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Prevalence and risk factors for VRE colonisation in a tertiary hospital in Melbourne, Australia: a cross sectional study.
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PMID:  23039285     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Vancomycin-resistant Enterococcus (VRE) has been established as a significant health-care associated problem since its first isolation in Australia in 1994. In this study, we measured the point prevalence and identified risk factors associated with vanB VRE colonisation in a tertiary care hospital in Melbourne, Australia where VRE has been endemic for 15 years.
METHODS: A hospital-wide point prevalence survey was conducted on October 13, 2008 with colonisation detected using rectal swab culture. Patient's demographic and medical information was collected through a review of medical records. Factors associated with VRE colonisation in univariate analysis were included in multivariate logistic regression model to adjust for confounding.
RESULTS: The prevalence of VRE colonisation on the day of screening was 17.5% (95% CI, 13.7 to 21.9). VRE was detected from patients in each ward with the prevalence ranging from 3% to 29%. Univariate analysis showed the use of any antibiotic, meropenem, ciprofloxacin, diarrhoea and longer length of hospital stay were associated with increased risk of VRE colonisation (p<0.05). However, age, sex, proximity to VRE positive cases, use of other antibiotics including cephalosporins, vancomycin were not associated with increased risk (P>0.05). Multivariate analysis showed the exposure to meropenem (p=0.004), age (≥65 years) (p=0.036) and length of stay ≥7 days (p<0.001) as independent predictors of VRE colonisation.
CONCLUSION: Our study suggests that exposure to antibiotics may have been more important than recent cross transmission for a high prevalence of vanB VRE colonisation at our hospital.
Authors:
Surendra Karki; Leanne Houston; Gillian Land; Pauline Bass; Rosaleen Kehoe; Sue Borrell; Kerrie Watson; Denis Spelman; Jacqueline Kennon; Glenys Harrington; Allen C Cheng
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Publication Detail:
Type:  Journal Article     Date:  2012-10-08
Journal Detail:
Title:  Antimicrobial resistance and infection control     Volume:  1     ISSN:  2047-2994     ISO Abbreviation:  Antimicrob Resist Infect Control     Publication Date:  2012  
Date Detail:
Created Date:  2012-12-17     Completed Date:  2012-12-18     Revised Date:  2013-04-18    
Medline Journal Info:
Nlm Unique ID:  101585411     Medline TA:  Antimicrob Resist Infect Control     Country:  England    
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Languages:  eng     Pagination:  31     Citation Subset:  -    
Affiliation:
Department of Epidemiology and Preventive Medicine, Infectious Disease Epidemiology Unit, Monash University, Melbourne, Australia. allen.cheng@monash.edu.
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Journal ID (nlm-ta): Antimicrob Resist Infect Control
Journal ID (iso-abbrev): Antimicrob Resist Infect Control
ISSN: 2047-2994
Publisher: BioMed Central
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Copyright ©2012 Karki et al.; licensee BioMed Central Ltd.
open-access:
Received Day: 11 Month: 7 Year: 2012
Accepted Day: 1 Month: 10 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 8 Month: 10 Year: 2012
Volume: 1First Page: 31 Last Page: 31
PubMed Id: 23039285
ID: 3523023
Publisher Id: 2047-2994-1-31
DOI: 10.1186/2047-2994-1-31

