Bremer Sebastian C B, Reinhardt Lars, Sobotta Michael, Hasselluhn Marie C, Lorf Thomas, Ellenrieder Volker, Schwörer Harald
Clinic for Gastroenterology and Gastrointestinal Oncology, University Medical Center Goettingen, Georg-August-University, Goettingen, Germany.
Liver Center Goettingen, University Medical Center Goettingen, Georg-August-University, Goettingen, Germany.
Front Med (Lausanne). 2018 Nov 19;5:320. doi: 10.3389/fmed.2018.00320. eCollection 2018.
Liver transplant recipients are frequently treated with proton pump inhibitors. Drug interactions have been described especially with respect to omeprazole. Due to the lower binding capacity of pantoprazole to CYP2C19 this drug became preferred and became the most used proton pump inhibitor in Germany. The data on the influence of pantoprazole on immunosuppressive drugs in liver transplant recipients a very scarce. The authors performed a single center analysis in liver transplant recipients on the effect of pantoprazole on the serum trough levels of different immunosuppressants. The trough levels were compared over a period of 1 year before and after start or stop of a continuous oral co-administration of 40 mg pantoprazole once daily. The serum trough levels of tacrolimus ( = 30), everolimus ( = 7), or sirolimus ( = 3) remain constant during an observation period of at least 1 year before and after co-administration of pantoprazole. None of the included patients needed a change of dosage of the observed immunosuppressants during the observation period. The oral co-administration of pantoprazole is safe in immunosuppressed liver transplant recipients according to the serum trough levels of tacrolimus, everolimus, and sirolimus. This analysis provides first data on the influence of pantoprazole on immunosuppressive drugs in liver transplant recipients.
肝移植受者经常接受质子泵抑制剂治疗。尤其是与奥美拉唑有关的药物相互作用已有报道。由于泮托拉唑对细胞色素P450 2C19的结合能力较低,这种药物成为首选,并成为德国使用最广泛的质子泵抑制剂。关于泮托拉唑对肝移植受者免疫抑制药物影响的数据非常稀少。作者对肝移植受者进行了一项单中心分析,以研究泮托拉唑对不同免疫抑制剂血清谷浓度的影响。在每天一次连续口服40 mg泮托拉唑开始或停止前后的1年时间内,对谷浓度进行了比较。在泮托拉唑联合给药前后至少1年的观察期内,他克莫司(n = 30)、依维莫司(n = 7)或西罗莫司(n = 3)的血清谷浓度保持恒定。在观察期内,纳入的患者均无需改变所观察免疫抑制剂的剂量。根据他克莫司、依维莫司和西罗莫司的血清谷浓度,泮托拉唑的口服联合给药在免疫抑制的肝移植受者中是安全的。该分析提供了关于泮托拉唑对肝移植受者免疫抑制药物影响的首批数据。