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vol.14 suppl.2Current status and recommendations on methicillin-resistant Staphylococcus aureus infection in Latin AmericaThe changing pattern of methicillin-resistant staphylococcus aureus clones in Latin America: implications for clinical practice in the region author indexsubject indexarticles search
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Brazilian Journal of Infectious Diseases

Print version ISSN 1413-8670

Braz J Infect Dis vol.14  supl.2 Salvador Dec. 2010

http://dx.doi.org/10.1590/S1413-86702010000800003 

ARTICLES

 

Epidemiology and surveillance of methicillin-resistant staphylococcus aureus in Latin America

 

 

Carlos MejíaI; Jeannete ZuritaII; Manuel Guzmán-BlancoIII

ILatin American Working Group on Gram Positive Resistance. Hospital Roosevelt, Guatemala City, Guatemala
IILatin American Working Group on Gram Positive Resistance. Hospital Vozandes, Quito, Ecuador
IIILatin American Working Group on Gram Positive Resistance. Centro Médico de Caracas, Caracas, Venezuela

Correspondence to

 

 


ABSTRACT

Surveillance systems monitoring the spread and divergence of methicillin-resistant Staphylococcus aureus (MRSA) strains are critical if preventive and therapeutic measures targeting MRSA infection are to be employed optimally. Surveillance provides information on the spread of MRSA, on the emergence of new strains within hospitals and communities, on the antibiotic resistance profile and virulence of strains, and on the risk factors associated with infection. These data help clinicians to provide appropriate empiric treatment of infections circulating in their region, leading to improved patient outcomes.
While information on MRSA epidemiology in Latin America is growing, significant gaps exist in the available data, especially in local areas where fewer resources are available for characterizing and reporting MRSA strains. Here, we describe current knowledge of healthcare- and community-associated MRSA epidemiology in the region, and provide recommendations for future development of surveillance systems with a view to providing robust data at regional, national and local levels.

Keywords: MRSA, epidemiology, surveillance, Latin America, resistance.


 

 

INTRODUCTION

The epidemiology of methicillin-resistant Staphylococcus aureus (MRSA) is constantly changing, and both circulating clones and their antibiotic resistance profiles vary considerably throughout regions and countries.1,2 Appropriate empiric treatment of infections, based on knowledge of local circulating pathogens, is known to lead to better patient outcomes.3,4 Therefore, epidemiologic information gathered through ongoing surveillance is essential to support clinicians and infection control committees in their efforts to prevent and treat infection.

Regular surveillance for MRSA in hospital settings in the USA and Europe has been organized since the late 1980s and early 1990s. Through surveillance measures, these regions documented anincreasing proportion of MRSA infections, with recent reports of over 50% of S. aureus isolates showing resistance to methicillin in some areas.5-8 Significantly, countries with strict infection control practices, such as The Netherlands and countries in the Scandinavian region, have maintained low rates of MRSA infection, even in hospitals.

In Latin America, awareness of the dangers posed by growing antimicrobial resistance motivated the first meeting of the Pan-American Conference on Antimicrobial Resistance in 1998 in Caraballeda, Venezuela.9 Following this meeting, a surveillance network was organized to monitor bacterial resistance across the region under the leadership of the Pan-American Health Organization (PAHO). Data quality is a central consideration in developing a reliable surveillance system for MRSA, and individual surveillance centers across Latin America are admitted to the network based on meeting appropriate levels of quality control, standardization and regular data reporting. These laboratories are supported by national and regional reference laboratories. A number of other surveillance studies are active in the region, including several run by pharmaceutical companies such as Bristol Myers Squibb (SENTRY), Wyeth (TEST), and Pfizer (RESISTNET and ZAAPS).

Despite these efforts, resources for monitoring the changing epidemiology of MRSA remain limited, and the true nature and extent of MRSA infections in the region are not well understood. Typically, only a few large hospitals with facilities available to perform microbiological surveillance are able to contribute data. In contrast, much of the population is served by small community healthcare centers without the resources to collect such information. Wider-reaching and coordinated programs to provide regular surveillance reports are needed to support clinicians and infection control committees faced with the challenges of treating and preventing infections due to MRSA. Only by emphasizing the collection of quality data at local levels will we be able to make better clinical decisions.

 

SURVEILLANCE OF S. AUREUS RESISTANCE

The overall goal of surveillance in public health is to provide information to decrease morbidity and mortality, and to improve health. This is achieved through ongoing systematic collection, analysis, interpretation and dissemination of data regarding a public health-related event. A surveillance system for MRSA could range from a simple system, in which data are collected from a single hospital, to a complex electronic system that receives and integrates data from multiple sources.10 Regardless of the form of data collection, the success of standardized surveillance in countries and regions depends on correct diagnosis of MRSA and identification of specific antimicrobial resistance patterns. Facilities must use appropriate quality standards to achieve these goals successfully, since decisions and recommendations for treatment can be based directly on laboratory results.

Surveillance of MRSA infections is important in both healthcare and community settings due to the continuously changing epidemiologic profile of MRSA. Although traditionally a nosocomial pathogen that infected those patients with known risk factors,11 the emergence of cases in the community setting has led to a classification of MRSA strains as either healthcare-associated MRSA (HA-MRSA) or community-associated MRSA (CA-MRSA).1,12-15 Healthcare- and community-associated MRSA have differing epidemiologic, clinical, therapeutic, microbiologic and genetic characteristics,16 and this has clear implications for their clinical management.

A complicating factor in interpreting epidemiological data comes from the use of different terms to describe MRSA appearing in hospital and community settings. Hospital-acquired MRSA and community-acquired MRSA have sometimes been used synonymously with the terms HA-MRSA and CA-MRSA. However, some infections acquired in hospitals may be derived from CA-MRSA strains, and infections acquired in the community may carry healthcareassociated risk factors.17 Recent expert guidance proposes that the terms 'hospital-acquired' and 'community-acquired' MRSA should be used to refer to the location of exposure to MRSA, whereas specific MRSA strains should be defined as HA-MRSA or CA-MRSA, depending on their microbiologic and genetic characteristics.18

 

MRSA IN HOSPITAL SETTINGS IN LATIN AMERICA

MRSA has become an endemic hospital pathogen in many countries. The US Centers for Disease Control and Prevention (CDC) report that MRSA infections now account for 63% of staphylococcal infections in the USA, after increasing from 2% in 1974 and 22% in 1995.19 In the Tigecycline Evaluation and Surveillance Trial (T.E.S.T.), in which data were collected from 33 centers in 11 Latin American countries (Argentina, Brazil, Chile, Colombia, Guatemala, Honduras, Jamaica, Mexico, Panama, Puerto Rico and Venezuela), the overall prevalence of MRSA (including HA- and CA-MRSA strains) among S. aureus isolates was 48.3% in 2004-2007.20 The SENTRY Antimicrobial Surveillance Program in Latin America revealed an increase in the prevalence of MRSA among staphylococcal infections in medical centers from 33.8% in 1997 to 40.2% in 2006,21 although these data are heavily weighted towards specific countries, with 41% of MRSA strains collected coming from Brazil. A number of other studies report nosocomial MRSA prevalence within Latin American countries, and these data point to differences in the pattern of resistance across the region (see Table 122-35). In a recent study, the prevalence of MRSA among S. aureus isolates from tertiary hospitals in Colombia, Ecuador, Peru, and Venezuela was found to be 45%, 28%, 62% and 26%, respectively. 36

Hospitalization, residence in long-term care facilities, surgery, hemodialysis, and contact with a person who has an MRSA infection, are all known risk factors for exposure to MRSA.1,16 MRSA infections were first reported in hospitals with high levels of oxacillin or methicillin use, and nosocomial MRSA now tends to be multidrug resistant. Healthcare-acquired MRSA is typically defined by an MRSA infection that occurs more than 48 hours following exposure to a healthcare setting,16 although a precise designation of an infecting strain is only available through diagnostic testing.

 

MRSA IN THE COMMUNITY IN LATIN AMERICA

The earliest report of MRSA acquired in a community setting in Latin America came from a hospital in Uruguay in 2001. Galiana and colleagues reported infections in four children without traditional risk factors for a nosocomial MRSA infection.37 Ribeiro and colleagues also provided an early report of CA-MRSA, where they described three strains isolated from patients with septic arthritis or skin and softtissue infections (SSTIs) between 2002 and 2003.38

A report of a large outbreak of CA-MRSA in Montevideo, Uruguay, suggests that CA-MRSA is a growing problem in Latin America. Between January 2002 and October 2003, more than 1,000 patients from a jail and the community were affected by this outbreak, resulting in 12 deaths. Furthermore, the number of cases increased substantially over a subsequent 22-month period.39 SSTIs were the most common infection, accounting for over 65% of the cases, but severe cases of pneumonia were also reported, resulting in four deaths.

