Original article
Screening for Methicillin-Resistant Staphylococcus aureus
An Analysis Based on Findings From the Hospital Infection Surveillance System (KISS), 2006–2021
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Background: Methicillin-resistant Staphylococcus aureus (MRSA) has become less common in Germany in recent years. In this paper, we report data from the MRSA module of the Hospital Infection Surveillance System (Krankenhaus-Infektionen-Surveillance-System, KISS) for the years 2006–2021. We also describe the association of MRSA rates with the frequency of patient screening for MRSA and discuss the findings.
Methods: Participation in the MRSA KISS module is voluntary. Once a year, the participating hospitals submit structural data, information on cases in which MRSA was detected (both colonizations and infections; both detected on admission and nosocomially acquired), and the number of nasal swabs taken for the detection of MRSA to the German National Reference Center for the Surveillance of Nosocomial Infections. Statistical analyses were performed with R software.
Results: The number of hospitals participating in the MRSA module rose from 110 in 2006 to 525 in 2021. From 2006 onward, the overall MRSA prevalence in German hospitals increased, reaching a maximum of 1.04 cases per 100 patients in 2012. The prevalence on admission fell by 44% from 0.96 in 2016 to 0.54 in 2021. The incidence density of nosocomial MRSA fell by an average of 12% per year, from 0.27 per 1000 patient-days in 2006 to 0.06 in 2021, while MRSA screening frequency increased sevenfold by 2021. The nosocomial incidence density was stable, independently of the screening frequency.
Conclusion: MRSA rates in German hospitals fell markedly from 2006 to 2021, reflecting a general trend. The incidence density was no higher in hospitals with a low or moderate screening frequency than in those with a high one. Thus, a targeted, risk-adapted MRSA screening strategy on hospital admission can be recommended.


Infections caused by methicillin-resistant Staphylococcus aureus (MRSA) continue to be a global challenge. Given the high morbidity and mortality associated with infections with S. aureus, including MRSA, the World Health Organization (WHO) considers research and development of new antibiotics to treat these pathogens a high priority (1). In Germany, section 23 of the Protection against Infection Act (Infektionsschutzgesetz, IfSG) requires hospitals to record specified nosocomial infections and multidrug-resistant organisms (MDROs), such as MRSA (2). Furthermore, direct detection of MRSA in blood cultures or cerebrospinal fluid (CSF) is reportable according to section 7 of the IfSG. In 2020, 1126 cases of invasive MRSA infections were reported to the Robert Koch Institute, which corresponds to an incidence of 1.4 per 100 000 population. In 2012, 4456 cases had been reported (incidence 5.4 per 100 000 population). Thus, the number of cases decreased statistically significantly by a factor of almost 4 within seven years (3, 4). Not only the number of cases, but also the proportion of MRSA in S. aureus isolates from clinical materials is steadily declining. A study on nosocomial infections in German intensive care units (ICUs) as part of the Hospital Infection Surveillance System (KISS, Krankenhaus-Infektionen-Surveillance-System) showed that the rate of MRSA in nosocomial infections caused by S. aureus fell from 33% to 20% in 10 years (5). This trend is also noted in the member countries of the European Union (EU). For example, in the EU, the proportion of MRSA in S. aureus isolates from blood cultures or cerebrospinal fluid declined from 19% in 2016 to 17% in 2020—a statistically significant decrease (6).
The aim of our study was to describe the developments in MRSA epidemiology in hospitals in Germany during the period from 2006 to 2021, to elucidate MRSA detection numbers in association with screening frequency and to critically evaluate the impact of hospital admission screening on the decline in the number of MRSA cases based on our findings. We also formulate recommendations for an adequate screening strategy.
Methods
Since 1997, the German national Hospital Infection Surveillance System (KISS) has served as a procedure to monitor nosocomial infections in Germany (7). Within the KISS framework, the MRSA-KISS module was established as a pathogen surveillance component in 2006 (8, 9). As with the other KISS modules, participation in the MRSA component is voluntary. This module can be used for collecting data on multidrug-resistant organisms, as required by section 23 of the German Protection against Infection Act (IfSG). The MRSA module collects information on MRSA detection among hospitalized patients for the entire hospital; rehabilitation hospitals are also eligible to participate in MRSA surveillance. Data collection and transmission to the National Reference Center (NRZ, Nationales Referenzzentrum) for Surveillance of Nosocomial Infections is performed via the online platform “webKess“ (9, 10).
