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
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
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
Good evening everyone . I will be discussing about the role of dair and stage 1 revision in cases of infected TKA
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)
As per this 2016 review in arthroplasty today where they analysed the infection rates across various joint registries … the incidence of ……………………….
The most widely used definition to establish pji was put forth by MSIS group in 2011 ………….
Out of all the parameters described TISSUE CULTURE has the highest sensitivity and specificity
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
Tsukayama in 1996 described a classification based on the time interval from index surgery …………..
And this classification also dictates treatment to a certain extent ……………………..
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
CCI … predicts the 10y survival rate depending on multiple host factors …
Finally the success of any rev. surgery also depends on the virulence of the infecting organism..
So coming to dair… this is one the early documented papers on DAIR
WHAT are the steps of a dair ??
The EFFORT group in 2019 has put forth some recent guidelines …. Where they say that…………………..
When it comes to dair……
So what constitutes an ideal dair ???
But this is rarely the scenario
Parvizi and colleagues in 2019 described crime 80 criteria to predict the preop risk of dair failure
So coming to the role of…….according to this 2012 article fro gallezzi institute Italy ..
As to the role of rifampicin…..
Although the conventional teaching is that dair should ideally be done in < 4 weeks…..grammatopolus in 2017….
Now After the dair is done… ..how do v define success ???
So if the dair fails next logical step is staged revision . -
Staged revision is usually done for chronically infected cases and many times the presentation is like this …
Coming to exposure….
Some modifications have been made over the years………