A retrospective cohort analysis comparing the effectiveness and safety of perioperative angiotensin II to adrenergic vasopressors as a first-line vasopressor in kidney transplant recipients.

George Urias, Jamie Benken, Hokuto Nishioka, Enrico Benedetti, Scott T Benken
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Abstract

Background: Perioperative adrenergic vasopressors in kidney transplantation have been linked to negative outcomes and arrhythmias. Synthetic angiotensin II (AT2S) could improve renal hemodynamics, preserve allograft function, and reduce arrhythmias.

Objective: We aimed to compare the effectiveness and safety of AT2S to adrenergic vasopressors when used for perioperative hypotension in kidney transplant.

Methods: This single-center, retrospective cohort study included adults with perioperative shock requiring AT2S or adrenergic agents as first-line vasopressors during kidney transplant. The primary outcome was the need for a second continuous infusion vasopressor agents beyond the first-line agent. Secondary outcomes assessed adverse events and early allograft outcomes.

Results: Twenty patients receiving AT2S and 60 patients receiving adrenergic vasopressor agents were included. Intraoperatively, 1 of 20 patients (5%) in the AT2S group needed a second continuous vasopressor compared to 7 of 60 patients (11.7%) who needed a second continuous vasopressor in the adrenergic vasopressor group (P = 0.672). Postoperatively, 1 of 20 patients (5%) in the AT2S group compared to 12 of 60 patients (20%) in the adrenergic vasopressor group required a second vasopressor (P = 0.168). There were significantly fewer arrhythmias (1/20 [5%] vs. 17/60 [28.3%]), P = 0.03) and ischemic complications (0/20 [0%] vs. 11/20 [18.3%], P = 0.031) in patients who received AT2S. There were no differences in immediate, slow, or delayed graft function or in discharge, 1-month, and 3-month glomerular filtration rates (p > 0.05). CONCLUSION AND RELEVANCE: Both AT2S and adrenergic vasopressors are effective for perioperative hypotension in kidney transplant, with AT2S showing a lower incidence of arrhythmias and ischemic complications.

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一项回顾性队列分析,比较了肾移植受者围手术期血管紧张素 II 和肾上腺素能血管抑制剂作为一线血管抑制剂的有效性和安全性。
背景:肾移植围手术期肾上腺素能血管加压药与不良预后和心律失常有关。合成血管紧张素 II(AT2S)可改善肾血流动力学、保护异体移植功能并减少心律失常:我们旨在比较 AT2S 与肾上腺素能血管加压药用于肾移植围手术期低血压的有效性和安全性:这项单中心回顾性队列研究纳入了肾移植围手术期休克、需要使用 AT2S 或肾上腺素类药物作为一线血管加压药物的成人患者。主要结果是除一线药物外是否需要第二次持续输注血管加压药。次要结果评估不良事件和早期异体移植结果:结果:纳入了20名接受AT2S治疗的患者和60名接受肾上腺素能血管加压剂治疗的患者。术中,AT2S组20名患者中有1名(5%)需要第二次持续使用血管加压药,而肾上腺素能血管加压药组60名患者中有7名(11.7%)需要第二次持续使用血管加压药(P = 0.672)。术后,AT2S 组 20 名患者中有 1 人(5%)需要使用第二台血管加压器,而肾上腺素能血管加压器组 60 名患者中有 12 人(20%)需要使用第二台血管加压器(P = 0.168)。接受 AT2S 的患者心律失常(1/20 [5%] vs. 17/60 [28.3%])和缺血性并发症(0/20 [0%] vs. 11/20 [18.3%],P = 0.031)明显较少。移植物功能的即时、缓慢或延迟以及出院、1 个月和 3 个月肾小球滤过率没有差异(P > 0.05)。结论和意义:AT2S和肾上腺素能血管加压药都能有效治疗肾移植围手术期低血压,其中AT2S的心律失常和缺血性并发症发生率较低。
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