Hepatic Medicine : Evidence and Research最新文献

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Chemical Risk Factors of Primary Liver Cancer: An Update. 原发性肝癌的化学危险因素:最新进展
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2021-01-05 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S278070
Adam Barsouk, Krishna Chaitanya Thandra, Kalyan Saginala, Prashanth Rawla, Alexander Barsouk
{"title":"Chemical Risk Factors of Primary Liver Cancer: An Update.","authors":"Adam Barsouk,&nbsp;Krishna Chaitanya Thandra,&nbsp;Kalyan Saginala,&nbsp;Prashanth Rawla,&nbsp;Alexander Barsouk","doi":"10.2147/HMER.S278070","DOIUrl":"https://doi.org/10.2147/HMER.S278070","url":null,"abstract":"<p><p>Primary liver cancer has the sixth highest incidence and fourth highest cancer mortality worldwide. Hepatitis B is the leading cause of liver cancer, though its incidence is decreasing with vaccination. Alcohol is the leading cause of liver transplant, cirrhosis, and cancer in the developed world, and is projected to surpass hepatitis B as the leading hepatic cancer etiology worldwide. Tobacco smoking has shown a positive association with liver cancer in a majority of studies, though not all. Aflatoxin, a mycotoxin produced by <i>Aspergillus</i>, is estimated to account for 3-20% of global liver cancer cases, 40% of which occur in sub-Saharan Africa. These statistics are confounded by the prevalence of hepatitis B, which may have a synergistic effect on hepatic carcinogenesis. Aflatoxin is ingested and likely inhaled from agricultural products, placing farmers, food processors, and textile workers in developing nations at risk. Vinyl-chloride is used in the production of PVC plastics and causes rare liver angiosarcoma, hepatocellular carcinoma, and other neoplasms. Arsenic and cadmium are naturally-occurring, hepatocarcinogenic metals with high occupational exposure in industries involving coal, metals, plastics, and batteries. Millions of laborers in waste-disposal and manufacturing are exposed to organic solvents and N-nitrosamines, which vary from carcinogenic (group 1) to possibly carcinogenic (group 2B) in their IARC designation. Insecticide DDT is possibly hepatocarcinogenic (group 2B), though continues to be used for malaria control in the developing world. While suggested by case reports, anabolic steroids and oral contraceptives have not been shown to increase liver cancer risk in large studies.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"179-188"},"PeriodicalIF":2.1,"publicationDate":"2021-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a3/0c/hmer-12-179.PMC7801911.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38820936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
Repurposing of N-Acetylcysteine for the Treatment of Dengue Virus-Induced Acute Liver Failure. n -乙酰半胱氨酸用于治疗登革病毒诱导的急性肝衰竭。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-11-03 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S263840
Gebrehiwot Gebremedhin Tafere, Dawit Zewdu Wondafrash, Filmon Beyenne Demoz
{"title":"Repurposing of N-Acetylcysteine for the Treatment of Dengue Virus-Induced Acute Liver Failure.","authors":"Gebrehiwot Gebremedhin Tafere,&nbsp;Dawit Zewdu Wondafrash,&nbsp;Filmon Beyenne Demoz","doi":"10.2147/HMER.S263840","DOIUrl":"https://doi.org/10.2147/HMER.S263840","url":null,"abstract":"<p><p>The prevalence of dengue infection-induced acute liver damage is increasing from time to time. Since it has no specific antiviral treatment in the world, people in endemic areas suffer more from dengue disorders. Thus, there is a need for searching options for the treatment of dengue-induced acute liver failure. N-acetylcysteine, which is used for the treatment of nasal congestion disorder and paracetamol overdose toxicity, could be used as a definitive therapy for dengue virus-induced acute liver disease. Therefore, this review discusses the therapeutic use of N-acetylcysteine for dengue-induced acute liver disease. Various case reports and case series showed that patients received NAC recovered from their clinical status. Additionally, a preclinical study showed that N-acetylcysteine has anti-dengue virus activity. Thus, N-acetylcysteine could be used as a definitive therapy in dengue virus-induced hepatitis. This might encourage researchers to further investigate the importance of N-acetylcysteine for dengue virus-induced hepatitis.