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Targeted versus universal antifungal prophylaxis among liver transplant recipients.

Identifieur interne : 000202 ( PubMed/Checkpoint ); précédent : 000201; suivant : 000203

Targeted versus universal antifungal prophylaxis among liver transplant recipients.

Auteurs : G A Eschenauer [États-Unis] ; E J Kwak ; A. Humar ; B A Potoski ; L G Clarke ; R K Shields ; R. Abdel-Massih ; F P Silveira ; P. Vergidis ; C J Clancy ; M H Nguyen

Source :

RBID : pubmed:25359455

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English descriptors

Abstract

Guidelines recommend targeted antifungal prophylaxis for liver transplant (LT) recipients based on tiers of risk, rather than universal prophylaxis. The feasibility and efficacy of tiered, targeted prophylaxis is not well established. We performed a retrospective study of LT recipients who received targeted prophylaxis (n = 145; voriconazole [VORI; 54%], fluconazole [8%], no antifungal [38%]) versus universal VORI prophylaxis (n = 237). Median durations of targeted and universal prophylaxis were 11 and 6 days, respectively (p < 0.0001). The incidence of invasive fungal infections (IFIs) in targeted and universal groups was 6.9% and 4.2% (p = 0.34). Overall, intra-abdominal candidiasis (73%) was the most common IFI. Posttransplant bile leaks (p = 0.001) and living donor transplants (p = 0.04) were independent risk factors for IFI. IFIs occurred in 6% of high-risk transplants who received prophylaxis and 4% of low-risk transplants who did not receive prophylaxis (p = 1.0). Mortality rates (100 days) were 10% (targeted) and 7% (universal) (p = 0.26); attributable mortality due to IFI was 10%. Compliance with prophylaxis recommendations was 97%. Prophylaxis was discontinued for toxicity in 2% of patients. Targeted antifungal prophylaxis in LT recipients was feasible and safe, effectively prevented IFIs and reduced the number of patients exposed to antifungals. Bile leaks and living donor transplants should be considered high-risk indications for prophylaxis.

DOI: 10.1111/ajt.12993
PubMed: 25359455


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pubmed:25359455

Le document en format XML

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<div type="abstract" xml:lang="en">Guidelines recommend targeted antifungal prophylaxis for liver transplant (LT) recipients based on tiers of risk, rather than universal prophylaxis. The feasibility and efficacy of tiered, targeted prophylaxis is not well established. We performed a retrospective study of LT recipients who received targeted prophylaxis (n = 145; voriconazole [VORI; 54%], fluconazole [8%], no antifungal [38%]) versus universal VORI prophylaxis (n = 237). Median durations of targeted and universal prophylaxis were 11 and 6 days, respectively (p < 0.0001). The incidence of invasive fungal infections (IFIs) in targeted and universal groups was 6.9% and 4.2% (p = 0.34). Overall, intra-abdominal candidiasis (73%) was the most common IFI. Posttransplant bile leaks (p = 0.001) and living donor transplants (p = 0.04) were independent risk factors for IFI. IFIs occurred in 6% of high-risk transplants who received prophylaxis and 4% of low-risk transplants who did not receive prophylaxis (p = 1.0). Mortality rates (100 days) were 10% (targeted) and 7% (universal) (p = 0.26); attributable mortality due to IFI was 10%. Compliance with prophylaxis recommendations was 97%. Prophylaxis was discontinued for toxicity in 2% of patients. Targeted antifungal prophylaxis in LT recipients was feasible and safe, effectively prevented IFIs and reduced the number of patients exposed to antifungals. Bile leaks and living donor transplants should be considered high-risk indications for prophylaxis.</div>
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<AbstractText>Guidelines recommend targeted antifungal prophylaxis for liver transplant (LT) recipients based on tiers of risk, rather than universal prophylaxis. The feasibility and efficacy of tiered, targeted prophylaxis is not well established. We performed a retrospective study of LT recipients who received targeted prophylaxis (n = 145; voriconazole [VORI; 54%], fluconazole [8%], no antifungal [38%]) versus universal VORI prophylaxis (n = 237). Median durations of targeted and universal prophylaxis were 11 and 6 days, respectively (p < 0.0001). The incidence of invasive fungal infections (IFIs) in targeted and universal groups was 6.9% and 4.2% (p = 0.34). Overall, intra-abdominal candidiasis (73%) was the most common IFI. Posttransplant bile leaks (p = 0.001) and living donor transplants (p = 0.04) were independent risk factors for IFI. IFIs occurred in 6% of high-risk transplants who received prophylaxis and 4% of low-risk transplants who did not receive prophylaxis (p = 1.0). Mortality rates (100 days) were 10% (targeted) and 7% (universal) (p = 0.26); attributable mortality due to IFI was 10%. Compliance with prophylaxis recommendations was 97%. Prophylaxis was discontinued for toxicity in 2% of patients. Targeted antifungal prophylaxis in LT recipients was feasible and safe, effectively prevented IFIs and reduced the number of patients exposed to antifungals. Bile leaks and living donor transplants should be considered high-risk indications for prophylaxis.</AbstractText>
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<CommentsCorrections RefType="Cites">
<RefSource>Transplantation. 2011 Aug 15;92(3):346-50</RefSource>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D008107" MajorTopicYN="N">Liver Diseases</DescriptorName>
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<QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName>
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<MeshHeading>
<DescriptorName UI="D016031" MajorTopicYN="N">Liver Transplantation</DescriptorName>
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<MeshHeading>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D014019" MajorTopicYN="N">Tissue Donors</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D066027" MajorTopicYN="Y">Transplant Recipients</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D014481" MajorTopicYN="N" Type="Geographic">United States</DescriptorName>
<QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName>
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<Keyword MajorTopicYN="N">complication: infectious</Keyword>
<Keyword MajorTopicYN="N">fungal</Keyword>
<Keyword MajorTopicYN="N">infection and infectious agents</Keyword>
<Keyword MajorTopicYN="N">infectious disease</Keyword>
<Keyword MajorTopicYN="N">liver transplantation/hepatology</Keyword>
<Keyword MajorTopicYN="N">liver transplantation: living donor</Keyword>
<Keyword MajorTopicYN="N">pharmacology</Keyword>
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<name sortKey="Humar, A" sort="Humar, A" uniqKey="Humar A" first="A" last="Humar">A. Humar</name>
<name sortKey="Kwak, E J" sort="Kwak, E J" uniqKey="Kwak E" first="E J" last="Kwak">E J Kwak</name>
<name sortKey="Nguyen, M H" sort="Nguyen, M H" uniqKey="Nguyen M" first="M H" last="Nguyen">M H Nguyen</name>
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<name sortKey="Eschenauer, G A" sort="Eschenauer, G A" uniqKey="Eschenauer G" first="G A" last="Eschenauer">G A Eschenauer</name>
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