Loading…
Non-invasive prenatal testing in Germany: a unique ethical and policy landscape
Non-invasive prenatal testing (NIPT) has been available commercially in Europe since approximately 2012. Currently, many countries are in the process of integrating NIPT into their publicly funded healthcare systems to screen for chromosomal aneuploidies such as trisomy 21 (Down syndrome), with a va...
Saved in:
Published in: | European journal of human genetics : EJHG 2023-05, Vol.31 (5), p.562-567 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93 |
---|---|
cites | cdi_FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93 |
container_end_page | 567 |
container_issue | 5 |
container_start_page | 562 |
container_title | European journal of human genetics : EJHG |
container_volume | 31 |
creator | Bowman-Smart, Hilary Wiesemann, Claudia Horn, Ruth |
description | Non-invasive prenatal testing (NIPT) has been available commercially in Europe since approximately 2012. Currently, many countries are in the process of integrating NIPT into their publicly funded healthcare systems to screen for chromosomal aneuploidies such as trisomy 21 (Down syndrome), with a variety of implementation models. In 2019, the German Federal Joint Committee (G-BA), which plays a significant role in overseeing healthcare decisions in Germany, recommended that NIPT be reimbursed through public insurance. Following this recommendation, NIPT will be offered on a case-by-case basis, when a pregnant woman, after being counselled, makes an informed decision that the test is necessary in her personal situation. This model differs significantly from many other European countries, where NIPT is being implemented either as a first-tier screening offer available for all pregnancies, or a contingent screen for those with a high probability of foetal aneuploidy (with varying probability cut-offs). In this paper we examine how this unique approach to implementing NIPT in Germany is produced by an ethical and policy landscape resulting from a distinctive cultural and historical context with a significant influence on healthcare decision-making. Due in part to the specific legal and regulatory environment, as well as strong objections from various stakeholders, Germany did not implement NIPT as a first-tier screen. However, as Germany does not currently publicly fund as standard other forms of prenatal aneuploidy screening (such as combined first trimester screening), neither can it be implemented as a screen contingent on specific probability cut-offs. We discuss how German policy reflects the echoes of the past shaping approaches to new biotechnologies, and the implications of this unique model for implementing NIPT in a public healthcare system. |
doi_str_mv | 10.1038/s41431-022-01256-x |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10172332</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2754048591</sourcerecordid><originalsourceid>FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93</originalsourceid><addsrcrecordid>eNpdkU1LJDEQhsOysqPu_gEPS2AvXqL57KT3soj4BYNe9Bwy6WrN0JPuTboH598bHR12hUAK6qmXeutF6IjRE0aFOc2SScEI5ZxQxlVFnr-gfSZ1RZQU5mupKTNEGiZm6CDnJaWlqdk3NBOVorURah_d3faRhLh2OawBDwmiG12HR8hjiI84RHwFaeXi5jd2eIrh7wQYxqfgC-Rig4e-C36Du1Jn7wb4jvZa12X48f4foofLi_vzazK_u7o5P5sTX1YeiWlMozT3vNUtW1S-PA1USOpB8dq3tRNSysq3Wja0BrXgzrMWlBFUe9XW4hD92eoO02IFjYc4JtfZIYWVSxvbu2D_78TwZB_7tS030VwIXhSO3xVSX1zl0a5C9tAVK9BP2XKtJJVG1aygvz6hy35Ksfiz3DCmtWHUFIpvKZ_6nBO0u20Yta-B2W1gtgRm3wKzz2Xo578-diMfCYkXXTGSLw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2811778108</pqid></control><display><type>article</type><title>Non-invasive prenatal testing in Germany: a unique ethical and policy landscape</title><source>PubMed Central (Open access)</source><source>Springer Nature</source><creator>Bowman-Smart, Hilary ; Wiesemann, Claudia ; Horn, Ruth</creator><creatorcontrib>Bowman-Smart, Hilary ; Wiesemann, Claudia ; Horn, Ruth</creatorcontrib><description>Non-invasive prenatal testing (NIPT) has been available commercially in Europe since approximately 2012. Currently, many countries are in the process of integrating NIPT into their publicly funded healthcare systems to screen for chromosomal aneuploidies such as trisomy 21 (Down syndrome), with a variety of implementation models. In 2019, the German Federal Joint Committee (G-BA), which plays a significant role in overseeing healthcare decisions in Germany, recommended that NIPT be reimbursed through public insurance. Following this recommendation, NIPT will be offered on a case-by-case basis, when a pregnant woman, after being counselled, makes an informed decision that the test is necessary in her personal situation. This model differs significantly from many other European countries, where NIPT is being implemented either as a first-tier screening offer available for all pregnancies, or a contingent screen for those with a high probability of foetal aneuploidy (with varying probability cut-offs). In this paper we examine how this unique approach to implementing NIPT in Germany is produced by an ethical and policy landscape resulting from a distinctive cultural and historical context with a significant influence on healthcare decision-making. Due in part to the specific legal and regulatory environment, as well as strong objections from various stakeholders, Germany did not implement NIPT as a first-tier screen. However, as Germany does not currently publicly fund as standard other forms of prenatal aneuploidy screening (such as combined first trimester screening), neither can it be implemented as a screen contingent on specific probability cut-offs. We discuss how German policy reflects the echoes of the past shaping approaches to new biotechnologies, and the implications of this unique model for implementing NIPT in a public healthcare system.