Crystal arthritides
Trauma
Gout
Soft tissue injury
Pseudogout
Spontaneous haemarthrosis
Fracture
Inflammatory arthritides
Rheumatoid arthritis
Infection
Psoriatic arthritis
Acute bacterial septic arthritis
Reactive arthritis including Reiter’s disease
Viral septic arthritis
Ankylosing spondylitis
Fungal septic arthritis
Enteropathic associated arthropathies
Mycobacterial septic arthritis
Lupus
Lyme disease
Familial mediterranean fever
Acute rheumatic fever
Other
Tumour/Metaplasia
Osteoarthritis
Pigmented villous nodular synovitis
Avascular necrosis
Synovial chondromatosis
Ochronosis
Sarcoma
Hypertrophic pulmonary osteoarthropathy
Septic arthritis is the invasion of a joint by a microorganism that generates a purulent response. In the majority of cases the responsible organism is a bacterium and acute bacterial septic arthritis will form the focus of this chapter, however other pathogens including viruses and fungi may also directly infect joints. Reactive arthritis is a separate condition whereby infection elsewhere in the body, commonly the upper respiratory tract, genitourinary system or bowel, leads to joint inflammation.
12.2 Risk Factors
Numerous risk factors exist for septic arthritis (Table 12.2), with skin infection being the most significant. Following arthroscopic surgery, septic arthritis is relatively uncommon with a reported incidence of 0.14 % [5], though infection following anterior cruciate ligament reconstruction is more common with 0.14–2.6 % of procedures affected [6]. The risk of joint infection following intra-articular corticosteroid injection is low with a reported incidence of 0.04 % [2]. Systemic conditions that are associated with the condition include diabetes mellitus, chronic renal failure, malignancy and alcohol abuse. Diabetic patients are at increased risk of septic arthritis due to immune system suppression, propensity to skin infections and ulceration, and the potential requirement for haemodialysis [7]. In a study from the Netherlands, increased age, particularly over 80 years, was associated with an increased risk of septic arthritis [5]. Conditions that lead to joint injury, in particular rheumatoid arthritis and to a lesser extent osteoarthritis, also confer an increased risk of joint infection [2]. The use of anti-tumour necrosis factor alpha (TNFα) therapies is reported to double the risk of septic arthritis in patients with rheumatoid disease [8]. Intravenous drug abusers are at greater risk than the general population of developing polymicrobial septic arthritis, potentially with atypical pathogens including fungi.
Table 12.2
Risk factors for septic arthritis
Extremes of age |
Low socioeconomic status |
Diabetes mellitus |
Chronic renal failure |
Malignancy |
Rheumatoid arthritis |
Osteoarthritis |
Alcohol abuse |
Intravenous drug abuse |
Knee surgery/intra-articular injection |
Cutaneous ulcers/skin infection |
Immunodeficiency |
12.3 Causative Agents
The aetiological agents for septic arthritis vary with age (Table 12.3), but in all age and risk groups, the principal causative organism is Staphylococcus aureus followed by other Gram-positive organisms, particularly streptococci [2]. S. aureus has a strong predilection for joints due to the presence of multiple microbial surface components that facilitate binding to joint extracellular matrix. Some strains of S. aureus (the Panton-Valentine Leukocidin complex) are producers of cytotoxins and can survive within neutrophils; these can be responsible for severe joint infections in otherwise healthy individuals [9]. The finding of methicillin resistant strains of S. aureus (MRSA) causing septic arthritis has been a particularly worrying trend over the past decade [2].
Table 12.3
Agents responsible for septic arthritis
Patient group | Aetiological agent | Source |
---|---|---|
Neonates | Group B streptococci | Maternal-foetal transmission |
Escherichia coli | ||
Staphylococcus aureus | ||
Children (<3 years old) | Streptococcus pyogenes | Bacteraemia |
Streptococcus pneumoniae | ||
Staphylococcus aureus | ||
Kingella kingae | ||
Haemophilus influenzae | ||
Adolescents | Neisseria gonorrhoea | |
Pseudomonas aeruginosa | ||
Kingella kingae | ||
Staphylococcus aureus | ||
Adults | Gonococci | Genitourinary tract or pharyngeal infection |
Staphylococcus aureus | Bacteraemia | |
Streptococci | ||
Haemophilus influenzae | ||
Pseudomonas aeruginosa | ||
Kingella kingae | ||
Moraxella osloensis | ||
Arcanobacterium haemolyticum | ||
Mycoplasma hominis | ||
Mycobacterium marinum | ||
Shigella sp | ||
Salmonella sp | ||
Ureaplasma urealyticum | ||
Bite wounds | ||
Human | Eikenella corrodens | |
Staphylococcus aureus | ||
Group B streptococci | ||
Oral anaerobes | ||
Rat | Staphylococcus aureus | |
Streptobacillus moniliformis | ||
Spirillum minus | ||
Streptococci | ||
Cat/dog | Staphylococcus aureus | |
Pasteurella multocida | ||
Pseudomonas sp | ||
Moraxella sp | ||
Haemophilus sp | ||
Elderly | Streptococci | |
Concomitant diseases | Enterobacter | |
Pseudomonas aeruginosa | ||
Serratia marcescens | ||
Salmonella sp | ||
Immunocompromised | Mycobacterium tuberculosis | |
Intra-articular injections | Mycobacterium kansasii | |
Arthroscopy | Mycobacterium marinum | |
HIV associated | Mycobacterium avium-intracellulare complex | |
Mycobacterium fortuitum | ||
Mycobacterium haemophilum | ||
Mycobacterium terrae | ||
Mycobacterium chelonae | ||
Nocardia asteroides | ||
Viruses | Parvovirus B19 | |
Hepatitis B or C | ||
Rubella | ||
Togavirus | ||
Chikungunya virus | ||
Varicella | ||
Mumps virus | ||
Adenovirus | ||
Coxsackie A9, B2, B3, B4 | ||
Retroviruses – HIV | ||
Epstein-Barr virus | ||
O’nyong nyong | ||
Ross River | ||
Barmah forest virus | ||
Ockelbo agent | ||
Fungi
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