Usefulness of Weekly Methicillin‐Resistant Staphylococcus aureus Screening
We evaluated the usefulness of adding weekly methicillin‐resistant Staphylococcus aureus (MRSA) screening to our established admission screening and clinical sampling in 4 acute care units of a university hospital. Our results suggest that weekly MRSA screening allows the detection of 56.1% of all cases of hospital‐acquired MRSA carriage. These cases would have remained undetected had admission screening and clinical sampling been the only types of surveillance in place.
Received March 17, 2009; accepted June 2, 2009; electronically published September 24, 2009.
During the past 4 decades, methicillin‐resistant Staphylococcus aureus (MRSA) has spread throughout the world, and many geographic areas have become highly endemic for MRSA colonization and infection, with resultant severe morbidity and mortality. Experts and policy makers recommend admission screening as one measure to control MRSA.1,2 Therefore, in most healthcare facilities, patients with MRSA colonization or infection are identified through admission screening or clinical samples during the hospital stay.3 This type of surveillance is not designed to detect true cross‐transmission rates, because patients who acquire MRSA and remain carriers without signs of infection are not recognized.4 The aim of our study was to evaluate the usefulness of weekly MRSA screening in 4 units of a university hospital.
Methods
The Besançon Hospital is a university‐affiliated hospital in France. For this study, data were collected for 5 years (from 2002 through 2006) in 4 units: a 15‐bed medical intensive care unit (ICU), a 15‐bed surgical ICU, a 12‐bed neurosurgery unit, and a 16‐bed general surgery unit. MRSA screening on admission and once a week thereafter (on a given day of the week) of all patients by systematic sampling of the anterior nares was recommended by the infection control department. MRSA isolates were also recovered from clinical samples obtained according to signs of infection. In addition to the screening program, standard infection control measures were used for patients with MRSA colonization or infection; these measures consisted of contact isolation of identified MRSA carriers in single rooms (or cohorts), use of dedicated material (gown, gloves, and if indicated, masks), and reinforcement of hand disinfection with alcohol‐based hand rub. MRSA cases were categorized as imported (involving patients whose screening or clinical sample tested positive for MRSA within 48 hours of hospitalization) or hospital acquired (involving patients whose admission screening had negative results for MRSA but whose subsequent screening or clinical sample had positive results for MRSA). A transmission index, defined as the ratio of the number of hospital‐acquired cases to the number of imported cases, was calculated. For example, a transmission index of 1.0 would indicate that, on average, each imported MRSA case generated one secondary (hospital‐acquired) MRSA case. Among hospital‐acquired MRSA cases, we distinguished 2 categories of patients: those who had positive results for MRSA only from a screening and those who had positive results for MRSA from a clinical sample (regardless of MRSA screening result). For each unit, the MRSA colonization pressure was calculated as the ratio of the number of MRSA‐positive patient‐days to the total number of patient‐days. Patients were considered to have MRSA colonization or infection from the date of recovery of the sample that yielded positive results to the date of hospital discharge.
Results
Of 8,101 patients admitted during the survey, 6,065 patients (74.9%) were screened for MRSA upon admission, representing 92.2% of the days of hospitalization. The rate of screening varied from 61.3% in the surgical unit to 82.7% in the medical ICU. The median number of screenings per patient (on admission and during the stay) was 3.03 (there were 2.9 screenings per patient in both ICUs, 3.1 screenings per patient in the general surgery unit, and 3.55 screenings per patient in the neurosurgical unit).
During the survey, 373 patients had positive test results for MRSA, giving an incidence of 4.31 MRSA cases per 1,000 patient‐days (6.15 MRSA cases per 100 hospitalizations). The distribution of MRSA cases is reported in the Table. Of the 373 patients, 148 (39.7%) acquired MRSA during their stay, whereas 225 (60.3%) were colonized on admission. Of the 148 cases of hospital‐acquired MRSA, 83 cases (56.1% of hospital‐acquired MRSA cases and 22.3 % of all MRSA cases) were detected only with weekly screening samples (excluding screening on admission). This proportion varied according to the departments: 6.1% in the general surgical unit, 23.3% in the medical ICU, 31.6% in the surgical ICU, and 43.5% in the neurosurgical unit. The global transmission index was 0.66 (0.28 in the general surgical unit, 0.71 in the medical ICU, 0.85 in the surgical ICU, and 2.07 in the neurosurgical unit). The total MRSA colonization pressure was 100.3 MRSA‐positive patient‐days per 1,000 patient‐days (54.9% of this colonization pressure was attributable to imported MRSA cases and 45.1% to hospital‐acquired MRSA cases). The 83 cases that were detected only with weekly MRSA screening were responsible for 13.0 MRSA‐positive patient‐days per 1,000 patient‐days (13.0% of total MRSA colonization pressure).