MRSA has since been identified as a cause of community-acquired infections throughout Latin America, although published data are limited to only a few countries and a few sites within those countries (Table 224,31,33,35,40-44). The proportion of MRSA infections caused by CA-MRSA clones differs across the region. In a recent study, 74% of MRSA isolates in Ecuador were found to be caused by clones with genotypic characteristics of CA-MRSA, whereas no CA-MRSA clones were observed among MRSA isolates from Peru.36 Surveillance of MRSA infections in the community, whether invasive or SSTIs, is important not only at the level of large hospitals, but also in small community hospitals and ambulatory clinics.

 

S. AUREUS WITH REDUCED SUSCEPTIBILITY TO VANCOMYCIN

Vancomycin and other glycopeptide antibiotics, such as teicoplanin, are commonly used to treat MRSA infections. However, reports of staphylococci with reduced susceptibility to vancomycin have begun to emerge worldwide,45 including in Latin America.46,47 The CDC defines S. aureus as having reduced susceptibility to vancomycin when the minimum inhibitory concentration (MIC) is 4 µg/mL or higher (intermediate susceptibility 4-8 µg/mL, resistance > 16 µg/mL).48-50 Despite this definition, recent reports indicate that patients infected with MRSA strains with a MIC > 1 µg/mL have a poor response to the usual prescribed doses of vancomycin.51

The earliest reports of S. aureus infections with reduced susceptibility to vancomycin were in patients with previous MRSA infections and exposure to multiple and prolonged courses of vancomycin.45,52 The first report of MRSA with reduced susceptibility to vancomycin in Latin America was in Brazil in 2001.46 Oliveira and colleagues screened 140 nosocomial isolates of MRSA and found five with a vancomycin MIC of 8 µg/mL, demonstrating reduced susceptibility. In the patients with infections due to these strains of MRSA, four patients had been treated with vancomycin for over 30 days, although one patient received only a 7-day course. Isolates with reduced vancomycin susceptibility have also been identified in the community.46,47 However, MRSA strains with reduced susceptibility to vancomycin do not appear to be increasing in the region. In a 10-year report from the SENTRY Antimicrobial Surveillance Program (1997-2006), which showed resistance to most antibiotics increasing across Latin America, the percentage of MRSA with vancomycin MIC > 1 µg/mL decreased from 96.6% in 1999-2001 to 92.3% in 2002-2006.21 Despite this apparent 'reversecreep', the potential importance of these strains requires that they still be included in future surveillance programs.

 

S. AUREUS WITH INDUCIBLE MLSB RESISTANCE

Antibiotics belonging to the macrolide-lincosamide-streptogramin B (MLSB) family are commonly used to treat staphylococcal infections, including S. aureus.53 CA-MRSA clones are usually susceptible to the lincosamide antibiotic clindamycin, which penetrates easily into the skin, making it particularly useful for the treatment of SSTIs.

Clindamycin kills bacteria by inhibiting ribosomal translocation and is active even in the presence of a high bacterial burden at the site of infection.54,55 However, MRSA strains have emerged containing a ribosomal target modification, which confers MLSB-inducible resistance to clindamycin. In the presence of low levels of erythromycin, clindamycin resistance is induced, which can lead to therapeutic failure.

The prevalence of MLSB-inducible resistance among MRSA clones is not widely reported. In a Brazilian study, 11.3% of S. aureus isolates were shown to have this phenotype,56 whereas 24.4% of MRSA isolates tested positive for MLSB-inducible resistance in a Turkish study.57

Surveillance techniques using standard susceptibility methods are liable to overlook clones with inducible resistance to clindamycin, but a double-disc diffusion test is now available, using clindamycin and erythromycin discs in close proximity, in order to observe this phenotype.53,58 In surveillance situations, positive results from double-disc diffusion tests should be disseminated quickly in order to allow clinicians to avoid the use of clindamycin in these patients.

 

MRSA MOLECULAR SURVEILLANCE

Molecular techniques, such as PCR, DNA sequencing and hybridization techniques, offer the potential for gathering a new level of detail in MRSA surveillance. For example, molecular surveillance provides a means to differentiate HA-MRSA from CA-MRSA, and allows the description of genetic variants in relation to clinical syndromes. Such findings can guide the implementation of preventive and therapeutic measures, improve patient management and reduce the impact of MRSA infections in both community and hospital settings. Rapid MRSA detection using molecular techniques, such as real-time PCR, is expected to have a significant clinical impact on patient outcome and on the costs for isolation and treatment.

