Most information on invasive Staphylococcus aureus infections comes from temperate countries. There are considerable knowledge gaps in epidemiology, treatment, drug resistance and outcome of invasive S. aureus infection in the tropics.
A prospective, observational study of S. aureus bacteraemia was conducted in a 1000-bed regional hospital in northeast Thailand over 1 year. Detailed clinical data were collected and final outcomes determined at 12 weeks, and correlated with antimicrobial susceptibility profiles of infecting isolates.
Ninety-eight patients with S. aureus bacteraemia were recruited. The range of clinical manifestations was similar to that reported from temperate countries. The prevalence of endocarditis was 14%. The disease burden was highest at both extremes of age, whilst mortality increased with age. The all-cause mortality rate was 52%, with a mortality attributable to S. aureus of 44%. Methicillin-resistant S. aureus (MRSA) was responsible for 28% of infections, all of which were healthcare-associated. Mortality rates for MRSA and methicillin-susceptible S. aureus (MSSA) were 67% (18/27) and 46% (33/71), respectively (p = 0.11). MRSA isolates were multidrug resistant. Only vancomycin or fusidic acid would be suitable as empirical treatment options for suspected MRSA infection.
S. aureus is a significant pathogen in northeast Thailand, with comparable clinical manifestations and a similar endocarditis prevalence but higher mortality than industrialised countries. S. aureus bacteraemia is frequently associated with exposure to healthcare settings with MRSA causing a considerable burden of disease. Further studies are required to define setting-specific strategies to reduce mortality from S. aureus bacteraemia, prevent MRSA transmission, and to define the burden of S. aureus disease and emergence of drug resistance throughout the developing world.
Citation: Nickerson EK, Hongsuwan M, Limmathurotsakul D, Wuthiekanun V, Shah KR, Srisomang P, et al. (2009) Staphylococcus aureus Bacteraemia in a Tropical Setting: Patient Outcome and Impact of Antibiotic Resistance. PLoS ONE 4(1): e4308. https://doi.org/10.1371/journal.pone.0004308
Editor: Adam J. Ratner, Columbia University, United States of America
Received: October 21, 2008; Accepted: December 22, 2008; Published: January 30, 2009
Copyright: © 2009 Nickerson et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The study was funded by the Wellcome Trust. EKN, MH, DL, VW, NJW, WC, NPD and SJP are funded by the Wellcome Trust. VGF is funded by National Institutes of Health award R01-AI068804. TEW is funded by National Institutes of Health award U54 AI057141 and by a Parker B. Francis Fellowship in Pulmonary Research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: All of the authors, except VGF, declare that they have no conflict of interest pertaining to this manuscript. Vance G. Fowler declares the potential conflict of interests: Grant or research support: Cubist, Merck, Theravance, Inhibitex, Cerexa, NIH; Paid consultant: Astellas, Biosynexus, Cubist, Inhibitex, Merck, Johnson & Johnson, Leo Pharmaceuticals; Speaker's Bureau: Cubist, Pfizer; Employment Duke University; Honoraria: Arpida, Astellas, Biosynexus, Cubist, Inhibitex, Merck, Nabi, Pfizer, Theravance, Ortho-McNeil; Membership on advisory committees or review panels, board membership, etc.: Cubist
The published literature on invasive Staphylococcus aureus disease is heavily skewed towards industrialised temperate countries, where it represents a major cause of community- and hospital-acquired infection , . Clinical management has been complicated by the increasing proportion of infections caused by methicillin-resistant S. aureus (MRSA), a problem that was initially limited to hospital-adapted strains but that has now extended to community-associated strains , . Attributable mortality rates for S. aureus bacteraemia (SAB) in the developed world are typically up to 30% –, and the costs of treating nosocomial infection, screening for MRSA carriage and changes in prescribing practices to include cover for MRSA are considerable. This situation has attracted huge public and media attention and receives significant research funding.
