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      Trends and three-year outcomes of hepatitis C virus–viremic donor heart transplant for hepatitis C virus–seronegative recipients

      research-article
      , MD a , , MS a , , ScM a , , BA a , , MD b , , PhD, MHS c , , MD, PhD c , d , , MD a , , MD a ,
      JTCVS Open
      Elsevier
      heart transplant, hepatitis C, outcomes, donor pool, aHR, adjusted hazard ratio, aOR, adjusted odds ratio, D+, HCV-viremic donor, D–, HCV-seronegative donor, DAAs, direct-acting antivirals, DCD, donation after circulatory death, ECMO, extracorporeal membranous oxygenation, HCV, hepatitis C virus, HT, heart transplant, IABP, intra-aortic balloon pump, IQR, interquartile range, LVAD, left ventricular assist device, MCS, mechanical circulatory support, R–, HCV-seronegative recipient, SRTR, Scientific Registry of Transplant Recipients

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          Abstract

          Objective

          Heart transplants (HTs) from hepatitis C virus (HCV)-viremic donors to HCV-seronegative recipients (HCV D+/R–) have good 6-month outcomes, but practice uptake and long-term outcomes overall and among candidates on mechanical circulatory support (MCS) have yet to be established.

          Methods

          Using the Scientific Registry of Transplant Recipients, we identified US adult HCV-seronegative HT recipients (R–) from 2015 to 2021. We classified donors as HCV-seronegative (D–) or HCV-viremic (D+). We used multivariable regression to compare post-HT extracorporeal membranous oxygenation, dialysis, pacemaker, acute rejection, and risk of post-HT mortality between HCV D+/R– and HCV D–/R–. Models were adjusted for donor, recipient, and transplant characteristics and center HT volume. We performed subgroup analyses of recipients bridged with MCS.

          Results

          From 2015 to 2021, the number of HCV D+/R– HT increased from 1 to 181 and the number of centers performing HCV D+/R– HT increased from 1 to 60. Compared with HCV D–/R– recipients, HCV D+/R– versus D–/R– recipients overall and among patients bridged with MCS had similar odds of post-HT extracorporeal membranous oxygenation, dialysis, pacemaker, and acute rejection; and mortality risk at 30 days, 1 year, and 3 years (all P > .05). High center HT volume but not HCV D+/R– volume (<5 vs >5 in any year) was associated with lower mortality for HCV D+/R– HT.

          Conclusions

          HCV D+/R– and D–/R– HT have similar outcomes at 3 years’ posttransplant. These results underscore the opportunity provided by HCV D+/R– HT, including among the growing population bridged with MCS, and the potential benefit of further expanding use of HCV+ allografts.

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          Most cited references24

          • Record: found
          • Abstract: found
          • Article: not found

          Big data in organ transplantation: registries and administrative claims.

          The field of organ transplantation benefits from large, comprehensive, transplant-specific national data sets available to researchers. In addition to the widely used Organ Procurement and Transplantation Network (OPTN)-based registries (the United Network for Organ Sharing and Scientific Registry of Transplant Recipients data sets) and United States Renal Data System (USRDS) data sets, there are other publicly available national data sets, not specific to transplantation, which have historically been underutilized in the field of transplantation. Of particular interest are the Nationwide Inpatient Sample and State Inpatient Databases, produced by the Agency for Healthcare Research and Quality. The USRDS database provides extensive data relevant to studies of kidney transplantation. Linkage of publicly available data sets to external data sources such as private claims or pharmacy data provides further resources for registry-based research. Although these resources can transcend some limitations of OPTN-based registry data, they come with their own limitations, which must be understood to avoid biased inference. This review discusses different registry-based data sources available in the United States, as well as the proper design and conduct of registry-based research.
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            Heart and Lung Transplants from HCV-Infected Donors to Uninfected Recipients

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              An Early Investigation of Outcomes with the New 2018 Donor Heart Allocation System in the United States

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                Author and article information

                Contributors
                Journal
                JTCVS Open
                JTCVS Open
                JTCVS Open
                Elsevier
                2666-2736
                03 November 2022
                December 2022
                03 November 2022
                : 12
                : 269-279
                Affiliations
                [a ]Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md
                [b ]Division of Infection Disease, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Md
                [c ]Division of Transplant Surgery, Department of Surgery, NYU Langone Health, New York, NY
                [d ]Scientific Registry of Transplant Recipients, Minneapolis, Minn
                Author notes
                []Address for reprints: Ahmet Kilic, MD, Department of Surgery, Johns Hopkins Medical Institutions, Sheikh Zayed Tower, Suite 7107, 1800 Orleans St, Baltimore, MD 21287. Akilic2@ 123456jhmi.edu
                Article
                S2666-2736(22)00372-2
                10.1016/j.xjon.2022.10.007
                9801334
                36590744
                aae63175-02c3-4bd9-abcb-e276e3b023bb
                © 2022 The Author(s)

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 21 July 2021
                : 17 October 2022
                : 24 October 2022
                Categories
                Adult: Transplantation

                heart transplant,hepatitis c,outcomes,donor pool,ahr, adjusted hazard ratio,aor, adjusted odds ratio,d+, hcv-viremic donor,d–, hcv-seronegative donor,daas, direct-acting antivirals,dcd, donation after circulatory death,ecmo, extracorporeal membranous oxygenation,hcv, hepatitis c virus,ht, heart transplant,iabp, intra-aortic balloon pump,iqr, interquartile range,lvad, left ventricular assist device,mcs, mechanical circulatory support,r–, hcv-seronegative recipient,srtr, scientific registry of transplant recipients

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