Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Liver failure treatment

However, if paracetamol is taken in overdose, the levels of quinoneimine exceed the ability of glutathione to convert it back to paracetamol and toxicity to the liver results. In some cases, if treatment is not initiated in time, severe toxicity results, leading to death by acute liver failure. Treatment of paracetamol overdose is by administration of N-acetylcysteine (Figure 5.8). This compound (the acetyl derivative of the essential amino acid cysteine) functions as an alternative source of thiol (—SH) groups, which act in a similar manner to glutathione to detoxify the quinoneimine. [Pg.118]

Ferrochelauise (EC 4.99.1.1). Activity greatly decreased in bone marrow and liver. High levels of protoporphyrin in erythrocytes, normoblasts and feces. Mild photodermatosis. Erythema and pruritis. Mild edema. Usually cholelithiasis. Sometimes liver failure. Treatment by oral administration of -carotene, and protection from UV light. Autosomal dominant. [Pg.534]

Circe Biomedical Lexington, MA HepatAssist liver support device Extracorporeal liver-failure treatment Hepatocyte bi eact(M s... [Pg.268]

University of Berlin Hybrid Organ GmbH, Berlin, Germany Modular Extracorporeal Liver Support System (MELS) Extracorporeal liver-failure treatment Hepatocyte bioreactors... [Pg.268]

A serious and potentially fatal adverse reaction to tolcapone ishepatic injury. Regular blood testing to monitor liver function is usually prescribed. The phys dan may order testing of serum transaminase levels at frequent intervals(eg, every 2 weeks for the first year and every 8 weeks thereafter). Treatment is discontinued if the ALT (SOFT) exceeds the upper normal limit or sgns or symptoms of liver failure develop. [Pg.271]

A black box warning for life-threatening liver failure was added to the prescribing information for nefazodone. Treatment with nefazodone should not be initiated in individuals with active liver disease or with elevated baseline serum transaminases. [Pg.799]

The Log-Rank Test is a statistical methodology for comparing the distribution of time until the occurrence of the event in independent groups. In toxicology, the most common event of interest is death or occurrence of a tumor, but it could just as well be liver failure, neurotoxicity, or any other event which occurs only once in an individual. The elapsed time from initial treatment or observation until the event is the event time, often referred to as survival time , even when the event is not death . [Pg.917]

Examples where use of the Log-Rank Test might be appropriate include comparing survival times in carcinogenity bioassay animals which are given a new treatment with those in the control group or comparing times to liver failure for several dose levels of a new NSAID where the animals are treated for 10 weeks or until cured, whichever comes first. [Pg.917]

Finally, if liver failure is chronic and extensive, the only treatment is liver transplantation. [Pg.221]

Cases of life-threatening hepatic failure have been reported in patients treated with nefazodone. The reported rate in the United States is about 1 case of liver failure resulting in death or transplant per 250,000 to 300,000 patient-years of nefazodone treatment. [Pg.1063]

Hepatotoxicity Itraconazole has been associated with rare cases of serious hepatotoxicity, including liver failure and death. Some of these cases had neither pre-existing liver disease, nor a serious underlying medical condition. If liver function tests are abnormal, discontinue treatment. In patients with raised liver enzymes or an active liver disease or who have experienced liver toxicity with other drugs, do not start treatment unless the expected benefit exceeds the risk of hepatic injury. In such cases, liver enzyme monitoring is necessary. [Pg.1686]

Hepatic failure Rare cases of liver failure, some leading to death or liver transplant, have occurred with the use of terbinafine for the treatment of onychomycosis in individuals with and without pre-existing liver disease. [Pg.1690]

Corticosteroids have no value in supportive therapy. Acute liver failure is the main problem and specific features noted below require treatment ... [Pg.632]

Although side effects of other stimulants respond to dose reduction or change in time of administration, PEM use can be associated with serious, irreversible liver damage. Postmarketing surveillance revealed abnormalities in liver function tests in 44 children receiving PEM acutely or chronically (Berkovitch et ah, 1995). Even more disturbing, 13 children on PEM experienced total liver failure—11 resulting in death or transplant within 4 weeks of failure. This exceeds the rate in the normal population by 4 to 17 times. Pemoline, therefore, is reserved for alternative treatment only if the patient fails to tolerate all three stimulants (MPH, DEX, and AMP) and subsequent trials of an-... [Pg.259]

There appears to be little difference between benzodiazepines and kava extract in anxiolytic activity. However, kava extracts seem to have fewer side effects. Two studies with more than 3000 patients each found unwanted events in about 2% of patients during treatment with kava extract. The more frequently reported side effects were gastrointestinal complaints, allergic skin reactions, headache, and photosensitivity (Pittler and Ernst, 2000). There have been isolated reports of hepatotoxicity and acute liver failure (Escher et ah, 2001). Kava may potentiate the sedative effects of other medications including barbiturates and benzodiazepines. Kava can also cause behavioral disinhibition in a minority of individuals, including children. The most common problem, which is usually associated with persistent and excessive usage, is a scaly skin rash called kava dermopathy, which is reversible. [Pg.373]

