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A new national antimicrobial resistance surveillance program in Singapore public hospitals that uses WHONET detected high levels of methicillin resistance among Staphylococcus aureus (35.3%), carbapenem resistance among Acinetobacter spp. (49.6%), and third-generation cephalosporin resistance among Klebsiella pneumoniae (35.9%) hospital isolates in 2006. Antimicrobial drug resistance is a major problem in Singapore.
Bacterial antimicrobial drug resistance is a worldwide problem that is exacerbated by the diminishing number of new antimicrobial drugs in the pharmaceutical pipeline (1,2). This is an emerging public health problem, especially in hospitals of the newly industrialized countries of Asia and the Pacific. In 2001, the World Health Organization (WHO) launched the first global strategy to counter this phenomenon (3), a key component of which is the development of surveillance programs to monitor trends in antimicrobial drug resistance and use (3).
Overarching surveillance programs monitoring antimicrobial drug–resistance trends on a national or regional level are present in Australia (4) and Europe (5). Such is not the case in Singapore, where surveillance efforts have generally been conducted only at the institutional level, with limited sharing and analysis of data. As a result, the actual scale of local antimicrobial drug resistance is not well defined. The Network for Antimicrobial Resistance Surveillance (Singapore), a voluntary group of healthcare professionals, was established in December 2005 to fill this gap.
A laboratory-based surveillance program was established in 2006 to monitor the antimicrobial drug–resistance trends of 6 common nosocomial pathogens: Staphylococcus aureus, Escherichia coli, Enterococcus spp., Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter spp. Excluding coagulase-negative staphylococci, these organisms collectively account for >90% of positive bacterial cultures from nosocomial infections locally.
All 6 public sector acute-care hospitals in Singapore—2 tertiary-care hospitals, 3 secondary-care hospitals, and 1 institution dedicated to pediatrics and obstetrics/gynecologic services only—participated in the program. These hospitals constitute ≈76.5% of the 8,205 acute-care hospital beds available in the country (6).
All clinical isolates submitted to the externally accredited microbiology laboratories of these hospitals in calendar year 2006 were recorded for this study. Four laboratories performed antimicrobial drug–susceptibility testing predominantly through disk-susceptibility testing, supplemented by VITEK 2 system (bioMérieux, Marcy l’Etoile, France), following guidelines of the Clinical Laboratory Standards Institute (CSLI) (7). One laboratory used the VITEK 2 system exclusively, following CLSI guidelines (7), and the sixth laboratory used disk-susceptibility testing, following guidelines for the calibrated dichotomous sensitivity method (8).
Microbiologic and demographic data were extracted every quarter from the laboratory information system of each participating institution and converted into a standard format by using WHONET 5 (WHO, Geneva, Switzerland). Data were collated and analyzed centrally, with duplicates eliminated according to CLSI guidelines (9). Hospital bed occupancy data were obtained from the published records of each institution.
Statistical analysis was performed by using Excel 2003 (Microsoft, Redmond, WA, USA). Clinical microbiologists of the respective hospitals verified the analyzed data. Combined antimicrobial drug–susceptibility data were analyzed for the target organisms in 3 ways: for all isolates, for blood culture isolates only, and for isolates from intensive care unit (ICU) settings. The same analysis was also separately performed for data from each institution.
The distribution of resistant organisms isolated in 2006 is shown in the Table. The incidence density of resistant organisms from clinical samples for 2006 is shown in the Figure. Antimicrobial drug resistance was generally more prevalent in ICUs, but there was marked interhospital variation in resistance percentages. The tertiary hospitals had high rates of antimicrobial drug resistance, whereas the pediatric and women’s hospital had much lower rates.
Antimicrobial drug resistance in the Enterobacteriaceae was prevalent for amoxicillin-clavulanate (K. pneumoniae 36.0%, E. coli 26.7%), ciprofloxacin, and third-generation cephalosporins (Table). Imipenem resistance was present in 0.2% (14 isolates) of K. pneumoniae. Ertapenem resistance was reported in 0.2% of all E. coli isolates and 0.9% of all K. pneumoniae isolates at the institutions that routinely test for this agent.
Despite the relatively small numbers of Acinetobacter spp. isolates compared with the other organisms, carbapenem-resistant Acinetobacter spp. were found in all ICUs at a high incidence density; as many as 69% of all isolates at 1 ICU were carbapenem resistant. Fully 18.2% of all Acinetobacter spp. were resistant to ampicillin/sulbactam, cephalosporins, carbapenems, ciprofloxacin, and aminoglycosides; these particular isolates were susceptible to only the polymyxins. Carbapenem resistance was also found in 9.6% of all P. aeruginosa isolates and in up to 27.2% of ICU isolates.
