INTRODUCTION
Methicillin-resistant Staphylococcus aureus (MRSA) is responsible for a substantial burden of illness due to healthcare- and community-associated infections. Within the European Union it is estimated that 150 000 patients per year have clinically relevant MRSA infections resulting in extra annual costs of €380 million [Reference Köck1]. Over the past two decades, there has been a shift away from acute-care hospitals with more healthcare being delivered in the outpatient setting, either at home or in long-term care facilities (LTCFs) [Reference Manzur and Gudiol2, Reference Manzur3]. Studies from different European countries have shown variable prevalence rates of MRSA colonization and predominance of MRSA genotypes often reflecting the national or local MRSA prevalence in acute-care hospitals [Reference Daeschlein4–Reference Eveillard16].
The aim of our study was to investigate the role of LTCFs as potential reservoirs for MRSA in the community. We conducted a prevalence study of MRSA colonization in a nationally representative sample of elderly residents of LTCFs in Luxembourg, to determine risk factors for colonization and to conduct molecular epidemiology of MRSA colonization isolates in the long-term care setting.
METHODS
Study population and epidemiological data collection
A nationally representative cross-sectional MRSA prevalence study in LTCF facilities was conducted from February to June 2010 in the Grand Duchy of Luxembourg. At the beginning of the study, in January 2010, 48 LTCFs with a total of 4688 beds (mean 98 beds per LTCF) were accredited by the Ministry of Family Affairs. According to national statistics (http://www.statistiques.public.lu), Luxembourg's elderly population (aged ⩾65 years) consisted of 70 046 persons in 2010, so that 67 beds/1000 elderly persons were available in publicly registered institutions.
Twenty-six LTCFs were selected at random using the random number generation function in Excel (Microsoft Corporation, USA) on three sequential sampling occasions until an approximate target of 1000 participants were recruited. Following an invitation by the Health Directorate, 19 (73%) LTCFs agreedto participate in the study. While one of the 19 LTCFs was physically adjacent to and associated with a hospital, the other LTFCs were not, and were geographically dispersed in different regions.
All residents of the nursing homes were informed by their local staff about the study and invited to participate subject to written informed consent given either by the elderly residents themselves or by an appropriate family member. The prevalence rate within the institution was communicated to individual LTCFs, but not individual test results. At the time of the study, there were no national guidelines on control procedures for positive MRSA residents. Ethical approval for the study was obtained from the national ethics committee. Demographic and risk factor data from all residents were collected using an anonymous paper questionnaire which was completed by nurses in the LTCFs prior to swab sampling. Data included date of sampling, date of residence, age in categories, sex, history of previous MRSA and decontamination, history of antibiotic therapies within the past year, hospitalization, comorbidities [chronic wounds, pressure sores (decubitus), urinary incontinence, urethral catheter, suprapubic catheter, diabetes, disorientated/dementia] and time allocated to essential care (minutes per week) according to the formal care assessment by the national dependency insurance.
Microbiological methods
For each resident, separate swabs for nose and throat were taken by the same nurse of the Health Directorate (in 18 LTCFs, respectively, in one LTCF by the infection control nurse) and additional swabs were taken if wounds were present. Urine samples were taken if the resident had a urethral or suprapubic catheter. Samples were transported on the same day to the laboratory for testing. Following incubation of pooled swabs in Todd-Hewitt enrichment broth (bioMérieux, France) for 18–24 h at 35 °C, 10 μl broth was plated onto chromID MRSA agar (bioMérieux) and incubated for 18–24 h at 35 °C. Putative green MRSA isolates were biochemically confirmed with the ID32 Staph gallery (bioMérieux). Following genomic DNA extraction by NucliSENS easyMAG (bioMérieux) an in-house multiplex real-time PCR on the LightCycler II platform (Roche Diagnostics, Germany) was used to simultaneously detect the presence of nuc and mecA genes, Panton–Valentine leukocidin (PVL) toxin coding gene and Toxic Shock Syndrome Toxin 1 (TSST-1) coding gene (see the Supplementary Material for a more detailed description). Isolates were tested by the disk diffusion method and the SIRSCAN automatic reader (i2a, Perols, France) for susceptibility to penicillin, cefoxitin, kanamycin, tobramycin, gentamicin, erythromycin, clindamycin, ciprofloxacin, rifampicin, tetracycline, fosfomycin, vancomycin, cotrimoxazole, furanes and mupirocin using CLSI breakpoints.
Molecular typing
All isolates were spa-typed using PCR conditions and the spa-F2 forward primer as described previously [Reference Oliveira17–Reference Baum19]. Analysis of spa sequences and assignment of spa-types were performed using the spa-typing plug-in tool of BioNumerics 5.10 (Applied Maths, Belgium). In addition, a selection of strains (one isolate of a particular spa-type per LTCF) was typed by multilocus sequence typing (MLST) [Reference Enright20].
Statistical analysis
All statistical testing was performed using Stata 10.1 (StataCorp., USA). Variation of the prevalence of MRSA colonization by LTCFs was assessed using StatXact-4 (Cytel Software Corp., USA). Risk factors for MRSA colonization were first estimated by univariate analysis and then by multiple logistic regression.
