Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2008 Jun;466(6):1388-91.
doi: 10.1007/s11999-008-0229-0. Epub 2008 Apr 18.

Hematogenous septic ankle arthritis

Affiliations

Hematogenous septic ankle arthritis

Paul D Holtom et al. Clin Orthop Relat Res. 2008 Jun.

Abstract

Ankle infection is a serious problem with limited published information on microbiology and associated morbidities. We describe the laboratory findings, microbiology, and occurrence of adjacent osteomyelitis in patients with hematogenous septic ankle arthritis. We retrospectively reviewed 30 patients with hematogenous septic arthritis of the ankle admitted over a 10-year period. Twenty-two patients were male and eight female. The mean age was 46 years (range, 23-67 years). C-reactive protein and erythrocyte sedimentation rate were elevated in all patients, but the peripheral white blood cell count was elevated in only 47% of patients. Staphylococcus aureus (S. aureus) was the most common pathogen, isolated in 13 (54%) of the 24 patients with positive cultures; four of these isolates (four of 24; 17% of positive cultures) were oxacillin-resistant. Four (17%) of the 24 patients with positive cultures had a mycobacterial infection. We identified adjacent osteomyelitis in 30% of patients, which was considerably associated with the presence of patient comorbidities. S. aureus is the most common pathogen in septic ankle arthritis and empiric antibiotic therapy is recommended. Adjacent osteomyelitis may be present and a high index of suspicion is necessary in patients with comorbidities.

Level of evidence: Level III, diagnostic study. See the Guidelines for Authors for a complete description of levels of evidence.

PubMed Disclaimer

References

    1. Dubost JJ, Soubrier M, De Champs C, Ristori JM, Bussiere JL, Sauvezie B. No changes in the distribution of organisms responsible for septic arthritis over a 20 year period. Ann Rheum Dis. 2002;61:267–269. doi: 10.1136/ard.61.3.267. - DOI - PMC - PubMed
    1. Eder L, Zisman D, Rosenbaum M, Rosner I. Clinical features and aetiology of septic arthritis in northern Israel. Rheumatology. 2005;44:1559–1563. doi: 10.1093/rheumatology/kei092. - DOI - PubMed
    1. Goldenberg DL, Reed JI. Bacterial arthritis. N Engl J Med. 1985;312:764–771. - PubMed
    1. Gupta MN, Sturrock RD, Field M. A prospective 2-year study of 75 patients with adult-onset septic arthritis. Rheumatology. 2001;40:24–30. doi: 10.1093/rheumatology/40.1.24. - DOI - PubMed
    1. 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;62:327–331. doi: 10.1136/ard.62.4.327. - DOI - PMC - PubMed