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Efficacy of L-ornithine-L-aspartate as an adjuvant therapy in cirrhotic patients with hepatic encephalopathy

机译:L-鸟氨酸-L-天冬氨酸作为肝性脑病肝硬化患者辅助治疗的疗效

摘要

OBJECTIVE: To evaluate the efficacy of L-ornithine-L-aspartate (LOLA) as an adjuvant therapy in cirrhotic patients with hepatic encephalopathy (HE).STUDY DESIGN: Randomized placebo controlled study.PLACE AND DURATION OF STUDY: The Aga Khan University Hospital, Karachi in the year 2003-2004.METHODOLOGY: Patients with HE were randomized to receive LOLA or placebo medicine as an adjuvant to treatment of HE. Number connection test-A (NCT-A), ammonia level, clinical grade of HE and duration of hospitalization were assessed.RESULTS: Out of 120 patients, there were 62 males with mean age of 57 11 years. Improvement in HE was higher (n=40, 66.7%) in LOLA group as compared to the placebo group (n=28, 46.7%, p=0.027). In patients with grade I or less encephalopathy, improvement was seen in 6 (35.3%) and 3 (20%) patients in LOLA and placebo groups respectively (p=0.667). Patients with HE grade II and above showed improvement in 34 (79.1%) and 25 (55.6%) cases in LOLA and placebo group respectively (p=0.019). On multivariate analysis patients with HE of grade II and above showed prothrombin time, creatinine level and use of LOLA influencing the outcome. Duration of hospitalization was 93.6 25.7 hours and 135.2 103.5 hours in LOLA and placebo groups respectively (p=0.025). No side effects were observed in either groups.CONCLUSION: In cirrhotic patients with advanced hepatic encephalopathy treatment with LOLA was safe and associated with relatively rapid improvement and shorter hospital stay.
机译:目的:评价左旋鸟氨酸-天冬氨酸(LOLA)作为肝硬化肝性脑病(HE)患者辅助治疗的疗效。研究设计:随机安慰剂对照研究。研究的地点和时间:阿加汗大学医院方法:2003年至2004年在卡拉奇市进行。方法:HE患者被随机分配接受LOLA或安慰剂药物作为HE的佐剂。结果:在120例患者中,有62例男性,平均年龄为57±11岁。与安慰剂组(n = 28,46.7%,p = 0.027)相比,LOLA组的HE改善更高(n = 40,66.7%)。在I级或以下脑病患者中,LOLA组和安慰剂组分别有6例(35.3%)和3例(20%)的患者得到了改善(p = 0.667)。 LOLA组和安慰剂组中,II级及以上的HE患者分别改善了34例(79.1%)和25例(55.6%)(p = 0.019)。在多变量分析中,II级及以上的HE患者显示凝血酶原时间,肌酐水平和使用LOLA影响结局。 LOLA组和安慰剂组的住院时间分别为93.6 25.7小时和135.2 103.5小时(p = 0.025)。结论:LOLA治疗肝硬化晚期肝性脑病患者是安全的,且病情相对较快改善且住院时间较短。

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