Native Joint Septic Arthritis: Epidemiology, Clinical Features, and Microbiological Causes in a New Zealand Population

被引:75
|
作者
Kennedy, Nicholas [1 ]
Chambers, Steven T. [2 ,4 ,5 ]
Nolan, Imogen [5 ]
Gallagher, Kate [2 ]
Werno, Anja [6 ]
Browne, Melanie [3 ]
Stamp, Lisa K. [1 ,5 ]
机构
[1] Christchurch Hosp, Dept Rheumatol Immunol & Allergy, Christchurch, New Zealand
[2] Christchurch Hosp, Dept Infect Dis, Christchurch, New Zealand
[3] Christchurch Hosp, Decis Support, Christchurch, New Zealand
[4] Univ Otago, Dept Pathol, Infect Dis, Christchurch 8140, New Zealand
[5] Univ Otago, Dept Med, Christchurch 8140, New Zealand
[6] Canterbury Hlth Labs, Microbiol, Christchurch, New Zealand
关键词
SEPTIC ARTHRITIS; EPIDEMIOLOGY; NEW ZEALAND; NATIVE JOINT; CRYSTAL ARTHROPATHY; INCREASING INCIDENCE; INFECTION;
D O I
10.3899/jrheum.150434
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To determine the epidemiology, clinical features, and microbiology of adult native joint septic arthritis in Canterbury, New Zealand, over a 5-year period in individuals with and without an underlying rheumatic disorder. Methods. Patients with native joint septic arthritis were identified retrospectively and classified by Newman's criteria. The clinical characteristics were described and comparisons made between those with and without underlying rheumatic disease. Results. Two hundred forty-eight cases of native joint septic arthritis (mean age 60, range 16-97 yrs) were identified with an overall incidence rate of 12.0/100,000/year (95% CI 10.6-13.6). Yearly incidence increased with age to a maximum of 73.4/100,000 in those > 90 years of age. Septic arthritis was iatrogenic in 16.9% of cases while 27% had an underlying inflammatory arthritis including gout (14.9%), calcium pyrophosphate disease (8.5%), and rheumatoid arthritis (4%). Few patients were taking immunosuppressant therapy, with just 1 taking a biological agent. Staphylococcus aureus was the most commonly identified organism. Those with underlying inflammatory arthritis were significantly older (73.6 yrs vs 55.6 yrs; p < 0.001), more likely to be female (55.2% vs 26.0%; p < 0.001), and to have septic polyarthritis (16.4% vs 4.4%; p = 0.002). The 30-day mortality was 2%, increasing to 6% at 90 days. Conclusion. The incidence of septic arthritis in Canterbury, New Zealand, is higher than in previous studies. Crystal arthropathy commonly coexisted with infection although autoimmune arthritis and immunosuppression was less of a factor than anticipated. (First Release
引用
收藏
页码:2392 / 2397
页数:6
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