Tanner A Melton, Molly W Fenske, Stacy A Bernard, Kristin C Cole, Kelly M Pennington, Adley I Lemke
{"title":"非诱导性巴昔昔单抗通过暂时停用他克莫司促进心胸移植患者肾脏恢复。","authors":"Tanner A Melton, Molly W Fenske, Stacy A Bernard, Kristin C Cole, Kelly M Pennington, Adley I Lemke","doi":"10.3390/medicines12030022","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction:</b> Reversible and irreversible nephrotoxicity are known complications of tacrolimus. Approaches to reduce the incidence of nephrotoxicity include the reduction or avoidance of tacrolimus but must be weighed against risk of rejection. Infrequently, basiliximab has been used outside of the induction period to facilitate temporary tacrolimus cessation in the setting of acute kidney injury (AKI). <b>Objective:</b> The primary objective of this study was to describe renal recovery after temporary tacrolimus cessation with non-induction basiliximab (NIB) compared to a matched cohort. <b>Methods:</b> We conducted a single-center study of adult cardiothoracic transplant recipients that received basiliximab beyond post-operative day 7 for temporary tacrolimus cessation in the setting of AKI between January 2019 and November 2023 and matched them to acontrol cohort. <b>Results:</b> Twelve patients underwent temporary tacrolimus cessation with NIB. In total, 7 (58%) patients achieved initial renal recovery at tacrolimus resumption compared to 15 (42%) patients in the matched cohort at an equivalent time point. No difference between treated rejection (17% vs. 19%, <i>p</i> = 0.80) or infection (75% vs. 50%, <i>p</i> = 0.32) was observed between tacrolimus cessation and its matched cohort. <b>Conclusions:</b> The use of NIB for tacrolimus cessation can allow for potential renal recovery after an AKI or in patients at risk of AKI. This approach does not appear to significantly increase the risk of rejection but may increase the risk of infection in the long term.</p>","PeriodicalId":74162,"journal":{"name":"Medicines (Basel, Switzerland)","volume":"12 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12452629/pdf/","citationCount":"0","resultStr":"{\"title\":\"Non-Induction Basiliximab to Facilitate Renal Recovery via Temporary Tacrolimus Cessation in Cardiothoracic Transplant Patients.\",\"authors\":\"Tanner A Melton, Molly W Fenske, Stacy A Bernard, Kristin C Cole, Kelly M Pennington, Adley I Lemke\",\"doi\":\"10.3390/medicines12030022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction:</b> Reversible and irreversible nephrotoxicity are known complications of tacrolimus. Approaches to reduce the incidence of nephrotoxicity include the reduction or avoidance of tacrolimus but must be weighed against risk of rejection. Infrequently, basiliximab has been used outside of the induction period to facilitate temporary tacrolimus cessation in the setting of acute kidney injury (AKI). <b>Objective:</b> The primary objective of this study was to describe renal recovery after temporary tacrolimus cessation with non-induction basiliximab (NIB) compared to a matched cohort. <b>Methods:</b> We conducted a single-center study of adult cardiothoracic transplant recipients that received basiliximab beyond post-operative day 7 for temporary tacrolimus cessation in the setting of AKI between January 2019 and November 2023 and matched them to acontrol cohort. <b>Results:</b> Twelve patients underwent temporary tacrolimus cessation with NIB. In total, 7 (58%) patients achieved initial renal recovery at tacrolimus resumption compared to 15 (42%) patients in the matched cohort at an equivalent time point. No difference between treated rejection (17% vs. 19%, <i>p</i> = 0.80) or infection (75% vs. 50%, <i>p</i> = 0.32) was observed between tacrolimus cessation and its matched cohort. <b>Conclusions:</b> The use of NIB for tacrolimus cessation can allow for potential renal recovery after an AKI or in patients at risk of AKI. This approach does not appear to significantly increase the risk of rejection but may increase the risk of infection in the long term.</p>\",\"PeriodicalId\":74162,\"journal\":{\"name\":\"Medicines (Basel, Switzerland)\",\"volume\":\"12 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12452629/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medicines (Basel, Switzerland)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/medicines12030022\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicines (Basel, Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/medicines12030022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
简介:可逆和不可逆肾毒性是已知的他克莫司并发症。减少肾毒性发生率的方法包括减少或避免使用他克莫司,但必须权衡排斥风险。在急性肾损伤(AKI)的情况下,basiliximab在诱导期之外用于促进暂时停止他克莫司。目的:本研究的主要目的是描述暂时停用他克莫司与非诱导性巴昔昔单抗(NIB)后肾脏恢复情况,并与匹配队列进行比较。方法:在2019年1月至2023年11月期间,我们对患有AKI的成人心胸移植受者进行了一项单中心研究,这些受者在术后第7天以上接受了巴昔昔单抗治疗,以暂时停止他克莫司,并将其与对照队列进行匹配。结果:12例患者在NIB的帮助下暂时停用他克莫司。总共有7例(58%)患者在恢复他克莫司后实现了初步肾脏恢复,而在相同的时间点,匹配队列中有15例(42%)患者实现了肾脏恢复。停止他克莫司治疗后的排斥反应(17% vs. 19%, p = 0.80)或感染(75% vs. 50%, p = 0.32)在他克莫司治疗组和匹配组之间没有差异。结论:停用他克莫司时使用NIB可使AKI后或有AKI风险的患者的肾脏恢复。这种方法似乎不会显著增加排异反应的风险,但从长远来看可能会增加感染的风险。
Non-Induction Basiliximab to Facilitate Renal Recovery via Temporary Tacrolimus Cessation in Cardiothoracic Transplant Patients.
Introduction: Reversible and irreversible nephrotoxicity are known complications of tacrolimus. Approaches to reduce the incidence of nephrotoxicity include the reduction or avoidance of tacrolimus but must be weighed against risk of rejection. Infrequently, basiliximab has been used outside of the induction period to facilitate temporary tacrolimus cessation in the setting of acute kidney injury (AKI). Objective: The primary objective of this study was to describe renal recovery after temporary tacrolimus cessation with non-induction basiliximab (NIB) compared to a matched cohort. Methods: We conducted a single-center study of adult cardiothoracic transplant recipients that received basiliximab beyond post-operative day 7 for temporary tacrolimus cessation in the setting of AKI between January 2019 and November 2023 and matched them to acontrol cohort. Results: Twelve patients underwent temporary tacrolimus cessation with NIB. In total, 7 (58%) patients achieved initial renal recovery at tacrolimus resumption compared to 15 (42%) patients in the matched cohort at an equivalent time point. No difference between treated rejection (17% vs. 19%, p = 0.80) or infection (75% vs. 50%, p = 0.32) was observed between tacrolimus cessation and its matched cohort. Conclusions: The use of NIB for tacrolimus cessation can allow for potential renal recovery after an AKI or in patients at risk of AKI. This approach does not appear to significantly increase the risk of rejection but may increase the risk of infection in the long term.