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International Journal of Environmental Research and Public Health logoLink to International Journal of Environmental Research and Public Health
. 2019 May 13;16(9):1660. doi: 10.3390/ijerph16091660

MRSA Point Prevalence among Health Care Workers in German Rehabilitation Centers: A Multi-Center, Cross-Sectional Study in a Non-Outbreak Setting

Melanie Schubert 1,*, Daniel Kämpf 1, Marlena Wahl 1, Samuel Hofmann 1, Maria Girbig 1, Lutz Jatzwauk 2, Claudia Peters 3, Albert Nienhaus 3,4, Andreas Seidler 1
PMCID: PMC6539477  PMID: 31086069

Abstract

People working in health care services have an increased risk of being infected with methicillin-resistant Staphylococcus aureus (MRSA), though little is known about the prevalence in rehabilitation centers. This cross-sectional study investigated the MRSA prevalence in employees from different rehabilitation centers and aimed to identify risk factors for MRSA transmission. We invited all staff (i.e., with and without patient contact from 22 participating rehabilitation centers; n = 2499) to participate. Study participation included a questionnaire on personal characteristics, lifestyle, personal and occupational risk factors for MRSA and nasal swabs taken by the study team. In total, 1005 persons participated in the study (response: 40.2%). Only four participants carried MRSA (0.40 (95% CI 0.00–1.00) per 100). MRSA carriage did not seem to be occupationally related, as it was found in different occupations with and without direct contact with MRSA patients, as well as in different clinics with different indications and patient clientele. We could not find a clear association between MRSA carriage and potential risk factors due to the low number of cases found. Genotyping revealed the spa types t032 (Barnim epidemic strain) and t1223. Our results suggest a low point prevalence of nasal MRSA colonization in a non-outbreak setting in employees from rehabilitation centers.

Keywords: health care workers, MRSA prevalence, rehabilitation centers, non-outbreak, risk factors

1. Introduction

Multi-resistant bacteria, such as the methicillin-resistant Staphylococcus aureus (MRSA), are important causes of nosocomial infections worldwide [1]. Whereas sufficient data for MRSA prevalence exist for acute care hospitals, this topic has been investigated only sparsely in rehabilitation centers. Rehabilitation centers usually provide care for patients that require further treatment to recover physiological or neurological functions, or to learn how to cope with residual impairments. Rehabilitation usually follows a holistic approach and is characterized by individuality, complexity, and multidisciplinarity. Thus, strict isolation of patients with MRSA (as in acute care hospitals) is usually not feasible for successful rehabilitation. For this reason, patients with MRSA might be refused by rehabilitation centers, and thus receive their rehabilitation late or not at all [2]. The handling of patients with MRSA has been subject to many debates, and recommendations have been proposed by several institutions [3,4,5,6]. In sum, an individual medical risk analysis with the aim to establish an optimal compromise between measures for the prevention of MRSA transmission and rehabilitation participation is recommended. Great emphasize is put on hygiene measures for staff and the patients. However, it has been shown that additional hygienic measures carry an additional substantial financial burden for rehabilitation centers, thereby lowering resources for rehabilitative core services [7].

Rehabilitation centers are often characterized by higher staff-patient contacts due to therapeutic measures. So far, there is only little data available for MRSA prevalence in health care workers (HCWs) in rehabilitation centers. A pooled analysis of studies from non-outbreak settings in Europe and the US showed a prevalence of MRSA carriage in HCWs of 1.8% (95% CI 1.34–2.50) [8]. In particular, Heudorf and colleagues observed MRSA prevalence of 0.6% in staff members from a German nursing home and geriatric rehabilitation unit. An Italian point prevalence study on MRSA colonization in wards with a mix of neurological, orthopedic, post-coma, and spinal cord injury cases found a prevalence of 3.1% [9]; this study observed MRSA colonization only among nurses but not among other HCWs. Moreover, a French study observed a MRSA prevalence of 10% among HWC staff and 20% among patients [10]. The highest MRSA prevalence was observed in assistant nurses, and occupations with more physical contact with patients were associated with a higher MRSA prevalence. The aim of this study was to determine the prevalence of MRSA in employees of different rehabilitation centers in a large multi-center setting in Germany and to identify risk factors for MRSA colonization.

