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dc.contributor.authorPlit M.en
dc.contributor.authorMalouf M.A.en
dc.contributor.authorGlanville A.R.en
dc.contributor.authorAboyoun C.L.en
dc.contributor.authorMorton J.M.en
dc.date.accessioned2021-05-14T10:50:38Zen
dc.date.available2021-05-14T10:50:38Zen
dc.date.copyright2006en
dc.date.created20060824en
dc.date.issued2012-10-17en
dc.identifier.citationJournal of Heart and Lung Transplantation. 25 (8) (pp 928-934), 2006. Date of Publication: August 2006.en
dc.identifier.issn1053-2498en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/32031en
dc.description.abstractBackground: Acute pulmonary allograft rejection (AR) is the most important risk factor for bronchiolitis obliterans syndrome (BOS), which is associated with reduced quality of life and decreased survival after lung transplantation (LTx). Trough (C0) cyclosporine (CyA) levels have a poor correlation with area-under-the-curve (AUC) measurements of cyclosporine exposure compared with 2-hour post-dose (C2) levels, but there are no published guidelines for C2 levels after LTx. Hence, we assessed the utility of C2 target levels to prevent AR. Method(s): Fifty consecutive de novo LTx patients (bilateral, 44; single, 3; heart-lung, 3; cystic fibrosis, 20; non-cystic fibrosis, 30) managed with CyA were assigned target C2 levels as follows: >800 mug/liter within 48 hours; >1,200 mug/liter from Week 1 to Month 1; >1,000 mug/liter in Month 2; >800 mug/liter in Month 3; >700 in mug/liter in Months 3 to 6; and >600 mug/liter thereafter. Surveillance transbronchial biopsies (TBBxs) were performed at 3, 6, 9 and 12 weeks. An intention-to-treat analysis was performed and results compared with our historic controls managed by C0 monitoring. Result(s): Fifteen of 50 (30%) LTx recipients developed AR on 23 of 171 TBBxs (Grade A2:A3 = 21:2) during follow-up (mean +/- SD) of 1,185 +/- 426 days (range, 16 to 1,790 days). Eighteen of 23 AR episodes occurred after sub-target C2 levels. The 30-day, 1-, 3- and 5-year actuarial survival rates were 98%, 94%, 82% and 77%, respectively. Thirteen of 48 (27%) evaluable LTx recipients developed BOS with 1-, 3- and 5-year freedom-from-BOS rates of 96%, 79% and 59%, respectively. Only 1 patient developed severe renal dysfunction. Conclusion(s): Achieving and maintaining target C2 levels after LTx is associated with reduced rates of AR and BOS, preservation of renal function, and excellent short-term survival rates when compared with historic controls. J Heart Lung Transplant. © 2006 International Society for Heart and Lung Transplantation.en
dc.languageEnglishen
dc.languageenen
dc.publisherElsevier USA (6277 Sea Harbor Drive, Orlando FL 32862 8239, United States)en
dc.titleCyclosporine C2 Target Levels and Acute Cellular Rejection After Lung Transplantation.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.healun.2006.03.020en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid16890113 [http://www.ncbi.nlm.nih.gov/pubmed/?term=16890113]en
dc.identifier.source44143002en
dc.identifier.institution(Glanville, Aboyoun, Plit, Malouf) St Vincent's Hospital, Darlinghurst, Sydney, NSW, Australia (Morton) Monash Medical Centre, Clayton, Vic., Australiaen
dc.description.addressA.R. Glanville, St Vincent's Hospital, Darlinghurst, Sydney, NSW, Australia. E-mail: aglanville@stvincents.com.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2012 Elsevier B.V., All rights reserved.en
dc.identifier.authoremailGlanville A.R.; aglanville@stvincents.com.auen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
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