Prevalence and risk factors for VRE colonisation in a tertiary hospital in Melbourne, Australia: a cross sectional study
Surendra Karki1 Email: Surendra.karki@monash.edu
Leanne Houston2 Email: Leanne.Houston@easternhealth.org.au
Gillian Land3 Email: G.Land@alfred.org.au
Pauline Bass3 Email: P.Bass@alfred.org.au
Rosaleen Kehoe3 Email: r.kehoe@alfred.org.au
Sue Borrell3 Email: S.Borrell@alfred.org.au
Kerrie Watson3 Email: K.Watson@alfred.org.au
Denis Spelman4 Email: D.Spelman@alfred.org.au
Jacqueline Kennon3 Email: J.Kennon@alfred.org.au
Glenys Harrington4 Email: infexion@ozemail.com.au
Allen C Cheng13 Email: allen.cheng@monash.edu
1Department of Epidemiology and Preventive Medicine, Infectious Disease Epidemiology Unit, Monash University, Melbourne, Australia
2Infection Control, Eastern Health, Melbourne, Australia
3Infection Prevention and Healthcare Epidemiology Infectious Diseases and Microbiology Unit, Alfred Health, Melbourne, Australia
4Infection Control Consultancy, Melbourne, Australia

Background

The emergence and spread of vancomycin-resistant Enterococcus (VRE) in health care settings has added risks and complexities in patient management. VRE can cause a variety of health care-associated infections, particularly bacteraemia and urinary tract infections. Most enterococcal infections are caused by two species, E. faecalis or E. faecium. VRE was first reported in Europe in 1986 and subsequently worldwide [1]. In Australia, the first case of VRE was reported in 1994 and by 1998 from all other major cities [2,3]. The predominant VRE genotype circulating in Australia is E. faecium vanB, in contrast to the vanA genotype which is predominant in the United States and Europe [3,4]. Recent surveys have shown an increase in the prevalence of vancomycin resistance in clinical isolates of enterococci in Australia [5]. A VRE prevalence as high as 19.1% was reported during an outbreak among hospital inpatients in Victoria [6]. Faecal colonisation with VRE in the community has been demonstrated in Australia but appears to be rare (prevalence 0.2%) although the vanB gene appears to be common in commensal bacteria including Clostridium spp [7-9].

Previous studies have identified various risk factors for VRE colonisation including advanced age, severe underlying illness, inter-hospital transfer, nursing home residency, extended hospitalization, specialized nutritional support, central venous catheterization, haematologic malignant tumours, solid organ allograft, chronic haemodialysis, antibiotic exposure to vancomycin, third-generation cephalosporins, metronidazole, antibiotics with anti-anaerobic activity, exposure to multiple antibiotics and prolonged duration of antibiotic therapy [10]. However, most of those studies involve high risk patients during outbreaks associated with vanA genotype. A previous study in Melbourne hospitals in 1998 identified broad spectrum antibiotics as significant risk factor for new colonisation with vanB VRE [11].

VRE colonisation can lead to infections which prolong hospital stay, increase the cost of care and increase morbidity and mortality [12,13]. The identification of modifiable risk factors may assist in identifying targets for intervention to reduce the incidence of VRE colonisation. In this study, we measured the prevalence of VRE colonisation in a hospital-wide point prevalence survey. We examined downstream risk factors for colonisation with implications for VRE control policies, including antibiotic exposure and patient placement, in a tertiary referral hospital in Melbourne, Australia where vanB VRE has been endemic for many years.


Methods
Setting and study design

The Alfred hospital is a major tertiary teaching hospital in Melbourne, Australia with 427 beds. The hospital provides general services as well as broad range of specialist care including referral services for trauma, cystic fibrosis and heart/lung transplantation, HIV/AIDS, bone marrow transplantation as well as specialist intensive care facilities.

We conducted a point prevalence survey on October 13, 2008 at the Alfred Hospital. All patients who were present in the hospital (including inpatients, patients in the emergency department, and day surgery but excluding psychiatry) at 8.00 a.m. were approached to participate. Patients were provided with information sheets (including advice about the potential consequences of VRE colonisation) and verbal consent was obtained for participation. Patients were included irrespective of known VRE status. Patients were excluded if they were not able to consent, were for palliative care only, had been discharged prior to being swabbed or they declined to participate. Single rectal swabs were primarily taken by nursing staff. Clinical data collection included demographic details, bed location of all patients, antibiotic use (at least 12 hours before the collection of rectal swab in current admission), ICU exposure, and previous hospital admissions in patients that were found to be positive for VRE.

