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首页> 外文期刊>The annals of pharmacotherapy >Hepatitis after intravenous injection of sublingual buprenorphine in acute hepatitis C carriers: report of two cases of disappearance of viral replication after acute hepatitis.
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Hepatitis after intravenous injection of sublingual buprenorphine in acute hepatitis C carriers: report of two cases of disappearance of viral replication after acute hepatitis.

机译:急性丙型肝炎携带者静脉注射舌下丁丙诺啡后的肝炎:两例急性肝炎后病毒复制消失的报道。

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摘要

OBJECTIVE: To report 2 cases of acute hepatitis related to intravenous administration of buprenorphine in hepatitis C-infected patients. CASE SUMMARY: Two patients, aged 33 and 50 years, respectively, who were hepatitis C virus (HCV) carriers were treated with sublingual buprenorphine 8 mg/day for addiction. Several years after initiation of buprenorphine, they were hospitalized because of clinical hepatitis with jaundice that developed after intravenous injection of buprenorphine. Serum alanine aminotransferase rose to 100 times the upper limit of normal (ULN) in the first patient and to 21 times the ULN in the second. As cofactors, the first patient had consumed alcohol, and the second patient took aspirin 600 mg in addition to the injection of buprenorphine 20 mg 4 days before the onset of jaundice. After stopping the intravenous injections, both patients continued sublingual buprenorphine therapy, with no relapse of hepatitis. Interestingly, in these 2 patients, buprenorphine-induced hepatitis was followed by the disappearance of HCV RNA. DISCUSSION: Most cases of hepatotoxicity related to buprenorphine have occurred in hepatitis C-infected patients. The main mechanism for buprenorphine-induced hepatitis is a mitochondrial defect, exacerbated by cofactors with additional potential to induce mitochondria dysfunction (eg, HCV, alcohol, concomitant medications). According to the Naranjo probability scale, buprenorphine was found to be the probable cause of acute hepatitis in both patients. In addition, we assessed the relationship between intravenous buprenorphine and acute hepatitis using 2 scales for causality assessment of hepatotoxicity (the Council for International Organizations of Medical Sciences scale and the Maria & Victorino scale). The diagnosis of intravenous buprenorphine-induced hepatitis was classified as probable in both cases. In addition, these 2 cases illustrate that acute hepatitis in a carrier of chronic HCV may occasionally facilitate the clearance of virus. CONCLUSIONS: Although buprenorphine is well tolerated when used at recommended sublingual doses, patients should be informed about the risk of acute hepatitis with misuse of the drug by the intravenous route. These cases illustrate that, in carriers of chronic HCV, acute hepatitis may modify the host's immunotolerance and facilitate clearance of the virus.
机译:目的:报告2例丙型肝炎感染者静脉注射丁丙诺啡相关的急性肝炎。病例摘要:两名分别为33岁和50岁的丙型肝炎病毒(HCV)携带者接受舌下丁丙诺啡8毫克/天的治疗,以致成瘾。丁丙诺啡开始使用后的几年,由于临床肝炎伴有静脉注射丁丙诺啡后出现黄疸,因此将其住院。第一位患者的血清丙氨酸氨基转移酶升高至正常上限(ULN)的100倍,第二位患者升高至正常值(ULN)的21倍。作为辅助因子,第一位患者饮酒,第二位患者在黄疸发作前4天服用丁丙诺啡20 mg,此外还服用阿司匹林600 mg。停止静脉注射后,两名患者继续进行舌下丁丙诺啡治疗,无肝炎复发。有趣的是,在这2例患者中,丁丙诺啡诱发的肝炎之后是HCV RNA的消失。讨论:大多数与丁丙诺啡有关的肝毒性病例发生在丙型肝炎感染患者中。丁丙诺啡引起的肝炎的主要机制是线粒体缺陷,辅因子加重了线粒体的功能,可能会诱发线粒体功能障碍(例如,HCV,酒精,药物)。根据Naranjo概率量表,发现丁丙诺啡是两名患者中急性肝炎的可能原因。另外,我们使用2种量表对肝毒性的因果关系评估(国际医学组织理事会量表和Maria&Victorino量表)评估了静脉丁丙诺啡与急性肝炎之间的关系。在两种情况下,静脉丁丙诺啡诱发的肝炎的诊断均被分类为可能。此外,这2例病例表明,慢性HCV携带者中的急性肝炎有时可能会促进病毒清除。结论:尽管丁丙诺啡以推荐的舌下剂量使用时耐受性良好,但应告知患者静脉途径滥用药物会导致急性肝炎的风险。这些案例说明,在慢性HCV携带者中,急性肝炎可能会改变宿主的免疫耐受性并促进病毒清除。

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