2. Materials and Methods

The study was conducted from September 2016 to May 2018. Ethical approval was obtained from the ethics committee of the TU Dresden (Clearance number EK 247062016). Methods were tested a priori with a pilot study in an acute care hospital in Dresden [11].

First, 34 rehabilitation centers in Saxony were invited, of which 10 participated in the study. These 10 rehabilitation centers employed 1173 persons altogether, of which 447 (38.1%) participated in the study. Twenty-four rehabilitation centers in Saxony refused to participate. Reasons for not participating, if named, were as follows: basic refusal to participate in studies of any kind (n = 1), not desired by the clinic management without specification (n = 3), fear regarding how to handle colonized staff and fear that a large number of employees would be on sick leave (n = 1), no one would participate (n = 1), expected high time expenditure (n = 1), no interest (n = 1), and no time (n = 1). Second, 66 rehabilitation centers from neighboring federal states, (i.e., Bavaria, Brandenburg, Saxony-Anhalt, and Thuringia) were also invited. Of these, 11 institutions participated in the study. One rehabilitation center contacted us through its own initiative.

In total, 22 German rehabilitation centers from different fields participated in the study. Specializations included addictions, cardiology, dermatology, gastroenterology, geriatrics, internal medicine, lymphology, mental trauma disorders, metabolic diseases, musculoskeletal disorders, neurology, orthopedics, oncology, pneumology, psychosomatics, psychotherapy, psychiatry, and rheumatic diseases. The number of employees within the rehabilitation centers ranged from 65–240.

The study process began with an anonymous invitation that was distributed to all employees of a participating rehabilitation center. The invitation included information about the study, an informed consent form, and a questionnaire. Standard questions on personal characteristics (e.g., gender, age, etc.) and work, as well as questions concerning occupational and personal risk factors for MRSA were incorporated into the questionnaire. Questions concerning MRSA risk factors were predominately derived from a review by Albrich and Harbarth [12], a questionnaire used for staff in nursing homes by the German Social Accident Insurance Institution for the Health and Welfare Services (Berufsgenossenschaft für Gesundheitsdienst und Wohlfahrtspflege―BGW) [13], and additional literature. Furthermore, an on-site information event performed by the study team was offered to each rehabilitation center.

For sampling of nasal swabs, the study team was on-site at the rehabilitation centers for 1–2 days. Participants were invited to an examination room, which was provided by each clinic. Before any measurements were taken, the informed consent and the completed questionnaire were collected and participants had an opportunity for asking questions. Then, samples were taken by a trained member of the study team using a swab from the anterior nares, which have been shown to be the main reservoir for MRSA [8]. Participants had the choice to either participate anonymously or to receive feedback of their MRSA status by mail to their private address.

Prior to the study, training seasons for sampling of nasal swabs were conducted. Samples were usually taken by the study physician (DK) or prospective physicians (MW, SH). Sampling was done in both nostrils using sterile transystem® cotton swabs (Hain LIFEscience GmbH, Nehren, Germany). One swab was used for both nostrils. Swab samples were analyzed by the Ostsächsische Labor according to the quality guidelines of the lab. The lab is accredited according to DAkkS: DIN EN ISO 15189. Prior to investigation of MRSA presence, broth enrichment media and MRSA selective agar plus non-selective blood agar were used in parallel. Swabs were plated on chromogenic agar plates selective for MRSA (BD BBL CHROMagar) and non-selective blood agar (Trypticase soy agar II with 5% sheep blood). In the case of no growth on the selective or blood agar, the enrichment broth was plated on the selective agar to culture low MRSA cell numbers. Suspicious colonies underwent phenotypical confirmation using an immunochromatic qualitative PBP2a assay (Alere) as well as antimicrobial susceptibility testing to measure MICs of oxacillin and cefoxitin using broth microdilution tests. In most cases, one single isolate was tested for MRSA unless colonies with different morphologies were present either on the selective or blood agar plate. Only S. aureus isolates suspicious for MRSA were further tested in the study and data concerning spa types of MSSA can therefore not be presented. Suspect MRSA isolates were definitively identified by the German National Reference Center for Staphylococci and Enterococci (Nationales Referenzzentrum für Staphylokokken und Enterokokken) in Wernigerode, Germany. The presence of mecA was detected in all samples.