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"173-178"},"PeriodicalIF":2.1,"publicationDate":"2020-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S263840","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38592834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Albumin Administration is Efficacious in the Management of Patients with Cirrhosis: A Systematic Review of the Literature. 白蛋白在肝硬化患者的治疗中是有效的:文献系统综述。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-10-27 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S264231
Giacomo Zaccherini, Manuel Tufoni, Mauro Bernardi
{"title":"Albumin Administration is Efficacious in the Management of Patients with Cirrhosis: A Systematic Review of the Literature.","authors":"Giacomo Zaccherini,&nbsp;Manuel Tufoni,&nbsp;Mauro Bernardi","doi":"10.2147/HMER.S264231","DOIUrl":"https://doi.org/10.2147/HMER.S264231","url":null,"abstract":"<p><p>The use of albumin in patients with cirrhosis has been extensively discussed over recent years. Current treatment approaches depend on targeting related complications, aiming to treat and/or prevent circulatory dysfunction, bacterial infections and multi-organ failure. Albumin has been shown to prolong survival and reduce complications in patients with cirrhosis. This review aims to ascertain whether the use of albumin is justified in patients with cirrhosis. A systematic review of randomized controlled trials (RCTs) and meta-analyses evaluating albumin use in patients with cirrhosis published between 1985 and February 2020 was conducted; the quality and risk of bias of the included studies were assessed. In total, 45 RCTs and 10 meta-analyses were included. Based on the included evidence, albumin is superior at preventing and controlling the incidence of cirrhosis complications vs other plasma expanders. Recent studies reported that long-term albumin administration to patients with decompensated cirrhosis improves survival with a 38% reduction in the mortality hazard ratio compared with standard medical treatment alone. Albumin infusions are justified for routine use in patients with cirrhosis, and the use of albumin either alone or in combination with other treatments leads to clinical benefits. Long-term administration of albumin should be considered in some patients.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"153-172"},"PeriodicalIF":2.1,"publicationDate":"2020-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S264231","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38672237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 14
Identifying High-Risk NASH Patients: What We Know so Far. 鉴别高危NASH患者:我们目前所知道的。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-08-21 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S265473
Marten Schulz, Frank Tacke
{"title":"Identifying High-Risk NASH Patients: What We Know so Far.","authors":"Marten Schulz,&nbsp;Frank Tacke","doi":"10.2147/HMER.S265473","DOIUrl":"https://doi.org/10.2147/HMER.S265473","url":null,"abstract":"<p><p>Steatosis is a condition of hepatic fat overload that is associated with overweight and the metabolic syndrome. Nonalcoholic fatty liver disease (NAFLD) has become the most common liver disease with a global impact on healthcare. A proportion of NAFLD patients develops nonalcoholic steatohepatitis (NASH), liver fibrosis, cirrhosis or hepatocellular carcinoma (HCC). Identifying patients at risk for potentially life-threatening complications is crucial in their prevention, surveillance and treatment. In addition to hepatic disease progression (cirrhosis, portal hypertension, HCC), NAFLD patients are also at risk of cardiovascular and metabolic diseases as well as extrahepatic malignancies. Liver fibrosis is related to morbidity and mortality in NASH patients, and biomarkers, imaging techniques (ultrasound, elastography, MRI) as well as liver biopsy help in diagnosing fibrosis. In this review, we discuss the tools for identifying patients at risk and their reasonable application in clinical routine in order to stratify prevention and treatment of this emerging disease.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"125-138"},"PeriodicalIF":2.1,"publicationDate":"2020-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S265473","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38525488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