The definitions used for data collection are as follows (8, 9): A patient in whom MRSA is detected in screening swabs (colonization) or isolated from clinical material (colonization or infection) is considered an MRSA case. Hospital cases, not patients with MRSA are counted, meaning that if a patient in whom MRSA was detected is readmitted after discharge from hospital, they are considered a new case. With regard to hospital cases overall (with and without detection of MRSA), we will use the term patients in the following for ease of understanding; however, the hospital admissions of the patients are counted (9). Each case of MRSA is only once considered for the hospital, meaning that if the patient is transferred to another department of the same hospital, the case is not counted again.
The number of MRSA hospital days is calculated from the day of diagnosis or detection of MRSA (date of swab or specimen collection) or from the day of admission, if MRSA had already been detected before hospital admission (9):
- until the day of discharge of the MRSA case (the day of discharge is counted)
- until the patient has no detectable MRSA colonization – as determined by the participating hospitals—for example, after collection of three MRSA-negative screening specimens on three consecutive days.
Participating hospitals are asked to submit once a year the following data on MRSA cases as well as hospital structural and process parameters:
- Number of patients admitted to the hospital per calendar years (number of cases)
- Patient days for a calendar year
- Rehabilitation facility available (yes/no)
- Number of nasal swabs (adjusted for patients yes/no, i.e. only one swab is counted per patient; a nasal swab is considered a screening swab)
- MRSA cases present on admission (MRSA known at the time of admission or MRSA isolated from screening swab or material collected within the first two days after admission)
- Nosocomial MRSA cases (MRSA isolated from swab or material collected from day three, i.e. later than day two, after admission)
- MRSA hospital days (assessment as defined above)
Based on the data submitted to the National Reference Center for the Surveillance of Nosocomial Infections (NRZ), the following measures are calculated:
- Overall prevalence (overall number of MRSA cases per 100 patients)
- Admission prevalence (number of MRSA cases present on admission per 100 patients)
- Incidence of nosocomial MRSA cases (number of nosocomial MRSA cases per 100 patients)
- Incidence density of nosocomial MRSA cases (number of nosocomial MRSA cases per 1000 patient days)
- Mean MRSA disease burden in the hospital (number of MRSA patient days per 100 patient days)
- Screening frequency (number of nasal swabs per 100 patient admissions; only one swab test during the hospital stay counts per patient)
These data are then analyzed at the German National Reference Center (NRZ); subsequently, the participating hospitals are provided with their own figures as well as the reference data.
For the period 2006–2021, we report the screening frequency in addition to these measures of MRSA epidemiology. For our data evaluation, we divided the screening frequency into four groups (categories/quartiles) of equal size, based on the frequency of nasal swabs performed. By analyzing overall MRSA prevalence and MRSA incidence density in the various categories, we were able to assess possible associations between epidemiological measures and screening frequency. Differences between categories were tested for significance using the Kruskal-Wallis test. For both overall MRSA prevalence and nosocomial MRSA incidence density, separate regression models were run to describe the temporal trend. Data analysis was performed using the open-source R statistical software (11).
We extrapolated the results of the MRSA surveillance data to all hospitals in Germany to estimate the overall burden of MRSA case in 2019 (the last calendar year before the start of the SARS-coronavirus 2 pandemic). German national hospital statistics data were used for this calculation (12)
Results
Since participation in KISS is voluntary, the number of reporting hospitals has fluctuated from year to year. Following the start of the MRSA module in 2006, 110 hospitals participated in this component. Since then, the number of participating hospitals has increased significantly, reaching a peak of 623 hospitals in 2018 which is about one third of all German hospitals. In 2021, 525 hospitals participated in the MRSA module.
Table 1 shows the development of MRSA epidemiology in German hospitals during the 16-year period from 2006 to 2021. In the pre-pandemic year 2019, the number of patient days included in the MRSA module corresponded to 41% of all patient days in German hospitals (the total number of patient days in 2019 was 139 million). On the assumption of an equal distribution of MRSA patient days in hospitals, the total number of MRSA patient days in Germany in 2019 was approximately 1.7 million, accounting for 1.2% of all annual patient days in German hospitals.