This situation strikes a sharp contrast with that in the developing world, where S. aureus is considered to be a less important cause of morbidity and mortality than other infectious diseases such as pneumococcal infections, malaria, HIV infection and tuberculosis. There are few studies of S. aureus infection in tropical countries that define disease epidemiology, the nature of clinical manifestations, outcome and drug resistance patterns. Yet the spread of pandemic clones of MRSA has major implications for the developing world, where facilities to determine antimicrobial resistance are lacking, expensive antibiotics required to treat MRSA are often not available and hospital infection control policies are limited. The availability of over-the-counter antibiotics in much of the tropical world is likely to be a major driver of drug resistance.
Here, we begin to fill our knowledge gaps with a study that describes the epidemiology, treatment and outcome from S. aureus bacteraemia in northeast Thailand, together with the incidence, place of acquisition and impact of MRSA infections.
Patients and Clinical methods
The Ethical and Scientific Review sub-committee of the Royal Thai Government Ministry of Public Health, and the Oxford Tropical Research Ethics Committee both approved the study. A prospective, observational study was conducted at Sappasithiprasong Hospital in northeast Thailand for a period of 1 year, from November 2006 to November 2007. This 1000-bed regional hospital has a catchment of 2 million people, the majority of whom are rice farmers and their families. The hospital provides a comprehensive clinical and laboratory service. Potential study patients were identified by daily screening of the blood culture results in the hospital diagnostic microbiology laboratory. Patients of any age with at least one clinically significant blood culture positive for a pure growth of S. aureus were enrolled into the study after providing written informed consent. Following recruitment, study investigators visited inpatients daily until discharge to record progress and management. Data were recorded on standardised forms adapted from those developed by Fowler et al . Clinical care was provided by the hospital physicians, independent of the research team. Study-specific investigations were a repeat blood culture taken 48–96 hours after the first culture positive for S. aureus and a transthoracic echocardiogram. Results of study investigations were given to hospital physicians caring for the patient. Echocardiograms on patients aged less than 14 years were performed by a paediatric echocardiographer (T.W.), while echocardiograms on the remainder were performed and/or reviewed by study investigators trained in adult echocardiography (E.K.N., W.M., H.B.). Final outcome was determined 12 weeks from the date the first culture positive for S. aureus was taken using a standardised telephone questionnaire.
Community-acquired infection was defined as admission to hospital with an illness consistent with invasive S. aureus disease and a positive S. aureus blood culture. Nosocomial infection was defined as a positive S. aureus blood culture taken more than 48 hours after admission for another condition. Non-nosocomial healthcare-associated infection was defined as community-acquired infection above but in an individual who had been in contact with healthcare services in the preceding year, using the criteria described by Fowler et al . Sites of S. aureus infection were established based on examination findings and referral to the medical notes, including investigation reports and operation notes. A history of an underlying chronic medical condition was recorded if documented in the medical notes. Outcomes at 12 weeks were defined as: (i) cure - clinically improved and no additional sites of infection present or suspected; (ii) unresolved infection - persistent features of infection with or without persistent positive cultures; (iii) death attributable to S. aureus - when death was due to S. aureus infection in a previously healthy individual or when S. aureus hastened death in the presence of an underlying condition such as cancer; or (iv) death due to other causes - when the S. aureus infection did not appear to contribute to death.
Antibiotic susceptibilities were performed by the hospital microbiology laboratory using the disk diffusion method . Susceptibilities reported to hospital physicians were penicillin, oxacillin, cefazolin, erythromycin, clindamycin and trimethoprim-sulphamethoxazole for methicillin-susceptible S. aureus (MSSA). For MRSA isolates, susceptibilities to vancomycin and fusidic acid were added. A total of 81/98 S. aureus isolates were available for further study, re-identified and stored at −80°C. An extended antibiotic susceptibility profile was determined in our research laboratory at the hospital using the disk diffusion method  to establish susceptibilities to other antibiotic agents with potential activity against the clinical isolates. This panel included cefoxitin, chloramphenicol, ciprofloxacin, clindamycin, erythromycin, fusidic acid, gentamicin, mupirocin, netilmicin, penicillin, rifampicin, trimethoprim-sulphamethoxazole, tetracycline and vancomycin. Isolates that were resistant to cefoxitin by disk diffusion were evaluated by oxacillin and vancomycin E-tests (AB Biodisk). Isolates were designated as MRSA based on an oxacillin E-test for 81 isolates, and based on the oxacillin disk diffusion assay performed by the hospital laboratory for the 17 isolates that were not available for further testing.