At the time of the survey, our VRE policy recommended the screening of all ward patients where a new case of VRE infection or colonisation was detected. There were no systemic screening practices for patients in high risk areas or testing of diarrhoeal stools prior to this study. Patients with known VRE colonisation or infection were isolated in single rooms with a dedicated toilet if they had faecal incontinence or diarrhoea. Healthcare workers were required to use gloves when entering the room, and gloves and gown if contact with body fluids was anticipated. Hospital floors were cleaned daily with 1000 part per million (ppm) sodium hypochlorite.

A nested case control (1:2) study was conducted to identify risk factors associated with VRE colonisation. A case was defined as a patient confirmed to be positive by standard microbiological methods for VRE isolated from rectal swabs taken for the point prevalence survey. A control was defined as a patient confirmed to be negative for VRE colonisation on the same survey. For each case, two unmatched controls were selected at random from eligible patients.

Microbiology

Rectal swabs were taken either by the patients themselves following instruction, or by nursing staff. The swabs were then plated onto bile aesculin media (BBL Enterococcosel agar, Cockeysville, MD) with vancomycin 6 μg/mL and incubated at 37°C for up to 72 hours. Enterococci species were identified using the VITEK-2 system (bioMérieux). Polymerase chain reaction was used to detect the vanA or vanB genes as described previously. [14] VRE colonisation was defined if an isolate of E. faecalis or E. faecium with vanA or vanB gene was detected. Ribotyping of the isolates was performed using the Riboprinter Microbial Characterization system as previously described [15,16].

Statistical methods

Standard statistical methods were used to summarize categorical and continuous measures and to compare proportions. Univariate analysis was performed to calculate unadjusted odds ratio. All variables with a p-value of <0.2 in univariate analysis were included in the multiple logistic regression model to examine independently associated risk factors for VRE colonisation. The association was considered statistically significant if p<0.05. Statistical analyses were performed using Stata statistical software (Version 10; Stata Corp, College Station, Texas).

Ethics

As this VRE survey represented a quality assurance activity, we did not obtain a formal ethical approval to perform the point prevalence survey. However, we counselled patients about the significance of VRE and provided written information, and obtained verbal consent to take rectal swabs from all patients and/or their relatives. We obtained approval from the Alfred Health Human Research Ethics Committee and Monash University Human Research Ethics Committee to retrieve demographic and clinical information from the medical records of patients for the case control study.


Results

A total of 434 patients were present in hospital at the time of survey. Among the total, 331 (77%) were screened for VRE colonisation; 103 patients (23%) could not be screened either due to refusal, discharge from hospital prior to the time of swabbing, patients not being present in the ward at the time of screening, or if the patient was for palliative care.

The prevalence of VRE colonisation on the day of screening was 58 of 331 patients (17.5%, 95% CI, 13.7% to 21.9%). The proportion of patients colonised with VRE was 3% in the emergency department and ranged from 8% to 29% in inpatient wards. Of the 58 VRE isolates, 57 were found to be Enterococcus faecium and one was Enterococcus faecalis. All the isolates were positive for vanB resistance genotype and no vanA resistance genotype was detected. All together, 9 ribotypes were detected with the majority of isolates belonging to either of the two ribotypes (S-7, n=25, 43%; S-5, n=23, 39%). However, more than 1 ribotype was present in all wards where there was more than one VRE-colonised patient present.

Of the total 58 patients found to be VRE colonised, 46 (79.3%) were not previously known to be VRE colonised and 12 (20.7%) were known to be previously colonised. A further 13 patients had a history of VRE colonisation but VRE was not detected on screening at the time of the survey.

Risk factors for VRE colonisation

We compared the exposure to probable risk factors in 58 cases and 116 controls.

