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Infected TKA
1. DAIR
2. Stage 1 revision
Dr Aditya Apte
Sunshine hospitals
• Foreign object
• Inefficient phagocytic response ,Neutrophil degranulation
• Frustrated phagocytosis
• Minimum infective conc. Of bacteria decreases by 10(5)
• INCIDENCE – (2016)
• Primary tka- 0.8 – 1.5 %
• Primary tha – 1 – 2.7 %
MSIS 2011 :
1. There is a sinus tract communicating with the prosthesis; or
2. A pathogen is isolated by culture from at least two separate tissue or
fluid samples obtained from the affected prosthetic joint; or
3. 4/6 of following :
a. Esr >30mm/hr , crp >10mg/l
b.Synovial wbc > 20,000
c. Synovial PMN % > 89 %
d. Presence of purulence in the affected joint
e. Isolation of microorganism in one culture
f. > 5 neutrophils / hpf in 5 hpf ( 400x magnification )
• 1. antibiotics
• 2. DAIR
• 3. two stage revision
• 4. single stage revision
• 5. arthrodesis , amputation
• Success rate –
• Time interval
• Immune status / comorbidity
• Virulence
I-Acute postoperative- < 4 weeks
II-Late chronic - > 4 weeks
III-Acute hematogenous
IV-Positive intra op culture – two or more positive intra op cultures
I,III- DAIR
II- Staged revision
IV- antibiotics
Mcpherson 1999
eg. II, B , 1
Mary charlson,1986 , New York
Success rate
• Coagulase neg staph
• Staph aureus
• Streptococci
• MRSA
DAIR
112 cases , success rate 78% at 3 years
• Excision of wound margins
• Debridement of necrotic soft tissues and debris
• Collection of pus samples from multiple sites
• Assess prosthesis integrity
• Exchange modular component
• Pulse lavage( HV + LP , 6-9L) + 0.05 % aqueous chlorhexidine solution
• Primary closure + drain
*Preoperative antibiotic omission – no longer recommended
• Empirical antibiotic therapy – best avoided
• inj vancomycin 1g bd + inj meropenem 500mg tds
• Reports- modified accordingly
• 6 weeks iv + upto 12 months oral
• No role of extended iv antibiotics
Contraindications for DAIR
• 1. Loose prosthesis
• 2. sinus tract
• 3. inability to close the wound
• 4. mrsa / polymicrobial
Ideal DAIR -
• 1. within 4 to 6 weeks
• 2. low virulence
• 3. non immunocompromised host
• 4. THOROUGH DEBRIDEMENT + poly exchange
• 5. 6-8 weeks of iv antibiotics
Worse prognosis :
1.SCORE > 3
2. S. aureus
1. intraarticular antibiotics ? X
2.Antibiotic impreg. Pellets ? X
3. NO ROLE OF MULTIPLE DAIRS
Role of rifampicin ? 2x450mg x 6weeks
1. Not time dependent…
Delphi criteria :
1. no infection recurrence caused by same strain
2. no subsequent surgical intervention
3. no infection related mortality
follow up- short – 2y
medium- 5y
long - > 10y
Stage 1 revision :
• Insall 1983- first two stage revision
• Booth – 74 %
Exposure
• Prior incision is used
• Multiple – lateral most
• Sinuses- incorporated and excised
• Avoid subcutaneous dissection
• Incision depth – upto deep fascia
“ most important step in revision is
DEBRIDEMENT.. If that is compromised all
subsequent surgeries will surely fail “ – J. Parvizi
• Preferably without tourniquet
• Better demarcation
• Excise all dead , necrotic tissue
Implant removal
• Poly – femur – tibia
• Specialised extractor sets
• Longitudnal force
• Implant –cement interface
• Antibiotic properties –
• Heat stable
• Broad spectrum
• Low risk of allergy
• Powder form ( homogenous distribution )
• Avoid vacuum mixing
• < 4g/40gm pmma
• vancomycin (2g), tobramycin( 2.4g), cefuroxime (1.5g) / 80 gm
• High initial release.. Constant elution over next few days
• Passive oppurtunism –
• Better elution properties on addition of a second antibiotic
• Addition of tobramycin in 40g pmma , improves the elution of
vancomycin
• Static spacer –
• Joint distraction
• Stability
• Articulating spacer –
• Reduced bone loss
• Allows partial wt bearing
• Better ROM
Articulating spacers
• 1.Cement on cement –
• Stainless steel mold for femur
• Stemmed all cement tibial tray
• Prevent interdigitation – tourniquet released
• 2.Cement on polyethylene –
• All cement femoral component + antibiotic cement coated thin tibia
poly
• Highest rates of reinfection
• 3. Metal on polyethelene –
• Reimplant femoral component + thin tibial poly
• Jamsen et al-
• All cement vs Hoffmann technique
• Better outcome -decreased blood loss
• Better post op KSS
1.Better than prostalac
2.no metal/poly surface
3.better antibiotic elution
Foil technique 2007 , IJO
1. Similar reinfection rates
2. Better rom ( 107 vs 84)
1. Small molecules- d aminoacids , n acetyl cysteine
2. Matrix targeting enzymes – dispersin B
• Thank you.

