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ANTIBIOTICS IN
SURGERY
PRESENTER: WANJE M. YAMU
FACILITATOR:DR.MUSAU
OUTLINE
 Definitions
 Classification of Antibiotics
 Use of antibiotics in surgery
- Prophylactic
- Therapeutic
 Classification of Surgical Wounds
 Causes and Prevention of Wound Infection
 Indiscriminate Use of Antibiotics
 Toxicity of Antibiotics
DEFINITIONS
 An antibiotic is a substance that has the
ability to kill or inhibit the growth or spread of
a micro-organism.
 Antibiotics are products of various species of
fungi that suppress growth or kill other micro-
organisms
Def cont
• Antibacterial-is any substance that destroys bacteria or
suppresses their growth.
• Antimicrobial-is a general term for synthetic agents
like drugs, chemicals or other substances that either kill
or slow the growth of microorganisms.
-It can be antibacterial drugs , antiviral agents ,
antifungal agents or antiparasitic agents.
Antibiotic Classification
a)mechanism of action
1.Cell wall synthesis inhibitors(inhibit
Peptidoglycan synthesis)
B-lactams-penicillins, cephalosporins,
carbapenems
Others-vancomycin, bacitracin
2. Protein synthesis inhibitors (interfere with 50s or
30s of rRNA)
Tetracyclines, aminoglycosides, macrolides,
Chloramphenicol,clindamycin
3. Folate antagonists(Sulphonamides)
Inhibit folate synthesis or reduction
e.g sulfamethoxazole, trimethoprim
4.Quinolones
DNA gyrase inhibitors
e.g levofloxacin, ciprofloxacin
5. Nitroimidazole e.g metronidazole
6. RNA polymerase inhibitor e.g Rifampicin
Classif Contd;
b)Mode of Action
•Bactericidal: Kill the micro-organism
•Bacteriostatic: Retard the growth/spread of the organism
Bacteriostatic Bactericidal
 Chloramphenicol Penicillins
 tetracyclines Aminoglycosides
 macrolides Cephalosporins
 Sulfonamide Quinolones
 clindamycin Metronidazole
Classifi Cont;
c) Based on Spectrum of Activity
- Narrow spectrum
- Extended spectrum
- Broad spectrum
Selection of antibiotics
• Requires knowledge of
-The organism involved and its sensitivity to a particular agent.
-The site of infection(CNS, bone, GIT, GUT)
-The safety of the agent.
-Patient factors e.g age, pregnancy, systemic illnesses,
hypersensitivity
-Availability, accessibility, affordability of the drug
NORMAL FLORA IN A NORMAL PERSON
IN THE COMMUNITY
ANATOMICAL SITE NORMAL FLORA
SKIN Staphylococcus, streptococcus,
propionibacteria
ORAL CAVITY ABOVE +, anaerobes (Actinomyces,
Bacteroides, Peptostreptococcus,
Fusobacterium, lactobacillus,
propionibacterium) & gram –ve rods
NASOPHARYNX Staph., strep., H. influenza & anaerobes
THORAX Staph, strep., & propionibacteria
GIT Flora of the nasopharynx+
enterobacteriaceae, Lactobacillus, candida
sp
URINARY TRACT Normally sterile
FEMALE GENITAL TRACT Lactobacillus sp.,strep. agalactiae
LIMBS Staph., strep., propionibacteria
A PERSON IN A HOSPITAL/ LONG-
TERM CARE FACILITY
UPPER
RESPIRATORY
TRACT
staph sp., anaerobes, Enterobacteriaceae (E. coli, klebsiella),
candida sp., pseudomonas sp.
SKIN Staph sp., Enterobacteriaceae
GIT Anaerobes , enterococcus sp( E. faecalis, E. faecium),
enterobacteriaceae( E. coli, klebsiella, salmonella, shigella),
candida sp., pseudomonas
GENITAL TRACT Candida species
ANTIBIOTICS FOR SURGICAL
PROPHYLAXIS
 Surgical antibiotic prophylaxis is defined as the use of antibiotics to
prevent anticipated infection at the surgical site.
 Indications for prophylaxis
 contaminated (risk of infection is 15%)and clean-contaminated (risk of
infection is 6%) wounds
 Clean wound in which implants or prosthesis are inserted
 Animal or human bite
 Open fracture
 Delay to cleaning >6 hrs
 Foot/hand wounds
 Wound length >5cm
 Crush injuries
 Wound involving body cavity/perineum
 Immunosuppressed pts
 Burns
NOTE: In our set up, every patient going to theatre has to be given prophylactic
antibiotics because of the high risk of infections/ bacterial contamination prior to
surgery.
