Septic arthritis

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Septic arthritis
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ICD-10 M00-M03
ICD-9 711.0
eMedicine med/3394 

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Septic arthritis

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Associate Editors-In-Chief: Jumana Nagarwala, M.D., Senior Staff Physician, Department of Emergency Medicine, Henry Ford Hospital and Cafer Zorkun, M.D., Ph.D. [1]

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Overview

Septic arthritis is the invasion of the joint space by an infectious agent which produces arthritis. The usual etiology is bacterial, but viral, mycobacterial, and fungal arthritis occur occasionally. Bacteria are either carried by the bloodstream from an infectious focus elsewhere, introduced by a skin lesion that penetrates the joint, or by extension from adjacent tissue (e.g. bone or bursae).

Etiology

Bacteria are carried by the bloodstream from an infectious focus elsewhere, introduced by a skin lesion that penetrates the joint, or by extension from adjacent tissue (e.g. bone or bursae).

Micro-organisms must reach the synovial membrane of a joint. This can happen in any of the following ways:

Bacteria that are commonly found to cause septic arthritis are:

In bacterial infection, Pseudomonas aeruginosa has been found to infect joints, especially in children who have sustained a puncture wound. This bacteria also causes endocarditis.[4]

Diagnosis

Septic arthritis should be considered whenever one is assessing a patient with joint pain. Usually only one joint is affected (monoarthritis) however in seeding arthritis, several joints can be affected simultaneously; this is especially the case when the infection is caused by staphylococcus or gonococcus bacteria.

The diagnosis of septic arthritic can be difficult as no test is able to completely rule out the possibility.

A number of factors should increase ones suspicion of the presence of an infection. In children these are: fever > 38.5 C, non weight bearing, serum WCBs > 12 x 10^9, ESR > 40 mm/hr, CRP > 20 mg/dL, a previous visit for the same.[5]

Diagnosis is by aspiration (giving a turbid, non-viscous fluid), Gram stain and culture of fluid from the joint, as well as tell-tale signs in laboratory testing (such as a highly elevated neutrophils (approx. 90%), ESR or CRP). A proportion of patients with septic arthritis have little in the way of fever or raised ESR, although the CRP is usually raised [6]

The Gram stain can rule in the diagnosis of septic arthritis however cannot exclude it.[7]

Treatment

Therapy is usually with intravenous antibiotics, analgesia and washout/aspiration of the joint to dryness.

Radiologic Findings

Traditionally, the diagnosis of septic arthritis was based on clinical assessment and prompt arthrocentesis. However, the clinical picture may be obscured by multiple confounding factors and a paucity of specific findings especially for the deep joints, ie. the hip or shoulder. Imaging can be used to confirm the diagnosis of septic arthritis and more importantly, imaging findings suggestive of septic arthritis can direct the clinician to a diagnosis that may not have been considered.

Plain film findings of septic arthritis include: joint effusion, soft tissue swelling, periarticular osteoporosis, loss of joint space, marginal and central erosions and bone ankylosis. CT is more sensitive than plain films for the detection of early bone destruction and effusion.

The role of MRI in the diagnosis of septic arthritis has been increasing in recent years in an effort to detect this entity earlier. Findings are usually evident within 24 hours following the onset of infection and include: synovial enhancement, perisynovial edema and joint effusion. Signal abnormalities in the bone marrow can indicate a concomitant osteomyelitis. The sensitivity and specificity of MRI for the detection of septic arthritis has been reported to be 100% and 77% respectively.

See also

References

  1. 1.0 1.1 O'Callaghan C, Axford JS (2004). Medicine, 2nd ed., Oxford: Blackwell Science. ISBN 0-632-05162-0. 
  2. 2.0 2.1 Kaandorp CJ, Dinant HJ, van de Laar MA, Moens HJ, Prins AP, Dijkmans BA (August 1997). "Incidence and sources of native and prosthetic joint infection: a community based prospective survey". Ann Rheum Dis. 56 (8): 470–5. PMID 9306869.
    Weston VC, Jones AC, Bradbury N, Fawthrop F, Doherty M (April 1999). "Clinical features and outcome of septic arthritis in a single UK Health District 1982-1991". Ann Rheum Dis. 58 (4): 214–9. PMID 10364899.
  3. Bowerman SG, Green NE, Mencio GA (August 1997). "Decline of bone and joint infections attributable to haemophilus influenzae type b". Clin Orthop Relat Res. (341): 128–33. PMID 9269165.
    Peltola H, Kallio MJ, Unkila-Kallio L (May 1998). "Reduced incidence of septic arthritis in children by Haemophilus influenzae type-b vaccination. Implications for treatment". J Bone Joint Surg Br. 80 (3): 471–3. PMID 9619939.
  4. Topics in Infectious Diseases Newsletter, August 2001, Pseudomonas aeruginosa.
  5. BestBets: Distinguishing between septic arthritis of the hip and transient synovitis in children.
  6. Geirsson AJ, Statkevicius S, Víkingsson A (May 2008). "Septic arthritis in Iceland 1990-2002: increasing incidence due to iatrogenic infections". Ann Rheum Dis. 67 (5): 638–43. doi:10.1136/ard.2007.077131. PMID 17901088.
  7. BestBets: Is a negative gram stain in suspected septic arthritis sufficient to rule out septic arthritis.

Additional Resources

  • Septic arthritis by William Brinkman, M.D., University of Washington Department of Radiology
  • Karchevsky M, Schweitzer ME, Morrison WB, Parellada JA. MRI findings of septic arthritis and associated osteomyelitis in adults. AJR 2004; 182:119-122.
  • Resnick D. Bone and joint imaging. Philadelphia, PA: WB Saunders Co; 1989; 744-749
  • Stoller DW, Tirman P, Bredella MA. Diagnostic imaging orthopaedics. Salt Lake City, UT: Amirsys; 2004; 4-99.
  • Edwards MS. "Osteomyelitis and Septic Arthritis"

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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .