71.18 Synovial White Cell Count For Diagnosis Of Septic Arthritis. Are Current Tests Appropriate?

K. Perera1, M. Armstrong1  1Eastern Health,Melbourne, VICTORIA, Australia

Introduction:

Septic arthritis is an emergency, potentially causing irreversible joint destruction and

disability. Synovial WCC and polymorphonuclear cell percentage is the best predictor of

septic arthritis likelihood. Yet, synovial WCC and differential are not routinely assessed.

We aim to investigate the incidence of this and develop correct synovial fluid analysis

practices.

Methods:

A retrospective analysis of native joints having had arthrocentesis for suspicion of septic

arthritis at Box Hill Hospital (BHH) between September 2011 and September 2013

inclusive. Recruitment was from the Eastern Health Decision Support Service (DSS), who

maintains a database compiled from all systems within Eastern Health; of which BHH is a

member.

The study was limited to large joints; this includes hip, knee and shoulder. All prosthetic

joints were excluded from the patient population.

All patient histories were examined for suspicion of septic arthritis and subsequent

arthrocentesis. Pathology records were accessed to determine incidence of cell count and

differential.

Results:

One hundred and thirty-six cases of joint aspirations were identified within the time frame,

of which sixty-seven fit our criteria for evaluation. All but two cases were delivered using

the DSS, which was limited to data compiled only until June 2013. The two remaining

cases were identified with a manual search of the radiology and pathology databases from

June to September 2013.

22 of the 67 joint aspirates studied did not have a cell count carried out. Four of these 22

cases had a diagnosis of septic arthritis. In five aspirates, there was a failure to confirm a

definite diagnosis and were thus conservatively treated as a septic joint. The remaining

acute joints in which no cell count was done were gout (7 cases), pseudogout (5 cases) and

rheumatoid arthritis (1 case).

Cell counts were not routinely detected for a variety of reasons. Eleven aspirates were

deemed too viscous, and in eight cases the sample had clotted prior to pathologist

assessment. Two cases had insufficient volume, and one sample was too bloodstained to

calculate a cell count and differential; likely due to traumatic aspiration.

Conclusion:

33% of acute monoarthritis’ evaluated over the study period failed to have a synovial fluid

WCC and differential. This may be due to inadequate samples, or lack of appropriate

collection tube. Better education is required for appropriate collection and test requesting

wherein a diagnosis of septic arthritis is in question.