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Volume 8, Number 2—February 2002


Antibiotic Resistance Patterns of Bacterial Isolates from Blood in San Francisco County, California, 1996-1999

Susan S. Huang*†Comments to Author , Brian J. Labus†‡, Michael C. Samuel†‡, Dairian T. Wan†, and Arthur L. Reingold†‡
Author affiliations: *University of California San Francisco, San Francisco, California, USA; †California Department of Health Services, San Francisco, California, USA; ‡University of California Berkeley, Berkeley, California, USA;

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EID Huang SS, Labus BJ, Samuel MC, Wan DT, Reingold AL. Antibiotic Resistance Patterns of Bacterial Isolates from Blood in San Francisco County, California, 1996-1999. Emerg Infect Dis. 2002;8(2):195-201.
AMA Huang SS, Labus BJ, Samuel MC, et al. Antibiotic Resistance Patterns of Bacterial Isolates from Blood in San Francisco County, California, 1996-1999. Emerging Infectious Diseases. 2002;8(2):195-201. doi:10.3201/eid0802.010102.
APA Huang, S. S., Labus, B. J., Samuel, M. C., Wan, D. T., & Reingold, A. L. (2002). Antibiotic Resistance Patterns of Bacterial Isolates from Blood in San Francisco County, California, 1996-1999. Emerging Infectious Diseases, 8(2), 195-201.


Countywide antibiotic resistance patterns may provide additional information from that obtained from national sampling or individual hospitals. We reviewed susceptibility patterns of selected bacterial strains isolated from blood in San Francisco County from January 1996 to March 1999. We found substantial hospital-to-hospital variability in proportional resistance to antibiotics in multiple organisms. This variability was not correlated with hospital indices such as number of intensive care unit or total beds, annual admissions, or average length of stay. We also found a significant increase in methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus, and proportional resistance to multiple antipseudomonal antibiotics. We describe the utility, difficulties, and limitations of countywide surveillance.

Many national sampling and hospital surveillance systems exist to monitor antimicrobial resistance patterns in bacteria (14). Previously, organisms resistant to multiple antibiotics were largely confined to hospital settings and were typically described through studies involving single hospitals or intensive care units (ICUs). These single-hospital studies often reported substantially different resistance patterns from one another (57). National surveillance systems provided key data on large-scale resistance trends, but, similarly, continued to show marked variability in proportional resistance among participating hospitals (13,8,9).

We hypothesized that countywide surveillance data would not only provide information on changes in bacterial antimicrobial resistance but also potentially identify hospital demographic data to account for interhospital variability in resistance patterns. Additionally, countywide surveillance should provide greater insight into the relationship between single hospitals and their neighboring communities as data accumulate to support the spread of resistant organisms from the hospital into the community and vice versa. Morgan et al. (8) reported data from Wales that 66% of patients colonized or infected with methicillin-resistant Staphylococcus aureus (MRSA) are being discharged to their homes, leading to risks of intrafamilial transmission (1012). Goetz et al. (6) showed that health-care workers similarly bring resistant organisms home. Additionally, outpatient dialysis units, rehabilitation centers, and outpatient intravascular devices have been shown to be reservoirs of colonization with MRSA and vancomycin-resistant Enterococcus (VRE) in many patients in the community (1316).

MRSA and VRE colonization and infection in the absence of hospital risk factors are also being increasingly recognized in the community (1722). Day-care centers and isolated communities may play a notable role (20,23). Patients colonized from these community reservoirs can subsequently cause hospital outbreaks after admission (24).

As hospital and community colonization and infection begin to exert pressure on one another, single-hospital surveillance data may become less useful in isolation. Countywide surveillance may provide more insight into the sources and extent of outbreaks and prompt focused investigations into the spread and containment of resistant organisms.

We conducted an observational study to evaluate the changes in antibiotic resistance in selected bacteria isolated from blood in San Francisco County, California, to determine if these changes were associated with specific hospital demographics and to define the utility, limitations, and potential areas of improvement in a county-based surveillance system.


