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Sepsis is a systemic disorder characterized by an inflammatory and immune-mediated response to infection. Aggressive and early fluid resuscitation, early antibiotic therapy, and source control are the cornerstones of sepsis management. See also Chapter 1, Resuscitation.
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Methicillin-Resistant Staphylococcus Aureus
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Methicillin-resistant Staphylococcus aureus (MRSA) was first recognized in the early 1960s shortly after the introduction of semisynthetic penicillins, such as methicillin. The mecA gene confers resistance to all β-lactam antibiotics such as methicillin, dicloxacillin, and many cephalosporins. MRSA infections are classified as either health care–associated MRSA (HA-MRSA) or community-associated MRSA (CA-MRSA). CA-MRSA strains have an additional Panton-Valentine leukocidin (PVL) toxin gene that allows production of necrotizing cytokines, increasing its invasiveness and virulence.
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HA-MRSA:
Hospital prevalence rates are as high as 60%.
Most common mode of transmission is patient-to-patient spread by health care workers with contaminated hands/gloves.
Risks for HA-MRSA include hospitalization, indwelling catheter, recent antibiotic therapy, and residence in a long-term care facility.
CA-MRSA:
Occurs primarily in the absence of health care exposure and often in otherwise healthy individuals.
Most common mode of transmission is skin-to-skin contact.
High-risk populations include day care attendees, athletes participating in contact sports, those living in close quarters (eg, military, prisoners), injection drug users and men having sex with men.
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KEY FACT
MRSA
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HA-MRSA: Most commonly presents as bacteremia or a device-associated infection.
CA-MRSA: Most common presentation is purulent (pus forming) skin/soft tissue infection.
Other presentations include necrotizing pneumonia, endocarditis, osteomyelitis (Figure 8.1).
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Suspect (and initiate treatment) based on risk factors and clinical presentation.
Gold standard is culture.
Polymerase chain reaction (PCR) is most accurate.
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HA-MRSA:
CA-MRSA:
Abscess: Incision and drainage (I&D) is the mainstay of therapy. Consider antibiotics for:
Abscess > 5 cm per or multiple lesions
Evidence of surrounding cellulitis
Associated comorbidities or immunosuppression such as diabetes or transplant patients
Systemic signs of infection
Lack of response to initial I&D
Trimethoprim-sulfamethoxazole, clindamycin, and doxycycline are typically safe in adults though each has its own side-effect profile.
Antibiotic choice should be guided whenever possible by a regional antibiogram.
Eradication of colonization: