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SURGICAL SITE INFECTION
Introduction
• Devastating surgical complication.
• Although reduced now
• CHALENGING PROBLEM
• Costly – patient & health care system.
Historical Aspects
• Pringle 1750 – “Antiseptic”
• Isaac Benedict Prevost 1807 – first proof of
microorganisms as the causation of sepsis.
• Louis Paster 1863 – Putrifaction is caused by
microbes from air.
• Joseph Lister – used antiseptic soln to prevent
putrifaction & demonstrated that pus is a
disaster rather than a sign of healing.
• Lister’s technique of sterilization, skin
preparation and washing became –
Foundation of “Antiseptic Surgery”.
• First step in development of
“Asepsis in surgery”.
• Introduction of antibiotics 1940 –
Streptococcal hospital infection disappeared.
• 1950s World wide epidemic of nosocomial
infection by Virulent resistant Staphylococcus.
Nosocomial Infection
• Develops during hospitalization
• Neither present nor incubating at the time of
patients admission.
• 50% involve surgical site infection.
National Nosocomial Infection Surveillance
(NNIS)
• Current version for SSI risk index scores each
operation by counting the risk factors:
1. Type of wound
2. ASA score of 3,4 or5 (Host defense)
3. Duration of surgery – lasting more than T-hours
Surgical site infection
• Postoperative wound developing signs of
inflammation or serous discharge is labeled
as “possibly infected”.
• Cruse et al 1977 classified wounds – 4
categories
1. Clean wound:
• No infection, no break in aseptic technique & no
hollow muscular organ opened.
2. Clean contaminated wound:
 Hollow muscular organ opened with minimal
organ spillage.
3. Contaminated wound:
 Hollow organ opened with gross spillage, acute
inflammation without pus, traumatic wounds
within 4 hours and major break in aseptic
technique.
4. Dirty wound:
 Perforated viscus, pus, traumatic wound more than 4
hours old.
• INFECTION RATE
1.5
7.7
15.2
40
0
5
10
15
20
25
30
35
40
1st Qtr
Clean
Clean contaminated
Contaminated
Dirty
• Infection in clean wounds – Surveillance &
research.
– < 1% Ideal.
– 1-2% can be acceptable.
– > 2% cause of concern.
• Monthly announcement– Everyone aware of
SSI
– Can reduce by 38% by appropriate feedback.
Rate of infection
• Purely a statistic for the surgeon.
• Total DISASTER for the patient.
• Sir Watson Jones 1962 – “Infection of one
clean case in a thousand is a disaster of the
first magnitude”.
• Even slight delay in healing, redness of skin, or
any other sign of wound infection – evidence
of failure.
Orthopaedic clean wound
• Too many variables
– Surgery of soft tissues alone or of bones
– With or without implants
– Emergency trauma or planned trauma cases
– Timing of surgery in trauma
– Reaming of medullary canal, primary plating.
– Stable and unstable fixation.
Post Operative infection?
• Primary or secondary?
• Possible to predict?
• High risk patients?
• Possible to prevent in best possible operative
conditions?
• All operative wounds get contaminated
during surgery – does not mean infection.
• Sources of contamination:
1. Surgeon & his team
2. Air in OT
3. Skin of patient & all OT personnel.
• Conversion of this contamination to
infection is to be avoided.
Depends upon:
• Virulence of the organisms
• Degree of contamination
• Presence of dead & devitalized tissue,
implants & suture material.
• Site of operation i.e. bone
• Duration of surgery
• HOST RESPONSE – Immunological status
SSI
• Story of germination of a seed in soil.
• 95% of bacteria reach – Via air by direct
sedimentation into the wound or the
instruments.
• Highest conc. – within the circle of surgical
team directly over the wound.
• No of bacteria directly proportional to the
increase in activity and number of the team –
max. at the time of induction, positioning and
extubation/ Closure.
• Staphylococcus aureus carrier – 30-50% of
general population.
• Every person sheds ~55,000 skin scales/min. –
10-20% contain live bacteria.
• Increase in shedding:
– Loose cotton scrub suits
– Higher temperature & humidity.
Gloves
• In a study of 1209 cases – 141 gloves were
found punctured.
• 18,000 Staph aureus can pass a single
puncture in 20min.
• 3-5 min hand scrub with antiseptic soln. is
essential.
• Double gloves – additional security.
• New cut resistant gloves.
Airborne bacteria
• Air handling systems of OT.
• Type of scrub suits worn.
