Although there are clinical features and laboratory results that are highly suggestive of septic arthritis, there is no single factor that is 100% sensitive or 100% specific for the diagnosis. The key to diagnosis is the level of clinical suspicion of a clinician experienced in the management of musculoskeletal disease. If clinical suspicion is high then it is imperative to treat for presumed septic arthritis, regardless of the results of blood tests or microbiology.[12]Coakley G, Mathews C, Field M, et al. BSR and BHPR, BOA, RCGP and BSAC guidelines for management of the hot swollen joint in adults. Rheumatology (Oxford). 2006 Aug;45(8):1039-41.
https://academic.oup.com/rheumatology/article/45/8/1039/1784962
http://www.ncbi.nlm.nih.gov/pubmed/16829534?tool=bestpractice.com
If a patient with signs or symptoms suggestive of infection is acutely deteriorating, clinicians should consider the possibility of sepsis and urgently undertake a systematic evaluation to identify those at risk of deterioration due to organ dysfunction, referring to local guidance where appropriate.[13]National Institute for Health and Care Excellence. Sepsis: recognition, diagnosis and early management. Sep 2017 [internet publication].
https://www.nice.org.uk/guidance/ng51
[14]Evans L, Rhodes A, Alhazzani W, et al. Surviving Sepsis Campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021 Nov 1;49(11):e1063-143.
https://www.doi.org/10.1097/CCM.0000000000005337
http://www.ncbi.nlm.nih.gov/pubmed/34605781?tool=bestpractice.com
See Sepsis in adults and Sepsis in children.
History
Septic arthritis usually presents with a short history of a hot, swollen, painful joint (or joints) with associated restriction of movement.[3]Weston VC, Jones AC, Bradbury N, et al. Clinical features and outcome of septic arthritis in a single UK health district 1982-1991. Ann Rheum Dis. 1999 Apr;58(4):214-9.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1752863/pdf/v058p00214.pdf
http://www.ncbi.nlm.nih.gov/pubmed/10364899?tool=bestpractice.com
[4]Gupta MN, Sturrock RD, Field M. A prospective 2-year study of 75 patients with adult-onset septic arthritis. Rheumatology (Oxford). 2001 Jan;40(1):24-30.
http://rheumatology.oxfordjournals.org/cgi/content/full/40/1/24
http://www.ncbi.nlm.nih.gov/pubmed/11157138?tool=bestpractice.com
Presentation may be more insidious in the context of a low-virulence organism or tuberculosis, or if the joint is prosthetic.[4]Gupta MN, Sturrock RD, Field M. A prospective 2-year study of 75 patients with adult-onset septic arthritis. Rheumatology (Oxford). 2001 Jan;40(1):24-30.
http://rheumatology.oxfordjournals.org/cgi/content/full/40/1/24
http://www.ncbi.nlm.nih.gov/pubmed/11157138?tool=bestpractice.com
[5]Gupta MN, Sturrock RD, Field M. Prospective comparative study of patients with culture proven and high suspicion of adult onset septic arthritis. Ann Rheum Dis. 2003 Apr;62(4):327-31.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754487/pdf/v062p00327.pdf
http://www.ncbi.nlm.nih.gov/pubmed/12634231?tool=bestpractice.com
In the context of underlying joint disease, a septic joint should be suspected if symptoms in the affected joint are out of proportion to the disease activity detected elsewhere. In up to 22% of cases septic arthritis is polyarticular.[2]Kaandorp CJ, Dinant HJ, van de Laar MA, et al. Incidence and sources of native and prosthetic joint infection: a community based prospective survey. Ann Rheum Dis. 1997 Aug;56(8):470-5.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1752430/pdf/v056p00470.pdf
http://www.ncbi.nlm.nih.gov/pubmed/9306869?tool=bestpractice.com
[6]Dubost JJ, Soubrier M, De Champs C, et al. No changes in the distribution of organisms responsible for septic arthritis over a 20 year period. Ann Rheum Dis. 2002 Mar;61(3):267-9.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754020/pdf/v061p00267.pdf
http://www.ncbi.nlm.nih.gov/pubmed/11830437?tool=bestpractice.com
Risk factors
Risk factors for the development of septic arthritis include rheumatoid arthritis, osteoarthritis, joint prostheses, low socioeconomic status, intravenous drug abuse, alcohol use disorder, diabetes, previous intra-articular corticosteroid injection, and the presence of cutaneous ulcers. In sexually active patients gonococcal arthritis may be suspected.[2]Kaandorp CJ, Dinant HJ, van de Laar MA, et al. Incidence and sources of native and prosthetic joint infection: a community based prospective survey. Ann Rheum Dis. 1997 Aug;56(8):470-5.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1752430/pdf/v056p00470.pdf
http://www.ncbi.nlm.nih.gov/pubmed/9306869?tool=bestpractice.com
[3]Weston VC, Jones AC, Bradbury N, et al. Clinical features and outcome of septic arthritis in a single UK health district 1982-1991. Ann Rheum Dis. 1999 Apr;58(4):214-9.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1752863/pdf/v058p00214.pdf
http://www.ncbi.nlm.nih.gov/pubmed/10364899?tool=bestpractice.com
[4]Gupta MN, Sturrock RD, Field M. A prospective 2-year study of 75 patients with adult-onset septic arthritis. Rheumatology (Oxford). 2001 Jan;40(1):24-30.
