Elsevier

Joint Bone Spine

Volume 71, Issue 4, July 2004, Pages 303-311
Joint Bone Spine

Original article
Streptococcal septic arthritis in adults. A study of 55 cases with a literature review

https://doi.org/10.1016/S1297-319X(03)00122-2Get rights and content

Abstract

Objectives. – To evaluate the rate of occurrence and characteristics of streptococcal septic arthritis.

Methods. – Retrospective single-center study of patients with bacteriologically documented septic arthritis admitted to a rheumatology department over a 20–year period.

Results. – Of 303 cases of septic arthritis, 55 (18%) were due to streptococci and 166 (55%) to Staphylococcus aureus (55%). As compared to patients with S. aureus arthritis, patients with streptococcal arthritis was more likely to be in female (56% vs. 36%, P < 0.006) and older than 60 years of age (71% vs. 58%), less likely to have comorbidities (36% vs. 56%), rheumatoid arthritis (5% vs. 19%, P < 0.01), or diabetes (2% vs. 15%, P < 0.01), and more likely to have cancer (13% vs. 7%). Involved joints and proportions of patients with arthritis in multiple joints were similar in two groups. Mortality was lower in the group with streptococcal infection (3.6% vs. 7.8%). The streptococci were distributed as follows: group A (n = 7), group B (n = 12), group C (n = 4), group D (n = 7), group F (n = 1), group G (n = 2), nongroupable (n = 14), nontypable (n = 1), and Streptococcus pneumoniae (n = 7). Groups A and B and nongroupable strains mainly affected women; group A selectively involved younger patients and group B very elderly patients. Comorbidity, most notably cancer, was common in patients with S. pneumoniae or group D streptococci. The portal of entry was often a skin lesion for groups A and B and a medical procedure for group D. Multiple joint involvement was common with groups A and B and prosthetic joint infection with groups B and C. Group A and S. pneumoniae were associated with severe systemic symptoms and extra articular foci of infection, whereas a smoldering course was more common with groups D and G and with nongroupable strains. Residual joint abnormalities were noted in half the patients, with no differences across groups.

Conclusions. – The features of streptococcal septic arthritis vary according to the group of the causative organism and differ from those of S. aureus arthritis.

Introduction

Staphylococcus aureus is responsible for over 60% of cases of bacteriologically documented nongonococcal septic arthritis [1]. Streptococci come in second position, with about 20% of cases on average and 30% in a recent study in the United Kingdom [2]. Although many streptococci can cause septic arthritis, most reports indicate the proportion of cases due to Streptococcus pneumoniae but provide no details on the other species. The characteristics of streptococcal septic arthritis have not been extensively evaluated. Available data come from small series or from anecdotal case-reports that were often selected because of an unusual presentation. A study of 51 cases seen in Thailand [3] showed that β-hemolytic streptococci were the most common organisms, with equal proportions of groups A, B, and G; however, detailed clinical information was not collected. Schattner and Vosti [4] recently studied 23 cases of septic arthritis due to β-hemolytic streptococci seen over a 12–year period. They found substantial differences among streptococcal groups: group A streptococci caused severe infections, often with septic shock, disseminated intravascular coagulation or necrotizing fasciitis, whereas group B streptococci were typically associated with involvement of multiple joints in patients with cancer or diabetes mellitus and group G streptococci with apparently mild infections.

Over the last 20 years, 55 patients with streptococcal septic arthritis were admitted to our rheumatology department. The objective of the present study was to evaluate the frequency and characteristics of streptococcal arthritis comparatively with arthritis due to S. aureus; to compare proportions of cases and clinical features among streptococcal groups; and to compare our findings to data from the literature.

Section snippets

Patients and methods

We retrospectively reviewed the medical charts of patients admitted for septic arthritis to the rheumatology department of the Clermont-Ferrand Teaching Hospital between 1979 and 1998. Only patients in whom the causative organism was recovered from joint specimens and/or blood cultures were included in the study. Patients with infections confined to the spine or sacroiliac joints were excluded.

