Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response
In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated...
Gespeichert in:
Veröffentlicht in: | Hepatology (Baltimore, Md.) Md.), 2007-12, Vol.46 (6), p.1732-1740 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1740 |
---|---|
container_issue | 6 |
container_start_page | 1732 |
container_title | Hepatology (Baltimore, Md.) |
container_volume | 46 |
creator | Kamal, Sanaa M. El Kamary, Samer S. Shardell, Michelle D. Hashem, Mohamed Ahmed, Imad N. Muhammadi, Mohamed Sayed, Khalifa Moustafa, Ashraf Hakem, Sarah Abdel Ibrahiem, Amany Moniem, Mohamed Mansour, Hoda Abdelaziz, Mohamed |
description | In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P < 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P < 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.) |
doi_str_mv | 10.1002/hep.21917 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69025981</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69025981</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</originalsourceid><addsrcrecordid>eNp10M9u1DAQBnALUdGlcOAFkC8gcUjrP0kcc0OrliJVag_lHE2S8cbIawc72yq3PkHVZ-RJcNmVeuLky--bGX-EfODslDMmzkacTgXXXL0iK14JVUhZsddkxYRiheZSH5O3Kf1ijOlSNG_IMVe6lLrRK_J4g5vFwYwDtX7GaDAGT8FNI_x5eBIdndwu0Wg7uLPR-ozoBLNFPyd6b-eRbtCHeZmQlrQfc9b2NJ-TyWwTXX-ltyPSGBzSYGiEyQ4U_EARoltoHhlc2ORIxDQFn_AdOTLgEr4_vCfk58X57fqyuLr-_mP97aroZSVVMQhkAApUI6oKKlVLFF3dNKBqbqDkAA2DJivdcNMpw3vTVbyTWsmGl0bJE_J5P3eK4fcO09xuberROfAYdqmtNRNVDmf4ZQ_7GFKKaNop2i3EpeWsfS6_zb9t_5Wf7cfD0F23xeFFHtrO4NMBQOrBmQi-t-nFac1rJZ-Xnu3dvXW4_H9je3l-s1_9F18qnhQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69025981</pqid></control><display><type>article</type><title>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library All Journals</source><creator>Kamal, Sanaa M. ; El Kamary, Samer S. ; Shardell, Michelle D. ; Hashem, Mohamed ; Ahmed, Imad N. ; Muhammadi, Mohamed ; Sayed, Khalifa ; Moustafa, Ashraf ; Hakem, Sarah Abdel ; Ibrahiem, Amany ; Moniem, Mohamed ; Mansour, Hoda ; Abdelaziz, Mohamed</creator><creatorcontrib>Kamal, Sanaa M. ; El Kamary, Samer S. ; Shardell, Michelle D. ; Hashem, Mohamed ; Ahmed, Imad N. ; Muhammadi, Mohamed ; Sayed, Khalifa ; Moustafa, Ashraf ; Hakem, Sarah Abdel ; Ibrahiem, Amany ; Moniem, Mohamed ; Mansour, Hoda ; Abdelaziz, Mohamed</creatorcontrib><description>In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P < 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P < 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.21917</identifier><identifier>PMID: 17943989</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antiviral agents ; Antiviral Agents - administration & dosage ; Biological and medical sciences ; Drug Administration Schedule ; Female ; Genotype ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - genetics ; Human viral diseases ; Humans ; Infectious diseases ; Interferon-alpha - administration & dosage ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Polyethylene Glycols ; Recombinant Proteins ; Ribavirin - administration & dosage ; RNA, Viral ; Viral diseases ; Viral hepatitis ; Viral Load</subject><ispartof>Hepatology (Baltimore, Md.), 2007-12, Vol.46 (6), p.1732-1740</ispartof><rights>Copyright © 2007 American Association for the Study of Liver Diseases</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</citedby><cites>FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.21917$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.21917$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19916731$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17943989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamal, Sanaa M.</creatorcontrib><creatorcontrib>El Kamary, Samer S.</creatorcontrib><creatorcontrib>Shardell, Michelle D.</creatorcontrib><creatorcontrib>Hashem, Mohamed</creatorcontrib><creatorcontrib>Ahmed, Imad N.</creatorcontrib><creatorcontrib>Muhammadi, Mohamed</creatorcontrib><creatorcontrib>Sayed, Khalifa</creatorcontrib><creatorcontrib>Moustafa, Ashraf</creatorcontrib><creatorcontrib>Hakem, Sarah Abdel</creatorcontrib><creatorcontrib>Ibrahiem, Amany</creatorcontrib><creatorcontrib>Moniem, Mohamed</creatorcontrib><creatorcontrib>Mansour, Hoda</creatorcontrib><creatorcontrib>Abdelaziz, Mohamed</creatorcontrib><title>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P < 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P < 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)</description><subject>Adult</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antiviral agents</subject><subject>Antiviral Agents - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Genotype</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - genetics</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Interferon-alpha - administration & dosage</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyethylene Glycols</subject><subject>Recombinant Proteins</subject><subject>Ribavirin - administration & dosage</subject><subject>RNA, Viral</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><subject>Viral Load</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M9u1DAQBnALUdGlcOAFkC8gcUjrP0kcc0OrliJVag_lHE2S8cbIawc72yq3PkHVZ-RJcNmVeuLky--bGX-EfODslDMmzkacTgXXXL0iK14JVUhZsddkxYRiheZSH5O3Kf1ijOlSNG_IMVe6lLrRK_J4g5vFwYwDtX7GaDAGT8FNI_x5eBIdndwu0Wg7uLPR-ozoBLNFPyd6b-eRbtCHeZmQlrQfc9b2NJ-TyWwTXX-ltyPSGBzSYGiEyQ4U_EARoltoHhlc2ORIxDQFn_AdOTLgEr4_vCfk58X57fqyuLr-_mP97aroZSVVMQhkAApUI6oKKlVLFF3dNKBqbqDkAA2DJivdcNMpw3vTVbyTWsmGl0bJE_J5P3eK4fcO09xuberROfAYdqmtNRNVDmf4ZQ_7GFKKaNop2i3EpeWsfS6_zb9t_5Wf7cfD0F23xeFFHtrO4NMBQOrBmQi-t-nFac1rJZ-Xnu3dvXW4_H9je3l-s1_9F18qnhQ</recordid><startdate>200712</startdate><enddate>200712</enddate><creator>Kamal, Sanaa M.