Data were double entered into a database. Data analysis was performed using Stata software version 9 (StataCorp, College Station, Texas). Categorical data were analysed using Fisher's exact test and for continuous data the Mann-Whitney U test was used. Reported p values are two-tailed. Kaplan-Meier survival curves were plotted for attributable and non-attributable deaths, and for S. aureus attributable deaths in children and adults (non-attributable deaths censored). These survival curves were compared using the log rank test.
A total of 106 patients fulfilled the inclusion criteria during the study period. Of these, 98 patients were recruited and 8 patients could not be studied either because they declined to consent to participate in the study (n = 6) or because they returned home to Lao PDR (across the Mekong River from Thailand) before the culture became positive and follow up was not possible (n = 2). The age of enrolled patients ranged from 1 day to 92 years (median 39 years). There were 61 (62%) adult and 37 paediatric patients (less than 18 years) (Table 1). A history of one or more underlying chronic medical conditions was documented in 57 cases (58%), with cardiac disease accounting for the greatest proportion (20 cases). A site of infection was identified in 59 (60%) patients.
Repeat blood cultures were performed within 48–96 hours of the first culture positive for S. aureus in 57 patients (58%, representing 79% of patients surviving to 4 days), of which 11 (19%) were still positive. After this time period, 56 further blood cultures were taken from 23 patients, which identified an additional 3 patients with persistently positive blood cultures. No vegetations were seen on transthoracic echocardiography performed on 11 of these 14 patients with persistently positive cultures. MRSA was responsible for persistently positive cultures significantly more often than MSSA infection (30% versus 8% respectively (p = 0.02)). Eight of 14 patients (57%) were receiving antibiotic therapy to which the organism was susceptible in vitro at the time the repeat blood culture was taken.
Prevalence of endocarditis
Echocardiography was performed in 49 out of 98 patients (50%). Although the aim of the study was to perform echocardiography on all patients, the remaining 49 patients were either discharged or died before an echocardiogram could be performed, were too sick to be taken to the echocardiography room, had a contraindication to transthoracic echocardiography, or the echocardiography machine or trained personnel were not available. However, there were no significant differences between those who did and did not undergo echocardiography in terms of pre-disposing cardiac conditions, co-morbidities, immunocompromise, age or presence of prosthetic material (data not shown). Seven of the 49 patients (14%) undergoing echocardiography had vegetations visualized. The affected valves were mitral (n = 3), aortic (n = 3) and tricuspid (n = 1). Two patients had definite endocarditis and 5 had possible endocarditis by modified Duke criteria , since taking 2 blood culture bottles is uncommon in the hospital. Among these 7 patients with endocarditis, 1 died. One additional patient with a history of injection drug use met clinical criteria for endocarditis, but died before echocardiography could be performed.
Over half of the infections (54%) were either nosocomial or non-nosocomial healthcare-associated. Nosocomial infections were most common in those aged less than 1 year old, accounting for 94% of cases. Infections related to devices were the third most common site of infection, accounting for 14% of all sites.
