Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/36072
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dc.contributor.authorDendle C.en
dc.contributor.authorMulley W.R.en
dc.contributor.authorPolkinghorne K.R.en
dc.contributor.authorHoldsworth S.R.en
dc.contributor.authorThursky K.en
dc.contributor.authorStuart R.L.en
dc.contributor.authorKanellis J.en
dc.contributor.authorGan P.-Y.en
dc.date.accessioned2021-05-14T12:13:20Zen
dc.date.available2021-05-14T12:13:20Zen
dc.date.copyright2019en
dc.date.created20190613en
dc.date.issued2019-06-13en
dc.identifier.citationTransplant Infectious Disease. 21 (3) (no pagination), 2019. Article Number: e13076. Date of Publication: June 2019.en
dc.identifier.issn1398-2273en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36072en
dc.description.abstractBackground: The aim of this study was to determine whether a composite score of simple immune biomarkers and clinical characteristics could predict severe infections in kidney transplant recipients. Method(s): We conducted a prospective study of 168 stable kidney transplant recipients who underwent measurement of lymphocyte subsets, immunoglobulins, and renal function at baseline and were followed up for 2 years for the development of any severe infections, defined as infection requiring hospitalization. A point score was developed to predict severe infection based on logistic regression analysis of factors in baseline testing. Result(s): Fifty-nine (35%) patients developed severe infection, 36 (21%) had two or more severe infections, and 3 (2%) died of infection. A group of 19 (11%) patients had the highest predicted infectious risk (>60%), as predicted by the score. Predictive variables were mycophenolate use, graft function, CD4+, and natural killer cell number. The level of immunosuppression score had an area under the receiver operating curve of 0.75 (95% CI: 0.67-0.83). Conclusion(s): Our level of immunosuppression score for predicting the development of severe infection over 2 years has sufficient prognostic accuracy for identification of high-risk patients. This data can inform research that examines strategies to reduce the risks of infection.Copyright © 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltden
dc.languageenen
dc.languageEnglishen
dc.publisherBlackwell Publishing Inc. (E-mail: subscrip@blackwellpub.com)en
dc.relation.ispartofTransplant Infectious Diseaseen
dc.titleA simple score can identify kidney transplant recipients at high risk of severe infection over the following 2 years.en
dc.typeArticleen
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/tid.13076en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid30875147 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30875147]en
dc.identifier.source627326281en
dc.identifier.institution(Dendle, Polkinghorne, Mulley, Gan, Kanellis, Stuart, Holdsworth) Centre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, VIC, Australia (Dendle, Stuart) Monash Infectious Diseases, Monash Health, Clayton, VIC, Australia (Polkinghorne, Mulley, Kanellis, Holdsworth) Department of Nephrology, Monash Medical Centre, Clayton, VIC, Australia (Polkinghorne) Department of Epidemiology and Preventive Medicine, Monash University, Prahran, VIC, Australia (Thursky) National Centre for Infections in Cancer, Peter MacCallum Cancer Centre, Melbourne, VIC, Australiaen
dc.description.addressC. Dendle, Centre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, VIC, Australia. E-mail: claire.dendle@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.subect.keywordsinfection risk kidney transplant risk lymphocytes natural killer cells scoreen
dc.identifier.authoremailDendle C.; claire.dendle@monash.eduen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptInfection Prevention and Epidemiology-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptNephrology-
crisitem.author.deptImmunology and Allergy-
crisitem.author.deptInfection Prevention and Epidemiology-
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