Descriptive statistics are shown for all data. Odds ratios and 95% confidence intervals were calculated using the exact method in Stata (StataCorp. 2011. Stata Statistical Software: Release 12. StataCorp LP, College Station, TX, USA).

Overall, 2499 employees were invited, of which 1005 participated in the study. Thus, the response rate was 40.2%. Within rehabilitation centers there was a huge variation in response rates, ranging from 15.2% to 75.0%. Most participants received the feedback by mail (n = 988); only 17 persons participated anonymously in the study.

3. Results

3.1. Charcterization of the Study Population

Mainly women participated in the study (82%, Table 1). Most participants were between 50 and 59 years old (31.2%) and were secondary school graduates (49.6%). Participants predominately lived in a partnership (78.8%). Mostly therapists (33.9%) participated in the study with a professional experience of 15–30 years (34.1%). Only about one-third (32.3%) reported having had close patient contact within the last four weeks.

Table 1.

Participant characteristics and methicillin-resistant Staphylococcus aureus (MRSA) risk factors.

Characteristics Number Percent
Total 1005 100
Sex
 Female 824 82.0
 Male 175 17.4
 Not reported 6 0.6
Age in years
 <20 6 0.6
 20–29 104 10.3
 30–39 229 22.8
 40–49 243 24.2
 50–59 314 31.2
 ≥60 88 8.8
 Not reported 21 2.1
Education
 Secondary school graduation 498 49.6
 High school, university entrance qualification 440 43.8
 Other 56 5.6
 No degree 1 0.1
 Not reported 10 1.0
Occupation
 Physician 104 10.3
 Nurse 140 13.9
 Therapist 338 33.6
 Medical technical assistant 28 2.8
 Transport service workers 3 0.3
 Cleaner 49 4.9
 Administrative personnel 148 14.7
 Others 186 18.5
 Not reported 9 0.9
Professional experience in years
 ≤1 73 7.3
 1–5 232 23.1
 6–10 145 14.4
 11–20 111 11.0
 21–40 343 34.1
 >41 95 9.5
 Not reported 6 0.6
Partnership
 Yes 792 78.8
 No 200 19.8
 Not reported 13 1.3
 Household Size
 One-person 199 19.8
 Multi-person 792 78.8
 Not reported 14 1.4
Work-related MRSA risk factors
Close contact with patients within the last 4 weeks
(washing, dressing, changing bandages, etc.)
 Yes 325 66.3
 No 666 32.3
 Not reported 14 1.4
Contact with MRSA patients within the last 4 weeks
 Yes 136 13.5
 No 320 31.8
 Unknown 542 53.9
 Not reported 7 0.7
Wearing protective gear when having contact with MRSA patients
 Yes, always 104 76.5
 Occasionally without 30 22.1
 Not reported 2 1.5
Protective gear worn when having contact with MRSA patients
 Surgical face mask, disposable gloves, and lab coat 79 58.1
 Surgical face mask and disposable gloves 12 8.8
 Disposable gloves 11 8.1
 Disposable gloves and lab coat 2 1.5
 Surgical face mask and lab coat 1 0.7
 Not applicable 2 1.5
 None reported 29 21.3
Working abroad
 Yes 15 1.5
 No 978 97.3
 Not reported 12 1.2
Private life-related MRSA risk factors
Caring for relatives at home
 Yes 72 7.2
 No 926 92.1
 Not reported 7 0.7
Contact with MRSA carriers
 Yes 14 1.4
 No 535 53.2
 Unknown 449 44.7
 Not reported 7 0.7
Contact with persons in need of care within the last 4 weeks
 Yes 137 13.6
 No 863 85.9
 Not reported 5 0.5
Working in the ambulant sector outside of work at rehabilitation center
 Yes 16 1.6
 No 984 97.9
 Not reported 5 0.5
Contact with farm animals
 Yes 89 8.9
 No 910 90.5
 Not reported 6 0.6
Contact with pets
 Yes 615 61.2
 No 387 38.5
 Not reported 3 0.3
Risk factors associated with health status
Chronic skin disease
 Yes, own diagnosis 14 1.4
 Yes, doctor’s diagnosis 97 9.7
 No 876 87.2
 Not reported 18 1.8
Chronic respiratory disease
 Yes, own diagnosis 25 2.5
 Yes, doctor’s diagnosis 90 9.0
 No 869 86.5
 Not reported 21 2.1
Diabetes mellitus
 Yes, own diagnosis 2 0.2
 Yes, doctor’s diagnosis 25 2.5
 No 951 94.6
 Not reported 27 2.7
Previous MRSA carriage
 Yes 17 1.7
 No 983 97.8
 Not reported 5 0.5
Use of antibiotics within the last12 months
 Yes 304 30.2
 No 690 68.7
 Not reported 11 1.1
Having had an operation within the last 30 days
 Yes 40 4.0
 No 959 95.4
 Not reported 6 0.6
Inpatient hospital treatment within the last 12 months
 Yes 95 9.5
 No 902 89.8
 Not reported 8 0.8

