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ANTIBIOTICS IN
SURGERY
PRESENTED BY-
DR. NESAR AHMAD
MODERATOR-
DR. SIMEEN USMANI
D/O JARAHAT, AKTC, AMU
ANTIBIOTICS
• Antibiotic is any substance of natural, synthetic or
semi-synthetic origin which kill (bactericidal) or
inhibit (bacteriostatic) the growth of bacteria
NORMAL FLORA
Group/mechanism of Action
1- Cell wall synthesis inhibitors
(inh. Peptidoglycan synthesis)
B-lactam- Penicillins/Cephalosporins
others- vancomycin/ bacitracin
2- cause leakage from cell
membranes
Polypeptides- polymyxins
Colistin, Bacitracin
3- Protein synthesis inhibitors
(interfere with 50s or 30s of rRNA)
Tetracyclines , Aminoglycoside ,
Macrolides, chloramphenicol
clindamycin
4- Folate Antagonists
Inhibitor folate synthesis or
reduction
e.g. Sulphonamides,
Trimethoprim
5- DNA gyrase inhibitors Fluoroquinolones e.g.
ciprofloxacin, levofloxacin
6- Nitroimidazole e.g. metronidazole
7-RNA polymerase inhibitor e.g. Rifampicin
Mode of action
Bacteriostatic
• Chloramphenicol
• Tetracyclines
• Macrolides
• Sulphonamides
• Clindamycin
Bactericidal
• Penicillins,
• Aminoglycosides
• Cephalosporins
• Metronidazole
• quinolones
Principles of Antibiotics in
Surgery
• Indication (prophylaxis vs. therapeutic)
• Susceptibility vs. empirical
• Pharmacodynamics
• Pharmacokinetic
• Combination
• Cost
• Availability
• Monitoring
Antibiotics Prophylaxis in Surgery
• use of antibiotic to prevent anticipated infection.
• Single dose regime, based on the most common
organism, which is given at the time of induction to
ensure the minimum inhibitory concentration during
skin incision – reduces risk of surgical site infection
(SSI) and post op infection
• Usually a single dose is sufficient. A second dose may
be required in the following situations:
a. in prolonged operations or when there is
excessive blood loss
b. when there is contamination during operation
• Giving more than 1 or 2 doses postoperatively is
generally not advised.
• Prophylaxis is generally recommended for clean
contaminated and contaminated operations
• In clean operation prophylaxis is also indicated under
certain conditions i.e. where there is prosthesis
implanted, high risk perforation where infection is
catastrophic e.g. neurosurgery or cardiac surgery.
Indications for prophylaxis in
surgery
• Wounds
- Clean contaminated and contaminated wound
- Clean wound in which implants or prosthesis are inserted
- Animal or Human bite
- Open fracture
- Foot/ Hand wounds
- Wound length > 5cm
- Crush
- Wound involving body cavity/ perineum
- Immuno-suppressed patient
- Burns
Classification of Surgical Wound
Choice of antibiotic
• The choice of the antibiotic for prophylaxis is based on
several factors.
• Always ask the patient about a prior history of antibiotic
allergy, as beta-lactams are the commonest type of
antibiotics used in prophylaxis.
• A history of severe penicillin allergy (anaphylaxis,
angioedema) means that cephalosporins are also
contraindicated, as there is a small but significant risk of
crossreaction.
•It is important to select an antibiotic with the narrowest
antibacterial spectrum required, to reduce the emergence
of multi-resistant pathogens and also because broad
spectrum antibiotics may be required later if the patient
develops serious sepsis.
• The use of 'third generation' cephalosporins such as
ceftriaxone and cefotaxime should therefore be avoided in
surgical prophylaxis.
• Often several antibiotics are equal in terms of antibacterial
spectrum, efficacy, toxicity, and ease of administration If
so, the least expensive drug should be chosen
• Commonly used surgical prophylactic antibiotics
include:
• intravenous 'first generation' cephalosporins -
cephazolin or cephalothin
• intravenous gentamicin
• intravenous or rectal metronidazole (if anaerobic
infection is likely)
• oral tinidazole (if anaerobic infection is likely)
• intravenous flucloxacillin (if methicillin-susceptible
staphylococcal infection is likely)
• intravenous vancomycin (if methicillin-resistant
staphylococcal infection is likely).
