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Infectious complications after heart transplantation in patients screened with gene expression profiling.

Identifieur interne : 000319 ( Main/Exploration ); précédent : 000318; suivant : 000320

Infectious complications after heart transplantation in patients screened with gene expression profiling.

Auteurs : Yasbanoo Moayedi [Canada] ; Carlos A. Gomez [États-Unis] ; Chun Po S. Fan [Canada] ; Robert J H. Miller [États-Unis] ; Paul E. Bunce [Canada] ; Maxime Tremblay-Gravel [États-Unis] ; Farid Foroutan [Canada] ; Cedric Manlhiot [Canada] ; James Yee [États-Unis] ; Michael A. Shullo [États-Unis] ; Kiran K. Khush [États-Unis] ; Heather J. Ross [Canada] ; Jose G. Montoya [États-Unis] ; Jeffrey J. Teuteberg [États-Unis]

Source :

RBID : pubmed:30704838

Descripteurs français

English descriptors

Abstract

BACKGROUND

The risk of infection after heart transplantation is highest within the first year and represents the leading cause of early mortality. In this cohort of patients enrolled in the Outcomes AlloMap Registry (OAR), we sought to describe infection episodes (IEp) resulting in hospitalization, in the early (<1 year) and late (≥1 year) post-transplant period and determine the impact of immunosuppression on incidence of infection.

METHODS

The primary aim was to assess the incidence and nature of IEp. The secondary aim was to evaluate the effect of potential risk factors, such as recipient age; sex; body mass index; panel-reactive antibodies; cytomegalovirus (CMV) primary mismatch; prednisone, tacrolimus, and sirolimus levels; and gene expression profile (GEP) score, in the development of IEp.

RESULTS

The OAR comprises 1,504 patients, of whom 220 patients (14.6%) had an IEp during a median follow-up period of 382 days (interquartile range [IQR] 230 to 579 days). The cause-specific 5-year hazard ratio for any infection was 2.029 (p = 0.12). The pattern of early infection was consistent with nosocomial and opportunistic causes, whereas later infection was consistent with late-onset opportunistic and community-acquired etiologies. Sixty-two percent of the infections occurred early. In the time-dependent analysis, higher prednisone dose (log prednisone, hazard ratio [HR] 1.30, p = 0.022) was the most significant risk factor for all IEp.

CONCLUSIONS

In the OAR cohort, the majority of infections occurred within 1 year after transplantation. Clinicians may consider more aggressive prednisone withdrawal in low-risk patients to reduce IEp.


DOI: 10.1016/j.healun.2019.01.006
PubMed: 30704838


Affiliations:


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Le document en format XML

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<term>Adult (MeSH)</term>
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<term>Cytomegalovirus Infections (epidemiology)</term>
<term>Female (MeSH)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Glucocorticoids (therapeutic use)</term>
<term>Heart Failure (etiology)</term>
<term>Heart Failure (mortality)</term>
<term>Heart Failure (surgery)</term>
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<term>Middle Aged (MeSH)</term>
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<term>Postoperative Complications (microbiology)</term>
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<term>Adulte (MeSH)</term>
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<term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Complications postopératoires (microbiologie)</term>
<term>Complications postopératoires (épidémiologie)</term>
<term>Défaillance cardiaque (chirurgie)</term>
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<term>Prednisone</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Complications postopératoires</term>
<term>Infections à cytomégalovirus</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Défaillance cardiaque</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Gene Expression Profiling</term>
<term>Hospitalization</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Risk Factors</term>
<term>Time Factors</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Analyse de profil d'expression de gènes</term>
<term>Facteurs de risque</term>
<term>Facteurs temps</term>
<term>Femelle</term>
<term>Hospitalisation</term>
<term>Humains</term>
<term>Mâle</term>
<term>Études de cohortes</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>The risk of infection after heart transplantation is highest within the first year and represents the leading cause of early mortality. In this cohort of patients enrolled in the Outcomes AlloMap Registry (OAR), we sought to describe infection episodes (IEp) resulting in hospitalization, in the early (<1 year) and late (≥1 year) post-transplant period and determine the impact of immunosuppression on incidence of infection.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>The primary aim was to assess the incidence and nature of IEp. The secondary aim was to evaluate the effect of potential risk factors, such as recipient age; sex; body mass index; panel-reactive antibodies; cytomegalovirus (CMV) primary mismatch; prednisone, tacrolimus, and sirolimus levels; and gene expression profile (GEP) score, in the development of IEp.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The OAR comprises 1,504 patients, of whom 220 patients (14.6%) had an IEp during a median follow-up period of 382 days (interquartile range [IQR] 230 to 579 days). The cause-specific 5-year hazard ratio for any infection was 2.029 (p = 0.12). The pattern of early infection was consistent with nosocomial and opportunistic causes, whereas later infection was consistent with late-onset opportunistic and community-acquired etiologies. Sixty-two percent of the infections occurred early. In the time-dependent analysis, higher prednisone dose (log prednisone, hazard ratio [HR] 1.30, p = 0.022) was the most significant risk factor for all IEp.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>In the OAR cohort, the majority of infections occurred within 1 year after transplantation. Clinicians may consider more aggressive prednisone withdrawal in low-risk patients to reduce IEp.</p>
</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">30704838</PMID>
<DateCompleted>
<Year>2020</Year>
<Month>11</Month>
<Day>10</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>11</Month>
<Day>10</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1557-3117</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>38</Volume>
<Issue>6</Issue>
<PubDate>
<Year>2019</Year>
<Month>06</Month>
</PubDate>
</JournalIssue>
<Title>The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation</Title>
<ISOAbbreviation>J Heart Lung Transplant</ISOAbbreviation>
</Journal>
<ArticleTitle>Infectious complications after heart transplantation in patients screened with gene expression profiling.</ArticleTitle>
<Pagination>
<MedlinePgn>611-618</MedlinePgn>
</Pagination>
<ELocationID EIdType="pii" ValidYN="Y">S1053-2498(19)30006-3</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.healun.2019.01.006</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND">The risk of infection after heart transplantation is highest within the first year and represents the leading cause of early mortality. In this cohort of patients enrolled in the Outcomes AlloMap Registry (OAR), we sought to describe infection episodes (IEp) resulting in hospitalization, in the early (<1 year) and late (≥1 year) post-transplant period and determine the impact of immunosuppression on incidence of infection.</AbstractText>
<AbstractText Label="METHODS">The primary aim was to assess the incidence and nature of IEp. The secondary aim was to evaluate the effect of potential risk factors, such as recipient age; sex; body mass index; panel-reactive antibodies; cytomegalovirus (CMV) primary mismatch; prednisone, tacrolimus, and sirolimus levels; and gene expression profile (GEP) score, in the development of IEp.</AbstractText>
<AbstractText Label="RESULTS">The OAR comprises 1,504 patients, of whom 220 patients (14.6%) had an IEp during a median follow-up period of 382 days (interquartile range [IQR] 230 to 579 days). The cause-specific 5-year hazard ratio for any infection was 2.029 (p = 0.12). The pattern of early infection was consistent with nosocomial and opportunistic causes, whereas later infection was consistent with late-onset opportunistic and community-acquired etiologies. Sixty-two percent of the infections occurred early. In the time-dependent analysis, higher prednisone dose (log prednisone, hazard ratio [HR] 1.30, p = 0.022) was the most significant risk factor for all IEp.</AbstractText>
<AbstractText Label="CONCLUSIONS">In the OAR cohort, the majority of infections occurred within 1 year after transplantation. Clinicians may consider more aggressive prednisone withdrawal in low-risk patients to reduce IEp.</AbstractText>
<CopyrightInformation>Copyright © 2019 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Moayedi</LastName>