Having contact with MRSA-patients within the last four weeks was reported by 13.5%, of which the majority (76.5%) also reported wearing protective gear at all times; 22.1% of participants had occasional contact without protective clothing, and two participants did not answer the question. When having contact with MRSA patients, the majority of participants (58.1%) reported wearing a surgical face mask, disposable gloves, and a lab coat.

In terms of private life risks, only a few participants had known contact with MRSA carriers (1.4%). Approximately 7.2% were caring for relatives at home and 13.6% had contact with persons in need of care within the last 4 weeks. Only 16 of 1005 reported working in the ambulant sector besides their work at the rehabilitation center. The majority of participants had contact with pets (61.2%). Contact with farm animals was reported by 8.9%.

Seventeen of 1005 participants had previously had MRSA in the past. About one-third (30.2%) of participants used antibiotics within the last 12 months. A hospital stay within the last 12 months was reported by 9.5%, and 4.0% had an operation within the last 30 days. About 10% reported suffering from chronic skin disease or chronic respiratory disease. Characteristics of study population are displayed in Table 1.

3.2. Prevalence of MRSA and Risk Factors

Four of 1005 participants tested positive as MRSA carriers during the examination, corresponding to a prevalence of 0.40% (95% CI 0.00–1.00). MRSA carriage was found in four different clinics with the following specializations: geriatrics, neurology, psychosomatics, and cardiology/oncology/gastroenterology. The MRSA carriers were working as a physician (n = 1) or as a cleaning staff member (n = 1), and the two remaining MRSA carriers stated having a job not listed in the questionnaire (i.e., geriatrics and psychosomatics, without any further specification). Professional experience ranged between MRSA carriers from less than 1 year (n = 1), 1–5 years (n = 1), 6–10 years (n = 1), and 15–30 years (n = 1). Three MRSA carriers were women and one was a man.

Two of the MRSA carriers had close contact with patients and MRSA patients within the last 4 weeks.

The contact with MRSA patients was always with protective work clothing (surgical face mask, disposable gloves, and lab coat). Two of the MRSA carriers did not know if they had contact with patients with MRSA.

One MRSA carrier reported working in the Czech Republic within the last 12 months. Regarding private-life factors, none of the four MRSA carriers were caring for relatives at home, had contact with MRSA carriers or with persons in need of care within the last 4 weeks, or worked in the ambulant sector outside work. Only one of the four MRSA carriers had contact with pets and none had contact with farm animals. For risk factors associated with health status, the following picture emerged: none of the MRSA carriers had a chronic skin or respiratory disease, diabetes mellitus, used antibiotics, or had an inpatient hospital stay within the last 12 months. One MRSA carrier had an operation within the last 30 days. Another carrier had a history of MRSA colonization.

Altogether, we could not find a clear association between MRSA carriage and potential risk factors due to the low sample size. We could not clearly identify risk factors for MRSA carriage, but the results did not contradict previous risk factor research. Having contact with patients with MRSA within the last four weeks, working abroad, previous MRSA carriage, and an operation within the last 30 days may increase the risk of MRSA carriage. Results are presented in Table 2.

Table 2.

Prevalence (odds ratios (ORs)) for MRSA risk factors.

