用纤维扫描评价β-地中海贫血感染丙型肝炎病毒儿童在雷地帕韦/索非布韦治疗前后肝纤维化的疗效

Aya Lotfy Yosef, Hanan H Soliman, G. Shiha, Mohiee Eldeen Abdelaziz Awad, Eslam E El-Hawary
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引用次数: 0

摘要

背景:地中海贫血儿童由于肝铁超载和丙型肝炎病毒(HCV)感染而发生肝纤维化。瞬时弹性成像(FibroScan)是评估地中海贫血患者肝纤维化的一种可靠的无创方法。使用ledipasvir/sofosbuvir (LED/SOF)直接作用抗病毒药物治疗可显著影响FibroScan肝硬度测量(LSM)。原创研究文章Yosef et al.;Ibrr, 11(3): 9-17, 2020;文章no.IBRR。目的:通过LSM无创纤维扫描评估多次输血感染HCV的β-地中海贫血儿童在通用LED/SOF治疗前后的肝纤维化情况。研究地点和时间:2017年11月至2019年5月,坦塔大学附属医院儿科血液科。方法:对50例经多次输血的慢性HCV感染的β-地中海贫血treatment-naϊve患儿(年龄12-18岁,体重≥35kg)进行临床评价、定量HCV PCR检测、FibroScan检查,并计算APRI、FIB4指数和AST/ ALT比值。除标准治疗外,给予通用LED/SOF (90/400 mg)治疗12周,治疗结束后再随访12周。结果:从治疗后第4周开始,所有研究患者的HCV PCR阳性变为阴性。治疗后,纤维扫描的LSM值显著降低(p值<0.001),中位降低率为19.4%。LSM值的显著降低在严重(F2)和晚期(F3)肝纤维化患者以及肝硬化患者(F4)中尤为突出。治疗后其他非侵袭性肝纤维化指标FIB-4指数、APRI评分和AST/ ALT比值均显著降低(p值分别<0.001、<0.001和0.020)。结论:为期12周的通用LED/SOF治疗可根除HCV感染,这与FibroScan的LSM显著降低有关,特别是那些基线肝纤维化分期较高的患者。
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Evaluation of Liver Fibrosis by FibroScan in β-Thalassemia Children Infected with Hepatitis C Virus Before and After Ledipasvir/Sofosbuvir Therapy
Background: Thalassemic children develop liver fibrosis because of liver iron overload and hepatitis C virus (HCV) infection. Transient elastography (FibroScan) can be a reliable non-invasive method for evaluating liver fibrosis in thalassemic patients. Treatment with ledipasvir/sofosbuvir (LED/SOF) direct acting antiviral agents can significantly affect liver stiffness measurement (LSM) by FibroScan. Original Research Article Yosef et al.; IBRR, 11(3): 9-17, 2020; Article no.IBRR.60361 10 Aims: To assess liver fibrosis by non-invasive FibroScan through LSM before and after generic LED/SOF therapy in multi-transfused β-thalassemic children infected with HCV. Place and Duration of Study: Pediatric Hematology Unit, Tanta University Hospital, from November 2017 to May 2019. Methodology: Fifty multi-transfused β-thalassemic treatment-naϊve children (aged 12-18 years and weighing ≥35kg) with chronic HCV infection were subjected to clinical evaluation, quantitative HCV PCR assay, FibroScan examination, and calculation of APRI, FIB4 index and AST/ ALT ratio. In addition to standard therapy, generic LED/SOF (90/400 mg) treatment was given for 12 weeks’ duration with follow up for further 12 weeks after end of treatment. Results: A positive HCV PCR was changed into negative for all studied patients starting from week 4 after treatment. There was highly significant reduction in the LSM values by FibroScan in the studied patients after therapy (p-value <0.001) with median reduction of 19.4 %. The significant reduction in LSM values was particularly prominent in patients with significant (F2) and advanced (F3) liver fibrosis stages as well as cirrhotic patients (F4). There was significant reduction in the values of other non-invasive liver fibrosis markers FIB-4 index, APRI score and AST/ ALT ratio (pvalue <0.001, <0.001 and 0.020 respectively) after therapy. Conclusion: Generic LED/SOF therapy for 12 weeks’ duration resulted in eradication of HCV infection that was associated with significant decrease in LSM by FibroScan particularly those with higher baseline liver fibrosis stages.
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