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Rational use of Antibiotics
Voodoo or science?
Antibiotics
2nd
most commonly prescribed
drugs
Voodoo
 A patient with fever & deranged LFT, on
Magnex & Tinidazole, shifted to hospital
 Started on Cefaxone/Oflox/Ampi/Metro
 Switched to Aug/Pip.tazo/O/M
 Switched to Clinda/P.t/O & antimalarials
 All within 48 hours of admission &
with MP reported negative
Facts
 50% antibiotics are used inappropriately
 Majority of acute diarrhea and acute
bronchitis episodes are not due to bacterial
infection
 UGI bleed and seizures are not due to
bacterial infection
 Antibiotics do not treat the patient, antibiotics
treat bacterial infection
Antibiotics
 Penicillins
 Cephalosporins
 Carbapenems
 Monobactams
 Aminoglycosides
 Quinolones
 Macrolides
 Tetracyclines
 Vancomycin
 Linezolid
 Teicoplanin
 Clindamycin
 Co-trimoxazole
 Metronidazole
 Chloramphenicol
 Rifampicin
 Nitrofurantoin
 Topical antibiotics :
Mupirocin, Polymyxin-B,
Bacitracin, Neomycin
Questions
 Is it infection?
 Is it bacterial infection?
 If yes, take appropriate samples first
 What is likely etiologic agent?
 What antibiotic?
Empiric antibiotic
Choice depends on:
 Severity of infection
 Susceptibility of presumed bacteria
 Patient factors
 Drug factors
 Cost
Severity
Oral antibiotic
 Always prefer
 Relatively mild infection
 After response to parenteral antibiotic
 Lower cost
 Lesser side-effects
 Increased acceptance
contd.
Severity
Parenteral antibiotic
 Severe infection or critically ill patient
 Ineffective oral antibiotic
 Large dose required
 Ensure bioavailability-
 Poor GI absorption
 UGI distress
 Meningitis/Endocarditis
 Costlier, more side-effects
Susceptibility of bacteria
 Aerobic gram-positive-
 Oral: Amox, Clox, Cephalexin, Co-trimox.
 IV: 1st
/3rd
gen. Cephalo., Vancomycin
 Aerobic gram-negative-
 Oral: Co-trimox., Quinolones
 IV: 3rd
gen. Cephalo., Pip.tazo, Aztreonam
 Anaerobes
 Oral/IV: Metronidazole, Clindamycin
Antibacterial spectrum of antibiotics
 Predominantly Gram positive
 Clox, Pen. G, 1st
gen. Ceph., Clindamycin
Vancomycin, Linezolid, Teicoplanin
 Only Anaerobes
 Metronidazole, Clindamycin
 Only Gram negative
 Aminoglycosides, Cipro/Oflox, Aztreonam
 Broad spectrum
 Augmentin, 3rd
gen. Ceph., Pip.tazo, Levoflox, Imipenem,
Meropenem, Chloramphenicol
Empiric antibiotics
 Severe acute GE: Cipro./Co-trimox.
 Acute UTI : Co-trimox./Cipro.
 Acute bronchitis : Co-trimox./Doxy./Azithro.
 Sepsis: 3rd
Cephalo/Pip.tazo/Meropenem
add Aminoglycoside
 IV line infection: Vancomycin/Linezolid
Patient factors
 h/o allergy
 Pregnancy: avoid Aminoglycosides & Doxycycline
 Deranged LFT: dose adjustment of Ceftriaxone, Clindamycin,
Metronidazole
 Deranged RFT: dose adjustment of Aminoglycosides,
Quinolones, Co-trimox., Vancomycin, all beta-lactams
 Deranged RFT: no dose adjustment of Ceftriaxone, Azithro.,
Clinda., Doxy., Metro.