In 2012, overall MRSA prevalence peaked with 1.04 cases per 100 patients, remaining for several years on this level before starting to continuously and significantly decrease in 2017 to 0.72 (−32%) and 0.54 (−50%) in 2019 and 2021, respectively (p<0.001). Admission prevalence and mean daily MRSA disease burden also followed this trend. The incidence of nosocomial MRSA cases declined steadily from 0.26 per 100 patients in 2006 to 0.04 per 100 patients in 2021. Nosocomial incidence density decreased by an average of 12% per year and was 0.06/1000 patient days in 2021 (Table 1). Figure 1 provides an overview of the development of MRSA epidemiology in hospitals and the frequency of screening (nasal swabs) for the period from 2006 to 2021.
For the further analyses, the frequency of nasal swabs per 100 hospital admissions was used as a marker for screening frequency and divided into four equally sized categories (quartiles 1–4). Since the screening frequencies varied from year to year, the categories differed between years/time periods. From 2006–2018, a steady increase in screening frequencies was observed; in 2013 a nasal swab was obtained from at least one quarter of patients for the first time; from 2019, screening frequencies have plateaued on a high level (Figure 1). The analyses included the year 2021 and the period 2013–2021. The categories used are presented in Table 2.
In 2021, hospitals with high screening frequencies had a significantly higher MRSA admission prevalence compared to hospitals with a low screening frequency (Kruskal-Wallis test p<0.0001). However, the same observation was not made for nosocomial incidence density, as it remained stable across all screening categories (p = 0.8402) (Table 3). When comparing these results with data from the 2013–2021 period, it can be seen that nosocomial incidence density was stable across all screening categories, consistent with the findings for the year 2021 alone (Table 3).
Discussion
A continuous decrease in nosocomial MRSA incidence is noted for the entire observation period and, since 2017, also a reduction in the overall and admission prevalence of MRSA (Table 1). Therefore, the epidemiological trend observed in other surveillance systems for Germany and Europe can also be applied to the MRSA incidence in German hospitals (5, 6, 13). Similar to Germany, a statistically significant reduction in the incidence of invasive MRSA infections has been shown in the United States. From 2005–2013, the nosocomial incidence of bloodstream infections caused by MRSA strain USA 100 decreased from 6.1 to 0.9/100 000 population and for strain USA 300 from 1.5 to 0.6/100 000 population (14). Globally, MRSA rates in S. aureus isolates from blood or cerebrospinal fluid vary widely; in the period 2000–2016, for example, it ranged between 0% and 98% in the Asia-Pacific region (15). Figure 2 provides an overview of 2019–2020 MRSA rates for selected countries (6, 16, 17). Multiple pathogen-specific and host-specific factors as well as the heterogeneity of health care and surveillance systems worldwide have been identified as causes of variation in MRSA rates.
Significantly fewer patients were treated in German hospitals in 2022 and 2021 compared to pre-pandemic years (12). The MRSA-KISS data also show that 8% fewer patients received care in 2021 compared to 2019 (last pre-pandemic calendar year) (Table 1). Elective hospital admissions, in particular, were deferred due to the SARS-CoV-2 pandemic. By contrast, patients with underlying chronic diseases who, for example, required dialysis or devices which are permanently left in place (such as an indwelling urinary catheter), continued to be admitted. Patients receiving dialysis on a regular basis or with indwelling urinary catheter or open wounds are at a higher risk of MRSA colonization (18). Nevertheless, admission prevalence continued to decline during the pandemic years. A meta-analysis concerned with the incidence of antimicrobial resistance in hospitals worldwide showed that the COVID-19 pandemic had no impact on the incidence density of MRSA (19); in the United States, the overall case rates for MRSA bloodstream infections remained stable between 2018 and 2020 (20). These observations made internationally during the years of the pandemic are reflected in the MRSA-KISS data.
