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Professor Stephanie Dancer
NHS Lanarkshire & Edinburgh Napier University, Scotland
Investigating an outbreak of surgical site infections
among Orthopaedic and Ophthalmology patients
Recognition of an outbreak
April 2009:
Sudden increase in infection rate for ‘clean’ surgical procedures for
orthopaedic patients receiving hip or knee prostheses;
There were also cases of acute endophthalmitis after eye surgery
Since our hospital reports such infections
promptly for surveillance purposes, a
sudden increase in infection rates ought to
have alerted Infection Control staff early;
BUT...there was no obvious ‘outbreak’
organism, so initial cases did not raise the
alarm as they should have done.
Dates of operation and onset of surgical site infection
for twenty orthopaedic and ophthalmic patients
Retrospective investigation
revealed possible missed cases!
Then there was a second surge of
cases because we had failed to
rectify the underlying cause
Orthopaedic patients
Fifteenorthopaedic patients were involved in the outbreak.
Eleven had knee or hip implant surgery (two were revisions).
The remainder were bilateral osteotomies; internal fixation of an ankle fracture;
bunion repair with screws; and a fasciotomy with external medullary fixation.
No obvious microbiological pathogen was found from submitted specimens
(wound swabs, aspirates, tissue, etc.)
Six patients required further surgery, e.g. wash-
outs; joint revision, etc.
One patient died.
One patient required two further attempts to
replace his knee prosthesis.
Ophthalmology patients
Phacoemulsificationis method of cataract surgery in which the internal
lens of the eye is emulsified using ultrasonic energy and replaced with
an intraocular lens implant.
Five patients who underwent cataract
surgery within the outbreak period suffered
post-operative endophthalmitis.
This is potentially devastating for the patient
since it can cause permament visual deficit
or even blindness.
All five patients required further surgery.
One sufferedpermament visual deficit.
Initial microbiology results
Orthopaedic specimens
Coagulase-negative staphylococci +/- Bacillus spp. with or without
faecal-type flora (different species)
Ophthalmology specimens
The only organisms retrieved from submitted
vitreous humour were coagulase-negative
staphylococci or Bacillus spp.
Bacillus spp. on blood agar
Gram-stain of staph
Actions taken
Outbreak committee convened!
Reviewof ward and theatre practices
Epidemiological analyses
Inspection of orthopaedic theatres
Reviewof microbiological results
Infectioncontrol audit, including hand hygiene
Maintenance services for laminar flow
Terminal cleans for orthopaedic wards
Antibiotic prophylaxis changed
Theatres deep cleaned
Increasedvigilance for further cases, with
additional microbiological investigations
Two months later: Resurgence of outbreak
with two cases of endophthalmitis
Outbreak committee reconvened, with medical director and hospital managers
Theatre staff volunteered concerns over damp and/or stained packs of surgical
instruments returning from sterile services provider
Staining was usually orange/brown in colour
We decided to audit damp and/or
discolouredpacks;
Packs were selected for microbiological
examination.
Surgical instruments used for high risk
surgery (eyes, orthopaedics and
vascular) were sent to another sterile
services provider ona temporary basis.
Microbiological examination of surgical sets
Level 1 laminar flow cabinet with Hepa-Afiltration
in a Category 3 room was disinfected and
allowed to run for 30 mins before processing;
Control settle plates positioned within the cabinet
Adapted from Widmer et al, J Hosp Infect 1992; Webster et al, AmJIC 2005
Pack and media bottles sprayed with disinfectant (Trigene) before placing in
the cabinet;
Gloved operator removes outer layer of pack;
Sterile gloves replace disposable gloves using aseptic technique
Microbiological sampling of surgical sets
Inner wrapping sampled with moistened sterile
swab and broth inoculated;
Wrappings folded back to sample inner box or
tray: swabs inoculated into broth;
Instruments sampled on untouched areas only:
swabs inoculated into broth
Adapted from Widmer et al, J Hosp Infect 1992; Webster et al, AmJIC 2005
Additional swab inoculated into broth to act as process and sterility control
Settle plates incubated aerobically for 48 hours;
Broths incubated for 5-7 days and sub-cultured if cloudy;
Terminal subcultures performedon clear broths at 7 days
Results discarded if any growth occurred on settle plates
Visual and microbiological findings from ‘sterile’ surgical packs
Pack type Visual
appearance
Culture from
wrappings
Culture from
instrument(s)
Ophthalmic set Damp; discoloured CNS CNS x2
Cystoscopy set Damp NG Bacillus & CNS x4
Hysteroscope Damp; discoloured NG Bacillus & CNS x2
Maxidriver set Normal NG Bacillus & CNS x4
Maxidriver set Damp Bacillus spp. Bacillus & CNS x4
Medullary set Damp NG Bacillus spp.
