What are the most frequent types of antibiotic resistance?
Which patients are at risk for infections with antibiotic-resistant organisms?
How are antibiotic-resistant organisms transmitted among patients?
What types of genes confer antibiotic resistance?
What types of isolation precautions exist, and when are they indicated?
Antibiotic resistance was described at the dawn of the antibiotic era. In Alexander Fleming's initial report of the antibacterial action of penicillin in 1929, he noted that it was usually inactive against enteric Gram-negative bacteria. In 1940, while engaged in isolating and purifying penicillin, Edward Abraham and Ernst Chain incidentally discovered that Escherichia coli produced penicillinase. While the global explosion and dissemination of antibiotic resistance in recent decades is alarming, perhaps it should not be too surprising. As most antibiotics are derived from substances produced by molds and bacteria to inhibit the growth of rival microorganisms, mechanisms of antibacterial resistance evolved before humans harnessed these compounds for medicinal use.
When antibiotics reduce populations of non-resistant organisms, resistant organisms are able to proliferate. Rates of invasive infections with drug-resistant bacteria increase after recent antibiotic exposure. Conversely, reduced use of antibiotics has been shown to decrease the prevalence of antibiotic-resistant organisms. Certain bacterial infections are now resistant to all antibiotics, with a limited number of promising antibiotics in the developmental pipeline.
Highly antibiotic-resistant organisms are usually thought of as exclusively hospital-acquired pathogens. However, community acquisition of resistant pathogens is on the rise, including methicillin-resistant Staphylococcus aureus (MRSA) and extended-spectrum beta-lactamase-producing Escherichia coli. This chapter reviews resistant bacteria of importance to the hospitalist, including the ESKAPE pathogens, for which there may be no effective drug therapy in the near future (Table 186-1).
Table 186-1 ESKAPE Pathogens: Multidrug-Resistant Bacteria Most Likely to Have No Effective Drug Therapy in the Immediate Future ||Download (.pdf)
Table 186-1 ESKAPE Pathogens: Multidrug-Resistant Bacteria Most Likely to Have No Effective Drug Therapy in the Immediate Future
- Enterococcus faecium (VRE)
- Staphylococcus aureus (MRSA)
- Klebsiella pneumoniae
- Acinetobacter baumannii
- Pseudomonas aeruginosa
- Enterobacter species
The medically important staphylococci may be divided into two main groups based on the rapid coagulase test, a measure of the ability of a staphylococcal colony to produce a clot in a tube of rabbit serum. Coagulase-negative staphylococci (principally Staphylococcus epidermidis) have little virulence aside from biofilm production, and generally only cause infections of medical devices, such as central venous catheters and joint prostheses. By contrast, Staphylococcus aureus (coagulase-positive) is innately pathogenic, and is one of the few bacteria that cause severe infection in both community and health care settings.
- A major strategy to reduce antibiotic resistance is to prescribe the narrowest spectrum antibiotic. For example, for documented methicillin-sensitive Staphylococcus aureus infection, preferred drugs for intravenous therapy are ...