0
Instructional Course Lecture   |    
Antimicrobial Resistance: Guidelines for the Practicing Orthopaedic Surgeon
Douglas R. Osmon, MD, MPH
View Disclosures and Other Information
An Instructional Course Lecture, American Academy of Orthopaedic Surgeons

Douglas R. Osmon, MD, MPH
Division of Infectious Diseases, Department of Internal Medicine, Mayo Clinic and Mayo Foundation, 200 First Street S.W., Rochester, MN 55905.

The author did not receive grants or outside funding in support of his research or preparation of this manuscript. He did not receive payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, educational institution, or other charitable or nonprofit organization with which the author is affiliated or associated.

Printed with permission of the American Academy of Orthopaedic Surgeons. This article, as well as other lectures presented at the Academy’s Annual Meeting, will be available in March 2002 in Instructional Course Lectures, Volume 51. The complete volume can be ordered online at www.aaos.org, or by calling 800-626-6726 (8 a.m.-5 p.m., Central time).

The Journal of Bone & Joint Surgery.  2001; 83:1891-1901 
5 Recommendations (Recommend) | 3 Comments | Saved by 3 Users Save Case
Antimicrobial resistance among pathogens, such as Staphylococcus aureus, coagulase-negative staphylococci, enterococci, and aerobic gram-negative bacilli, is pervasive in the community and hospital setting. Every practicing orthopaedist faces on a daily basis the increasing problem of antimicrobial resistance in the effort to prevent or treat nosocomial infections. Recognizing the scope of the problem; understanding the mechanisms of antimicrobial resistance as well as the epidemiology, prevention, and treatment of infections due to resistant organisms; and knowing the proposed solutions to these problems will optimize the orthopaedic surgeon’s ability to manage multidrug-resistant nosocomial pathogens.
 
Anchor for JumpAnchor for JumpTABLE I:  Common Nosocomial Antibiotic-Resistant Microorganisms Encountered by the Orthopaedic Surgeon
*Methicillin-resistant Staphylococcus aureus. †Infrequent pathogen in such infections. ‡Some non-Candida albicans species, such as Candida krusei, are also resistant.
MicroorganismInfections Commonly Involving Microorganism as PathogenAntibiotics Frequently Resisted by Microorganism
Staphylococcus aureusSurgical wound infectionPenicillin
OsteomyelitisMethicillin, oxacillin
Infection around prosthetic joint Vancomycin (rare)
Infectious arthritisAminoglycosides*
Osteomyelitis, footFluoroquinolones*
Traumatic open fractureCotrimoxazole*
Coagulase-negative StaphylococcusSurgical wound infectionPenicillin
Osteomyelitis associated with foreign body Methicillin, oxacillin
Infection around prosthetic joint Vancomycin (rare)
Septic arthritis following arthroscopyAminoglycosides*
Fluoroquinolones*
Cotrimoxazole*
Clindamycin*
Enterococcus speciesOsteomyelitis, footPenicillin (Enterococcus faecium)
Vancomycin (Enterococcus faecium)
Gentamicin
Pseudomonas aeruginosaSurgical wound infectionPiperacillin
Traumatic osteomyelitisCeftazidime
Chronic osteomyelitis, footImipenem
Aminoglycosides
Fluoroquinolones
Enterobacter speciesSurgical wound infectionCeftazidime
OsteomyelitisCefotaxime
Chronic osteomyelitis, foot
Stenotrophomonas maltophiliaTraumatic osteomyelitisImipenem
Ceftazidime
Fluoroquinolones
Aminoglycosides
Bacteroides speciesOsteomyelitis, foot Penicillin
Clindamycin
Candida speciesMusculoskeletal system infections†Fluconazole‡
 
Anchor for JumpAnchor for JumpTABLE II:  Comparison of Antimicrobial Resistance of Selected Pathogens in Bloodstream Isolates from Nosocomial and Community-Acquired Infections*
*Reproduced, with modification, from: Pfaller MA, Jones RN, Doern GV, Kugler K. Bacterial pathogens isolated from patients with bloodstream infection: frequencies of occurrence and antimicrobial susceptibility patterns from the SENTRY antimicrobial surveillance program (United States and Canada, 1997). Antimicrob Agents Chemother. 1998;42:1762-70. Reprinted with permission.
OrganismAntimicrobial AgentPercent Resistant
Nosocomial InfectionsCommunity-Acquired Infections
Staphylococcus aureusOxacillin31.025.1
Coagulase-negative StaphylococcusOxacillin68.041.5
Enterococcus speciesVancomycin20.0?7.1
Enterobacter cloacaeCeftazidime38.519.2
Pseudomonas aeruginosaCeftazidime?7.8?1.9
Imipenem13.7?5.8
Escherichia coliCeftazidime?7.3?0.6
Ciprofloxacin?1.7?1.1
 
Anchor for JumpAnchor for JumpTABLE III:  Mechanisms of Resistance and Their Genetic Basis for Common Nosocomial Antibiotic-Resistant Microorganisms Encountered by Orthopaedic Surgeons*
*Reproduced, with modification, from: Virk A, Steckelberg JM. Clinical aspects of antimicrobial resistance. Mayo Clinic Proc. 2000;75:200-14. Reprinted with permission.
Mechanism of ResistanceAntibioticGenetic BasisExamples of Microorganism and Antibiotic Combinations
Enzymatic inhibitionb-lactamsPlasmid-mediated and chromosomalStaphylococci species-penicillin, Enterobacter species-ceftazidime, Stenotrophomonas maltophilia-imipenem
AminoglycosidesGram-negative bacilli or highly gentamicin-resistant Enterococci
Permeability-uptakeb-lactamsChromosomalPseudomonas aeruginosa-b-lactams
AminoglycosidesStaphylococcus aureus, gram-negative bacilli, enterococci-aminoglycosides
Porin channelsb-lactamsChromosomalPseudomonas aeruginosa, Stenotrophomonas maltophilia
Carbapenems
Drug efflux mechanismsb-lactamsPlasmid-mediated or chromosomalPseudomonas aeruginosa,Staphylococcus aureus
Fluoroquinolones
Tetracycline
Target-site alteration
(Altered penicillin-binding protein)b-lactamsPlasmid-mediatedStaphylococcus aureus-methicillin
(Altered oligopeptide)GlycopeptidePlasmid-mediated or constitutiveEnterococci resistant to vancomycin
Competitive inhibition by overproduction of p-aminobenzoic acid or altered dihydropteroate synthaseSulfonamidesPlasmid-mediatedStaphylococcus aureus, Escherichia coli
DNA gyrase mutationFluoroquinolonesChromosomal or plasmid (Klebsiella pneumoniae)-mediatedPseudomonas aeruginosa, Staphylococcus aureus
 
Anchor for JumpAnchor for JumpTABLE IV:  Selected Recommendations by the Centers for Disease Control for the Prudent Use of Vancomycin in the Practice of an Orthopaedic Surgeon*
*Adapted from the Recommendations of the Hospital Infection Control Practices Advisory Committee of the Centers for Disease Control9.
Situations in which the use of vancomycin is appropriate or acceptable
Treatment of serious infection caused by b-lactam-resistant gram-positive organism
Treatment of infection caused by gram-positive microorganisms in patients who have serious allergies to b-lactam antimicrobials
When antibiotic-associated colitis fails to respond to metronidazole therapy or is severe and potentially life-threatening
Prophylaxis as recommended by the American Heart Association for endocarditis following certain procedures in patients at high risk for endocarditis
Prophylaxis for major surgical procedures involving implantation of prosthetic materials or devices at institutions that have a high rate of infections caused by methicillin-resistant Staphylococcus aureus or methicillin-resistant coagulase-negative staphylococci
Situations in which the use of vancomycin should be discouraged
Routine surgical prophylaxis other than that in a patient who has a life-threatening allergy to b-lactam antibiotics
Treatment in response to positive findings for coagulase-negative staphylococcus on a single blood culture if other blood cultures performed during the same time-frame have negative findings
Continued empiric use for presumed infection in patients who have negative findings for b-lactam-resistant gram-positive organisms on culture
Systemic or local prophylaxis for infection or colonization of indwelling central or peripheral intravenous catheters
Eradication of methicillin-resistant Staphylococcus aureus colonization
Primary treatment of antibiotic-associated colitis
Treatment for infection caused by b-lactam-sensitive organisms in patients who have renal failure (when the decision is based on dosing convenience)
Topical application or irrigation
 