Discussion
We explored the usefulness of weekly MRSA screening in 4 units of a university hospital: 2 adult ICUs, 1 neurosurgical unit, and 1 general surgery unit. This last unit is a dedicated cohort facility that is mainly dedicated to orthopedic patients with infection and some other surgical patients with infection. We have previously demonstrated that having this dedicated cohort facility is useful in the reduction of MRSA cross‐transmission.5 Weekly MRSA screening allowed the identification of 83 MRSA carriers who would have remained undetected by the combination of MRSA screening upon admission and clinical samples obtained according to signs of infection during hospitalization. These 83 MRSA carriers represent 22.3% of all patients with MRSA colonization or infection. This rate increases to 29.3% if we omit the general surgical unit, where most of the patients with MRSA colonization or infection were classified as imported because of the mode of recruitment of this unit (some patients were admitted after discovery of an infection in another surgical unit). This 22.3% of MRSA cases was responsible for 13.0% of the total MRSA colonization pressure. The difference between these 2 rates is linked to the prolonged length of stay associated with MRSA infection, compared with the length of stay associated with simple MRSA colonization (data not shown).
An MRSA control program has been implemented in all high‐risk units of our hospital, including the 4 units that participated in this study. Because the control program was not perfectly implemented, MRSA cross‐transmission occurred. However, the transmission index (0.66) was relatively low: 3 cases of imported MRSA were needed to observe 2 new hospital‐acquired MRSA cases. This transmission index was similar to those reported in facilities that applied a similar design of MRSA control (including weekly screening).6‐8
Our study has a number of limitations. Only 74.9% of admitted patients were screened. Even if most of the unscreened patients had a limited length of stay (less than 2 days) in the units considered, this represents a potential bias in the calculation of the true MRSA colonization pressure. We did not obtain surveillance cultures from healthcare workers, who may carry a substantial reservoir of MRSA that limits the success of control measures.9 We did not perform audits on the application of hygiene procedures, especially hand hygiene observation. Finally, this retrospective study was not designed to determine the efficiency of weekly MRSA screening, compared with the efficiency of simple admission screening, in the reduction of MRSA acquisition.
In conclusion, our results suggest that weekly MRSA screening allows the detection of a significant proportion of MRSA cases that would have remained undetected with screening on admission only. These MRSA cases are likely to facilitate the spread of MRSA and could represent a major impediment to MRSA control.10,11 The introduction of weekly MRSA screening requires a careful assessment of MRSA epidemiology and may be useful in ICUs and similar units.
Acknowledgments
Potential conflicts of interest. All authors report no conflicts of interest relevant to this article.
References
- 1. Diekema DJ, Edmond MB. Look before you leap: active surveillance for multidrug‐resistant organisms. Clin Infect Dis 2007; 44:1101–1107.
- 2. Weber SG, Huang SS, Oriola S, et al. Legislative mandates for use of active surveillance cultures to screen for methicillin‐resistant Staphylococcus aureus and vancomycin‐resistant enterococci: position statement from the Joint SHEA and APIC Task Force. Infect Control Hosp Epidemiol 2007; 28:249–260.
- 3. 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; 299:1149–1157.
- 4. Talon D, Bertrand X. Methicillin‐resistant Staphylococcus aureus in geriatric patients: usefulness of screening in a chronic care setting. Infect Control Hosp Epidemiol 2001; 22:505–509.
- 5. Talon D, Vichard P, Muller A, Bertin M, Jeunet L, Bertrand X. Modelling the usefulness of a dedicated cohort facility to prevent the dissemination of MRSA. J Hosp Infect 2003; 54:57–62.
- 6. Jeyaratnam D, Whitty CJ, Phillips K, et al. Impact of rapid screening tests on acquisition of methicillin‐resistant Staphylococcus aureus: cluster randomised crossover trial. BMJ 2008; 336:927–930.
- 7. Trautmann M, Pollitt A, Loh U, et al. Implementation of an intensified infection control program to reduce MRSA transmissions in a German tertiary care hospital. Am J Infect Control 2007; 35:643–649.
- 8. Cunningham R, Jenks P, Northwood J, Wallis M, Ferguson S, Hunt S. Effect on MRSA transmission of rapid PCR testing of patients admitted to critical care. J Hosp Infect 2007; 65:24–28.
- 9. Ben‐David D, Mermel LA, Parenteau S. Methicillin‐resistant Staphylococcus aureus transmission: the possible importance of unrecognized healthcare worker carriage. Am J Infect Control 2008; 36:93–97.
- 10. Lucet JC, Paoletti X, Lolom I, et al. Successful long‐term program for controlling methicillin‐resistant Staphylococcus aureus in intensive care units. Intensive Care Med 2005; 31:1051–1057.
- 11. Muto CA, Jernigan JA, Ostrowsky BE, et al. SHEA guideline for preventing nosocomial transmission of multidrug‐resistant strains of Staphylococcus aureus and Enterococcus. Infect Control Hosp Epidemiol 2003; 24:362–386.
