• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肝移植受者的24小时类固醇无激素免疫抑制方案

Twenty-four hour steroid avoidance immunosuppressive regimen in liver transplant recipients.

作者信息

Ju Wei-qiang, Guo Zhi-yong, Ling Xiaoting, He Xiao-shun, Wu Lin-wei, Tai Qiang, Hu An-bin, Han Ming, Zhu Xiao-feng

机构信息

From the Organ Transplant Center, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

出版信息

Exp Clin Transplant. 2012 Jun;10(3):258-62. doi: 10.6002/ect.2010.0127.

DOI:10.6002/ect.2010.0127
PMID:22631063
Abstract

OBJECTIVES

To investigate the efficacy and safety of an immunosuppressive regimen of steroid avoidance in combination with induction therapy and tacrolimus in liver transplant recipients.

MATERIALS AND METHODS

Eighty-two adult liver transplant recipients were randomized into 2 groups: standard protocol group (n=41) in which steroids were withdrawn 3 months after the operation, and a 24-hour steroid avoidance group (n=41) in which steroids were eliminated within 24 hours. The incidence of acute rejections, infections (bacterial, fungal, and cytomegalovirus), and metabolic complications were analyzed between the groups.

RESULTS

The incidence of early posttransplant diabetes mellitus and the average dosage of insulin consumption among diabetic recipients were significantly higher in recipients in the standard protocol group than in the 24-hour avoidance group (P < .05). In addition, the incidence of hypertension and infection during the follow-up were also higher in patients of the standard protocol group (P < .05). The incidence of hypertension in the early posttransplant period, hyperlipemia, and acute rejection during the follow-up were comparable between the groups (P > .05).

CONCLUSIONS

Twenty-four hour steroid avoidance combined with induction therapy and tacrolimus maintenance is a safe and efficient immunosuppression strategy that can significantly reduce posttransplant infections and other complications owing to long-term use of steroids, without increasing the risk of acute rejection.

摘要

目的

探讨在肝移植受者中,避免使用类固醇联合诱导治疗及他克莫司的免疫抑制方案的疗效和安全性。

材料与方法

82例成年肝移植受者被随机分为两组:标准方案组(n = 41),术后3个月停用类固醇;24小时类固醇避免组(n = 41),在24小时内停用类固醇。分析两组之间急性排斥反应、感染(细菌、真菌和巨细胞病毒)及代谢并发症的发生率。

结果

标准方案组受者移植后早期糖尿病的发生率及糖尿病受者胰岛素平均使用剂量显著高于24小时避免组(P < 0.05)。此外,标准方案组患者随访期间高血压和感染的发生率也更高(P < 0.05)。两组之间移植后早期高血压、高脂血症的发生率及随访期间急性排斥反应的发生率相当(P > 0.05)。

结论

24小时类固醇避免联合诱导治疗及他克莫司维持治疗是一种安全有效的免疫抑制策略,可显著降低因长期使用类固醇导致的移植后感染及其他并发症,且不增加急性排斥反应的风险。

