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Long-Acting Lipoglycopeptides

GENERAL PRINCIPLES

Long-acting lipoglycopeptides are bactericidal antibiotics that inhibit bacterial cell wall biosynthesis, similar to vancomycin. Their spectrum of activity includes gram-positive aerobic pathogens only.

These agents are characterized by extremely long terminal half-lives and are currently FDA-approved for skin/soft tissue infections.

TREATMENT

• Dalbavancin (1500 mg single dose or 1000 mg IV on day 1 followed by 500 mg IV on day 8 to complete the course of therapy) has a terminal half-life of 346 hours. Dalbavancin is active against staphylococci (including MRSA), streptococci, and enterococci. Susceptibility to dalbavancin can be reliably inferred from vancomycin.

• Oritavancin (1200 mg IV administered once to complete therapy) has a terminal half-life of 245 hours. Oritavancin is active against staphylococci (including MRSA), streptococci, and enterococci (including VRE).

SPECIAL CONSIDERATIONS

Adverse events include nausea, diarrhea, vomiting, headache, dizziness, pruritus, and infusion-related reactions. In clinical trials, more dalbavancin-treated patients had alanine LFT elevation greater than three times the upper limit of normal than patients treated with a comparative agent. Dalbavancin may also cause acute kidney injury.

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Source: Ancha S., Auberle C., Cash D., Harsh M., Hickman J., Kounga C.. The Washington Manual of Medical Therapeutics, 37th edition, LWW, 2022. —1250p.. 1250
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