Neonatal Screening for Treatable and Untreatable Disorders: Prospective Parents' Opinions
In the Netherlands, in 2007, the national newborn screening program was expanded from 3 to 17 disorders that met the World Health Organization's Wilson and Jungner screening criteria, especially regarding treatability. The decision of whether to add diseases to the program is generally based on...
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description | In the Netherlands, in 2007, the national newborn screening program was expanded from 3 to 17 disorders that met the World Health Organization's Wilson and Jungner screening criteria, especially regarding treatability. The decision of whether to add diseases to the program is generally based on experts' advice, whereas the opinion of those whom it concerns--prospective parents--remains unknown. In this study, we investigated the opinion of prospective parents concerning newborn screening for disorders that are incurable yet treatable to some extent or even untreatable.
A structured questionnaire that consisted of 3 parts in which similar questions were posed about treatable, less treatable, and untreatable childhood-onset disorders was posted on the Web site of a national pregnancy fair.
A total of 1631 prospective parents filled out the questionnaire, 259 of whom were excluded. In contrast to current policy, respondents showed a positive attitude toward inclusion of less treatable (88%) or untreatable childhood-onset disorders (73%) within the national newborn screening program. Respondents who already had children at the time of completing the questionnaire were even more in favor of screening for especially untreatable disorders. The most important reason mentioned was to prevent a long diagnostic quest. Obtaining information to enable reproductive choices in future pregnancies was hardly mentioned.
Prospective parents in the Dutch population seem interested in newborn screening for untreatable childhood-onset disorders; therefore, we argue that additional debate of pros and cons is needed among policy makers, health care professionals, and consumers. |
doi_str_mv | 10.1542/peds.2009-0269 |
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A structured questionnaire that consisted of 3 parts in which similar questions were posed about treatable, less treatable, and untreatable childhood-onset disorders was posted on the Web site of a national pregnancy fair.
A total of 1631 prospective parents filled out the questionnaire, 259 of whom were excluded. In contrast to current policy, respondents showed a positive attitude toward inclusion of less treatable (88%) or untreatable childhood-onset disorders (73%) within the national newborn screening program. Respondents who already had children at the time of completing the questionnaire were even more in favor of screening for especially untreatable disorders. The most important reason mentioned was to prevent a long diagnostic quest. Obtaining information to enable reproductive choices in future pregnancies was hardly mentioned.
Prospective parents in the Dutch population seem interested in newborn screening for untreatable childhood-onset disorders; therefore, we argue that additional debate of pros and cons is needed among policy makers, health care professionals, and consumers.</description><identifier>ISSN: 0031-4005</identifier><identifier>EISSN: 1098-4275</identifier><identifier>DOI: 10.1542/peds.2009-0269</identifier><identifier>PMID: 20026497</identifier><identifier>CODEN: PEDIAU</identifier><language>eng</language><publisher>United States: Am Acad Pediatrics</publisher><subject>Age of Onset ; Attitude to Health ; Babies ; Child ; Child, Preschool ; Cross-Sectional Studies ; Cystic Fibrosis - diagnosis ; Cystic Fibrosis - genetics ; Cystic Fibrosis - therapy ; Female ; Genetic Testing - standards ; Genetic Testing - trends ; Humans ; Infant, Newborn ; Male ; Medical disorders ; Medical screening ; Muscular Dystrophy, Duchenne - diagnosis ; Muscular Dystrophy, Duchenne - genetics ; Muscular Dystrophy, Duchenne - therapy ; Neonatal Screening - organization & administration ; Netherlands ; Parent attitudes ; Parents - psychology ; Pediatrics ; Phenylketonurias - diagnosis ; Phenylketonurias - genetics ; Phenylketonurias - therapy ; Professional-Family Relations ; Program Evaluation ; Qualitative research ; Risk Assessment ; Surveys and Questionnaires ; Treatment Failure ; Treatment Outcome</subject><ispartof>Pediatrics (Evanston), 2010-01, Vol.125 (1), p.e99-e106</ispartof><rights>Copyright American Academy of Pediatrics Jan 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-4b98752273207273f999e8c5206d0d4f1c39e5a14691e37a0da8bf774155852b3</citedby><cites>FETCH-LOGICAL-c360t-4b98752273207273f999e8c5206d0d4f1c39e5a14691e37a0da8bf774155852b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20026497$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Plass, Anne Marie Catharina</creatorcontrib><creatorcontrib>van El, Carla Geertruida</creatorcontrib><creatorcontrib>Pieters, Toine</creatorcontrib><creatorcontrib>Cornel, Martina Cornelia</creatorcontrib><title>Neonatal Screening for Treatable and Untreatable Disorders: Prospective Parents' Opinions</title><title>Pediatrics (Evanston)</title><addtitle>Pediatrics</addtitle><description>In the Netherlands, in 2007, the national newborn screening program was expanded from 3 to 17 disorders that met the World Health Organization's Wilson and Jungner screening criteria, especially regarding treatability. The decision of whether to add diseases to the program is generally based on experts' advice, whereas the opinion of those whom it concerns--prospective parents--remains unknown. In this study, we investigated the opinion of prospective parents concerning newborn screening for disorders that are incurable yet treatable to some extent or even untreatable.
