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Antibiotics in ENT Surgery

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Antibiotics in ENT Surgery Magdy M. Amin RIAD Professor of Otolaryngology. Ain shames University Senior Lecturer in Otolaryngology University of Dundee – PowerPoint PPT presentation

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Title: Antibiotics in ENT Surgery


1
Antibiotics in ENT Surgery
  • Magdy M. Amin RIAD
  • Professor of Otolaryngology.
  • Ain shames University
  • Senior Lecturer in Otolaryngology
  • University of Dundee

2
Prophylactic antibiotics
  • Prophylaxis with antibiotics has decreased the
    high incidence of wound infection after head and
    neck operations that involve incisions through
    oral or pharyngeal mucosa.
  • Prophylactic administration of antibiotics can
    decrease postoperative morbidity, shorten
    hospitalization, and reduce overall costs
    attributable to infections.

3
Prophylactic antibiotics
  • Many antibiotics require a single dose given
    within 30 minutes of skin incision to provide
    adequate tissue concentration throughout the
    operation.
  • Additional doses during the procedure are
    advisable if surgery is prolonged (i. e, gt4 h),
    major blood loss occurs, or an antimicrobial with
    a short half-life is used

4
The aim of prophylaxis
  • The aim of prophylaxis is to augment host defense
    mechanisms at the time of bacterial invasion,.
  • Prophylaxis is an attempt to attack organisms
    before they have a chance to induce infection.
  • Previous surgery (i. e, scarring) and radiation
    injury decrease host defenses.
  • Likewise, certain medical conditions, such as
    diabetes mellitus or HIV, predispose the patient
    to infection because of diminished host response.

5
Choosing an antibiotic for prophylaxis
  • Choosing an antibiotic for prophylaxis is
    multi-factorial and should be based on the
    following
  • Type of operation
  • Kinetics and toxicity of the drugs
  • Microbiologic characteristics of the operative
    site
  • Antibiotic sensitivities specific to the
    particular hospital environment

6
Choosing an antibiotic for prophylaxis
  • If a number of drugs appear equally acceptable
    for prophylaxis, the agent least likely to be
    used for definitive therapy in postoperative
    wound infection should be chosen.
  • This strategy should minimize the selection of
    organisms resistant to valuable therapeutic
    agents.

7
Choosing an antibiotic for prophylaxis
  • The regimen chosen should be compatible with
    findings from the hospital's infection control
    wound surveillance report.
  • This regimen is particularly important in
    hospitals with high incidence of infection with
    methicillin-resistant organisms (eg, S aureus
    MRSA, S epidermidis MRSE) or with newly
    vancomycin-resistant organisms.

8
CLASSIFICATION OF OPERATIONClass Definition
  • Clean Operations
  • in which no inflammation is encountered .
  • The respiratory, alimentary or genitourinary
    tracts are not entered.
  • There is no break in aseptic operating theatre
    technique.

9
Non contaminated head and neck surgery
  • Non contaminated surgery refers to violation of
    prepared skin only and no mucosal exposure or
    incision (eg, neck dissection, parotidectomy,
    thyroidectomy).

10
Non contaminated head and neck surgery
  • Clean surgical procedures are those in which no
    infection exists prior to surgery.
  • During surgery, sterility of the wound is
    maintained.
  • Following closure of the wound at completion of
    surgery, the wound is never again exposed to
    direct contact with bacteria.
  • The risk of postoperative wound infection under
    these circumstances is less than 5.

11
CLASSIFICATION OF OPERATIONClass Definition
  • Clean-contaminated Operations
  • in which the respiratory, alimentary or
    genitourinary tracts are entered
  • but without significant spillage.

12
CLASSIFICATION OF OPERATIONClass Definition
  • Contaminated Operations
  • where acute inflammation (without pus) is
    encountered.
  • or where there is visible contamination of the
    wound.
  • Examples include gross spillage from a hollow
    viscus during the operation
  • or compound/open injuries operated on within four
    hours.

13
CLASSIFICATION OF OPERATIONClass Definition
  • Dirty Operations
  • In the presence of pus.
  • where there is a previously perforated hollow
    viscus,
  • or compound/open injuries more than four hours
    old.

14
PROBABILITY OF WOUND INFECTION BY TYPE OF WOUND
AND RISK INDEX
  • Risk
    Index
  • 0 1
    2
  • Clean 1.0 2.3
    5.4
  • Clean-contam. 2.1 4.0 9.5
  • Contaminated 3.4 6.8 13.2

15
ENT SURGERY
  • Head and neck surgery - A Antibiotic prophylaxis
    is recommended
  • Head and neck surgery - clean C Antibiotic
    prophylaxis is not recommended There is no
    evidence of effectiveness from RCTs
  • Ear surgery - clean A Antibiotic prophylaxis is
    not recommended There is no evidence of
    effectiveness from RCTs
  • Nose or sinus surgery C Antibiotic prophylaxis is
    not recommended There is evidence of no
    effectiveness from RCTs
  • Tonsillectomy C Antibiotic prophylaxis is not
    recommended There is no evidence of effectiveness
    of prophylaxis from RCTs. The cited trials are of
    treatment for seven days after tonsillectomy, not
    prophylaxis.