In Vitro Intraductal MRI and T2 Mapping of Cholangiocarcinoma Using Catheter Coils. 使用导管线圈对胆管癌进行体外导管内磁共振成像和 T2 映像分析
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-07-27 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S266841
Narong Khuntikeo, Attapol Titapun, Nittaya Chamadol, Wuttisak Boonphongsathien, Prakasit Sa-Ngiamwibool, Simon D Taylor-Robinson, Christopher A Wadsworth, Shuo Zhang, Evdokia M Kardoulaki, Richard R A Syms
{"title":"In Vitro Intraductal MRI and T2 Mapping of Cholangiocarcinoma Using Catheter Coils.","authors":"Narong Khuntikeo, Attapol Titapun, Nittaya Chamadol, Wuttisak Boonphongsathien, Prakasit Sa-Ngiamwibool, Simon D Taylor-Robinson, Christopher A Wadsworth, Shuo Zhang, Evdokia M Kardoulaki, Richard R A Syms","doi":"10.2147/HMER.S266841","DOIUrl":"10.2147/HMER.S266841","url":null,"abstract":"<p><strong>Aim: </strong>Diagnostic imaging of early-stage cholangiocarcinoma is challenging. A previous in vitro study of fixed-tissue liver resection specimens investigated T2 mapping as a method of exploiting the locally increased signal-to-noise ratio (SNR) of duodenoscope coils for improved quantitative magnetic resonance imaging (MRI), despite their non-uniform sensitivity. This work applies similar methods to unfixed liver specimens using catheter-based receivers.</p><p><strong>Methods: </strong>Ex vivo intraductal MRI and T2 mapping were carried out at 3T on unfixed resection specimens obtained from cholangiocarcinoma patients immediately after surgery using a catheter coil based on a thin-film magneto-inductive waveguide, inserted directly into an intrahepatic duct.</p><p><strong>Results: </strong>Polypoid intraductal cholangiocarcinoma was imaged using fast spin-echo sequences. High-resolution T2 maps were extracted by fitting of data obtained at different echo times to mono-exponential models, and disease-induced changes were correlated with histopathology. An increase in T2 was found compared with fixed specimens and differences in T2 allowed the resolution of tumour tissue and malignant features such as polypoid morphology.</p><p><strong>Conclusion: </strong>Despite their limited field of view, useful data can be obtained using catheter coils, and T2 mapping offers an effective method of exploiting their local SNR advantage without the need for image correction.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"107-114"},"PeriodicalIF":2.1,"publicationDate":"2020-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397475/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38278467","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Oral Administration of Weissella confusa on Fecal and Plasma Ethanol Concentrations, Lipids and Glucose Metabolism in Wistar Rats Fed High Fructose and Fat Diet. 口服鸢尾草对高果糖高脂饲料Wistar大鼠粪便和血浆乙醇浓度、脂质和葡萄糖代谢的影响。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-06-26 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S254195
Fouad M F Elshaghabee, Darab Ghadimi, Diana Habermann, Michael de Vrese, Wilhelm Bockelmann, Hans-Jürgen Kaatsch, Knut J Heller, Jürgen Schrezenmeir
{"title":"Effect of Oral Administration of <i>Weissella confusa</i> on Fecal and Plasma Ethanol Concentrations, Lipids and Glucose Metabolism in Wistar Rats Fed High Fructose and Fat Diet.","authors":"Fouad M F Elshaghabee,&nbsp;Darab Ghadimi,&nbsp;Diana Habermann,&nbsp;Michael de Vrese,&nbsp;Wilhelm Bockelmann,&nbsp;Hans-Jürgen Kaatsch,&nbsp;Knut J Heller,&nbsp;Jürgen Schrezenmeir","doi":"10.2147/HMER.S254195","DOIUrl":"https://doi.org/10.2147/HMER.S254195","url":null,"abstract":"<p><strong>Background and purpose: </strong>In previous investigations, <i>Weissella confusa</i> was shown to lack the metabolic pathway from fructose to mannitol and to produce ethanol when cultivated in the presence of fructose. Hence, we assessed the effect of oral administration of <i>W. confusa</i> (strain NRRL-B-14171) on blood and fecal ethanol concentrations, glucose and lipid metabolism and traits of the metabolic syndrome in Wistar rats (n=27) fed diets with two different fat and fructose levels and with or without the addition of <i>W. confusa</i> during a total intervention time of 15 weeks (105 days).