Biancofiore Gianni, Bindi Maria L, Miccoli Mario, Cerutti Elisabetta, Lavezzo Bruna, Pucci Laura, Bisà Massimo, Esposito Massimo, Meacci Luca, Mozzo Roberto, Stratta Chiara, Penno Giuseppe, Baggiani Angelo, Filipponi Franco
Liver Transplant Anaesthesia and Critical Care, P. Kaisserli ICU, Azienda Ospedaliera Universitaria Pisana, Ospedale Cisanello, 56100, Pisa, Italy.
Epidemiology and Biostatistics Unit, Department of Experimental Pathology, University School of Medicine, Pisa, Italy.
J Anesth. 2015 Jun;29(3):426-432. doi: 10.1007/s00540-014-1951-2. Epub 2014 Nov 30.
Acute kidney injury remains a serious complication after orthotopic liver transplantation. To date, several 'renal-protective' agents have been explored in this setting but with conflicting and disappointing results. Therefore, our aim is to evaluate the effects of fenoldopam in liver transplant patients with an established renal injury.
In this prospective study, intravenous fenoldopam 0.1 µg/kg/min was administered to consecutive liver transplant patients with postoperative (within 7 days from surgery) stage 2 acute kidney injury (AKI) according to the Acute Kidney Injury Network classification. Actual glomerular filtration rate (GFR; calculated by the iohexol plasma clearance), serum creatinine (SCr) and cystatin C (SCyC) were used to assess the effect of the medication on the patients.
During the study, 295 patients underwent liver transplant. Fifty-one patients (17.6%) met the inclusion criteria and the data from 48 patients were analysed. SCr and SCyC levels decreased (p < 0.001 after 48 h; p < 0.0001 after 72 h) and GFR increased (p < 0.001 after 24 h; p < 0.0001 after 72 h). When compared to a cohort of comparable patients with AKI from our historical series, the patients in the present study showed better SCr and SCyC levels. It was not necessary to discontinue the infusion of fenoldopam in any patient because of the occurrence of adverse events potentially attributable to it.
We showed that fenoldopam was capable of improving some renal function parameters in postoperative liver transplantation patients with on-going AKI. This preliminary study now sets the stage for a multicenter, randomized, placebo-controlled trial in order to provide definite evidence.
急性肾损伤仍是原位肝移植术后的严重并发症。迄今为止,已在此背景下探索了几种“肾脏保护”药物,但结果相互矛盾且令人失望。因此,我们的目的是评估非诺多泮对已发生肾损伤的肝移植患者的影响。
在这项前瞻性研究中,根据急性肾损伤网络分类,对连续的术后(手术后7天内)2期急性肾损伤(AKI)肝移植患者静脉输注非诺多泮,剂量为0.1μg/kg/min。采用实际肾小球滤过率(GFR;通过碘海醇血浆清除率计算)、血清肌酐(SCr)和胱抑素C(SCyC)评估药物对患者的影响。
研究期间,295例患者接受了肝移植。51例患者(17.6%)符合纳入标准,对48例患者的数据进行了分析。SCr和SCyC水平下降(48小时后p<0.001;72小时后p<0.0001),GFR升高(24小时后p<0.001;72小时后p<0.0001)。与我们历史系列中具有可比性的AKI患者队列相比,本研究中的患者SCr和SCyC水平更好。由于未发生可能归因于非诺多泮的不良事件,因此无需在任何患者中停止输注。
我们表明,非诺多泮能够改善正在发生AKI的肝移植术后患者的一些肾功能参数。这项初步研究为多中心、随机、安慰剂对照试验奠定了基础,以便提供确凿证据。