Fu Dahai, Li Jin, Zeng Guanglan, Tang Maozhi
Department of Nephrology, Wushan County People's Hospital of Chongqing, Chongqing, China.
Urinary Nephropathy Center, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Front Pharmacol. 2024 Dec 11;15:1522558. doi: 10.3389/fphar.2024.1522558. eCollection 2024.
Data about the safety of ACEI/ARB use in early (<3 months) posttransplant period are restricted and remain controversial.
This systematic review and meta-analysis included searches of PubMed, Embase and CENTRAL from inception to 31 November 2023, for studies to compare the safety (transplant outcomes and postoperative complications) of ACEI/ARB with non-ACEI/ARB (other antihypertensive medications) initiation in early post kidney transplant period.
Of 1,247 citations identified, 13 eligible studies involving 1919 patients were enrolled for analyses. In short- or long-term observations, there were no differences on pooled serum creatinine between ACEI/ARB and non-ACEI/ARB groups whether initiated within 1 or 1-3 months posttransplant, however, initiation of ACEI/ARB within the first month posttransplant had an advantage effect on the mean creatinine clearance. Early initiation of ACEI/ARB posttransplant reduced the risks of patient death (RR 0.60, = 0.009) and graft loss (RR 0.54, = 0.0002). For postoperative complications, there were no significant differences in acute rejection risk (RR 0.87, = 0.58), delayed graft function risk (RR 1.00, = 0.93), hemoglobin level (MD -0.32 mg/Dl, = 0.46) or urinary protein excretion (MD -0.10 g/24 h, = 0.16) between two groups. However, the ACEI/ARB group had higher incidence of hyperkalemia (RR 2.43, = 0.02).
Early initiation of ACEI/ARB within 3 months posttransplant proved to be basically safe and has renal function recovery benefits, however, hyperkalemia needs to be noted.
关于肾移植术后早期(<3个月)使用血管紧张素转换酶抑制剂(ACEI)/血管紧张素Ⅱ受体阻滞剂(ARB)安全性的数据有限且仍存在争议。
本系统评价和荟萃分析检索了从数据库建立至2023年11月31日的PubMed、Embase和CENTRAL数据库,以比较肾移植术后早期开始使用ACEI/ARB与非ACEI/ARB(其他抗高血压药物)的安全性(移植结局和术后并发症)。
在识别出的1247篇文献中,纳入13项符合条件的研究,共1919例患者进行分析。在短期或长期观察中,无论在移植后1个月内还是1 - 3个月内开始使用,ACEI/ARB组和非ACEI/ARB组的合并血清肌酐水平均无差异,然而,在移植后第一个月内开始使用ACEI/ARB对平均肌酐清除率有有益影响。移植后早期开始使用ACEI/ARB可降低患者死亡风险(风险比[RR]0.60,P = 0.009)和移植物丢失风险(RR 0.54,P = 0.0002)。对于术后并发症,两组在急性排斥反应风险(RR 0.87,P = 0.58)、移植肾功能延迟恢复风险(RR 1.00,P = 0.93)、血红蛋白水平(平均差[MD] -0.32mg/Dl,P = 0.46)或尿蛋白排泄(MD -0.10g/24小时,P = 0.16)方面无显著差异。然而,ACEI/ARB组高钾血症的发生率更高(RR 2.43,P = 0.02)。
移植后3个月内早期开始使用ACEI/ARB基本安全,且对肾功能恢复有益,但需注意高钾血症。