Sofosbuvir for the treatment of hepatitis C virus infection

Results of published phase III trials of sofosbuvir in combination with ribavirin or peginterferon-ribavirin are summarized in Appendix 1 (available at www.cmaj.ca/lookup/suppl /doi: 10.1503/cmaj.l40151/-/DCl). In the NEUTRINO trial, 5 327 treatment- naive patients with HCV infection received sofosb...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Canadian Medical Association journal (CMAJ) 2015-02, Vol.187 (3), p.203-204
Hauptverfasser: Rolland, Sébastien, Vachon, Marie-Louise
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 204
container_issue 3
container_start_page 203
container_title Canadian Medical Association journal (CMAJ)
container_volume 187
creator Rolland, Sébastien
Vachon, Marie-Louise
description Results of published phase III trials of sofosbuvir in combination with ribavirin or peginterferon-ribavirin are summarized in Appendix 1 (available at www.cmaj.ca/lookup/suppl /doi: 10.1503/cmaj.l40151/-/DCl). In the NEUTRINO trial, 5 327 treatment- naive patients with HCV infection received sofosbuvir plus peginterferon-ribavirin for 12 weeks. Most (89%) had HCV genotype 1 infection, and the remainder had HCV genotype 4, 5 or 6 infection. The sustained virologic response rate at 12 weeks was 90%. Among patients with cirrhosis, the sustained virologic response rate was 80%, which is the highest rate reported in that population. Sofosbuvir in combination with ribavirin was investigated in treatment-naive patients with HCV genotype 2 or 3 infection in the FISSION trial, an open-label randomized active-control trial.5 A sustained virologic response rate of 67% at 12 weeks was observed in both the sofosbuvir-ribavirin and the peginterferon- ribavirin arms. In the POSITRON trial,6 patients with HCV genotype 2 or 3 infection who were intolerant of or ineligible for interferon treatment were randomly assigned to either the sofosbuvir-ribavirin ann or the matching placebo arm. The sustained virologic response rate at 12 weeks was 78% in the intervention group and 0% in the placebo group. The data pertaining to sofosbuvir support its use as part of combination therapy in the treatment of chronic HCV genotype IM infection. Whether combined with ribavirin alone, with peginterferon and ribavirin, or with other direct-acting antiviral agents, sofosbuvir will likely have a large impact on the treatment of HCV infection. Studies assessing the safety and efficacy of sofosbuvir in traditionally difficult-to-treat populations (e.g., patients receiving liver transplantation or hemodialysis, people with hemophilia and those with HIV/HCV co-infection) are currently underway. Combinations of sofosbuvir with other direct-acting antiviral agents are also being evaluated.11-14 Other promising interferon-free combinations that do not involve sofosbuvir are also in development.
doi_str_mv 10.1503/cmaj.140151
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4330143</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A401507791</galeid><sourcerecordid>A401507791</sourcerecordid><originalsourceid>FETCH-LOGICAL-c640t-a57cff1f54e5d4c7f9b995fc174a7b34ec06adb59910e783d12513bfbec8872f3</originalsourceid><addsrcrecordid>eNqV0l2L1DAUBuAgijuOXnkvRUEU6Zg0SdMiCMvgx8Ki4Op1SNOTmQxtM5uki_57U2ZdpzI3ttBC-vTktOdF6CnBK8Ixfat7tVsRhgkn99CCsKrKC1rU99ECVwXOac3KM_QohB1OBy3EQ3RWcIwLXtIFenfljAvNeGN9ZpzP4hay6EHFHoaYOZNtYa-ijTZk6yyhMWR2MKCjdcNj9MCoLsCT2_sS_fj44fv6c3759dPF-vwy1yXDMVdcaGOI4Qx4y7QwdVPX3GgimBINZaBxqdqG1zXBICrakoIT2pgGdFWJwtAlen-oux-bHlqdOvOqk3tve-V_SaesnD8Z7FZu3I1klGKSLkv06raAd9cjhCh7GzR0nRrAjUGSkgtasJKKRF_8Q3du9EP6vEnVgqaOyr9qozqQ6Ye4tK-eisrzaRBYiJoklZ9QGxggNekGMDYtz_zzE17v7bU8RqsTKJ0t9FafrPp69kIyEX7GjRpDkBdX3_7Dfpnbl0d2C6qL2-C6cUpGmMM3B6i9C8GDuZscwXJKsJwSLA8JTvrZ8bDv7J_I0t-IzeZu</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1659738726</pqid></control><display><type>article</type><title>Sofosbuvir for the treatment of hepatitis C virus infection</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Journals@Ovid Complete</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Rolland, Sébastien ; Vachon, Marie-Louise</creator><creatorcontrib>Rolland, Sébastien ; Vachon, Marie-Louise</creatorcontrib><description>Results of published