All bacterial strains recovered from blood were identified from available microbiology department records of all 13 hospitals in San Francisco County from January 1, 1996, to March 31, 1999. For three hospitals (4,5,9), data from 1996 had been purged and were no longer available. For each isolate, data were collected on organism type and susceptibility pattern. Information was also obtained on the ward, age, and gender of the patient. Only the first positive blood culture of a given species was included for a single patient throughout the study period, regardless of susceptibility pattern. Cultures positive for S. epidermidis were considered representative of clinical bacteremia if at least two isolates with identical susceptibility patterns were obtained from a minimum of two separate sets of blood cultures. Each such set was considered a single bacteremic event. All other cultures positive for S. epidermidis were excluded, as were other common skin contaminants (e.g., Propionibacterium acnes, Peptostreptococcus, Corynebacterium).

All but one hospital used automated systems (VITEK [bioMerieux Vitek, Hazelwood, MO] or Microscan [Baxter Laboratories, West Sacramento, CA]) for the susceptibility testing of gram-negative bacteria. All hospitals used Kirby-Bauer disk-diffusion techniques for the evaluation of susceptibility profiles for Streptococcus pneumoniae and other streptococcal species according to National Committee for Clinical Laboratory Standards (NCCLS) guidelines. Kirby-Bauer results were supplemented by e-testing. One hospital (12) performed all susceptibility testing using Kirby-Bauer disk-diffusion techniques. All microbiology laboratories used MIC breakpoints established by the NCCLS. The annual number of blood culture sets processed by each microbiology laboratory was also obtained.

Data from five hospitals were obtained as text files or Microsoft Excel (Redmond, WA) files and subsequently imported into a Microsoft Access (Redmond, WA) database. Data from four hospitals were obtained in printed form, scanned as image files, converted into text files using TextBridge Pro 98 (ScanSoft Inc., Peabody, MA), and imported into the database. All scanned entries were verified for accuracy. Data from the remaining four hospitals were obtained from stored index cards, entered manually into the database, and verified for accurate entry.

We also obtained bed size and census data for all 13 hospitals in San Francisco County. Total hospital admissions were tabulated from quarterly administrative records from 1996 through 1998. For each hospital, average length of hospital stay was obtained from publicly available resources (25).

Data Analyses

The number of isolates for each species was tabulated for each year and for the entire study period. Only species for which the total number of countywide isolates exceeded 100 during the study period were further evaluated. For each organism, proportional annual resistance to an antibiotic was calculated as the yearly number of organisms with intermediate or full resistance divided by the total number of organisms isolated in San Francisco County that year. Because of laboratory variability in susceptibility testing, not all isolates are included in descriptions of proportional resistance.

Means were calculated from the annual countywide percentages in each of the 4 years studied. Percent annual resistance was determined for any antibiotic tested in ≥50 isolates and analyzed for increasing or decreasing annual trend from 1996 through 1999. Data for 1999 were based on the first quarter culture results. Strains with full or intermediate resistance to an antibiotic were counted as resistant in all statistical analyses.

Organisms demonstrating increasing or decreasing annual resistance to a given antibiotic (p<0.05) were further described by calculating mean proportional resistance over the study period according to categories of hospital, ward, patient age (in 10-year intervals), and patient gender. Spearman rank tests were used to determine any correlation between hospital indices (beds, annual admissions, average length of stay) and proportional antibiotic resistance. P values were not adjusted for the effect of multiple comparisons. P values remained unchanged with respect to alpha level (0.05) after removal of the three hospitals missing data from 1996.


A total of 11,573 bacterial strains were recovered from blood cultures by the 13 hospitals. After excluding duplicate cultures, we had 8,072 remaining clinical isolates.

Information on hospital size, census, and blood culture volume is provided in Table 1. Despite being distinct and nonadjoining, hospitals 4 and 5 are reported together because of unified microbiology and administrative centers. Hospital 13 is a skilled nursing facility. On average, 74,600 sets of blood cultures were processed each year in San Francisco County; 9.9% of these were positive for bacterial species.

