Infection-control measures reduce transmission of vancomycin-resistant enterococci in an endemic setting

被引:131
作者
Montecalvo, MA
Jarvis, WR
Uman, J
Shay, DK
Petrullo, C
Rodney, K
Gedris, C
Horowitz, HW
Wormser, GP
机构
[1] New York Med Coll, Div Infect Dis, Valhalla, NY 10595 USA
[2] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[3] Westchester Cty Med Ctr, Dept Microbiol, Valhalla, NY 10595 USA
关键词
D O I
10.7326/0003-4819-131-4-199908170-00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Vancomycin-resistant enterococci (VRE) are nosocomial pathogens in many U.S. hospitals. Objective: To determine whether enhanced infection-control strategies reduce transmission of VRE in an endemic setting. Design: Prospective cohort study. Setting: Adult oncology inpatient unit. Patients: 259 patients evaluated during use of enhanced infection-control strategies and 184 patients evaluated during use of standard infection-control practices. Interventions: Patient surveillance cultures were taken, patients were assigned to geographic cohorts, nurses were assigned to patient cohorts, gowns and gloves were worn on room entry, compliance with infection-control procedures was monitored, patients were educated about VRE transmission, patients taking antimicrobial agents were evaluated by an infectious disease specialist, and environmental surveillance was performed. Measurements: VRE infection rates, VRE colonization rates, and changes in antimicrobial use. Results: During use of enhanced infection-control strategies, incidence of VRE bloodstream infections decreased significantly (0.45 patients per 1000 patient-days compared with 2.1 patients per 1000 patient-days; relative rate ratio, 0.22 [95% CI, 0.05 to 0.92]; P = 0.04), as did VRE colonization (10.3 patients per 1000 patient-days compared with 20.7 patients per 1000 patient-days; relative rate ratio, 0.5 [CI, 0.33 to 0.75]; P < 0.001). Use of all antimicrobial agents except clindamycin and amikacin was significantly reduced. Conclusion: Enhanced infection-control strategies reduced VRE transmission in an oncology unit in which VRE were endemic.
引用
收藏
页码:269 / 272
页数:4
相关论文
共 17 条
[1]  
Anderson RL, 1997, INFECT CONT HOSP EP, V18, P195
[2]  
[Anonymous], 1993, MMWR-MORBID MORTAL W, V42, P597
[3]   OUTBREAK OF MULTIDRUG-RESISTANT ENTEROCOCCUS-FAECIUM WITH TRANSFERABLE VANB CLASS VANCOMYCIN RESISTANCE [J].
BOYCE, JM ;
OPAL, SM ;
CHOW, JW ;
ZERVOS, MJ ;
POTTERBYNOE, G ;
SHERMAN, CB ;
ROMULO, RLC ;
FORTNA, S ;
MEDEIROS, AA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (05) :1148-1153
[4]  
*CONTR PRACT ADV C, 1995, MMWR-MORBID MORTAL W, V44, P1
[5]   VANCOMYCIN-RESISTANT ENTEROCOCCUS-FAECIUM BACTEREMIA - RISK-FACTORS FOR INFECTION [J].
EDMOND, MB ;
OBER, JF ;
WEINBAUM, DL ;
PFALLER, MA ;
HWANG, T ;
SANFORD, MD ;
WENZEL, RP .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (05) :1126-1133
[6]   CDC DEFINITIONS FOR NOSOCOMIAL INFECTIONS, 1988 [J].
GARNER, JS ;
JARVIS, WR ;
EMORI, TG ;
HORAN, TC ;
HUGHES, JM .
AMERICAN JOURNAL OF INFECTION CONTROL, 1988, 16 (03) :128-140
[7]   OUTBREAK OF VANCOMYCIN-RESISTANT, AMPICILLIN-RESISTANT, AND AMINOGLYCOSIDE-RESISTANT ENTEROCOCCUS-FAECIUM BACTEREMIA IN AN ADULT ONCOLOGY UNIT [J].
MONTECALVO, MA ;
HOROWITZ, H ;
GEDRIS, C ;
CARBONARO, C ;
TENOVER, FC ;
ISSAH, A ;
COOK, P ;
WORMSER, GP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (06) :1363-1367
[8]   ENTEROCOCCI RESISTANT TO MULTIPLE ANTIMICROBIAL AGENTS, INCLUDING VANCOMYCIN - ESTABLISHMENT OF ENDEMICITY IN A UNIVERSITY MEDICAL-CENTER [J].
MORRIS, JG ;
SHAY, DK ;
HEBDEN, JN ;
MCCARTER, RJ ;
PERDUE, BE ;
JARVIS, W ;
JOHNSON, JA ;
DOWLING, TC ;
POLISH, LB ;
SCHWALBE, RS .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (04) :250-259
[9]   COMPARISON OF GENOMIC DNAS OF DIFFERENT ENTEROCOCCAL ISOLATES USING RESTRICTION ENDONUCLEASES WITH INFREQUENT RECOGNITION SITES [J].
MURRAY, BE ;
SINGH, KV ;
HEATH, JD ;
SHARMA, BR ;
WEINSTOCK, GM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (09) :2059-2063
[10]   Manipulation of a hospital antimicrobial formulary to control an outbreak of vancomycin-resistant enterococci [J].
Quale, J ;
Landman, D ;
Saurina, G ;
Atwood, E ;
DiTore, V ;
Patel, K .
CLINICAL INFECTIOUS DISEASES, 1996, 23 (05) :1020-1025