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Infected total knee arthroplasty

  • 1. Infected TKA 1. DAIR 2. Stage 1 revision Dr Aditya Apte Sunshine hospitals
  • 2. • Foreign object • Inefficient phagocytic response ,Neutrophil degranulation • Frustrated phagocytosis • Minimum infective conc. Of bacteria decreases by 10(5)
  • 3. • INCIDENCE – (2016) • Primary tka- 0.8 – 1.5 % • Primary tha – 1 – 2.7 %
  • 4. MSIS 2011 : 1. There is a sinus tract communicating with the prosthesis; or 2. A pathogen is isolated by culture from at least two separate tissue or fluid samples obtained from the affected prosthetic joint; or 3. 4/6 of following : a. Esr >30mm/hr , crp >10mg/l b.Synovial wbc > 20,000 c. Synovial PMN % > 89 % d. Presence of purulence in the affected joint e. Isolation of microorganism in one culture f. > 5 neutrophils / hpf in 5 hpf ( 400x magnification )
  • 5.
  • 6. • 1. antibiotics • 2. DAIR • 3. two stage revision • 4. single stage revision • 5. arthrodesis , amputation • Success rate – • Time interval • Immune status / comorbidity • Virulence
  • 7. I-Acute postoperative- < 4 weeks II-Late chronic - > 4 weeks III-Acute hematogenous IV-Positive intra op culture – two or more positive intra op cultures I,III- DAIR II- Staged revision IV- antibiotics
  • 10. Success rate • Coagulase neg staph • Staph aureus • Streptococci • MRSA
  • 11. DAIR 112 cases , success rate 78% at 3 years
  • 12. • Excision of wound margins • Debridement of necrotic soft tissues and debris • Collection of pus samples from multiple sites • Assess prosthesis integrity • Exchange modular component • Pulse lavage( HV + LP , 6-9L) + 0.05 % aqueous chlorhexidine solution • Primary closure + drain
  • 13. *Preoperative antibiotic omission – no longer recommended • Empirical antibiotic therapy – best avoided • inj vancomycin 1g bd + inj meropenem 500mg tds • Reports- modified accordingly • 6 weeks iv + upto 12 months oral • No role of extended iv antibiotics
  • 14. Contraindications for DAIR • 1. Loose prosthesis • 2. sinus tract • 3. inability to close the wound • 4. mrsa / polymicrobial
  • 15. Ideal DAIR - • 1. within 4 to 6 weeks • 2. low virulence • 3. non immunocompromised host • 4. THOROUGH DEBRIDEMENT + poly exchange • 5. 6-8 weeks of iv antibiotics
  • 16. Worse prognosis : 1.SCORE > 3 2. S. aureus
  • 17. 1. intraarticular antibiotics ? X 2.Antibiotic impreg. Pellets ? X 3. NO ROLE OF MULTIPLE DAIRS
  • 18. Role of rifampicin ? 2x450mg x 6weeks
  • 19. 1. Not time dependent…
  • 20. Delphi criteria : 1. no infection recurrence caused by same strain 2. no subsequent surgical intervention 3. no infection related mortality follow up- short – 2y medium- 5y long - > 10y
  • 21. Stage 1 revision : • Insall 1983- first two stage revision • Booth – 74 %
  • 22. Exposure • Prior incision is used • Multiple – lateral most • Sinuses- incorporated and excised • Avoid subcutaneous dissection • Incision depth – upto deep fascia
  • 23.