</creator><creator>El Kamary, Samer S.</creator><creator>Shardell, Michelle D.</creator><creator>Hashem, Mohamed</creator><creator>Ahmed, Imad N.</creator><creator>Muhammadi, Mohamed</creator><creator>Sayed, Khalifa</creator><creator>Moustafa, Ashraf</creator><creator>Hakem, Sarah Abdel</creator><creator>Ibrahiem, Amany</creator><creator>Moniem, Mohamed</creator><creator>Mansour, Hoda</creator><creator>Abdelaziz, Mohamed</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>IQODW</scope><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></search><sort><creationdate>200712</creationdate><title>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</title><author>Kamal, Sanaa M. ; El Kamary, Samer S. ; Shardell, Michelle D. ; Hashem, Mohamed ; Ahmed, Imad N. ; Muhammadi, Mohamed ; Sayed, Khalifa ; Moustafa, Ashraf ; Hakem, Sarah Abdel ; Ibrahiem, Amany ; Moniem, Mohamed ; Mansour, Hoda ; Abdelaziz, Mohamed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antiviral agents</topic><topic>Antiviral Agents - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Genotype</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - genetics</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Interferon-alpha - administration & dosage</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyethylene Glycols</topic><topic>Recombinant Proteins</topic><topic>Ribavirin - administration & dosage</topic><topic>RNA, Viral</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamal, Sanaa M.</creatorcontrib><creatorcontrib>El Kamary, Samer S.</creatorcontrib><creatorcontrib>Shardell, Michelle D.</creatorcontrib><creatorcontrib>Hashem, Mohamed</creatorcontrib><creatorcontrib>Ahmed, Imad N.</creatorcontrib><creatorcontrib>Muhammadi, Mohamed</creatorcontrib><creatorcontrib>Sayed, Khalifa</creatorcontrib><creatorcontrib>Moustafa, Ashraf</creatorcontrib><creatorcontrib>Hakem, Sarah Abdel</creatorcontrib><creatorcontrib>Ibrahiem, Amany</creatorcontrib><creatorcontrib>Moniem, Mohamed</creatorcontrib><creatorcontrib>Mansour, Hoda</creatorcontrib><creatorcontrib>Abdelaziz, Mohamed</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kamal, Sanaa M.</au><au>El Kamary, Samer S.</au><au>Shardell, Michelle D.</au><au>Hashem, Mohamed</au><au>Ahmed, Imad N.</au><au>Muhammadi, Mohamed</au><au>Sayed, Khalifa</au><au>Moustafa, Ashraf</au><au>Hakem, Sarah Abdel</au><au>Ibrahiem, Amany</au><au>Moniem, Mohamed</au><au>Mansour, Hoda</au><au>Abdelaziz, Mohamed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2007-12</date><risdate>2007</risdate><volume>46</volume><issue>6</issue><spage>1732</spage><epage>1740</epage><pages>1732-1740</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P < 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P < 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17943989</pmid><doi>10.1002/hep.21917</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0270-9139 |
ispartof | Hepatology (Baltimore, Md.), 2007-12, Vol.46 (6), p.1732-1740 |
issn | 0270-9139 1527-3350 |
language | eng |
recordid | cdi_proquest_miscellaneous_69025981 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals |
subjects | Adult Antibiotics. Antiinfectious agents. Antiparasitic agents Antiviral agents Antiviral Agents - administration & dosage Biological and medical sciences Drug Administration Schedule Female Genotype Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - genetics Human viral diseases Humans Infectious diseases Interferon-alpha - administration & dosage Male Medical sciences Middle Aged Pharmacology. Drug treatments Polyethylene Glycols Recombinant Proteins Ribavirin - administration & dosage RNA, Viral Viral diseases Viral hepatitis Viral Load |
title | Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T13%3A48%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pegylated%20interferon%20alpha%E2%80%902b%20plus%20ribavirin%20in%20patients%20with%20genotype%204%20chronic%20hepatitis%20C:%20The%20role%20of%20rapid%20and%20early%20virologic%20response&rft.jtitle=Hepatology%20(Baltimore,%20Md.)&rft.au=Kamal,%20Sanaa%20M.&rft.date=2007-12&rft.volume=46&rft.issue=6&rft.spage=1732&rft.epage=1740&rft.pages=1732-1740&rft.issn=0270-9139&rft.eissn=1527-3350&rft.coden=HPTLD9&rft_id=info:doi/10.1002/hep.21917&rft_dat=%3Cproquest_cross%3E69025981%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=69025981&rft_id=info:pmid/17943989&rfr_iscdi=true |