GUIDELINES FOR SURGICAL
PROPHYLACTIC ANTIBIOTICS
PROCEDURE SUGGESTED ANTIBIOTIC
1. GI surgery
2. HBS surgery
IV Cefoperazone 1g PLUS IV
Metronidazole 500mg
1. Hernia repair with mesh
(includes laparoscopic repair)
2. Breast
(not recommended for minor excision)
3.Burns
IV Cloxacillin 1g
Vascular Operation IV Ampicillin/Sulbactam 1.5g
Neurosurgery IV Ceftriaxone 1g AND
IV Metronidazole 500mg
Urogenital IV Amoxycillin / clavulanate 1.2g
Route and timing of antibiotic
administration
• Oral or rectal antibiotics need to be given earlier to ensure
adequate tissue concentrations during surgery.
• Metronidazole suppositories are commonly used in bowel surgery
and must be given 2-4 hours before it begins.
• Topical antibiotics are not recommended, with the exceptions of
ophthalmic or burns surgery.
• Prophylactic antibiotics are usually given intravenously as a bolus on
induction of anaesthesia to ensure adequate tissue concentrations
at the time of surgical incision.
• Intramuscular antibiotics are less commonly used than intravenous
antibiotics. They are typically given at the time of pre-medication so
that peak tissue levels are attained at the most critical time, the
time of surgical incision.
Therapeutic Antibiotics
Therapeutic antibiotics is given to fight infection
that is already established.
1. Establish a Clinical Diagnosis and the need for Antibiotics base
on history and physical examination
2. Determine the Urgency of the situation
•Non-urgent situation: mild infection or chronic infection
•Urgent situation:- Suspected severe infection
3. Obtain an appropriate clinical specimens for examination, culture
and sensitivity
4. Remove barrier to cure by
- Debridement
- sequestrectomy
- I & D
- Good wound care
5. Determine the most likely organism causing the
infection
6. If multiple antibiotics are available to treat
pathogen,
choose the best agent
Prior antibiotic allergies
Antibiotic penetration
Potential side effects
Medical condition of the patient
7- Antibiotic combination can be considered to achieve
Synergism
8. Assess effectiveness of antibiotic therapy
- Clinical assessment –
↓ temperature - 48 hrs for BC antibiotics
3 - 4days for BS drugs
- Inflammatory markers – signif. ↓CRP < 25 % from the baseline
within 24 hrs.
- Contagiousness of patient –
BC 24 hrs.
BS 5 days
9. Initial therapy may need modification after culture results are
available
Modification not necessary if there is significant Relief of
symptoms
Narrow spectrum of antibiotics should be used (to decrease the
risk of colonization)
Therapeutic
Antibiotics:
PRINCIPLES
C&S
Combination Pharmaco-
dynamics
Host status
Prevent
resistance
Multiple
pathogens
Site of
infection
Synergism/
Additive
therapy
Definitive
Specific to organism
isolated in C & S
Empirical
Initiation of treatment prior
to determination of a firm
diagnosis
THERAPEUTIC
ANTIBIOTICS
EMPIRIC THERAPY
• When to start ?
• Risk of surgical infection is high - based on the underlying
disease process (e.g. perforated appendicitis) [prophylaxis
empiric]
• Significant contamination during surgery has occurred (e.g.
considerable spillage of colon contents)
• In critically ill patients – potential site of infection has been
identified
• Severe sepsis or septic shock
• Short course (3-5 days)
• Stop if the presence of a local site or systemic infection is not
revealed
Systemic Inflammatory Response
Syndrome (SIRS)
• Empiric antibiotics are not indicated for all
patients with SIRS
• Indications for antibiotic therapy include the
following:
• Suspected or diagnosed infectious etiology (e.g.
