甲泼尼龙加N乙酰半胱氨酸或己酮茶碱加N乙酰半胱氨酸治疗重度酒精性肝炎患者的短期疗效

K. Regmi, A. Mishra, S. Kc, D. Sharma, J. K. Shrestha, Sushil Prajapati, D. Khadka
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摘要

重度酒精性肝炎(AH)是一种急性酒精性肝损伤。通常表现为胎儿疾病,短期(28天)死亡率非常高(30-50%)。本研究于2016年5月至2017年7月在Bir医院肝脏科进行。主要目的是找出判别功能(DF)≥32的严重酒精性肝炎患者的28天死亡率。这是一项前瞻性、比较性、随机介入医院研究。方法:选取符合诊断标准的110例重度酒精性肝炎患者,随机分为奇数组和偶数组。1组给予甲基强的松龙治疗,2组给予己酮可可碱治疗,疗程28 d。两组均添加N型乙酰半胱氨酸。甲强的松龙组在第7天计算里尔评分,评分≤0.45的患者继续甲强的松龙治疗28天,否则停止治疗。第28天收集数据。他们的生存、药物并发症和死亡原因进行了比较。结果:甲泼尼龙组平均发病年龄为40.21±10.5岁,己酮可可碱组平均发病年龄为42.1±12.1岁。两组并发症均为恶心、呕吐、腹胀、厌食和肢体肿胀。然而,甲基强的松龙组高血糖(16.4%)和肾功能损害(9.1%)更为常见。甲泼尼龙组28 d内死亡率为34.5%,己酮可可碱组为37.8%。两组的常见死亡原因均为肝性脑病、肝肾综合征、败血症或原因不明。结论:酒精性肝炎是酒精性肝病的常见表现,两组均有较高的短期死亡率,但药物不良反应在甲基强的松龙组更为常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Short term outcome in severe alcoholic hepatitis patients treated with Methylprednisolone plus N acetylcysteine or Pentoxifylline plus N acetylcysteine
Introduction: Severe Alcoholic hepatitis (AH) is an acute form of alcohol induced liver injury. Often it present as fetal diseases with very high (30-50%) short term (28 days) mortality. This study was conducted from period May 2016 to July 2017 in Liver unit, Bir hospital. The main objective was to find out 28 days mortality in patients with severe alcoholic hepatitis who had Discriminant function (DF) ≥ 32. This was a prospective, comparative, randomized interventional hospital based study. Methodology: Hundred and ten diagnosed patients of severe alcoholic hepatitis who fulfilled the criteria were enrolled and randomized into two groups (odd number and even number). Group 1 received methylprednisolone and group 2 received pentoxifylline for 28 days. In both groups N acetylcysteine were added. Lille score was calculated in methylprednisolone group at day 7 and patients with score of ≤ 0.45 were continued methylprednisolone for total 28 days otherwise stopped. Data were recollected at day 28. They were compared in relation to survival, complications of drugs and causes of mortality. Results: Mean age of presentation were 40.21±10.5 yrs in methylprednisolone and 42.1±12.1 yrs in pentoxifylline group. In both groups complications were nausea, vomiting, bloating, anorexia and swelling of limb. However, hyperglycemia (16.4%) and renal impairment (9.1%) were more common in methylprednisolone group. Mortality rates were 34.5% in methylprednisolone and 37.8% in pentoxifylline group within 28 days. Common causes of death in both groups were hepatic encephalopathy, hepatorenal syndrome, sepsis or the cause was undetermined. Conclusion: Alcoholic hepatitis is common manifestation of alcoholic liver disease with high short term mortality in both the groups however adverse effects of drugs are more common in methylprednisolone groups.
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