Hostname: page-component-8448b6f56d-wq2xx Total loading time: 0 Render date: 2024-04-23T23:19:38.702Z Has data issue: false hasContentIssue false

Antianaerobic Antibiotic Therapy Promotes Overgrowth of Antibiotic-Resistant, Gram-Negative Bacilli and Vancomycin-Resistant Enterococci in the Stool of Colonized Patients

Published online by Cambridge University Press:  02 January 2015

Anita Bhalla
Affiliation:
Infectious Diseases Division, University Hospitals of Cleveland, Cleveland, Ohio
Nicole J. Pultz
Affiliation:
Infectious Diseases Section, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, Ohio
Amy J. Ray
Affiliation:
Department of Medicine, University Hospitals of Cleveland, Cleveland, Ohio
Claudia K. Hoyen
Affiliation:
Pediatrics Department, Rainbow Babies and Childrens Hospital, Cleveland, Ohio
Elizabeth C. Eckstein
Affiliation:
Infectious Diseases Section, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, Ohio
Curtis J. Donskey*
Affiliation:
Infectious Diseases Section, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, Ohio
*
Infectious Diseases Section, Louis Stokes Cleveland Veterans Affairs Medical Center, 10701 East Boulevard, Cleveland, OH 44106

Abstract

Background and Objective:

Antianaerobic antibiotic therapy promotes persistent high-density growth of vancomycin-resistant enterococci (VRE) in the stool of colonized patients. We tested the hypothesis that antibiotic regimens with potent antianaerobic activity promote overgrowth of coexisting antibiotic-resistant, gram-negative bacilli in the stool of VRE-colonized patients.

Design:

Eight-month prospective study examining the effect of antibiotic therapy on the stool density of gram-negative bacilli resistant to ceftazidime, ciprofloxacin, or piperacillin/tazobactam.

Setting:

A Department of Veterans Affairs medical center including an acute care hospital and nursing home.

Patients:

All VRE-colonized patients with at least 3 stool samples available for analysis.

Results:

One-hundred forty stool samples were obtained from 37 study patients. Forty-nine (61%) of 80 stool samples obtained during therapy with an antianaerobic regimen were positive for an antibiotic-resistant, gram-negative bacillus, whereas only 14 (23%) of 60 samples obtained 4 or more weeks after completion of such therapy were positive (P < .001). Twenty-four (65%) of the 37 patients had one or more stool cultures positive for a gram-negative bacillus resistant to ciprofloxacin, ceftazidime, or piperacillin/tazobactam. The density of these organisms was higher during therapy with antianaerobic regimens than in the absence of such therapy for at least 2 weeks (mean ± standard deviation, 5.6 ± 1.4 and 3.9 ± 0.71 log10 organisms/g; P < .001).

Conclusion:

Limiting the use of antianaerobic antibiotics in VRE-colonized patients may reduce the density of colonization with coexisting antibiotic-resistant, gram-negative bacilli.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2003