Molecular techniques are fundamental to a successful surveillance system, especially within reference facilities, and their introduction into regional laboratories would provide opportunities for quick and reliable identification of MRSA isolates at a local level. However, they also require considerable resources, including expensive instrumentation and skilled technicians. Consequently, the use of molecular approaches is limited in some Latin American countries, especially in less developed regions where resources are limited.

 

RECOMMENDATIONS FOR LOCAL, NATIONAL AND REGIONAL SURVEILLANCE OF MRSA

In Latin America, MRSA surveillance conducted by Emerging Infections Programs or Hospital Infection Programs must have two principal goals:

1) To monitor and report the incidence and epidemiologic characteristics of healthcare-acquired and community-acquired MRSA infections.

2) To assess and report the molecular epidemiologic patterns of HA- and CA-MRSA.

Implementation of a robust surveillance system is dependent on the use of appropriate monitoring and reporting procedures. Isolates may be obtained from patients receiving routine clinical care for suspected infections, or from a broader screening strategy monitoring asymptomatic colonization by active surveillance.59 Microbiologic data from patients receiving routine clinical care can be used to assess the incidence of infection in certain populations, the clinical impact of infection and the success of prevention strategies. An active surveillance program may be used for early detection and monitoring of MRSA in high-risk patient populations,60 with the nares being a reliable source of cultures to identify MRSA.60

Successful monitoring of MRSA requires data collection to be both extensive and accurate. In this regard, robust quality control procedures are of high importance, and reference laboratories are needed to provide definitive results. Susceptibility testing should be incorporated into surveillance systems, including MIC determination for vancomycin, and detection of inducible clindamycin resistance. Rapid detection methods for MRSA, such as chromogenic agar and real-time PCR-based tests, may reduce the time to positive diagnosis by 2-3 days. Automated software, such as WHONET, can be used for efficient data collection and analysis.

Appropriate reporting procedures should include regular surveillance updates through local, regional and national publications, alongside early warning systems to inform clinicians, pharmacists and hospital directors of local outbreaks in their regions. Internet updates, including clinical data and demographic information, are useful in this regard, as they are both rapid and wide-reaching. Within hospitals, the Clinical and Laboratory Standards Institute (CLSI) recommends preparation of antimicrobial susceptibility reports that are specific to the facility, and provides specific recommendations on how to prepare these reports and the key information to be included within them.61 Reports should be monitored routinely for evidence of developing resistance patterns.59 In addition to local dissemination of surveillance information, communication between surveillance networks in Latin America is vital if information is to be spread quickly across the region.

An important aspect of developing successful surveillance systems is the appropriate training of personnel, from microbiologists involved in monitoring MRSA to clinicians providing patient care. Infection control committees should be charged with ensuring the use of monitoring techniques that are appropriate to the local setting, and with providing updated information to inform clinicians of the evolving epidemiology in their region.

In summary, surveillance is an important tool that assists in the implementation of different preventive and therapeutic measures to combat MRSA infections in the community and in hospitals. With accurate surveillance information, clinicians in Latin America would be able to effect appropriate antibiotic treatment for MRSA infections, having regard for likely antibiotic-resistance profiles and community-or healthcare-associated characteristics of strains within their region.

 

 

ACKNOWLEDGEMENTS

Financial support

Pfizer Inc., New York, NY, USA, provided support for meetings of the Latin American Working Group on Gram Positive Resistance. Pfizer Inc. had no involvement in the collection, analysis and interpretation of data, in the writing of the manuscripts, or in the decision to submit the articles for publication.

Manuscript preparation

The support provided by Choice Pharma (Hitchin, UK), funded by Pfizer Inc., consisted of manuscript formatting and writing assistance.

 

DISCLOSURES

C. Mejía: Advisory Board member for Pfizer and Abbott; consultant for Pfizer; received funding from Tibotec for HIV research, from Avexa for studies in HIV treatment, and from Merck for participation in the SMART study.

J. Zurita: Advisory Board member and consultant for Pfizer; received research grant from Wyeth.

M. Guzmán-Blanco: Advisory Board member for Pfizer, Merck and BD; consultant for Pfizer, Wyeth and Janssen; received research funding from Wyeth and Merck.

 

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Correspondence to:
Carlos Mejía
Infectious Diseases Division Hospital Roosevelt
Calz Roosevelt Z-11 Guatemala City, Guatemala
Phone: +502-244401086 Fax: +502-24710341
E-mail: mejia_villatoro@hotmail.com