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2
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本文引用的文献

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Glecaprevir-Pibrentasvir for 8 or 12 Weeks in HCV Genotype 1 or 3 Infection.格卡瑞韦哌仑他韦片治疗 8 或 12 周用于治疗 1 型或 3 型丙型肝炎病毒感染。
N Engl J Med. 2018 Jan 25;378(4):354-369. doi: 10.1056/NEJMoa1702417.
2
Safety and efficacy of sofosbuvir-containing regimens in hepatitis C-infected patients with impaired renal function.含索磷布韦方案在肾功能受损的丙型肝炎感染患者中的安全性和有效性。
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3
Sofosbuvir and Velpatasvir for HCV Genotype 2 and 3 Infection.索磷布韦和维帕他韦治疗 2 型和 3 型丙型肝炎病毒感染。
N Engl J Med. 2015 Dec 31;373(27):2608-17. doi: 10.1056/NEJMoa1512612. Epub 2015 Nov 17.
4
An update on the management of chronic hepatitis C: 2015 Consensus guidelines from the Canadian Association for the Study of the Liver.慢性丙型肝炎管理的最新进展:加拿大肝病研究协会 2015 年共识指南。
Can J Gastroenterol Hepatol. 2015 Jan-Feb;29(1):19-34. doi: 10.1155/2015/692408. Epub 2015 Jan 13.
5
Does Therapeutic Drug Monitoring of Ribavirin in HCV Genotype 3 Treatment With Sofosbuvir and Ribavirin Still Have a Role?在索磷布韦和利巴韦林治疗丙型肝炎病毒3型时,利巴韦林的治疗药物监测是否仍有作用?
Ther Drug Monit. 2015 Aug;37(4):550-1. doi: 10.1097/FTD.0000000000000161.
6
Sofosbuvir and ribavirin in HCV genotypes 2 and 3.索磷布韦和利巴韦林治疗 2 型和 3 型丙型肝炎病毒。
N Engl J Med. 2014 May 22;370(21):1993-2001. doi: 10.1056/NEJMoa1316145. Epub 2014 May 4.
7
Peginterferon alfa-2a with or without low-dose ribavirin for treatment-naive patients with hepatitis C virus genotype 2 receiving haemodialysis: a randomised trial.聚乙二醇干扰素 alfa-2a 联合或不联合低剂量利巴韦林治疗初治丙型肝炎病毒基因型 2 接受血液透析的患者:一项随机试验。
Gut. 2015 Feb;64(2):303-11. doi: 10.1136/gutjnl-2014-307080. Epub 2014 Apr 19.
8
Pharmacokinetics of tacrolimus during pregnancy.环孢素 A 在妊娠期的药代动力学。
Ther Drug Monit. 2012 Dec;34(6):660-70. doi: 10.1097/FTD.0b013e3182708edf.
9
Pharmacokinetics, safety, and tolerability of ribavirin in hemodialysis-dependent patients.依赖血液透析患者中利巴韦林的药代动力学、安全性和耐受性。
Eur J Clin Pharmacol. 2012 Apr;68(4):415-8. doi: 10.1007/s00228-011-1137-x. Epub 2011 Oct 27.
10
Pegylated interferon alpha-2a plus low-dose ribavirin for the retreatment of dialysis chronic hepatitis C patients who relapsed from prior interferon monotherapy.聚乙二醇化干扰素α-2a联合小剂量利巴韦林用于对先前干扰素单药治疗后复发的透析慢性丙型肝炎患者进行再治疗。
Gut. 2009 Feb;58(2):314-6. doi: 10.1136/gut.2008.165076.

利巴韦林诱发的贫血降低了一名接受血液透析的丙型肝炎患者的他克莫司血药浓度。

Ribavirin-induced anaemia reduced tacrolimus level in a hepatitis C patient receiving haemodialysis.

作者信息

Liu Hin-Yee, Cheung Catherine Yuen Shan, Cooper Susan Elizabeth

机构信息

Dialysis Unit, Fraser Health, Abbotsford, British Columbia, Canada.

出版信息

BMJ Case Rep. 2018 Apr 18;2018:bcr-2017-222477. doi: 10.1136/bcr-2017-222477.

DOI:10.1136/bcr-2017-222477
PMID:29669765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5911140/
Abstract

A 37-year-old man with hepatitis C virus (HCV) genotype 3A developed renal failure. In 2007, the patient received a renal transplant and started receiving tacrolimus (Tac); the transplant subsequently failed. In April 2015, the patient restarted haemodialysis and in May initiated sofosbuvir 400 mg and ribavirin 400 mg daily. Baseline Tac level was 6.6 ng/mL and haemoglobin (Hb) was 10.3 g/dL. The patient then left the country for vacation and Hb was found to be dramatically low at 3.7 g/dL on return on 5 August. Ribavirin was put on hold, while darbepoetin dose was increased. On 23 August, Tac level was found undetectable; hence, dosage was increased. Hb eventually bounced back to >10 g/dL in October and Tac to 7.2 ng/mL; ribavirin was restarted at 200 mg three times weekly. HCV RNA level was undetectable at 3 months and remained undetectable 12 weeks after therapy finished.

摘要

一名37岁的丙型肝炎病毒(HCV)基因3A感染者出现了肾衰竭。2007年,该患者接受了肾移植,并开始使用他克莫司(Tac);随后移植失败。2015年4月,患者重新开始血液透析,并于5月开始每日服用400毫克索磷布韦和400毫克利巴韦林。基线Tac水平为6.6纳克/毫升,血红蛋白(Hb)为10.3克/分升。该患者随后出国度假,8月5日回国时发现Hb大幅降至3.7克/分升。利巴韦林暂停使用,同时增加了促红细胞生成素的剂量。8月23日,发现Tac水平检测不到;因此,增加了剂量。Hb最终在10月回升至>10克/分升,Tac升至7.2纳克/毫升;利巴韦林以每周三次、每次200毫克的剂量重新开始使用。治疗3个月时HCV RNA水平检测不到,治疗结束12周后仍检测不到。