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Vollaard, EJ, Clasener, HAL. Colonization resistance. Antimicrob Agents Chemother 1994;38:409414.Google Scholar
2.Donskey, CJ, Chowdhry, TK, Hecker, MT, et al.Effect of antibiotic therapy on the density of vancomycin-resistant enterococci in the stool of colonized patients. N Engl J Med 2000;343:19251932.Google Scholar
3.Freter, R, Brickner, H, Botney, M, et al.Mechanisms that control bacterial populations in continuous-flow culture models of mouse large intestinal flora. Infect Immun 1983;39:676685.Google Scholar
4.Donskey, CJ, Hanrahan, JA, Hutton, RA, Rice, LB. Effect of parenteral antibiotic administration on persistence of vancomycin-resistant Enterococcus faecium in the mouse gastrointestinal tract. J Infect Dis 1999;180:384390.Google Scholar
5.Wilson, KH. The microecology of Clostridium difficile. Clin Infect Dis 1993;15(suppl 4):S214S218.Google Scholar
6.Louie, TJ. Preservation of colonization resistance parameters during empiric therapy with aztreonam in the febrile neutropenic patient. Reviews of Infectious Diseases 1985;7(suppl 4):S747S761.Google Scholar
7.Samonis, G, Gikas, A, Anaissie, EJ, et al.Prospective evaluation of effects of broad-spectrum antibiotics on gastrointestinal yeast colonization of humans. Antimicrob Agents Chemother 1993;37:5153.Google Scholar
8.Hoyen, CK, Pultz, NJ, Paterson, DL, Aron, DC, Donskey, CJ. Effect of parenteral antibiotic administration on the establishment of intestinal colonization with extended-spectrum β-lactamase-producing Klebsiella pneumoniae in mice. Antimicrob Agents Chemother. In press.Google Scholar
9.Donskey, CJ, Ray, AJ, Hoyen, CK, Fuldauer, PD, Aron, DC, Bonomo, RA. Colonization and infection with multiple nosocomial pathogens in patients colonized with vancomycin-resistant Enterococcus. Infect Control Hosp Epidemiol 2003;24:242245.Google Scholar
10.Ray, AJ, Pultz, NJ, Bhalla, A, Aron, DC, Donskey, CJ. Coexistence of vancomycin-resistant enterococci and Staphylococcus aureus in the intestinal tracts of hospitalized patients. Clin Infect Dis. In press.Google Scholar
11.Bodey, GP, Fainstein, V, Garcia, I, Rosenbaum, B, Wong, Y. Effect of broad-spectrum cephalosporins on the microbial microbiota of recipients. J Infect Dis 1983;148:892897.Google Scholar
12.Kager, L, Liljeqvist, L, Malmborg, AS, Nord, CE. Effect of clindamycin prophylaxis on the colonic microflora in patients undergoing colorectal surgery. Antimicrob Agents Chemother 1981;20:736740.CrossRefGoogle ScholarPubMed
13.Nord, CE, Brismar, B, Hasholm-Tengve, B, Tunevall, G. Effect of piperacillin/tazobactam therapy on intestinal microflora. Scand J Infect Dis 1992;24:209213.Google Scholar
14.Mulligan, ME, Citron, D, Gabay, E, et al.Alterations in human fecal flora, including ingrowth of Clostridium difficile, related to cefoxitin therapy. Antimicrob Agents Chemother 1984;26:343346.CrossRefGoogle ScholarPubMed
15.Edlund, C, Barkholt, L, Olsson-Liljequist, B, Nord, CE. Effect of vancomycin on intestinal flora of patients who have previously received antimicrobial therapy. Clin Infect Dis 1997:25:729732.Google Scholar
16.Nord, CE, Heimdahl, A, Kager, L, Malmborg, AS. The impact of different antimicrobial agents on the normal gastrointestinal microflora of humans. Reviews of Infectious Diseases 1984;6(suppl 1) :S270S196.CrossRefGoogle ScholarPubMed
17.Sakata, H, Fujita, K, Yoshioka, H. The effect of antimicrobial agents on fecal flora of children. Antimicrob Agents Chemother 1986;29:225229.Google Scholar
18.Edlund, C, Nord, CE. Effect of quinolones on intestinal ecology. Drugs 1999;58(suppl 2):6570.Google Scholar
19.Bacher, KSchaeffer, M, Lode, H, Nord, CE, Borner, K, Koeppe, P. Multiple dose pharmacokinetics, safety, and effects on faecal microflora, of cefepime in healthy volunteers. J Antimicrob Chemother 1992;30:365375.Google Scholar
20.Vollaard, EJ, Clasener, HA, Janssen, AJ. Co-trimoxazole impairs colonization resistance in healthy volunteers. J Antimicrob Chemother 1992;30:685691.CrossRefGoogle ScholarPubMed
21.National Committee for Clinical Laboratory Standards. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically. Wayne, PA: National Committee for Clinical Laboratory Standards; 1993: Approved standard M7-A3.Google Scholar
22.Ray, AJ, Hoyen, CK, Taub, TF, Eckstein, EC, Donskey, CJ. Nosocomial transmission of vancomycin-resistant enterococci from surfaces. JAMA 2002;287:14001401.CrossRefGoogle ScholarPubMed
23.Hecker, MT, Aron, DC, Patel, NP, Lehman, MK, Donskey, CJ. Unnecessary use of antimicrobials in hospitalized patients: current patterns of misuse with an emphasis on the antianaerobic spectrum of activity. Arch Intern Med 2003;163:972978.Google Scholar