RESULTS
In 19 LTCFs, 1962 residents (mean 103 per LTCF) were invited to participate. Swab samples with epiemiological questionnaires were collected from 954 residents yielding an overall effective participation rate of 48·6%. Participation varied significantly by LTCF (see Table 1) with a range from 15·2% to 90·3% (Pearson's χ2, P < 0·0001). Women comprised 71·3% of the participants and 46% were aged ⩾85 years. Overall, 69 residents were colonized by MRSA yielding a prevalence rate of 7·2% [95% confidence interval (CI) 5·7–9·1]. MRSA colonization did not vary significantly between LTCFs (range 0–16·7%; Monte Carlo estimate of exact P value of Pearson's χ2 test, P = 0·185).
Number of residents invited to participate, participants and MRSA-positive residents by long-term care facility (LTCF)
In univariate analysis, significant risk factors for MRSA colonization were length of stay [odds ratio (OR) of starting residency before 2007: 1·93, 95% CI 1·16–3·20], known history of MRSA (OR 9·30, 95% CI 4·49–19·29), weekly care administered (⩾24 h: OR 8·08, 95% CI 3·26–20·00), any antibiotic therapy in the preceding year (OR 3·87, 95% CI 2·20–6·82), β-lactam therapy in the preceding year (OR 2·34, 95% CI 1·39–3·96), quinolone therapy in the preceding year (OR 2·74, 95% CI 1·63–4·61), pressure sores (OR 4·01, 95% CI 1·75–9·20), urinary incontinence (OR 2·30, 95% CI 1·39–3·81) and suprapubic catheter (OR 3·96, 95% 1·73–9·07). Age, sex, hospitalization in the preceding year, macrolide therapy in the preceding year, chronic wounds, urethral catheter, diabetes and disorientation were not associated with MRSA colonization (P > 0·05) in univariate analysis.
In multivariate analysis (Table 2), previous history of MRSA (OR 7·20, 95% CI 3·19–16·27), quinolone therapy in the previous year (OR 2·27, 95% CI 1·17–4·41) and ⩾24 h care administered per week (OR 4·29, 95% CI 1·18–15·56) remained independently associated with MRSA colonization.
Univariate and multivariate logistic regression analysis of risk factors associated with MRSA colonization in long-term care facility residents
OR, Odds ratio; CI, confidence interval.
For the 69 isolates submitted to spa-typing, 17 different spa-types were obtained (Supplementary Table S2). One isolate was not typable because the sequence of one of its repeats was too short for type assignment. Thirty-nine (57·3%) isolates belonged to spa-type 003, the remaining spa-types all accounting for <5% of isolates. The distribution of spa-types differed significantly by LTCF (exact P value = 0·0308), indicating a certain clustering effect and possibly transmission within LTCFs.
MLST on 31 isolates yielded eight different sequence types belonging to six clonal complexes (CC): CC5 (21 isolates), CC8 (four isolates), CC22 (two isolates), CC45 (one isolate), CC59 (one isolate) and CC398 (two isolates). Interestingly isolates of spa-type t003 could be further discriminated by MLST into ST710 (four isolates) and ST225 (14 isolates). Five (7·2%) isolates belonged to livestock associated spa-types t899 and t3106: one isolate of each of these two spa-types were confirmed as having sequence type (ST)398.
All isolates were resistant to β-lactams, 96% to ciprofloxacin, 75% to kanamycin and tobramycin, 72% to erythromycin, 68% to clindamycin, 10% to mupirocin, 7% to cotrimoxazole and tetracycline. None of the isolates was resistant to gentamicin, rifampicin and furanes. Resistance to the kanamycin, tobramycin, erythromycin and clindamycin was associated with CC5 (exact χ2 test, P < 0·001) and resistance to tetracycline and cotrimoxazole with CC398 (exact χ2 test, P < 0·001). Six of seven isolates resistant to mupirocin were clustered in a single institution.
DISCUSSION
The MRSA colonization prevalence of 7·2% observed in the current study in Luxembourg ranks in the middle of prevalences reported by similar studies in other European countries since 2000 (Table 3); our prevalence rate was generally lower than in Belgium and France, but generally higher than in Germany. Direct comparisons between countries and studies are difficult, because of differing sampling and microbiological methodologies, differing ‘case-mix’ populations, and possibly also because of different financing mechanisms of dependency care and LTCF provision. Due to their small number and limited geographical scope, studies presented in Table 3 are unlikely to yield a representative picture of the actual MRSA colonization rates in LTCFs throughout Europe. Difficulties in comparing MRSA prevalence rates in hospitals and other healthcare institutions included differences in timing of screening (on admission or during hospital stay), selection criteria (all admissions or patients at high risk for MRSA) and anatomical sampling sites [Reference Dulon21].
Compilation of MRSA prevalence studies in long-term care facility/nursing home residents in Europe published on PubMed between 2000 and 2011
LTCF, Long-term care facility.