Anchor for JumpAnchor for JumpTABLE V:  Percent Resistance of Bloodstream Isolates Reported by Pfaller et al.81 in 1998
Antimicrobial AgentPercent Resistant
Staphylococcus aureus Coagulase-Negative Staphylococci
Penicillin89.886.6
Oxacillin26.256.9
Vancomycin?0.0?0.0
Gentamicin13.740.0
Ciprofloxacin28.242.5
Clindamycin24.042.9
Cotrimoxazole10.844.5
In 1990, the National Foundation for Infectious Diseases stated that the estimated cost of nosocomial infections due to antimicrobial-resistant pathogens in the United States was as high as $4 billion annually and that antimicrobial resistance and emerging infections were the most important problems in the prevention and control of infectious diseases1,2. In 1995, in New York City alone, treatment of methicillin-resistant Staphylococcus aureus infections cost $500 million and the infections were responsible for 1409 deaths1. In 1998, Burke stated in an editorial in the Journal of the American Medical Association: "The need for responsible antibiotic use stewardship to quell microbial resistance should have no disputants. Indeed, there have been so many clarion calls for action to halt the increasing resistance to antimicrobials that further emphasis seems redundant."3 Despite numerous attempts by individuals, groups, and national and international organizations to notify the medical community and the public of the seriousness of the problem, antimicrobial resistance continues to increase1,4-19.
Since the advent of sulfonamides and penicillin in the 1930s and 1940s, specific antimicrobial resistance has been an issue. Penicillin-resistant staphylococci developed in the 1940s and 1950s. Methicillin resistance developed in the 1960s, and aminoglycoside resistance among Pseudomonas aeruginosa isolates was first seen in the late 1960s and 1970s. In the last decade, multidrug resistance has become frequent among nosocomial pathogens (that is, Staphylococcus aureus, coagulase-negative Staphylococcus, and Enterococcus and Enterobacter species) (Table I). In addition, antimicrobial resistance (methicillin resistance among staphylococci, vancomycin resistance among enterococci, and third-generation-cephalosporin and fluoroquinolone resistance among Pseudomonas aeruginosa, Enterobacter cloacae, and Escherichia coli) has become common in community-acquired isolates (Table II).
Antimicrobial resistance can be intrinsic (naturally occurring in a specific organism) or acquired through genetic mutation. Microorganisms have multiple mechanisms, each with its own genetic basis, by which they express antimicrobial resistance19,20 (Table III). Although the production of enzymes that inhibit an antimicrobial is the most common mechanism of antibiotic resistance, other mechanisms include altered membrane permeability or porin channels (proteins within the outer membrane of bacteria that are arranged to allow the passage of antimicrobials), target-protein alteration on the cell wall, and active efflux of the antibiotic from inside to outside the cell. An understanding of common antimicrobial resistance mechanisms can help to guide the orthopaedic surgeon with regard to the expected spectrum of activity of an antimicrobial. For example, ampicillin-sulbactam, a b-lactam-b-lactamase inhibitor combination, would be expected to be active against penicillin-resistant Staphylococcus aureus because the mechanism of penicillin resistance among Staphylococcus aureus is penicillinase production. However, ampicillin-sulbactam would not be expected to be active against penicillin-resistant enterococci, whose typical mechanism of resistance to penicillin is altered penicillin-binding proteins.
Antimicrobial resistance is increasing for a variety of reasons12,13,19. These include suboptimal use of antimicrobials for prophylaxis and treatment of infection, prolonged hospitalization, increased number and duration of intensive-care-unit stays, multiple comorbidities in hospitalized patients, increased use of invasive devices and catheters, ineffective infection-control practices, noncompliance with infection-control practices, transfer of colonized patients from hospital to hospital, grouping of colonized patients in long-term-care facilities, antibiotic use in agriculture, and increasing national and international travel. In general, the level of antibiotic resistance is dependent on the proportion of resistant organisms introduced into the hospital from the community, the proportion that becomes resistant spontaneously or as a result of antibiotic use, and the proportion that is spread from person to person5. All of these factors must be addressed in order to control the spread of antimicrobial-resistant organisms within the hospital.
Community-acquired antimicrobial resistance is increasing in large part because of the widespread suboptimal use of antibiotics in the outpatient setting and the use of antibiotics in animal husbandry and agriculture1,5,10,13,19,21-23. Additional factors include an increase in global travel that permits widespread transmission of resistant organisms by infected and colonized individuals; grouping of colonized persons in day-care facilities and long-term-care facilities; and an increase in the prevalence of chronic diseases in society, making individuals more susceptible to colonization or infection24-30.
Approximately 50% of the prescriptions given to adults and children for the treatment of an upper respiratory tract infection, a common indication for outpatient antibiotic therapy, are estimated to be unnecessary31,32. Numerous studies of animals and humans have shown an association between antibiotic use and the emergence of antibiotic resistance10,21-23. In addition, the use of certain types of antibiotics may increase the burden of antibiotic-resistant organisms in patients who are already colonized with these organisms33. It is estimated that 160 million prescriptions are written for antibiotics each year in the United States. This represents 22.7 million kilograms (25,022 tons), 50% of which is used in humans and 50%, in animals5. Antimicrobial use in animals and agriculture is frequent and includes agents such as virginiamycin (similar to the recently released streptogramin combination, quinupristin/dalfopristin) and avoparcin (a glycopeptide that is used on animal farms in Europe and as a result may be linked to the emergence of vancomycin-resistant enterococci)19,34. Many experts and groups have recently reviewed the principles of proper antimicrobial use in humans and have examined means to decrease the use of antimicrobials in agriculture and animal husbandry1,5,9-13,19.
Once hospitalized patients have been colonized or infected with antibiotic-resistant microorganisms, the spread of such organisms is promoted by the administration of broad-spectrum antimicrobials (often in already ill patients in the intensive care unit), by the use of ineffective infection-control measures (most often due to noncompliance by health-care workers), and by the increasing use of invasive devices and procedures such as mechanical ventilators and central venous catheters. The keys to controlling the spread of antimicrobial resistance in the hospital are prompt, effective treatment of an established infection, including optimal empiric and directed antimicrobial therapy as well as surgical management, and adherence to common, inexpensive infection-control measures, such as hand-washing between visits with patients and compliance with isolation procedures. In addition, an active program of infection control and surveillance as well as multiple strategies to promote antimicrobial stewardship in the hospital, based on the hospital’s culture and infrastructure, are also important means with which to control the spread of nosocomial antimicrobial-resistant microorganisms15,35.

Vancomycin-Resistant Enterococci

Enterococci were classified as group-D streptococci until the mid-1980s when nucleic acid studies showed that they were not genetically related to streptococci36. Enterococci are gram-positive aerobic cocci that are facultatively anaerobic and can appear alone or in pairs and chains on gram stain37. They are easily identified by the clinical microbiology laboratory. Currently, enterococci have their own genus, Enterococcus, which contains twelve species. Two of them, Enterococcus faecalis (80% to 90% of Enterococcus infections) and Enterococcus faecium (5% to 10% of Enterococcus infections), are the most common species that cause infection in humans. Enterococcus faecium is most often associated with vancomycin resistance37.
Enterococci are normal flora of the human gastrointestinal tract, but because they can survive in many environments they can also be found in soil, food, and water37. It is the ability of enterococci to survive for extended periods of time in harsh environments that allows their easy dissemination in the hospital when strict adherence to infection-control measures such as hand-washing are not followed by health-care providers.
Enterococci are not as virulent as Staphylococcus aureus or group-A streptococci. Their virulence lies in their intrinsic resistance to the common antimicrobials (for example, cephalosporins) used in hospitals today. Hospitalized patients may become colonized with enterococci after exposure to these antimicrobials38. Although enterococci cause a variety of both community-acquired and nosocomial infections (for example, bacteremia, urinary tract infection, infective endocarditis, and intra-abdominal infection), osteomyelitis, septic arthritis, and infection around a prosthetic joint are not commonly due to enterococci39-46. Orthopaedists usually encounter these organisms in association with soft-tissue or foot infections in patients with diabetes mellitus, peripheral neuropathy, or vascular insufficiency41 (Table I). In this setting, enterococci are often part of a polymicrobial infection.
Enterococci are intrinsically resistant to a number of antimicrobials, including cephalosporins, clindamycin, antistaphylococcal penicillins, tetracyclines, macrolides, and cotrimoxazole36-38. Most enterococci have low-level resistance to penicillins. As such, penicillin and vancomycin are bacteriostatic when used as monotherapy in susceptible isolates. Aminoglycosides, such as gentamicin or streptomycin in combination with penicillin or vancomycin, are useful because of their in vitro synergism and are bactericidal for most susceptible strains. Thus, for patients who require bactericidal therapy to treat an enterococcal infection (for example, enterococcal infective endocarditis), the treatment of choice historically has been penicillin or vancomycin in combination with gentamicin or streptomycin37. Penicillin or vancomycin alone historically has been standard therapy for other types of enterococcal infections. In the last fifteen years, enterococci (usually Enterococcus faecium) have acquired high-level resistance to penicillin and aminoglycosides as well as to vancomycin. Typically, vancomycin-resistant enterococci are also resistant to penicillin and aminoglycosides, leaving the clinician with no approved antimicrobial therapy for vancomycin-resistant enterococci (until the recent approval of linezolid and quinupristin/dalfopristin)47-52.
Vancomycin-resistant enterococci were first reported in Europe in 198636. Between 1989 and 1993, the Centers for Disease Control and Prevention reported that vancomycin resistance had increased from 0.3% to 7.9% of all enterococcal isolates and from 0.4% to 13.6% of intensive-care-unit enterococcal isolates in the United States53. In 2000, the Centers for Disease Control reported that 24.7% of nosocomial enterococcal infections in intensive care units in the United States were vancomycin-resistant, a 40% increase compared with the rate in the 1994-to-1998 time-period6. Most patients are colonized (in the gastrointestinal tract), not infected, with vancomycin-resistant enterococci. Vancomycin-resistant enterococci, however, can and do cause types of infections similar to those caused by vancomycin-susceptible strains. Investigators have reported that the rate of mortality from bacteremia due to vancomycin-resistant enterococci is higher than that associated with vancomycin-sensitive strains, but whether this increase in mortality is due to vancomycin resistance or to other factors remains controversial54-56. It is estimated that it costs at least $25,000 more to treat an episode of vancomycin-resistant bacteremia than it does to treat an episode of vancomycin-susceptible bacteremia. Similar data are not available for osteomyelitis or infection around prosthetic joints due to vancomycin-resistant enterococci57.
The factors believed to contribute to the acquisition of vancomycin-resistant enterococci include exposure to antimicrobials, prolonged hospitalization, an intensive-care-unit stay, proximity to a patient colonized or infected with vancomycin-resistant enterococci, care by a nurse who is also caring for a patient who is colonized or infected with vancomycin-resistant enterococci, medical comorbidities such as renal failure, and hospitalization in an institution that has a high proportion of patients who are colonized with vancomycin-resistant enterococci36,58,59. The role of exposure to vancomycin itself in the acquisition of vancomycin-resistant enterococci is controversial in part because of difficulties with the selection of controls and adjustments for potential confounders in published studies60. Thus, the prompt isolation of colonized patients and strict adherence to infection-control policies are important for control of the nosocomial spread of this microorganism61.
The emergence of vancomycin-resistant enterococci has raised concern about the need to prevent organisms from becoming resistant to vancomycin. Prevention of vancomycin resistance is important because of the limited therapeutic options that are available and, probably more importantly, because of the potential for transfer of genes for vancomycin resistance from enterococci to other nosocomial pathogens (for example, Staphylococcusaureus)9,62-64. Given the virulence of Staphylococcusaureus and its prominence as the most common nosocomial pathogen, vancomycin-resistant Staphylococcus aureus would be a major threat to public health.
The Centers for Disease Control presented recommendations for preventing the spread of vancomycin resistance9. These included guidelines concerning the prudent use of intravenous and oral vancomycin. Particular points of interest to the orthopaedic surgeon are shown in Table IV. It should be stressed that the guidelines include a recommendation to limit perioperative prophylaxis with vancomycin to a maximum of two doses for so-called clean orthopaedic surgery involving the implantation of prosthetic material at institutions with a high rate of superficial or deep surgical wound infections due to methicillin-resistant staphylococci or in patients with severe b-lactam allergies. Thus, the orthopaedist must have a close working relationship with the infection-control officer and know the microbiological characteristics of the orthopaedic surgical wound infections at his or her hospital. In addition, a detailed allergy history and targeted penicillin skin-testing may decrease the need to give vancomycin to patients with a history of allergy to penicillin or cephalosporin65. Although the Centers for Disease Control did not comment on the definition of a "high rate" of infections due to methicillin-resistant staphylococci, an American Academy of Orthopaedic Surgeons advisory statement indicated that vancomycin may be appropriate as a prophylactic antimicrobial for patients undergoing joint replacement at institutions that have identified a substantial prevalence (for example, >10% to 20%) of methicillin-resistant Staphylococcus aureus and coagulase-negative staphylococci among orthopaedic patients8. Cefazolin is still used as the standard perioperative prophylactic agent for patients undergoing total joint replacement at my institution66. Vancomycin is also inappropriate for antimicrobial prophylaxis prior to dental procedures in patients with a total joint replacement. An advisory panel consisting of members of both the American Academy of Orthopaedic Surgeons and the American Dental Association recommended the use of clindamycin, not vancomycin, when a dentist or orthopaedist wants antibiotic prophylaxis to be administered before a high-risk dental procedure in a patient with a total joint replacement and an allergy to penicillin67.
It should also be noted that the Centers for Disease Control discouraged the use of vancomycin solution for topical application or irrigation. Hanssen and I recently reviewed the utility of topical antibiotic irrigation in total joint replacement66. It is my opinion that the use of vancomycin-impregnated bone cement in total joint replacement surgery and vancomycin-impregnated beads in surgery for the treatment of osteomyelitis should be limited to patients with an established infection rather than be employed as routine prophylaxis against infection. This opinion was based on the finding of gentamicin resistance in patients in Europe who had been managed prophylactically with gentamicin-containing bone cement68.
The Centers for Disease Control also recommended education of hospital staff with regard to the problem of vancomycin resistance, early detection and prompt reporting of vancomycin-resistant enterococci by the clinical microbiology laboratory, and implementation of appropriate infection-control measures. The Centers for Disease Control did not comment on which of the intervention strategies would be most useful in altering the prescribing practices of physicians. The Centers for Disease Control did recommend that use of vancomycin be monitored through the hospital’s quality-improvement process or as part of the drug-utilization review by the pharmacy and therapeutics committee and the medical staff.
The Centers for Disease Control made the following recommendations for dealing with hospitalized patients who are found to be colonized or infected with vancomycin-resistant enterococci9.
Place the patient with a vancomycin-resistant enterococcal infection or colonization in a private room or with other patients who have vancomycin-resistant enterococci colonization.
Wear clean, nonsterile gloves when treating a patient with vancomycin-resistant enterococci.
Wear a clean, nonsterile gown if substantial contact with a patient who has vancomycin-resistant enterococci is anticipated or if contact with stool or wound drainage is likely.
Remove the gloves and gown before leaving the patient’s room and wash hands with an antiseptic soap or waterless antiseptic agent.
Avoid contact with potentially contaminated environmental surfaces (such as a doorknob or curtain) after glove and gown removal and hand-washing.
Restrict the use of routine medical instruments (such as a stethoscope or blood pressure cuff) to a single patient or group of patients with vancomycin-resistant enterococci.
Obtain a stool culture or rectal swab culture from roommates of patients who are found to have vancomycin-resistant enterococci.
As the duration of gastrointestinal tract colonization with vancomycin-resistant enterococci may be indefinite, each hospital must adopt a policy for when and under what circumstances to remove a patient colonized with vancomycin-resistant enterococci from isolation9. In addition, each hospital should implement a system to promptly reinstitute isolation of a patient with vancomycin-resistant enterococcal colonization when the patient is readmitted to the hospital.