相似文献

1
Twenty-four hour steroid avoidance immunosuppressive regimen in liver transplant recipients.肝移植受者的24小时类固醇无激素免疫抑制方案
Exp Clin Transplant. 2012 Jun;10(3):258-62. doi: 10.6002/ect.2010.0127.
2
Steroid avoidance reduce the cost of morbidities after live-donor renal allotransplants: a prospective, randomized, controlled study.避免使用类固醇可降低活体供肾肾移植术后并发症的成本:一项前瞻性、随机、对照研究。
Exp Clin Transplant. 2011 Apr;9(2):121-7.
3
Interleukin-2 receptor antibody (basiliximab) for immunosuppressive induction therapy after liver transplantation: a protocol with early elimination of steroids and reduction of tacrolimus dosage.白细胞介素-2受体抗体(巴利昔单抗)用于肝移植后免疫抑制诱导治疗:一项早期停用类固醇并减少他克莫司剂量的方案
Liver Transpl. 2004 Jun;10(6):728-33. doi: 10.1002/lt.20144.
4
[Two-dose steroid combined with two-dose daclizumab and tacrolimus regimen in liver transplant recipients].肝移植受者中两剂类固醇联合两剂达利珠单抗和他克莫司方案
Zhonghua Wai Ke Za Zhi. 2009 Jul 15;47(14):1064-6.
5
Early steroid withdrawal protocol with basiliximab, cyclosporine and mycophenolate mofetil in renal-transplant recipients.肾移植受者中使用巴利昔单抗、环孢素和霉酚酸酯的早期类固醇撤药方案。
Int Immunopharmacol. 2006 Dec 20;6(13-14):1984-92. doi: 10.1016/j.intimp.2006.07.018. Epub 2006 Aug 10.
6
Steroid elimination within 24 hours after orthotopic liver transplantation: effectiveness and tolerability.肝移植术后 24 小时内类固醇的消除:疗效和耐受性。
Hepatobiliary Pancreat Dis Int. 2012 Apr;11(2):137-42. doi: 10.1016/s1499-3872(12)60138-6.
7
Basiliximab induction in adult liver transplant recipients with 93% rejection-free patient and graft survival at 24 months.巴利昔单抗用于成人肝移植受者诱导治疗,24个月时患者和移植物无排斥生存率达93%。
Transplant Proc. 2006 Dec;38(10):3633-5. doi: 10.1016/j.transproceed.2006.10.110.
8
Thymoglobulin Versus Basiliximab Induction Therapy in Low-Risk Kidney Transplant Recipients: A Single-Center Experience.低风险肾移植受者中胸腺球蛋白与巴利昔单抗诱导治疗的单中心经验
Transplant Proc. 2018 Jun;50(5):1285-1288. doi: 10.1016/j.transproceed.2018.02.088.
9
Comparative study of the cellular pharmacodynamics of tacrolimus in renal transplant recipients treated with and without basiliximab.比较他克莫司在接受和未接受巴利昔单抗治疗的肾移植受者中的细胞药代动力学。
Cell Transplant. 2012;21(2-3):565-70. doi: 10.3727/096368911X605493.
10
Efficacy and safety of basiliximab with a tacrolimus-based regimen in liver transplant recipients.巴利昔单抗联合他克莫司方案在肝移植受者中的疗效和安全性
Transplantation. 2004 Sep 27;78(6):886-91. doi: 10.1097/01.tp.0000134970.92694.68.

引用本文的文献

1
New-Onset Diabetes Mellitus (NODM) After Liver Transplantation (LT): The Ultimate Non-diabetogenic Immunosuppressive Therapy.肝移植后新发糖尿病(NODM):终极非致糖尿病性免疫抑制疗法
Cureus. 2022 Mar 29;14(3):e23635. doi: 10.7759/cureus.23635. eCollection 2022 Mar.
2
Glucocorticosteroid-free versus glucocorticosteroid-containing immunosuppression for liver transplanted patients.肝移植患者使用不含糖皮质激素与含糖皮质激素的免疫抑制治疗对比
Cochrane Database Syst Rev. 2018 Apr 9;4(4):CD007606. doi: 10.1002/14651858.CD007606.pub4.
3
Post-Liver Transplantation Diabetes Mellitus: A Review of Relevance and Approach to Treatment.
肝移植后糖尿病:相关性及治疗方法综述
Diabetes Ther. 2018 Apr;9(2):521-543. doi: 10.1007/s13300-018-0374-8. Epub 2018 Feb 6.
4
Efficacy and Safety of a Steroid-Free Immunosuppressive Regimen after Liver Transplantation for Hepatocellular Carcinoma.肝细胞癌肝移植术后无类固醇免疫抑制方案的疗效与安全性
Gut Liver. 2016 Jul 15;10(4):604-10. doi: 10.5009/gnl15017.