Do fluoroquinolones predispose patients to Clostridium difficile associated disease?: A review of the evidence

被引:53
作者
Deshpande, Abhishek [1 ,2 ]
Pant, Chaitanya [3 ]
Jain, Anil [1 ]
Fraser, Thomas G. [1 ]
Rolston, David D. K. [1 ]
机构
[1] Cleveland Clin, Inst Med, Dept Gen Internal Med, A91,9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Kent State Univ, Sch Biomed Sci, Kent, OH 44242 USA
[3] Louisiana State Univ Hlth Sci Ctr, Shreveport, LA 71105 USA
关键词
Clostridium difflicile; diarrhea; fluoroquinolones;
D O I
10.1185/030079908X253735
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Clostridium difficile, associated diarrhea (CDAD) is an important cause of hospital-acquired diarrhea, and increasingly of community-acquired diarrhea. The occurrence of CDAD in the hospitalized patient is associated with increased length of stay, morbidity, mortality, and healthcare costs. Exposure to antimicrobials is the single most important predisposing factor for acquiring CDAD. The data suggesting that fluoroquinolones are an important risk factor for CDAD is becoming stronger. Also, different fluoroquinolones may pose different risks for CDAD development. Objectives: The aim of this commentary is to summarize the literature as it relates to the role that fluoroquinolones may have in CDAD. Methods: PubMed and Ovid MEDLINE were searched using the terms fluoroquinolones, ciprofloxacin, levofloxacin, gatifloxacin, and moxifloxacin in combination with C. difficile, CDAD, pseudomembranous colitis and antibiotic associated diarrhea. Results: The evidence for an association between fluoroquinolone use and CDAD, especially CDAD due to the hypervirulent NAP1 strain or the polymerase chain reaction ribotype 027, is becoming stronger. Conclusions: Fluoroquinolones appear to predispose patients to CDAD. The data are suggestive but not conclusive. More studies are needed to define the role that fluoroquinolones play in the development of CDAD. Meticulous and enhanced infection control practices at all times and the judicious use of antimicrobials will help contain the epidemic of CDAD.
引用
收藏
页码:329 / 333
页数:5
相关论文
共 28 条
[1]   Correlation of disease severity with fecal toxin levels in patients with Clostridium difficile-associated diarrhea and distribution of PCR ribotypes and toxin yields in vitro of corresponding isolates [J].
Åkerlund, T ;
Svenungsson, B ;
Lagergren, Å ;
Burman, LG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (02) :353-358
[2]  
[Anonymous], 2007, Clin Infect Dis
[3]   Moxifloxacin therapy as a risk factor for clostridium difficile-associated disease during an outbreak: Attempts to control a new epidemic strain [J].
Biller, Priscilla ;
Shank, Beth ;
Lind, Leah ;
Brennan, Meghan ;
Tkatch, Lisa ;
Killgore, George ;
Thompson, Angela ;
McDonald, L. Clifford .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2007, 28 (02) :198-201
[4]  
DAN M, 1989, AM J MED, V87, P479
[5]   High-level resistance to moxifloxacin and gatifloxacin associated with a novel mutation in gyrB in toxin-A-negative, toxin-B-positive Clostridium difficile [J].
Drudy, Denise ;
Quinn, Teresa ;
O'Mahony, Rebecca ;
Kyne, Lorraine ;
O'Gaora, Peadar ;
Fanning, Seamus .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 58 (06) :1264-1267
[6]   DIAGNOSIS AND TREATMENT OF CLOSTRIDIUM-DIFFICILE COLITIS [J].
FEKETY, R ;
SHAH, AB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (01) :71-75
[7]   Outbreak of Clostridium difficile infection in a long-term care facility:: Association with gatifloxacin use [J].
Gaynes, R ;
Rimland, D ;
Killum, E ;
Lowery, HK ;
Johnson, TM ;
Killgore, G ;
Tenover, FC .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (05) :640-645
[8]   CLOSTRIDIUM-DIFFICILE ASSOCIATED DIARRHEA AND COLITIS IN ADULTS - A PROSPECTIVE CASE-CONTROLLED EPIDEMIOLOGIC-STUDY [J].
GERDING, DN ;
OLSON, MM ;
PETERSON, LR ;
TEASLEY, DG ;
GEBHARD, RL ;
SCHWARTZ, ML ;
LEE, JT .
ARCHIVES OF INTERNAL MEDICINE, 1986, 146 (01) :95-100
[9]   Clindamycin, cephalosporins, fluoroquinolones, and Clostridium difficile-associated diarrhea:: This is an antimicrobial resistance problem [J].
Gerding, DN .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (05) :646-648
[10]  
Jones EM, 1997, LANCET, V349, P1176, DOI 10.1016/S0140-6736(05)63056-5