Various causes have been attributed to the generally noted decline in MRSA. Apart from a potentially reduced biological fitness of drug-resistant S. aureus strains compared to drug-sensitive S. aureus, as well as a change in how antibiotics are used (21, 22, 23), the decline in MRSA could be due to various bundles of infection prevention and control (IPC) measures. In 1999 and 2014, the Commission for Hospital Hygiene and Infection Prevention (KRINKO, Kommission für Krankenhaushygiene und Infektionsprävention) published recommendations for MRSA-related IPC measures to be taken in hospitals and care facilities (18, 24). These recommendations include enhancing basic hygiene and hand disinfection compliance. In addition, KRINKO supports targeted admission screening for patients at risk of MRSA and recommends the preparation of an infection control plan for each hospital, taking into account the local situation and country-specific recommendations for MRSA admission screening (18).
Notwithstanding this recommendation and a steady decline in MRSA incidence, screening frequency has increased in German hospitals over time since 2006 to remain at a high level since 2019 (Figure 1). One reason for this could be that targeted screening of patients with an increased risk of MRSA—for example, re-admissions with known history of MRSA or admissions or transfers from facilities with known endemic or suspected MRSA occurrence (18, 24)—is considered to be more time-consuming to implement than screening entire departments or the entire hospital. What is more, MRSA detected during hospitalization is classified as nosocomially acquired in patients who have not undergone admission screening. To address this issue, admission screening has been expanded in some hospitals. Furthermore, hospitals could use a comprehensive MRSA screening strategy for promotional purposes, as the media keeps reporting on alleged successes of universal admission screening. In these reports, however, reference is often made to the Netherlands, despite the fact that only risk-based screening is performed there (25).
Finally, it appears that there is still a widespread perception that universal admission screening is an evidence-based IPC measure. However, this view is refuted or critically discussed in various studies (26, 27, 28, 29, 30). Likewise, MRSA-KISS figures reported in recent years indicate that hospitals with low or moderate screening frequencies did not see an increase in the number of nosocomial MRSA cases detected. For example, for the year 2021, the admission prevalence for a hospital was found to be significantly higher if the hospital was in the 4th quartile with respect to the frequency of admission swabs instead of the first quartile. However, the incidence density of nosocomial MRSA was found to be stable at 0.04/1000 patient days, independent of the screening frequency (Table 3). Thus, the question arises whether a high screening frequency is necessary at all. Rather, IPC measures appear to be increasingly implemented successfully to prevent nosocomially acquired MRSA cases. Risk-adapted targeted MRSA admission screening can help to conserve staff capacities and laboratory resources. Therefore, such a screening strategy appears to be useful, especially in view of the stable epidemiological situation.
Limitations
The following limitations apply to the surveillance survey within the German National Nosocomial Infections Surveillance System (KISS): First, the number of hospitals participating in the MRSA-KISS module varied over time, and this may have influenced MRSA rates. The number of participating hospitals was rather stable from 2017 to 2019, but decreased during the SARS-CoV-2 pandemic.
Second, statements can only be made for participating hospitals. It remains unclear whether these can be considered representative of all hospitals in Germany. However, the number of hospitals participating in MRSA KISS surveillance is by no means insignificant—even in the first pandemic year of 2020, one-third of all approximately 1,900 hospitals participated (12).
The MRSA-KISS findings reflect the general epidemiological trend of declining MRSA incidence rates. For this reason, a stable database can be assumed despite the limitations mentioned above (6).
Conclusion
A significant decrease in MRSA cases in German hospitals has been observed for the period 2006–2021. The incidence density of nosocomial MRSA is not associated with screening frequency. This means that the probability of nosocomial transmission of MRSA is not increased in hospitals with a low number of nasal swabs per 100 patients. Given the lack of a preventive effect and the resource consumption associated with a high screening frequency, a targeted screening strategy focused on patients at increased risk of MRSA should be preferred over universal MRSA admission screening.
Conflict of interest statement
The authors declare that no conflict of interest exists.
Manuscript received on 23 January 2023, revised version accepted on 27 April 2023.
Translated from the original German by Ralf Thoene, MD.