Staphylococci

Staphylococcus aureus has been recognized as a major human pathogen since the 1880s69,70. Staphylococci are gram-positive aerobic cocci that usually are seen in clusters on gram stain. Staphylococcus aureus produces microcapsules and surface proteins, some of which are being used to create vaccines that may be employed to prevent infection71. Staphylococcusaureus is one of the most virulent and common nosocomial pathogens, in part because of its extensive ability to produce enzymes and toxins71,72. Staphylococcusaureus can both colonize and infect humans. Colonization can occur at birth. The major site of colonization is the anterior nares72. As many as 30% to 50% of healthy adults are colonized, and 10% to 20% may be persistently colonized. Colonization with Staphylococcus aureus is a risk factor for subsequent Staphylococcusaureus infection73-75. Clinical infections caused by Staphylococcusaureus are numerous and include some of the most common infections managed by orthopaedic surgeons (Table I).
Coagulase-negative staphylococci include fifteen different species, of which Staphylococcus epidermidis, Staphylococcus saprophyticus, and increasingly Staphylococcus lugdunensis are major pathogens in humans76-78. Coagulase-negative staphylococci, of which Staphylococcus epidermidis is the most numerous, are normal human skin flora. Most infections due to coagulase-negative staphylococci are nosocomially acquired and develop around an indwelling medical device (such as a joint prosthesis) or as a complication of an invasive medical procedure (such as arthroscopy) in part because of the ability of these organisms to produce a biofilm76,79,80. However, there are exceptions to this rule, such as urinary tract infections due to Staphylococcus saprophyticus in healthy young women.
Acquired antimicrobial resistance among staphylococci has been a problem since the advent of penicillin and sulfonamides. Currently, approximately 90% of staphylococci produce b-lactamase and therefore are penicillin resistant81,82 (Table V). Infections with methicillin-resistant Staphylococcusaureus have become increasingly common despite attempts to limit their spread through strict infection-control practices6,76,81,82. Between the time-period of 1994 to 1998 and the year 1999, the prevalence of methicillin-resistant Staphylococcusaureus among all intensive-care-unit isolates reported to the Centers for Disease Control increased by 40%6. Methicillin resistance among coagulase-negative staphylococci was even more prevalent, although the number of intensive-care-unit isolates with methicillin-resistant coagulase-negative staphylococci reported to the Centers for Disease Control increased by only 4% during that same time-period6.
Unfortunately, methicillin or oxacillin resistance confers cross-resistance to all other b-lactam antimicrobials including cefazolin76,82. In addition, methicillin-resistant isolates are often resistant to other antistaphylococcal agents, such as cotrimoxazole, clindamycin, and fluoroquinolones, leaving vancomycin as the primary and standard treatment option for serious methicillin-resistant staphylococcal infections, such as osteomyelitis and infection around a prosthetic joint. De novo rifampin resistance is uncommon among methicillin-resistant staphylococci, but like most, if not all, fluoroquinolones, this agent should not be used as monotherapy against staphylococci because of the rapid emergence of resistance during therapy76. Use of rifampin in combination with other agents for the treatment of bone and joint infections remains controversial because of a lack of data showing superior efficacy with its use. Furthermore, rifampin has gastrointestinal side effects and drug-drug interactions, which make it difficult to use83-90. The new antimicrobials, linezolid and quinupristin/dalfopristin, also have in vitro activity against methicillin-resistant staphylococci and resistance to them remains uncommon49,91. Their role in the treatment of methicillin-resistant staphylococcal infections remains to be determined.
In addition, it is important to point out that many methicillin-resistant isolates are also resistant to aminoglycosides at the standard concentrations used to predict in vivo activity for parenteral administration. It remains unknown whether the high concentrations of an aminoglycoside that can be achieved without nephrotoxicity or ototoxicity by means of local delivery in antibiotic-impregnated bone cement will be effective against these resistant strains or will promote antibiotic resistance or an infection with otherwise metabolically inactive strains92.
Vancomycin resistance among certain coagulase-negative staphylococci has been recognized for some time, but it remains a rare clinical problem93-96. Unfortunately, Staphylococcusaureus with intermediate resistance to vancomycin has recently been reported in studies from Japan and the United States97-104. The resistance is low level, is associated with clinical failures, and typically has occurred in patients with methicillin-resistant Staphylococcusaureus infections that have been treated with prolonged courses of parenteral vancomycin. Although Staphylococcus aureus with intermediate resistance to vancomycin remains a relatively rare problem, there is a potential for a serious public health threat. Microbiology laboratories are aware of appropriate methods to detect vancomycin or other antimicrobial resistance105, and the Centers for Disease Control and other organizations have presented guidelines for the prevention of these infections7,8. These guidelines include recommendations to improve antimicrobial use and microbiology laboratory methods to detect strains of Staphylococcus aureus with intermediate resistance to vancomycin as well as information on how to obtain approval of investigational antimicrobial agents through the Centers for Disease Control. In addition, methods to prevent the nosocomial transmission of intermediately vancomycin-resistant Staphylococcus aureus include immediate notification of the responsible clinician by the microbiology laboratory; immediate notification of the Centers for Disease Control and the appropriate state health department; and implementation of specific isolation procedures, including the use of dedicated health-care workers to work one-on-one with infected patients. There is an urgent need for additional research on novel strategies to prevent staphylococcal infections, including decolonization with mupirocin to eliminate nasal colonization and nosocomial staphylococcal infections, and on the development of antistaphylococcal vaccines106-111.

Solutions to the Bacterial Resistance Issue

Many individuals and groups have proposed solutions to the global threat of antimicrobial resistance1,3,5,10,12,13,15,18. These proposals include the assurance of the use of appropriate antimicrobials through a multidisciplinary approach; the institution of antimicrobial-resistance surveillance programs; the implementation of aggressive infection-control programs in hospitals; education of physicians and paramedical staff; computer-based monitoring of and feedback on the use of antimicrobial agents; professional review of hospitals by oversight agencies, such as the Joint Commission on Accreditation of Healthcare Organizations; increased funding for clinical and basic research; and regulatory reform. The reader is referred to the individual references for specific details. Common elements in most recommendations include improved antimicrobial use (in humans, animals, and the agriculture industry), education of the health-care community regarding antimicrobial resistance, and improved infection-control practices within hospitals. Achieving these goals will require financial resources; individual, institutional, and governmental support; and improved information services within the health-care industry.
Institute of Medicine. Forum on Emerging Infections. Antimicrobial resistance: issues and options: workshop report. Harrison PF, Lederberg J, editors. Washington, DC: National Academy Press; 1998. p 8-74. 
 
The National Foundation for Infectious Diseases. Biological terrorist attacks, antimicrobial resistance are growing global threats. Double Helix,1998;23: 4. 234  1998 
 
Burke JP. Antibiotic resistance—squeezing the balloon? [editorial]. JAMA,1998;280: 1270-1. 2801270  1998  [PubMed]
 
Garvin KL, Hinrichs SH,Urban JA. Emerging antibiotic-resistant bacteria. Their treatment in total joint arthroplasty. Clin Orthop,1999;369: 110-23. 369110  1999  [PubMed]
 
Wenzel RP,Edmond MB. Managing antibiotic resistance. N Engl J Med,2000;343: 1961-3. 3431961  2000  [PubMed]
 
National Nosocomial Infections Surveillance (NNIS) system report, data summary from January 1992-April 2000, issued June 2000. Am J Infect Control,2000;28: 429-48. 28429  2000  [PubMed]
 
Interim guidelines for prevention and control of Staphylococcal infection associated with reduced susceptibility to vancomycin. MMWR Morb Mortal Wkly Rep,1997;46: 626-8, 635. 46626  1997  [PubMed]
 
American Academy of Orthopaedic Surgeons. Advisory statement. The use of prophylactic antibiotics in orthopaedic medicine and the emergence of vancomycin-resistant bacteria. 1998. www.aaos.org/wordhtml/papers/advistmt/vancomyc.htm. 
 
