Department of Gastroenterology, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo - São Paulo (SP), Brazil.
Department of Nephrology, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo - São Paulo (SP), Brazil.
Crit Care Sci. 2023 Mar 1;35(1):11-18. doi: 10.5935/2965-2774.20230336-en.
To explain the rationale and protocol of the methods and analyses to be used in the LIVER-PAM randomized clinical trial, which seeks to understand whether a higher mean arterial pressure is capable of reducing the incidence of renal dysfunction postoperatively after liver transplantation.
LIVER-PAM is an open-label, randomized, controlled, singlecenter clinical trial. Patients randomized to the intervention group will have a mean arterial pressure of 85 - 90mmHg in the initial 24 hours of postoperative management, while patients in the control group will have a mean arterial pressure of 65 - 70mmHg in the same period. A sample of 174 patients will be required to demonstrate a 20% reduction in the absolute incidence of renal dysfunction, with a power of 80% and an alpha of 0.05.
If a 20% reduction in the absolute incidence of renal dysfunction in the postoperative period of liver transplantation is achieved with higher target mean arterial pressure in the first 24 hours, this would represent an inexpensive and simple therapy for improving current outcomes in the management of liver transplant patients.ClinicalTrials.gov Registry: NCT05068713.
解释 LIVER-PAM 随机临床试验中将要使用的方法和分析的原理和方案,该试验旨在了解更高的平均动脉压是否能够降低肝移植术后肾功能障碍的发生率。
LIVER-PAM 是一项开放标签、随机、对照、单中心临床试验。干预组患者在术后管理的最初 24 小时内的平均动脉压将为 85-90mmHg,而对照组患者在同一时期的平均动脉压将为 65-70mmHg。需要 174 例患者的样本,以证明术后肾功能障碍的绝对发生率降低 20%,具有 80%的功效和 0.05 的α值。
如果在肝移植术后的前 24 小时内通过更高的目标平均动脉压实现术后肾功能障碍的绝对发生率降低 20%,这将代表一种廉价且简单的治疗方法,可改善目前肝移植患者管理的结果。
ClinicalTrials.gov 注册号:NCT05068713。