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Effect of alcoholic liver disease and hepatitis C infection on waiting list and posttransplant mortality and transplant survival benefit

dc.contributor.authorLucey, Michael R.en_US
dc.contributor.authorSchaubel, Douglas E.en_US
dc.contributor.authorGuidinger, Mary K.en_US
dc.contributor.authorTome, Santiagoen_US
dc.contributor.authorMerion, Robert M.en_US
dc.date.accessioned2009-08-12T15:36:43Z
dc.date.available2010-10-05T18:27:30Zen_US
dc.date.issued2009-08en_US
dc.identifier.citationLucey, Michael R.; Schaubel, Douglas E.; Guidinger, Mary K.; Tome, Santiago; Merion, Robert M. (2009). "Effect of alcoholic liver disease and hepatitis C infection on waiting list and posttransplant mortality and transplant survival benefit Presented in part at the 2008 American Transplant Congress in Toronto, Ontario, Canada. The views expressed herein are those of the authors and not necessarily those of the U.S. Government. Potential conflicts of interest: Dr. Lucey is a consultant for Astellas. He also received grants from Novartis, Human Genome Sciences, Vertex, Bristol-Myers Squibb, Roche, and Schering-Plough. ." Hepatology 50(2): 400-406. <http://hdl.handle.net/2027.42/63562>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/63562
dc.description.abstractDisease-specific analysis of liver transplant survival benefit, which encompasses both pre- and posttransplant events, has not been reported. Therefore, we evaluated the effect of alcoholic liver disease (ALD) and hepatitis C virus (HCV) infection on waiting list mortality, posttransplant mortality, and the survival benefit of deceased donor liver transplantation using United States data from the Scientific Registry of Transplant Recipients on 38,899 adults placed on the transplant waiting list between September 2001 and December 2006. Subjects were classified according to the presence/absence of HCV and ALD. Cox regression was used to estimate waiting list mortality and posttransplant mortality separately. Survival benefit was assessed using sequential stratification. Overall, the presence of HCV significantly increased waiting list mortality, with a covariate-adjusted hazard ratio (HR) for HCV-positive (HCV+) compared with HCV-negative (HCV−) HR = 1.19 ( P = 0.0001). The impact of HCV+ was significantly more pronounced ( P = 0.001) among ALD-positive (ALD+) patients (HR = 1.36; P < 0.0001), but was still significant among ALD-negative (ALD−) patients (HR = 1.11; P = 0.02). The contrast between ALD+ and ALD− waiting list mortality was significant only among HCV+ patients (HR = 1.14; P = 0.006). Posttransplant mortality was significantly increased among HCV+ (versus HCV−) patients (HR = 1.26; P = 0.0009), but not among ALD+ (versus ALD−) patients. Survival benefit of transplantation was significantly decreased among HCV+ compared with HCV− recipients with model for end-stage liver disease (MELD) scores 9-29, but was significantly increased at MELD ≥30. ALD did not influence the survival benefit of transplantation at any MELD score. Conclusion: Except in patients with very low or very high MELD scores, HCV status has a significant negative impact on the survival benefit of liver transplantation. In contrast, the presence of ALD does not influence liver transplant survival benefit. (H EPATOLOGY 2009.)en_US
dc.format.extent185310 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titleEffect of alcoholic liver disease and hepatitis C infection on waiting list and posttransplant mortality and transplant survival benefiten_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arbor, MI ; Department of Surgery, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan, Ann Arbor, MI ; Scientific Registry of Transplant Recipients, Ann Arbor, MIen_US
dc.contributor.affiliationotherDepartment of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI ; fax: 608-265-5677 ; Section of Gastroenterology and Hepatology, University of Wisconsin School of Medicine and Public Health, H6/516 CSC, 600 Highland Avenue, Madison, WI 53792-5124en_US
dc.contributor.affiliationotherArbor Research Collaborative for Health, Ann Arbor, MIen_US
dc.contributor.affiliationotherScientific Registry of Transplant Recipients, Ann Arbor, MI ; Department of Internal Medicine, Universitario de Santiago de Compostela, Santiago, Spainen_US
dc.identifier.pmid19472315en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/63562/1/23007_ftp.pdf
dc.identifier.doi10.1002/hep.23007en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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