phase III trials of sofosbuvir in combination with ribavirin or peginterferon-ribavirin are summarized in Appendix 1 (available at www.cmaj.ca/lookup/suppl /doi: 10.1503/cmaj.l40151/-/DCl). In the NEUTRINO trial, 5 327 treatment- naive patients with HCV infection received sofosbuvir plus peginterferon-ribavirin for 12 weeks. Most (89%) had HCV genotype 1 infection, and the remainder had HCV genotype 4, 5 or 6 infection. The sustained virologic response rate at 12 weeks was 90%. Among patients with cirrhosis, the sustained virologic response rate was 80%, which is the highest rate reported in that population. Sofosbuvir in combination with ribavirin was investigated in treatment-naive patients with HCV genotype 2 or 3 infection in the FISSION trial, an open-label randomized active-control trial.5 A sustained virologic response rate of 67% at 12 weeks was observed in both the sofosbuvir-ribavirin and the peginterferon- ribavirin arms. In the POSITRON trial,6 patients with HCV genotype 2 or 3 infection who were intolerant of or ineligible for interferon treatment were randomly assigned to either the sofosbuvir-ribavirin ann or the matching placebo arm. The sustained virologic response rate at 12 weeks was 78% in the intervention group and 0% in the placebo group. The data pertaining to sofosbuvir support its use as part of combination therapy in the treatment of chronic HCV genotype IM infection. Whether combined with ribavirin alone, with peginterferon and ribavirin, or with other direct-acting antiviral agents, sofosbuvir will likely have a large impact on the treatment of HCV infection. Studies assessing the safety and efficacy of sofosbuvir in traditionally difficult-to-treat populations (e.g., patients receiving liver transplantation or hemodialysis, people with hemophilia and those with HIV/HCV co-infection) are currently underway. Combinations of sofosbuvir with other direct-acting antiviral agents are also being evaluated.11-14 Other promising interferon-free combinations that do not involve sofosbuvir are also in development.</description><identifier>ISSN: 0820-3946</identifier><identifier>EISSN: 1488-2329</identifier><identifier>DOI: 10.1503/cmaj.140151</identifier><identifier>PMID: 25002563</identifier><identifier>CODEN: CMAJAX</identifier><language>eng</language><publisher>Canada: Joule Inc</publisher><subject>Antiviral Agents - therapeutic use ; Dosage and administration ; Drug therapy ; Genotype ; Genotype &amp; phenotype ; Hepacivirus - genetics ; Hepatitis ; Hepatitis C ; Hepatitis C - drug therapy ; Humans ; Medical treatment ; Practice ; Sofosbuvir ; Uridine Monophosphate - analogs &amp; derivatives ; Uridine Monophosphate - therapeutic use</subject><ispartof>Canadian Medical Association journal (CMAJ), 2015-02, Vol.187 (3), p.203-204</ispartof><rights>COPYRIGHT 2015 Joule Inc.</rights><rights>Copyright 8872147 Canada Inc. Feb 17, 2015</rights><rights>2015 8872147 Canada Inc. or its licensors 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c640t-a57cff1f54e5d4c7f9b995fc174a7b34ec06adb59910e783d12513bfbec8872f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330143/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330143/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25002563$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rolland, Sébastien</creatorcontrib><creatorcontrib>Vachon, Marie-Louise</creatorcontrib><title>Sofosbuvir for the treatment of hepatitis C virus infection</title><title>Canadian Medical Association journal (CMAJ)</title><addtitle>CMAJ</addtitle><description>Results of published phase III trials of sofosbuvir in combination with ribavirin or peginterferon-ribavirin are summarized in Appendix 1 (available at www.cmaj.ca/lookup/suppl /doi: 10.1503/cmaj.l40151/-/DCl). In the NEUTRINO trial, 5 327 treatment- naive patients with HCV infection received sofosbuvir plus peginterferon-ribavirin for 12 weeks. Most (89%) had HCV genotype 1 infection, and the remainder had HCV genotype 4, 5 or 6 infection. The sustained virologic response rate at 12 weeks was 90%. Among patients with cirrhosis, the sustained virologic response rate was 80%, which is the highest rate reported in that population. Sofosbuvir in combination with ribavirin was