Antibiotic resistance and therapy
MRSA accounted for 28% (n = 27) of SAB, with no significant difference in rate between adults and children (26% versus 30% respectively; p = 0.82). The MRSA cases were either nosocomial (n = 21, 78%) or non-nosocomial healthcare-associated (n = 6, 22%). Of the 71 MSSA cases, 44 (62%) were community-acquired, 8 (11%) were non-nosocomial healthcare-associated, and 19 (27%) were nosocomial. There was a significant difference in MRSA rates on the intensive care units compared with the general wards: 57% versus 16%, respectively (p<0.001). The impact of MRSA on effective prescribing of antibiotic therapy is summarised in Table 2. Patients infected with MSSA were more likely than patients infected with MRSA to receive an antibiotic to which the organism was susceptible before the culture results became available (67/71 (94%) versus 4/27 (15%) respectively, p<0.001). The median number of days to starting antibiotic therapy to which the organism was susceptible in vitro was 0 (interquartile range (IQR) 0–0) days and 3 (IQR, 2–4) days for MSSA and MRSA, respectively (p<0.001). Once culture results were available, 70 out of 73 survivors (96%) received an antibiotic that covered the infecting isolate. The median duration of parenteral treatment given to survivors from the day the first culture positive for S. aureus was taken was 17 (IQR 12–24) days, with no difference in duration for patients infected with MSSA versus MRSA (p = 0.26). All MRSA isolates were susceptible to vancomycin by E-test (minimum inhibitory concentration ≤2 µg/ml). Of the 17 patients with normal renal function who received vancomycin, 13 (76%) received adequate vancomycin doses by manufacturer's recommendations. Measurement of vancomycin drug levels was not available in the hospital.
Antibiotic resistance patterns are summarised in Table 3. Over 90% of MRSA isolates were resistant to ciprofloxacin, erythromycin, gentamicin, netilmicin, tetracycline and trimethoprim-sulphamethoxazole, and 65% were resistant to clindamycin. Vancomycin and fusidic acid had the lowest rates of resistance.
The overall mortality rate at 12 weeks was 52% (n = 51), and the S. aureus attributable mortality rate was 44% (n = 43). There was insufficient information to determine the cause of death in 1 case. Most deaths (39/51, 76%) occurred in hospital or at home on the day of discharge, as relatives commonly take moribund patients home to die (n = 12). S. aureus bacteraemia accounted for 1% of all in-patient deaths at Sappasithiprasong hospital during the study period. Overall mortality increased significantly with age (p<0.001) (Figure 1). There was a significant difference between the overall mortality rate in children compared to adults (32% versus 64%, p = 0.003). The association between overall mortality and increasing age remained highly significant when adjusted for underlying co-morbidities or immunosuppression (p = 0.001). The mortality rates for MRSA and MSSA were 67% (18/27) and 46% (33/71), respectively (p = 0.11). There was no significant difference in mortality between patients with and without identified sites of infection, (47% and 59% respectively, p = 0.31). Mortality amongst patients with repeated blood cultures positive for S. aureus was 43% (6/14). The median number of days to death in those patients whose death was attributable to S. aureus was 3 (IQR, 1–6) days compared with 47 (IQR, 25–68) days in those with non-attributable deaths (p<0.001). Significant differences were noted on survival curve analysis of attributable mortality rates in adults and children (p = 0.01) (Figure 2), and in the timing of death for S. aureus attributable and non-attributable deaths (p = 0.001) (Figure 3). There was no difference in times to death comparing patients infected with MSSA versus MRSA (data not shown). At 12 weeks, 44 patients (45%) were cured, and 3 patients (3%) had unresolved infection (empyema thoracis, infected pacemaker, and osteomyelitis).
Age distribution and age-specific mortality rates and disease burden for 98 cases of S. aureus bacteraemia studied in Ubon Ratchathani, NE Thailand. Overall mortality increased significantly with age (p<0.001), analysing age as a continuous variable.
Kaplan-Meier survival curves comparing adult and paediatric patients with respect to S. aureus attributable deaths (p = 0.01). Non-attributable deaths were censored.
