Teicoplanin 

1. Introduction

Teicoplanin is a glycopeptide antibiotic used primarily against serious Gram-positive infections, especially when resistance or intolerance to β-lactams exists.

  • Give loading dose.
  • Do NOT use for Gram-negative sepsis.
  • Prefer in:
    • High vancomycin MIC
    • Vancomycin intolerance
    • Long-term therapy (osteomyelitis)

2. Classification

  • Bactericidal
  • Time-dependent killing
  • Concentration-dependent post-antibiotic effect (PAE)

Other glycopeptides:

  • Vancomycin
  • Telavancin
  • Dalbavancin
  • Oritavancin


3. Mechanism of Action 

Teicoplanin inhibits cell wall synthesis.

 Molecular Mechanism:

  • Prevents:
    • Transglycosylation
    • Transpeptidation
  • Blocks peptidoglycan cross-linking
  • Leads to bacterial cell death


4. Antimicrobial Spectrum

 Strong Activity Against:

  • MRSA
  • MSSA
  • Coagulase-negative staphylococci
  • Streptococci
  • Enterococci (not VRE)
  • Clostridium spp.
  • Corynebacterium

 No Activity Against:

  • Gram-negative bacteria
  • Anaerobic Gram-negatives
  • Atypicals

Not effective against VanA-type VRE.


5. Pharmacokinetics 

Parameter

Teicoplanin

Bioavailability (oral)

Poor (used IV/IM)

Volume of distribution

Good tissue penetration

Elimination

Renal

Dialyzable

Minimally

Clinical Implications:

  • Once daily dosing possible
  • Requires loading dose
  • Dose adjust in renal failure
  • Safe in hepatic dysfunction


6. Renal Failure Adjustment

CrCl

Adjustment

>60

Normal

30–60

Reduce frequency

<30

Extend interval

Hemodialysis

Give after dialysis


7. Therapeutic Drug Monitoring (TDM)

Not mandatory in mild infections but recommended in:

  • Endocarditis
  • Osteomyelitis
  • Bacteremia
  • Renal dysfunction
  • Obesity


8. Clinical Indications

  • MRSA Bacteremia
  • Infective Endocarditis,Often combined with gentamicin
  • Catheter-Related Bloodstream Infection
  • Bone & Joint Infection
  • Skin & Soft Tissue Infection
  • Peritonitis (PD-related)


9. Adverse Effects

 Common

  • Rash
  • Fever
  • Injection site pain

 Nephrotoxicity

  • Less than vancomycin but possible.
  • Ototoxicity-Rare.
  • Thrombocytopenia-Occasional.
  • Red Man Syndrome?Much rarer than vancomycin.


10. Resistance Mechanisms

  1. Altered D-Ala-D-Lac (VanA type)
  2. Thickened cell wall (VISA-like phenotype)
  3. Reduced penetration