Risk Factor MRSA Positive (n) MRSA Negative (n) OR 95% CI
No (Reference) Yes No (Reference) Yes
Work-related risk factors
Close contact with patients within the last 4 weeks 2 2 664 323 2.1 0.1–28.5
Contact with MRSA patients within the last 4 weeks 2 2 860 134 6.4 0.5–89.0
Working abroad 3 1 975 14 23.2 0.4–305.5
Private life-related MRSA risk factors
Caring for relatives at home 4 0 922 72 - -
Contact with MRSA carriers 4 0 980 14 - -
Contact with persons in need of care within the last 4 weeks 4 0 859 137 - -
Working in the ambulant sector outside of work 4 0 980 16 - -
Contact with farm animals 4 0 906 89 - -
Contact with pets 3 1 384 614 0.2 0.0–2.6
Risk factors associated with health status
Chronic skin disease 4 0 872 111 - -
Chronic respiratory disease 4 0 865 115 - -
Diabetes mellitus 4 0 947 27
Previous MRSA carriage 3 1 980 16 20.4 0.4–266.8
Antibiotics use within the last12 months 3 0 687 304 - -
Operation within the last 30 days 3 1 956 39 8.2 0.2–103.8
Inpatient hospital treatment within the last 12 months 4 0 898 95 - -

3.3. MRSA Genotyping

Genotyping revealed the MRSA spa types t032 (CC22, mecA positive) and t223 (CC22, mecA positive). The spa type t032 occurred in a clinic for geriatrics and a clinic for cardiology/oncology/ gastroenterology. The tetracycline-resistant MRSA spa type t223 was observed in a psychosomatic rehab center with psychotherapy. Unfortunately, we were unable to genotype the fourth MRSA-positive sample.

4. Discussion

The present study investigated the prevalence of MRSA in 22 rehabilitation centers with different specializations. Only four of 1005 participants were colonized with MRSA (0.4%, 95% CI 0.0–1.0%). This corresponds to results of the German nursing home and geriatric rehabilitation unit, which showed a prevalence of MRSA in HCWs of 0.6% [14]. For HCWs working in German acute care hospitals, prevalence rates of 2.3–5.3% have been described [15,16,17,18]. This suggests that MRSA prevalence might be generally lower in rehabilitation centers than in acute care clinics. Nevertheless, we also recently studied MRSA prevalence in an acute care hospital in a small pilot study. Here only 1 in 180 (0.6%) employees, or 1 of 149 (0.7%) persons with close patient contact, carried MRSA [11]. A general decrease in MRSA has been observed for Germany and Europe [19,20]. Thus, the low observed MRSA prevalence may also reflect this decrease.

MRSA colonization was observed in four different rehabilitation centers with the following different specialties: geriatrics, neurology, psychosomatics, and a mix of cardiac/oncological/gastroenterological cases. Geriatrics and neurology have been described as high risk units for MRSA for patients. In contrast, psychosomatic clinics and units with cardiac/oncological/gastroenterological cases are considered low risk MRSA areas [21,22]. One MRSA carrier was a physician, one worked as a cleaner, and two stated as having a job not listed in the questionnaire. Only two of the four MRSA carriers had close contact with patients and MRSA patients within the last 4 weeks (neurology and geriatrics). Thus, it is possible that MRSA transmission may have occurred indirectly. MRSA strains have a high tenacity and die off slowly (i.e., they can survive for longer than 6 months) [23]. MRSA can be found on general surfaces such as beds, floor, linen, curtains, and overbed tables [24]. Boyce and colleagues showed that environmental contamination with MRSA occurred in 69% of colonized patients [25]. Moreover, it has been shown that 42% of persons not having direct contact with MRSA patients but touching contaminated surfaces had MRSA on the gloves. This may suggest that MRSA transmission might have occurred from contaminated surfaces without having direct patient contact in two cases. Thus, strict hygiene measures, including routine disinfection of contact surfaces, are essential for limiting MRSA transmission [3,24]. However, since we do not have data on patient clientele and patient MRSA status, we cannot make an assumption about transmission pathways. Moreover, MRSA transmission may have also occurred outside the centers.

When investigating risk factors for MRSA carriage, we could not find a clear association between MRSA carriage and potential personal and occupational risk factors due to the low number of MRSA carriers in the study sample―only four HCWs carried MRSA. Nevertheless, the results are not contradictory to previous research on MRSA risk factors. Having contact with patients with MRSA within the last four weeks, working abroad, known history of MRSA carriage, and having had an operation within the last 30 days may increase the risk of MRSA carriage. These are well known risk factors for MRSA transmission in HCWs [15,26].

