought the reasons for not attending information and screening sessions.
The nonattender questionnaire was distributed at 24 workplaces and completed by 872 individuals. The most common reason for not attending sessions, accounting for 70.1%, was practical (e.g., unaware of session, too busy, or unavailable). Other relatively common reasons were that the individual had low iron levels or were a blood donor (14.9%), or that hemochromatosis was considered unimportant (12.2%). Insurance concerns were very rarely cited as the reason for nonattendance (1.0%).
The nonattender data presented here indicate that concerns about insurance, anxiety, and use of genetic information are not major factors for why people did not attend workplace information and screening sessions for hereditary hemochromatosis. Practical barriers were the major reasons identified. This highlights that when implementing screening programs, as many practical barriers as possible need to be overcome, so that a maximum number of people who would like to be informed about screening are given the opportunity to do so.</abstract><cop>United States</cop><pmid>23098241</pmid><doi>10.1089/gtmb.2012.0247</doi><tpages>4</tpages></addata></record> |
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subjects | Anxiety Blood Donors Data processing Early Diagnosis Female Genetic screening Genetic Testing Hemochromatosis Hemochromatosis - diagnosis Hemochromatosis - epidemiology Hemochromatosis - genetics Hemochromatosis - prevention & control Humans Inventories Iron Iron - blood Iron - metabolism Male Mass Screening - organization & administration Mass Screening - psychology Mutation Surveys and Questionnaires Workplace |
title | Why do people choose not to have screening for hemochromatosis? |
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