* This study was conducted in hospitals, nursing homes and geriatric rehabilitation centres. The prevalence indicated refers to nursing homes only, but risk factors indicated in multivariate analysis are not limited to nursing home residents.
† Study was conducted in a geriatric unit associated with a teaching hospital.
LTCFs in Luxembourg are classified into two types: ‘maison de soins’ (or nursing homes using the terminology of Ribbe et al. [Reference Ribbe22]) which offer a higher level of care to mainly dependent and frail elderly with chronic diseases, disabilities and/or dementia, and CIPA (‘centre intégré pour personnes âgées’ or integrated centre for the elderly) whose residents at admission more often require no or very little care, but who may remain in the same institution if the care-load increases as they get older. CIPAs are thus a mixture of the two categories of nursing and residential homes according to the terminology of Ribbe et al. [Reference Ribbe22]. Given that a large proportion of residents in our study came from such CIPAs (LTCFs were selected at random in our study), it is clear that the average dependency level was probably lower than in the Belgian study which focused on nursing homes only [Reference Denis14]. The MRSA colonization rate in highly dependent residents (needing ⩾24 h of care per week, Table 2) in our study was 17·5% which is closer to the prevalence reported in Belgium.
In a recent national MRSA prevalence survey conducted in Luxembourgish hospitals in 2008, a lower prevalence rate of 3·7% was found (A. M. Ternes & J. C. Schmit, unpublished report) suggesting that asymptomatic carriage in LTCFs is likely to be an important reservoir for MRSA. Again comparisons between prevalence rates and hospitals should be interpreted with caution, as screening in hospitals was performed on admission, whereas our study participants were sampled on average a long time after admission.
While four out of five major hospital-acquired MRSA clonal complexes (CC5, CC8, CC22, CC30, CC45) [Reference Deurenberg, Vink and Kalenic23, Reference Wolters24] were detected in our study, we observed a large predominance (>75%) of strains belonging to CC5 (mainly of spa-type t003 or variants thereof, corresponding to ST225, ST710 or more rarely ST5). This dominance of CC5 strains was also found in the national hospital survey in Luxembourg in 2008, although to a lesser extent: t003 or variants thereof corresponded to 65% of isolates. This is in marked contrast to the MRSA genotype distribution in Luxembourg in 2003, when strains belonging to CC8 (spa-type t008) were largely predominant in hospitals [Reference Schuh25]. Thus we have observed at a rather rapid time-scale a local strain replacement by a new lineage that has recently emerged in hospitals in central Europe (Germany, Denmark, Switzerland, Czech Republic) [Reference Nubel26]. Why this rapid strain emergence has taken place is unclear. However, it is interesting to note that in comparison to previously prevalent CC8 strains, currently dominating CC5 strains tend additionally to be resistant to clindamycin, erythromycin and tobramycin. In our study, reported treatment with these antibiotics was rare and colonization with MRSA was only associated with fluoroquinolones and almost all strains belonging to CC5 and CC8 shared this phenotype. This illustrates that the epidemiology of MRSA in Europe and elsewhere is constantly changing and that molecular surveillance shared via the internet is crucial to provide early warning of emerging strains, cross-border spread and importation by travel [Reference Grundmann27].
Our study had several limitations. Despite a relatively high consent rate (49%), the use of informed consent most likely led to a selection bias in the patients sampled which could have led to an underestimate of the prevalence of MRSA. The wide range of the participation rate between LTCFs was probably to some extent due to the relative priority that our study was given by the various LTCF management staff who were instructed to inform residents by providing them with study leaflets and explaining the purpose of the study. Moreover, because of the cross-sectional nature of the study, transmission within LTCFs could not be assessed. Clustering of spa-types by LTCF, for example, could be also due to referral biases from different hospitals or geographical areas which have distinct spa-types.
To the best of our knowledge our study is the first to report recently identified livestock associated-MRSA belonging to CC398 [Reference van Loo28] in LTCF residents. Whether residents were colonized prior to entering or during residency cannot be easily determined because we did not collect any information on contact with livestock, farms or handling raw meat [Reference Waters29]. It should, however, be noted that the LTCFs where these strains were detected were located in more rural areas.
While we saw some evidence of MRSA transmission occurring within institutes, the typing methodology used in our study (spa-typing, MLST and antibiotic resistance typing) was not sufficiently discriminant to investigate chains of transmission, particularly for the highly prevalent t003 strains. To address this, we plan to conduct full genome sequencing [Reference Harris30] in order to develop single nucleotide polymorphism assays that can differentiate prevalent clones of CC5 strains further. However, we did observe a small degree of clustering, particularly of mupirocin resistance in one LTCF, but it is unclear whether this was due to transmission of resistant strains or multiply acquired resistance due to antibiotic selection pressure.
SUPPLEMENTARY MATERIAL
For supplementary material accompanying this paper visit http://dx.doi.org/10.1017/S0950268812001999.
ACKNOWLEDGEMENTS
We thank the participating residents, staff at nursing homes and members of the national group for the prevention of nosocomial infections (GNPIN) for comments and support. This study was financially supported by a research grant from the Luxembourg government.
DECLARATION OF INTEREST
None.