http://rheumatology.oxfordjournals.org/cgi/content/full/40/1/24
http://www.ncbi.nlm.nih.gov/pubmed/11157138?tool=bestpractice.com
[6]Dubost JJ, Soubrier M, De Champs C, et al. No changes in the distribution of organisms responsible for septic arthritis over a 20 year period. Ann Rheum Dis. 2002 Mar;61(3):267-9.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754020/pdf/v061p00267.pdf
http://www.ncbi.nlm.nih.gov/pubmed/11830437?tool=bestpractice.com
[7]Sharp JT, Lidsky MD, Duffy J, et al. Infectious arthritis. Arch Intern Med. 1979 Oct;139(10):1125-30.
http://www.ncbi.nlm.nih.gov/pubmed/485744?tool=bestpractice.com
[8]Meijers KA, Dijkmans BA, Hermans J, et al. Non-gonococcal infectious arthritis: a retrospective study. J Infect. 1987 Jan;14(1):13-20.
http://www.ncbi.nlm.nih.gov/pubmed/3819454?tool=bestpractice.com
The incidence of MRSA is increasing in North America.[15]Arnold SR, Elias D, Buckingham SC, et al. Changing patterns of acute hematogenous osteomyelitis and septic arthritis: emergence of community-associated methicillin-resistant Staphylococcus aureus. J Pediatr Orthop. 2006 Nov-Dec;26(6):703-8.
http://www.ncbi.nlm.nih.gov/pubmed/17065930?tool=bestpractice.com
Those patients particularly at risk are recent inpatients, nursing home residents, and those with leg ulceration or indwelling urinary catheters. Tuberculous arthritis is also becoming more frequent and should be suspected in immunocompromised people and in those from regions where tuberculosis is prevalent.
Examination
The characteristic features of an infected joint are swelling, warmth, tenderness, and a significant reduction in the range of movement. The presence or absence of a fever is not a reliable indicator of joint sepsis.[3]Weston VC, Jones AC, Bradbury N, et al. Clinical features and outcome of septic arthritis in a single UK health district 1982-1991. Ann Rheum Dis. 1999 Apr;58(4):214-9.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1752863/pdf/v058p00214.pdf
http://www.ncbi.nlm.nih.gov/pubmed/10364899?tool=bestpractice.com
[4]Gupta MN, Sturrock RD, Field M. A prospective 2-year study of 75 patients with adult-onset septic arthritis. Rheumatology (Oxford). 2001 Jan;40(1):24-30.
http://rheumatology.oxfordjournals.org/cgi/content/full/40/1/24
http://www.ncbi.nlm.nih.gov/pubmed/11157138?tool=bestpractice.com
[5]Gupta MN, Sturrock RD, Field M. Prospective comparative study of patients with culture proven and high suspicion of adult onset septic arthritis. Ann Rheum Dis. 2003 Apr;62(4):327-31.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754487/pdf/v062p00327.pdf
http://www.ncbi.nlm.nih.gov/pubmed/12634231?tool=bestpractice.com
[6]Dubost JJ, Soubrier M, De Champs C, et al. No changes in the distribution of organisms responsible for septic arthritis over a 20 year period. Ann Rheum Dis. 2002 Mar;61(3):267-9.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754020/pdf/v061p00267.pdf
http://www.ncbi.nlm.nih.gov/pubmed/11830437?tool=bestpractice.com
Laboratory investigations
If septic arthritis is suspected, it is mandatory to aspirate the joint to obtain a sample of synovial fluid before antimicrobial therapy is started.[11]Earwood JS, Walker TR, Sue GJC. Septic arthritis: diagnosis and treatment. Am Fam Physician. 2021 Dec 1;104(6):589-97.