UTI, pneumonia, cellulitis)
• Neutropenia or other immunocompromised
states
• Asplenia - Due to the potential for
overwhelming postsplenectomy infection
• Abdominal trauma – 3rd generation
Cephalosporins, Cefuroxime, Augmentin, Unasyn
• Perforated viscus, Peritonitis - 3rd generation
Cephalosporins & Flagyl
• Breast abscess (S. aureus) – Cloxacillin
• Mycotic pseudoaneurysm – Cloxacillin
• Prostethic graft infection - 3rd generation
Cephalosporins
• MRSA - Vancomycin
DURATION OF THERAPY
• Duration should be long enough to prevent relapse yet
not excessive, as it can increase side effects and
resistance
• Factors such as decreasing trend of WBCs and lack of
fever guide the length of therapy
• The search for extra abdominal source of infection or a
residual /ongoing source of intra abdominal infection
should be sought
DURATION OF THERAPY
• Penetrating GI trauma without extensive contamination
• 12-24hours
• Perforated/gangrenous appendicitis
• 3-5days
• Peritoneal soilage due to perforated viscus with
moderate degrees of contamination
• 5-7days
• Extensive peritoneal soilage/immunocompromised host
• 7-14days
SIDE EFFECTS/TOXICITY
Antibiotic Side Effects
Penicillins • Allergy , diarrhoea
Cephalosporins • Allergy, thrombophlebitis
Aminoglycosides • Hearing loss
• Vertigo
• Renal dysfunction
Carbapenems • Seizures (Imipenem)
• Rashes
Macrolides • Prolonged QT interval
(Erythromycin)
• Hearing loss, • Jaundice
Clindamycin Diarrhoa/ rash
levofloxacin headache, dizziness or
lightheadedness.
ANTIBIOTIC RESISTANCE
• Resistance of a microorganism to an antimicrobial
agent to which it was previously sensitive
• Resistant organisms are able to withstand attack by
antimicrobial medicines so that standard treatments
become ineffective and infections persist and may
spread to others
ANTIBIOTIC RESISTANCE
Intrinsic/Natural resistance -
• Drug target is not present in the bacteria’s metabolic
pathways
e.g. Gram –ve bacilli are normally unaffected by
Penicillin G
Acquired resistance -
• Mutation – is a stable and heritable genetic change that
occurs spontaneously and randomly among
microorganisms
• Gene transfer (infectious resistance) - Transfer of genetic
material from resistant to susceptible organisms
(plasmids, bacteriophages)
Main factors contributing to resistance are:
• Excess antibiotic usage
• Incorrect use of broad spectrum agents
• Incorrect dosing
• Non compliance
Prevention of Drug resistance
1. No indiscreminate and inediquate or unduly
prolonged use of antibiotics should be made
2. Prefer rapidly acting and selective antibiotics
whenever possible
3. Use combination of antibiotics whenever prolonged
therapy is undertaken e.g. TB, HIV-AIDS
4. Infection by organisms notorious for developing
resistance, e.g. Staph.aureus, E.coli, M.Tuberculosis,
Proteus etc. must be treated
Common pathogens antibiotic
susceptibility
 SSI for a skin wound at any site:
1. Staph aureus - 90% remains sensitive to flucloxacillin,
macrolides and clindamycin.
2. Beta haemolytic streptococci - 90% remains sensitive to
penicillin, macrolides and clindamycin
 Head and neck surgery:
Oral anaerobes - 95% remains sensitive to metronidazole
and co-amoxyclav
Operations below the waist:
1. Anaerobes - 95% remains sensitive to metronidazole
and co-amoxyclav
2. E. coli and other entrobacteriaceae - Complex
resistance, but 90% remains sensitive to second
generation cephalosporins, gentamicin or beta lactam.
Insertion of prosthesis, graft or shunt:
1. Coagulase negative Staph - 90% remains sensitive to
flucloxacillin, clindamycin or microlides.
2. Staph aureus - 2/3 are MRSA but beta lactam
antibiotics are still appropriate.
Conclusion
• Prophylactic antibiotic should be given in clean
surgery which involves prosthetic implants, in clean-
contaminated and contaminated surgeries
• Prophylactic antibiotics should be administered within
1 hour prior to incision
• Therapeutic antibiotic should be started for dirty
wound
• Empirical therapy should be altered according to the
sensitivity of the culture
• Escalation and de-escalation of antibiotics should be
done based on clinical response and aided by culture
and sensitivity results
• Therapeutic drug monitoring is done in antibiotics
with narrow therapeutic range (Amikacin, Gentamycin,
Vancomycin)
• Allergic reactions include anaphylaxis, fever, rashes,
nephritis, granulocytopenia & hemolytic anemia are
possible side effects of Penicillins and Cephalosporins
• Appropriate choice of antibiotics, dosage, compliance
should be ensured to avoid emergence of resistance
Thanks all for
listening

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Antibiotics in surgery Dr Nesar Ahmad, AKTC, AMU

  • 1.
