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Advances in cirrhosis: Optimizing the management of hepatic encephalopathy 被引量:3
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作者 Andy Liu Ryan B Perumpail +3 位作者 radhika kumari Zobair M Younossi Robert J Wong Aijaz Ahmed 《World Journal of Hepatology》 CAS 2015年第29期2871-2879,共9页
Hepatic encephalopathy(HE) is a major complication of cirrhosis resulting in significant socioeconomic burden, morbidity, and mortality. HE can be further subdivided into covert HE(CHE) and overt HE(OHE). CHE is a sub... Hepatic encephalopathy(HE) is a major complication of cirrhosis resulting in significant socioeconomic burden, morbidity, and mortality. HE can be further subdivided into covert HE(CHE) and overt HE(OHE). CHE is a subclinical, less severe manifestation of HE and requires psychometric testing for diagnosis. Due to the time consuming screening process and lack of standardized diagnostic criteria, CHE is frequently underdiagnosed despite its recognized role as a precursor to OHE. Screening for CHE with the availability of the Stroop test has provided a pragmatic method to promptly diagnose CHE. Management of acute OHE involves institution of lactulose, the preferred first-line therapy. In addition, prompt recognition and treatment of precipitating factors is critical as it may result in complete resolution of acute episodes of OHE. Treatment goals include improvement of daily functioning, evaluation for liver transplantation, and prevention of OHE recurrence. For secondary prophylaxis, intolerance to indefinite lactulose therapy may lead to non-adherence and has been identified as a precipitating factor for recurrent OHE. Rifaximin is an effective add-on therapy to lactulose for treatment and prevention of recurrent OHE. Recent studies have demonstrated comparable efficacy of probiotic therapy to lactulose use in both primary prophylaxis and secondary prophylaxis. 展开更多
关键词 Overt HEPATIC ENCEPHALOPATHY LACTULOSE RIFAXIMIN HEPATIC ENCEPHALOPATHY Covert HEPATICENCEPHALOPATHY
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Sofosbuvir Use in the Setting of End-stage Renal Disease:A Single Center Experience 被引量:2
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作者 Avin Aggarwal Eric R.Yoo +5 位作者 Ryan B.Perumpail George Cholankeril radhika kumari Tami J.Daugherty Alex S.Lapasaran Aijaz Ahmed 《Journal of Clinical and Translational Hepatology》 SCIE 2017年第1期23-26,共4页
Background and Aims:Patients with chronic hepatitis C (CHC) and end-stage renal disease (ESRD) who are dialysisdependent form a unique group,in which safety,tolerability and efficacy of sofosbuvir (SOF)-based direct-a... Background and Aims:Patients with chronic hepatitis C (CHC) and end-stage renal disease (ESRD) who are dialysisdependent form a unique group,in which safety,tolerability and efficacy of sofosbuvir (SOF)-based direct-acting antivirals (DAAs) need further evaluation.Methods:We performed a retrospective analysis of 14 patients with CHC and ESRD on dialysis who received 15 courses of SOF-based therapy.We evaluated dose escalation to standard-dose SOF in this proof-of-principle experience.Results:Sustained virological response (defined as undetectable viral load at 12 weeks,SVR-12) was achieved in 13 out of the 15 (86.7%) treatment courses.Seven (46.6%) patients received reduced half dose as conservative proof-of-principal to mitigate potential toxicity.In 13 out of 15 treatment courses,patients completed the designated treatment duration.One patient was treated twice and developed SVR-12 with the retreatment.One patient was lost to follow-up and counted as a non-responder.Premature discontinuations were not due to DAA-related adverse effects.There were no reports of severe adverse effects or drug interactions.Conclusion:We treated CHC patients with ESRD using dose escalation to standard-dose SOF in this proof-of-principle experience and achieved SVR rates comparable to general population. 展开更多
关键词 Hepatitis C End-stage renal disease Sofosbuvir Direct-acting antivirals
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