A structured questionnaire that consisted of 3 parts in which similar questions were posed about treatable, less treatable, and untreatable childhood-onset disorders was posted on the Web site of a national pregnancy fair.
A total of 1631 prospective parents filled out the questionnaire, 259 of whom were excluded. In contrast to current policy, respondents showed a positive attitude toward inclusion of less treatable (88%) or untreatable childhood-onset disorders (73%) within the national newborn screening program. Respondents who already had children at the time of completing the questionnaire were even more in favor of screening for especially untreatable disorders. The most important reason mentioned was to prevent a long diagnostic quest. Obtaining information to enable reproductive choices in future pregnancies was hardly mentioned.
Prospective parents in the Dutch population seem interested in newborn screening for untreatable childhood-onset disorders; therefore, we argue that additional debate of pros and cons is needed among policy makers, health care professionals, and consumers.</description><subject>Age of Onset</subject><subject>Attitude to Health</subject><subject>Babies</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cross-Sectional Studies</subject><subject>Cystic Fibrosis - diagnosis</subject><subject>Cystic Fibrosis - genetics</subject><subject>Cystic Fibrosis - therapy</subject><subject>Female</subject><subject>Genetic Testing - standards</subject><subject>Genetic Testing - trends</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Medical disorders</subject><subject>Medical screening</subject><subject>Muscular Dystrophy, Duchenne - diagnosis</subject><subject>Muscular Dystrophy, Duchenne - genetics</subject><subject>Muscular Dystrophy, Duchenne - therapy</subject><subject>Neonatal Screening - organization & administration</subject><subject>Netherlands</subject><subject>Parent attitudes</subject><subject>Parents - psychology</subject><subject>Pediatrics</subject><subject>Phenylketonurias - diagnosis</subject><subject>Phenylketonurias - genetics</subject><subject>Phenylketonurias - therapy</subject><subject>Professional-Family Relations</subject><subject>Program Evaluation</subject><subject>Qualitative research</subject><subject>Risk Assessment</subject><subject>Surveys and Questionnaires</subject><subject>Treatment Failure</subject><subject>Treatment Outcome</subject><issn>0031-4005</issn><issn>1098-4275</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkMtLxDAQh4Mouj6uHqV48dR18moab-IbRBfUg6eQtlONdNOadBX_e1vWF14yyfDNj8lHyC6FKZWCHXZYxSkD0CmwTK-QCQWdp4IpuUomAJymAkBukM0YXwBASMXWycYwwDKh1YQ83mDrbW-b5K4MiN75p6RuQ3IfcOgWDSbWV8mD73_epy62ocIQj5JZaGOHZe_eMJnZgL6PB8lt57xrfdwma7VtIu581S3ycH52f3KZXt9eXJ0cX6clz6BPRaFzJRlTnIEazlprjXkpGWQVVKKmJdcoLRWZpsiVhcrmRa2UoFLmkhV8ixwsc7vQvi4w9mbuYolNYz22i2gUF4xRnuuB3P9HvrSL4IflDGM5z3IOfICmS6gcPhcD1qYLbm7Dh6FgRuVmVG5G5WZUPgzsfaUuijlWP_i349_EZ_f0_O4CjgnO9sGV8c-VMmmoQa35J6HAjCQ</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Plass, Anne Marie Catharina</creator><creator>van El, Carla Geertruida</creator><creator>Pieters, Toine</creator><creator>Cornel, Martina Cornelia</creator><general>Am Acad Pediatrics</general><general>American Academy of Pediatrics</general><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>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>20100101</creationdate><title>Neonatal Screening for Treatable and Untreatable Disorders: Prospective Parents' Opinions</title><author>Plass, Anne Marie Catharina ; van El, Carla Geertruida ; Pieters, Toine ; Cornel, Martina Cornelia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-4b98752273207273f999e8c5206d0d4f1c39e5a14691e37a0da8bf774155852b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Age of Onset</topic><topic>Attitude to Health</topic><topic>Babies</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cross-Sectional Studies</topic><topic>Cystic Fibrosis - diagnosis</topic><topic>Cystic Fibrosis - genetics</topic><topic>Cystic Fibrosis - therapy</topic><topic>Female</topic><topic>Genetic Testing - standards</topic><topic>Genetic Testing - trends</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Medical disorders</topic><topic>Medical screening</topic><topic>Muscular Dystrophy, Duchenne - diagnosis</topic><topic>Muscular Dystrophy, Duchenne - genetics</topic><topic>Muscular Dystrophy, Duchenne - therapy</topic><topic>Neonatal Screening - organization & administration</topic><topic>Netherlands</topic><topic>Parent attitudes</topic><topic>Parents - psychology</topic><topic>Pediatrics</topic><topic>Phenylketonurias - diagnosis</topic><topic>Phenylketonurias - genetics</topic><topic>Phenylketonurias - therapy</topic><topic>Professional-Family Relations</topic><topic>Program Evaluation</topic><topic>Qualitative research</topic><topic>Risk Assessment</topic><topic>Surveys and Questionnaires</topic><topic>Treatment Failure</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Plass, Anne Marie Catharina</creatorcontrib><creatorcontrib>van El, Carla Geertruida</creatorcontrib><creatorcontrib>Pieters, Toine</creatorcontrib><creatorcontrib>Cornel, Martina Cornelia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Physical Education Index</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatrics (Evanston)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Plass, Anne Marie Catharina</au><au>van El, Carla Geertruida</au><au>Pieters, Toine</au><au>Cornel, Martina Cornelia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neonatal Screening for Treatable and Untreatable Disorders: Prospective Parents' Opinions</atitle><jtitle>Pediatrics (Evanston)</jtitle><addtitle>Pediatrics</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>125</volume><issue>1</issue><spage>e99</spage><epage>e106</epage><pages>e99-e106</pages><issn>0031-4005</issn><eissn>1098-4275</eissn><coden>PEDIAU</coden><abstract>In the Netherlands, in 2007, the national newborn screening program was expanded from 3 to 17 disorders that met the World Health Organization's Wilson and Jungner screening criteria, especially regarding treatability. The decision of whether to add diseases to the program is generally based on experts' advice, whereas the opinion of those whom it concerns--prospective parents--remains unknown. In this study, we investigated the opinion of prospective parents concerning newborn screening for disorders that are incurable yet treatable to some extent or even untreatable.
A structured questionnaire that consisted of 3 parts in which similar questions were posed about treatable, less treatable, and untreatable childhood-onset disorders was posted on the Web site of a national pregnancy fair.
A total of 1631 prospective parents filled out the questionnaire, 259 of whom were excluded. In contrast to current policy, respondents showed a positive attitude toward inclusion of less treatable (88%) or untreatable childhood-onset disorders (73%) within the national newborn screening program. Respondents who already had children at the time of completing the questionnaire were even more in favor of screening for especially untreatable disorders. The most important reason mentioned was to prevent a long diagnostic quest. Obtaining information to enable reproductive choices in future pregnancies was hardly mentioned.
Prospective parents in the Dutch population seem interested in newborn screening for untreatable childhood-onset disorders; therefore, we argue that additional debate of pros and cons is needed among policy makers, health care professionals, and consumers.</abstract><cop>United States</cop><pub>Am Acad Pediatrics</pub><pmid>20026497</pmid><doi>10.1542/peds.2009-0269</doi></addata></record> |
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subjects | Age of Onset Attitude to Health Babies Child Child, Preschool Cross-Sectional Studies Cystic Fibrosis - diagnosis Cystic Fibrosis - genetics Cystic Fibrosis - therapy Female Genetic Testing - standards Genetic Testing - trends Humans Infant, Newborn Male Medical disorders Medical screening Muscular Dystrophy, Duchenne - diagnosis Muscular Dystrophy, Duchenne - genetics Muscular Dystrophy, Duchenne - therapy Neonatal Screening - organization & administration Netherlands Parent attitudes Parents - psychology Pediatrics Phenylketonurias - diagnosis Phenylketonurias - genetics Phenylketonurias - therapy Professional-Family Relations Program Evaluation Qualitative research Risk Assessment Surveys and Questionnaires Treatment Failure Treatment Outcome |
title | Neonatal Screening for Treatable and Untreatable Disorders: Prospective Parents' Opinions |
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