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Toxicity Research Foundation
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Liver Damage Research | See downloads for: Adobe Files |
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Antibiotic-associated hepatitis:
update from 1990 OBJECTIVE: To review the literature on the recent available
evidence of antibiotic-associated acute liver injury. DATA SOURCES:
All published articles from January 1990 to July 1995 were extracted
from the monthly updated HEPATOX database. Additional articles were
found using MEDLINE, EMBASE, and PASCAL searches. Hepatic injuries
associated with antituberculous, antimycotic, antiviral, antiprotozoal,
and antiseptic compounds were excluded form this review. STUDY
SELECTION: As the amount of literature was large, only case reports,
series and epidemiologic data were used. Results from clinical trials
were reviewed only when other information was available. DATA
EXTRACTION: Original articles were reviewed to select relevant
material. Information regarding the clinical description, histologic
features, severity, outcome, and possible risk factors was extracted.
Data on incidence were provided by epidemiologic studies or
spontaneous reporting to regulatory agencies. DATA SYNTHESIS:
Antibiotic-associated acute injury is rare, with an incidence not
exceeding 1 case 10,000 users for most drugs. Among beta-lactams,
amoxicillin/clavulanic acid and penicillinase-resistant penicillins
are associated with predominant and sometimes protracted cholestasis.
The hepatotoxic potential of all available erythromycin salts is
confirmed, and recent evidence suggests that roxithromycin could be
added to the list of antibiotic-induced liver injury. Among
fluoroquinolones, only ciprofloxacin has been associated with serious
hepatitis. Trimethoprim/sulfamethoxazole-induced hepatitis often
reported, but trimethoprim alone also appears as a possible cause of
acute liver injury. Finally, acute bile duct injuries and ductopenia
have been described with several antibiotics. CONCLUSIONS: The most
important recent information is the possibility of protracted liver
cholestasis with bile duct injuries induced by several antibiotics,
particularly penicillinase-resistant penicillins, and the
identification of new potentially hepatotoxic antibiotics, namely,
roxithromycin, ciprofloxacin, and trimethoprim.
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