Hirano Yutaka, Sugimoto Seiichiro, Mano Toshifumi, Kurosaki Takeshi, Miyoshi Kentaroh, Otani Shinji, Yamane Masaomi, Kobayashi Motomu, Miyoshi Shinichiro, Oto Takahiro
Department of General Thoracic Surgery, Okayama University Hospital, Okayama City, Okayama, Japan.
Department of Organ Transplant Center, Okayama University Hospital, Okayama City, Okayama, Japan.
Ann Transplant. 2017 Aug 11;22:484-492. doi: 10.12659/aot.904225.
BACKGROUND Although administration of tacrolimus, whether by the enteric, sublingual, or continuous intravenous routes, has some limitations, twice-daily bolus intravenous tacrolimus administration has been shown to be beneficial in optimizing efficacy and safety after lung transplantation. However, at present, the duration of bolus intravenous tacrolimus administration is limited, and the effects of prolonged bolus intravenous tacrolimus administration remain unknown. Our study was aimed at assessing the safety and efficacy of prolonged twice-daily bolus intravenous tacrolimus administration in the early phase after lung transplantation. MATERIAL AND METHODS We retrospectively investigated the data of 62 recipients of lung transplantation who had received twice-daily bolus intravenous administration of tacrolimus, followed by oral tacrolimus, after lung transplantation at our institution between January 2011 and October 2015. RESULTS The median duration of bolus intravenous tacrolimus administration was 19 days (4-72 days). The target trough level was achieved in 89% of the patients by day 3. Acute kidney injury occurred in 27% of the patients during bolus intravenous tacrolimus. Two patients (3%) had neurotoxicity, necessitating discontinuation of tacrolimus. Suspected acute rejection requiring steroid pulse therapy occurred in 21% of patients during the follow-up period. Eight patients (13%) developed chronic lung allograft dysfunction during the follow-up period. The 1-year and 5-year survival rates after lung transplantation were 95% and 76%, respectively. CONCLUSIONS These results suggest that prolonged bolus intravenous tacrolimus administration in the early phase after lung transplantation is a safe and effective alternative to enteric, sublingual, or continuous intravenous administration.
尽管他克莫司的给药方式,无论是经肠内、舌下还是持续静脉途径,都存在一些局限性,但每日两次静脉推注他克莫司已被证明在优化肺移植后的疗效和安全性方面是有益的。然而,目前,静脉推注他克莫司的给药持续时间有限,延长静脉推注他克莫司给药的效果仍不清楚。我们的研究旨在评估肺移植术后早期延长每日两次静脉推注他克莫司给药的安全性和疗效。
我们回顾性调查了2011年1月至2015年10月期间在我们机构接受肺移植的62例患者的数据,这些患者在肺移植后接受了每日两次静脉推注他克莫司,随后口服他克莫司。
静脉推注他克莫司的中位给药持续时间为19天(4 - 72天)。到第3天时,89%的患者达到了目标谷浓度。在静脉推注他克莫司期间,27%的患者发生了急性肾损伤。两名患者(3%)出现神经毒性,需要停用他克莫司。在随访期间,21%的患者发生了疑似急性排斥反应,需要进行类固醇冲击治疗。在随访期间,8名患者(13%)发生了慢性肺移植功能障碍。肺移植后的1年和5年生存率分别为95%和76%。
这些结果表明,肺移植术后早期延长静脉推注他克莫司给药是肠内、舌下或持续静脉给药的一种安全有效的替代方法。