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VANCOMYCIN
Lakshmi Narayana M.
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• Introduction
• Mechanism of action
• Pharmacokinetics
• Indications
• Recommended dosing schedule
• contraindications
• Possible side effects
• Acquired resistance
Introduction • Vancomycin is an antibiotic used to treat a no. of
bacterial infections
• Vancomycin was first discovered in 1950 and was
approved by the Federal Drug and Agency (FDA) in
1958
• It is extracted from soil bacteria S. orientalis
• It is a glycopeptide antibiotic used to treat infections
caused by gram-positive bacteria
• Named vancomycin because it was going to vanquish
penicillinase producing S. aureus
Mechanism
of action
• Vancomycin acts by inhibiting proper cell wall
synthesis in Gram-positive bacteria
• InhibitCell wall synthesis by binding with ala-D-ala
• Inhibit trans glycosylase.
• Alter cell membrane permeability
• Cell become susceptible to lysis
Pharmacokinetics ABSORPTION:
– Vancomycin is poorly absorbed orally in GIT
– When given parenterally drug distributes widely into tissues
– Cmax 63mcg/ml.
– Tmax is 1h
DISTRIBUTION:
– 55% protein bound.
– Vd is 0.3 to 0.43 L/kg
– Distributes well into pleural ,pericardial synovial fluid.
ELIMINATION
– Intravenous: about 75% is excreted in urine by GFR (in 24
hours) as a unchanged.
– Mean half life is 4-6hours
– Oral: faeces
Indications
• Treatment of serious infections caused by susceptible
organisms resistant to penicillin's MRSA (methicillin-
resistant S. aureus)and MRSE (multidrug-resistant
Staphylococcus epidermidis)
• For treatment of infections caused by Gram-positive
microorganisms in patients with serious allergies to beta-
lactam antimicrobials
• Antibacterial prophylaxis for endocarditis following
certain procedures in penicillin-hypersensitive individuals
at high risk
• Vancomycin is considered a last resort medication for the
treatment of septicemia and lower respiratory tract, skin,
and bone infections caused by Gram-positive bacteria
• Vancomycin has been the gold standard for treating
hospital acquired infections such as: ventilator associated
pneumonia, Bacteremia (septicemia), Catheter associated
urinary tract infection, Central line associated blood
stream infections, Surgical site infections (SSI)
Recommended
dosing
schedule
• ≥ 1 month – 6 years: 40mg/kg/day divided every 6
hours
• > 6 years – 18 years: 40mg/kg/day divided every 8
hours
• > 18 years: 15mg/kg/dose every 12 hours
• Uncomplicated Infections: 10-15 mg/kg q12h1
• Serious Infections:Consider loading dose of 25mg/kg
iv, followed by 15-20 mg/kg 8-12h (45-60mg/kg/day
divided 12h or 8h)
Contraindications • Hypersensitive to drug.
• Caution if renal impairment
• Caution if concurrent nephrotoxic agent use
• Caution if hearing impairment
• Caution if concurrent ototoxic agent use
• Caution in elderly pts
• PregnancyCategory C for parenteral route
• May use while breastfeeding;
Patients with Renal disease, inflammatory bowel
disorders may have an increased chance of adverse
effects
Possible
side effects
• Fever
• Chills
• Flushing
• Phlebitis
• Ototoxicity**
• Nephrotoxicity**
• Rapid iv infusion may cause diffuse flushing (red man
syndrome)**
• Anaphylaxis/anaphylactoid reaction (Allergy)
Acquired
resistance
• The alteration to the terminal amino acid residues of the
NAM/NAG-peptide subunits, under normal conditions, D-
ala-D-ala, to which vancomycin binds.This loss of just one
point of interaction results in a 1000-fold decrease in
affinity
• Three main resistance variants have been characterised to
date among resistant Enterococcus faecium and E.
faecalis populations:
 VanA - enterococcal resistance to vancomycin
and teicoplanin; inducible on exposure to these
agents
 VanB - lower-level enterococcal resistance; inducible
by vancomycin, but strains may remain susceptible to
teicoplanin
 VanC - least clinically important; enterococci resistant
only to vancomycin; constitutive resistance
Bullet points • Helpful in MRSA (methicillin-resistant S. aureus)and
MRSE (multidrug-resistant Staphylococcus epidermidis)
• A last resort medication for the treatment of
septicemia and lower respiratory tract, skin, and bone
infections caused by Gram-positive bacteria
• Gold standard for hospital acquired diseases.