Recommendations for preventing the spread of vancomycin resistance. Recommendations of the Hospital Infection Control Practices Advisory Committee (HICPAC). MMWR Morb Mortal Wkly Rep,1995;44: 1-13. 441  1995  [PubMed]
 
Report of the ASM task force on antibiotic resistance. Antimicrob Agents Chemother,1995;Suppl: 1-23. Suppl1  1995  [PubMed]
 
Fishman NO,Brennan PJ. Optimizing use of antimicrobial agents: pitfalls and consequences of inappropriate therapy. JCOM,1997;4: 25-33. 425  1997 
 
Goldmann DA, Weinstein RA, Wenzel RP, Tablan OC, Duma RJ, Gaynes RP, Schlosser J,Martone WJ. Strategies to prevent and control the emergence and spread of antimicrobial-resistant microorganisms in hospitals. A challenge to hospital leadership. JAMA,1996;275: 234-40. 275234  1996  [PubMed]
 
Shlaes DM, Gerding DN, John JF Jr, Craig WA, Bornstein DL, Duncan RA, Eckman MR, Farrer WE, Greene WH, Lorian V, Levy S, McGowan JE Jr, Paul SM, Ruskin J, Tenover FC,Watanakunakorn C. Society for Healthcare Epidemiology of America and Infectious Diseases Society of America Joint Committee on the Prevention of Antimicrobial Resistance: guidelines for the prevention of antimicrobial resistance in hospitals. Infect Control Hosp Epidemiol,1997;18: 275-91. 18275  1997  [PubMed]
 
McGowan JE Jr,Tenover FC. Control of antimicrobial resistance in the health care system. Infect Dis Clin North Am,1997;11: 297-311. 11297  1997  [PubMed]
 
Kollef MH,Fraser VJ. Antibiotic resistance in the intensive care unit. Ann Intern Med,2001;134: 298-314. 134298  2001  [PubMed]
 
Swartz MN. Use of antimicrobial agents and drug resistance [editorial]. N Engl J Med,1997;337: 491-2. 337491  1997  [PubMed]
 
Gold HS,Moellering RC Jr. Antimicrobial-drug resistance. N Engl J Med,1996;335: 1445-53.. 3351445  1996  [PubMed]
 
Chopra I, Hodgson J, Metcalf B,Poste G. New approaches to the control of infections caused by antibiotic-resistant bacteria. An industry perspective. JAMA,1996;275: 401-3. 275401  1996  [PubMed]
 
Virk A,Steckelberg JM. Clinical aspects of antimicrobial resistance. Mayo Clin Proc,2000;75: 200-14. 75200  2000  [PubMed]
 
Walsh C. Molecular mechanisms that confer antibacterial drug resistance. Nature,2000;406: 775-81. 406775  2000  [PubMed]
 
Levy SB, FitzGerald GB,Macone AB. Changes in intestinal flora of farm personnel after introduction of tetracycline-supplemented feed on a farm. N Engl J Med,1976;295: 583-8. 295583  1976  [PubMed]
 
McGowan JE Jr. Antimicrobial resistance in hospital organisms and its relation to antibiotic use. Rev Infect Dis,1983;5: 1033-48. 51033  1983  [PubMed]
 
Barton MD. Antibiotic use in animal feed and its impact on human health. Nutr Res Rev,2000;13: 279-99. 13279  2000  [PubMed]
 
Bradley SF. Issues in the management of resistant bacteria in long-term-care facilities. Infect Control Hosp Epidemiol,1999;20: 362-6. 20362  1999  [PubMed]
 
Kunin CM. Resistance to antimicrobial drugs—a worldwide calamity. Ann Intern Med,1993;118: 557-61. 118557  1993  [PubMed]
 
Tauxe RV, Puhr ND, Wells JG, Hargrett-Bean N,Blake PA. Antimicrobial resistance of Shigella isolates in the USA: the importance of international travelers. J Infect Dis,1990;162: 1107-11. 1621107  1990  [PubMed]
 
Smith KE, Besser JM, Hedberg CW, Leano FT, Bender JB, Wicklund JH, Johnson BP, Moore KA,Osterholm MT. Quinolone-resistant Campylobacter jejuni infections in Minnesota, 1992-1998. Investigation Team. N Engl J Med,1999;340: 1525-32. 3401525  1999  [PubMed]
 
Clavo-Sanchez AJ, Giron-Gonzalez JA, Lopez-Prieto D, Canueto-Quintero J, Sanchez-Porto A, Vergara-Campos A, Marin-Casanova P,Cordoba-Dona JA. Multivariate analysis of risk factors for infection due to penicillin-resistant and multidrug-resistant Streptococcus pneumoniae: a multicenter study. Clin Infect Dis,1997;24: 1052-9. 241052  1997  [PubMed]
 
Doone JL, Klespies SL,Sabella C. Risk factors for penicillin-resistant systemic pneumococcal infections in children. Clin Pediatr (Phila),1997;36: 187-91. 36187  1997  [PubMed]
 
Hofmann J, Cetron MS, Farley MM, Baughman WS, Facklam RR, Elliott JA, Deaver KA,Breiman RF. The prevalence of drug-resistant Streptococcus pneumoniae in Atlanta. N Engl J Med,1995;333: 481-6. 333481  1995  [PubMed]
 
Faryna A, Wergowske GL,Goldenberg K. Impact of therapeutic guidelines on antibiotic use by residents in primary care clinics. J Gen Intern Med,1987;2: 102-7. 2102  1987  [PubMed]
 
Gonzales R, Steiner JF,Sande MA. Antibiotic prescribing for adults with colds, upper respiratory tract infections, and bronchitis by ambulatory care physicians. JAMA,1997;278: 901-4. 278901  1997  [PubMed]
 
Donskey CJ, Chowdhry TK, Hecker MT, Hoyen CK, Hanrahan JA, Hujer AM, Hutton-Thomas RA, Whalen CC, Bonomo RA,Rice LB. Effect of antibiotic therapy on the density of vancomycin-resistant enterococci in the stool of colonized patients. N Engl J Med,2000;343: 1925-32. 3431925  2000  [PubMed]
 
Murray BE. Vancomycin-resistant enterococci. Am J Med,1997;102: 284-93. 102284  1997  [PubMed]
 
John JF Jr, Fishman NO. Programmatic role of the infectious diseases physician in controlling antimicrobial costs in the hospital. Clin Infect Dis,1997;24: 471-85. 24471  1997  [PubMed]
 
Murray BE. Vancomycin-resistant enterococcal infections. N Engl J Med,2000;342: 710-21. 342710  2000  [PubMed]
 
Moellering RC. Enterococcus species, Streptococcus bovis, and Leuconostoc species. In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone; 2000. p 2147-56. 
 
Moellering RC Jr. Vancomycin-resistant enterococci. Clin Infect Dis,1998;26: 1196-9. 261196  1998  [PubMed]
 
Lew DP,Waldvogel FA. Osteomyelitis. N Engl J Med,1997;336: 999-1007. 336999  1997  [PubMed]
 
Sapico FL. Microbiology and antimicrobial therapy of spinal infections. Orthop Clin North Am,1996;27: 9-13. 279  1996  [PubMed]
 
Lipsky BA. Osteomyelitis of the foot in diabetic patients. Clin Infect Dis,1997;25: 1318-26. 251318  1997  [PubMed]
 
Goldenberg DL. Septic arthritis. Lancet,1998;351: 197-202. 351197  1998  [PubMed]
 
Smith JW,Piercy EA. Infectious arthritis. Clin Infect Dis,1995;20: 225-30. 20225  1995  [PubMed]
 
Steckelberg JM, Osmon DR. Prosthetic joint infection. In: Waldvogel FA, Bisno AL, editors. Infections associated with indwelling medical devices. 3rd ed. Washington, DC: ASM Press; 2000. p 173-209. 
 
Ryan MJ, Kavanagh R, Wall PG,Hazleman BL. Bacterial joint infections in England and Wales: analysis of bacterial isolates over a four year period. Br J Rheumatol,1997;36: 370-3. 36370  1997  [PubMed]
 
Patzakis MJ, Wilkins J, Kumar J, Holtom P, Greenbaum B,Ressler R. Comparison of the\ results of bacterial cultures from multiple sites in chronic osteomyelitis of long bones. A prospective study. J Bone Joint Surg Am,1994;76: 664-6. 76664  1994  [PubMed]
 
Winston DJ, Emmanouilides C, Kroeber A, Hindler J, Bruckner DA, Territo MC,Busuttil RW. Quinupristin/dalfopristin therapy for infections due to vancomycin-resistant Enterococcus faecium. Clin Infect Dis,2000;30: 790-7. 30790  2000  [PubMed]
 
Lundstrom TS,Sobel JD. Antibiotics for gram-positive bacterial infections. Vancomycin, teicoplanin, quinupristin/dalfopristin, and linezolid. Infect Dis Clin North Am,2000;14: 463-74. 14463  2000  [PubMed]
 
Clemett D,Markham A. Linezolid. Drugs,2000;59: 815-27.. 59815  2000  [PubMed]
 
Linezolid (Zyvox). Med Lett Drugs Ther,2000;42: 45-6. 4245  2000  [PubMed]
 
Chien JW, Kucia ML,Salata RA. Use of linezolid, an oxazolidinone, in the treatment of multidrug-resistant gram-positive bacterial infections. Clin Infect Dis,2000;30: 146-51. 30146  2000  [PubMed]
 
Moellering RC, Linden PK, Reinhardt J, Blumberg EA, Bompart F,Talbot GH. The efficacy and safety of quinupristin/dalfopristin for the treatment of infections caused by vancomycin-resistant Enterococcus faecium. Synercid Emergency-Use Study Group. J Antimicrob Chemother,1999;44: 251-61. 44251  1999  [PubMed]
 
Nosocomial enterococci resistant to vancomycin—United States, 1989-1993. MMWR Morb Mortal Wkly Rep,1993;42: 597-9. 42597  1993  [PubMed]
 
French GL. Enterococci and vancomycin resistance. Clin Infect Dis,1998;27 Suppl 1: 75-83. 27 Suppl 175  1998 
 
Garbutt JM, Ventrapragada M, Littenberg B,Mundy LM. Association between resistance to vancomycin and death in cases of Enterococcus faecium bacteremia. Clin Infect Dis,2000;30: 466-72. 30466  2000  [PubMed]
 
Bhavnani SM, Drake JA, Forrest A, Deinhart JA, Jones RN, Biedenbach DJ,Ballow CH. A nationwide, multicenter, case-control study comparing risk factors, treatment, and outcome for vancomycin-resistant and -susceptible enterococcal bacteremia. Diagn Microbiol Infect Dis,2000;36: 145-58.. 36145  2000  [PubMed]
 
Stosor V, Peterson LR, Postelnick M,Noskin GA. Enterococcus faecium bacteremia: does vancomycin resistance make a difference?. Arch Intern Med,1998;158: 522-7.. 158522  1998  [PubMed]
 
Dever LL, China C, Eng RH, O’Donovan C,Johanson WG Jr. Vancomycin-resistant Enterococcus faecium in a Veterans Affairs Medical Center: association with antibiotic usage. Am J Infect Control,1998;26: 40-6. 2640  1998  [PubMed]
 
Linden PK,Miller CB. Vancomycin-resistant enterococci: the clinical effect of a common nosocomial pathogen. Diagn Microbiol Infect Dis,1999;33: 113-20. 33113  1999  [PubMed]
 
Carmeli Y, Samore MH,Huskins C. The association between antecedent vancomycin treatment and hospital-acquired vancomycin-resistant enterococci: a meta-analysis. Arch Intern Med,1999;159: 2461-8. 1592461  1999  [PubMed]
 
Montecalvo MA, Jarvis WR, Uman J, Shay DK, Petrullo C, Rodney K, Gedris C, Horowitz HW,Wormser GP. Infection-control measures reduce transmission of vancomycin-resistant enterococci in an endemic setting. Ann Intern Med,1999;131: 269-72. 131269  1999  [PubMed]
 
Noble WC, Virani Z,Cree RG. Co-transfer of vancomycin and other resistance genes from Enterococcus faecalis NCTC 12201 to Staphylococcus aureus. FEMS Microbiol Lett,1992;72: 195-8. 72195  1992  [PubMed]
 
Leclercq R, Derlot E, Weber M, Duval J,Courvalin P. Transferable vancomycin and teicoplanin resistance in Enterococcus faecium. Antimicrob Agents Chemother,1989;33: 10-5. 3310  1989  [PubMed]
 
