Institute of Clinical Medical Science, China Medical University.
Department of Psychiatry & Brain Disease Research Center, China Medical University Hospital, Taichung.
Medicine (Baltimore). 2021 Jun 4;100(22):e26218. doi: 10.1097/MD.0000000000026218.
This study evaluated the severe hepatic outcome (SHO) in patients with schizophrenia and viral hepatitis who received antipsychotics.Using the nationwide Taiwan National Health Insurance Research Database, patients first diagnosed with schizophrenia between 2002 and 2013 were identified. Patients diagnosed with schizophrenia who had viral hepatitis, including hepatitis B virus (HBV) or hepatitis C virus (HCV), were designated as the viral hepatitis group. A control group without viral hepatitis was matched for age, sex, and index year in a 2:1 ratio. Patients with severe hepatic outcomes before enrollment were excluded. The 2 cohorts were observed until December 31, 2013. The primary endpoint was occurrence of a SHO, including liver cancer, liver failure, liver decompensation, or transplantation.Among the 16,365 patients newly diagnosed with schizophrenia between January 2002 and December 2013, we identified 614 patients with viral hepatitis and 1228 matched patients without viral hepatitis. Of these 1842 patients, 41 (2.22%) developed SHOs, including 26 (4.23%) in the viral hepatitis group and 15 (1.22%) in the control group, during the mean follow-up period of 3.71 ± 2.49 years. Cox proportional hazard analysis indicated that the SHO risk increased by 3.58 (95% confidence interval [CI]: 1.859-6.754; P < .001) in patients with schizophrenia and viral hepatitis. Moreover, patients with schizophrenia having HCV had a higher SHO risk than those without viral hepatitis (hazard ratio: 5.07, 95% CI: 1.612-15.956; P < .0001). Patients having both schizophrenia and viral hepatitis, especially HCV, had a higher risk of SHOs.
这项研究评估了接受抗精神病药物治疗的患有精神分裂症和病毒性肝炎的患者的严重肝脏结局 (SHO)。使用全国性的台湾全民健康保险研究数据库,确定了 2002 年至 2013 年间首次被诊断患有精神分裂症的患者。患有病毒性肝炎(包括乙型肝炎病毒 [HBV] 或丙型肝炎病毒 [HCV])的患者被指定为病毒性肝炎组。以 2:1 的比例按年龄、性别和索引年份与无病毒性肝炎的对照组相匹配。排除了入组前患有严重肝脏结局的患者。两组患者均观察至 2013 年 12 月 31 日。主要终点是发生 SHO,包括肝癌、肝功能衰竭、肝代偿失调或肝移植。在 2002 年 1 月至 2013 年 12 月期间新诊断患有精神分裂症的 16365 名患者中,我们确定了 614 名患有病毒性肝炎的患者和 1228 名匹配的无病毒性肝炎患者。在这 1842 名患者中,41 名(2.22%)发生了 SHO,其中病毒性肝炎组 26 名(4.23%),对照组 15 名(1.22%),平均随访时间为 3.71±2.49 年。Cox 比例风险分析表明,患有精神分裂症和病毒性肝炎的患者 SHO 风险增加了 3.58(95%置信区间 [CI]:1.859-6.754;P<.001)。此外,患有 HCV 的精神分裂症患者 SHO 风险高于无病毒性肝炎的患者(风险比:5.07,95%CI:1.612-15.956;P<.0001)。患有精神分裂症和病毒性肝炎,特别是 HCV 的患者 SHO 风险更高。