Tibial Nail set Normal NG Bacillus x2
Phacoemulsifier Normal NG CNS
Strabismus set Discoloured NG Bacillus spp.
Phacoemulsifier Damp; discoloured NG Bacillus & CNS x3
Fasciotomy set Slightly discoloured NG Bacillus x2
Microbiological results from all 20 patients
Twelve specimens grew CNS, three of which also had faecal-type flora
One specimen grew CNS and Bacillus sp.
One specimen (vitreous humour) grew Bacillus sp.
Four specimens grew faecal-type flora only
One specimen grew methicillin-susceptible Staphylococcus aureus
There were no microbiological results for one patient
Six patients had aspirates/tissue sent from subsequent surgical revision:
Of these, three specimens grew CNS alone
One grew Bacillus sp.
There was no growth from specimens from two patients
All patients were treated with vancomycin and gentamicin
Further actions following microbiological findings
Immediate site visit to the sterile services provider!
We found:
drab and dusty autoclave area, with poorly maintained fabric;
no wash hand basin facilities within the autoclave area;
no evidence of baffle plates or functioning indicators in the autoclaves;
sterilisedpackages were stored on, or just off, the floor of the autoclave area;
lack of assurance for adequate drying/cooling of packages;
metal gurneys used to transfer sterilised sets between autoclave and transfer cart
were corrodedwith rust.
We set up a Healthboard Sterile Services
Governance Committee, for better communication
between sterile services, managers and NHS staff.
We review all aspects of procurement, cleaning,
sterilisation and repair of surgical instruments used
across the Healthboard. In addition, all sterile sets
are routinely inspected and signed off by a senior
theatre nurse on delivery at the theatre complex.
What did we do?
Actions agreed by sterile services
provider and hospital managers
Sterile services:
Staff training review
Hand hygiene practices
Electronic tracking
Incident reporting process
Hospital:
Monitoring of sterile packs on receipt from provider
Computer based notification of faulty; missing; damaged or wet packs
Surgical site infection surveillance for high-risk specialties
BOTH:
Creation of a governance committee to oversee sterile services
Review fault notifications and trends
Review new kit; missing kit; fast track service and overall
turnaround times
WHY were there no cases among
vascular graft patients?
Surgical prophylaxis for orthopaedics was:
CEFUROXIME
Surgical prophylaxis for cataract surgery was:
CEFUROXIME
....but surgical prophylaxis for vascular surgery is:
VANCOMYCIN
Conclusion
Faulty processing of reusable surgical instruments has serious
clinical implications for patients
Surgical sets should always be carefully inspected on reception. There
should be close collaboration between decontamination, theatre and
infection control staff, particularly if sterile services are located off-site.
This presentation has
highlighted the importance of
surgical instrument processing
by sterile sevice facilities
Acknowledgements
We would like to acknowledge the huge amount of work performed
by managers, clinicians, infection control, theatre and
decontaminationstaff, some of which continues with regular
meetings and audit exercises.
Without support from all the staff involved, we would not have been
able to produce the relevant action plans or set up a long-term
specialist group to safe-guard future practices.
Surgical site infection rates have remained within the expected
range for Scotland over the last five years
Dancer SJ, Stewart M, Coulombe C, Virdi M, Gregori A. (2012) Investigation of increased surgical
site infections among Orthopaedic and Ophthalmology patients. J Hosp Infect 81: 231-38.