Uttley AH, George RC, Naidoo J, Woodford N, Johnson AP, Collins CH, Morrison D, Gilfillan AJ, Fitch LE,Heptonstall J. High-level vancomycin-resistant enterococci causing hospital infections. Epidemiol Infect,1989;103: 173-8. 103173  1989  [PubMed]
 
Li JT, Markus PJ, Osmon DR, Estes L, Gosselin VA,Hanssen AD. Reduction of vancomycin use in orthopedic patients with a history of antibiotic allergy. Mayo Clin Proc,2000;75: 902-6. 75902  2000  [PubMed]
 
Hanssen AD,Osmon DR. The use of prophylactic antimicrobial agents during and after hip arthroplasty. Clin Orthop,1999;369: 124-38. 369124  1999  [PubMed]
 
Advisory statement. Antibiotic prophylaxis for dental patients with total joint replacements. American Dental Association; American Academy of Orthopaedic Surgeons. J Am Dent Assoc,1997;128: 1004-8. 1281004  1997  [PubMed]
 
Hope PG, Kristinsson KG, Norman P,Elson RA. Deep infection of cemented total hip arthroplasties caused by coagulase-negative staphylococci. J Bone Joint Surg Br,1989;71: 851-5. 71851  1989  [PubMed]
 
Ogston A. Micrococcus poisoning. J Anat Physiol,1882;17: 24-58. 1724  1882  [PubMed]
 
Classics in infectious diseases. "On abscesses". Alexander Ogston (1844-1929). Rev Infect Dis,1984;6: 122-8. 6122  1984  [PubMed]
 
Lowy FD. Staphylococcus aureus infections. N Engl J Med,1998;339: 520-32. 339520  1998  [PubMed]
 
Waldvogel FA. Staphylococcus aureus (including staphylococcal toxic shock). In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone; 2000. p 2069-92. 
 
von Eiff C, Becker K, Machka K, Stammer H,Peters G. Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med,2001;344: 11-16. 34411  2001  [PubMed]
 
Archer GL,Climo MW. Staphylococcus aureus bacteremia—consider the source [editorial]. N Engl J Med,2001;344: 55-6. 34455  2001  [PubMed]
 
Wenzel RP,Perl TM. The significance of nasal carriage of Staphylococcus aureus and the incidence of postoperative wound infection. J Hosp Infect,1995;31: 13-24. 3113  1995  [PubMed]
 
Archer GL. Staphylococcus epidermidis and other coagulase-negative staphylococci. In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone; 2000. p 2092-100. 
 
Ferevenza FC, Contreras GE, Garratt KN,Steckelberg JM. Staphylococcus lugdunensis endocarditis: a complication of vasectomy? . Mayo Clin Proc,1999;74: 1227-30. 741227  1999  [PubMed]
 
Sampathkumar P, Osmon DR,Cockerill FR 3rd. Prosthetic joint infection due to Staphylococcus lugdunensis. Mayo Clin Proc,2000;75: 511-2. 75511  2000  [PubMed]
 
Costerton JW, Stewart PS,Greenberg EP. Bacterial biofilms: a common cause of persistent infections. Science,1999;284: 1318-22. 2841318  1999  [PubMed]
 
Rupp ME,Archer GL. Coagulase-negative staphylococci: pathogens associated with medical progress. Clin Infect Dis,1994;19: 231-43. 19231  1994  [PubMed]
 
Pfaller MA, Jones RN, Doern GV,Kugler K. Bacterial pathogens isolated from patients with bloodstream infection: frequencies of occurrence and antimicrobial susceptibility patterns from the SENTRY antimicrobial surveillance program (United States and Canada, 1997). Antimicrob Agents Chemother,1998;42: 1762-70. 421762  1998  [PubMed]
 
Raad I, Alrahwan A,Rolston K. Staphylococcus epidermidis: emerging resistance and need for alternative agents. Clin Infect Dis,1998;26: 1182-7. 261182  1998  [PubMed]
 
Bahl D, Miller DA, Leviton I, Gialanella P, Wolin MJ, Liu W, Perkins R,Miller MH. In vitro activities of ciprofloxacin and rifampin alone and in combination against growing and nongrowing strains of methicillin-susceptible and methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother,1997;41: 1293-7. 411293  1997  [PubMed]
 
Drancourt M, Stein A, Argenson JN, Zannier A, Curvale G,Raoult D. Oral rifampin plus ofloxacin for treatment of Staphylococcus-infected orthopedic implants. Antimicrob Agents Chemother,1993;37: 1214-8. 371214  1993  [PubMed]
 
Drancourt M, Stein A, Argenson JN, Roiron R, Groulier P,Raoult D. Oral treatment of Staphylococcus spp. infected orthopaedic implants with fusidic acid or ofloxacin in combination with rifampicin. J Antimicrob Chemother,1997;39: 235-40. 39235  1997  [PubMed]
 
Hershberger E, Aeschlimann JR, Moldovan T,Rybak MJ. Evaluation of bactericidal activities of LY333328, vancomycin, teicoplanin, ampicillin-sulbactam, trovafloxacin, and RP59500 alone or in combination with rifampin or gentamicin against different strains of vancomycin-intermediate Staphylococcus aureus by time-kill curve methods. Antimicrob Agents Chemother,1999;43: 717-21. 43717  1999  [PubMed]
 
Norden CW. Experimental chronic staphylococcal osteomyelitis in rabbits: treatment with rifampin alone and in combination with other antimicrobial agents. Rev Infect Dis,1983;5 Suppl 3: 491-4. 5 Suppl 3491  1983 
 
Norden CW, Bryant R, Palmer D, Montgomerie JZ,Wheat J. Chronic osteomyelitis caused by Staphylococcus aureus: controlled clinical trial of nafcillin therapy and nafcillin-rifampin therapy. South Med J,1986;79: 947-51. 79947  1986  [PubMed]
 
Zimmerli W, Widmer AF, Blatter M, Frei R,Ochsner PE. Role of rifampin for treatment of orthopedic implant-related staphylococcal infections: a randomized controlled trial. Foreign-Body Infection (FBI) Study Group. JAMA,1998;279: 1537-41. 2791537  1998  [PubMed]
 
Zavasky DM,Sande MA. Reconsideration of rifampin: a unique drug for a unique infection [editorial]. JAMA,1998;279: 1575-7. 2791575  1998  [PubMed]
 
Quinupristin/dalfopristin. Med Lett Drugs Ther,1999;41: 109-10. 41109  1999  [PubMed]
 
Proctor RA,Peters G. Small colony variants in staphylococcal infections: diagnostic and therapeutic implications. Clin Infect Dis,1998;27: 419-22. 27419  1998  [PubMed]
 
Froggatt JW, Johnston JL, Galetto DW,Archer GL. Antimicrobial resistance in nosocomial isolates of Staphylococcus haemolyticus. Antimicrob Agents Chemother,1989;33: 460-6. 33460  1989  [PubMed]
 
Sieradzki K, Villari P,Tomasz A. Decreased susceptibilities to teicoplanin and vancomycin among coagulase-negative methicillin-resistant clinical isolates of staphylococci. Antimicrob Agents Chemother,1998;42: 100-7. 42100  1998  [PubMed]
 
Veach LA, Pfaller MA, Barrett M, Koontz FP,Wenzel PP. Vancomycin resistance in Staphylococcus haemolyticus causing colonization and bloodstream infection. J Clin Microbiol,1990;28: 2064-8. 282064  1990  [PubMed]
 
Schwalbe RS, Stapleton JT,Gilligan PH. Emergence of vancomycin resistance in coagulase-negative staphylococci. N Engl J Med,1987;316: 927-31. 316927  1987  [PubMed]
 
Reduced susceptibility of Staphylococcus aureus to vancomycin—-Japan, 1996. MMWR Morb Mortal Wkly Rep,1997;46: 624-6. 46624  1997  [PubMed]
 
Staphylococcus aureus with reduced susceptibility to vancomycin—-United States, 1997. MMWR Morb Mortal Wkly Rep,1997;46: 765-6. 46765  1997  [PubMed]
 
Hiramatsu K, Aritaka N, Hanaki H, Kawasaki S, Hosoda Y, Hori S, Fukuchi Y,Kobayashi I. Dissemination in Japanese hospitals of strains of Staphylococcus aureus heterogeneously resistant to vancomycin. Lancet,1997;350: 1670-3. 3501670  1997  [PubMed]
 
Paterson DL. Reduced susceptibility of Staphylococcus aureus to vancomycin—a review of current knowledge. Commun Dis Intell,1999;23: 69-73.. 2369  1999  [PubMed]
 
Sieradzki K, Roberts RB, Haber SW,Tomasz A. The development of vancomycin resistance in a patient with methicillin-resistant Staphylococcus aureus infection. N Engl J Med,1999;340: 517-23. 340517  1999  [PubMed]
 
Smith TL, Pearson ML, Wilcox KR, Cruz C, Lancaster MV, Robinson-Dunn B, Tenover FC, Zervos MJ, Band JD, White E,Jarvis WR. Emergence of vancomycin resistance in Staphylococcus aureus. Glycopeptide-Intermediate Staphylococcus aureus Working Group. N Engl J Med,1999;340: 493-501.. 340493  1999  [PubMed]
 
Waldvogel FA. New resistance in Staphylococcus aureus [editorial]. N Engl J Med,1999;340: 556-7. 340556  1999  [PubMed]
 
Staphylococcus aureus with reduced susceptibility to vancomycin—Illinois, 1999. MMWR Morb Mortal Wkly Rep,2000;48: 1165-7. 481165  2000  [PubMed]
 
Laboratory capacity to detect antimicrobial resistance, 1998. MMWR Morb Mortal Wkly Rep,2000;48: 1167-71. 481167  2000  [PubMed]
 
Edmond MB, Wenzel RP,Pasculle AW. Vancomycin-resistant Staphylococcus aureus: perspectives on measures needed for control. Ann Intern Med,1996;124: 329-34. 124329  1996  [PubMed]
 
Reagan DR, Doebbeling BN, Pfaller MA, Sheetz CT, Houston AK, Hollis RJ,Wenzel RP. Elimination of coincident Staphylococcus aureus nasal and hand carriage with intranasal application of mupirocin calcium ointment. Ann Intern Med,1991;114: 101-6. 114101  1991  [PubMed]
 
Gernaat-van der Sluis AJ, Hoogenboom-Verdegaal AM, Edixhoven PJ,Spies-van Rooijen NH. Prophylactic mupirocin could reduce orthopedic wound infections. 1,044 patients treated with mupirocin compared with 1,260 historical controls. Acta Orthop Scand,1998;69: 412-4. 69412  1998  [PubMed]
 
Hudson IR. The efficacy of intranasal mupirocin in the prevention of staphylococcal infections: a review of recent experience. J Hosp Infect,1994;27: 81-98. 2781  1994  [PubMed]
 
Kluytmans JA, Mouton JW, Ijzerman EP, Vandenbroucke-Grauls CM, Maat AW, Wagenvoort JH,Verbrugh HA. Nasal carriage of Staphylococcus aureus as a major risk factor for wound infections after cardiac surgery. J Infect Dis,1995;171: 216-9. 171216  1995  [PubMed]
 