Principles of Antibiotics Prophylaxis in
Surgery
1. Timing- within 30 min-1 hr of making incision; often during
induction of anesthesia- so that adequate blood and tissue levels are
present at the time skin incision is made.
Timing is dependent on the half life of the antibiotic used; most of the
times it falls within the above range.
2.Mechanism/Mode of action- bactericidal preferred over bacteriostatic.
3. Spectrum- The antibiotic selected should only cover the likely
pathogens- narrowest antibacterial spectrum required
Principles of Prophylaxis Continued
4.Route- IV because of the need for fast onset
5.Duration- once STAT dose. Repeat dose once if
surgery takes longer than 4 hrs, when there is
contamination during operation or when there is
more than 1.5 L of blood loss.
6. Dosage- should be high dose( maximum dose)
Goals of Antibiotic Prophylaxis
1.Reduce the incidence of surgical site infections
2.Minimize the effect on the patient’s normal bacterial flora
3.Minimize adverse effects of antibiotics
4.Minimize the emergence of antibiotics resistant strains of
bacteria
PLEASE NOTE
• Antibiotic prophylaxis is not a substitute of aseptic technique.
GUIDELINES FOR SURGICAL
PROPHYLACTIC ANTIBIOTIC
PROCEDURE SUGGESTED ANTIBIOTIC
GI SURGERY IV ceftriaxone 1g + iv metronidazole
500mg
HERNIA REPAIR, BREAST(major excision),
BURNS
IV Cloxacillin 1g
VASCULAR OPERATION IV Ampicillin/ sulbactam 1.5 g
NEUROSURGERY IV Ceftriaxone 1g + iv metronidazole
500mg
UROLOGY IV amoxicillin/ clavulanate 1.2 g
Therapeutic Antibiotics
Given to fight infection that is already established
Principles Of Therapeutic Antibiotic Use
1. Establish a clinical diagnosis and the need for antibiotic use based on hx and physical
examination
2. Determine the urgency of the situation
- non- urgent: mild infection or chronic infection
- Urgent situation: suspected severe infection
3.Obtain appropriate clinical specimens for examination, culture and sensitivity
4. Remove barrier to cure thru
-debridement
-Incision & drainage
-Good wound care
5. Determine the most likely organism causing infection
-focus of infection – age
- epidemiologic features -prior culture data
6. Choose the best agent available to treat the pathogen.
7. Antibiotic combination can be considered to achieve synergism
8. Assess effectiveness of antibiotic therapy
-decrease in temp within 48 hrs after adm of antibiotics
-decrease in inflammatory markers like CRP( 25% from baseline)
within 24 hrs
9.Initial therapy may need to be modified after culture results.
Empirical Antibiotic Therapy
• Initiation of treatment before isolation of an organism.
• Empirical antibiotic use is mostly based on the doctor’s experience.
• When to start:
– When risk of surgical infection is high- based on underlying disease
process. (e.g. Perforated appendicitis).
– Significant contamination during surgery has occurred. e.g.
considerable spillage of colon contents
– In critically ill patients when potential site for infections has been
identified
– Severe sepsis or septic shock
• Usually is a short course (3-5 days)
• Stop if presence of a local site infection or systemic infection is not
identified.
Indications for empirical therapy
• Suspected or diagnosed infectious etiology
e.g. UTI, pneumonia, cellulitis
• Neutropenia or other immunocompromised
states
• Asplenia- due to the potential of
overwhelming post splenectomy infections
Indications for empirical therapy
Con’t
Abdominal trauma- 3rd gen cephalosporin(
ceftriaxone…)
Perforated viscus, peritonitis – 3rd gen
cephalosporins & flagyl
 Breast abscess (S.aureus)- cloxacillin
Mycotic pseudo aneurysm- cloxacillin
Prosthetic graft infection-3rd generation cephalosporin
Duration of therapy
• Should be long enough to prevent relapse yet not excessive as can increase side
effects and resistance
• Antibiotic use post-operatively normally takes 3-5 days. It is based on the
likelihood of infections after surgery.
• Factors such as decreasing WBC and lack of fever guide therapy
• For instance:
-Penetrating GI trauma without extensive contamination (12-24 hours)
-Perforated/gangrenous appendicitis (3-5 days)
-Peritoneal soilage due to perforated viscus with moderate degree of contamination
(5-7 days)
-Extensive peritoneal soilage/ immunocompromised host (7-14 days)
CLASSIFICATION OF SURGICAL
WOUNDS
1.CLEAN WOUND ( <5% infection rate)
-wound made under ideal operating condition
-No entry into hollow viscus i.e the oropharyngeal cavity, lumen of the respiratory, alimentary or
genitourinary tract.
-Inflammation is not encountered
-No break in sterile technique occurs
-Example: hernia repair, breast biopsy, thyroidectomy
2. CLEAN-CONTAMINATED .(2-8% Infxn rate)
-Hollow viscous entered without significant spillage
-no inflammation
-minor breaks in the aseptic technique
–Example: appendectomy, biliary tract
3.CONTAMINATED WOUND (15-20% infxn rate)
- includes open, fresh and traumatic wounds
-uncontrolled spillage from viscous
-operations with major breaks in the aseptic technique
- incisions encountering acute, non purulent inflammation e.g in cholecystitis or cystitis
-other examples: penetrating abd trauma, enterotomy during bowel obstruction, large tissue injuries
4. DIRTY WOUND( 30-40% infxn rate)
-Traumatic wounds ( >4 hrs old)
-untreated uncontrolled spillage
-severe inflammation
-perforated viscera or operations involving clinically evident infxns e.g pus in the wound
-wounds containing foreign bodies or devitalized tissue.
CAUSES OF WOUND INFECTION
• Combination of bacterial numbers and virulence that overcome local host
defenses.
• Bacterial factors:-
– Type of bacteria
– Numbers of inoculums ≥105.
– Toxins produced by pathogen
– Organism ability to resist phagocytosis and intra-cellular destruction
CAUSES OF WOUND INFECTION
cont
• Local wound factors:-
– Inhibition of local defense mechanisms
– Presence of foreign bodies
– Strangulation of tissues
– Presence of dead tissue, haematomas or seromas
CAUSES OF WOUND INFECTION cont.
Patient Factors:
• Very young and very old
• Reduced blood flow to wound – vascular disease, anemia
• Inhibition of cellular function – malignancy states, trauma
• Immunocompromised states
PREVENTION OF WOUND INFECTION
• Avoidance of bacterial contamination- aseptic technique
• Environmental factors: theatre design to limit airborne
contamination. Use of ultraviolet light for decontamination of
theatre, lamina flow of ventilation systems, limiting of traffic
within operating room.
• Sterilization techniques
Prevention of Wound Infection: Pre-
operative preparation of patient
• Pre-op shower using antibacterial soap- for elective cases
• Treatment of all cutaneous and any other infection before elective
procedures
• Hair removal – extensive hair removal should not be done. If needed (e.g
to prevent adherence of dressings), it should be done on the operating table
because minor skin injury enhances superficial bacterial colonisation.
• Skin preparation–adequate cleaning (5-7 min) using
chlorhexidine/povidine-iodine and draping (antimicrobial incision drape)
are vital.
Operating room team and discipline-
prevention of wound infections
• Wear clean scrub suits, cap and mask.
• Scrub hands and forearms with antimicrobial
soap
• Careful wearing of gowns and gloves
• Change punctured or torn gloves
Dangers of Indiscriminate Use of
Antibiotics
 Changes of normal flora of body --> overgrowth of
resistant organisms with development of drug
resistance
 - Masking serious infection without eradicating it (e.g.
abscess)
 - Direct Drug Toxicity
 - Alteration of individual and hospital bacterial ecology
 - Higher cost of treatment
 - False sense of security
Antibiotic resistance
 Resistance of a micro-organism to an antimicrobial agent to which it was
previously sensitive.
 Intrinsic – drug target is not present in the bacteria’s metabolic pathways
 Acquired- mutation, transfer of genetic material from the resistant to
susceptible organisms (plasmids, transposons, bacteriophages)
 Factors contributing to resistance
 Excess antibiotic use(over a long period)
 Incorrect use of broad spectrum agents
 Incorrect dosing
 Non compliance
Toxicity of commonly use
Antibiotics
References
• Medscape
• Bertram G. Katzung: basic and clinical
pharmacology, 9th Edition. Lange Medical
Books 2002
• Previous Slides
THANK YOU

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Antibiotics in surgery DR. SHILULI

  • 1. ANTIBIOTICS IN SURGERY PRESENTER: WANJE M. YAMU FACILITATOR:DR.MUSAU
  • 2. OUTLINE  Definitions  Classification of Antibiotics  Use of antibiotics in surgery - Prophylactic - Therapeutic  Classification of Surgical Wounds  Causes and Prevention of Wound Infection  Indiscriminate Use of Antibiotics  Toxicity of Antibiotics
  • 3. DEFINITIONS  An antibiotic is a substance that has the ability to kill or inhibit the growth or spread of a micro-organism.  Antibiotics are products of various species of fungi that suppress growth or kill other micro- organisms
  • 4. Def cont • Antibacterial-is any substance that destroys bacteria or suppresses their growth. • Antimicrobial-is a general term for synthetic agents like drugs, chemicals or other substances that either kill or slow the growth of microorganisms. -It can be antibacterial drugs , antiviral agents , antifungal agents or antiparasitic agents.
  • 5. Antibiotic Classification a)mechanism of action 1.Cell wall synthesis inhibitors(inhibit Peptidoglycan synthesis) B-lactams-penicillins, cephalosporins, carbapenems Others-vancomycin, bacitracin 2. Protein synthesis inhibitors (interfere with 50s or 30s of rRNA) Tetracyclines, aminoglycosides, macrolides, Chloramphenicol,clindamycin 3. Folate antagonists(Sulphonamides) Inhibit folate synthesis or reduction e.g sulfamethoxazole, trimethoprim 4.Quinolones DNA gyrase inhibitors e.g levofloxacin, ciprofloxacin 5. Nitroimidazole e.g metronidazole 6. RNA polymerase inhibitor e.g Rifampicin
  • 6.
  • 7. Classif Contd; b)Mode of Action •Bactericidal: Kill the micro-organism •Bacteriostatic: Retard the growth/spread of the organism Bacteriostatic Bactericidal  Chloramphenicol Penicillins  tetracyclines Aminoglycosides  macrolides Cephalosporins  Sulfonamide Quinolones  clindamycin Metronidazole
  • 8. Classifi Cont; c) Based on Spectrum of Activity - Narrow spectrum - Extended spectrum - Broad spectrum
  • 9. Selection of antibiotics • Requires knowledge of -The organism involved and its sensitivity to a particular agent. -The site of infection(CNS, bone, GIT, GUT) -The safety of the agent. -Patient factors e.g age, pregnancy, systemic illnesses, hypersensitivity -Availability, accessibility, affordability of the drug
  • 10. NORMAL FLORA IN A NORMAL PERSON IN THE COMMUNITY ANATOMICAL SITE NORMAL FLORA SKIN Staphylococcus, streptococcus, propionibacteria ORAL CAVITY ABOVE +, anaerobes (Actinomyces, Bacteroides, Peptostreptococcus, Fusobacterium, lactobacillus, propionibacterium) & gram –ve rods NASOPHARYNX Staph., strep., H. influenza & anaerobes THORAX Staph, strep., & propionibacteria GIT Flora of the nasopharynx+ enterobacteriaceae, Lactobacillus, candida sp URINARY TRACT Normally sterile FEMALE GENITAL TRACT Lactobacillus sp.,strep. agalactiae LIMBS Staph., strep., propionibacteria
  • 11. A PERSON IN A HOSPITAL/ LONG- TERM CARE FACILITY UPPER RESPIRATORY TRACT staph sp., anaerobes, Enterobacteriaceae (E. coli, klebsiella), candida sp., pseudomonas sp. SKIN Staph sp., Enterobacteriaceae GIT Anaerobes , enterococcus sp( E. faecalis, E. faecium), enterobacteriaceae( E. coli, klebsiella, salmonella, shigella), candida sp., pseudomonas GENITAL TRACT Candida species
  • 12. ANTIBIOTICS FOR SURGICAL PROPHYLAXIS  Surgical antibiotic prophylaxis is defined as the use of antibiotics to prevent anticipated infection at the surgical site.  Indications for prophylaxis  contaminated (risk of infection is 15%)and clean-contaminated (risk of infection is 6%) wounds  Clean wound in which implants or prosthesis are inserted  Animal or human bite  Open fracture
  • 13.  Delay to cleaning >6 hrs  Foot/hand wounds  Wound length >5cm  Crush injuries  Wound involving body cavity/perineum  Immunosuppressed pts  Burns NOTE: In our set up, every patient going to theatre has to be given prophylactic antibiotics because of the high risk of infections/ bacterial contamination prior to surgery.
  • 14. Principles of Antibiotics Prophylaxis in Surgery 1. Timing- within 30 min-1 hr of making incision; often during induction of anesthesia- so that adequate blood and tissue levels are present at the time skin incision is made. Timing is dependent on the half life of the antibiotic used; most of the times it falls within the above range. 2.Mechanism/Mode of action- bactericidal preferred over bacteriostatic. 3. Spectrum- The antibiotic selected should only cover the likely pathogens- narrowest antibacterial spectrum required
  • 15. Principles of Prophylaxis Continued 4.Route- IV because of the need for fast onset 5.Duration- once STAT dose. Repeat dose once if surgery takes longer than 4 hrs, when there is contamination during operation or when there is more than 1.5 L of blood loss. 6. Dosage- should be high dose( maximum dose)
  • 16. Goals of Antibiotic Prophylaxis 1.Reduce the incidence of surgical site infections 2.Minimize the effect on the patient’s normal bacterial flora 3.Minimize adverse effects of antibiotics 4.Minimize the emergence of antibiotics resistant strains of bacteria PLEASE NOTE • Antibiotic prophylaxis is not a substitute of aseptic technique.
  • 17. GUIDELINES FOR SURGICAL PROPHYLACTIC ANTIBIOTIC PROCEDURE SUGGESTED ANTIBIOTIC GI SURGERY IV ceftriaxone 1g + iv metronidazole 500mg HERNIA REPAIR, BREAST(major excision), BURNS IV Cloxacillin 1g VASCULAR OPERATION IV Ampicillin/ sulbactam 1.5 g NEUROSURGERY IV Ceftriaxone 1g + iv metronidazole 500mg UROLOGY IV amoxicillin/ clavulanate 1.2 g
  • 18. Therapeutic Antibiotics Given to fight infection that is already established
  • 19. Principles Of Therapeutic Antibiotic Use 1. Establish a clinical diagnosis and the need for antibiotic use based on hx and physical examination 2. Determine the urgency of the situation - non- urgent: mild infection or chronic infection - Urgent situation: suspected severe infection 3.Obtain appropriate clinical specimens for examination, culture and sensitivity 4. Remove barrier to cure thru -debridement -Incision & drainage -Good wound care
  • 20. 5. Determine the most likely organism causing infection -focus of infection – age - epidemiologic features -prior culture data 6. Choose the best agent available to treat the pathogen. 7. Antibiotic combination can be considered to achieve synergism 8. Assess effectiveness of antibiotic therapy -decrease in temp within 48 hrs after adm of antibiotics -decrease in inflammatory markers like CRP( 25% from baseline) within 24 hrs 9.Initial therapy may need to be modified after culture results.
  • 21. Empirical Antibiotic Therapy • Initiation of treatment before isolation of an organism. • Empirical antibiotic use is mostly based on the doctor’s experience. • When to start: – When risk of surgical infection is high- based on underlying disease process. (e.g. Perforated appendicitis). – Significant contamination during surgery has occurred. e.g. considerable spillage of colon contents – In critically ill patients when potential site for infections has been identified – Severe sepsis or septic shock • Usually is a short course (3-5 days) • Stop if presence of a local site infection or systemic infection is not identified.
