86 patients (70.5%) were diagnosed with transient synovitis. All the 7 re-admissions were from this group. Only one of the re-admissions was diagnosed with confirmed septic arthritis. 4 patients (3.3%) were diagnosed with definite septic arthritis with positive cultures from the hip, and 1 (0.8%) with probable septic arthritis (negative culture). The presence of the clinical predictors was compared between the transient synovitis and septic arthritis groups, using Fisher’s exact test. Only the raised temperature and CRP were found to be significantly different (p<
0.05). Only two children (40%) with confirmed septic arthritis had four or more predictors (one had all five, and the other was able to partially weight bear). The third child had a raised temperature and CRP, and the fourth had a raised temperature only. The fifth patient (20%) was diagnosed with probable septic arthritis. His cultures were negative, but he was already on intravenous antibiotics. This patient did not have any of the predictors on admission (temperature was 38.3°C, CRP 10.7). However, he spiked a temperature of 40°C 24 hours post admission despite being on antibiotics, and his CRP increased to 34.5mg/L. In the transient synovitis group, two patients (2.2%) had positive five predictors, but were proven to have transient synovitis secondary to a urinary tract infection and gastroenteritis. 47 patients (51.6%) did not have any of the predictors, and 6 patients (6.6%) had three or more positive predictors.
Establishing the diagnosis in a child presenting with an atraumatic limp can be challenging. There is particular difficulty distinguishing septic arthritis (SA) from transient synovitis (TS) and consequently clinical prediction algorithms have been devised to differentiate the conditions using the presence of fever, raised erythrocyte sedimentation rate (ESR), raised white cell count (WCC) and inability to weight bear. Within Europe measurement of the ESR has largely been replaced with assessment of C-reactive protein (CRP) as an acute phase protein. We have evaluated the utility of including CRP in a clinical prediction algorithm to distinguish TS from SA. All children with a presentation of ‘atraumatic limp’ and a proven effusion on hip ultrasound between 2004 and 2009 were included. Patient demographics, details of the clinical presentation and laboratory investigations were documented to identify a response to each of four variables (Weight bearing status, WCC >12,000 cells/m3, CRP >20mg/L and Temperature >38.5 degrees C. The definition of SA was based upon microscopy and culture of the joint fluid collected at arthrotomy.Background
Method