Figure 1

Thumbnail of All bacterial species that were isolated from blood in &gt;100 persons, January 1996 through March 1999, all hospitals in San Francisco County, California. Each bar is divided by yearly totals. Total number of isolates obtained during the study period is given above each bar. MRSA = methicillin-resistant Staphylococcus aureus; VRE = vancomycin-resistant Enterococcus.

Figure 1. All bacterial species that were isolated from blood in >100 persons, January 1996 through March 1999, all hospitals in San Francisco County, California. Each bar is divided by yearly totals. Total...

Of the 8,072 isolates, Staphylococcus aureus (1,858), Escherichia coli (1,634), and S. pneumoniae (725) were the most common organisms. The numbers of S. aureus, Enterococcus faecalis, Bacteroides fragilis, E. coli, and Serratia marcescens increased annually during the 4-year period. Fourteen species had >100 isolates and were considered for further analysis (Figure 1). These 14 organisms accounted for 85% to 86% of all yearly totals.

Gram-Positive Organisms

Figure 2

Thumbnail of Increase in percentage of Staphylococcus aureus isolates resistant to methicillin and increase in percent of Enterococcus faecium resistant to vancomycin on a yearly basis from 1996 through the first quarter of 1999. Number of isolates per year, regardless of susceptibility, appears above each bar. Tests of trend showed significant increases in percent resistance for both organisms.

Figure 2. Increase in percentage of Staphylococcus aureus isolates resistant to methicillin and increase in percent of Enterococcus faecium resistant to vancomycin on a yearly basis from 1996 through the first quarter of...

The proportion of MRSA and E. faecium resistant to vancomycin (VRE faecium) increased annually (Figure 2). Countywide, the proportion of MRSA isolates rose from 18.1% (1996) to 26.1% (1999) (p<0.001). In total, MRSA constituted 22.4% of all S. aureus isolates, including 19.6% of emergency department isolates and 15.9% of isolates in the outpatient setting (Table 2). Methicillin resistance in S. aureus isolates was <15% in patients <20 years of age and >20% in all other age groups, with the exception of 30- to 39-year-olds (17.6%) (Table 3). Proportional resistance did not vary by patient gender.

During the study period, 124 VRE isolates and 157 vancomycin-sensitive Enterococcus isolates were unspeciated. Among the speciated E. faecium isolates, the percentage resistant to vancomycin rose from 0% to 66.7% in the 4-year period (p<0.001). VRE faecium was most frequently isolated from inpatient adult wards, but six isolates were cultured from emergency department and outpatient settings. Over 66% of E. faecium isolates from skilled nursing facilities were resistant to vancomycin (Table 2). VRE isolates exceeded 40% in all age groups with the exception of ≤10-year-olds (22.2%) (Table 3). Of note, VRE faecium isolates showed increasing annual resistance to doxycycline (from 30% to 68%; p = 0.02).

Figure 3

Thumbnail of Plot of the number of methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) isolates by hospital day of admission. An early peak is noted, corresponding to patients entering the hospital with MRSA or VRE bacteremia. Subsequent cases likely represent nosocomial acquisition.

Figure 3. Plot of the number of methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) isolates by hospital day of admission. An early peak is noted, corresponding to patients entering the hospital with...

Even after the skilled nursing facility (hospital 13) was excluded, the percentage of MRSA and VRE faecium isolates varied substantially among individual hospitals (MRSA 12.5% to 37.5%, VRE faecium 12.5% to 80.0%). There was no correlation between proportional resistance and number of ICU or total hospital beds, number of annual admissions, or average length of ICU or total hospital stay. However, for both organisms, there was increasing proportional resistance among adult wards in the following order: outpatient wards, emergency department, medical and surgical floors, medical and surgical ICUs, and skilled nursing facility wards. Notably, a substantial number of VRE and MRSA isolates were cultured within the first 24 to 48 hours of hospital admission (Figure 3).

Of the 678 isolates of S. pneumoniae, 13.6% were resistant to penicillin. Proportional resistance increased from 10.8% (21 isolates) in 1996 to 14.6% (27 isolates) in 1998, but this increase was not statistically significant. Proportional resistance was highest at the extremes of age (16.4% in patients >70 years of age and 19.3% in patients <10 years of age (Table 3).