• Air bacterial count in ordinary OT varies from
50 – 500 colony meter cube
• “A Sterile air operating room” &
Concept of “Rapid Unimpeded Down flow of
Filtered Air and Exhaust Ventilated Whole
Body Suit” – Sir John Charnley
Microbiological facts:
1. Airborne bacterial contamination is directly
related to number & activity of people in OR.
2. Inversely related to the effectiveness of
personnel garment barrier & no. of air
exchange / hour.
3. Air borne bacteria are agglomerated on
inanimate particles size from 2-10 microns.
4. Almost always gram positive corresponding
to skin flora.
Methods of cleaning air
1. Laminar air flow – clean, filtered air with
frequent whole air exchange.
2. Ultraviolet light system
3. Vacuum body exhaust system
4. Garment barrier.
5. HEPA (High Efficacy Particle Air filter) –
removing 99.9% particles larger than 0.3
microns. (Bacteria - .5-10.5)
Laminar flow
• Super-high air turn over (400-600) in a laminar
flow room – “Air broom” action.
• Flow – Horizontal or Vertical.
• Conventional OR – 12-25 air exchanges each
hour – Federal standards.
• “Unobstructed” – If not –
positive pressure is generated
• Doors kept closed.
• Air temperature – 21.1 to 24.4 C
– Lower temperatures are preferred.
• Humidity: 50%
– Prevent static electricity and
– Decrease perspiration
– Decreased viability of bacteria
Garment Barrier
• AORN recommends:
– Pant suit or one piece suit with ankle closure &
shoe covers.
– All hair covered by cap or hood
– Face mask – high microbial filtration efficacy.
• Micro porous textile – disposable/reusable –
use in gown & drape barrier systems.
• Standard cotton scrub suit or drapes –
– pore size 100 microns
– Sheds more bacteria
“Cheese grater” effect.
– “Bellows” action
– Wet
• Microporous material is superior as:
– Resistance to blood & water
– Abrasion resistant
– Lint free
– Memory free
– High degree of drapability.
• e.g Polypropylene
nonwoven gown.
Host defense mechanism
• Skin test score
• Serum albumin level
• Age of the patient
– Prediction regarding susceptibility to infection
• Other factors
– Diabetes, Old age, Obesity, Rh Arthritis,
– Major implant surgery
– AIDS
• Protein calorie malnutrition – most imp.
factor.
• Clean wound infection rate in
– Diabetics – 10.5%
– With obesity – 13.5%
– With malnutrition 16.5%
• Polytrauma patients.
• These compromised situations - decision
regarding early operative intervention has to
weigh against possibility of infection.
Organisms
• 60% of SSI – Gram +ve bacteria esp. Staph
aureus and epidermidis.
• 20% - Gram –ve bacteria like E.Coli,
Pseudomonas, Klebsiella etc.
• Precise bacteriological diagnosis
– 6 aerobic and anaerobic cultures.
– Enriched media for at least 2 weeks.
• 90% of implant surgeries result from
intraoperative contamination.
• 50% of these become clinically evident 3
months after surgery
• Many of these caused by low virulence
organisms like Staph epidermidis and other
anaerobes.
• Steady increase in G –ve bacteria – more
difficult to treat as is resistant Staph aureus.
• 2-8 million inoculums of Staph aureus injected
develop infection.
• Only 100 organisms in presence of foreign
body.
• Main reservoir – human body.
• Nasal carriers – 30-50% of general population.
• Glycocalyx biofilms:
– Bacteria get adhered to implant surface.
Susceptibility of bone to infection
• Limited soft tissue space
• Blood supply favoring necrosis
• Inadequate mechanism to reabsorb necrotic
bone
• Increased duration of surgery
Role of prophylactic antibiotics
• Tengve et al reported
– 16.9% rate of infection with no antibiotics.
– 1.8% with prophylactic antibiotics.
• Antibiotics given before bacterial inoculation
– Inhibit growth of bacteria
• After inoculation
– Prevent overt clinical signs of infection, but
bacteria can always be isolated from the wound.
Pathophysiology
• As a response to operative trauma
– Maximum exudation occurs in the first 6 hrs and
– Contamination occurs at the time of surgery
• Antibiotic must be present in the circulation &
into hematoma throughout the operation in
sufficient concentration – to kill these
bacteria.
Prophylactic antibiotic
• Started just before surgery
• Ideal conc. in serum during surgery should be
4% of MIC in a healthy individual.
8% in a compromised patient.
• No extra advantage of continuing for 5 or
more days over limited therapy. (Stone et al)
Topical antibiotics
• Willson et al 1991 – Topical triple antibiotic
soln.- Neuromycin, polymyxin and bacitracin.
• Bacitracin – allergic rxn so stopped.
• Simple good wash with NS or RL is very
effective.