Corresponding author
Dr. med. Miriam Wiese-Posselt, MPH
Charité – Universitätsmedizin Berlin
Institut für Hygiene und Umweltmedizin
Campus Benjamin Franklin
Hindenburgdamm 27
12203 Berlin, Germany
miriam.wiese-posselt@charite.de
Cite this as:
Wiese-Posselt M, Saydan S, Schwab F, Behnke M, Kola A, Kramer TS, Gastmeier P, Maechler F: Screening for methicillin-resistant Staphylococcus aureus—an analysis based on findings from the Hospital Infection Surveillance System (KISS), 2006–2021. Dtsch Arztebl Int 2023; 120: 447–53. DOI: 10.3238/arztebl.m2023.0117
German National Reference Center for the Surveillance of Nosocomial Infections at the Institute of Hygiene and Environmental Medicine, Charité – University Medicine Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany: Selin Saydan, Dr. rer. medic. Frank Schwab, Dr. rer. medic. Michael Behnke, Prof. Dr. med. Petra Gastmeier, Dr. med. Friederike Maechler
1. | World Health Organization: Prioritization of pathogens to guide discovery, research and development of new antibiotics for drug-resistant bacterial infections, including tuberculosis. Report 2017. www.apps.who.int/iris/handle/10665/311820 (last accessed on 11 April 2023). |
2. | Robert Koch-Institut: Surveillance nosokomialer Infektionen sowie die Erfassung von Krankheitserregern mit speziellen Resistenzen und Multiresistenzen. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2013; 56: 580–3 CrossRef MEDLINE |
3. | Robert Koch-Institut: Infektionsepidemiologisches Jahrbuch meldepflichtiger Krankheiten für 2012. Berlin: RKI 2013; 202–4. www.rki.de/DE/Content/Infekt/Jahrbuch/Jahrbuch_2012.pdf?__blob=publicationFile (last accessed on 11 April 2023). |
4. | Robert Koch-Institut: Infektionsepidemiologisches Jahrbuch meldepflichtiger Krankheiten für 2020. Berlin: RKI 2012; 156–9. www.rki.de/DE/Content/Infekt/Jahrbuch/Jahrbuch_2020.pdf?__blob=publicationFile (last accessed on 11 April 2023). |
5. | Kramer TS, Schroder C, Behnke M, et al.: Decrease of methicillin resistance in Staphylococcus aureus in nosocomial infections in Germanya prospective analysis over 10 years. J Infect 2019; 78: 215–9 CrossRef MEDLINE |
6. | European Centre for Disease Prevention and Control, European Antimicrobial Resistance Surveillance Network (EARS-Net): Antimicrobial resistance surveillance in Europe 2022 (2020 data). Table 7a. 2022. www.ecdc.europa.eu/sites/default/files/documents/Joint-WHO-ECDC-AMR-report-2022.pdf (last accessed on 11 April 2023). |
7. | Nationales Referenzzentrum für Surveillance von nosokomialen Infektionen: KISS – Krankenhaus-Infektions-Surveillance-System. www.nrz-hygiene.de/kiss (last accessed on 11 April 2023). |
8. | Chaberny IF, Sohr D, Ruden H, Gastmeier P: Development of a surveillance system for methicillin-resistant Staphylococcus aureus in German hospitals. Infect Control Hosp Epidemiol 2007; 28: 446–52 CrossRef MEDLINE |
9. | Nationales Referenzzentrum für Surveillance von nosokomialen Infektionen: MRSA-KISS Protokoll, 2018. www.nrz-hygiene.de/KISS-Modul/KISS/MRSA (last accessed on 11 April 2023). |
10. | Nationales Referenzzentrum für Surveillance von nosokomialen Infektione: WebKess – Portal für KISS. www.nrz-hygiene.de/projekte (last accessed on 11 April 2023). |
11. | The R Project for Statistical Computing. www.r-project.org/ (last accessed on 11 April 2023). |
12. | Statistisches Bundesamt. Destatis: Krankenhausreport 2021. www.destatis.de/DE/Themen/Gesellschaft-Umwelt/Gesundheit/Krankenhaeuser/_inhalt.html#sprg234206 (last accessed on 11 April 2023). |
13. | Layer F, Strommenger B, Cuny C, Werner G: Eigenschaften, Häufigkeit und Verbreitung von MRSA in Deutschland – Zur Situation 2019/2020. Epid Bull 2021; 40: 3–12. |
14. | See I, Mu Y, Albrecht V, et al.: Trends in incidence of methicillin-resistant Staphylococcus aureus bloodstream infections differ by strain type and healthcare exposure, United States, 2005–2013. Clin Infect Dis 2020; 70: 19–25 CrossRef MEDLINE PubMed Central |