This study shows that SAB is an important cause of morbidity and mortality in northeast Thailand. The all-cause and S. aureus-attributable mortality rates in our study, 52% and 44% respectively, are considerably higher than mortality rates for SAB reported from temperate industrialised countries –. A study of SAB conducted in the USA by Fowler et al  found an all-cause and attributable mortality of 22% (157/724) and 12% (86/724), respectively, but this excluded deaths that occurred before culture results were available. The addition of these cases would have given an all-cause and S. aureus-attributable mortality rate of 33% and 23%, respectively. Published studies of all-cause bacteraemia in Asia have identified S. aureus as a major cause of bacteraemia, accounting for both community-acquired and hospital-acquired disease –. If our data showing that S. aureus accounts for 1% of all in-patient deaths is representative of this populous region (half the world's population lives within 2000 miles of northeast Thailand), then S. aureus would be a major contributor to preventable mortality worldwide. To our knowledge this is the first published prospective study to focus on SAB in tropical Asia. This is noteworthy because papers describing all-cause bacteraemia in Asia rarely give details by causative organism, resulting in an under-appreciation of the morbidity and mortality burden due to S. aureus in the tropics. Sappasithiprasong Hospital is the regional hospital for the province with referrals from clinics and hospitals in the province, but also provides primary care services to a large local population so accurate estimates of disease incidence were not possible.
In our study, SAB was most common at the extremes of age, a similar pattern to that described in a temperate industrialised country , . Among the 17 patients under 1 year of age, 16 (94%) had hospital-acquired infections and nearly a third (29%) were premature or very low birth weight babies. This suggests the particular vulnerability to acquiring nosocomial SAB of children less than 1 year of age requiring multiple interventions and prolonged stays in hospital. A higher incidence in those aged under 1 year and the predominance of nosocomial infections in this age group has been described in Denmark . The increase in numbers of cases and mortality with age also mirror the rise in co-morbidities with age, as noted in Denmark .
The broad range of clinical manifestations seen in patients with SAB in industrialised countries was observed in this series. Our findings suggest that the burden of S. aureus disease in the tropics exceed current perceptions, and demonstrate that serious invasive infections are common. This has an important bearing on antimicrobial therapy because management of deep infections and bacteraemia requires effective antimicrobial therapy whereas drainage of superficial pus collections can result in cure irrespective of antibiotic therapy .
The rapid deterioration and short median time to death (3 days) of patients dying from S. aureus septicaemia meant that echocardiograms could not be performed in half of the patients. However, the prevalence of echocardiographically-confirmed endocarditis of 14% (7/49) is comparable to that seen in industrialised countries , , which has important implications for many tropical countries where restricted or delayed access to echocardiography is liable to be an issue. Our prevalence may be an underestimate since those patients who died earlier may have been more likely to have endocarditis. A quarter of the patients with endocarditis died, which is at the lower end of the mortality range reported for S. aureus endocarditis (25–47%)  and may be a further indication that a number of patients who died prior to echocardiography had undiagnosed endocarditis. The heart valves affected by endocarditis were predominantly left-sided, which is in keeping with the low number of intravenous drug users in our study. Half the patients with endocarditis were teenagers, which is a younger age group than typically seen in industrialised temperate countries ,  but is described in other tropical countries , , often as a result of rheumatic heart disease and uncorrected congenital heart disease. However, none of our patients with endocarditis had known valvular abnormalities.
MRSA was responsible for nearly one third of cases of SAB, all of which were healthcare-associated. Although community-associated MRSA is a major problem elsewhere, we find no evidence for this in our setting where a clone defined by multilocus sequence typing as sequence type 239 predominates . Over half of our patients had healthcare-associated infections which suggests that SAB in Thailand is strongly related to healthcare, mirroring industrialised countries , . Although there are comprehensive hospital infection control guidelines in Sappasithiprasong hospital, implementing these is difficult due to a bed occupancy rate that often exceeds 100% and a lack of infrastructure, such as a scarcity of isolation rooms and only two hand wash basins on each of the general wards. However, alcohol hand rub is available in the intensive care units. Addressing such infection control measures would require a significant increase in investment, although this would be offset by reducing the expense of nosocomial infections. Our finding that over half the infections were healthcare-associated indicates that hospital infection control is an important area for clinical, microbiological and economic research if improvements are to be made.
