IB WCS 37
SURGICAL INFECTION
Dr J Ho
Surgery
Wed 02-10-02
OUTLINE
- What is surgical infection?
- Pathogenesis
- Spread of surgical infection
- Sepsis, Bacteraemia & Septicaemia
- Diagnosis
- Treatment
Nosocomial infection & infection control
- (Wound infection)
- Prophylactic antibiotics
Specific types of surgical infection
- Wound infection
- Furuncle & carbuncle
- Cellulitis
- Myositis (localised & spreading)
- Necrotising fasciitis
Principles of Antiobiotic Therapy
SURGICAL INFECTION
A surgical infection is an infection that
- Unlikely to respond to non-surgical treatment (it usually must be excised or drained)
- Occupies an unvascularised space in tissue (e.g. appendicitis, empyema, gas gangrene and abscesses)
- Occurs in an previously operated/ trauma site
PATHOGENESIS
Three common elements
- Infectious agent
- Susceptible host
- Closed unperfused space
Host's body defence mechanisms vs. bacteria in the environment (body surface, GIT)
1. Infectious Agent
Aerobic
- Gram positive: streptococci, staphylococcus aureus
- Gram negative: E. coli, klebsiella, pseudomonas
Anaerobic: bacteroides (low/ absent oxygen)
- Opportunistic
: pseudomonas, fungi etc (infection cause by bacteria that is normal flora in healthy individual); esp. in nosocomial infection
- Community-acquired
vs. hospital-acquired (nosocomial): more virulent/ resistant to Tx in nosocomial
2. Susceptible Host
Body defence mechanism
- Local
defence mechanism: skin, mucous membrane, cilia, GIT (compromised in (1) Trauma (2) Viral infection - makes surface inflamed and more permeable)
- Specific
immunity: cell mediated and hormonal mediated
- Non-specific
immunity: white cells (phagocytes, macrophages)
Immunosuppressed host
- Immunodeficiency disorders: acquired, congenital
- Burn,
trauma
- Chronic
disease: DM, CRF, cirrhosis liver
- Malignancy
- Iatrogenic
: steroid, cytotoxic agent (kill BM cells as well as ca cells)
3. Closed Space
- Poorly vascularised place in tissue (wound)
- Natural space
CYCLE OF EVENTS
- Entry
of micro-organisms into the body
- Apposition
to the host cell
- Overcoming
local defences
- Accumulation
& spread
- Outwitting the immune response;
- Inducing cellular injury - the manifestation of disease: fever, leukocytosis, specific acute phase proteins;
- Persistence
SPREAD OF SURGICAL INFECTIONS
1. Necrotising infections
- Spread along anatomically defined paths
- Eg. Clostridial myonecrosis (through muscle plane), necrotising fasciitis (bacteria kills fascia and spreads along fascia, not limited to one plane), cellulitis (through subcutaneous plane)
2. Abscess
- Accumulation of dead WBC causing pus - exerts pressure on surrounding body tissue
- Breaching of natural boundary -> fistulas or sinuses
3. Phlegmons and superficial infections
- Phlegmon: diffuse inflammation of the soft or CT due to infection
- Oedema
- Superficial infection - eg. Cellulitis
4. Via lymphatic system
- Lymphangitis: streptococcal
5. Via bloodstream
- IV drug abuse: empyema, endocarditis
- Brain abscess, liver abscess
SEPSIS, BACTERAEMIA & SEPTICAEMIA
BACTERAEMIA
- Bacteria in blood
- Transient bacteraemia: usually of no clinical significance except in patients with prosthesis or RHD (bacteria reside prosthesis/ damaged heart valves -> IE)
SEPTICAEMIA
- A serious infection resulting from both bacteraemia and toxaemia (bacterial toxins in blood)
- Gram -ve
: endotoxin (eg. E Coli) ®
peripheral dilatation, increased cellular permeability
- Systemic inflammatory response syndrome (SIRS)
- Pyrexia (> 380C) or hypothermia (< 360C)
- Tachycardia (hypotension)
- Tachypnoea
- Leukocytosis: increase WBC (>12) or leucopenia (<4)
SEPSIS
- Sepsis = SIRS + Documented source of infection
- Severe
sepsis = Sepsis + Dysfunction of one or more organs (liver, kidney, intestine, lung, heart; multiple organ failure = high mortality; may remove infective source but Pt dies due to organ failure)
DIAGNOSIS
- Aim of investigation: ID source of sepsis
1. Physical examination
2. Blood test
- Limited use: cannot tell source, can only tell if sepsis is present
- WBC
- Blood gas analysis: metabolic acidosis
- Coagulation profile: impairment of coagulation due to stimulation of body's coagulation system
3. Body fluid culture
- Blood culture : the best evidence of sepsis (aerobic & anaerobic cultures)
4. Imaging studies
- CXR: chest infection (also bone + jt swelling = jt infection)
- CT (Dx, anat location) + US (liver, children/ thin adult for appendicitis)
- Radionucleide scan: eg. WBC scan, attach isotope to WBC (injection), scan few hours later, shows WBC going to area of infection
TREATMENT
- Principle of Tx: any septic focus amenable to surgical therapy should be excised or drained