Gram-Negative Organisms

Countywide, E. coli (1,634 isolates), Klebsiella pneumoniae (428 isolates), and Pseudomonas aeruginosa (260 isolates) were the most frequently isolated gram-negative bacilli. This was true in all inpatient and outpatient wards with the exception of skilled nursing facilities, where Proteus mirabilis was the most common gram-negative isolate after E. coli. Proportional resistance by ward for selective gram-negative organisms is shown in Table 4.

Among E. coli isolates, resistance to trimethoprim-sulfamethoxazole averaged 28% and resistance to ciprofloxacin averaged 3%. There was no resistance to fluoroquinolones among E. coli isolates from pediatric wards. Increasing annual resistance to ticarcillin-clavulanate was seen in both E. coli (6% to 16%, p = 0.03) and K. pneumoniae (0% to 18%, p = 0.007) isolates.

Figure 4

Thumbnail of Yearly percent resistance to ciprofloxacin, ceftazidime, imipenem, and piperacillin in Pseudomonas aeruginosa isolates from blood. Increasing proportional resistance occurred in three of the four antibiotics commonly used to treat this organism. Annual number of isolates tested to each antibiotic is given at the top of each graph.

Figure 4. Yearly percent resistance to ciprofloxacin, ceftazidime, imipenem, and piperacillin in Pseudomonas aeruginosa isolates from blood. Increasing proportional resistance occurred in three of the four antibiotics commonly used to treat this organism....

P. aeruginosa isolates showed increasing annual countywide resistance to ciprofloxacin (7% to 21%, p = 0.005), ceftazidime (6% to 16%, p = 0.02), and imipenem (2% to 18%, p = 0.004) (Figure 4). Resistance to each of these three antibiotics exceeded 10% in adult ICU and adult medical and surgical wards. In fact, in these settings, ciprofloxacin resistance approached 20% countywide. No isolates resistant to ciprofloxacin were cultured from pediatric wards (Table 4). Resistance to gentamicin (15%) and piperacillin-tazobactam (12%) also increased but was not statistically significant.

There were 182 E. cloacae and 116 S. marcescens isolates from January 1996 through March 1999. Ciprofloxacin resistance averaged 4% among E. cloacae isolates and 6% among S. marcescens isolates. S. marcescens isolates also showed increasing annual proportional resistance to gentamicin (0% to 14%, p = 0.02) and piperacillin (4% to 29%, p = 0.01).

Resistance to ceftazidime, which can be predictive of inducible and extended-spectrum-beta-lactamases, was found in the following overall mean proportions in the study period: E. coli (1%), P. mirabilis (1%), K. pneumoniae (1%), S. marcescens (8%), P. aeruginosa (13%), and E. cloacae (39%). Only P. aeruginosa isolates demonstrated an increasing linear annual trend (p = 0.02).


San Francisco County has a population of approximately 735,000 and covers 46.7 square miles (26). It comprises multiple racial and ethnic groups (black 10.9%, Hispanic 13.9%, Asian 29.1%, and Native American 0.5%) and is served by 13 hospitals. We have shown that county surveillance of bacterial resistance is a useful addition to local hospital surveillance, particularly as antibiotic resistant bacteria increasingly spread from hospital to hospital and into the community at large.

Across the county, annual proportions of MRSA and VRE isolates significantly increased over the 4-year period. Pseudomonal strains resistant to fluoroquinolones, ceftazidime, or imipenem also increased annually. These data allow us to distinguish countywide outbreaks and trends from single-hospital changes in resistance patterns, and enable infection control efforts to expand or narrow to the appropriate scale. With awareness programs, county surveillance can broaden physicians’ knowledge of their hospital’s effects on the community, as well as the effects of neighboring hospitals on resistance patterns in their particular hospital.

