Clindamycin Antimicrobial Coverage
Clindamycin provides excellent coverage against anaerobic bacteria and gram-positive organisms, including most Staphylococcus aureus strains and streptococci, but has no activity against most gram-negative aerobic bacteria. 1
Spectrum of Activity
Gram-Positive Bacteria
- Staphylococcus aureus (methicillin-susceptible strains) 1
- Streptococcus pneumoniae (penicillin-susceptible strains) 1
- Streptococcus pyogenes (Group A Streptococcus) 1
- Staphylococcus epidermidis (methicillin-susceptible strains) 1
- Streptococcus agalactiae (Group B Streptococcus) 1
- Other streptococci (Group C, G) 2
- Streptococcus anginosus, mitis, and oralis 1
Anaerobic Bacteria
- Clostridium perfringens 1
- Peptostreptococcus anaerobius 1
- Fusobacterium species (F. necrophorum, F. nucleatum) 1
- Prevotella melaninogenica 1
- Bacteroides fragilis 3
- Actinomyces israelii 1
- Clostridium clostridioforme 1
- Eggerthella lenta 1
- Finegoldia (Peptostreptococcus) magna 1
- Micromonas (Peptostreptococcus) micros 1
- Prevotella bivia and intermedia 1
- Cutibacterium acnes 1
Key Clinical Applications
Clindamycin is indicated for treating serious infections caused by susceptible organisms in:
Skin and soft tissue infections 2
- Particularly effective against S. aureus and streptococcal infections
- Used for MRSA when susceptible 2
- Combined with penicillin for Group A streptococcal necrotizing fasciitis
- Suppresses toxin production in streptococcal toxic shock syndrome
Bone and joint infections 1
- Acute hematogenous osteomyelitis caused by S. aureus
- Adjunctive therapy in chronic bone/joint infections
Respiratory tract infections 1
- Pneumonia, empyema, lung abscess caused by anaerobes and susceptible streptococci
- Endometritis, tubo-ovarian abscess, pelvic inflammatory disease
- Often combined with gentamicin for polymicrobial coverage
Intra-abdominal infections 1
- Peritonitis and intra-abdominal abscesses caused by anaerobes
Important Limitations
No activity against:
Resistance concerns:
Pharmacology Highlights
- Mechanism of action: Inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S ribosomal subunit 1
- Bacteriostatic rather than bactericidal 1
- Excellent tissue penetration with wide distribution in body fluids and tissues 6
- Half-life: 2-3 hours in normal adults, allowing dosing at 6-8 hour intervals 6
- Metabolism: Predominantly by CYP3A4 with minor contribution from CYP3A5 7
Clinical Pearls
- Clindamycin is particularly valuable for its ability to suppress toxin production in streptococcal and staphylococcal infections 2
- When treating necrotizing fasciitis caused by Group A streptococci, clindamycin should be combined with penicillin for optimal efficacy 2
- For polymicrobial infections, clindamycin is often combined with agents effective against gram-negative bacteria (e.g., aminoglycosides, fluoroquinolones) 2
- The most significant adverse effect is Clostridioides difficile-associated diarrhea (pseudomembranous colitis) 1
Clindamycin remains a valuable antibiotic for treating serious gram-positive and anaerobic infections, particularly when beta-lactams cannot be used or when toxin suppression is desirable.