Clinical presentation of postoperative
infection
• 3 types of presentation:
1. Early – within 8 weeks
2. Delayed – 8 weeks – 1 year.
3. Late – after 1 year.
• Early further 4 types (Mukhopadaya)
i. Imminent within 48 hrs
ii. 3-9 days i.e. before suture removal
iii. 10-21st
day and
iv. 3-8 weeks.
Classical presentation
• Disproportionate pain
• Fever >102 F
• Wound – signs of local cellulitis
• Mild to moderate serosanguineous discharge.
Seen only when antibiotics and anti
inflammatory are not given.
Common presentation
• Severe pain
• Fever not responding to high doses of drugs
• Frank purulent discharge
• Wound already partially opened up due to cut
through sutures.
Late infection
• Go home with apparently normal wound
healing
• Return with chronic discharging sinus
• Persistent tachycardia
• Pain not presenting complaint.
Diagnosis of infection
• Fever and Leukocytosis – not always helpful.
• Thrombotic index
• “Leukergy” – based on the phenomenon
– WBCs agglomerate in the peripheral blood of
patients with inflammatory disease.
– Percentage of agglomerated cells correlate with
the severity of infection.
– Rapid and inexpensive.
• Persistent elevation of ESR –
– Suggests infection
– Neither very sensitive nor specific.
• ESR with CRP
• Results better but still unreliable.
• Bone scan – more accurate.
Treatment
• Immediate action.
• Discharging fluid to be sent for –
– Gram staining,
– Culture & sensitivity.
• Broad spectrum antibiotic along with
aminoglycoside started – no relief in 24 hrs –
• Open and debride thoroughly.
• Always better to debride than wait for
antibiotics to act.
• Wound always closed by loose intermittent
sutures or by secondary suturing later.
• A well fixed implant can be left as such.
• Loose implant – removal or refixation or
Exfixation.
• Implants once infected needs removal
• Well fixed implant left in place till fracture
unites.
• Plate fixation – Early diagnosis and removal –
extensive cortical necrosis.
• Non union is not due to infection but
inadequate fixation.
• Sir John Charnley 1982
“Because of the tragic seriousness of post
operative infection, I regard it as our duty to
continue in the future to study to eliminate
post operative infection by any means or
combination of means, whatever, I say
eliminate deliberately because I have not yet
abandoned the hope that some way we’ll
achieve this target”
Thank You!

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Surgical site infection (2)

  • 2. Introduction • Devastating surgical complication. • Although reduced now • CHALENGING PROBLEM • Costly – patient & health care system.
  • 3. Historical Aspects • Pringle 1750 – “Antiseptic” • Isaac Benedict Prevost 1807 – first proof of microorganisms as the causation of sepsis. • Louis Paster 1863 – Putrifaction is caused by microbes from air. • Joseph Lister – used antiseptic soln to prevent putrifaction & demonstrated that pus is a disaster rather than a sign of healing.
  • 4. • Lister’s technique of sterilization, skin preparation and washing became – Foundation of “Antiseptic Surgery”. • First step in development of “Asepsis in surgery”. • Introduction of antibiotics 1940 – Streptococcal hospital infection disappeared. • 1950s World wide epidemic of nosocomial infection by Virulent resistant Staphylococcus.
  • 5. Nosocomial Infection • Develops during hospitalization • Neither present nor incubating at the time of patients admission. • 50% involve surgical site infection.
  • 6. National Nosocomial Infection Surveillance (NNIS) • Current version for SSI risk index scores each operation by counting the risk factors: 1. Type of wound 2. ASA score of 3,4 or5 (Host defense) 3. Duration of surgery – lasting more than T-hours
  • 7. Surgical site infection • Postoperative wound developing signs of inflammation or serous discharge is labeled as “possibly infected”. • Cruse et al 1977 classified wounds – 4 categories 1. Clean wound: • No infection, no break in aseptic technique & no hollow muscular organ opened.
  • 8. 2. Clean contaminated wound:  Hollow muscular organ opened with minimal organ spillage. 3. Contaminated wound:  Hollow organ opened with gross spillage, acute inflammation without pus, traumatic wounds within 4 hours and major break in aseptic technique.
  • 9. 4. Dirty wound:  Perforated viscus, pus, traumatic wound more than 4 hours old. • INFECTION RATE 1.5 7.7 15.2 40 0 5 10 15 20 25 30 35 40 1st Qtr Clean Clean contaminated Contaminated Dirty
  • 10. • Infection in clean wounds – Surveillance & research. – < 1% Ideal. – 1-2% can be acceptable. – > 2% cause of concern. • Monthly announcement– Everyone aware of SSI – Can reduce by 38% by appropriate feedback.