  • 22. Indications for empirical therapy • Suspected or diagnosed infectious etiology e.g. UTI, pneumonia, cellulitis • Neutropenia or other immunocompromised states • Asplenia- due to the potential of overwhelming post splenectomy infections
  • 23. Indications for empirical therapy Con’t Abdominal trauma- 3rd gen cephalosporin( ceftriaxone…) Perforated viscus, peritonitis – 3rd gen cephalosporins & flagyl  Breast abscess (S.aureus)- cloxacillin Mycotic pseudo aneurysm- cloxacillin Prosthetic graft infection-3rd generation cephalosporin
  • 24. Duration of therapy • Should be long enough to prevent relapse yet not excessive as can increase side effects and resistance • Antibiotic use post-operatively normally takes 3-5 days. It is based on the likelihood of infections after surgery. • Factors such as decreasing WBC and lack of fever guide therapy • For instance: -Penetrating GI trauma without extensive contamination (12-24 hours) -Perforated/gangrenous appendicitis (3-5 days) -Peritoneal soilage due to perforated viscus with moderate degree of contamination (5-7 days) -Extensive peritoneal soilage/ immunocompromised host (7-14 days)
  • 25. CLASSIFICATION OF SURGICAL WOUNDS 1.CLEAN WOUND ( <5% infection rate) -wound made under ideal operating condition -No entry into hollow viscus i.e the oropharyngeal cavity, lumen of the respiratory, alimentary or genitourinary tract. -Inflammation is not encountered -No break in sterile technique occurs -Example: hernia repair, breast biopsy, thyroidectomy 2. CLEAN-CONTAMINATED .(2-8% Infxn rate) -Hollow viscous entered without significant spillage -no inflammation -minor breaks in the aseptic technique –Example: appendectomy, biliary tract
  • 26. 3.CONTAMINATED WOUND (15-20% infxn rate) - includes open, fresh and traumatic wounds -uncontrolled spillage from viscous -operations with major breaks in the aseptic technique - incisions encountering acute, non purulent inflammation e.g in cholecystitis or cystitis -other examples: penetrating abd trauma, enterotomy during bowel obstruction, large tissue injuries 4. DIRTY WOUND( 30-40% infxn rate) -Traumatic wounds ( >4 hrs old) -untreated uncontrolled spillage -severe inflammation -perforated viscera or operations involving clinically evident infxns e.g pus in the wound -wounds containing foreign bodies or devitalized tissue.
  • 27. CAUSES OF WOUND INFECTION • Combination of bacterial numbers and virulence that overcome local host defenses. • Bacterial factors:- – Type of bacteria – Numbers of inoculums ≥105. – Toxins produced by pathogen – Organism ability to resist phagocytosis and intra-cellular destruction
  • 28. CAUSES OF WOUND INFECTION cont • Local wound factors:- – Inhibition of local defense mechanisms – Presence of foreign bodies – Strangulation of tissues – Presence of dead tissue, haematomas or seromas
  • 29. CAUSES OF WOUND INFECTION cont. Patient Factors: • Very young and very old • Reduced blood flow to wound – vascular disease, anemia • Inhibition of cellular function – malignancy states, trauma • Immunocompromised states
  • 30. PREVENTION OF WOUND INFECTION • Avoidance of bacterial contamination- aseptic technique • Environmental factors: theatre design to limit airborne contamination. Use of ultraviolet light for decontamination of theatre, lamina flow of ventilation systems, limiting of traffic within operating room. • Sterilization techniques
  • 31. Prevention of Wound Infection: Pre- operative preparation of patient • Pre-op shower using antibacterial soap- for elective cases • Treatment of all cutaneous and any other infection before elective procedures • Hair removal – extensive hair removal should not be done. If needed (e.g to prevent adherence of dressings), it should be done on the operating table because minor skin injury enhances superficial bacterial colonisation. • Skin preparation–adequate cleaning (5-7 min) using chlorhexidine/povidine-iodine and draping (antimicrobial incision drape) are vital.
  • 32. Operating room team and discipline- prevention of wound infections • Wear clean scrub suits, cap and mask. • Scrub hands and forearms with antimicrobial soap • Careful wearing of gowns and gloves • Change punctured or torn gloves
  • 33. Dangers of Indiscriminate Use of Antibiotics  Changes of normal flora of body --> overgrowth of resistant organisms with development of drug resistance  - Masking serious infection without eradicating it (e.g. abscess)  - Direct Drug Toxicity  - Alteration of individual and hospital bacterial ecology  - Higher cost of treatment  - False sense of security
  • 34. Antibiotic resistance  Resistance of a micro-organism to an antimicrobial agent to which it was previously sensitive.  Intrinsic – drug target is not present in the bacteria’s metabolic pathways  Acquired- mutation, transfer of genetic material from the resistant to susceptible organisms (plasmids, transposons, bacteriophages)  Factors contributing to resistance  Excess antibiotic use(over a long period)  Incorrect use of broad spectrum agents  Incorrect dosing  Non compliance
  • 35. Toxicity of commonly use Antibiotics
  • 36. References • Medscape • Bertram G. Katzung: basic and clinical pharmacology, 9th Edition. Lange Medical Books 2002 • Previous Slides