Fattom AI, Naso R. Staphylococcal vaccines: a realistic dream. Ann Med,1996;28: 43-6. 2843  1996  [PubMed]
 

Submit a comment

Topics

Anchor for JumpAnchor for JumpTABLE I:  Common Nosocomial Antibiotic-Resistant Microorganisms Encountered by the Orthopaedic Surgeon
*Methicillin-resistant Staphylococcus aureus. †Infrequent pathogen in such infections. ‡Some non-Candida albicans species, such as Candida krusei, are also resistant.
MicroorganismInfections Commonly Involving Microorganism as PathogenAntibiotics Frequently Resisted by Microorganism
Staphylococcus aureusSurgical wound infectionPenicillin
OsteomyelitisMethicillin, oxacillin
Infection around prosthetic joint Vancomycin (rare)
Infectious arthritisAminoglycosides*
Osteomyelitis, footFluoroquinolones*
Traumatic open fractureCotrimoxazole*
Coagulase-negative StaphylococcusSurgical wound infectionPenicillin
Osteomyelitis associated with foreign body Methicillin, oxacillin
Infection around prosthetic joint Vancomycin (rare)
Septic arthritis following arthroscopyAminoglycosides*
Fluoroquinolones*
Cotrimoxazole*
Clindamycin*
Enterococcus speciesOsteomyelitis, footPenicillin (Enterococcus faecium)
Vancomycin (Enterococcus faecium)
Gentamicin
Pseudomonas aeruginosaSurgical wound infectionPiperacillin
Traumatic osteomyelitisCeftazidime
Chronic osteomyelitis, footImipenem
Aminoglycosides
Fluoroquinolones
Enterobacter speciesSurgical wound infectionCeftazidime
OsteomyelitisCefotaxime
Chronic osteomyelitis, foot
Stenotrophomonas maltophiliaTraumatic osteomyelitisImipenem
Ceftazidime
Fluoroquinolones
Aminoglycosides
Bacteroides speciesOsteomyelitis, foot Penicillin
Clindamycin
Candida speciesMusculoskeletal system infections†Fluconazole‡
Anchor for JumpAnchor for JumpTABLE II:  Comparison of Antimicrobial Resistance of Selected Pathogens in Bloodstream Isolates from Nosocomial and Community-Acquired Infections*
*Reproduced, with modification, from: Pfaller MA, Jones RN, Doern GV, Kugler K. Bacterial pathogens isolated from patients with bloodstream infection: frequencies of occurrence and antimicrobial susceptibility patterns from the SENTRY antimicrobial surveillance program (United States and Canada, 1997). Antimicrob Agents Chemother. 1998;42:1762-70. Reprinted with permission.
OrganismAntimicrobial AgentPercent Resistant
Nosocomial InfectionsCommunity-Acquired Infections
Staphylococcus aureusOxacillin31.025.1
Coagulase-negative StaphylococcusOxacillin68.041.5
Enterococcus speciesVancomycin20.0?7.1
Enterobacter cloacaeCeftazidime38.519.2
Pseudomonas aeruginosaCeftazidime?7.8?1.9
Imipenem13.7?5.8
Escherichia coliCeftazidime?7.3?0.6
Ciprofloxacin?1.7?1.1
Anchor for JumpAnchor for JumpTABLE III:  Mechanisms of Resistance and Their Genetic Basis for Common Nosocomial Antibiotic-Resistant Microorganisms Encountered by Orthopaedic Surgeons*
*Reproduced, with modification, from: Virk A, Steckelberg JM. Clinical aspects of antimicrobial resistance. Mayo Clinic Proc. 2000;75:200-14. Reprinted with permission.
Mechanism of ResistanceAntibioticGenetic BasisExamples of Microorganism and Antibiotic Combinations
Enzymatic inhibitionb-lactamsPlasmid-mediated and chromosomalStaphylococci species-penicillin, Enterobacter species-ceftazidime, Stenotrophomonas maltophilia-imipenem
AminoglycosidesGram-negative bacilli or highly gentamicin-resistant Enterococci
Permeability-uptakeb-lactamsChromosomalPseudomonas aeruginosa-b-lactams
AminoglycosidesStaphylococcus aureus, gram-negative bacilli, enterococci-aminoglycosides
Porin channelsb-lactamsChromosomalPseudomonas aeruginosa, Stenotrophomonas maltophilia
Carbapenems
Drug efflux mechanismsb-lactamsPlasmid-mediated or chromosomalPseudomonas aeruginosa,Staphylococcus aureus
Fluoroquinolones
Tetracycline
Target-site alteration
(Altered penicillin-binding protein)b-lactamsPlasmid-mediatedStaphylococcus aureus-methicillin
(Altered oligopeptide)GlycopeptidePlasmid-mediated or constitutiveEnterococci resistant to vancomycin
Competitive inhibition by overproduction of p-aminobenzoic acid or altered dihydropteroate synthaseSulfonamidesPlasmid-mediatedStaphylococcus aureus, Escherichia coli
DNA gyrase mutationFluoroquinolonesChromosomal or plasmid (Klebsiella pneumoniae)-mediatedPseudomonas aeruginosa, Staphylococcus aureus
Anchor for JumpAnchor for JumpTABLE IV:  Selected Recommendations by the Centers for Disease Control for the Prudent Use of Vancomycin in the Practice of an Orthopaedic Surgeon*
*Adapted from the Recommendations of the Hospital Infection Control Practices Advisory Committee of the Centers for Disease Control9.
Situations in which the use of vancomycin is appropriate or acceptable
Treatment of serious infection caused by b-lactam-resistant gram-positive organism
Treatment of infection caused by gram-positive microorganisms in patients who have serious allergies to b-lactam antimicrobials
When antibiotic-associated colitis fails to respond to metronidazole therapy or is severe and potentially life-threatening
Prophylaxis as recommended by the American Heart Association for endocarditis following certain procedures in patients at high risk for endocarditis
Prophylaxis for major surgical procedures involving implantation of prosthetic materials or devices at institutions that have a high rate of infections caused by methicillin-resistant Staphylococcus aureus or methicillin-resistant coagulase-negative staphylococci
Situations in which the use of vancomycin should be discouraged
Routine surgical prophylaxis other than that in a patient who has a life-threatening allergy to b-lactam antibiotics
Treatment in response to positive findings for coagulase-negative staphylococcus on a single blood culture if other blood cultures performed during the same time-frame have negative findings
Continued empiric use for presumed infection in patients who have negative findings for b-lactam-resistant gram-positive organisms on culture
Systemic or local prophylaxis for infection or colonization of indwelling central or peripheral intravenous catheters
Eradication of methicillin-resistant Staphylococcus aureus colonization
Primary treatment of antibiotic-associated colitis
Treatment for infection caused by b-lactam-sensitive organisms in patients who have renal failure (when the decision is based on dosing convenience)
Topical application or irrigation
Anchor for JumpAnchor for JumpTABLE V:  Percent Resistance of Bloodstream Isolates Reported by Pfaller et al.81 in 1998
Antimicrobial AgentPercent Resistant
Staphylococcus aureus Coagulase-Negative Staphylococci
Penicillin89.886.6
Oxacillin26.256.9
Vancomycin?0.0?0.0
Gentamicin13.740.0
Ciprofloxacin28.242.5
Clindamycin24.042.9
Cotrimoxazole10.844.5
Institute of Medicine. Forum on Emerging Infections. Antimicrobial resistance: issues and options: workshop report. Harrison PF, Lederberg J, editors. Washington, DC: National Academy Press; 1998. p 8-74. 
 
The National Foundation for Infectious Diseases. Biological terrorist attacks, antimicrobial resistance are growing global threats. Double Helix,1998;23: 4. 234  1998 
 
Burke JP. Antibiotic resistance—squeezing the balloon? [editorial]. JAMA,1998;280: 1270-1. 2801270  1998  [PubMed]
 
Garvin KL, Hinrichs SH,Urban JA. Emerging antibiotic-resistant bacteria. Their treatment in total joint arthroplasty. Clin Orthop,1999;369: 110-23. 369110  1999  [PubMed]
 
Wenzel RP,Edmond MB. Managing antibiotic resistance. N Engl J Med,2000;343: 1961-3. 3431961  2000  [PubMed]
 
National Nosocomial Infections Surveillance (NNIS) system report, data summary from January 1992-April 2000, issued June 2000. Am J Infect Control,2000;28: 429-48. 28429  2000  [PubMed]
 
Interim guidelines for prevention and control of Staphylococcal infection associated with reduced susceptibility to vancomycin. MMWR Morb Mortal Wkly Rep,1997;46: 626-8, 635. 46626  1997  [PubMed]
 
American Academy of Orthopaedic Surgeons. Advisory statement. The use of prophylactic antibiotics in orthopaedic medicine and the emergence of vancomycin-resistant bacteria. 1998. www.aaos.org/wordhtml/papers/advistmt/vancomyc.htm. 
 
Recommendations for preventing the spread of vancomycin resistance. Recommendations of the Hospital Infection Control Practices Advisory Committee (HICPAC). MMWR Morb Mortal Wkly Rep,1995;44: 1-13. 441  1995  [PubMed]
 
Report of the ASM task force on antibiotic resistance. Antimicrob Agents Chemother,1995;Suppl: 1-23. Suppl1  1995  [PubMed]
 
Fishman NO,Brennan PJ. Optimizing use of antimicrobial agents: pitfalls and consequences of inappropriate therapy. JCOM,1997;4: 25-33. 425  1997 
 
Goldmann DA, Weinstein RA, Wenzel RP, Tablan OC, Duma RJ, Gaynes RP, Schlosser J,Martone WJ. Strategies to prevent and control the emergence and spread of antimicrobial-resistant microorganisms in hospitals. A challenge to hospital leadership. JAMA,1996;275: 234-40. 275234  1996  [PubMed]
 
Shlaes DM, Gerding DN, John JF Jr, Craig WA, Bornstein DL, Duncan RA, Eckman MR, Farrer WE, Greene WH, Lorian V, Levy S, McGowan JE Jr, Paul SM, Ruskin J, Tenover FC,Watanakunakorn C. Society for Healthcare Epidemiology of America and Infectious Diseases Society of America Joint Committee on the Prevention of Antimicrobial Resistance: guidelines for the prevention of antimicrobial resistance in hospitals. Infect Control Hosp Epidemiol,1997;18: 275-91. 18275  1997  [PubMed]
 
McGowan JE Jr,Tenover FC. Control of antimicrobial resistance in the health care system. Infect Dis Clin North Am,1997;11: 297-311. 11297  1997  [PubMed]
 
Kollef MH,Fraser VJ. Antibiotic resistance in the intensive care unit. Ann Intern Med,2001;134: 298-314. 134298  2001  [PubMed]
 
Swartz MN. Use of antimicrobial agents and drug resistance [editorial]. N Engl J Med,1997;337: 491-2. 337491  1997  [PubMed]
 
Gold HS,Moellering RC Jr. Antimicrobial-drug resistance. N Engl J Med,1996;335: 1445-53.. 3351445  1996  [PubMed]
 
Chopra I, Hodgson J, Metcalf B,Poste G. New approaches to the control of infections caused by antibiotic-resistant bacteria. An industry perspective. JAMA,1996;275: 401-3. 275401  1996  [PubMed]
 