1. Incision & drainage
- Superficial
abscess: surgical drainage (MUST drain abscess - oedema, tender, erythema, fluctuation); if no surrounding cellulitis, do not need ABX
- Deep
abscesses: CT or ultrasound guided percutaneous catheter drainage; surgical drainage (then Tx with ABX, can change abscess from emergency to elective need for operation)
- If very obese, in bowel, use CT (difficult to localise with US)
- Eg. Cholecystitis (remove gallbladder); Appendicitis (remove appendix); Colonic diverticulitis (remove that part of the colon)
2. Excision
- Eg. Appendectomy, cholecystectomy etc
- Elective excision: prevent recurrence (eg. Cholecystitis with gallstones, if no cholecystectomy, then Pt will present later with another attack)
- Appendicitis: cannot treat with ABX, need appendectomy
- Many times use both excision and ABX (eg. cholecystitis: usually only need cholecystectomy and no ABX, but if severe infection need to have cholecystectomy and ABX)
3. ABX
- Not necessary for simple surgical infections that respond to incision and drainage alone (eg. furuncles and uncomplicated wound infection)
- Infections likely to spread or persist require antibiotic therapy
- Empirical treatment à definitive treatment according to culture result
4. Other support of body systems
- Esp. if Pt already septic ®
IV fluid, nutrition, circulatory support (inotropes) etc.
NOSOCOMIAL INFECTION & INFECTION CONTROL
- Nosocomial infection = Hospital acquired infection: surgical team, operating room, bacteria harboured by patient before operation
REDUCING NOSOCOMIAL INFECTIONS IN SURGICAL PT'S
1. Surgical Team
- Operating room attire: caps, mask, gown & gloves
- Surgical behaviour (1) Aseptic operating technique (2) Cutaneous or respiratory infection (3) Hand scrubbing
- Hand washing: mandatory after all contact with infected patients
2. Operating Room
- Design of operating room: e.g. ventilation (+ve pressure in OT)
- Sterilisation of equipment and instrument
3. Patient
- Treat pre-existing infection before elective operation
- Skin commensals (1) Preoperative showers or baths (2) Body hair: prefer clipping because shaving causes microcuts; immediately before operation (3) Skin included in operating field: antiseptic cleansing
- Universal precautions: any procedure involving close contact with any patient or patient's body fluid (blood, urine, faeces or saliva) should be performed by personnel wearing gloves or other protective devices
PROPHYLACTIC ABX
- Aim: to reduce surgical wound infection
Principles
1. Choose antibiotics for the expected type of contamination
- Use "first-line" antibiotics to reduce emergence of resistance strain
- Consider cost-effectiveness, efficacy and safety
- Eg. (1) Urological operation: according to urine culture (2) Colorectal operation: gram negative aerobes and anaerobes (3) Prosthetic placement: staphylococcus aureus
2. Use antibiotics only if the risk of infection justifies their use
- Not indicated for clean operation like hernia repair (except placement of prosthesis or patient with rheumatic heart disease or prosthetic heart valve)
3. Appropriate doses, time & route
- To achieve a therapeutic level in the blood and tissue before surgical incision
- Intravenous: amount varies with body type of Pt
- Less than 2 hours before operation: at induction of anaesthesia
4. Stop dosing before the risk of side effects outweighs benefits
- Stopped a few hours after operation
- Prevent resistant strains emerging
SPECIFIC TYPES OF SURGICAL WOUND INFECTION
WOUND INFECTION
- Due to bacterial contamination during/ after a surgical procedure (usu. only subcut tiss)
- Risk µ
wound class (usu. day 5-10 post-op)
- Clinical features: fever, wound pain, oedema, erythema, discharge
Infection Rate (%)
- Clean (hernia repair, sebaceous cyst) 1.5
- Clean contaminated (elective cholecystectomy, cholectomy with time for bowel preparation) 7.7
- Contaminated
(perforated appendix, bowel obstruction needing emergency cholectomy with now time for bowel preparation) 15.2
- Dirty
(LI bowel perforation - faeces inside peritoneal cavity) 40.0
Risk factors
- Abdominal operation
- Operation > 2 hours (
difficulty,
planes opened,
bacterial exposure)
- Contaminated operation
- ³
3 pre-existing medical conditions
Prevention measures
- Careful operative technique
- Reduction of contamination: eg. Clean large bowel before operation
- Prophylactic antibiotics
- Contaminated wound: delayed primary closure or secondary closure (eg. Delayed primary: if leave open, clean for few days and then suture again; Delayed secondary: if leave open, clean, leave to heal without sutures)
- Treatment: open the wound for drainage; wound swab