  • 11. Rate of infection • Purely a statistic for the surgeon. • Total DISASTER for the patient. • Sir Watson Jones 1962 – “Infection of one clean case in a thousand is a disaster of the first magnitude”. • Even slight delay in healing, redness of skin, or any other sign of wound infection – evidence of failure.
  • 12. Orthopaedic clean wound • Too many variables – Surgery of soft tissues alone or of bones – With or without implants – Emergency trauma or planned trauma cases – Timing of surgery in trauma – Reaming of medullary canal, primary plating. – Stable and unstable fixation.
  • 13. Post Operative infection? • Primary or secondary? • Possible to predict? • High risk patients? • Possible to prevent in best possible operative conditions?
  • 14. • All operative wounds get contaminated during surgery – does not mean infection. • Sources of contamination: 1. Surgeon & his team 2. Air in OT 3. Skin of patient & all OT personnel. • Conversion of this contamination to infection is to be avoided.
  • 15. Depends upon: • Virulence of the organisms • Degree of contamination • Presence of dead & devitalized tissue, implants & suture material. • Site of operation i.e. bone • Duration of surgery • HOST RESPONSE – Immunological status
  • 16. SSI • Story of germination of a seed in soil. • 95% of bacteria reach – Via air by direct sedimentation into the wound or the instruments. • Highest conc. – within the circle of surgical team directly over the wound. • No of bacteria directly proportional to the increase in activity and number of the team – max. at the time of induction, positioning and extubation/ Closure.
  • 17. • Staphylococcus aureus carrier – 30-50% of general population. • Every person sheds ~55,000 skin scales/min. – 10-20% contain live bacteria. • Increase in shedding: – Loose cotton scrub suits – Higher temperature & humidity.
  • 18. Gloves • In a study of 1209 cases – 141 gloves were found punctured. • 18,000 Staph aureus can pass a single puncture in 20min. • 3-5 min hand scrub with antiseptic soln. is essential. • Double gloves – additional security. • New cut resistant gloves.
  • 19. Airborne bacteria • Air handling systems of OT. • Type of scrub suits worn. • Air bacterial count in ordinary OT varies from 50 – 500 colony meter cube • “A Sterile air operating room” & Concept of “Rapid Unimpeded Down flow of Filtered Air and Exhaust Ventilated Whole Body Suit” – Sir John Charnley
  • 20. Microbiological facts: 1. Airborne bacterial contamination is directly related to number & activity of people in OR. 2. Inversely related to the effectiveness of personnel garment barrier & no. of air exchange / hour. 3. Air borne bacteria are agglomerated on inanimate particles size from 2-10 microns. 4. Almost always gram positive corresponding to skin flora.
  • 21. Methods of cleaning air 1. Laminar air flow – clean, filtered air with frequent whole air exchange. 2. Ultraviolet light system 3. Vacuum body exhaust system 4. Garment barrier. 5. HEPA (High Efficacy Particle Air filter) – removing 99.9% particles larger than 0.3 microns. (Bacteria - .5-10.5)
  • 22. Laminar flow • Super-high air turn over (400-600) in a laminar flow room – “Air broom” action. • Flow – Horizontal or Vertical. • Conventional OR – 12-25 air exchanges each hour – Federal standards. • “Unobstructed” – If not – positive pressure is generated • Doors kept closed.
  • 23. • Air temperature – 21.1 to 24.4 C – Lower temperatures are preferred. • Humidity: 50% – Prevent static electricity and – Decrease perspiration – Decreased viability of bacteria
  • 24. Garment Barrier • AORN recommends: – Pant suit or one piece suit with ankle closure & shoe covers. – All hair covered by cap or hood – Face mask – high microbial filtration efficacy. • Micro porous textile – disposable/reusable – use in gown & drape barrier systems.
  • 25. • Standard cotton scrub suit or drapes – – pore size 100 microns – Sheds more bacteria “Cheese grater” effect. – “Bellows” action – Wet
  • 26. • Microporous material is superior as: – Resistance to blood & water – Abrasion resistant – Lint free – Memory free – High degree of drapability. • e.g Polypropylene nonwoven gown.
  • 27. Host defense mechanism • Skin test score • Serum albumin level • Age of the patient – Prediction regarding susceptibility to infection • Other factors – Diabetes, Old age, Obesity, Rh Arthritis, – Major implant surgery – AIDS
  • 28. • Protein calorie malnutrition – most imp. factor. • Clean wound infection rate in – Diabetics – 10.5% – With obesity – 13.5% – With malnutrition 16.5% • Polytrauma patients. • These compromised situations - decision regarding early operative intervention has to weigh against possibility of infection.