https://www.aafp.org/pubs/afp/issues/2021/1200/p589.html
http://www.ncbi.nlm.nih.gov/pubmed/34913662?tool=bestpractice.com
A contraindication to simple aspiration is the presence of a joint prosthesis. Under these circumstances it is recommended that any invasive procedure should be undertaken under sterile conditions in an operating room, and therefore referral to an orthopedic surgeon is recommended. It is also recommended that patients with suspected tuberculous arthritis be referred to an orthopedic surgeon, and synovial biopsy may be indicated to confirm the diagnosis.
Neither overlying cellulitis nor anticoagulation is an absolute contraindication to joint aspiration. Specialist help should be sought if the attending physician feels uncomfortable performing arthrocentesis under either of these conditions.
Synovial fluid should be sent for immediate Gram stain, white cell count, and subsequent culture. Blood cultures are also recommended at initial presentation before the start of antibiotic therapy.
The serum white cell count, erythrocyte sedimentation rate, and C-reactive protein may be helpful both in the diagnosis and the monitoring of treatment. It is therefore recommended that these investigations be performed routinely if septic arthritis is suspected.
Electrolytes and liver function tests may be performed to indicate whether there is systemic sepsis.
If the history or examination suggests an alternative, nonarticular source of infection then appropriate samples should be taken and sent for culture.
Procalcitonin (PCT) can help identify bacterial infection, and serial measurements may indicate response to therapy.[18]Sager R, Kutz A, Mueller B, et al. Procalcitonin-guided diagnosis and antibiotic stewardship revisited. BMC Med. 2017 Jan 24;15(1):15.
https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-017-0795-7
http://www.ncbi.nlm.nih.gov/pubmed/28114931?tool=bestpractice.com
However, serum PCT is not yet recommended as a routine diagnostic tool.[19]Mathews CJ, Coakley G; British Society for Rheumatology. Hot joint update 2017. Mar 2017 [internet publication].
https://www.rheumatology.org.uk/Portals/0/Documents/Guidelines/Audit%20tools/Hot_Joint_guideline_update_2017.pdf
Radiological imaging
There are no radiological investigations that have been found to be reliable in the diagnosis of septic arthritis.[20]Nijhof MW, Oyen WJ, van Kampen A, et al. Evaluation of infections of the locomotor system with indium-111-labeled human IgG scintigraphy. J Nucl Med. 1997 Aug;38(8):1300-5.
http://jnm.snmjournals.org/cgi/reprint/38/8/1300
http://www.ncbi.nlm.nih.gov/pubmed/9255172?tool=bestpractice.com
[21]Karchevsky M, Schweitzer ME, Morrison WB, et al. MRI findings of septic arthritis and associated osteomyelitis in adults. Am J Roentgenol. 2004 Jan;182(1):119-22.
http://www.ajronline.org/doi/full/10.2214/ajr.182.1.1820119
http://www.ncbi.nlm.nih.gov/pubmed/14684523?tool=bestpractice.com
However, it is recommended that a baseline plain radiograph be performed to establish any underlying joint disease at presentation.[22]American College of Radiology. ACR appropriateness criteria: suspected osteomyelitis, septic arthritis, or soft tissue infection (excluding spine and diabetic foot). 2022 [internet publication].
https://acsearch.acr.org/docs/3094201/Narrative
Magnetic resonance imaging may be helpful if associated osteomyelitis is suspected.[22]American College of Radiology. ACR appropriateness criteria: suspected osteomyelitis, septic arthritis, or soft tissue infection (excluding spine and diabetic foot). 2022 [internet publication].
https://acsearch.acr.org/docs/3094201/Narrative
If hip sepsis is suspected, it is suggested that aspiration be performed under ultrasound guidance.