Vancomycin

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Vancomycin

  • 2. Now you follow… • Introduction • Mechanism of action • Pharmacokinetics • Indications • Recommended dosing schedule • contraindications • Possible side effects • Acquired resistance
  • 3. Introduction • Vancomycin is an antibiotic used to treat a no. of bacterial infections • Vancomycin was first discovered in 1950 and was approved by the Federal Drug and Agency (FDA) in 1958 • It is extracted from soil bacteria S. orientalis • It is a glycopeptide antibiotic used to treat infections caused by gram-positive bacteria • Named vancomycin because it was going to vanquish penicillinase producing S. aureus
  • 4. Mechanism of action • Vancomycin acts by inhibiting proper cell wall synthesis in Gram-positive bacteria • InhibitCell wall synthesis by binding with ala-D-ala • Inhibit trans glycosylase. • Alter cell membrane permeability • Cell become susceptible to lysis
  • 5. Pharmacokinetics ABSORPTION: – Vancomycin is poorly absorbed orally in GIT – When given parenterally drug distributes widely into tissues – Cmax 63mcg/ml. – Tmax is 1h DISTRIBUTION: – 55% protein bound. – Vd is 0.3 to 0.43 L/kg – Distributes well into pleural ,pericardial synovial fluid. ELIMINATION – Intravenous: about 75% is excreted in urine by GFR (in 24 hours) as a unchanged. – Mean half life is 4-6hours – Oral: faeces
  • 6. Indications • Treatment of serious infections caused by susceptible organisms resistant to penicillin's MRSA (methicillin- resistant S. aureus)and MRSE (multidrug-resistant Staphylococcus epidermidis) • For treatment of infections caused by Gram-positive microorganisms in patients with serious allergies to beta- lactam antimicrobials • Antibacterial prophylaxis for endocarditis following certain procedures in penicillin-hypersensitive individuals at high risk • Vancomycin is considered a last resort medication for the treatment of septicemia and lower respiratory tract, skin, and bone infections caused by Gram-positive bacteria • Vancomycin has been the gold standard for treating hospital acquired infections such as: ventilator associated pneumonia, Bacteremia (septicemia), Catheter associated urinary tract infection, Central line associated blood stream infections, Surgical site infections (SSI)
  • 7. Recommended dosing schedule • ≥ 1 month – 6 years: 40mg/kg/day divided every 6 hours • > 6 years – 18 years: 40mg/kg/day divided every 8 hours • > 18 years: 15mg/kg/dose every 12 hours • Uncomplicated Infections: 10-15 mg/kg q12h1 • Serious Infections:Consider loading dose of 25mg/kg iv, followed by 15-20 mg/kg 8-12h (45-60mg/kg/day divided 12h or 8h)
  • 8. Contraindications • Hypersensitive to drug. • Caution if renal impairment • Caution if concurrent nephrotoxic agent use • Caution if hearing impairment • Caution if concurrent ototoxic agent use • Caution in elderly pts • PregnancyCategory C for parenteral route • May use while breastfeeding; Patients with Renal disease, inflammatory bowel disorders may have an increased chance of adverse effects
  • 9. Possible side effects • Fever • Chills • Flushing • Phlebitis • Ototoxicity** • Nephrotoxicity** • Rapid iv infusion may cause diffuse flushing (red man syndrome)** • Anaphylaxis/anaphylactoid reaction (Allergy)
  • 10. Acquired resistance • The alteration to the terminal amino acid residues of the NAM/NAG-peptide subunits, under normal conditions, D- ala-D-ala, to which vancomycin binds.This loss of just one point of interaction results in a 1000-fold decrease in affinity • Three main resistance variants have been characterised to date among resistant Enterococcus faecium and E. faecalis populations:  VanA - enterococcal resistance to vancomycin and teicoplanin; inducible on exposure to these agents  VanB - lower-level enterococcal resistance; inducible by vancomycin, but strains may remain susceptible to teicoplanin  VanC - least clinically important; enterococci resistant only to vancomycin; constitutive resistance
  • 11. Bullet points • Helpful in MRSA (methicillin-resistant S. aureus)and MRSE (multidrug-resistant Staphylococcus epidermidis) • A last resort medication for the treatment of septicemia and lower respiratory tract, skin, and bone infections caused by Gram-positive bacteria • Gold standard for hospital acquired diseases.