Viesselmann Chris W, Descourouez Jillian L, Jorgenson Margaret R, Radke Nancy A, Odorico Jon S
Department of Pharmacy, University of Wisconsin Hospital and Clinics, Madison, Wisconsin.
Division of Transplant, Department of Surgery, University of Wisconsin Hospital and Clinics, Madison, Wisconsin.
Pharmacotherapy. 2016 Mar;36(3):335-41. doi: 10.1002/phar.1718. Epub 2016 Mar 11.
To examine the clinical significance of clotrimazole troche discontinuation on tacrolimus trough levels and risk of allograft rejection after pancreas transplantation.
Retrospective cohort study.
Academic medical center.
Sixty-five pancreas transplant recipients (simultaneous pancreas-kidney transplants [39 patients], pancreas after kidney transplants [4 patients], and pancreas transplant alone [22 patients]) who were discharged after transplantation receiving a maintenance immunosuppressive regimen of tacrolimus, mycophenolate, and prednisone, and a clotrimazole troche to prevent oral mucosal candidiasis; per protocol, the clotrimazole troche was discontinued at 3 months after transplantation.
Patients were followed for 1 year after transplantation. The primary outcome measure was the difference in tacrolimus trough level before and after discontinuation of the clotrimazole troche. The secondary outcome measure was the difference in tacrolimus trough level when patients were stratified by the cohort that had a documented rejection episode 3-12 months after transplantation (rejection group) and the cohort that did not experience a rejection episode (no-rejection group). The incidence of rejection was evaluated in relation to mean tacrolimus trough concentrations above or below a protocol-defined level of significance (6 ng/ml). For the primary outcome, the mean tacrolimus trough level before discontinuation of the clotrimazole troche was significantly higher than the mean trough level after discontinuation (mean ± SD 9.6 ± 3.0 ng/ml vs 7.1 ± 2.6 ng/ml, p = 0.000003). For the secondary outcome, the mean tacrolimus trough level difference before and after clotrimazole troche discontinuation remained significant in both the no-rejection group (9.5 ± 3.0 ng/ml vs 7.4 ± 2.4 ng/ml, p = 0.00007) and rejection group (10.9 ± 3.3 ng/ml vs 4.1 ± 2.5 ng/ml, p = 0.0008). Between groups, the mean tacrolimus serum trough level after clotrimazole troche discontinuation was lower in the rejection group (4.1 ± 2.5 ng/ml) than that in the no-rejection group (7.4 ± 2.4 ng/ml; p = 0.005). The mean tacrolimus trough level difference between before and after discontinuation was greater in the rejection group (6.8 ± 1.5 ng/ml) versus the no-rejection group (2.1 ± 3.8 ng/ml, p = 0.009). Tacrolimus trough levels below 6 ng/ml (19 patients) after clotrimazole troche discontinuation were associated with an increased incidence of rejection episodes within 3-12 months after transplantation (odds ratio 12, 95% confidence interval 1.24-115.91, p = 0.032) versus trough levels of 6 ng/ml or higher (46 patients).
Clotrimazole troche discontinuation at 3 months after transplantation may cause significant tacrolimus trough level reductions. In addition, when trough levels are below 6 ng/ml, these fluctuations may contribute to the occurrence of allograft rejection.
探讨停用克霉唑含片对胰腺移植后他克莫司谷浓度及移植肾排斥反应风险的临床意义。
回顾性队列研究。
学术医疗中心。
65例胰腺移植受者(胰肾联合移植[39例]、肾移植后胰腺移植[4例]、单纯胰腺移植[22例]),移植后出院,接受他克莫司、霉酚酸酯和泼尼松维持免疫抑制方案,并使用克霉唑含片预防口腔黏膜念珠菌病;按照方案,移植后3个月停用克霉唑含片。
对患者进行移植后1年的随访。主要观察指标为停用克霉唑含片前后他克莫司谷浓度的差异。次要观察指标为根据移植后3 - 12个月有记录的排斥反应发作的队列(排斥组)和未经历排斥反应发作的队列(无排斥组)对患者进行分层时他克莫司谷浓度的差异。根据他克莫司谷浓度高于或低于方案定义的显著水平(6 ng/ml)评估排斥反应的发生率。对于主要观察指标,停用克霉唑含片前他克莫司的平均谷浓度显著高于停用后(平均值±标准差9.6±3.0 ng/ml对7.1±2.6 ng/ml,p = 0.000003)。对于次要观察指标,在无排斥组(9.5±3.0 ng/ml对7.4±2.4 ng/ml,p = 0.00007)和排斥组(10.9±3.3 ng/ml对4.1±2.5 ng/ml,p = 0.0008)中,停用克霉唑含片前后他克莫司的平均谷浓度差异均有统计学意义。两组之间,停用克霉唑含片后排斥组他克莫司血清谷浓度(4.1±2.5 ng/ml)低于无排斥组(7.4±2.4 ng/ml;p = 0.005)。排斥组停用前后他克莫司平均谷浓度差异(6.8±1.5 ng/ml)大于无排斥组(2.1±3.8 ng/ml,p = 0.009)。停用克霉唑含片后他克莫司谷浓度低于6 ng/ml(19例患者)与移植后3 - 12个月内排斥反应发作发生率增加相关(比值比12,95%置信区间1.24 - 115.91,p = 0.032),而谷浓度为6 ng/ml或更高(46例患者)。
移植后3个月停用克霉唑含片可能导致他克莫司谷浓度显著降低。此外,当谷浓度低于6 ng/ml时,这些波动可能导致移植肾排斥反应的发生。