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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1007/s00268-011-1078-7</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">73978</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2011-73978</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">García-Gil, F. A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-8275-7191</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Celsior Versus University of Wisconsin Preserving Solutions for Liver Transplantation: Postreperfusion Syndrome and Outcome of a 5-Year Prospective Randomized Controlled Study</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2011</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Background: Celsior solution (CS) is a high-sodium, low-potassium, low-viscosity extracellular solution that has been used for liver graft preservation in recent years, although experience with it is still limited. We performed an open-label randomized active-controlled trial comparing CS with the University of Wisconsin solution (UW) for liver transplantation (LT), with a follow-up period of 5 years.
Methods: Adult transplant recipients (n = 102) were prospectively randomized to receive either CS (n = 51) or UW (n = 51). The two groups were comparable with respect to donor and recipient characteristics. The primary outcome measure was the incidence of postreperfusion syndrome (PRS). Secondary outcome measures included primary nonfunction (PNF) or primary dysfunction (PDF), liver retransplantation, and graft and patient survival. Other secondary outcome measures were days in the intensive care unit (ICU) and the rates of acute rejection, chronic rejection, infectious complications, postoperative reoperations, and vascular and biliary complications.
Results In all, 14 posttransplant variables revealed no significant differences between the groups. There were no cases of PNF or PDF. The incidence of PRS was 5.9% in the CS group and 21.6% in the UW group (P = 0.041). After reperfusion, CS revealed greater control of serum potassium (P = 0.015), magnesium levels (P = 0.005), and plasma glucose (P = 0.042) than UW. Respective patient survivals at 3, 12, and 60 months were 95.7, 87.2, and 82.0% for the CS group and 95.7, 83.3, and 66.6% for the UW group (P = 0.123).
Conclusions

While retaining the same degree of safety and effectiveness as UW for LT, CS may yield postliver graft reperfusion benefits, as shown in this study by a significant reduction in the incidence of PRS and greater metabolic control.</subfield>
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    <subfield code="9">info:eu-repo/semantics/closedAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="a">2.362</subfield>
    <subfield code="b">2011</subfield>
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  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">SURGERY</subfield>
    <subfield code="b">48 / 199 = 0.241</subfield>
    <subfield code="c">2011</subfield>
    <subfield code="d">Q1</subfield>
    <subfield code="e">T1</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Serrano, M. T.</subfield>
    <subfield code="0">(orcid)0000-0002-7119-2244</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Fuentes-Broto, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-2656-6750</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Arenas, J.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">García, J. J.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-9507-6478</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Güemes, A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-4437-2581</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Bernal, V.</subfield>
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    <subfield code="a">Campillo, A.</subfield>
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    <subfield code="a">Sostres, C.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Araiz, J. J.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-6033-2216</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Royo, P.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Simón, M. A.</subfield>
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    <subfield code="1">1005</subfield>
    <subfield code="2">410</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmacología y Fisiolog.</subfield>
    <subfield code="c">Área Fisiología</subfield>
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    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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    <subfield code="1">1004</subfield>
    <subfield code="2">090</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Cirugía,Ginecol.Obstetr.</subfield>
    <subfield code="c">Área Cirugía</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">35, 7 (2011), 1598-1607</subfield>
    <subfield code="p">World j. surg.</subfield>
    <subfield code="t">WORLD JOURNAL OF SURGERY</subfield>
    <subfield code="x">0364-2313</subfield>
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