Additionally, county surveillance that includes subcategorization of isolates by ward is invaluable in identifying patients at high risk and locations for transmission of resistant bacteria. Not surprisingly, we report our highest proportion of MRSA and VRE isolates from ICU and nursing home units. Nevertheless, ward variability across hospitals was substantial. Large interhospital differences can lead to further study of ward practices that foster or abate transmission. Awareness can prompt hospital infection control personnel to ensure well-described preventive measures such as swabbing and isolation precautions for VRE and MRSA in ICU settings (2730) and nasopharyngeal swabbing and eradication of MRSA in hemodialysis wards (1,31). We also identify several MRSA and VRE isolates from outpatient and emergency department settings. Whether or not these represent true community-acquired strains or strains from patients recently released from hospital settings, they suggest that highly resistant bacterial outpatient infections and infectivity are increasing, a result consistent with recent studies (19,21,22).

We also evaluated whether the wide variability in the proportions of resistant bacteria among San Francisco hospitals was linked to hospital indices. In contrast to previous nationwide sampling studies, none of this variability was correlated with the number of hospital ICU beds (3), total beds (1,2,31), annual admissions (32), or annual mean length of stay. This may be due to our small number of hospitals, leading to limited power to detect such correlations. Alternatively, local community and hospital factors (e.g., increasing care of moderately ill patients at home [8], increasing home intravenous antibiotics [15], active transfer of patients between hospitals [33,34], and community-acquired resistant organisms) may now be diminishing the effect of hospital size, census and length of stay on proportional resistance.

There are many additional advantages to a countywide surveillance system for antimicrobial resistance. First, it can help reassess therapy. The 28% trimethoprim-sulfamethoxazole resistance in E. coli raises questions about the optimal empiric treatment of urinary tract infections in patients at high risk for bacteremia or urosepsis. Likewise, distinguishing resistance in the outpatient versus inpatient setting can guide empiric therapy in the appropriate setting.

Second, in studying a larger populace, we can obtain sufficient numbers to study uncommon organisms. Similarly, countywide surveillance provides a means to identify and confirm novel resistant pathogens. In our study, one MRSA isolate with intermediate resistance to vancomycin and three vancomycin-resistant S. epidermidis isolates were noted in microbiology laboratory reports. As with the organisms recently reported in the United States (3537), these were reported from nontertiary hospitals. Nevertheless, our reports are unconfirmed and likely represent laboratory error. However, if surveillance could be expedited to real-time use, such reports could be investigated and confirmed rather than dismissed. At its worst, this suggests that highly resistant organisms may be escaping deserved attention and reaction.

Third, countywide surveillance engenders further hypotheses and research regarding interhospital and community transmission of resistant organisms. For example, our finding that 20% of emergency department S. aureus isolates are methicillin-resistant provides a flag to further study which county areas have the highest percentages of resistant S. aureus and which risk factors are involved (e.g., recent hospital admission [21,22], associated hemodialysis centers [8,38] or nursing homes [21,22], or intravenous drug use [39]). The finding that P. mirabilis bacteremia is more common in nursing home wards raises questions about preventing urinary tract infections in that setting. The relative lack of fluoroquinolone resistance in pediatric gram-negative isolates is likely due to the avoidance of fluoroquinolones in children because of potential detrimental cartilage effects. The study of fluoroquinolone-resistant organisms during the transition years from pediatric to adult medicine may provide insight into the quantity and duration of antibiotic needed to produce selection pressure, as well as the speed and durability of emerging resistance.

Our surveillance method had several limitations. Chart review would have been an invaluable addition in distinguishing between community-acquired and recent hospital or nursing home acquisition of resistant organisms. Second, we did not collect or confirm isolates; thus, although our results reflect microbiologic data actually presented to ordering physicians, they are subject to laboratory differences in speciation and susceptibility determination. Notably, not all organisms were fully speciated or tested against the antibiotics of interest. Fortunately, this occurred in a small proportion of bacteria. Third, we do not provide information on antibiotic use, which is known to be a major determinant of bacterial antibiotic resistance. Fourth, countywide trends can be driven by trends seen in the largest hospitals, particularly since smaller hospitals often lack sufficient numbers of isolates to make statistical analyses meaningful. This was notable for our data on proportional increases in VRE, which was largely driven by three hospitals. On the contrary, MRSA trends were not limited to a few hospitals, nor were they limited to the largest hospitals in the county. No hospital showed a significant decreasing trend in the proportion of MRSA isolates.

