Search results for "EPA"

showing 10 items of 8995 documents

The impact of antibiotic resistance on the efficacy of three 7-day regimens againstHelicobacter pylori

2000

Background: Antibiotic resistance affects the success of anti-Helicobacter pylori therapies and varies greatly from country to country. Aim: To compare the efficacy of three short-term triple regimens in relation to H. pylori primary resistance in our region. Methods: We enrolled 210 H. pylori-positive dyspeptic patients for this randomized, open, parallel-group study. Three arms of 70 patients each received the following 1-week regimens: (1) ranitidine bismuth citrate 400 mg b.d. + clarithromycin 250 mg b.d. + metronidazole 500 mg b.d. (RCM); (2) bismuth subcitrate 240 mg b.d. + amoxycillin 1000 mg b.d. + metronidazole 500 mg b.d. (BAM); (3) omeprazole 20 mg o.d. + clarithromycin 250 mg b.…

medicine.medical_specialtyHepatologybiologybusiness.industryGastroenterologyDrug resistanceHelicobacter pyloriAmoxicillinbiology.organism_classificationGastroenterologySurgeryMetronidazoleBismuth SubcitrateClarithromycinInternal medicinemedicinePharmacology (medical)businessOmeprazolemedicine.drugAntibacterial agentAlimentary Pharmacology & Therapeutics
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Basal release of nitric oxide in the mesenteric artery in portal hypertension and cirrhosis: Role of dimethylarginine dimethylaminohydrolase

2013

Background and Aim Increased basal release of nitric oxide (NO) in the splanchnic circulation contributes to elevated plasma levels of NO observed in decompensated cirrhosis. We evaluated in rat mesenteric arteries whether the differences in basal release of NO, revealed by asymmetric dimethylarginine (ADMA)- and NG-nitro-L-arginine methyl ester (L-NAME)-induced contractions, were associated with changes in messenger RNA (mRNA) expression of endothelial NO synthase (eNOS) and dimethylarginine dimethylaminohydrolases (DDAHs). Methods Rat small mesenteric arteries from 14 Sham-control, from 14 with partial portal vein ligation (PPVL), and from 14 with bile duct excision (BDE)-induced cirrhosi…

medicine.medical_specialtyHepatologybiologybusiness.industryGastroenterologyVasodilationmedicine.diseasebiology.organism_classificationApaminNitric oxidechemistry.chemical_compoundEndocrinologymedicine.anatomical_structurechemistryEnosInternal medicinemedicinePortal hypertensionbusinessAsymmetric dimethylarginineMesenteric arteriesArteryJournal of Gastroenterology and Hepatology
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P0760 : PNPLA3 rs738409 I748M is associated with steatohepatitis in non obese subjects with hepatitis C

2015

medicine.medical_specialtyHepatologybiologybusiness.industryHepacivirusFatty liverHepatitis Cmedicine.diseasebiology.organism_classificationGastroenterologyObesityMembrane proteinInternal medicineGenotypebiology.proteinMedicineLipaseSteatohepatitisbusinessJournal of Hepatology
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HCV E1E 2‐ MF 59 vaccine in chronic hepatitis C patients treated with PEG ‐ IFN α2a and R ibavirin: a randomized controlled trial

2013

Hepatitis C virus (HCV) vaccines may be able to increase viral clearance in combination with antiviral therapy. We analysed viral dynamics and HCV-specific immune response during retreatment for experienced patients in a phase Ib study with E1E2MF59 vaccine. Seventy-eight genotype 1a/1b patients [relapsers (30), partial responders (16) and nonresponders (32) to interferon-(IFN)/ribavirin-(RBV)] were randomly assigned to vaccine (V:23), Peg-IFNα2a-180-ug/qw and ribavirin 1000-1200-mg/qd for 48 weeks (P/R:25), or their combination (P/R + V:30). Vaccine (100 μg/0.5 mL) was administered intramuscularly at week 0-4-8-12-24-28-32-36. Neutralizing of binding (NOB) antibodies and lymphocyte prolife…

medicine.medical_specialtyHepatologybiologybusiness.industryT cellHepatitis C virusRibavirinmedicine.disease_causeVirologyGastroenterologyVaccinationchemistry.chemical_compoundInfectious Diseasesmedicine.anatomical_structurechemistryInterferonVirologyInternal medicinePEG ratiomedicinebiology.proteinAntibodybusinessViral loadmedicine.drugJournal of Viral Hepatitis
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A 10-day levofloxacin-based therapy in patients with resistant infection: A controlled trial