Methicillin resistance occurred in 35.3% of all S. aureus isolates. Methicillin-resistant S. aureus (MRSA) strains showed correspondingly high resistance levels to macrolides (90.2%), ciprofloxacin (93.9%), and trimethoprim-sulfamethoxazole (49.9%). Vancomycin resistance was reported in 0.8% of all enterococci.
Based on incidence density calculations, MRSA was the predominant drug-resistant pathogen at all hospitals. It had the highest incidence density for blood and ICU cultures (0.31/1,000 inpatient-days and 4.48/1,000 ICU inpatient-days, respectively) among all organisms surveyed. Third-generation cephalosporin-resistant K. pneumoniae was the predominant gram-negative resistant pathogen, with an incidence density of 0.19/1,000 and 3.21/1,000 inpatient days for blood and ICU cultures, respectively.
A comparison between organisms isolated from blood cultures and other cultures demonstrated statistically significant differences with regard to percentage resistance for S. aureus, P. aeruginosa, and the Enterobacteriaceae. The reason for these finding is not evident. In general, ≈10% of all resistant organisms were isolated from blood cultures.
This is the first comprehensive national survey of antimicrobial drug resistance in Singapore public hospitals. We believe that our findings represent the endemic antimicrobial drug resistance situation in our hospitals; quarterly data analysis did not show any overt outbreak. These results, although new, are not surprising. Previous regional surveys and local studies had already hinted at the extent of the problem in Singapore (10–12). Similar data have also been reported from other countries in the Asia Pacific region (10,11).
Use of both incidence density and percentage resistance enabled a more nuanced analysis of the scale of the problem. Although almost half of all Acinetobacter spp. clinical isolates were resistant to imipenem, the relative rarity of isolating this organism from clinical specimens renders it a smaller problem compared with MRSA or quinolone-resistant Enterobacteriaceae outside the ICU setting.
In comparison with similar data from Europe (5) and Australia (4), prevalence of resistance in gram-negative organisms is much higher but prevalence of vancomycin-resistant enterococci is lower. MRSA rates are comparable to those in some countries in southern Europe (5) but higher than those in Australia. The reasons for the differences in antimicrobial drug–resistant patterns might be related to infection control practices or to timing of the introduction of resistant organisms. However, more research is needed to clarify these differences.
There are several limitations of this work. First, the inability to segregate nosocomial and community infections prevented a more detailed analysis of antimicrobial drug–resistance issues pertaining to community and hospital settings. Second, the use of different laboratory standards and methods potentially adds a degree of inaccuracy in the analyses. Third, routine laboratory data did not enable us to distinguish the different mechanisms of resistance, particularly among gram-negative bacteria, or to determine the presence of any predominant clone responsible for the high endemic levels of antimicrobial resistance.
Nevertheless, the results can serve to direct any national effort aimed toward reducing the antimicrobial resistance problems of local hospitals. The issues of MRSA in general and carbapenem-resistant Acinetobacter spp. and P. aeruginosa in local ICUs are particularly pressing. Continued surveillance will also serve as an impartial feedback on the efforts of infection control programs for the future. For a small city-state, comprehensive national surveillance is relatively easier for Singapore than for larger countries. Such surveillance of clinical microbiology isolates is a critical first step toward controlling the growing worldwide threat of antimicrobial drug resistance, and WHONET is a useful tool in this respect.
We thank the many dedicated staff who have helped with data collection and technical assistance, in particular, Winnie Lee, Dale Andrew Fisher, and Mee-Lee Tan.
This work was funded by the following grants: SingHealth Foundation Grant 2006, Ministry of Health Healthcare Quality Improvement Fund 2006, and Educational grants from Pfizer Singapore, Wyeth, and AstraZeneca.
Dr Hsu is an infectious diseases physician at the Yong Loo Lin School of Medicine, National University of Singapore. His research interests include the genetics and epidemiology of MRSA as well as nosocomial antimicrobial drug resistance.
Suggested citation for this article: Hsu L-Y, Tan T-Y, Jureen R, Koh T-H, Krishnan P, Lin RT-P, et al. Antimicrobial drug resistance in Singapore hospitals. Emerg Infect Dis [serial on the Internet]. 2007 Dec [date cited]. Available from http://www.cdc.gov/EID/content/13/12/1944.htm