Virk A,Steckelberg JM. Clinical aspects of antimicrobial resistance. Mayo Clin Proc,2000;75: 200-14. 75200  2000  [PubMed]
 
Walsh C. Molecular mechanisms that confer antibacterial drug resistance. Nature,2000;406: 775-81. 406775  2000  [PubMed]
 
Levy SB, FitzGerald GB,Macone AB. Changes in intestinal flora of farm personnel after introduction of tetracycline-supplemented feed on a farm. N Engl J Med,1976;295: 583-8. 295583  1976  [PubMed]
 
McGowan JE Jr. Antimicrobial resistance in hospital organisms and its relation to antibiotic use. Rev Infect Dis,1983;5: 1033-48. 51033  1983  [PubMed]
 
Barton MD. Antibiotic use in animal feed and its impact on human health. Nutr Res Rev,2000;13: 279-99. 13279  2000  [PubMed]
 
Bradley SF. Issues in the management of resistant bacteria in long-term-care facilities. Infect Control Hosp Epidemiol,1999;20: 362-6. 20362  1999  [PubMed]
 
Kunin CM. Resistance to antimicrobial drugs—a worldwide calamity. Ann Intern Med,1993;118: 557-61. 118557  1993  [PubMed]
 
Tauxe RV, Puhr ND, Wells JG, Hargrett-Bean N,Blake PA. Antimicrobial resistance of Shigella isolates in the USA: the importance of international travelers. J Infect Dis,1990;162: 1107-11. 1621107  1990  [PubMed]
 
Smith KE, Besser JM, Hedberg CW, Leano FT, Bender JB, Wicklund JH, Johnson BP, Moore KA,Osterholm MT. Quinolone-resistant Campylobacter jejuni infections in Minnesota, 1992-1998. Investigation Team. N Engl J Med,1999;340: 1525-32. 3401525  1999  [PubMed]
 
Clavo-Sanchez AJ, Giron-Gonzalez JA, Lopez-Prieto D, Canueto-Quintero J, Sanchez-Porto A, Vergara-Campos A, Marin-Casanova P,Cordoba-Dona JA. Multivariate analysis of risk factors for infection due to penicillin-resistant and multidrug-resistant Streptococcus pneumoniae: a multicenter study. Clin Infect Dis,1997;24: 1052-9. 241052  1997  [PubMed]
 
Doone JL, Klespies SL,Sabella C. Risk factors for penicillin-resistant systemic pneumococcal infections in children. Clin Pediatr (Phila),1997;36: 187-91. 36187  1997  [PubMed]
 
Hofmann J, Cetron MS, Farley MM, Baughman WS, Facklam RR, Elliott JA, Deaver KA,Breiman RF. The prevalence of drug-resistant Streptococcus pneumoniae in Atlanta. N Engl J Med,1995;333: 481-6. 333481  1995  [PubMed]
 
Faryna A, Wergowske GL,Goldenberg K. Impact of therapeutic guidelines on antibiotic use by residents in primary care clinics. J Gen Intern Med,1987;2: 102-7. 2102  1987  [PubMed]
 
Gonzales R, Steiner JF,Sande MA. Antibiotic prescribing for adults with colds, upper respiratory tract infections, and bronchitis by ambulatory care physicians. JAMA,1997;278: 901-4. 278901  1997  [PubMed]
 
Donskey CJ, Chowdhry TK, Hecker MT, Hoyen CK, Hanrahan JA, Hujer AM, Hutton-Thomas RA, Whalen CC, Bonomo RA,Rice LB. Effect of antibiotic therapy on the density of vancomycin-resistant enterococci in the stool of colonized patients. N Engl J Med,2000;343: 1925-32. 3431925  2000  [PubMed]
 
Murray BE. Vancomycin-resistant enterococci. Am J Med,1997;102: 284-93. 102284  1997  [PubMed]
 
John JF Jr, Fishman NO. Programmatic role of the infectious diseases physician in controlling antimicrobial costs in the hospital. Clin Infect Dis,1997;24: 471-85. 24471  1997  [PubMed]
 
Murray BE. Vancomycin-resistant enterococcal infections. N Engl J Med,2000;342: 710-21. 342710  2000  [PubMed]
 
Moellering RC. Enterococcus species, Streptococcus bovis, and Leuconostoc species. In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone; 2000. p 2147-56. 
 
Moellering RC Jr. Vancomycin-resistant enterococci. Clin Infect Dis,1998;26: 1196-9. 261196  1998  [PubMed]
 
Lew DP,Waldvogel FA. Osteomyelitis. N Engl J Med,1997;336: 999-1007. 336999  1997  [PubMed]
 
Sapico FL. Microbiology and antimicrobial therapy of spinal infections. Orthop Clin North Am,1996;27: 9-13. 279  1996  [PubMed]
 
Lipsky BA. Osteomyelitis of the foot in diabetic patients. Clin Infect Dis,1997;25: 1318-26. 251318  1997  [PubMed]
 
Goldenberg DL. Septic arthritis. Lancet,1998;351: 197-202. 351197  1998  [PubMed]
 
Smith JW,Piercy EA. Infectious arthritis. Clin Infect Dis,1995;20: 225-30. 20225  1995  [PubMed]
 
Steckelberg JM, Osmon DR. Prosthetic joint infection. In: Waldvogel FA, Bisno AL, editors. Infections associated with indwelling medical devices. 3rd ed. Washington, DC: ASM Press; 2000. p 173-209. 
 
Ryan MJ, Kavanagh R, Wall PG,Hazleman BL. Bacterial joint infections in England and Wales: analysis of bacterial isolates over a four year period. Br J Rheumatol,1997;36: 370-3. 36370  1997  [PubMed]
 
Patzakis MJ, Wilkins J, Kumar J, Holtom P, Greenbaum B,Ressler R. Comparison of the\ results of bacterial cultures from multiple sites in chronic osteomyelitis of long bones. A prospective study. J Bone Joint Surg Am,1994;76: 664-6. 76664  1994  [PubMed]
 
Winston DJ, Emmanouilides C, Kroeber A, Hindler J, Bruckner DA, Territo MC,Busuttil RW. Quinupristin/dalfopristin therapy for infections due to vancomycin-resistant Enterococcus faecium. Clin Infect Dis,2000;30: 790-7. 30790  2000  [PubMed]
 
Lundstrom TS,Sobel JD. Antibiotics for gram-positive bacterial infections. Vancomycin, teicoplanin, quinupristin/dalfopristin, and linezolid. Infect Dis Clin North Am,2000;14: 463-74. 14463  2000  [PubMed]
 
Clemett D,Markham A. Linezolid. Drugs,2000;59: 815-27.. 59815  2000  [PubMed]
 
Linezolid (Zyvox). Med Lett Drugs Ther,2000;42: 45-6. 4245  2000  [PubMed]
 
Chien JW, Kucia ML,Salata RA. Use of linezolid, an oxazolidinone, in the treatment of multidrug-resistant gram-positive bacterial infections. Clin Infect Dis,2000;30: 146-51. 30146  2000  [PubMed]
 
Moellering RC, Linden PK, Reinhardt J, Blumberg EA, Bompart F,Talbot GH. The efficacy and safety of quinupristin/dalfopristin for the treatment of infections caused by vancomycin-resistant Enterococcus faecium. Synercid Emergency-Use Study Group. J Antimicrob Chemother,1999;44: 251-61. 44251  1999  [PubMed]
 
Nosocomial enterococci resistant to vancomycin—United States, 1989-1993. MMWR Morb Mortal Wkly Rep,1993;42: 597-9. 42597  1993  [PubMed]
 
French GL. Enterococci and vancomycin resistance. Clin Infect Dis,1998;27 Suppl 1: 75-83. 27 Suppl 175  1998 
 
Garbutt JM, Ventrapragada M, Littenberg B,Mundy LM. Association between resistance to vancomycin and death in cases of Enterococcus faecium bacteremia. Clin Infect Dis,2000;30: 466-72. 30466  2000  [PubMed]
 
Bhavnani SM, Drake JA, Forrest A, Deinhart JA, Jones RN, Biedenbach DJ,Ballow CH. A nationwide, multicenter, case-control study comparing risk factors, treatment, and outcome for vancomycin-resistant and -susceptible enterococcal bacteremia. Diagn Microbiol Infect Dis,2000;36: 145-58.. 36145  2000  [PubMed]
 
Stosor V, Peterson LR, Postelnick M,Noskin GA. Enterococcus faecium bacteremia: does vancomycin resistance make a difference?. Arch Intern Med,1998;158: 522-7.. 158522  1998  [PubMed]
 
Dever LL, China C, Eng RH, O’Donovan C,Johanson WG Jr. Vancomycin-resistant Enterococcus faecium in a Veterans Affairs Medical Center: association with antibiotic usage. Am J Infect Control,1998;26: 40-6. 2640  1998  [PubMed]
 
Linden PK,Miller CB. Vancomycin-resistant enterococci: the clinical effect of a common nosocomial pathogen. Diagn Microbiol Infect Dis,1999;33: 113-20. 33113  1999  [PubMed]
 
Carmeli Y, Samore MH,Huskins C. The association between antecedent vancomycin treatment and hospital-acquired vancomycin-resistant enterococci: a meta-analysis. Arch Intern Med,1999;159: 2461-8. 1592461  1999  [PubMed]
 
Montecalvo MA, Jarvis WR, Uman J, Shay DK, Petrullo C, Rodney K, Gedris C, Horowitz HW,Wormser GP. Infection-control measures reduce transmission of vancomycin-resistant enterococci in an endemic setting. Ann Intern Med,1999;131: 269-72. 131269  1999  [PubMed]
 
Noble WC, Virani Z,Cree RG. Co-transfer of vancomycin and other resistance genes from Enterococcus faecalis NCTC 12201 to Staphylococcus aureus. FEMS Microbiol Lett,1992;72: 195-8. 72195  1992  [PubMed]
 
Leclercq R, Derlot E, Weber M, Duval J,Courvalin P. Transferable vancomycin and teicoplanin resistance in Enterococcus faecium. Antimicrob Agents Chemother,1989;33: 10-5. 3310  1989  [PubMed]
 
Uttley AH, George RC, Naidoo J, Woodford N, Johnson AP, Collins CH, Morrison D, Gilfillan AJ, Fitch LE,Heptonstall J. High-level vancomycin-resistant enterococci causing hospital infections. Epidemiol Infect,1989;103: 173-8. 103173  1989  [PubMed]
 
Li JT, Markus PJ, Osmon DR, Estes L, Gosselin VA,Hanssen AD. Reduction of vancomycin use in orthopedic patients with a history of antibiotic allergy. Mayo Clin Proc,2000;75: 902-6. 75902  2000  [PubMed]
 
Hanssen AD,Osmon DR. The use of prophylactic antimicrobial agents during and after hip arthroplasty. Clin Orthop,1999;369: 124-38. 369124  1999  [PubMed]
 
Advisory statement. Antibiotic prophylaxis for dental patients with total joint replacements. American Dental Association; American Academy of Orthopaedic Surgeons. J Am Dent Assoc,1997;128: 1004-8. 1281004  1997  [PubMed]
 
Hope PG, Kristinsson KG, Norman P,Elson RA. Deep infection of cemented total hip arthroplasties caused by coagulase-negative staphylococci. J Bone Joint Surg Br,1989;71: 851-5. 71851  1989  [PubMed]
 
Ogston A. Micrococcus poisoning. J Anat Physiol,1882;17: 24-58. 1724  1882  [PubMed]
 
Classics in infectious diseases. "On abscesses". Alexander Ogston (1844-1929). Rev Infect Dis,1984;6: 122-8. 6122  1984  [PubMed]
 
Lowy FD. Staphylococcus aureus infections. N Engl J Med,1998;339: 520-32. 339520  1998  [PubMed]
 
Waldvogel FA. Staphylococcus aureus (including staphylococcal toxic shock). In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone; 2000. p 2069-92. 
 
von Eiff C, Becker K, Machka K, Stammer H,Peters G. Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med,2001;344: 11-16. 34411  2001  [PubMed]
 
Archer GL,Climo MW. Staphylococcus aureus bacteremia—consider the source [editorial]. N Engl J Med,2001;344: 55-6. 34455  2001  [PubMed]
 
Wenzel RP,Perl TM. The significance of nasal carriage of Staphylococcus aureus and the incidence of postoperative wound infection. J Hosp Infect,1995;31: 13-24. 3113  1995  [PubMed]
 
Archer GL. Staphylococcus epidermidis and other coagulase-negative staphylococci. In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone; 2000. p 2092-100. 
 