Ssi outbreak 2009 (4)

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Ssi outbreak 2009 (4)

  • 1. Professor Stephanie Dancer NHS Lanarkshire & Edinburgh Napier University, Scotland Investigating an outbreak of surgical site infections among Orthopaedic and Ophthalmology patients
  • 2. Recognition of an outbreak April 2009: Sudden increase in infection rate for ‘clean’ surgical procedures for orthopaedic patients receiving hip or knee prostheses; There were also cases of acute endophthalmitis after eye surgery Since our hospital reports such infections promptly for surveillance purposes, a sudden increase in infection rates ought to have alerted Infection Control staff early; BUT...there was no obvious ‘outbreak’ organism, so initial cases did not raise the alarm as they should have done.
  • 3. Dates of operation and onset of surgical site infection for twenty orthopaedic and ophthalmic patients
  • 4. Retrospective investigation revealed possible missed cases! Then there was a second surge of cases because we had failed to rectify the underlying cause
  • 5. Orthopaedic patients Fifteenorthopaedic patients were involved in the outbreak. Eleven had knee or hip implant surgery (two were revisions). The remainder were bilateral osteotomies; internal fixation of an ankle fracture; bunion repair with screws; and a fasciotomy with external medullary fixation. No obvious microbiological pathogen was found from submitted specimens (wound swabs, aspirates, tissue, etc.) Six patients required further surgery, e.g. wash- outs; joint revision, etc. One patient died. One patient required two further attempts to replace his knee prosthesis.
  • 6. Ophthalmology patients Phacoemulsificationis method of cataract surgery in which the internal lens of the eye is emulsified using ultrasonic energy and replaced with an intraocular lens implant. Five patients who underwent cataract surgery within the outbreak period suffered post-operative endophthalmitis. This is potentially devastating for the patient since it can cause permament visual deficit or even blindness. All five patients required further surgery. One sufferedpermament visual deficit.
  • 7. Initial microbiology results Orthopaedic specimens Coagulase-negative staphylococci +/- Bacillus spp. with or without faecal-type flora (different species) Ophthalmology specimens The only organisms retrieved from submitted vitreous humour were coagulase-negative staphylococci or Bacillus spp. Bacillus spp. on blood agar Gram-stain of staph
  • 8. Actions taken Outbreak committee convened! Reviewof ward and theatre practices Epidemiological analyses Inspection of orthopaedic theatres Reviewof microbiological results Infectioncontrol audit, including hand hygiene Maintenance services for laminar flow Terminal cleans for orthopaedic wards Antibiotic prophylaxis changed Theatres deep cleaned Increasedvigilance for further cases, with additional microbiological investigations
  • 9. Two months later: Resurgence of outbreak with two cases of endophthalmitis Outbreak committee reconvened, with medical director and hospital managers Theatre staff volunteered concerns over damp and/or stained packs of surgical instruments returning from sterile services provider Staining was usually orange/brown in colour We decided to audit damp and/or discolouredpacks; Packs were selected for microbiological examination. Surgical instruments used for high risk surgery (eyes, orthopaedics and vascular) were sent to another sterile services provider ona temporary basis.
  • 10.
  • 11.