  • 24. “ most important step in revision is DEBRIDEMENT.. If that is compromised all subsequent surgeries will surely fail “ – J. Parvizi • Preferably without tourniquet • Better demarcation • Excise all dead , necrotic tissue
  • 25. Implant removal • Poly – femur – tibia • Specialised extractor sets • Longitudnal force • Implant –cement interface
  • 26.
  • 27.
  • 28. • Antibiotic properties – • Heat stable • Broad spectrum • Low risk of allergy • Powder form ( homogenous distribution ) • Avoid vacuum mixing • < 4g/40gm pmma • vancomycin (2g), tobramycin( 2.4g), cefuroxime (1.5g) / 80 gm • High initial release.. Constant elution over next few days
  • 29. • Passive oppurtunism – • Better elution properties on addition of a second antibiotic • Addition of tobramycin in 40g pmma , improves the elution of vancomycin
  • 30. • Static spacer – • Joint distraction • Stability • Articulating spacer – • Reduced bone loss • Allows partial wt bearing • Better ROM
  • 31.
  • 32. Articulating spacers • 1.Cement on cement – • Stainless steel mold for femur • Stemmed all cement tibial tray • Prevent interdigitation – tourniquet released
  • 33. • 2.Cement on polyethylene – • All cement femoral component + antibiotic cement coated thin tibia poly • Highest rates of reinfection
  • 34. • 3. Metal on polyethelene – • Reimplant femoral component + thin tibial poly
  • 35.
  • 36.
  • 37. • Jamsen et al- • All cement vs Hoffmann technique • Better outcome -decreased blood loss • Better post op KSS
  • 38.
  • 39.
  • 40. 1.Better than prostalac 2.no metal/poly surface 3.better antibiotic elution
  • 42.
  • 43. 1. Similar reinfection rates 2. Better rom ( 107 vs 84)
  • 44.
  • 45. 1. Small molecules- d aminoacids , n acetyl cysteine 2. Matrix targeting enzymes – dispersin B

Editor's Notes

  1. Good evening everyone . I will be discussing about the role of dair and stage 1 revision in cases of infected TKA
  2. Whenever a foreign object is implanted inside the body it leads to a phagocytic response – neutrophil degran. Loss of defensins- frustrated phagocytosis – ultimately the MIC decreases by 10 (5)
  3. As per this 2016 review in arthroplasty today where they analysed the infection rates across various joint registries … the incidence of ……………………….
  4. The most widely used definition to establish pji was put forth by MSIS group in 2011 ………….
  5. Out of all the parameters described TISSUE CULTURE has the highest sensitivity and specificity
  6. So after a tka has been diagnosed as infected there are multiple ways in which on can proceed.. ..and the choice of treatment depends on multiple factors… But the successs of these depend on 3 main factors
  7. Tsukayama in 1996 described a classification based on the time interval from index surgery ………….. And this classification also dictates treatment to a certain extent ……………………..
  8. Another classification that is actually derived from the cerny mader classification of OM … mcpherson classi. Where each joint is classified according to the infection type/ host properties / local factors For eg. II B 1
  9. CCI … predicts the 10y survival rate depending on multiple host factors …
  10. Finally the success of any rev. surgery also depends on the virulence of the infecting organism..
  11. So coming to dair… this is one the early documented papers on DAIR
  12. WHAT are the steps of a dair ??
  13. The EFFORT group in 2019 has put forth some recent guidelines …. Where they say that…………………..
  14. When it comes to dair……
  15. So what constitutes an ideal dair ??? But this is rarely the scenario
  16. Parvizi and colleagues in 2019 described crime 80 criteria to predict the preop risk of dair failure
  17. So coming to the role of…….according to this 2012 article fro gallezzi institute Italy ..
  18. As to the role of rifampicin…..
  19. Although the conventional teaching is that dair should ideally be done in < 4 weeks…..grammatopolus in 2017….
  20. Now After the dair is done… ..how do v define success ???
  21. So if the dair fails next logical step is staged revision . -
  22. Staged revision is usually done for chronically infected cases and many times the presentation is like this … Coming to exposure….
  23. Some modifications have been made over the years………