Whole and partial liver transplants have become the treatments of choice for patients with imminent liver failure. Advances in surgical techniques and immune suppression are responsible for this progress. Treatments for liver diseases were unknown in the 1960s. Despite our improved knowledge of the function and physiology of the liver, one of every 10 individuals in the U.S. has been or will be diagnosed with liver disease. Hepatitis C virus (HCV) is a public health problem approximately 170 million people are infected worldwide, and 8,000 to 10,000 deaths per year... [Pg.146]

Two cases of fatal fulminant hepatic failure have been described in previously healthy women aged 30 and 32 years who presented with jaundice 4 and 5 months respectively after starting to take propylthiouracil for Graves hyperthyroidism (51). Another case of fatal fulminant liver failure with cholestatic jaundice 2 weeks after the start of treatment with propylthiouracil 100 mg tds has been described (52). [Pg.339]

Assurance of good renal and hepatic function is mandatory before beginning treatment with the fibrates (22). Serum transaminase changes are regularly seen and hepatitis occurs (23). Several cases of hepatitis due to fenofibrate have been reviewed (24) and it has also been observed with etofibrate (25). One case of liver failure, probably due to beclobrate, has been reported (SEDA-13, 1324 26). Liver biopsies showed a lymphoplasmacytic infiltrate in all of five cases of chronic hepatitis associated with fibrates (27). [Pg.536]

Terbinafine (Lamisil) is an allylamine antifungal agent that has been shown to be quite effective for the treatment of onychomycosis. Recommended oral dosing consists of 250 mg daily for 6 weeks for fingernail infections and 12 weeks for toenail infections. Recent reports of serious hepatic toxicity, including liver failure and death, have led to recommendations that patients receiving terbinafine for onychomycosis be monitored closely with periodic laboratory evaluations for possible hepatic dysfunction. [Pg.1449]

Besides glucose, other analytes of clinical value can be possibly quantified by noninvasive spectral analysis. In vivo concentrations of lactate and urea are examples. The concentration of lactate in blood is used clinically to follow intensive care treatments, to identify cardiac or liver failure, to determine hypoxia of tissues from atherosclerosis, and to detect bacterial infection. In vivo urea levels are valuable for optimizing hemodialysis treatments and tracking the accumulation of toxins for people with end-stage renal failure or recent kidney transplant recipients. [Pg.333]

Liver failure is a fatal disease and liver transplantation is the only established treatment however, donor shortages remain problematic. Liver failure is potentially reversible because of liver regeneration [11] so considerable work has been done over many years to develop effective liver-support devices and various hepatic support systems using hepatocytes have been developed. Liver-engineered constructs can be also applied to the development of drugs to treat many diseases. The impact will be... [Pg.434]

There is no official register of MCS fatalities, but within MCS circles cases of death are reported (especially in the United States and Canada). These are often MCS patients who die from suicide, fatal reactions (such as anaphylactic shock or an allergic reaction) or due to complications from being unable to undergo traditional methods of treatment, such as chemotherapy. Severe MCS patients can sustain fatal organ damage. Officially these patients die from heart, kidney or liver failure. In these cases the cause is rarely described as MCS. [Pg.47]

Lactitol 40 is a disaccharide that has been used in the management of hepatic encephalopathy, a major neuropsychiatric complication of both acute and chronic liver failure. It has mild laxative properties and is used to reduce the production and absorption of gut-derived neurotoxic substances symptomatic of hepatic encephalopathy. Although long considered a first-line pharmacological treatment, there is a lack of sufficient evidence to support lactitol s efficacy and continued use when weighed against other suitable therapeutic alternatives such as oral antibiotics <2006MI94>. [Pg.715]

In this chapter Case studies levels 1-3 explore the management of a patient with alcoholic liver disease. The patient has alcoholic liver cirrhosis and first presents with alcohol withdrawal (Case study level 1), then the patient s risk of bleeding and treatment for the maintenance of alcohol abstinence are considered (Case study level 2). The patient then goes on to develop encephalopathy (Case study level 3). Case studies levels Ma and Mb consider two patients one presents with TB and the other liver failure. [Pg.338]


See other pages where Liver failure treatment is mentioned: [Pg.666]    [Pg.762]    [Pg.666]    [Pg.762]    [Pg.257]    [Pg.66]    [Pg.468]    [Pg.957]    [Pg.184]    [Pg.676]    [Pg.166]    [Pg.91]    [Pg.636]    [Pg.301]    [Pg.37]    [Pg.225]    [Pg.1011]    [Pg.16]    [Pg.146]    [Pg.426]    [Pg.119]    [Pg.165]    [Pg.159]    [Pg.426]    [Pg.108]    [Pg.488]    [Pg.363]   
See also in sourсe #XX -- [ Pg.2644 , Pg.2646 ]




SEARCH



Liver failure

© 2024 chempedia.info