In this study, two different MRSA spa types of the epidemic strain CC22 (mecA positive) were identified: t032 and t223. The Barnim epidemic strain (t023) was observed in the rehabilitation centers with geriatric patients and a mix of cardiological/oncological/gastroenterological cases. This strain is a classical nosocomial MRSA strain that is spread throughout Germany [20,27]. Rehabilitation centers usually provide care following treatment in an acute care hospital. Thus, the spread of MRSA between hospitals and rehabilitation centers is likely to occur. Indeed, the Barnim epidemic strain has been shown to be the second most frequent epidemic strain in patients from rehabilitation centers with neurologic, orthopedics, internal medicine, and geriatric units [28]. The spa type t223 occurred in a psychosomatic rehabilitation center. This strain is associated with community-acquired MRSA and has only been observed sporadically before 2014 [20]. A recent analysis by the Robert Koch Institute showed a trend for increasing tetra-cycline resistant MRSA in recent years, where it has been observed among asylum seekers in central reception centers [20].

One study limitation was the low response rate of 40.2%. The variation in response was rather large, ranging from 15.2% to 75.0% within the single rehabilitation centers. Mainly women participated in the study (82%). Most participants were between 50–59 years (31.2%) followed by 40–49 years (24.2%), 30–39 years (22.8%), under 30 years (10.9%), and over 60 years (8.8%). Unfortunately, we do not have information about the general employee characteristics of the rehabilitation centers. However, according to the German Federal Statistical Office (DESTATIS), about 77% of health personnel in prevention and rehabilitation centers were women in 2016 [29]. Moreover, the age structure of study participants generally corresponds to the age structure of rehabilitation staff in Germany, as monitored by DESTATIS. In the year 2016, the majority of staff working in prevention and rehabilitation centers were between 50–60 years (31.4%) followed by 40–50 years (24.0%), 30–40 years (19.0%), under 30 years (14.9%), and over 60 years (10.7%). Thus, the characteristics of our study population generally correspond to that of nationwide rehabilitation staff characteristics, suggesting little bias. Another limitation of the study is the lack of environmental samples in the participating centers. A further study limitation is that we only tested employees, and not patients. Data on patient MRSA status would have made it possible to test assumptions about possible transmission paths [30]. Moreover, we only sampled the anterior nares for MRSA. This may have led to an underestimation of MRSA prevalence because it has been shown that screening other body sites (e.g., throat and axilla) increases MRSA yield over nares alone [31]. The study was also underpowered due to the (unexpectedly) low sample of MRSA carriers. Due to the low prevalence of MRSA carriage in this population, a huge sample size is required to generate robust data for identifying risk factors for MRSA transmission.

5. Conclusions

Our results suggest a low point prevalence of MRSA in employees from German rehabilitation centers in a non-outbreak setting. MRSA carriage was a rare event found in different occupations among workers with and without direct contact with MRSA patients, as well as in different clinics with different specializations and caring for different patient clientele. Due to the low prevalence of MRSA, risk factors for MRSA carriage could not be evaluated. Altogether, the results correspond to the recently reported trend of decreasing MRSA prevalence in Europe.

Acknowledgments

The authors wish to extend their very special thanks to Katrin Liesk-Biskop and Philipp Heinrich for their great support during the study conduct. We thank Gilda Gudacker from the Labor Ostsachsen for support. We are grateful for the comments of the anonymous reviewers.

Author Contributions

Conceptualization: A.S., M.S., D.K., and M.G.; methodology: A.S., M.S., D.K., and M.G.; validation: M.S., M.W., and S.H.; formal analysis: M.S.; investigation: M.S., D.K., M.W., and S.H.; data curation: M.W. and S.H.; writing—original draft preparation: M.S.; writing—review and editing: M.S., D.K., M.W., S.H., M.G., L.J., C.P., A.N., and A.S.; supervision: A.S.; project administration: M.S.

Funding

This research was funded by the Statutory Accident Insurance and Prevention in Health and Welfare Services, Hamburg, Germany.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

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