  • 2. ANTIBIOTICS IN SURGERY PRESENTED BY- DR. NESAR AHMAD MODERATOR- DR. SIMEEN USMANI D/O JARAHAT, AKTC, AMU
  • 3. ANTIBIOTICS • Antibiotic is any substance of natural, synthetic or semi-synthetic origin which kill (bactericidal) or inhibit (bacteriostatic) the growth of bacteria
  • 5. Group/mechanism of Action 1- Cell wall synthesis inhibitors (inh. Peptidoglycan synthesis) B-lactam- Penicillins/Cephalosporins others- vancomycin/ bacitracin 2- cause leakage from cell membranes Polypeptides- polymyxins Colistin, Bacitracin 3- Protein synthesis inhibitors (interfere with 50s or 30s of rRNA) Tetracyclines , Aminoglycoside , Macrolides, chloramphenicol clindamycin 4- Folate Antagonists Inhibitor folate synthesis or reduction e.g. Sulphonamides, Trimethoprim 5- DNA gyrase inhibitors Fluoroquinolones e.g. ciprofloxacin, levofloxacin 6- Nitroimidazole e.g. metronidazole 7-RNA polymerase inhibitor e.g. Rifampicin
  • 6.
  • 7.
  • 8. Mode of action Bacteriostatic • Chloramphenicol • Tetracyclines • Macrolides • Sulphonamides • Clindamycin Bactericidal • Penicillins, • Aminoglycosides • Cephalosporins • Metronidazole • quinolones
  • 9. Principles of Antibiotics in Surgery • Indication (prophylaxis vs. therapeutic) • Susceptibility vs. empirical • Pharmacodynamics • Pharmacokinetic • Combination • Cost • Availability • Monitoring
  • 10. Antibiotics Prophylaxis in Surgery • use of antibiotic to prevent anticipated infection. • Single dose regime, based on the most common organism, which is given at the time of induction to ensure the minimum inhibitory concentration during skin incision – reduces risk of surgical site infection (SSI) and post op infection
  • 11. • Usually a single dose is sufficient. A second dose may be required in the following situations: a. in prolonged operations or when there is excessive blood loss b. when there is contamination during operation • Giving more than 1 or 2 doses postoperatively is generally not advised.
  • 12. • Prophylaxis is generally recommended for clean contaminated and contaminated operations • In clean operation prophylaxis is also indicated under certain conditions i.e. where there is prosthesis implanted, high risk perforation where infection is catastrophic e.g. neurosurgery or cardiac surgery.
  • 13. Indications for prophylaxis in surgery • Wounds - Clean contaminated and contaminated wound - Clean wound in which implants or prosthesis are inserted - Animal or Human bite - Open fracture - Foot/ Hand wounds - Wound length > 5cm - Crush - Wound involving body cavity/ perineum - Immuno-suppressed patient - Burns
  • 15. Choice of antibiotic • The choice of the antibiotic for prophylaxis is based on several factors. • Always ask the patient about a prior history of antibiotic allergy, as beta-lactams are the commonest type of antibiotics used in prophylaxis. • A history of severe penicillin allergy (anaphylaxis, angioedema) means that cephalosporins are also contraindicated, as there is a small but significant risk of crossreaction.
  • 16. •It is important to select an antibiotic with the narrowest antibacterial spectrum required, to reduce the emergence of multi-resistant pathogens and also because broad spectrum antibiotics may be required later if the patient develops serious sepsis. • The use of 'third generation' cephalosporins such as ceftriaxone and cefotaxime should therefore be avoided in surgical prophylaxis. • Often several antibiotics are equal in terms of antibacterial spectrum, efficacy, toxicity, and ease of administration If so, the least expensive drug should be chosen
  • 17. • Commonly used surgical prophylactic antibiotics include: • intravenous 'first generation' cephalosporins - cephazolin or cephalothin • intravenous gentamicin • intravenous or rectal metronidazole (if anaerobic infection is likely) • oral tinidazole (if anaerobic infection is likely) • intravenous flucloxacillin (if methicillin-susceptible staphylococcal infection is likely) • intravenous vancomycin (if methicillin-resistant staphylococcal infection is likely).