Until 1989, joint fluid specimens were seeded on Schaedler broth (Institut Pasteur Production), Eugon

Rate of occurrence

Between 1979 and 1998, 303 patients were admitted to our department for bacteriologically documented septic arthritis. A streptococcus was recovered in 55 patients, representing 18% of all patients with septic arthritis and 20% of patients with nontuberculous nongonococcal septic arthritis. During the same time period, 166 patients had septic arthritis due to S. aureus.

The distribution of causative organisms showed little change over time. However, the proportion of streptococcal infections

Discussion

Over the 20–year study period, 55 patients with streptococcal septic arthritis were admitted to our rheumatology department. These patients represented 18% of all cases of bacteriologically documented septic arthritis and 20% of cases of nontuberculous nongonococcal septic arthritis. Similar proportions have been found in other case-series [5], [6], [7], [8], [9], [10], [11], [12], [13], [14], [15], [16], [17], [18], [19], [20], [21], [22], [23], [24], [25], [26], [27], [28], [29], [30], [31],

References (62)

  • R.J Argen et al.

    Suppurative arthritis. Clinical features of 42 cases

    Arch Intern M

    (1996)
  • A Baitch

    Recent observations of acute suppurative arthritis

    Clin Orthop

    (1962)
  • C Cooper et al.

    Bacterial arthritis in an English health district a 10 year review

    Ann Rheum Dis

    (1986)
  • U Deesomchok et al.

    Clinical study of culture-proven cases of non-gonococcal arthritis

    J Med Assoc Thai

    (1990)
  • B Delcambre et al.

    Les arthrites septiques non tuberculeuses (spondylodiscites exclues)

    Rhumatologie

    (1982)
  • D.L Goldenberg et al.

    Treatment of septic arthritis. Comparison of needle aspiration and surgery as initial modes of joint drainage

    Arthritis Rheum

    (1975)
  • G Ho et al.

    Therapy for septic arthritis

    JAMA

    (1982)
  • J.P Huaux et al.

    Les arthrites septiques à germes banals de l’adulte

    Acta Orthop Belg

    (1986)
  • C.J.E Kaandorp et al.

    Incidence and sources of native and prosthetic joint infection: a community based prospective survey

    Ann Rheum Dis

    (1997)
  • L Le Dantec et al.

    Peripheral pyogenic arthritis. A study of one hundred seventy-nine cases

    Rev Rhum [Engl Ed]

    (1996)
  • L Lidgren et al.

    Twenty-nine cases of bacterial arthritis

    Acta Orthop Scand

    (1973)
  • B.M Manshady et al.

    Septic arthritis in a general hospital 1966–1977

    J Rheumatol

    (1980)
  • H Mielants et al.

    Long-term functional results of the non-surgical treatment of common bacterial infections of joints

    Scand J Rheumatol

    (1982)
  • D.S Morgan et al.

    An 18 year clinical review of septic arthritis from tropical Australia

    Epidemiol Infect

    (1996)
  • J.H Newman

    Review of septic arthritis throughout the antibiotic era

    Ann Rheum Dis

    (1976)
  • R.H.J Peters et al.

    Bacterial arthritis in a district hospital

    Clin Rheumatol

    (1992)
  • J Rosenthal et al.

    Acute nongonococcal infectious arthritis. Evaluation of risk factors, therapy and outcome

    Arthritis Rheum

    (1980)
  • A.S Russel et al.

    Septic arthritis

    Ann Rheum Dis

    (1972)
  • A Ryckewaert et al.

    Les arthrites aiguës suppurées métastatiques à germes identifiés

    Sem Hôp Paris

    (1972)
  • A Ryckewaert et al.

    Arthrites bactériennes aiguës suppurées après injections intra-articulaires de dérivés cortisoniques

    Rev Rhum Mal Ostéoartic

    (1973)
  • H Serre et al.

    Les arthrites infectieuses des membres à germes banals

    Rev Rhum Mal Ostéoartic

    (1973)
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