Drug factors
 Bactericidal: cell-wall active agents e.g. beta-
lactams, aminoglycosides, Vanco.
or DNA active agents e.g. Quinolones
 Bacteriostatic: inhibit protein synthesis
e.g.Macrolides, Co-trimox., Doxycycline, Clindamycin
 No difference in an immunocompetent host, but
bactericidal agents preferred in an
immunocompromised host or for
meningeal/endocardial/endovascular infections
 Aminoglycosides & Quinolones show concentration
dependent killing
Combination of antibiotics
 Multiple potential pathogens-
intra-abdominal abscess, diabetic foot infection,
aspiration pneumonia, neutropenic fever,
septic shock
 Synergism:
 Block sequential steps in metabolism- Co-trimox.
 Inhibition of enzyme activation- beta-lactam & beta
lactamase inhibitor
 Increase uptake- beta-lactams & aminoglycoside
 Decrease emergence of resistance:
Pseudomonas
Side-effects of drugs
 Ceftriaxone- cholecystitis
 Imipenem- seizures
 Vancomycin- Red man syndrome, mild nephrotoxicity
 Aminoglycosides- nephrotoxicity & ototoxicity
 Macrolides- UGI distress
 Clindamycin- GI distress, diarrhoea
 Doxycycline- phototoxicity, teeth discoloration
 Metronidazole- metallic taste, stomatitis,
seizures/encephalopathy with deranged LFT
 Co-trimoxazole- allergy, photosensitivity, raised Cr.
 Chloramphenicol- BM suppression, Grey baby syndrome
Cost x 5 days- oral & IV- Rs.
 Augmentin- 550
 Clindamycin- 360
 Linezolid- 750
 Ciprofloxacin- 90
 Ofloxacin- 50/95
 Levofloxacin- 360
 Cefuroxime- 360
 Augmentin- 2750
 Clindamycin- 1800
 Linezolid- 5000
 Ciprofloxacin-1000
 Ofloxacin- 1550
 Levofloxacin- 1000
 Cefuroxime- 1665
Better use of Antibiotics
 Use when required, i.e. do not use when not required
 Empiric antibiotics based on empiric bacteria & local
susceptibility profile
 Use only necessary & appropriate combination
 Newer doesn’t mean better
 Scale up/down based on lab. results
 Switch from IV to oral ASAP
 Drugs can cause fever & can change hematologic
parameters

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Rationaluseofantibiotics 150109060106-conversion-gate02

  • 1. Rational use of Antibiotics Voodoo or science?
  • 3. Voodoo  A patient with fever & deranged LFT, on Magnex & Tinidazole, shifted to hospital  Started on Cefaxone/Oflox/Ampi/Metro  Switched to Aug/Pip.tazo/O/M  Switched to Clinda/P.t/O & antimalarials  All within 48 hours of admission & with MP reported negative
  • 4. Facts  50% antibiotics are used inappropriately  Majority of acute diarrhea and acute bronchitis episodes are not due to bacterial infection  UGI bleed and seizures are not due to bacterial infection  Antibiotics do not treat the patient, antibiotics treat bacterial infection
  • 5. Antibiotics  Penicillins  Cephalosporins  Carbapenems  Monobactams  Aminoglycosides  Quinolones  Macrolides  Tetracyclines  Vancomycin  Linezolid  Teicoplanin  Clindamycin  Co-trimoxazole  Metronidazole  Chloramphenicol  Rifampicin  Nitrofurantoin  Topical antibiotics : Mupirocin, Polymyxin-B, Bacitracin, Neomycin
  • 6. Questions  Is it infection?  Is it bacterial infection?  If yes, take appropriate samples first  What is likely etiologic agent?  What antibiotic?
  • 7. Empiric antibiotic Choice depends on:  Severity of infection  Susceptibility of presumed bacteria  Patient factors  Drug factors  Cost
  • 8. Severity Oral antibiotic  Always prefer  Relatively mild infection  After response to parenteral antibiotic  Lower cost  Lesser side-effects  Increased acceptance contd.