  • 18. GUIDELINES FOR SURGICAL PROPHYLACTIC ANTIBIOTICS PROCEDURE SUGGESTED ANTIBIOTIC 1. GI surgery 2. HBS surgery IV Cefoperazone 1g PLUS IV Metronidazole 500mg 1. Hernia repair with mesh (includes laparoscopic repair) 2. Breast (not recommended for minor excision) 3.Burns IV Cloxacillin 1g Vascular Operation IV Ampicillin/Sulbactam 1.5g Neurosurgery IV Ceftriaxone 1g AND IV Metronidazole 500mg Urogenital IV Amoxycillin / clavulanate 1.2g
  • 19. Route and timing of antibiotic administration • Oral or rectal antibiotics need to be given earlier to ensure adequate tissue concentrations during surgery. • Metronidazole suppositories are commonly used in bowel surgery and must be given 2-4 hours before it begins. • Topical antibiotics are not recommended, with the exceptions of ophthalmic or burns surgery. • Prophylactic antibiotics are usually given intravenously as a bolus on induction of anaesthesia to ensure adequate tissue concentrations at the time of surgical incision. • Intramuscular antibiotics are less commonly used than intravenous antibiotics. They are typically given at the time of pre-medication so that peak tissue levels are attained at the most critical time, the time of surgical incision.
  • 20. Therapeutic Antibiotics Therapeutic antibiotics is given to fight infection that is already established.
  • 21. 1. Establish a Clinical Diagnosis and the need for Antibiotics base on history and physical examination 2. Determine the Urgency of the situation •Non-urgent situation: mild infection or chronic infection •Urgent situation:- Suspected severe infection 3. Obtain an appropriate clinical specimens for examination, culture and sensitivity 4. Remove barrier to cure by - Debridement - sequestrectomy - I & D - Good wound care
  • 22. 5. Determine the most likely organism causing the infection 6. If multiple antibiotics are available to treat pathogen, choose the best agent Prior antibiotic allergies Antibiotic penetration Potential side effects Medical condition of the patient 7- Antibiotic combination can be considered to achieve Synergism
  • 23. 8. Assess effectiveness of antibiotic therapy - Clinical assessment – ↓ temperature - 48 hrs for BC antibiotics 3 - 4days for BS drugs - Inflammatory markers – signif. ↓CRP < 25 % from the baseline within 24 hrs. - Contagiousness of patient – BC 24 hrs. BS 5 days 9. Initial therapy may need modification after culture results are available Modification not necessary if there is significant Relief of symptoms Narrow spectrum of antibiotics should be used (to decrease the risk of colonization)
  • 25. Definitive Specific to organism isolated in C & S Empirical Initiation of treatment prior to determination of a firm diagnosis THERAPEUTIC ANTIBIOTICS
  • 26. EMPIRIC THERAPY • When to start ? • Risk of surgical infection is high - based on the underlying disease process (e.g. perforated appendicitis) [prophylaxis empiric] • Significant contamination during surgery has occurred (e.g. considerable spillage of colon contents) • In critically ill patients – potential site of infection has been identified • Severe sepsis or septic shock • Short course (3-5 days) • Stop if the presence of a local site or systemic infection is not revealed
  • 27. Systemic Inflammatory Response Syndrome (SIRS) • Empiric antibiotics are not indicated for all patients with SIRS • Indications for antibiotic therapy include the following: • Suspected or diagnosed infectious etiology (e.g. UTI, pneumonia, cellulitis) • Neutropenia or other immunocompromised states • Asplenia - Due to the potential for overwhelming postsplenectomy infection
  • 28. • Abdominal trauma – 3rd generation Cephalosporins, Cefuroxime, Augmentin, Unasyn • Perforated viscus, Peritonitis - 3rd generation Cephalosporins & Flagyl • Breast abscess (S. aureus) – Cloxacillin • Mycotic pseudoaneurysm – Cloxacillin • Prostethic graft infection - 3rd generation Cephalosporins • MRSA - Vancomycin
  • 29. DURATION OF THERAPY • Duration should be long enough to prevent relapse yet not excessive, as it can increase side effects and resistance • Factors such as decreasing trend of WBCs and lack of fever guide the length of therapy • The search for extra abdominal source of infection or a residual /ongoing source of intra abdominal infection should be sought
  • 30. DURATION OF THERAPY • Penetrating GI trauma without extensive contamination • 12-24hours • Perforated/gangrenous appendicitis • 3-5days • Peritoneal soilage due to perforated viscus with moderate degrees of contamination • 5-7days • Extensive peritoneal soilage/immunocompromised host • 7-14days
  • 31. SIDE EFFECTS/TOXICITY Antibiotic Side Effects Penicillins • Allergy , diarrhoea Cephalosporins • Allergy, thrombophlebitis Aminoglycosides • Hearing loss • Vertigo • Renal dysfunction Carbapenems • Seizures (Imipenem) • Rashes Macrolides • Prolonged QT interval (Erythromycin) • Hearing loss, • Jaundice Clindamycin Diarrhoa/ rash levofloxacin headache, dizziness or lightheadedness.