16
ADMINISTRATION OF INTRAVENOUS PROPHYLACTIC
ANTIBIOTICS
  • Prophylaxis should be started preoperatively in
    most circumstances
  • ideally within 30 minutes of the induction of
    anesthesia.

17
ADMINISTRATION OF INTRAVENOUS PROPHYLACTIC
ANTIBIOTICS
  • Antibiotic prophylaxis should be administered
    immediately before or during a procedure.
  • Prophylactic antibiotics should be administered
    intravenously.
  • The single dose of antibiotic for prophylactic
    use is, in most circumstances, the same as would
    be used therapeutically.

18
ADMINISTRATION OF INTRAVENOUS PROPHYLACTIC
ANTIBIOTICS
  • An additional dose of prophylactic agent is not
    indicated in adults, unless there is blood loss
    of up to 1500 ml during surgery or haemodilution
    of up to 15 ml/kg.
  • Fluid replacement bags should not be primed with
    prophylactic antibiotics because of the potential
    risk of contamination and calculation errors.

19
Duration of Perioperative Antibiotic Use
  • 1. Prophylactic perioperative antibiotics should
    be started prior to skin incision for maximal
    benefit.

20
Duration of Perioperative Antibiotic Use
  • 2. There is no advantage to continuation of
    perioperative antibiotics beyond 24 to 48 hours
    postoperatively has ever been demonstrated.

21
Duration of Perioperative Antibiotic Use
  • The possible exception to this is metronidazole
  • because metronidazole may enter abscess spaces
    better than other antibiotics.
  • its prolonged use has been associated with less
    severe postoperative infections in one study.

22
Prophylactic Antibiotic Regimens for Major
Clean-Contaminated
  • Clindamycin 600 mg IV within 1 hour of surgery,
    4 additional doses Q6H following surgery.
  • The antibiotic may alternatively be given for a
    full 48 hours postoperatively.
  • there is no compelling evidence that the
    additional 24 hours confers any additional
    benefit.

23
Prophylactic Antibiotic Regimens for Major
Clean-Contaminated
  • 2. Augmentine 1.5 grams IV within 1 hour of
    surgery .
  • and 8 additional doses at 6-hour intervals
    following surgery.

24
Prophylactic Antibiotic Regimens for Major
Clean-Contaminated
  • 3. Cefazolin 2.0 grams IV within 1 hour of
    surgery.
  • and 3 postoperative doses at 8-hour intervals.
  • This regimen may be extended to a total of 48
    hours postoperatively.

25
Prophylactic Antibiotic Regimens for Major
Clean-Contaminated
  • 4. Cefazolin/metronidazole cefazolin 1 gm IV 1
    hour prior to surgery
  • then 1 gram IV every 8 hours postoperatively
    for a total of 6 doses.
  • and metronidazole 900 mg IV 1 hour prior to
    surgery
  • then 900 mg IV every 8 hours postoperatively
    for a total of 6 doses.

26
ENT SURGERYAntibiotic prophylaxis is
recommended in
  • A Head and neck surgery (clean-contaminated/cont
    aminated)
  • Antibiotic prophylaxis is not recommended in
  • A Ear surgery (clean)
  • C Head and neck surgery (clean)
  • C Nose or sinus surgery
  • C Tonsillectomy

27
Contaminated head and neck surgery
  • Contaminated surgery refers to transmucosal
    operations (eg, composite resection, glossectomy,
    maxillectomy).
  • Saliva contains 108 bacteria per milliliter, 90
    of which are anaerobic. Ninety-six percent of
    wound infections in the head and neck are
    polymicrobial.

28
Contaminated head and neck surgery
  • Organisms involving oropharyngeal flora
    included
  • anaerobic organisms (Bacteroides, 76)
  • gram-negative rods (eg, Escherichia coli and
    Klebsiella, Serratia, and Proteus species)
  • gram-positive organisms (ie, Staphylococcus,
    Streptococcus).

29
Contaminated head and neck surgery
  • Clindamycin (600 mg PO/IV q8h for 4 doses) is the
    recommended antibiotic to prevent anaerobic wound
    contamination in extensive surgeries of the head
    and neck.
  • Appropriate antibiotic choices also include a
    combination of ampicillin and sulbactam (3 g IV
    followed by 1.5 g q8h for 3 doses)
  • combination Ancef and Flagyl.
  • As an oral mouth rinse, use of clindamycin (75-mg
    caps stirred in 8 oz of tap water) or
    chlorhexidine (Peridex) provides rapid and
    sustained reductions in the concentrations of
    aerobic and anaerobic oral flora.

30
Facial fractures
  • Open fractures have an increased incidence of
    infection in the absence of antibiotic
    prophylaxis when compared to closed or open
    fractures treated with prophylactic antibiotics.

