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Ribavirin Impairs Salivary gland function During Combination Treatment With Pegylated Interferon Alfa-2a In HEpatitis C patients

机译:利巴韦林与聚乙二醇化干扰素Alfa-2a联合治疗丙型肝炎患者期间唾液腺功能受损

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Background: Xerostomia is a common adverse event of unknown etiology observed during pegylated interferon (PegIFN)/Ribavirin (Rbv) treatment. Objectives: To assess the frequency and mechanisms of xerostomia during PegIFN/Rbv therapy. Patients and Methods: Thirty-one na?ve patients with chronic hepatitis C consecutively received PegIFN-α2a (180 μg/week) plus Rbv (800-1200 mg/day). The controls were 10 patients with chronic hepatitis B who received PegIFN-α2a (180 μg/week). During treatment and follow-up, all patients underwent basal and masticatory stimulated sialometry, otorhinolaryngoiatric (ORL) examination, and a questionnaire survey to subjectively assess symptoms of oral dryness. Results: Twenty-seven patients on PegIFN/Rbv and 4 on PegIFN (87% vs. 40%, P = 0.006) reported xerostomia. Thirty patients on PegIFN/Rbv combination therapy and 2 patients on monotherapy had ORL signs of salivary gland hypofunction (97% vs. 20%, P < 0.0001). Mean basal (A) and stimulated (B) salivary flow rates (mL/min) progressively decreased during PegIFN/Rbv treatment (A, 0.49 at baseline vs. 0.17 at the end of treatment, P < 0.0001; B, 1.24 at baseline vs. 0.53 at the end of treatment, P = 0.0004). At week 24 following PegIFN/Rbv treatment, salivary flow rates were similar to baseline (A, 0.53 at the end of follow-up vs. 0.49 at baseline; B, 1.19 at the end of follow-up vs. 1.24 at baseline). Salivary function was unaffected in monotherapy patients. Conclusions: Rbv causes salivary gland hypofunction in hepatitis C patients receiving PegIFN/Rbv therapy, which promptly reverts to normal upon cessation of treatment. Implication for health policy/practice/research/medical education: The implications of the present study can be useful to correctly manage the side effects of Ribavirin. Indeed Ribavirin is not only a key player of the current standard of care regimen for chronic hepatitis C, but will also remain crucial for achieving optimal sustained virological response rates once the first and second generation of directly acting antiviral agents become available worldwide. Please cite this paper as: Aghemo A, Rumi MG, Monico S, Banderali M, Russo A, Ottaviani F, et al. Ribavirin Impairs Salivary Gland Function in Hepatitis C Patients During Combination Treatment With Pegylated Interferon Alfa-2a. Hepat Mon. 2011; 11(11):918-24.DOI:10.5812/kowsar.1735143X.733.
机译:背景:口干症是在聚乙二醇干扰素(PegIFN)/利巴韦林(Rbv)治疗期间观察到的病因不明的常见不良事件。目的:评估PegIFN / Rbv治疗期间口干症的发生频率和机制。患者和方法:31名初治的慢性丙型肝炎患者连续接受PegIFN-α2a(180μg/周)和Rbv(800-1200 mg /天)。对照组为10例接受PegIFN-α2a(180μg/周)的慢性乙型肝炎患者。在治疗和随访期间,所有患者均接受了基础和咀嚼刺激的唾液酸测定法,耳鼻咽喉科(ORL)检查和问卷调查,以主观评估口腔干燥的症状。结果:27例接受PegIFN / Rbv的患者和4例接受PegIFN的患者(87%比40%,P = 0.006)报告有口干症。接受PegIFN / Rbv联合治疗的30例患者和接受单一疗法的2例患者存在唾液腺功能减退的ORL征象(97%vs. 20%,P <0.0001)。在PegIFN / Rbv治疗期间,唾液平均基础流速(A)和刺激流速(B)逐渐降低(A,基线时为0.49,治疗结束时为0.17,P <0.0001; B,基线时为1.24,VS 0.53在治疗结束时,P = 0.0004)。 PegIFN / Rbv治疗后第24周,唾液流速与基线相似(A,随访结束时为0.53,基线为0.49; B,随访结束时为1.19,基线时为1.24)。单药治疗患者的唾液功能不受影响。结论:Rbv导致接受PegIFN / Rbv治疗的丙型肝炎患者唾液腺功能低下,在停止治疗后可迅速恢复正常。对健康政策/实践/研究/医学教育的意义:本研究的意义对于正确管理利巴韦林的副作用可能是有用的。确实,利巴韦林不仅是当前慢性丙型肝炎治疗方案标准的关键参与者,而且一旦第一代和第二代直接作用的抗病毒药物在全球范围内普及,对于保持最佳的持续病毒学应答率也将至关重要。请将本文引用为:Aghemo A,Rumi MG,Monico S,Banderali M,Russo A,Ottaviani F等。利巴韦林在聚乙二醇化干扰素Alfa-2a联合治疗期间损害丙型肝炎患者的唾液腺功能。肝星期一2011; 11(11):918-24.DOI:10.5812 / kowsar.1735143X.733。

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