KEY POINTS
- Clindamycin (Cleocin) is a lincosamide antibiotic, which inhibits protein synthesis in susceptible bacteria by binding to the 50S ribosomal subunit
- Available as injectable, oral and topical
- Typical oral dose is 150 to 450 mg per DOSE every 6 hrs
- Typical IV dose is 600 to 2,700 mg per DAY divided in 2 to 4 doses
- Has activity versus Gram positive organisms like Streptococcus species and Staphylococcus species
- Typically covers community-associated MRSA but not health care-associated MRSA
- Has activity versus anaerobic organisms, but not versus Clostridium difficile
- Not great for Bacteroides fragilis
- Has the ability to inhibit bacterial toxin synthesis
- At times added to other agents for this purpose in the treatment of necrotizing staphylococcal or streptococcal infections
- Commonly considered for use when a beta-lactam is not an option (e.g., penicillin allergy present)
- Has many uses, including surgical prophylaxis, skin and soft tissue infections, community acquired pneumonia and more
- Highly associated with Clostridium difficile infection
- Even has a U.S. Boxed Warning of: “Can cause severe and possibly fatal colitis”
- The D Test is use with clindamycin to test for inducible resistance in MRSA
Photo Credit: www.microbeonline.com (click the pic for their article)
RESOURCES
- IV Clindamycin Package Insert
- Oral Clindamycin Package Insert
- 2015 CDC STD Guideline
- IDSA Practice Guidelines
- Comparison of CA-MRSA and HA-MRSA
- Ways to Improve Insights into Clindamycin Pharmacology and Pharmacokinetics Tailored to Practice
- Clindamycin versus Trimethoprim–Sulfamethoxazole for Uncomplicated Skin Infections
- Increasing clindamycin resistance in group A streptococcus
- Clindamycin STAT Pearls