Significantly higher proportions of cases had prior exposure to one or more antibiotics (odds ratio (OR) 3.83, 95% CI 1.79 to 8.54). Similarly, cases had a longer length of hospital stay compared to controls (P<0.001). Patients with VRE colonisation were more likely to have been admitted for ≥7 days (OR 4.86, 95% CI 2.30 to 10.51). Univariate analyses identified prior exposure to any antibiotic (p <0.001), exposure to meropenem (p=0.001), ciprofloxacin (p=0.03), diarrhoea (p=0.03) as associated with the detection of VRE colonisation (Table  1). However, the prior use of vancomycin (p=0.33), ticarcillin-clavulanate (p=0.11), pipericillin-tazobactam (p=0.07), metronidazole (p=0.16) and any cephalosporins were not associated with colonisation status. Proximity to other VRE positive cases either in same side of the ward or located within next 2 rooms was not associated with VRE colonisation (p>0.05) (Table  1).

In a multivariate logistic regression model, exposure to meropenem (adjusted OR; 12.24, 95% CI 2.24 to 66.77), age ≥ 65years (adjusted OR 2.19, 95% CI 1.05 to 4.58) and length of stay ≥7 days (adjusted OR 4.69, 95% CI 2.25 to 9.73) were independently associated with VRE colonisation (Table  2). After adjusting for age ≥ 65years, length of stay ≥7 days and exposure to meropenem, exposure to any antibiotic other than meropenem (compared to patients that did not receive any antibiotics) was independently associated with VRE colonisation (adjusted OR 2.95, 95% CI 1.27 to 6.88). In total, 16 (9.2%) patients in case–control study were from emergency department and short stay units. A sensitivity analysis excluding the patients in these units did not alter any of the above effects, significantly.


Discussion

We conducted a hospital-wide point prevalence survey to measure the prevalence of VRE, as our previous surveillance activities were targeted to patients felt to be at risk and therefore may have resulted in selection biases. In this survey, we confirmed that vanB VRE is endemic in inpatients at our hospital. We found a lower prevalence in short stay areas, such as the emergency department (3%) and the short stay unit, but prevalence was 8-29% in other inpatient areas. This is higher than reported by previous studies conducted at Melbourne hospitals [11,17-19]. This is also in contrast to previous studies demonstrating that VRE colonisation was restricted to particular high risk inpatient areas [11]. Our finding that 80% of the VRE colonised patients in the survey were newly detected cases demonstrates that the previous screening strategy of surveying patients only on wards when a new clinical isolate of VRE was detected is inadequate.

Prima facie, our results suggest that antibiotic selection pressures appear to play a larger role in determining VRE colonisation than cross-transmission at our institution. Exposure to antibiotics, particularly meropenem, was strongly associated with VRE colonisation; this is consistent with previous studies suggesting that antibiotic regimens with activity against anaerobic bacteria are potent risk factors in the development of VRE [20-22]. The vanB gene is known to be present in commensal enteric bacteria such as Clostridium, and transmission of this gene to E. faecium has been demonstrated in vivo[23]. In other studies, a variety of other antibiotics have been implicated as risk factors for VRE colonisation, including vancomycin, metronidazole, piperacillin-tazobactam, ticarcillin-clavulanate and third generation cephalosporins [24-26]. However, our analysis comparing meropenem and non-meropenem antibiotic use with no antibiotic use showed the exposure to antibiotics other than meropenem is also associated with VRE colonisation. Thus, our study may have been underpowered to detect differences at the level of individual antibiotics other than meropenem.

We found ambiguous evidence regarding the extent of cross transmission of VRE, which has been shown to be important in previous studies [27,28]. We did not find proximity to other VRE colonised patients to be a risk factor for VRE detection. However, this does not exclude the possibility of cross transmission contributing to endemicity, as transmission may have occurred prior to the time of the survey and would not be detected with frequent patient movements. Conversely, the finding that ribotyping only demonstrated two large clones of VRE in patients does not necessarily implicate extensive cross transmission. If transmission was significant, we would expect a lower diversity among individual wards; however, we found that in all wards with at least two VRE colonised patients had at least two ribotypes. We did not have access to pulsed field gel electrophoresis, regarded as the gold standard for epidemiological investigations of VRE [29].

The purpose of this study was to examine “downstream” exposures that had implications for VRE control policies, rather than patient-specific “upstream” risk factors that are not modifiable. However, we did find older age and longer length of stay in hospital as independent predictor of VRE colonisation. This is reflected in the low colonisation rate in patients with a short length of stay, including emergency and short stay units.

A strength of this study is that we conducted a hospital-wide survey including a broad range of patients, thus minimizing selection biases [30]. A limitation of this cross-sectional study is that we were not able to determine the timing of acquisition of VRE in the patients identified as being colonised; therefore, patients may have acquired VRE in the remote past, with antibiotic use merely amplifying existing colonisation. In addition, we do not have data on patient co-morbidities, previous invasive procedures, and indwelling devices, which may have confounded our findings. We chose to perform rectal swabs due to practical reasons but previous studies have demonstrated that the sensitivity of these specimens is around 79%, we might have missed detection of few patients with low VRE density [31,32]. We did not perform separate broth enrichment before the agar plate culture, which may lead to an underestimation of the true prevalence [33]. This may have resulted in misclassification bias in assigning VRE colonised patients as controls and bias the case control study towards the null hypothesis. As the sensitivity of VRE detection is likely to be related to bacterial density, it is likely that detection of VRE in screening is the product of two processes, that of new acquisition of VRE (whether by endogenous generation or exogenous exposure) and amplification of existing low level colonisation by antibiotics [34].


Conclusions

The endemic and high prevalence of vanB VRE in our setting may have been maintained by higher exposure to antibiotics. Although cross transmission remains a possibility and is supported by predominance of two large clones of VRE, colonisation status did not appear to be associated with proximity to other colonised patients. Our data suggest that antibiotic stewardship efforts may be more effective in reducing the spread of VRE in our hospital.


Competing interests

The authors declare that they have no competing interests.


Authors’ contributions

The point prevalence study was designed by GH, LH, GL, PB, SB, RK, DS. The study was primarily co-ordinated by LH with support from GH, LH, GL, PB, SB, RK, including identifying patients, co-ordinating swab collection and collecting data on cases. DS oversaw microbiological testing and typing. LH and KW managed the data and performed the initial analysis of cases. AC and SK designed and analysed the case control study with assistance from JK and DS. SK collected the data on controls and drafted the manuscript. All authors interpreted the results and revised the manuscript.


Acknowledgements

We thank ward staff at the Alfred Hospital for assisting in this survey, microbiology staff including Lisa Liolios for processing specimens and performing vanA and vanB PCR and the staff at the Microbiological Diagnostic Unit (The University of Melbourne) for performing ribotyping.


