Disease | encephalopathy |
Comorbidity | C0023895|liver disease |
Sentences | 25 |
PubMedID- 20880508 | Many theories have been advanced to explain the encephalopathy associated with chronic liver disease and with the less common acute form. |
PubMedID- 25586470 | Objectives: rifaximin is approved for the reduction of hepatic encephalopathy (he) recurrence in patients with chronic liver disease (cld); however, few studies have evaluated the benefit of adding rifaximin to lactulose for treatment of acute he. |
PubMedID- 26029995 | Objectives: acute liver failure is a life-threatening condition with sudden onset liver injury, decreased liver functions, hepatic encephalopathy, and coagulopathy in patients without preexisting liver disease. |
PubMedID- 21741091 | Rifaximin received new labeling for reduction in the risk of the recurrence of overt hepatic encephalopathy (he) in patients with advanced liver disease in march of 2010. |
PubMedID- 25374704 | In addition to this case, there are two other reports of metronidazole-induced encephalopathy in patients with liver disease. |
PubMedID- 23978689 | Alf is characterized by coagulopathy and hepatic encephalopathy (he) in a patient without pre-existing liver disease. |
PubMedID- 21384402 | Additional studies are warranted to evaluate the effects of ast-120 on hepatic encephalopathy in patients with advanced liver disease. |
PubMedID- 25867912 | Comparison of once a day rifaximin to twice a day dosage in the prevention of recurrence of hepatic encephalopathy in patients with chronic liver disease. |
PubMedID- 26098218 | In the intestine, bacterial urease converts host-derived urea to ammonia and carbon dioxide, contributing to hyperammonemia-associated neurotoxicity and encephalopathy in patients with liver disease. |
PubMedID- 24498036 | These data have been routinely collected since january 2001 and include non-aids malignancies, pancreatitis, severe liver disease with hepatic encephalopathy (grade 3 or 4), cardio- and cerebrovascular events (i.e. |
PubMedID- 22228885 | The aim of this study was to evaluate scientific evidence for the effectiveness and safety of lola infusions for treatment of clinical hepatic encephalopathy in patients with chronic liver disease. |
PubMedID- 25908985 | These include hepatic encephalopathy in patients with advanced liver disease, vascular bypass of the liver, valproic acid or cyclophosphamide poisoning, herpes simplex infection, and gastrointestinal bacterial overgrowth. |
PubMedID- 25068951 | Acute liver failure (alf) is an uncommon clinical syndrome that often has a course associated with rapidly progressive multiorgan failure and devastating complications like coagulopathy and encephalopathy in patients without previous liver disease. |
PubMedID- 24665321 | The sudden onset and rapid reversibility of encephalopathy in liver disease suggest that it has a metabolic origin, so that the liver cannot detoxify the portal venous blood. |
PubMedID- 20335583 | Methods: in this randomized, double-blind, placebo-controlled trial, we randomly assigned 299 patients who were in remission from recurrent hepatic encephalopathy resulting from chronic liver disease to receive either rifaximin, at a dose of 550 mg twice daily (140 patients), or placebo (159 patients) for 6 months. |
PubMedID- 21959704 | Minimal encephalopathy was originally associated with chronic liver disease but is increasingly associated with most other chronic diseases and particularly with diabetes and also chronic disorders in other organs: kidneys, lungs, thyroid and with obesity. |
PubMedID- 20728575 | No state specifically mentioned hepatic encephalopathy or patients with advanced liver disease. |
PubMedID- 21705899 | Objective: hyperammonemia is a major contributing factor to the encephalopathy associated with liver disease. |
PubMedID- 24133449 | Alf results from the acute and rapid loss of hepatocyte function, and is associated with coagulopathy [international normalized ratio (inr) >1.5] and hepatic encephalopathy (he) in a patient without pre-existing liver disease. |
PubMedID- 25733099 | The primary outcome was drug-induced alf (defined as coagulopathy and hepatic encephalopathy without underlying chronic liver disease), determined by hepatologists who reviewed medical records of all kpnc members with inpatient diagnostic and laboratory criteria suggesting potential alf. |
PubMedID- 25849554 | Briefly, acute hepatic injury manifestated as increasing jaundice (serum tbil>85 umol/l) and coagulopathy (pta <40%) in patients with previously diagnosed or undiagnosed chronic liver diseases, complicated by ascites and/or encephalopathy within 4 weeks. |
PubMedID- 22447259 | Acute liver failure (alf) (sometimes referred to as fulminant hepatic failure) is a clinical syndrome from a variety of causes resulting from rapid loss in hepatocyte function, typically associated with coagulopathy and encephalopathy in a patient without preexisting liver disease or cirrhosis. |
PubMedID- 22867045 | All opioid drugs can precipitate or aggravate hepatic encephalopathy in patients with severe liver disease, thus requiring cautious use and careful monitoring. |
PubMedID- 26426612 | Hepatitis b virus (hbv) infection is a global health problem, with a seroprevalence varying from 1.7% (latin america) to 11.3% (east asia and pacific).1 hbv infection is associated with an increased risk of cirrhosis, hepatic decompensation, and hepatocellular carcinoma.2 hepatic decompensation may be gradual or acute, which is termed acute-on-chronic liver failure (aclf).3 patients with chronic hepatitis b (chb) may experience a severe acute exacerbation of the disease that progresses into liver failure, which is defined as acute-on-chronic hepatitis b liver failure (achblf), manifesting as jaundice and coagulopathy (international normalized ratio [inr] > 1.5) complicated within 4 weeks by ascites and/or encephalopathy in a patient with chronic liver disease.3,4 liver transplantation is the only curative therapeutic option for aclf, with a 5-year survival rate of 85%. |
PubMedID- 25374719 | Acute liver failure is characterized by the rapid development of severe liver injury with impaired synthetic function and hepatic encephalopathy in a patient without obvious, previous liver disease. |
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