  • 12. Microbiological examination of surgical sets Level 1 laminar flow cabinet with Hepa-Afiltration in a Category 3 room was disinfected and allowed to run for 30 mins before processing; Control settle plates positioned within the cabinet Adapted from Widmer et al, J Hosp Infect 1992; Webster et al, AmJIC 2005 Pack and media bottles sprayed with disinfectant (Trigene) before placing in the cabinet; Gloved operator removes outer layer of pack; Sterile gloves replace disposable gloves using aseptic technique
  • 13. Microbiological sampling of surgical sets Inner wrapping sampled with moistened sterile swab and broth inoculated; Wrappings folded back to sample inner box or tray: swabs inoculated into broth; Instruments sampled on untouched areas only: swabs inoculated into broth Adapted from Widmer et al, J Hosp Infect 1992; Webster et al, AmJIC 2005 Additional swab inoculated into broth to act as process and sterility control Settle plates incubated aerobically for 48 hours; Broths incubated for 5-7 days and sub-cultured if cloudy; Terminal subcultures performedon clear broths at 7 days Results discarded if any growth occurred on settle plates
  • 14. Visual and microbiological findings from ‘sterile’ surgical packs Pack type Visual appearance Culture from wrappings Culture from instrument(s) Ophthalmic set Damp; discoloured CNS CNS x2 Cystoscopy set Damp NG Bacillus & CNS x4 Hysteroscope Damp; discoloured NG Bacillus & CNS x2 Maxidriver set Normal NG Bacillus & CNS x4 Maxidriver set Damp Bacillus spp. Bacillus & CNS x4 Medullary set Damp NG Bacillus spp. Tibial Nail set Normal NG Bacillus x2 Phacoemulsifier Normal NG CNS Strabismus set Discoloured NG Bacillus spp. Phacoemulsifier Damp; discoloured NG Bacillus & CNS x3 Fasciotomy set Slightly discoloured NG Bacillus x2
  • 15. Microbiological results from all 20 patients Twelve specimens grew CNS, three of which also had faecal-type flora One specimen grew CNS and Bacillus sp. One specimen (vitreous humour) grew Bacillus sp. Four specimens grew faecal-type flora only One specimen grew methicillin-susceptible Staphylococcus aureus There were no microbiological results for one patient Six patients had aspirates/tissue sent from subsequent surgical revision: Of these, three specimens grew CNS alone One grew Bacillus sp. There was no growth from specimens from two patients All patients were treated with vancomycin and gentamicin
  • 16. Further actions following microbiological findings Immediate site visit to the sterile services provider! We found: drab and dusty autoclave area, with poorly maintained fabric; no wash hand basin facilities within the autoclave area; no evidence of baffle plates or functioning indicators in the autoclaves; sterilisedpackages were stored on, or just off, the floor of the autoclave area; lack of assurance for adequate drying/cooling of packages; metal gurneys used to transfer sterilised sets between autoclave and transfer cart were corrodedwith rust.
  • 17. We set up a Healthboard Sterile Services Governance Committee, for better communication between sterile services, managers and NHS staff. We review all aspects of procurement, cleaning, sterilisation and repair of surgical instruments used across the Healthboard. In addition, all sterile sets are routinely inspected and signed off by a senior theatre nurse on delivery at the theatre complex. What did we do?
  • 18. Actions agreed by sterile services provider and hospital managers Sterile services: Staff training review Hand hygiene practices Electronic tracking Incident reporting process Hospital: Monitoring of sterile packs on receipt from provider Computer based notification of faulty; missing; damaged or wet packs Surgical site infection surveillance for high-risk specialties BOTH: Creation of a governance committee to oversee sterile services Review fault notifications and trends Review new kit; missing kit; fast track service and overall turnaround times
  • 19. WHY were there no cases among vascular graft patients? Surgical prophylaxis for orthopaedics was: CEFUROXIME Surgical prophylaxis for cataract surgery was: CEFUROXIME ....but surgical prophylaxis for vascular surgery is: VANCOMYCIN
  • 20.
  • 21. Conclusion Faulty processing of reusable surgical instruments has serious clinical implications for patients Surgical sets should always be carefully inspected on reception. There should be close collaboration between decontamination, theatre and infection control staff, particularly if sterile services are located off-site. This presentation has highlighted the importance of surgical instrument processing by sterile sevice facilities
  • 22. Acknowledgements We would like to acknowledge the huge amount of work performed by managers, clinicians, infection control, theatre and decontaminationstaff, some of which continues with regular meetings and audit exercises. Without support from all the staff involved, we would not have been able to produce the relevant action plans or set up a long-term specialist group to safe-guard future practices. Surgical site infection rates have remained within the expected range for Scotland over the last five years Dancer SJ, Stewart M, Coulombe C, Virdi M, Gregori A. (2012) Investigation of increased surgical site infections among Orthopaedic and Ophthalmology patients. J Hosp Infect 81: 231-38.