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  • Acetaminophen-induced acute liver failure: results of a United States multicenter, prospective study.

Acetaminophen-induced acute liver failure: results of a United States multicenter, prospective study.

Hepatology (Baltimore, Md.) (2005-12-01)
Anne M Larson, Julie Polson, Robert J Fontana, Timothy J Davern, Ezmina Lalani, Linda S Hynan, Joan S Reisch, Frank V Schiødt, George Ostapowicz, A Obaid Shakil, William M Lee
摘要

Severe acetaminophen hepatotoxicity frequently leads to acute liver failure (ALF). We determined the incidence, risk factors, and outcomes of acetaminophen-induced ALF at 22 tertiary care centers in the United States. Detailed prospective data were gathered on 662 consecutive patients over a 6-year period fulfilling standard criteria for ALF (coagulopathy and encephalopathy), from which 275 (42%) were determined to result from acetaminophen liver injury. The annual percentage of acetaminophen-related ALF rose during the study from 28% in 1998 to 51% in 2003. Median dose ingested was 24 g (equivalent to 48 extra-strength tablets). Unintentional overdoses accounted for 131 (48%) cases, intentional (suicide attempts) 122 (44%), and 22 (8%) were of unknown intent. In the unintentional group, 38% took two or more acetaminophen preparations simultaneously, and 63% used narcotic-containing compounds. Eighty-one percent of unintentional patients reported taking acetaminophen and/or other analgesics for acute or chronic pain syndromes. Overall, 178 subjects (65%) survived, 74 (27%) died without transplantation, and 23 subjects (8%) underwent liver transplantation; 71% were alive at 3 weeks. Transplant-free survival rate and rate of liver transplantation were similar between intentional and unintentional groups. In conclusion, acetaminophen hepatotoxicity far exceeds other causes of acute liver failure in the United States. Susceptible patients have concomitant depression, chronic pain, alcohol or narcotic use, and/or take several preparations simultaneously. Education of patients, physicians, and pharmacies to limit high-risk use settings is recommended.

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Sigma-Aldrich
咖啡因, anhydrous, 99%, FCC, FG
Sigma-Aldrich
咖啡因, powder, ReagentPlus®
Supelco
咖啡因, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
咖啡因标准液 溶液, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
咖啡因, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
咖啡因, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Sigma-Aldrich
咖啡因, Sigma Reference Standard, vial of 250 mg
Supelco
熔点标准品 235-237°C, analytical standard
Supelco
咖啡因标准液 溶液, analytical standard, 1.0 mg/mL in methanol
Supelco
Mettler-Toledo® 校准物质 ME 18872,咖啡因, traceable to primary standards (LGC)
Sigma-Aldrich
咖啡因, anhydrous, tested according to Ph. Eur.
Sigma-Aldrich
咖啡因, meets USP testing specifications, anhydrous
Sigma-Aldrich
咖啡因, BioXtra
咖啡因, European Pharmacopoeia (EP) Reference Standard
咖啡因, European Pharmacopoeia (EP) Reference Standard