References
Uttley AH,Collins CH,Naidoo J,George RC,Vancomycin-resistant enterococciLancetYear: 1988157582891921
Kamarulzaman A,Tosolini FA,Boquest AL,Geddes JE,Richards MJ,Vancomycin-resistant Enterococcus faecium in a liver transplant patientAust NZ J MedYear: 199525560
Bell J,Turnidge J,Coombs G,O'Brien F,Emergence and epidemiology of vancomycin-resistant enterococci in AustraliaCommun Dis IntellYear: 1998222492529823687
Deshpande LM,Fritsche TR,Moet GJ,Biedenbach DJ,Jones RN,Antimicrobial resistance and molecular epidemiology of vancomycin-resistant enterococci from North America and Europe: a report from the SENTRY antimicrobial surveillance programDiagn Microbiol Infect DisYear: 20075816317010.1016/j.diagmicrobio.2006.12.02217368801
Christiansen KJ,Turnidge JD,Bell JM,George NM,Pearson JC,Prevalence of antimicrobial resistance in Enterococcus isolates in Australia, 2005: report from the Australian Group on Antimicrobial ResistanceCommun Dis IntellYear: 20073139239718268880
Cooper E,Paull A,O'Reilly M,Characteristics of a large cluster of vancomycin-resistant enterococci in an Australian hospitalInfect Control Hosp EpidemiolYear: 20022315115310.1086/50202711918122
Ballard SA,Pertile KK,Lim M,Johnson PD,Grayson ML,Molecular characterization of vanB elements in naturally occurring gut anaerobesAntimicrob Agents ChemotherYear: 2005491688169410.1128/AAC.49.5.1688-1694.200515855482
Padiglione AA,Grabsch EA,Olden D,Hellard M,Sinclair MI,Fairley CK,Grayson ML,Fecal colonisation with vancomycin-resistant enterococci in AustraliaEmerg Infect DisYear: 2000653453610.3201/eid0605.00051411202974
Graham M,Ballard SA,Grabsch EA,Johnson PD,Grayson ML,High rates of fecal carriage of nonenterococcal vanB in both children and adultsAntimicrob Agents ChemotherYear: 2008521195119710.1128/AAC.00531-0718180361
DeLisle S,Perl TM,Vancomycin-resistant enterococci: a road map on how to prevent the emergence and transmission of antimicrobial resistanceChestYear: 2003123504S518S10.1378/chest.123.5_suppl.504S12740236
Padiglione AA,Wolfe R,Grabsch EA,Olden D,Pearson SH,Franklin C,Spelman D,Mayall B,Johnson PDR,Grayson ML,Risk factors for new detection of vancomycin-resistant enterococci in acute-care hospitals that employ strict infection control proceduresAntimicrob Agents ChemotherYear: 2003472492249810.1128/AAC.47.8.2492-2498.200312878510
Joels CS,Matthews BD,Sigmon LB,Hasan R,Lohr CE,Kercher KW,Norton J,Sing RF,Heniford BT,Clinical characteristics and outcomes of surgical patients with vancomycin-resistant enterococcal infectionsAm SurgYear: 20036951451912852510
DiazGranados CA,Zimmer SM,Klein M,Jernigan JA,Comparison of mortality associated with vancomycin-resistant and vancomycin-susceptible enterococcal bloodstream infections: a meta-analysisClin Infect DisYear: 20054132733310.1086/43090916007529
Dutka-Malen S,Evers S,Courvalin P,Detection of glycopeptide resistance genotypes and identification to the species level of clinically relevant enterococci by PCRJ Clin MicrobiolYear: 19953314347615777
Bruce J,Automated system rapidly identifies and characterizes microorganisms in foodFood TechnolYear: 1996507781
Price CS,Huynh H,Paule S,Hollis RJ,Noskin GA,Pfaller MA,Peterson LR,Comparison of an automated ribotyping system to restriction endonuclease analysis and pulsed-field gel electrophoresis for differentiating vancomycin-resistant Enterococcus faecium isolatesJ Clin MicrobiolYear: 2002401858186110.1128/JCM.40.5.1858-1861.200211980978
Burrell LJ,Grabsch EA,Padiglione AA,Grayson ML,Prevalence of colonisation with vancomycin-resistant enterococci (VRE) among haemodialysis outpatients in Victoria: implications for screeningMedical Journal of AustraliaYear: 200518249249215865598
Grayson ML,Grabsch EA,Johnson PDR,Olden D,Aberline M,Li HY,Hogg G,Abbott M,Kerr PG,Outcome of a screening program for vancomycin-resistant enterococci in a hospital in VictoriaMedical Journal of AustraliaYear: 199917113313610474604