SPECIFIC TYPES
1. Furuncle & Carbuncle
- Furuncle: infected hair follicles
- Carbuncles
: starts @ furuncles, spread through dermis/ subcut tissue in a myriad of connecting tunnels; freq. back of neck (strong aponeurosis, if open there are pockets of pus, therefore cannot do incision and drainage, therefore need excision); poorly-controlled DM (need control to prevent recurrence)
- Organisms: staphylococci & anaerobic diphtheroids
- Treatment (1) Furuncle: incision & drainage (do not need ABX) (2) Carbuncles: excision & antibiotics
2. Cellulitis
- Common invasive non-suppurative infection of connective tissue (no fluctuation)
- Usually caused by streptococci
- Clinical finding (1) Erythematous, oedematous skin (2) May cause lymphangitis
- Treatment
(1) Rest, elevation, packs (2) ABX
3. Myositis
- Types (1) Localised (2) Diffuse
- Organisms (1) Staphylococcus aureus (2) Clostridium (gas gangrene)
- Gas Gangrene
: (1) < 3 d after inj (2) Rapidly increasing wound pain (3) Oedema (4) Purulent exudate (5) Crepitus: gas inside tissue (6) Profound toxaemia (7) Extensive underlying muscle necrosis: compartment syndrome
- Treatment
(1) Extensive surgical debridement: cut muscle away, amputation (2) Hyperbaric oxygen: organisms relatively anaerobic (3) ABX: usu. Tx combination
- MUST have debridement with ABX (hyperbaric oxygen if facilities allow)
4. Necrotising Fasciitis
- An invasive infection of fascia
- Usually caused by multiple pathogens (1) Microaerophilic streptococci (2) Staphylococci (30 Gram-negative bacteria: klebsiella, pseudomonas (4) Anaerobes: bacteroides (5) Clostridium
- Pathogenesis
: infectious thrombosis of vessels passing between skin and deep circulation -> skin necrosis as well as necrosis of underlying fascia and subcutaneous tissue
- Clinical
features (1) Skin: haemorrhagic bullae (2) Fascial necrosis: usually wider than the skin appearance indicates (3) Crepitus (4) Toxic patient
- Treatment
(1) Surgical debridement: remove all avascular skin and fascia; may require repeated debridement (2) ABX: broad-spectrum (3) Circulatory support: blood or plasma transfusion
PRINCIPLES OF ABX THERAPY
Indicated?
- Surgeon decides ®
clinical impression, that a microbial infection probably exists
Which organism?
- A guess as to which microorganisms are most likely to cause the suspected infection
- Based on clinical grounds: the suspected type of infection; known types of organisms involved and local pattern
Specimen culture
- Relevant culture should be taken (blood, sputum, urine etc) before start of treatment to provide a microbiological diagnosis
- Culture not helpful after start of empirical ABX
- May have atypical organisms involved
Which agent?
- Selects the drug that is most likely to be effective against the suspected organisms ("empirical" therapy)
- Because culture result will require a number of days to be available and treatment cannot be delayed till availability of result
- Choice: depends on local antibiotics sensitivity pattern
- Can be single agent (against one organism or broad-spectrum antibiotics against a wide spectrum of organisms) or combined agents (against both aerobic and anaerobic organisms)
- In principle: should be specific; avoid overuse of broad-spectrum antibiotics except in life-threatening situation (to reduce emergence of resistant strains)
Route?
- Make sure that the drug can reach the site of active infection in adequate concentration
- Types of drug used (different route of administration): depends on pharmacological properties
- Whether patient can eat (if so, use oral preparation)
- Life threatening infection: require intravenous route to ensure very high blood level of antibiotics
Dosage?
- Usually calculated according to body weight
- Some drugs, e.g. aminoglycoside, serum drug level can be checked
- Adjusted (1) Children (2) Liver impairment (3) Renal impairment - drugs excreted through kidneys: may need adjustment of dosage in patients with renal impairment or failure
Duration?
- Determined in part by clinical response and past experience and in part by laboratory indications of suppression or elimination of infection
- Example: subsidence of fever; negative culture
- A course of antibiotics: five to seven days (longer with fungal infection)
Agent adjustment
- Clinical response: no clinical response to initial empirical therapy; may no longer need ABX if no need for; inotropes for circulatory support, etc. (most commonly used indication)
- Culture results indicate resistance of microorganisms to antibiotics used and evidence of persistence of infection (no need to change antibiotics if good clinical response) (good in complicated situations: > 1 organism)