Fluoroquinolone therapy and idiosyncratic acute liver injury: a population-based study

被引:51
作者
Paterson, J. Michael [1 ,4 ,7 ]
Mamdani, Muhammad M. [1 ,5 ,6 ]
Manno, Michael [1 ]
Juurlink, David N. [1 ,2 ,3 ]
机构
[1] Inst Clin Evaluat Sci, Toronto, ON, Canada
[2] Sunnybrook Res Inst, Toronto, ON, Canada
[3] Univ Toronto, Dept Med, Toronto, ON, Canada
[4] Univ Toronto, Dept Hlth Policy Management & Evaluat, Toronto, ON, Canada
[5] Univ Toronto, Leslie Dan Fac Pharm, Toronto, ON, Canada
[6] St Michaels Hosp, Keenan Res Ctr, Li Ka Shing Knowledge Inst, Toronto, ON M5B 1W8, Canada
[7] McMaster Univ, Dept Family Med, Hamilton, ON L8S 4L8, Canada
基金
加拿大健康研究院;
关键词
RISK; FEATURES;
D O I
10.1503/cmaj.111823
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Although fluoroquinolones are sometimes associated with mild, transient elevations in aminotransferase levels, serious acute liver injury is uncommon. Regulatory warnings have identified moxifloxacin as presenting a particular risk of hepatotoxicity. Thus, we examined the risk of idiosyncratic acute liver injury associated with the use of moxifloxacin relative to other selected antibiotic agents. Methods: We conducted a population-based, nested, case-control study using health care data from Ontario for the period April 2002 to March 2011. We identified cases as outpatients aged 66 years or older with no history of liver disease, and who were admitted to hospital for acute liver injury within 30 days of receiving a prescription for 1 of 5 broad-spectrum antibiotic agents: moxifloxacin, levofloxacin, ciprofloxacin, cefuroxime axetil or clarithromycin. For each case, we selected up to 10 age-and sex-matched controls from among patients who had received a study antibiotic, but who were not admitted to hospital for acute liver injury. We calculated odds ratios (ORs) to determine the association between admission to hospital and previous exposure to an antibiotic agent, using clarithromycin as the reference. Results: A total of 144 patients were admitted to hospital for acute liver injury within 30 days of receiving a prescription for one of the identified drugs. Of these patients, 88 (61.1%) died while in hospital. After multivariable adjustment, use of either moxifloxacin (adjusted OR 2.20, 95% confidence interval [CI] 1.21-3.98) or levo floxacin (adjusted OR 1.85, 95% CI 1.01-3.39) was associated with an increase in risk of acute liver injury relative to the use of clarithromycin. We saw no such risk associated with the use of either ciprofloxacin or cefuroxime axetil. Interpretation: Among older outpatients with no evidence of liver disease, moxifloxacin and levofloxacin were associated with an increased risk of acute liver injury relative to clarithromycin.
引用
收藏
页码:1565 / 1570
页数:6
相关论文
共 28 条
[1]   Drug-induced liver injury:: An analysis of 461 incidences submitted to the Spanish Registry over a 10-year period [J].
Andrade, RJ ;
Lucena, MI ;
Fernández, MC ;
Pelaez, G ;
Pachkoria, K ;
García-Ruiz, E ;
García-Munoz, B ;
González-Grande, R ;
Pizarro, A ;
Durán, JA ;
Jiménez, M ;
Rodrigo, L ;
Romero-Gomez, M ;
Navarro, JM ;
Planas, R ;
Costa, J ;
Borras, A ;
Soler, A ;
Salmerón, J ;
Martin-Vivaldi, R .
GASTROENTEROLOGY, 2005, 129 (02) :512-521
[2]  
[Anonymous], 1999, DRUG SAF AV TROV TRO
[3]  
[Anonymous], 2008, NOT DET TEQ GAT WITH
[4]  
Brinker A., 2006, FDA JOINT M ANT DRUG
[5]  
Canadian Institute of Health Information, 2009, INT STAT CLASS DIS R, V10th
[6]   Risk Factors for Idiosyncratic Drug-Induced Liver Injury [J].
Chalasani, Naga ;
Bjornsson, Einar .
GASTROENTEROLOGY, 2010, 138 (07) :2246-2259
[7]   Causes, Clinical Features, and Outcomes From a Prospective Study of Drug-induced Liver Injury in the United States [J].
Chalasani, Naga ;
Fontana, Robert J. ;
Bonkovsky, Herbert L. ;
Watkins, Paul B. ;
Davern, Timothy ;
Serrano, Jose ;
Yang, Hongqiu ;
Rochon, James .
GASTROENTEROLOGY, 2008, 135 (06) :1924-1934
[8]   A province-level risk factor analysis of fluoroquinolone consumption patterns in Canada (2000-06) [J].
Glass, Shiona K. ;
Pearl, David L. ;
McEwen, Scott A. ;
Finley, Rita .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2010, 65 (09) :2019-2027
[9]  
Health Canada, 2010, UPD LAB ANT AV MOX R
[10]  
Hoofnagle Jay H, 2004, Hepatology, V40, P773, DOI 10.1002/hep.20445