investigated in treatment-naive patients with HCV genotype 2 or 3 infection in the FISSION trial, an open-label randomized active-control trial.5 A sustained virologic response rate of 67% at 12 weeks was observed in both the sofosbuvir-ribavirin and the peginterferon- ribavirin arms. In the POSITRON trial,6 patients with HCV genotype 2 or 3 infection who were intolerant of or ineligible for interferon treatment were randomly assigned to either the sofosbuvir-ribavirin ann or the matching placebo arm. The sustained virologic response rate at 12 weeks was 78% in the intervention group and 0% in the placebo group. The data pertaining to sofosbuvir support its use as part of combination therapy in the treatment of chronic HCV genotype IM infection. Whether combined with ribavirin alone, with peginterferon and ribavirin, or with other direct-acting antiviral agents, sofosbuvir will likely have a large impact on the treatment of HCV infection. Studies assessing the safety and efficacy of sofosbuvir in traditionally difficult-to-treat populations (e.g., patients receiving liver transplantation or hemodialysis, people with hemophilia and those with HIV/HCV co-infection) are currently underway. Combinations of sofosbuvir with other direct-acting antiviral agents are also being evaluated.11-14 Other promising interferon-free combinations that do not involve sofosbuvir are also in development.</description><subject>Antiviral Agents - therapeutic use</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Genotype</subject><subject>Genotype &amp; phenotype</subject><subject>Hepacivirus - genetics</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C - drug therapy</subject><subject>Humans</subject><subject>Medical treatment</subject><subject>Practice</subject><subject>Sofosbuvir</subject><subject>Uridine Monophosphate - analogs &amp; derivatives</subject><subject>Uridine Monophosphate - therapeutic use</subject><issn>0820-3946</issn><issn>1488-2329</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqV0l2L1DAUBuAgijuOXnkvRUEU6Zg0SdMiCMvgx8Ki4Op1SNOTmQxtM5uki_57U2ZdpzI3ttBC-vTktOdF6CnBK8Ixfat7tVsRhgkn99CCsKrKC1rU99ECVwXOac3KM_QohB1OBy3EQ3RWcIwLXtIFenfljAvNeGN9ZpzP4hay6EHFHoaYOZNtYa-ijTZk6yyhMWR2MKCjdcNj9MCoLsCT2_sS_fj44fv6c3759dPF-vwy1yXDMVdcaGOI4Qx4y7QwdVPX3GgimBINZaBxqdqG1zXBICrakoIT2pgGdFWJwtAlen-oux-bHlqdOvOqk3tve-V_SaesnD8Z7FZu3I1klGKSLkv06raAd9cjhCh7GzR0nRrAjUGSkgtasJKKRF_8Q3du9EP6vEnVgqaOyr9qozqQ6Ye4tK-eisrzaRBYiJoklZ9QGxggNekGMDYtz_zzE17v7bU8RqsTKJ0t9FafrPp69kIyEX7GjRpDkBdX3_7Dfpnbl0d2C6qL2-C6cUpGmMM3B6i9C8GDuZscwXJKsJwSLA8JTvrZ8bDv7J_I0t-IzeZu</recordid><startdate>20150217</startdate><enddate>20150217</enddate><creator>Rolland, Sébastien</creator><creator>Vachon, Marie-Louise</creator><general>Joule Inc</general><general>CMA Impact, Inc</general><general>8872147 Canada Inc</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>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M3G</scope><scope>MBDVC</scope><scope>NAPCQ</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></search><sort><creationdate>20150217</creationdate><title>Sofosbuvir for the treatment of hepatitis C virus infection</title><author>Rolland, Sébastien ; Vachon, Marie-Louise</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c640t-a57cff1f54e5d4c7f9b995fc174a7b34ec06adb59910e783d12513bfbec8872f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antiviral Agents - therapeutic use</topic><topic>Dosage and administration</topic><topic>Drug therapy</topic><topic>Genotype</topic><topic>Genotype &amp; phenotype</topic><topic>Hepacivirus - genetics</topic><topic>Hepatitis</topic><topic>Hepatitis C</topic><topic>Hepatitis C - drug therapy</topic><topic>Humans</topic><topic>Medical treatment</topic><topic>Practice</topic><topic>Sofosbuvir</topic><topic>Uridine Monophosphate - analogs &amp; derivatives</topic><topic>Uridine Monophosphate - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rolland, Sébastien</creatorcontrib><creatorcontrib>Vachon, Marie-Louise</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business &amp; Current Affairs Database</collection><collection>Canadian Business &amp; Current Affairs Database (Alumni Edition)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>CBCA Reference &amp; Current Events</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</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><jtitle>Canadian Medical Association journal (CMAJ)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rolland, Sébastien</au><au>Vachon, Marie-Louise</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sofosbuvir for the treatment of hepatitis C virus infection</atitle><jtitle>Canadian Medical Association journal (CMAJ)</jtitle><addtitle>CMAJ</addtitle><date>2015-02-17</date><risdate>2015</risdate><volume>187</volume><issue>3</issue><spage>203</spage><epage>204</epage><pages>203-204</pages><issn>0820-3946</issn><eissn>1488-2329</eissn><coden>CMAJAX</coden><abstract>Results of published phase III trials of sofosbuvir in combination with ribavirin or peginterferon-ribavirin are summarized in Appendix 1 (available at www.cmaj.ca/lookup/suppl /doi: 10.1503/cmaj.l40151/-/DCl). In the NEUTRINO trial, 5 327 treatment- naive patients with HCV infection received sofosbuvir plus peginterferon-ribavirin for 12 weeks. Most (89%) had HCV genotype 1 infection, and the remainder had HCV genotype 4, 5 or 6 infection. The sustained virologic response rate at 12 weeks was 90%. Among patients with cirrhosis, the sustained virologic response rate was 80%, which is the highest rate reported in that population. Sofosbuvir in combination with ribavirin was investigated in treatment-naive patients with HCV genotype 2 or 3 infection in the FISSION trial, an open-label randomized active-control trial.5 A sustained virologic response rate of 67% at 12 weeks was observed in both the sofosbuvir-ribavirin and the peginterferon- ribavirin arms. In the POSITRON trial,6 patients with HCV genotype 2 or 3 infection who were intolerant of or ineligible for interferon treatment were randomly assigned to either the sofosbuvir-ribavirin ann or the matching placebo arm. The sustained virologic response rate at 12 weeks was 78% in the intervention group and 0% in the placebo group. The data pertaining to sofosbuvir support its use as part of combination therapy in the treatment of chronic HCV genotype IM infection. Whether combined with ribavirin alone, with peginterferon and ribavirin, or with other direct-acting antiviral agents, sofosbuvir will likely have a large impact on the treatment of HCV infection. Studies assessing the safety and efficacy of sofosbuvir in traditionally difficult-to-treat populations (e.g., patients receiving liver transplantation or hemodialysis, people with hemophilia and those with HIV/HCV co-infection) are currently underway. Combinations of sofosbuvir with other direct-acting antiviral agents are also being evaluated.11-14 Other promising interferon-free combinations that do not involve sofosbuvir are also in development.</abstract><cop>Canada</cop><pub>Joule Inc</pub><pmid>25002563</pmid><doi>10.1503/cmaj.140151</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0820-3946
ispartof Canadian Medical Association journal (CMAJ), 2015-02, Vol.187 (3), p.203-204
issn 0820-3946
1488-2329
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4330143
source MEDLINE; DOAJ Directory of Open Access Journals; Journals@Ovid Complete; PubMed Central; Alma/SFX Local Collection
subjects Antiviral Agents - therapeutic use
Dosage and administration
Drug therapy
Genotype
Genotype & phenotype
Hepacivirus - genetics
Hepatitis
Hepatitis C
Hepatitis C - drug therapy
Humans
Medical treatment
Practice
Sofosbuvir
Uridine Monophosphate - analogs & derivatives
Uridine Monophosphate - therapeutic use
title Sofosbuvir for the treatment of hepatitis C virus infection
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T05%3A12%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sofosbuvir%20for%20the%20treatment%20of%20hepatitis%20C%20virus%20infection&rft.jtitle=Canadian%20Medical%20Association%20journal%20(CMAJ)&rft.au=Rolland,%20S%C3%A9bastien&rft.date=2015-02-17&rft.volume=187&rft.issue=3&rft.spage=203&rft.epage=204&rft.pages=203-204&rft.issn=0820-3946&rft.eissn=1488-2329&rft.coden=CMAJAX&rft_id=info:doi/10.1503/cmaj.140151&rft_dat=%3Cgale_pubme%3EA401507791%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1659738726&rft_id=info:pmid/25002563&rft_galeid=A401507791&rfr_iscdi=true