<ForeName>Yasbanoo</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>Section of Heart Failure, Cardiac Transplant, and Mechanical Circulatory Support, Department of Medicine, Stanford University, Stanford, California, USA; Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gomez</LastName>
<ForeName>Carlos A</ForeName>
<Initials>CA</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, Stanford University, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fan</LastName>
<ForeName>Chun Po S</ForeName>
<Initials>CPS</Initials>
<AffiliationInfo>
<Affiliation>Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Miller</LastName>
<ForeName>Robert J H</ForeName>
<Initials>RJH</Initials>
<AffiliationInfo>
<Affiliation>Section of Heart Failure, Cardiac Transplant, and Mechanical Circulatory Support, Department of Medicine, Stanford University, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bunce</LastName>
<ForeName>Paul E</ForeName>
<Initials>PE</Initials>
<AffiliationInfo>
<Affiliation>Department of Medicine, Division of Infectious Disease, University Health Network, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tremblay-Gravel</LastName>
<ForeName>Maxime</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Section of Heart Failure, Cardiac Transplant, and Mechanical Circulatory Support, Department of Medicine, Stanford University, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Foroutan</LastName>
<ForeName>Farid</ForeName>
<Initials>F</Initials>
<AffiliationInfo>
<Affiliation>Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Manlhiot</LastName>
<ForeName>Cedric</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Yee</LastName>
<ForeName>James</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>CareDx, Inc., Brisbane, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Shullo</LastName>
<ForeName>Michael A</ForeName>
<Initials>MA</Initials>
<AffiliationInfo>
<Affiliation>department of Medicine, West Virginia University, Morgantown, West Virginia, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Khush</LastName>
<ForeName>Kiran K</ForeName>
<Initials>KK</Initials>
<AffiliationInfo>
<Affiliation>Section of Heart Failure, Cardiac Transplant, and Mechanical Circulatory Support, Department of Medicine, Stanford University, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ross</LastName>
<ForeName>Heather J</ForeName>
<Initials>HJ</Initials>
<AffiliationInfo>
<Affiliation>Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Montoya</LastName>
<ForeName>Jose G</ForeName>
<Initials>JG</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, Stanford University, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Teuteberg</LastName>
<ForeName>Jeffrey J</ForeName>
<Initials>JJ</Initials>
<AffiliationInfo>
<Affiliation>Section of Heart Failure, Cardiac Transplant, and Mechanical Circulatory Support, Department of Medicine, Stanford University, Stanford, California, USA. Electronic address: jeff.teuteberg@stanford.edu.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2019</Year>
<Month>01</Month>
<Day>07</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>J Heart Lung Transplant</MedlineTA>
<NlmUniqueID>9102703</NlmUniqueID>
<ISSNLinking>1053-2498</ISSNLinking>
</MedlineJournalInfo>
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<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005938">Glucocorticoids</NameOfSubstance>
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<RegistryNumber>0</RegistryNumber>
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</Chemical>
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</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015331" MajorTopicYN="N">Cohort Studies</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003586" MajorTopicYN="N">Cytomegalovirus Infections</DescriptorName>
<QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<MeshHeading>
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<MeshHeading>
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<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
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<MeshHeading>
<DescriptorName UI="D006333" MajorTopicYN="N">Heart Failure</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
<QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName>
<QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016027" MajorTopicYN="N">Heart Transplantation</DescriptorName>
<QualifierName UI="Q000009" MajorTopicYN="Y">adverse effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006760" MajorTopicYN="N">Hospitalization</DescriptorName>
</MeshHeading>
<MeshHeading>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D011183" MajorTopicYN="N">Postoperative Complications</DescriptorName>
<QualifierName UI="Q000453" MajorTopicYN="Y">epidemiology</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
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<DescriptorName UI="D012307" MajorTopicYN="N">Risk Factors</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">AlloMap</Keyword>
<Keyword MajorTopicYN="Y">cytomegalovirus</Keyword>
<Keyword MajorTopicYN="Y">heart transplantation</Keyword>
<Keyword MajorTopicYN="Y">immunosuppression</Keyword>
<Keyword MajorTopicYN="Y">infectious episode</Keyword>
<Keyword MajorTopicYN="Y">survival</Keyword>
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<Month>04</Month>
<Day>17</Day>
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<Month>12</Month>
<Day>19</Day>
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<name sortKey="Bunce, Paul E" sort="Bunce, Paul E" uniqKey="Bunce P" first="Paul E" last="Bunce">Paul E. Bunce</name>
<name sortKey="Fan, Chun Po S" sort="Fan, Chun Po S" uniqKey="Fan C" first="Chun Po S" last="Fan">Chun Po S. Fan</name>
<name sortKey="Foroutan, Farid" sort="Foroutan, Farid" uniqKey="Foroutan F" first="Farid" last="Foroutan">Farid Foroutan</name>
<name sortKey="Manlhiot, Cedric" sort="Manlhiot, Cedric" uniqKey="Manlhiot C" first="Cedric" last="Manlhiot">Cedric Manlhiot</name>
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<name sortKey="Khush, Kiran K" sort="Khush, Kiran K" uniqKey="Khush K" first="Kiran K" last="Khush">Kiran K. Khush</name>
<name sortKey="Miller, Robert J H" sort="Miller, Robert J H" uniqKey="Miller R" first="Robert J H" last="Miller">Robert J H. Miller</name>
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</country>
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