31
Facial fractures
  • Antibiotic prophylaxis significantly reduce the
    incidence of postoperative infections in facial
    fractures, especially mandible fractures of the
    body.
  • The infection rates in zygoma fractures, LeFort
    fractures, and mandibular subcondylar fractures
    are similar.

32
Disadvantages of antibiotics
  • It promotes antibiotic resistance and contributes
    to super infection.
  • Antibiotic use is also costly and associated with
    allergic reactions, toxic reactions, and adverse
    effects
  • The use of antibiotics may encourage laxity of
    good surgical technique.

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Penicillin
  • Mechanism of action
  • Exerts action on actively dividing cells by
    causing abnormal cell wall development
  • Inhibits third stage of cell wall synthesis
  • Resistance
  • Alterations in penicillin-binding proteins
  • Inability to penetrate bacterial cell walls
  • Enzymatic hydrolysis of penicillin molecule

36
Penicillin
  • Spectrum
  • Gram-positive cocci - Group A and group B
    Streptococcus
  • Gram-positive bacilli - Corynebacterium
    diphtheriae
  • Gram-negative cocci - Neisseria meningitidis
  • Gram-negative bacilli - Streptobacillus
    moniliformis
  • Anaerobes - Clostridium, Bacteroides,
    Fusobacterium, and Peptostreptococcus species
  • Miscellaneous - Treponema pallidum and
    Leptospira, Enterobacter, and Acinetobacter
    species

37
Penicillin
  • Adverse reactions
  • Hypersensitivity (1-5)
  • Irritant properties that affect the peripheral
    nervous system
  • Nephropathy - Allergic reaction manifested by
    interstitial nephritis and hypokalemia

38
Cephalosporin
  • Mechanism of action
  • Inhibits third step of bacterial wall synthesis
  • Binds to specific proteins on cell membranes
  • Alters cell permeability
  • Inhibits protein synthesis
  • Releases autolysins
  • Resistance - Decrease in bacterial cell wall
    permeability to antibiotics and production of
    beta-lactamase

39
Cephalosporin
  • Spectrum
  • First generation (eg, Ancef, Keflin, Kefzol) -
    Have the greatest degree of activity against
    gram-positive organisms, such as Staphylococcus
    and Streptococcus (not MRSA) have the same
    coverage against gram-positive, anaerobic, and
    aerobic bacilli as penicillin
  • Second generation (eg, Ceclor, Zinacef, Mefoxin)
    - Less active against gram-positive bacteria, but
    have an advantage against Haemophilus influenzae
    organisms and some gram-negative bacilli,
    including Proteus and Enterobacter species
  • Third generation (eg, Ceftazidime, Cefotaxime,
    Cefoperazone) - Have the greatest activity
    against gram-negative aerobes, with variable
    activity against Pseudomonas organisms

40
Cephalosporin
  • Adverse reactions
  • Hypersensitivity - Highest incidence in those
    allergic to penicillin
  • Hematologic - Neutropenia, leukopenia, and
    thrombopenia
  • GI disturbances - Nausea, vomiting, anorexia, and
    diarrhea
  • Reversible renal impairment

41
Erythromycin
  • Mechanism of action - Inhibits bacterial protein
    synthesis
  • Resistance
  • Alteration in protein component of 50s ribosomal
    subunit
  • Plasmid-mediated resistance

42
Erythromycin
  • Spectrum
  • Similar to that of penicillin G
  • Effective against Mycoplasma, Legionella, and
    Actinomyces species
  • Combined with sulfisoxazole to make Pediazole,
    which is used in the pediatric population
  • Effective against H influenzae organisms
  • Adverse reactions
  • GI disturbances
  • Hypersensitivity
  • Cholestatic hepatitis

43
Clindamycin
  • Mechanism of action Binds to 50s ribosomal
    subunit, thereby inhibiting protein synthesis
  • Resistance Similar to that of erythromycin

44
Clindamycin
  • Spectrum
  • Active against most aerobic and anaerobic
    gram-positive organisms
  • Anaerobic gram-negative organisms
  • although some staphylococcal organisms have
    developed resistance

45
Clindamycin
  • Adverse reactions
  • Pseudomembranous colitis
  • Mild nausea and diarrhea
  • Hypersensitivity
  • Leukopenia Transient increase
  • Hepatotoxicity (rare)

46
Metronidazole (Flagyl)
  • Mechanism of action
  • Reduced intracellularly to its active metabolite
    that is bactericidal
  • May be administered orally, intravenously, or
    rectally
  • Metabolized in the liver and excreted by the
    kidneys

47
Metronidazole (Flagyl)
  • Adverse reactions (most of which are dose related
    and are not seen with regular short-term use)
  • CNS toxicity
  • GI disturbance
  • Neutropenia
  • Drug fever
  • Synergistic alcohol effect
  • Prolonged activated partial thromboplastin time
    (aPTT)

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