</p><p><strong>Materials and methods: </strong>From week 1 to 6, rats were given a medium fructose and fat (MFru-MF) diet containing 28% fructose and 10% fat without the addition of <i>W. confusa</i> (control group, n=13) or mixed with 30 g per kg diet of lyophilized <i>W. confusa</i> (10.56 ± 0.20 log CFU/g; <i>W. confusa</i> group, n=14). From week 7 to 15, the percentage of dietary fructose and fat in the control and <i>W. confusa</i> group was increased to 56% and 16%, respectively (high fructose-high fat (HFru-HF) diet).</p><p><strong>Results: </strong>In HFru-HF-fed rats, <i>W. confusa</i> was detected in feces, regardless of whether <i>W. confusa</i> was added to the diet or not, but not in rats receiving the MFru-MF diet without added <i>W. confusa</i> or in an additional control group (n=10) fed standard rat food without fructose, increased fat content and <i>W. confusa</i>. This indicates that fecal <i>W. confusa</i> may be derived from orally administered <i>W. confusa</i> as well as - in the case of high fructose and fat intake and obesity of rats - from the intestinal microbiota. As shown by multifactorial ANOVA, blood ethanol, the relative liver weight, serum triglycerides, and serum cholesterol as well as fecal ethanol, ADH, acetate, propionate and butyrate, but not lactate, were significantly higher in the <i>W. confusa -</i> compared to the control group.</p><p><strong>Discussion: </strong>This is the first in vivo trial demonstrating that heterofermentative lactic acid bacteria lacking the mannitol pathway (like <i>W. confusa</i>) can increase fecal and blood ethanol concentrations in mammals on a high fructose-high fat diet. This may explain why <i>W. confusa</i> resulted in hyperlipidemia and may promote development of NAFLD in the host.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"93-106"},"PeriodicalIF":2.1,"publicationDate":"2020-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S254195","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38118619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
In vitro Differentiation of Human TERT-Transfected Multi-Lineage Progenitor Cells (MLPC) into Immortalized Hepatocyte-Like Cells. 人tert转染多系祖细胞(MLPC)向永生化肝细胞样细胞的体外分化。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-06-11 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S245916
Daniel P Collins, Joel H Hapke, Rajagopal N Aravalli, Clifford J Steer
{"title":"In vitro Differentiation of Human TERT-Transfected Multi-Lineage Progenitor Cells (MLPC) into Immortalized Hepatocyte-Like Cells.","authors":"Daniel P Collins,&nbsp;Joel H Hapke,&nbsp;Rajagopal N Aravalli,&nbsp;Clifford J Steer","doi":"10.2147/HMER.S245916","DOIUrl":"https://doi.org/10.2147/HMER.S245916","url":null,"abstract":"<p><strong>Background: </strong>Research directed towards drug development, metabolism, and liver functions often utilize primary hepatocytes (PH) for preliminary in vitro studies. Variability in the in vitro functionality of PH and the unsuitability of hepatocarcinoma cells for these studies have driven researchers to look to ESC, iPS, and other stem cell types using differentiation protocols to provide more reliable and available cells. This study describes the development of hepatocyte-like cells through the in vitro differentiation of human TERT-immortalized cord blood-derived multi-lineage progenitor cells (MLPC). The E12 clonal cell line derived from polyclonal TERT-transfected cells was used throughout the study.</p><p><strong>Methods: </strong>E12 MLPC were subjected to a three-step differentiation protocol using alternating combinations of growth factors, cytokines, and maturational factors. Cells at various stages of differentiation were analyzed for consistency with PH by morphology, immunohistochemistry, urea production, and gene expression.