Department of Anesthesiology, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Department of Anesthesiology, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China; Department of Anesthesiology, Yancheng Third People's Hospital, Yancheng, Jiangsu, China.
J Clin Anesth. 2021 Dec;75:110498. doi: 10.1016/j.jclinane.2021.110498. Epub 2021 Sep 3.
To determine the effect of dexmedetomidine on acute kidney injury (AKI) following endovascular aortic repair (EVAR) for Stanford type B aortic dissection (TBAD).
Randomized, double-blind, placebo-controlled, pilot study.
University Hospital.
102 TBAD patients undergoing EVAR procedures were enrolled. Patients with dissection involving aortic arch or renal artery were excluded.
Patients were randomly assigned, in a 1:1 ratio, to a dexmedetomidine group (intravenous dexmedetomidine 0.4 μg/kg/h immediately after anesthesia induction and 0.1 μg/kg/h after extubation, which was maintained until 24 h) or a normal saline control group.
The primary outcome was the incidence of AKI within the first two days after surgery, based on the Acute Kidney Injury Network (AKIN) criteria. The secondary outcomes included serum cystatin C and estimated glomerular filtration rate on postoperative days 1, 2, and 7, and in-hospital need for renal replacement therapy (RRT). Long-term outcomes included RRT and all-cause mortality.
Ninety-eight patients completed the study (dexmedetomidine, n = 48; control, n = 50). AKIN stage 1 AKI occurred in 3/48 (6.3%) patients receiving dexmedetomidine, compared with 11/50 (22%) patients receiving normal saline (odds ratio = 0.24, 95% CI: 0.07 to 0.89, P = 0.041). This difference remained significant after adjusting for baseline covariates (adjusted odds ratio = 0.21, 95% CI: 0.05 to 0.84; P = 0.028). Dexmedetomidine led to a lower serum cystatin C on postoperative day 1 (median [IQR] mg/L: 1.31 [1.02-1.72] vs. 1.58 [1.28-1.96]). There were no between-group differences in other secondary or long-term outcomes. During the follow-up (median = 28.4 months), 1 patient in the dexmedetomidine group and 3 patients in the control group required RRT.
Dexmedetomidine reduced the incidence of AKI in TBAD patients after EVAR procedures. The long-term benefits of dexmedetomidine in this patient population warrant further investigation.
ChiCTR-IPR-15006372.
确定右美托咪定对 Stanford 型 B 型主动脉夹层(TBAD)患者血管内修复术后急性肾损伤(AKI)的影响。
随机、双盲、安慰剂对照、初步研究。
大学医院。
102 例 TBAD 患者接受血管内修复术。排除涉及主动脉弓或肾动脉的夹层患者。
患者按 1:1 比例随机分配至右美托咪定组(麻醉诱导后立即静脉注射右美托咪定 0.4μg/kg/h,拔管后 0.1μg/kg/h,持续至 24 小时)或生理盐水对照组。
主要结局是根据急性肾损伤网络(AKIN)标准,术后 2 天内 AKI 的发生率。次要结局包括术后第 1、2、7 天的血清胱抑素 C 和估算肾小球滤过率,以及院内需要肾脏替代治疗(RRT)。长期结局包括 RRT 和全因死亡率。
98 例患者完成研究(右美托咪定组,n=48;对照组,n=50)。右美托咪定组 3/48(6.3%)患者发生 AKIN 1 期 AKI,生理盐水组 11/50(22%)患者发生(比值比=0.24,95%CI:0.07 至 0.89,P=0.041)。调整基线协变量后,差异仍有统计学意义(调整比值比=0.21,95%CI:0.05 至 0.84;P=0.028)。右美托咪定组术后第 1 天血清胱抑素 C 水平较低(中位数[IQR]mg/L:1.31[1.02-1.72]vs.1.58[1.28-1.96])。其他次要和长期结局两组间无差异。在随访期间(中位数=28.4 个月),右美托咪定组 1 例患者和对照组 3 例患者需要 RRT。
右美托咪定可降低 TBAD 患者血管内修复术后 AKI 的发生率。右美托咪定在该患者人群中的长期获益需要进一步研究。
ChiCTR-IPR-15006372。