Victorian Advisory Committee on Infection ControlVancomycin Resistant Enterococci (VRE) in Victorian Health FacilitiesYear: 2008Victorian Department of Health, Melbourne http://www.health.vic.gov.au/infectionprevention/downloads/vre-report.pdf, accessed June 10, 2012.
Al-Nassir WN,Sethi AK,Li YJ,Pultz MJ,Riggs MM,Donskey CJ,Both oral metronidazole and oral vancomycin promote persistent overgrowth of vancomycin-resistant enterococci during treatment of Clostridium difficile-associated diseaseAntimicrob Agents ChemotherYear: 2008522403240610.1128/AAC.00090-0818443120
Carmeli Y,Eliopoulos GM,Samore MH,Antecedent treatment with different antibiotic agents as a risk factor for vancomycin-resistant enterococcusEmerg Infect DisYear: 2002880280710.3201/eid0808.01041812141965
MacIntyre CR,Empson M,Boardman C,Sindhusake D,Lokan J,Brown GV,Risk factors for colonisation with vancomycin-resistant enterococci in a Melbourne hospitalInfect Control Hosp EpidemiolYear: 20012262462910.1086/50183311776348
Launay A,Ballard SA,Johnson PDR,Grayson ML,Lambert T,Transfer of vancomycin resistance transposon Tn1549 from Clostridium symbiosum to Enterococcus spp. in the gut of gnotobiotic miceAntimicrob Agents ChemotherYear: 2006501054106210.1128/AAC.50.3.1054-1062.200616495268
Askarian M,Afkhamzadeh R,Monabbati A,Daxboeck F,Assadian O,Risk factors for rectal colonisation with vancomycin-resistant enterococci in Shiraz, IranInt J Infect DisYear: 20081217117510.1016/j.ijid.2007.04.02017855141
Loeb M,Salama S,Armstrong-Evans M,Capretta G,Olde J,A case–control study to detect modifiable risk factors for colonisation with vancomycin-resistant enterococciInfect Control Hosp EpidemiolYear: 19992076076310.1086/50158010580629
Gordts B,Van Landuyt H,Ieven M,Vandamme P,Goossens H,Vancomycin-resistant enterococci colonising the intestinal tracts of hospitalized patientsJ Clin MicrobiolYear: 199533284228468576330
Byers KE,Anglim AM,Anneski CJ,Germanson TP,Gold HS,Durbin LJ,Simonton BM,Farr BM,A hospital epidemic of vancomycin-resistant Enterococcus: risk factors and controlInfect Control Hosp EpidemiolYear: 20012214014710.1086/50188011310691
Zhou Q,Moore C,Eden S,Tong A,McGeer A,Factors associated with acquisition of vancomycin-resistant enterococci (VRE) in roommate contacts of patients colonised or infected with VRE in a tertiary care hospitalInfect Control Hosp EpidemiolYear: 20082939840310.1086/58718718419360
Gordillo ME,Singh KV,Murray BE,Comparison of Ribotyping and Pulsed-Field Gel-Electrophoresis for Subspecies Differentiation of Strains of Enterococcus-FaecalisJ Clin MicrobiolYear: 199331157015748314998
Cole SR,Platt RW,Schisterman EF,Chu HT,Westreich D,Richardson D,Poole C,Illustrating bias due to conditioning on a colliderInt J EpidemiolYear: 20103941742010.1093/ije/dyp33419926667
Weinstein JW,Tallapragada S,Farrel P,Dembry LM,Comparison of rectal and perirectal swabs for detection of colonisation with vancomycin-resistant enterococciJ Clin MicrobiolYear: 1996342102128748308
D'Agata EMC,Gautam S,Green WK,Tang YW,High rate of false-negative results of the rectal swab culture method in detection of gastrointestinal colonisation with vancomycin-resistant enterococciClin Infect DisYear: 20013416717211740703
Ieven M,Vercauteren E,Descheemaeker P,van Laer F,Goossens H,Comparison of direct plating and broth enrichment culture for the detection of intestinal colonisation by glycopeptide-resistant enterococci among hospitalized patientsJ Clin MicrobiolYear: 1999371436144010203501
Padiglione AA,Grabsch E,Wolfe R,Gibson K,Grayson ML,The prevalence of fecal colonisation with VRE among residents of long-term-care facilities in Melbourne, AustraliaInfect Control Hosp EpidemiolYear: 20012257657810.1086/50195511732788