2004

Background & Aims: Antibiotic resistance is a major issue in anti– Helicobacter pylori treatment. This study was aimed at assessing the efficacy of 2 therapies in patients with resistant H pylori infection. Methods: Patients who had failed 1 or more eradication regimens underwent upper gastrointestinal endoscopy and 2 antral and 2 corpus biopsy specimens were taken for histology and culture. Metronidazole, clarithromycin, and amoxicillin resistance were determined by E-test. Patients were randomly assigned to 2 therapies: 1 group received pantoprazole 40 mg, amoxicillin 1 g, levofloxacin 250 mg, all twice daily for 10 days, and the other group was treated with omeprazole 20 mg twice daily f…

medicine.medical_specialtyHepatologybiologymedicine.diagnostic_testbusiness.industryUrea breath testGastroenterologyHelicobacter pyloriAmoxicillinbiology.organism_classificationGastroenterologySurgeryMetronidazoleLevofloxacinClarithromycinInternal medicinemedicinebusinessOmeprazolemedicine.drugPantoprazoleClinical Gastroenterology and Hepatology
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Head-to-head comparison of 1-week triple regimens combining ranitidine or omeprazole with two antibiotics to eradicate Helicobacter pylori

1999

Background : Triple therapies containing omeprazole and ranitidine have been shown to be equivalent in eradicating H. pylori infection, but have been assessed either separately or head-to-head, only in small trials. Aim : To carry out a large randomized controlled study comparing omeprazole and ranitidine combined with two antibiotic combinations for 1 week. Methods : Three hundred and twenty H. pylori-positive patients were randomly subdivided into four equal-sized groups and received one of the following treatments: OAM = omeprazole 20 mg b.d. + amoxycillin 1 g b.d. + metronidazole 500 mg b.d.; RAM = ranitidine 300 mg b.d. + amoxycillin 1 g b.d. + metronidazole 500 mg b.d.; OAC = omeprazo…

medicine.medical_specialtyHepatologybiologymedicine.drug_classbusiness.industrySpirillaceaeAntibioticsGastroenterologyProton-pump inhibitorHelicobacter pyloribiology.organism_classificationGastroenterologySurgeryRanitidineClarithromycinInternal medicinemedicinePharmacology (medical)businessOmeprazolemedicine.drugAntibacterial agentAlimentary Pharmacology & Therapeutics
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On the Visual Diagnosis of Human Taeniasis by Capsule Endoscopy

2018

medicine.medical_specialtyHepatologybusiness.industry030231 tropical medicineGastroenterologyTaenia saginatamedicine.diseaseCapsule Endoscopylaw.invention03 medical and health sciences0302 clinical medicineCapsule endoscopylawmedicineAnimalsHumansTaeniasis030211 gastroenterology & hepatologyRadiologybusinessTaeniasisClinical Gastroenterology and Hepatology
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Interferon-α for chronic hepatitis C: An analysis of pretreatment clinical predictors of response

1994

To identify predictors of short-term and sustained ALT normalization after interferon treatment in adult patients with chronic hepatitis C, we performed a metanalysis of individual patients'data, with construction and cross-validation of a prediction rule, in 361 patients from two randomized trials. In one trial, 116 subjects with transfusion-related chronic hepatitis C were treated with lymphoblastoid interferon (5 MU/m 2 three times a week for 2 mo, then 3 MU/m 2 three times a week for 4 or 10 mo)

medicine.medical_specialtyHepatologybusiness.industryAlpha interferonGastroenterologylaw.inventionRandomized controlled trialChronic hepatitislawInterferonInternal medicineInterferon αImmunologymedicineViral diseaseLymphoblastoid InterferonbusinessInterferon alfamedicine.drugHepatology
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Evidence recommending antiviral therapy in hepatitis C

2014

medicine.medical_specialtyHepatologybusiness.industryAlternative medicineAntiviral therapyMEDLINEHepatitis CHepatitis C Chronicmedicine.diseaseGastroenterologyAntiviral AgentsInternal medicinemedicineHumansbusinessJournal of Hepatology
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A double-blind, randomized, dose response study testing the pharmacological efficacy of synthetic porcine secretin

2000

Background: Biologically derived porcine secretin has been used as a diagnostic agent in clinical gastrointestinal practice for many years. Pure synthetic porcine secretin is now available for investigational clinical use. Aim: To compare the pharmacology of synthetic porcine secretin and biologically derived porcine secretin in healthy volunteers. Methods: Secretin stimulation tests were performed in 12 volunteer subjects in a double-blind, randomized, Latin square crossover design study comparing three doses of synthetic porcine secretin (0.05, 0.2, and 0.4 μg/kg) with a standard dose of biologically derived porcine secretin (1 CU/kg). Duodenal aspirates were analysed for total volume and…

medicine.medical_specialtyHepatologybusiness.industryBicarbonateGastroenterologyPeptide hormonedigestive systemCrossover studydigestive system diseasesDose Response StudySecretinchemistry.chemical_compoundfluids and secretionsEndocrinologymedicine.anatomical_structurechemistryGastrointestinal hormoneInternal medicinemedicinePharmacology (medical)businessPancreasVolunteerhormones hormone substitutes and hormone antagonistsAlimentary Pharmacology & Therapeutics
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