Significant delays in receiving effective antibiotic therapy were seen with MRSA bacteraemia compared with MSSA bacteraemia. Vancomycin is available in this setting but is not used in the empiric regimen for a patient with suspected bacterial sepsis unless they are already known to be MRSA positive. Monitoring of vancomycin levels is not possible at Sappasithiprasong Hospital, which may lead doctors to give lower doses to reduce the perceived risk of toxicity. The mortality rates for patients with MRSA who received effective and ineffective empirical antibiotics were 0% and 69%, respectively, indicating the importance of early effective treatment. There was a median delay in effective antibiotic therapy of 3 days for MRSA patients. Delays in treating SAB are known to have an adverse effect on outcome . The common usage of ampicillin and gentamicin as empirical therapy in children under the age of 1 year should be revised in light of our finding that 53% of SAB cases in this age group were MRSA and all MRSA strains were resistant to gentamicin. Although alternative antibiotics to vancomycin may be appropriate therapy for MRSA, in our setting the high rates of resistance found on susceptibility testing indicate that these alternatives would not be effective.
This study has demonstrated that S. aureus is a significant pathogen in northeast Thailand, with comparable clinical manifestations and a similar endocarditis prevalence but higher mortality than industrialised countries. The factors contributing to this high death rate, such as delayed presentation to hospital and the early management of sepsis, require further evaluation. The majority of infections were associated with exposure to healthcare settings and MRSA was associated with a considerable burden of disease and a high mortality. Revisions to the empirical prescribing practices to include MRSA therapy could be associated with significant benefit. An initiative to raise the profile of infection control is needed, together with work to characterise the burden and causes of hospital-acquired infections, including patient-to-patient transmission of MRSA, such that cost-effective solutions can be devised appropriate to this setting.
Conceived and designed the experiments: EKN DL VW VGF WC NPJD SJP. Performed the experiments: EKN MH DL VW KRS PS WM TW NT HB SJP. Analyzed the data: EKN DL TEW. Wrote the paper: EKN VGF TEW NJW SJP. Contributed to and approved manuscript: MH DL VW KRS PS WM TW NT HB WC NPJD.
- 1. Lowy FD (1998) Staphylococcus aureus infections. N Engl J Med 339: 520–532.
- 2. Wisplinghoff H, Bischoff T, Tallent SM, Seifert H, Wenzel RP, et al. (2004) Nosocomial bloodstream infections in US hospitals: analysis of 24,179 cases from a prospective nationwide surveillance study. Clin Infect Dis 39: 309–317.
- 3. Wallin TR, Hern HG, Frazee BW (2008) Community-associated methicillin-resistant Staphylococcus aureus. Emerg Med Clin North Am 26: 431–455, ix.
- 4. Powell JP, Wenzel RP (2008) Antibiotic options for treating community-acquired MRSA. Expert Rev Anti Infect Ther 6: 299–307.
- 5. Hill PC, Birch M, Chambers S, Drinkovic D, Ellis-Pegler RB, et al. (2001) Prospective study of 424 cases of Staphylococcus aureus bacteraemia: determination of factors affecting incidence and mortality. Intern Med J 31: 97–103.
- 6. Das I, O'Connell N, Lambert P (2007) Epidemiology, clinical and laboratory characteristics of Staphylococcus aureus bacteraemia in a university hospital in UK. J Hosp Infect 65: 117–123.
- 7. McClelland RS, Fowler VG Jr, Sanders LL, Gottlieb G, Kong LK, et al. (1999) Staphylococcus aureus bacteremia among elderly vs younger adult patients: comparison of clinical features and mortality. Arch Intern Med 159: 1244–1247.
- 8. Fowler VG Jr, Olsen MK, Corey GR, Woods CW, Cabell CH, et al. (2003) Clinical identifiers of complicated Staphylococcus aureus bacteremia. Arch Intern Med 163: 2066–2072.