Areas for improvement include methods to computerize microbiologic data storage in a universal format. This would expedite surveillance and allow real-time collection and identification of unusually resistant organisms, as well as provide sentinel data regarding countywide outbreaks. In addition, linking of patient information to microbiologic data would have expedited acquisition of sex, gender, and ward information. Furthermore, despite NCCLS guidelines, a fair amount of variability exists in laboratory practices and susceptibility panels. Further standardization of these practices would help ensure the reliability of merging data among hospitals.

Without a doubt, the greatest utility of countywide surveillance lies in its ability to ask screening questions that prompt a more thorough investigation of specific hospitals, wards, or age groups at particular risk for acquiring or transmitting highly resistant organisms.

We have shown how several such questions were raised by our surveillance of bacteremias in San Francisco County and described its many advantages. We have further defined our limitations and difficulties in performing such surveillance, in the hope that this will be helpful to further similar surveillance efforts.

At the time of this study, Dr. Huang was a categorical resident in Internal Medicine at the University of California San Francisco Medical Center. She has since completed a Master of Public Health at the Harvard School of Public Health and is pursuing a fellowship in infectious diseases at Brigham & Women's Hospital and Massachusetts General Hospital, Boston, Massachusetts. Her current research interests are in the field of bacterial antibiotic resistance.


We thank the following persons for their extensive assistance in our data collection: Lisa Gelling, Gretchen Rothrock, May Ma, Ray Fung, Hiroshi Takahashi, Kathy Alzate, Maureen Bergondy, Lynn Gok, Martha Eason, Tom Newman, Sandra Cruz, Keith Hadley, Margaret Wong, Laura Gutierrez, Diane Ciucci, Stella Jeong, Tom Hicks, Mary York, George Brooks, Andy Brown, Jane Jang, Ken Lee, Michael Fitzgerald, and Alexander Hines.

Financial support for this study was provided by the California Emerging Infections Program, a joint project of the California Department of Health Services, University of California Berkeley School of Public Heath, and the Centers for Disease Control and Prevention.


