Segamwenge Innocent Lule, Bernard Miriam Kaunanele
Department of Internal Medicine, Intermediate Hospital Oshakati, Oshakati, Namibia.
Case Reports Hepatol. 2018 May 10;2018:1270716. doi: 10.1155/2018/1270716. eCollection 2018.
To describe the clinical characteristics of patients presenting with fulminant liver failure after varying periods of exposure to Efavirenz containing antiretroviral medications.
We report a series of 4 patients with human immunodeficiency virus (HIV) infection who were admitted with acute liver failure (ALF) over a 6-month period. All these patients had been treated with a range of Efavirenz containing antiretroviral regimens and were negative for hepatitis A, B, and C infections as well as other opportunistic infections, all were negative for autoimmune hepatitis, and none had evidence of chronic liver disease or use of alcohol or herbal medications. Information on patient clinical characteristics, current antiretroviral regimen, CD4 count, HIV-1 RNA levels, and clinical chemistry parameters was collected. Informed consent was provided.
During a 6-month period, four patients without other known risk factors for acute hepatitis presented with symptomatic drug-induced liver injury with varying symptoms and outcomes. The pattern of liver injury was hepatocellular for all the 4 cases. Liver biopsies were done for all the four cases and the results showed a heavy mixed inflammatory cell infiltrate with eosinophils. For three patients withdrawal of Efavirenz from their antiretroviral regimen was sufficient to restore transaminase levels to normal and led to improvement of clinical symptoms. For one patient his clinical course was characterized by fulminant liver failure and fluctuating episodes of hepatic encephalopathy which ultimately resulted in his death.
Hepatotoxicity of Efavirenz is not as rare as previously described in the literature and does actually present with fatal outcomes. The key message to note is that frequent monitoring of liver enzymes should be done at initiation of antiretroviral therapy and should continue throughout the treatment period.
描述在接触含依非韦伦的抗逆转录病毒药物不同时间段后出现暴发性肝衰竭患者的临床特征。
我们报告了一系列4例人类免疫缺陷病毒(HIV)感染患者,他们在6个月内因急性肝衰竭(ALF)入院。所有这些患者都接受过一系列含依非韦伦的抗逆转录病毒治疗方案,甲型、乙型和丙型肝炎感染以及其他机会性感染检测均为阴性,自身免疫性肝炎检测均为阴性,且均无慢性肝病证据,未使用酒精或草药。收集了患者的临床特征、当前抗逆转录病毒治疗方案、CD4细胞计数、HIV-1 RNA水平和临床化学参数等信息。已获得知情同意。
在6个月期间,4例无其他已知急性肝炎危险因素的患者出现了有症状的药物性肝损伤,症状和结局各不相同。4例患者的肝损伤模式均为肝细胞型。对所有4例患者均进行了肝活检,结果显示有大量混合性炎性细胞浸润,伴有嗜酸性粒细胞。对于3例患者,从其抗逆转录病毒治疗方案中停用依非韦伦足以使转氨酶水平恢复正常,并导致临床症状改善。对于1例患者,其临床病程以暴发性肝衰竭和肝性脑病波动发作为特征,最终导致死亡。
依非韦伦的肝毒性并不像文献中先前描述的那样罕见,实际上确实会导致致命后果。需要注意的关键信息是,在开始抗逆转录病毒治疗时应频繁监测肝酶,并应在整个治疗期间持续监测。