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作 者:邱源旺[1] 黄利华[1] 华海涌[2] 牛雪花 吴鹏飞 吴杭源[1] 朱宏英[1] 杨小娟[1] 姚上志[1] 李燚光[1]
机构地区:[1]无锡市传染病医院肝病科,214000 [2]江苏省寄生虫病防治研究所 [3]昆山第三人民医院消化内科
出 处:《中华传染病杂志》2012年第4期231-234,共4页Chinese Journal of Infectious Diseases
基 金:江苏省卫生厅血地寄防应用性科研课题资助项目(X200913)
摘 要:目的观察恩替卡韦(ETV)治疗合并HBV感染的晚期血吸虫病的疗效及安全性。方法将确诊的60例合并HBV感染的晚期血吸虫病患者分为ETV治疗组30例,大黄治疗组30例(拒绝接受抗病毒治疗),两组在常规治疗基础上分别加用ETV、大黄蛰虫丸治疗,疗程均为52周。比较两组HA、PCⅢ、ⅣC、LN、纤维连接蛋白(FN)等肝纤维化指标及ALT、HBVDNA、Child—Pugh评分结果。分析采用意向性治疗原则(ITT)方法,计量数据和计数数据分别采用t检验和X2检验。结果治疗52周时,ETV治疗组患者HA、PCⅢ、IVC、LN、FN均明显改善,与大黄治疗组比较,差异均有统计学意义(t=3.952、3.765、3.857、3.122、3.735,均Pd0.05);ETV治疗组部分患者肝组织肝纤维化程度改善,与大黄治疗组比较,差异有统计学意义(X2=11.207,P〈0.05);ETV治疗组患者ALT、HBVDNA、Child-Pugh评分结果较大黄治疗组明显下降,两组比较,差异均有统计学意义(t=3.287、4.382、3.872,均P〈0.05);ETV治疗组ALT复常率、HBVDNA在检测水平以下的比率较大黄治疗组明显升高,两组比较,差异有统计学意义(X2=17.376、39.095,均P〈0.05);且ETV治疗组未出现严重不良反应。结论ETV治疗合并HBV感染的晚期血吸虫病患者安全有效。Objective To evaluate the efficacy and safety profiles of entecavir (ETV) in patients with advanced schistosomiasis and hepatitis B virus (HBV) co-infection. Methods Totally sixty patients with advanced schistosomiasis and HBV co-infection were enrolled in this study. The patients were divided into ETV treatment group (n=30) and rhubarb treatment group who refused to receive antiviral treatment (n= 30). The patients were treated with ETV or rhubarb thelepus ball on the basis of routine supportive therapy for 52 weeks. The hepatic fibrosis markers (e. g. hyaluronic acid, type Ⅲ procollagen, type Ⅳ collagen, laminin and fibronectin), alanine transaminase (ALT), HBV DNA, Child-Pugh score between two groups were compared. Intention to treat (ITT) population was used for analysis. The measurement data and the enumeration data were analyzed by t test and X2 test, respectively. Results After 52-week treatment, the hepatic fibrosis markers (hyaluronic acid, type Ⅲ procollagen, type Ⅳ collagen, laminin and fibronectin) were significantly improved in ETV treatment group compared to the rhubarb treatment group (t = 3. 952, 3.765, 3.857, 3. 122 and 3. 735,respectively; all P〈0.05), and the fibrosis of liver tissue in ETV treatment group was significantly improved compared with rhubarb treatment group (X2 = 11. 207, P〈0.05 ). The ALT level, HBV DNA, Child-Pugh score after 52-weeks treatment in ETV treatment group were statistically reduced compared with rhubarb treatment group (t=3. 287, 4. 382 and 3. 872, respectively; all P〈0.05), meanwhile, the ALT normalization rate and HBV DNA undetectable rate were significantly increased in ETV treatment group (X2 = 17. 376 and 39. 095, respectively; both P〈0.05). In addition, no obvious adverse reaction was observed during ETV treatment. Conclusion Entecavir is safe and effective in patients with advanced schistosomiasis and HBV co-infection.
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