  1. Panlilio AL, Culver DH, Gaynes RP, Banerjee S, Henderson TS, Tolson JS, Methicillin-resistant Staphylococcus aureus in U.S. hospitals 1975-1991. Infect Control Hosp Epidemiol. 1992;13:5826.PubMed
  2. Centers for Disease Control and Prevention. Nosocomial enterococci resistant to vancomycin—United States, 1989-1993. MMWR Morb Mortal Wkly Rep. 1993;42:5979.PubMed
  3. Itokazu GS, Quinn JP, Bell-Dixon C, Kahan FM, Weinstein RA. Antimicrobial resistance rates among aerobic gram-negative bacilli recovered from patients in intensive-care units: evaluation of a national postmarketing surveillance program. Clin Infect Dis. 1996;23:77984.PubMed
  4. Lugeon C, Blanc DS, Wenger A. Molecular epidemiology of methicillin-resistant Staphylococcus aureus at a low-incidence hospital over a 4-year period. Infect Control Hosp Epidemiol. 1995;16:2607.PubMed
  5. Quale J, Landmann D, Atwood E, Kreiswirth B, Willey BM, Ditore V, Experience with a hospital-wide outbreak of vancomycin-resistant enterococci. Am J Infect Control. 1996;24:3729. DOIPubMed
  6. Goetz A, Posey K, Fleming J, Jacobs S, Boody L, Wagener MM, Methicillin-resistant Staphylococcus aureus in the community: a hospital-based study. Infect Control Hosp Epidemiol. 1999;20:68991. DOIPubMed
  7. Coque TM, Tomakyo JF, Ricke SC, Okhyusen PC, Murray BE. Vancomycin-resistant enterococci from nosocomial, community, and animal sources in the United States. Antimicrob Agents Chemother. 1996;40:26059.PubMed
  8. Morgan M, Evans-Williams D, Salmon R, Hosein I, Looker DN, Howard A. The population impact of MRSA in a country: the national survey of MRSA in Wales, 1997. J Hosp Infect. 2000;44:22739. DOIPubMed
  9. Archibald L, Phillips L, Monnet D, McGowan JE Jr, Tenover F, Gaynes R, Antimicrobial resistance in isolates from inpatients and outpatients in the United States: increasing importance of the intensive care unit. Clin Infect Dis. 1997;24:2215.
  10. Hollis RJ, Barr JL, Doebbeling GN, Pfaller MA, Wenzel RP. Familial carriage of methicillin-resistant Staphylococcus aureus and subsequent infection in a premature neonate. Clin Infect Dis. 1995;21:32832.PubMed
  11. Masterton RG, Coia JE, Notman AW, Kempton-Smith L, Cookson BD. Refractory methicillin-resistant Staphylococcus aureus carriage associated with contamination of the home environment. J Hosp Infect. 1995;29:3189. DOIPubMed
  12. Lindenmayer HM, Schoenfeld S, O’Grady R, Carney JK. Methicillin-resistant Staphylococcus aureus in a high school wrestling team and the surrounding community. Arch Intern Med. 1998;158:8959. DOIPubMed
  13. Bonilla HF, Zervos MA, Lyons MJ, Bradley SF, Hedderwick SA, Ramsey MA, Colonization with vancomycin-resistant Enterococcus faecium: comparison of a long-term care unit with an acute-care hospital. Infect Control Hosp Epidemiol. 1997;18:3339.PubMed
  14. Piraino B. Staphylococcus aureus infections in dialysis patients: focus on prevention. ASAIO J. 2000;46:S137. DOIPubMed
  15. Steinberg JP, Clark CC, Hackman BO. Nosocomial and community acquired Staphylococcus aureus bacteremias from 1980 to 1993: impact of intravascular devices and methicillin resistance. Clin Infect Dis. 1996;23:2559.PubMed
  16. Beltrami EM, Singer DA, Fish L, Manning K, Young S, Banerjee SN, Risk factors for acquisition of vancomycin-resistant enterococci among patients on a renal ward during a community hospital outbreak. Am J Infect Control. 2000;28:2825. DOIPubMed
  17. Wendt C, Krause C, Xander LU, Loffler D, Floss H. Prevalence of colonization with vancomycin-resistant enterococci in various population groups in Berlin, Germany. J Hosp Infect. 1999;42:193200. DOIPubMed
  18. Bonten MJ, Slaughter S, Hayden MK, Nathan C, van Voorhis J, Weinstein RA. External sources of vancomycin-resistant enterococci for intensive care units. Crit Care Med. 1998;26:20014. DOIPubMed
  19. Herold BC, Immergluck LC, Maranan MC, Lauderdale DS, Gaskin RE, Boyle-Vavra S, Community-acquired methicillin-resistant Staphylococcus aureus in children with no identified predisposing risk. JAMA. 1998;279:5938. DOIPubMed
  20. Maguire GP, Arthur AD, Boustead PJ, Dwyer B, Currie BJ. Emerging epidemic of community-acquired methicillin-resistant Staphylococcus aureus infection in the northern territory. Med J Aust. 1996;164:7123.