  • 29. Organisms • 60% of SSI – Gram +ve bacteria esp. Staph aureus and epidermidis. • 20% - Gram –ve bacteria like E.Coli, Pseudomonas, Klebsiella etc. • Precise bacteriological diagnosis – 6 aerobic and anaerobic cultures. – Enriched media for at least 2 weeks.
  • 30. • 90% of implant surgeries result from intraoperative contamination. • 50% of these become clinically evident 3 months after surgery • Many of these caused by low virulence organisms like Staph epidermidis and other anaerobes. • Steady increase in G –ve bacteria – more difficult to treat as is resistant Staph aureus.
  • 31. • 2-8 million inoculums of Staph aureus injected develop infection. • Only 100 organisms in presence of foreign body. • Main reservoir – human body. • Nasal carriers – 30-50% of general population. • Glycocalyx biofilms: – Bacteria get adhered to implant surface.
  • 32. Susceptibility of bone to infection • Limited soft tissue space • Blood supply favoring necrosis • Inadequate mechanism to reabsorb necrotic bone • Increased duration of surgery
  • 33. Role of prophylactic antibiotics • Tengve et al reported – 16.9% rate of infection with no antibiotics. – 1.8% with prophylactic antibiotics. • Antibiotics given before bacterial inoculation – Inhibit growth of bacteria • After inoculation – Prevent overt clinical signs of infection, but bacteria can always be isolated from the wound.
  • 34. Pathophysiology • As a response to operative trauma – Maximum exudation occurs in the first 6 hrs and – Contamination occurs at the time of surgery • Antibiotic must be present in the circulation & into hematoma throughout the operation in sufficient concentration – to kill these bacteria.
  • 35. Prophylactic antibiotic • Started just before surgery • Ideal conc. in serum during surgery should be 4% of MIC in a healthy individual. 8% in a compromised patient. • No extra advantage of continuing for 5 or more days over limited therapy. (Stone et al)
  • 36. Topical antibiotics • Willson et al 1991 – Topical triple antibiotic soln.- Neuromycin, polymyxin and bacitracin. • Bacitracin – allergic rxn so stopped. • Simple good wash with NS or RL is very effective.
  • 37. Clinical presentation of postoperative infection • 3 types of presentation: 1. Early – within 8 weeks 2. Delayed – 8 weeks – 1 year. 3. Late – after 1 year. • Early further 4 types (Mukhopadaya) i. Imminent within 48 hrs ii. 3-9 days i.e. before suture removal iii. 10-21st day and iv. 3-8 weeks.
  • 38. Classical presentation • Disproportionate pain • Fever >102 F • Wound – signs of local cellulitis • Mild to moderate serosanguineous discharge. Seen only when antibiotics and anti inflammatory are not given.
  • 39. Common presentation • Severe pain • Fever not responding to high doses of drugs • Frank purulent discharge • Wound already partially opened up due to cut through sutures.
  • 40. Late infection • Go home with apparently normal wound healing • Return with chronic discharging sinus • Persistent tachycardia • Pain not presenting complaint.
  • 41. Diagnosis of infection • Fever and Leukocytosis – not always helpful. • Thrombotic index • “Leukergy” – based on the phenomenon – WBCs agglomerate in the peripheral blood of patients with inflammatory disease. – Percentage of agglomerated cells correlate with the severity of infection. – Rapid and inexpensive.
  • 42. • Persistent elevation of ESR – – Suggests infection – Neither very sensitive nor specific. • ESR with CRP • Results better but still unreliable. • Bone scan – more accurate.
  • 43. Treatment • Immediate action. • Discharging fluid to be sent for – – Gram staining, – Culture & sensitivity. • Broad spectrum antibiotic along with aminoglycoside started – no relief in 24 hrs – • Open and debride thoroughly. • Always better to debride than wait for antibiotics to act.
  • 44. • Wound always closed by loose intermittent sutures or by secondary suturing later. • A well fixed implant can be left as such. • Loose implant – removal or refixation or Exfixation. • Implants once infected needs removal • Well fixed implant left in place till fracture unites.
  • 45. • Plate fixation – Early diagnosis and removal – extensive cortical necrosis. • Non union is not due to infection but inadequate fixation.
  • 46. • Sir John Charnley 1982 “Because of the tragic seriousness of post operative infection, I regard it as our duty to continue in the future to study to eliminate post operative infection by any means or combination of means, whatever, I say eliminate deliberately because I have not yet abandoned the hope that some way we’ll achieve this target”