- 9. NCCLS (2004) National Committee for Clinical Laboratory Standards. Performance Standards for Antimicrobial Susceptibility Testing; Fourteenth Informational Supplement (M100-S14) 24: 40–47.
- 10. Li JS, Sexton DJ, Mick N, Nettles R, Fowler VG Jr, et al. (2000) Proposed modifications to the Duke criteria for the diagnosis of infective endocarditis. Clin Infect Dis 30: 633–638.
- 11. Singhi S, Ray P, Mathew JL, Jayashree M (2008) Nosocomial bloodstream infection in a pediatric intensive care unit. Indian J Pediatr 75: 25–30.
- 12. Karunakaran R, Raja NS, Ng KP, Navaratnam P (2007) Etiology of blood culture isolates among patients in a multidisciplinary teaching hospital in Kuala Lumpur. J Microbiol Immunol Infect 40: 432–437.
- 13. Phetsouvanh R, Phongmany S, Soukaloun D, Rasachak B, Soukhaseum V, et al. (2006) Causes of community-acquired bacteremia and patterns of antimicrobial resistance in Vientiane, Laos. Am J Trop Med Hyg 75: 978–985.
- 14. Frederiksen MS, Espersen F, Frimodt-Moller N, Jensen AG, Larsen AR, et al. (2007) Changing epidemiology of pediatric Staphylococcus aureus bacteremia in Denmark from 1971 through 2000. Pediatr Infect Dis J 26: 398–405.
- 15. Benfield T, Espersen F, Frimodt-Moller N, Jensen AG, Larsen AR, et al. (2007) Increasing incidence but decreasing in-hospital mortality of adult Staphylococcus aureus bacteraemia between 1981 and 2000. Clin Microbiol Infect 13: 257–263.
- 16. Lee MC, Rios AM, Aten MF, Mejias A, Cavuoti D, et al. (2004) Management and outcome of children with skin and soft tissue abscesses caused by community-acquired methicillin-resistant Staphylococcus aureus. Pediatr Infect Dis J 23: 123–127.
- 17. Chang FY, MacDonald BB, Peacock JE Jr, Musher DM, Triplett P, et al. (2003) A prospective multicenter study of Staphylococcus aureus bacteremia: incidence of endocarditis, risk factors for mortality, and clinical impact of methicillin resistance. Medicine (Baltimore) 82: 322–332.
- 18. Mylonakis E, Calderwood SB (2001) Infective endocarditis in adults. N Engl J Med 345: 1318–1330.
- 19. Hogevik H, Olaison L, Andersson R, Lindberg J, Alestig K (1995) Epidemiologic aspects of infective endocarditis in an urban population. A 5-year prospective study. Medicine (Baltimore) 74: 324–339.
- 20. Nkomo VT (2007) Epidemiology and prevention of valvular heart diseases and infective endocarditis in Africa. Heart 93: 1510–1519.
- 21. Dhawan A, Grover A, Marwaha RK, Khattri HN, Anand IS, et al. (1993) Infective endocarditis in children: profile in a developing country. Ann Trop Paediatr 13: 189–194.
- 22. Feil EJ, Nickerson EK, Chantratita N, Wuthiekanun V, Srisomang P, et al. (2008) Rapid detection of the pandemic methicillin-resistant Staphylococcus aureus clone ST 239, a dominant strain in Asian hospitals. J Clin Microbiol 46: 1520–1522.
- 23. Fowler VG Jr, Miro JM, Hoen B, Cabell CH, Abrutyn E, et al. (2005) Staphylococcus aureus endocarditis: a consequence of medical progress. Jama 293: 3012–3021.
- 24. Wyllie DH, Walker AS, Peto TE, Crook DW (2007) Hospital exposure in a UK population, and its association with bacteraemia. J Hosp Infect 67: 301–307.
- 25. Lodise TP, McKinnon PS, Swiderski L, Rybak MJ (2003) Outcomes analysis of delayed antibiotic treatment for hospital-acquired Staphylococcus aureus bacteremia. Clin Infect Dis 36: 1418–1423.