  21. Cookson BD. Methicillin-resistant Staphylococcus aureus in the community: new battlefronts, or are the battles lost? Infect Control Hosp Epidemiol. 2000;21:398403. DOIPubMed
  22. Martone WJ. Spread of vancomycin-resistant enterococci: why did it happen in the United States? Infect Control Hosp Epidemiol. 1998;19:53945.PubMed
  23. Adcock PM, Pastor P, Medley F, Patterson JE, Murphy TV. Methicillin-resistant Staphylococcus aureus in two child care centers. J Infect Dis. 1998;178:57780.PubMed
  24. O’Brien FG, Pearman JW, Cracey M, Riley TV, Grubb WB. Community strain of methicillin-resistant Staphylococcus aureus involved in a hospital outbreak. J Clin Microbiol. 1999;37:285862.PubMed
  25. Office of Statewide Health Planning and Development. Quarterly individual hospital financial data for California, Sacramento, California, 1996-98, Quarters 1-4, Vol 2: Bay area. Sacramento (CA): The Office; 1999. Available at URL:
  26. U.S. Census Bureau. the official statistics. Estimates of the population of cities with populations of 100,000 and greater. November 1997. Available at URL:
  27. Farr BM. Hospital wards spreading vancomycin-resistant enterococci to intensive care units: returning coals to Newcastle. Crit Care Med. 1998;26:19423. DOIPubMed
  28. Montecalvo MA, Jarvis WR, Uman J, Shay DK, Petrullo C, Rodney K, Infection-control measures reduce transmission of vancomycin-resistant enterococci in an endemic setting. Ann Intern Med. 1999;131:26972.PubMed
  29. Jernigan JA, Titus MG, Groschel DH, Getchell-White S, Farr BM. Effectiveness of contact isolation during a hospital outbreak of methicillin-resistant Staphylococcus aureus. Am J Epidemiol. 1996;143:496504.PubMed
  30. Fridkin SK. Increasing prevalence of antimicrobial resistance in intensive care units. Crit Care Med. 2001;29(Suppl):N648. DOIPubMed
  31. Osono E, Takahashi M, Kurihara S, Ohwada K, Sakurai Y, Onoda N, Effects of “isolating hemodialysis” on prevention of methicillin-resistant Staphylococcus aureus cross-infection in a hemodialysis unit. Clin Nephrol. 2000;54:12833.PubMed
  32. Haley RW, Hightower AW, Khabbaz RF, Thornsberry C, Martone WJ, Allen JR, The emergence of methicillin-resistant Staphylococcus aureus infections in United States hospitals. Ann Intern Med. 1982;97:297308.PubMed
  33. McNeeley DF, Brown AE, Noel GJ, Chung M, de Lencastre H. An investigation of vancomycin-resistant Enterococcus faecium within the pediatric service of a large urban medical center. Pediatr Infect Dis J. 1998;17:1848. DOIPubMed
  34. Chow JW, Kuritza A, Shlaes DM, Green M, Sahm DF, Zervos MJ. Clonal spread of vancomycin-resistant Enterococcus faecium between patients in three hospitals in two states. J Clin Microbiol. 1993;31:160911.PubMed
  35. Del’Alamo L, Cereda RF, Tosin I, Miranda EA, Sader HS. Antimicrobial susceptibility of coagulase-negative staphylococci and characterization of isolates with reduced susceptibility to glycopeptides. Diagn Microbiol Infect Dis. 1999;34:18591. DOIPubMed
  36. Garrett DO, Jochimsen E, Murfitt K, Hill B, McAllister S, Nelson P, The emergence of decreased susceptibility to vancomycin in Staphylococcus epidermidis. Infect Control Hosp Epidemiol. 1999;20:1635. DOIPubMed
  37. Smith TL, Pearson ML, Wilcox KR, Cruz C, Lancaster MV, Robinson-Dunn B, Emergence of vancomycin resistance in Staphylococcus aureus. Glycopeptide-Intermediate Staphylococcus aureus Working Group. N Engl J Med. 1999;340:493501. DOIPubMed
  38. Zimakoff J, Bangsgaard Pederseon F, Bergen L, Baago-Nielsen J, Daldorph B, Espersen F, Staphylococcus aureus carriage and infections among patients in four haemo- and peritoneal-dialysis centers in Denmark. J Hosp Infect. 1996;33:289300. DOIPubMed
  39. Saravolatz LD, Markowitz N, Arking L, Pohlod MS, Fisher E, Arbor A. Methicillin-resistant Staphylococcus aureus. Ann Intern Med. 1982;96:116.PubMed



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DOI: 10.3201/eid0802.010102

Table of Contents – Volume 8, Number 2—February 2002


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