</p><p><strong>Results: </strong>E12 MLPC were shown to significantly change morphology with each stage of differentiation. Coincidental with the morphological changes in the cells, immunohistochemistry data documented the differentiation to committed endoderm by the expression of SOX-17 and GATA-4; the progression to committed hepatocyte-like cells by the expression of a large number of markers including α-fetoprotein and albumin; and the final differentiation by the expression of nuclear and cytoplasmic HNF4. Fully differentiated cells demonstrated gene expression, urea production, and immunohistochemistry consistent with PH. A methodology and medium formulation to continuously expand the E12-derived hepatocyte-like cells is described.</p><p><strong>Conclusion: </strong>The availability of immortalized hepatocyte-like cell lines could provide a consistent tool for the study of hepatic diseases, drug discovery, and the development of cellular therapies for liver disorders. Utilization of these techniques could provide a basis for the development of bridge therapies for liver failure patients awaiting transplant.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"79-92"},"PeriodicalIF":2.1,"publicationDate":"2020-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S245916","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38109340","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Update on Emerging Treatment Options for Primary Biliary Cholangitis. 原发性胆道胆管炎的最新治疗方案。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-05-25 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S205431
Maria T Aguilar, David M Chascsa
{"title":"Update on Emerging Treatment Options for Primary Biliary Cholangitis.","authors":"Maria T Aguilar,&nbsp;David M Chascsa","doi":"10.2147/HMER.S205431","DOIUrl":"https://doi.org/10.2147/HMER.S205431","url":null,"abstract":"<p><p>Primary biliary cholangitis (PBC) is a rare autoimmune cholestatic liver disease that may progress to fibrosis or cirrhosis. Treatment options are currently limited. Ursodeoxycholic acid (UDCA) remains first-line therapy and has been proven to normalize serum biochemistries, halt histologic disease progression, and lead to patient survival comparable to the general population. Obeticholic acid (OCA) was recently approved as adjunct therapy in PBC patients with inadequate response or intolerance to UDCA. However, OCA has been associated with worsening pruritus in clinical studies which may limit its use in this patient population. Several studies are currently underway to address the lack of treatment options for PBC. Of these, fibrates, which have been used in Japan for over a decade, have produced promising results. Furthermore, as currently approved therapies for PBC do not address the potentially debilitating clinical symptoms of PBC such as pruritus and fatigue, supplemental therapy is often required for symptom control.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"69-77"},"PeriodicalIF":2.1,"publicationDate":"2020-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S205431","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38051519","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Elbasvir/Grazoprevir for HCV Infection in Russia: A Randomized Trial. Elbasvir/Grazoprevir治疗俄罗斯HCV感染:一项随机试验
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-04-21 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S241418
Konstantin Zhdanov, Vasily Isakov, Eduard Burnevich, Svetlana Kizhlo, Igor Bakulin, Vadim Pokrovsky, Liwen Liang, Peggy Hwang, Rohit Talwani, Barbara A Haber, Michael N Robertson