  • 9. Severity Parenteral antibiotic  Severe infection or critically ill patient  Ineffective oral antibiotic  Large dose required  Ensure bioavailability-  Poor GI absorption  UGI distress  Meningitis/Endocarditis  Costlier, more side-effects
  • 10. Susceptibility of bacteria  Aerobic gram-positive-  Oral: Amox, Clox, Cephalexin, Co-trimox.  IV: 1st /3rd gen. Cephalo., Vancomycin  Aerobic gram-negative-  Oral: Co-trimox., Quinolones  IV: 3rd gen. Cephalo., Pip.tazo, Aztreonam  Anaerobes  Oral/IV: Metronidazole, Clindamycin
  • 11. Antibacterial spectrum of antibiotics  Predominantly Gram positive  Clox, Pen. G, 1st gen. Ceph., Clindamycin Vancomycin, Linezolid, Teicoplanin  Only Anaerobes  Metronidazole, Clindamycin  Only Gram negative  Aminoglycosides, Cipro/Oflox, Aztreonam  Broad spectrum  Augmentin, 3rd gen. Ceph., Pip.tazo, Levoflox, Imipenem, Meropenem, Chloramphenicol
  • 12. Empiric antibiotics  Severe acute GE: Cipro./Co-trimox.  Acute UTI : Co-trimox./Cipro.  Acute bronchitis : Co-trimox./Doxy./Azithro.  Sepsis: 3rd Cephalo/Pip.tazo/Meropenem add Aminoglycoside  IV line infection: Vancomycin/Linezolid
  • 13. Patient factors  h/o allergy  Pregnancy: avoid Aminoglycosides & Doxycycline  Deranged LFT: dose adjustment of Ceftriaxone, Clindamycin, Metronidazole  Deranged RFT: dose adjustment of Aminoglycosides, Quinolones, Co-trimox., Vancomycin, all beta-lactams  Deranged RFT: no dose adjustment of Ceftriaxone, Azithro., Clinda., Doxy., Metro.
  • 14. Drug factors  Bactericidal: cell-wall active agents e.g. beta- lactams, aminoglycosides, Vanco. or DNA active agents e.g. Quinolones  Bacteriostatic: inhibit protein synthesis e.g.Macrolides, Co-trimox., Doxycycline, Clindamycin  No difference in an immunocompetent host, but bactericidal agents preferred in an immunocompromised host or for meningeal/endocardial/endovascular infections  Aminoglycosides & Quinolones show concentration dependent killing
  • 15. Combination of antibiotics  Multiple potential pathogens- intra-abdominal abscess, diabetic foot infection, aspiration pneumonia, neutropenic fever, septic shock  Synergism:  Block sequential steps in metabolism- Co-trimox.  Inhibition of enzyme activation- beta-lactam & beta lactamase inhibitor  Increase uptake- beta-lactams & aminoglycoside  Decrease emergence of resistance: Pseudomonas
  • 16. Side-effects of drugs  Ceftriaxone- cholecystitis  Imipenem- seizures  Vancomycin- Red man syndrome, mild nephrotoxicity  Aminoglycosides- nephrotoxicity & ototoxicity  Macrolides- UGI distress  Clindamycin- GI distress, diarrhoea  Doxycycline- phototoxicity, teeth discoloration  Metronidazole- metallic taste, stomatitis, seizures/encephalopathy with deranged LFT  Co-trimoxazole- allergy, photosensitivity, raised Cr.  Chloramphenicol- BM suppression, Grey baby syndrome
  • 17. Cost x 5 days- oral & IV- Rs.  Augmentin- 550  Clindamycin- 360  Linezolid- 750  Ciprofloxacin- 90  Ofloxacin- 50/95  Levofloxacin- 360  Cefuroxime- 360  Augmentin- 2750  Clindamycin- 1800  Linezolid- 5000  Ciprofloxacin-1000  Ofloxacin- 1550  Levofloxacin- 1000  Cefuroxime- 1665
  • 18. Better use of Antibiotics  Use when required, i.e. do not use when not required  Empiric antibiotics based on empiric bacteria & local susceptibility profile  Use only necessary & appropriate combination  Newer doesn’t mean better  Scale up/down based on lab. results  Switch from IV to oral ASAP  Drugs can cause fever & can change hematologic parameters