UCL Institute of Liver and Digestive Health, Royal Free Hospital, University College London, London, UK.
Mallinckrodt Pharmaceuticals, Bedminster, NJ, USA.
Aliment Pharmacol Ther. 2020 Jul;52(2):351-358. doi: 10.1111/apt.15836. Epub 2020 Jun 4.
Hepatorenal syndrome and acute kidney injury are common complications of decompensated cirrhosis, and terlipressin is recommended as first-line vasoconstrictor therapy. However, data on its use outside of clinical trials are lacking.
To assess practice patterns and outcomes around vasoconstrictor use for hepatorenal syndrome in UK hospitals.
This was a multicentre chart review study. Data were extracted from medical records of patients diagnosed with hepatorenal syndrome and treated by vasoconstrictor drugs between January 2013 and December 2017 at 26 hospitals in the United Kingdom. The primary outcome was improvement of kidney function, defined as complete response (serum creatinine improved to ≤1.5 mg/dL), partial response (serum creatinine reduction of ≥20% but >1.5 mg/dL) and overall response (complete or partial response). Other outcomes included need for dialysis, mortality, liver transplantation and adverse events.
Of the 225 patients included in the analysis, 203 (90%) were treated with terlipressin (median duration, 6 days; range: 2-24 days). Mean (±standard deviation) serum creatinine at vasopressor initiation was 3.25 ± 1.64 mg/dL. Terlipressin overall response rate was 73%. Overall response was higher in patients with mild acute kidney injury (baseline serum creatinine <2.25 mg/dL), compared to those with moderate (serum creatinine ≥2.25 mg/dL and <3.5 mg/dL) or severe (serum creatinine ≥3.5 mg/dL). Ninety-day survival was 86% for all patients (93% for overall responders vs 66% for treatment nonresponders, P < 0.0001).
Terlipressin is the most commonly prescribed vasoconstrictor for patients with hepatorenal syndrome in the United Kingdom. Treatment with terlipressin in patients with less severe acute kidney injury (serum creatinine <2.25 mg/dL) was associated with higher treatment responses, and 90-day survival.
肝肾综合征和急性肾损伤是代偿性肝硬化的常见并发症,特利加压素被推荐作为一线血管收缩剂治疗药物。然而,临床试验之外的特利加压素使用数据尚缺乏。
评估英国医院肝肾综合征血管收缩剂使用的实践模式和结果。
这是一项多中心病历回顾性研究。数据从英国 26 家医院的病历中提取,纳入 2013 年 1 月至 2017 年 12 月期间接受血管收缩药物治疗的肝肾综合征患者。主要结局为肾功能改善,定义为完全应答(血清肌酐改善至≤1.5mg/dL)、部分应答(血清肌酐降低≥20%但>1.5mg/dL)和总应答(完全或部分应答)。其他结局包括需要透析、死亡率、肝移植和不良反应。
在纳入分析的 225 例患者中,203 例(90%)接受特利加压素治疗(中位治疗时间 6 天;范围:2-24 天)。血管加压素治疗开始时的平均(±标准差)血清肌酐为 3.25±1.64mg/dL。特利加压素的总应答率为 73%。与中度(血清肌酐≥2.25mg/dL 且<3.5mg/dL)或重度(血清肌酐≥3.5mg/dL)急性肾损伤患者相比,轻度急性肾损伤(基线时血清肌酐<2.25mg/dL)患者的总体应答率更高。所有患者 90 天生存率为 86%(总应答者为 93%,治疗无应答者为 66%,P<0.0001)。
特利加压素是英国治疗肝肾综合征患者最常开的血管收缩剂。在血清肌酐<2.25mg/dL 的较不严重的急性肾损伤患者中使用特利加压素与更高的治疗应答率和 90 天生存率相关。