{"title":"Elbasvir/Grazoprevir for HCV Infection in Russia: A Randomized Trial.","authors":"Konstantin Zhdanov,&nbsp;Vasily Isakov,&nbsp;Eduard Burnevich,&nbsp;Svetlana Kizhlo,&nbsp;Igor Bakulin,&nbsp;Vadim Pokrovsky,&nbsp;Liwen Liang,&nbsp;Peggy Hwang,&nbsp;Rohit Talwani,&nbsp;Barbara A Haber,&nbsp;Michael N Robertson","doi":"10.2147/HMER.S241418","DOIUrl":"https://doi.org/10.2147/HMER.S241418","url":null,"abstract":"Purpose Hepatitis C virus (HCV) infection is a major healthcare concern in Russia, where almost 5 million individuals are viremic. Elbasvir/grazoprevir is a fixed-dose combination therapy for the treatment of HCV genotype 1 and genotype 4 infection. The present analysis aimed to assess the safety and efficacy of elbasvir/grazoprevir in individuals with HCV infection enrolled at Russian study sites in the C-CORAL study. Patients and Methods C-CORAL (Protocol PN-5172-067; NCT02251990) was a Phase 3, placebo-controlled, double-blind study conducted throughout Asia and Russia. Treatment-naive participants with chronic HCV infection were randomly assigned to receive immediate or deferred treatment with elbasvir 50 mg/grazoprevir 100 mg once daily for 12 weeks. Participants in the immediate-treatment group received elbasvir/grazoprevir for 12 weeks, and those in the deferred-treatment group received placebo for 12 weeks, followed by open-label elbasvir/grazoprevir for 12 weeks. The primary endpoint was sustained virologic response at 12 weeks after completion of therapy (SVR12). Results One hundred and nineteen Russian participants were randomized (immediate-treatment group, n=88; deferred-treatment group, n=31). Most participants were white (99%) with HCV genotype 1b infection (97%) and mild-to-moderate (F0–F2) fibrosis (70%). SVR12 was achieved by 98.9% participants in the immediate-treatment group and by 100% of those receiving deferred elbasvir/grazoprevir in the deferred-treatment group. One participant relapsed with nonstructural protein 5A (NS5A) L28M and Y93H resistance-associated substitutions at baseline and at time of failure. Drug-related adverse events were reported by 19% of participants receiving elbasvir/grazoprevir in the immediate-treatment group and by 16% of those receiving placebo in the deferred-treatment group. No serious adverse event or deaths occurred, and no participant discontinued treatment owing to an adverse event. Conclusion Elbasvir/grazoprevir for 12 weeks was highly effective in treatment-naive Russian individuals with HCV genotype 1b infection.","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"61-68"},"PeriodicalIF":2.1,"publicationDate":"2020-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S241418","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37901244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Clinical Implications of Thrombocytopenia for the Cirrhotic Patient. 肝硬化患者血小板减少症的临床意义。
IF 2.1
Hepatic Medicine : Evidence and Research Pub Date : 2020-04-14 eCollection Date: 2020-01-01 DOI: 10.2147/HMER.S244596
Samuel H Sigal, Zachary Sherman, Arun Jesudian
{"title":"Clinical Implications of Thrombocytopenia for the Cirrhotic Patient.","authors":"Samuel H Sigal,&nbsp;Zachary Sherman,&nbsp;Arun Jesudian","doi":"10.2147/HMER.S244596","DOIUrl":"https://doi.org/10.2147/HMER.S244596","url":null,"abstract":"<p><p>Thrombocytopenia is a frequent complication in patients with cirrhosis. As many as 84% of patients with cirrhosis have thrombocytopenia, and it is an independent variable indicative of advanced disease and poor prognosis. Although there is great concern that it may aggravate bleeding during surgical procedures, there is limited evidence to inform decisions regarding the treatment of cirrhotic patients with thrombocytopenia undergoing invasive procedures. Finally, there is evidence that platelets play a significant role in liver regeneration. In this report, the clinical implications of thrombocytopenia in cirrhotic patients are reviewed. The utility of platelet counts in the prognosis of cirrhosis and relationship to complications of advanced liver disease, including portal hypertension, esophageal varices, and hepatocellular carcinoma. The impact of low platelet counts on bleeding complications during invasive procedures is outlined. Finally, the role of platelets and potential adverse impact in liver regeneration is reviewed.</p>","PeriodicalId":12917,"journal":{"name":"Hepatic Medicine : Evidence and Research","volume":"12 ","pages":"49-60"},"PeriodicalIF":2.1,"publicationDate":"2020-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/HMER.S244596","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37878455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 18
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