15. | Lim WW, Wu P, Bond HS, et al.: Determinants of methicillin-resistant Staphylococcus aureus (MRSA) prevalence in the Asia-Pacific region: a systematic review and meta-analysis. J Glob Antimicrob Resist 2019; 16: 17–27 CrossRef MEDLINE PubMed Central |
16. | Sriram A, Kalanxhi E, Kapoor G, et al.: State of the world‘s antibiotics 2021: a global analysis of antimicrobial resistance and its drivers. Center for Disease Dynamics, Economics & Policy, Washington DC. 2021. https://onehealthtrust.org/wp-content/uploads/2021/02/SOWA_01.02.2021_Low-Res.pdf (last accessed on 10 May 2023). |
17. | OneHealthTrust. ResistanceMap: Antibiotic resistance. 2023. www.resistancemap.onehealthtrust.org/AntibioticResistance.php (last accessed on 13 April 2023). |
18. | Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut: Empfehlungen zur Prävention und Kontrolle von Methicillin-resistenten Staphylococcus aureus-Stämmen (MRSA) in medizinischen und pflegerischen Einrichtungen. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2014; 57: 696–732 CrossRef |
19. | Langford BJ, Soucy JR, Leung V, et al.: Antibiotic resistance associated with the COVID-19 pandemic: a systematic review and meta-analysis. Clin Microbiol Infect 2023; 29: 302–9 CrossRef MEDLINE PubMed Central |
20. | Centers for Disease Control and Prevention (CDC), Atlanta, USA: COVID-19 U.S. Impact on Antimicrobial Resistance; Special Report 2022. www.cdc.gov/drugresistance/pdf/covid19-impact-report-508.pdf (last accessed on 11 April 2023). |
21. | Touati A, Bellil Z, Barache D, Mairi A: Fitness cost of antibiotic resistance in staphylococcus aureus: a systematic review. Microb Drug Resist 2021; 27: 1218–31 CrossRef MEDLINE |
22. | Renggli L, Gasser M, Pluss-Suard C, Kronenberg A: Consumption of anti-meticillin-resistant Staphylococcus aureus antibiotics in Swiss hospitals is associated with antibiotic stewardship measures. J Hosp Infect 2021; 117: 165–71 CrossRef MEDLINE |
23. | Lawes T, Lopez-Lozano JM, Nebot CA, et al.: Effects of national antibiotic stewardship and infection control strategies on hospital-associated and community-associated meticillin-resistant Staphylococcus aureus infections across a region of Scotland: a non-linear time-series study. Lancet Infect Dis 2015; 15: 1438–49 CrossRef MEDLINE |
24. | Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut: Empfehlungen zur Prävention und Kontrolle von Methicillin-resistenten Staphylococcus-aureus–Stämmen (MRSA) in Krankenhäusern und anderen medizinischen Einrichtungen. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 1999; 42: 954–58 CrossRef |
25. | Rijksinstituut voor Volksgezondheid en Milieu: MRSA – Maatregelen, 24–11–2020. www.rivm.nl/mrsa (last accessed on 30 March 2023). |
26. | Harbarth S, Fankhauser C, Schrenzel J, et al.: Universal screening for methicillin-resistant Staphylococcus aureus at hospital admission and nosocomial infection in surgical patients. JAMA 2008; 299: 1149–57 CrossRef MEDLINE |
27. | Huang SS, Septimus E, Kleinman K, et al.: Targeted versus universal decolonization to prevent ICU infection. N Engl J Med 2013; 368: 2255–65 CrossRef MEDLINE |
28. | Huskins WC, Huckabee CM, O‘Grady NP, et al.: Intervention to reduce transmission of resistant bacteria in intensive care. N Engl J Med 2011; 364: 1407–18 CrossRef MEDLINE PubMed Central |
29. | Derde LPG, Cooper BS, Goossens H, et al.: Interventions to reduce colonisation and transmission of antimicrobial-resistant bacteria in intensive care units: an interrupted time series study and cluster randomised trial. Lancet Infect Dis 2014; 14: 31–9 CrossRef MEDLINE |
30. | Fatkenheuer G, Hirschel B, Harbarth S: Screening and isolation to control meticillin-resistant Staphylococcus aureus: sense, nonsense, and evidence. Lancet 2015; 385: 1146–9 CrossRef MEDLINE |