  • 32. ANTIBIOTIC RESISTANCE • Resistance of a microorganism to an antimicrobial agent to which it was previously sensitive • Resistant organisms are able to withstand attack by antimicrobial medicines so that standard treatments become ineffective and infections persist and may spread to others
  • 33. ANTIBIOTIC RESISTANCE Intrinsic/Natural resistance - • Drug target is not present in the bacteria’s metabolic pathways e.g. Gram –ve bacilli are normally unaffected by Penicillin G Acquired resistance - • Mutation – is a stable and heritable genetic change that occurs spontaneously and randomly among microorganisms • Gene transfer (infectious resistance) - Transfer of genetic material from resistant to susceptible organisms (plasmids, bacteriophages)
  • 34. Main factors contributing to resistance are: • Excess antibiotic usage • Incorrect use of broad spectrum agents • Incorrect dosing • Non compliance
  • 35. Prevention of Drug resistance 1. No indiscreminate and inediquate or unduly prolonged use of antibiotics should be made 2. Prefer rapidly acting and selective antibiotics whenever possible 3. Use combination of antibiotics whenever prolonged therapy is undertaken e.g. TB, HIV-AIDS 4. Infection by organisms notorious for developing resistance, e.g. Staph.aureus, E.coli, M.Tuberculosis, Proteus etc. must be treated
  • 36. Common pathogens antibiotic susceptibility  SSI for a skin wound at any site: 1. Staph aureus - 90% remains sensitive to flucloxacillin, macrolides and clindamycin. 2. Beta haemolytic streptococci - 90% remains sensitive to penicillin, macrolides and clindamycin  Head and neck surgery: Oral anaerobes - 95% remains sensitive to metronidazole and co-amoxyclav
  • 37. Operations below the waist: 1. Anaerobes - 95% remains sensitive to metronidazole and co-amoxyclav 2. E. coli and other entrobacteriaceae - Complex resistance, but 90% remains sensitive to second generation cephalosporins, gentamicin or beta lactam. Insertion of prosthesis, graft or shunt: 1. Coagulase negative Staph - 90% remains sensitive to flucloxacillin, clindamycin or microlides. 2. Staph aureus - 2/3 are MRSA but beta lactam antibiotics are still appropriate.
  • 38. Conclusion • Prophylactic antibiotic should be given in clean surgery which involves prosthetic implants, in clean- contaminated and contaminated surgeries • Prophylactic antibiotics should be administered within 1 hour prior to incision • Therapeutic antibiotic should be started for dirty wound • Empirical therapy should be altered according to the sensitivity of the culture • Escalation and de-escalation of antibiotics should be done based on clinical response and aided by culture and sensitivity results
  • 39. • Therapeutic drug monitoring is done in antibiotics with narrow therapeutic range (Amikacin, Gentamycin, Vancomycin) • Allergic reactions include anaphylaxis, fever, rashes, nephritis, granulocytopenia & hemolytic anemia are possible side effects of Penicillins and Cephalosporins • Appropriate choice of antibiotics, dosage, compliance should be ensured to avoid emergence of resistance