Ferevenza FC, Contreras GE, Garratt KN,Steckelberg JM. Staphylococcus lugdunensis endocarditis: a complication of vasectomy? . Mayo Clin Proc,1999;74: 1227-30. 741227  1999  [PubMed]
 
Sampathkumar P, Osmon DR,Cockerill FR 3rd. Prosthetic joint infection due to Staphylococcus lugdunensis. Mayo Clin Proc,2000;75: 511-2. 75511  2000  [PubMed]
 
Costerton JW, Stewart PS,Greenberg EP. Bacterial biofilms: a common cause of persistent infections. Science,1999;284: 1318-22. 2841318  1999  [PubMed]
 
Rupp ME,Archer GL. Coagulase-negative staphylococci: pathogens associated with medical progress. Clin Infect Dis,1994;19: 231-43. 19231  1994  [PubMed]
 
Pfaller MA, Jones RN, Doern GV,Kugler K. Bacterial pathogens isolated from patients with bloodstream infection: frequencies of occurrence and antimicrobial susceptibility patterns from the SENTRY antimicrobial surveillance program (United States and Canada, 1997). Antimicrob Agents Chemother,1998;42: 1762-70. 421762  1998  [PubMed]
 
Raad I, Alrahwan A,Rolston K. Staphylococcus epidermidis: emerging resistance and need for alternative agents. Clin Infect Dis,1998;26: 1182-7. 261182  1998  [PubMed]
 
Bahl D, Miller DA, Leviton I, Gialanella P, Wolin MJ, Liu W, Perkins R,Miller MH. In vitro activities of ciprofloxacin and rifampin alone and in combination against growing and nongrowing strains of methicillin-susceptible and methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother,1997;41: 1293-7. 411293  1997  [PubMed]
 
Drancourt M, Stein A, Argenson JN, Zannier A, Curvale G,Raoult D. Oral rifampin plus ofloxacin for treatment of Staphylococcus-infected orthopedic implants. Antimicrob Agents Chemother,1993;37: 1214-8. 371214  1993  [PubMed]
 
Drancourt M, Stein A, Argenson JN, Roiron R, Groulier P,Raoult D. Oral treatment of Staphylococcus spp. infected orthopaedic implants with fusidic acid or ofloxacin in combination with rifampicin. J Antimicrob Chemother,1997;39: 235-40. 39235  1997  [PubMed]
 
Hershberger E, Aeschlimann JR, Moldovan T,Rybak MJ. Evaluation of bactericidal activities of LY333328, vancomycin, teicoplanin, ampicillin-sulbactam, trovafloxacin, and RP59500 alone or in combination with rifampin or gentamicin against different strains of vancomycin-intermediate Staphylococcus aureus by time-kill curve methods. Antimicrob Agents Chemother,1999;43: 717-21. 43717  1999  [PubMed]
 
Norden CW. Experimental chronic staphylococcal osteomyelitis in rabbits: treatment with rifampin alone and in combination with other antimicrobial agents. Rev Infect Dis,1983;5 Suppl 3: 491-4. 5 Suppl 3491  1983 
 
Norden CW, Bryant R, Palmer D, Montgomerie JZ,Wheat J. Chronic osteomyelitis caused by Staphylococcus aureus: controlled clinical trial of nafcillin therapy and nafcillin-rifampin therapy. South Med J,1986;79: 947-51. 79947  1986  [PubMed]
 
Zimmerli W, Widmer AF, Blatter M, Frei R,Ochsner PE. Role of rifampin for treatment of orthopedic implant-related staphylococcal infections: a randomized controlled trial. Foreign-Body Infection (FBI) Study Group. JAMA,1998;279: 1537-41. 2791537  1998  [PubMed]
 
Zavasky DM,Sande MA. Reconsideration of rifampin: a unique drug for a unique infection [editorial]. JAMA,1998;279: 1575-7. 2791575  1998  [PubMed]
 
Quinupristin/dalfopristin. Med Lett Drugs Ther,1999;41: 109-10. 41109  1999  [PubMed]
 
Proctor RA,Peters G. Small colony variants in staphylococcal infections: diagnostic and therapeutic implications. Clin Infect Dis,1998;27: 419-22. 27419  1998  [PubMed]
 
Froggatt JW, Johnston JL, Galetto DW,Archer GL. Antimicrobial resistance in nosocomial isolates of Staphylococcus haemolyticus. Antimicrob Agents Chemother,1989;33: 460-6. 33460  1989  [PubMed]
 
Sieradzki K, Villari P,Tomasz A. Decreased susceptibilities to teicoplanin and vancomycin among coagulase-negative methicillin-resistant clinical isolates of staphylococci. Antimicrob Agents Chemother,1998;42: 100-7. 42100  1998  [PubMed]
 
Veach LA, Pfaller MA, Barrett M, Koontz FP,Wenzel PP. Vancomycin resistance in Staphylococcus haemolyticus causing colonization and bloodstream infection. J Clin Microbiol,1990;28: 2064-8. 282064  1990  [PubMed]
 
Schwalbe RS, Stapleton JT,Gilligan PH. Emergence of vancomycin resistance in coagulase-negative staphylococci. N Engl J Med,1987;316: 927-31. 316927  1987  [PubMed]
 
Reduced susceptibility of Staphylococcus aureus to vancomycin—-Japan, 1996. MMWR Morb Mortal Wkly Rep,1997;46: 624-6. 46624  1997  [PubMed]
 
Staphylococcus aureus with reduced susceptibility to vancomycin—-United States, 1997. MMWR Morb Mortal Wkly Rep,1997;46: 765-6. 46765  1997  [PubMed]
 
Hiramatsu K, Aritaka N, Hanaki H, Kawasaki S, Hosoda Y, Hori S, Fukuchi Y,Kobayashi I. Dissemination in Japanese hospitals of strains of Staphylococcus aureus heterogeneously resistant to vancomycin. Lancet,1997;350: 1670-3. 3501670  1997  [PubMed]
 
Paterson DL. Reduced susceptibility of Staphylococcus aureus to vancomycin—a review of current knowledge. Commun Dis Intell,1999;23: 69-73.. 2369  1999  [PubMed]
 
Sieradzki K, Roberts RB, Haber SW,Tomasz A. The development of vancomycin resistance in a patient with methicillin-resistant Staphylococcus aureus infection. N Engl J Med,1999;340: 517-23. 340517  1999  [PubMed]
 
Smith TL, Pearson ML, Wilcox KR, Cruz C, Lancaster MV, Robinson-Dunn B, Tenover FC, Zervos MJ, Band JD, White E,Jarvis WR. Emergence of vancomycin resistance in Staphylococcus aureus. Glycopeptide-Intermediate Staphylococcus aureus Working Group. N Engl J Med,1999;340: 493-501.. 340493  1999  [PubMed]
 
Waldvogel FA. New resistance in Staphylococcus aureus [editorial]. N Engl J Med,1999;340: 556-7. 340556  1999  [PubMed]
 
Staphylococcus aureus with reduced susceptibility to vancomycin—Illinois, 1999. MMWR Morb Mortal Wkly Rep,2000;48: 1165-7. 481165  2000  [PubMed]
 
Laboratory capacity to detect antimicrobial resistance, 1998. MMWR Morb Mortal Wkly Rep,2000;48: 1167-71. 481167  2000  [PubMed]
 
Edmond MB, Wenzel RP,Pasculle AW. Vancomycin-resistant Staphylococcus aureus: perspectives on measures needed for control. Ann Intern Med,1996;124: 329-34. 124329  1996  [PubMed]
 
Reagan DR, Doebbeling BN, Pfaller MA, Sheetz CT, Houston AK, Hollis RJ,Wenzel RP. Elimination of coincident Staphylococcus aureus nasal and hand carriage with intranasal application of mupirocin calcium ointment. Ann Intern Med,1991;114: 101-6. 114101  1991  [PubMed]
 
Gernaat-van der Sluis AJ, Hoogenboom-Verdegaal AM, Edixhoven PJ,Spies-van Rooijen NH. Prophylactic mupirocin could reduce orthopedic wound infections. 1,044 patients treated with mupirocin compared with 1,260 historical controls. Acta Orthop Scand,1998;69: 412-4. 69412  1998  [PubMed]
 
Hudson IR. The efficacy of intranasal mupirocin in the prevention of staphylococcal infections: a review of recent experience. J Hosp Infect,1994;27: 81-98. 2781  1994  [PubMed]
 
Kluytmans JA, Mouton JW, Ijzerman EP, Vandenbroucke-Grauls CM, Maat AW, Wagenvoort JH,Verbrugh HA. Nasal carriage of Staphylococcus aureus as a major risk factor for wound infections after cardiac surgery. J Infect Dis,1995;171: 216-9. 171216  1995  [PubMed]
 
Fattom AI, Naso R. Staphylococcal vaccines: a realistic dream. Ann Med,1996;28: 43-6. 2843  1996  [PubMed]
 
Accreditation Statement
These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
CME Activities Associated with This Article
Submit a Comment
Please read the other comments before you post yours. Contributors must reveal any conflict of interest.
Comments are moderated and will appear on the site at the discretion of JBJS editorial staff.

* = Required Field
(if multiple authors, separate names by comma)
Example: John Doe




Related Articles
Related Cases
Related Content
Topic Collections
Related Audio and Videos
PubMed Articles
Genetic basis for in vivo daptomycin resistance in enterococci.
The New England journal of medicine: Issue date- 2011 Sep 8
Intervention to reduce transmission of resistant bacteria in intensive care.
The New England journal of medicine: Issue date- 2011 Apr 14
Clinical Trials
Readers of This Also Read...
jbjs jobs
12/22/2011
VA - Charleston Area Medical Center
12/22/2011
ME - Central Maine Medical Center
12/22/2011
Maine - Central Maine Medical Center