</description><identifier>ISSN: 1018-4813</identifier><identifier>EISSN: 1476-5438</identifier><identifier>DOI: 10.1038/s41431-022-01256-x</identifier><identifier>PMID: 36509835</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Aneuploidy ; Decision making ; Down syndrome ; Down's syndrome ; Ethics ; Female ; Germany ; Health care ; Health care policy ; Health insurance ; Health Policy ; Humans ; Life Style ; Pregnancy ; Prenatal diagnosis ; Prenatal Diagnosis - ethics ; Prenatal Diagnosis - methods ; Public health ; Reimbursement ; Trisomy ; Ultrasonic imaging</subject><ispartof>European journal of human genetics : EJHG, 2023-05, Vol.31 (5), p.562-567</ispartof><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93</citedby><cites>FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93</cites><orcidid>0000-0002-8260-0346 ; 0000-0002-5714-3905</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172332/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172332/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36509835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bowman-Smart, Hilary</creatorcontrib><creatorcontrib>Wiesemann, Claudia</creatorcontrib><creatorcontrib>Horn, Ruth</creatorcontrib><title>Non-invasive prenatal testing in Germany: a unique ethical and policy landscape</title><title>European journal of human genetics : EJHG</title><addtitle>Eur J Hum Genet</addtitle><description>Non-invasive prenatal testing (NIPT) has been available commercially in Europe since approximately 2012. Currently, many countries are in the process of integrating NIPT into their publicly funded healthcare systems to screen for chromosomal aneuploidies such as trisomy 21 (Down syndrome), with a variety of implementation models. In 2019, the German Federal Joint Committee (G-BA), which plays a significant role in overseeing healthcare decisions in Germany, recommended that NIPT be reimbursed through public insurance. Following this recommendation, NIPT will be offered on a case-by-case basis, when a pregnant woman, after being counselled, makes an informed decision that the test is necessary in her personal situation. This model differs significantly from many other European countries, where NIPT is being implemented either as a first-tier screening offer available for all pregnancies, or a contingent screen for those with a high probability of foetal aneuploidy (with varying probability cut-offs). In this paper we examine how this unique approach to implementing NIPT in Germany is produced by an ethical and policy landscape resulting from a distinctive cultural and historical context with a significant influence on healthcare decision-making. Due in part to the specific legal and regulatory environment, as well as strong objections from various stakeholders, Germany did not implement NIPT as a first-tier screen. However, as Germany does not currently publicly fund as standard other forms of prenatal aneuploidy screening (such as combined first trimester screening), neither can it be implemented as a screen contingent on specific probability cut-offs. We discuss how German policy reflects the echoes of the past shaping approaches to new biotechnologies, and the implications of this unique model for implementing NIPT in a public healthcare system.</description><subject>Aneuploidy</subject><subject>Decision making</subject><subject>Down syndrome</subject><subject>Down's syndrome</subject><subject>Ethics</subject><subject>Female</subject><subject>Germany</subject><subject>Health care</subject><subject>Health care policy</subject><subject>Health insurance</subject><subject>Health Policy</subject><subject>Humans</subject><subject>Life Style</subject><subject>Pregnancy</subject><subject>Prenatal diagnosis</subject><subject>Prenatal Diagnosis - ethics</subject><subject>Prenatal Diagnosis - methods</subject><subject>Public health</subject><subject>Reimbursement</subject><subject>Trisomy</subject><subject>Ultrasonic imaging</subject><issn>1018-4813</issn><issn>1476-5438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkU1LJDEQhsOysqPu_gEPS2AvXqL57KT3soj4BYNe9Bwy6WrN0JPuTboH598bHR12hUAK6qmXeutF6IjRE0aFOc2SScEI5ZxQxlVFnr-gfSZ1RZQU5mupKTNEGiZm6CDnJaWlqdk3NBOVorURah_d3faRhLh2OawBDwmiG12HR8hjiI84RHwFaeXi5jd2eIrh7wQYxqfgC-Rig4e-C36Du1Jn7wb4jvZa12X48f4foofLi_vzazK_u7o5P5sTX1YeiWlMozT3vNUtW1S-PA1USOpB8dq3tRNSysq3Wja0BrXgzrMWlBFUe9XW4hD92eoO02IFjYc4JtfZIYWVSxvbu2D_78TwZB_7tS030VwIXhSO3xVSX1zl0a5C9tAVK9BP2XKtJJVG1aygvz6hy35Ksfiz3DCmtWHUFIpvKZ_6nBO0u20Yta-B2W1gtgRm3wKzz2Xo578-diMfCYkXXTGSLw</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Bowman-Smart, Hilary</creator><creator>Wiesemann, Claudia</creator><creator>Horn, Ruth</creator><general>Nature Publishing Group</general><general>Springer International