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Drug-Induced Liver Disease [Hardcover]

Neil Kaplowitz (Editor), Laurie D. DeLeve (Editor)


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Book Description

October 16, 2002 0824708113 978-0824708115 1

Featuring more than 4100 references, Drug-Induced Liver Disease will be an invaluable reference for gastroenterologists, hepatologists, family physicians, internists, pathologists, pharmacists, pharmacologists, and clinical toxicologists, and graduate and medical school students in these disciplines.


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Editorial Reviews

From The New England Journal of Medicine

Books and articles entitled Drug-Induced Liver Disease have always held promise but ultimately disappointed, since they have never delivered a plausible account of the mechanisms involved. So why should this 700-page, beautifully presented book be any better? Our understanding of the mechanisms of how drugs cause liver disease has advanced enormously, and the past decade has seen an explosion of new information concerning the immunology, toxicology, and pharmacology of liver disease. Simultaneously, there has been a substantial increase in the number of drugs on the market, with the result that drugs are now the most common cause of acute liver failure, accounting for up to half of cases. Clinically, there are still diagnostic and therapeutic challenges, and diagnoses are more often based on "implication" than on certainty. It is therefore fitting that this book should appear now. It is authoritative, with contributions by experts in basic sciences as well as by clinical hepatologists. The first part of the book deals with mechanisms and the roles of cytochrome P-450, antioxidants, cytokines, and growth factors in hepatic regeneration, repair, and fibrosis. No book on liver disease can be complete without a discussion of the mechanisms of cell death, and here the current knowledge of apoptosis has provided much-needed insight into the induction of cell death by drugs. The roles of membrane transport and hepatotoxicity due to mitochondrial injury are also discussed. Although drugs and chemicals can cause hepatic damage directly, evidence is fast accumulating of an indirect effect by inflammatory mediators released by nonparenchymal cells, particularly macrophages, endothelial cells, stellate cells, and infiltrating leukocytes. Nevertheless, the mechanisms whereby a particular drug may cause a particular type of damage may not be obvious, and the book includes an axiomatic summary to serve as a guide for the generalist. Overall, hepatocellular injury has a much less favorable prognosis (particularly if there is jaundice) and is more likely to produce life-threatening illness than would be expected on the basis of a cholestatic picture. Diagnosis and management are discussed with particular attention to the spectrum of disease. There are helpful comments on the identification and diagnosis of problems caused by specific drugs, backed up by information about the histopathological features. Despite the expected overlap in the histologic pictures of these drug-specific problems, the reader comes away with a better understanding, albeit from the pathologist's point of view. The usual drugs associated with hepatotoxicity are discussed, but the authors also venture into alternative medicines, vitamins, natural hepatotoxins, and occupational and environmental causes -- all of which are now potential and important hazards. The science discussed in the early chapters is used to inform the reader about possibly damaging mechanisms -- an indication of a well-edited book. It was refreshing to see a whole chapter devoted to the regulatory perspective, which outlines the path a new drug takes from discovery to established use -- a process that may take many years. Extensive and rigorous testing of drugs in animals and premarketing trials are a frequent cause of the early termination of a drug's developmental program, particularly if hepatotoxicity is detected. Sadly, even these large testing programs, often involving several thousand patients, cannot always detect an idiosyncratic event that may occur in 1 of every 10,000 to 100,000 patients. The editors emphasize the importance of randomized, double-blind, prospective, multigroup clinical trials as the gold standard for reducing unwanted bias and confounding factors. Postmarketing data for the first two years after the release of a drug on the risk associated with it, its optimal use, and its administration over longer periods are absolutely crucial. In summary, this book provides an excellent and authoritative account of the whole subject, from basic science to the clinical manifestations of drug-induced disease. It will be used by gastroenterologists, liver specialists, and basic scientists as their regular reference but will also be dipped into by other clinicians when they are confronted with an unusual case of liver disease. I was definitely not disappointed. Parveen J. Kumar, M.D.
Copyright © 2003 Massachusetts Medical Society. All rights reserved. The New England Journal of Medicine is a registered trademark of the MMS.

Product Details

  • Hardcover: 784 pages
  • Publisher: Informa Healthcare; 1 edition (October 16, 2002)
  • Language: English
  • ISBN-10: 0824708113
  • ISBN-13: 978-0824708115
  • Product Dimensions: 10.4 x 7.2 x 1.6 inches
  • Shipping Weight: 3 pounds
  • Amazon Best Sellers Rank: #3,060,125 in Books (See Top 100 in Books)

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Inside This Book (learn more)
First Sentence:
Drug-induced liver disease represents an important problem for the following major reasons: (1) approximately 1000 drugs have been implicated in causing liver disease at least on rare occasion (1); (2) in the United States drug-induced liver disease is the most common cause of acute liver failure, accounting for one-third to one-half of cases (2,3); although acetaminophen accounts for the bulk of these, other drugs are still a more frequent cause of acute liver failure than viral hepatitis and other causes; (3) in addition, drug-induced liver disease represents an important diagnostic/therapeutic challenge for physicians caring for patients presenting with liver disorders, since it can mimic all forms of acute or chronic liver disease; (4) the frequency and economic impact of this problem is a major challenge for the pharmaceutical industry and regulatory bodies, especially since the toxic potential of some drugs is not evident in Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
oxaprozin glucuronide, isomeric conjugates, antidiabetic troglitazone, trifluoroacetylated neoantigens, monoacetyl hydrazine, tolmetin glucuronide, nonhepatotoxic regioisomer, beclobric acid, hepatotoxicant exposure, dihydralazine hepatitis, zomepirac glucuronide, hepatic sinusoidal endothelial cells, acyl glucuronides, furosemide glucuronide, liver protein adducts, canalicular conjugate export pump, protein neoantigens, nonparenchymal liver cells, intramolecular acyl migration, liver neoantigens, ipso adducts, stereoselective degradation, xenobiotic carboxylic acids, acyl glucuronide conjugates, acyl glucuronidation
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Ann Intern Med, Biochem Pharmacol, Pharmacol Exp Ther, Drug Metab Dispos, Biol Chem, United States, Clin Pharmacol Ther, Arch Intern Med, Chem Res Toxicol, Toxicol Appl Pharmacol, Clin Invest, Cancer Res, New York, Semin Liver Dis, Arthritis Rheum, Dig Dis Sci, Proc Natl Acad Sci, Mol Pharmacol, Clin Gastroenterol, Gastroenterol Clin Biol, United Kingdom, Ann Pharmacother, Arch Biochem Biophys, Biochem Biophys Res Commun, Gastroenterol Hepatol
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