Tables
[TableWrap ID: T1] Table 1 

Factors associated with VRE detection in cases and controls (Univariate analysis)


Variables Cases Controls Unadjusted OR P value
Participants
58
116
-
-
Age ≥ 65 (years)
35 (60.3%)
56 (48.2%)
1.63 (0.82 to 3.26)
0.13
Male
36 (62.1%)
74 (63.8%)
0.92 (0.46 to 1.88)
0.82
Antibiotics
 
 
 
 
Exposure to any antibiotic
45 (77.6%)
55 (47.4%)
3.83 (1.79 to 8.54)
<0.001
Meropenem
8 (13.8%)
2 (1.7%)
9.12 (1.71 to 89.92)
0.001
Antibiotics other than meropenem
39 (67.2%)
54 (46.5%)
4.5 (2.06 to 10.71)
0.001
Vancomycin
13 (22.4%)
19 (16.38%)
1.47 (0.61 to 3.46)
0.33
Teicoplanin
2 (3.4%)
2 (1.7%)
2.03 (0.14 to 28.63)
0.47
Any cephalosporin
19 (32.8%)
32 (27.6%)
1.27 (0.60 to 2.66)
0.47
Ceftriaxone
11 (18.9%)
24 (20.7%)
0.89 (0.36 to 2.11)
0.78
Cefotaxime
2 (3.4%)
0
-
-
Ceftazidime
5 (8.6%)
4 (3.4%)
2.64 (0.54 to 13.79)
0.14
Cefepime
1 (1.7%)
6 (5.2%)
0.32 (0.01 to 2.76)
0.27
Metronidazole
5 (8.6%)
19 (16.4%)
0.48 (0.13 to 1.43)
0.16
Ciprofloxacin
11 (18.9%)
9 (7.8%)
2.78 (0.96 to 8.11)
0.03
Ticarcillin-clavulanate
11 (18.9%)
12 (10.3%)
2.02 (0.74 to 5.41)
0.11
Ampicillin
1 (1.7%)
3 (2.6%)
0.66 (0.01 to 8.45)
0.72
Gentamicin
2 (3.4%)
9 (7.8%)
0.42 (0.04 to 2.16)
0.27
Piperacillin-tazobactam
5 (8.6%)
3 (2.6%)
3.55 (0.65 to 23.53)
0.07
Other factors
 
 
 
 
ICU admission
18 (31.1%)
26 (22.4%)
1.55 (0.71 to 3.33)
0.21
Within 2 rooms of positive case
30 (62.5%)
54 (65.8%)
0.86 (0.38 to 1.94)
0.69
On same side as positive case
48 (82.8%)
83 (77.6%)
1.38 (0.57 to 3.53)
0.43
Diarrhoea
12 (21.1%)
11 (9.5%)
2.54 (0.94 to 6.85)
0.03
Length of stay (Median days)
11.5 (7–30)
6.0 (3–13)
-
<0.001
Length of stay ≥7 days 43 (74.2%) 43 (37.1%) 4.86 (2.30 to 10.51) <0.001

[TableWrap ID: T2] Table 2 

Factors associated with VRE detection in cases and controls (multivariate analysis)


Risk factor Adjusted OR (95% CI) p value
Meropenem
12.24 (2.24 to 66.77)
0.004
Age (≥65 years)
2.19 (1.05 to 4.58)
0.036
Length of stay ≥7 days 4.69 (2.25 to 9.73) <0.001


Article Categories:
  • Research

Keywords: VRE, Colonisation, Acquisition, Prevalence, Risk factors, Australia, VanB, Antibiotics.

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