Publishing</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8260-0346</orcidid><orcidid>https://orcid.org/0000-0002-5714-3905</orcidid></search><sort><creationdate>20230501</creationdate><title>Non-invasive prenatal testing in Germany: a unique ethical and policy landscape</title><author>Bowman-Smart, Hilary ; Wiesemann, Claudia ; Horn, Ruth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aneuploidy</topic><topic>Decision making</topic><topic>Down syndrome</topic><topic>Down's syndrome</topic><topic>Ethics</topic><topic>Female</topic><topic>Germany</topic><topic>Health care</topic><topic>Health care policy</topic><topic>Health insurance</topic><topic>Health Policy</topic><topic>Humans</topic><topic>Life Style</topic><topic>Pregnancy</topic><topic>Prenatal diagnosis</topic><topic>Prenatal Diagnosis - ethics</topic><topic>Prenatal Diagnosis - methods</topic><topic>Public health</topic><topic>Reimbursement</topic><topic>Trisomy</topic><topic>Ultrasonic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bowman-Smart, Hilary</creatorcontrib><creatorcontrib>Wiesemann, Claudia</creatorcontrib><creatorcontrib>Horn, Ruth</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of human genetics : EJHG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bowman-Smart, Hilary</au><au>Wiesemann, Claudia</au><au>Horn, Ruth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-invasive prenatal testing in Germany: a unique ethical and policy landscape</atitle><jtitle>European journal of human genetics : EJHG</jtitle><addtitle>Eur J Hum Genet</addtitle><date>2023-05-01</date><risdate>2023</risdate><volume>31</volume><issue>5</issue><spage>562</spage><epage>567</epage><pages>562-567</pages><issn>1018-4813</issn><eissn>1476-5438</eissn><abstract>Non-invasive prenatal testing (NIPT) has been available commercially in Europe since approximately 2012. Currently, many countries are in the process of integrating NIPT into their publicly funded healthcare systems to screen for chromosomal aneuploidies such as trisomy 21 (Down syndrome), with a variety of implementation models. In 2019, the German Federal Joint Committee (G-BA), which plays a significant role in overseeing healthcare decisions in Germany, recommended that NIPT be reimbursed through public insurance. Following this recommendation, NIPT will be offered on a case-by-case basis, when a pregnant woman, after being counselled, makes an informed decision that the test is necessary in her personal situation. This model differs significantly from many other European countries, where NIPT is being implemented either as a first-tier screening offer available for all pregnancies, or a contingent screen for those with a high probability of foetal aneuploidy (with varying probability cut-offs). In this paper we examine how this unique approach to implementing NIPT in Germany is produced by an ethical and policy landscape resulting from a distinctive cultural and historical context with a significant influence on healthcare decision-making. Due in part to the specific legal and regulatory environment, as well as strong objections from various stakeholders, Germany did not implement NIPT as a first-tier screen. However, as Germany does not currently publicly fund as standard other forms of prenatal aneuploidy screening (such as combined first trimester screening), neither can it be implemented as a screen contingent on specific probability cut-offs. We discuss how German policy reflects the echoes of the past shaping approaches to new biotechnologies, and the implications of this unique model for implementing NIPT in a public healthcare system.</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>36509835</pmid><doi>10.1038/s41431-022-01256-x</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-8260-0346</orcidid><orcidid>https://orcid.org/0000-0002-5714-3905</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1018-4813 |
ispartof | European journal of human genetics : EJHG, 2023-05, Vol.31 (5), p.562-567 |
issn | 1018-4813 1476-5438 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10172332 |
source | PubMed Central (Open access); Springer Nature |
subjects | Aneuploidy Decision making Down syndrome Down's syndrome Ethics Female Germany Health care Health care policy Health insurance Health Policy Humans Life Style Pregnancy Prenatal diagnosis Prenatal Diagnosis - ethics Prenatal Diagnosis - methods Public health Reimbursement Trisomy Ultrasonic imaging |
title | Non-invasive prenatal testing in Germany: a unique ethical and policy landscape |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T11%3A04%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Non-invasive%20prenatal%20testing%20in%20Germany:%20a%20unique%20ethical%20and%20policy%20landscape&rft.jtitle=European%20journal%20of%20human%20genetics%20:%20EJHG&rft.au=Bowman-Smart,%20Hilary&rft.date=2023-05-01&rft.volume=31&rft.issue=5&rft.spage=562&rft.epage=567&rft.pages=562-567&rft.issn=1018-4813&rft.eissn=1476-5438&rft_id=info:doi/10.1038/s41431-022-01256-x&rft_dat=%3Cproquest_pubme%3E2754048591%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c431t-8d8d572c2f7f1b6cb6c7e0340ce529cf9a34446cf74d09e5b2ac1fe58307c5f93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2811778108&rft_id=info:pmid/36509835&rfr_iscdi=true |