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Annals of the Rheumatic Diseases 2009;68:1074-1075; doi:10.1136/ard.2008.098335
Copyright © 2009 BMJ Publishing Group Ltd & European League Against Rheumatism.

Diagnostic value of procalcitonin for differentiation between bacterial infection and non-infectious inflammation in febrile patients with active adult-onset Still’s disease

D-Y Chen1,2, Y-M Chen1,2, W-L Ho1,2, H-H Chen1,2, G-H Shen3, J-L Lan1,2

1 Yang-Ming University and Chung-Hsing University, Taipei, Taiwan
2 Division of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan
3 Chung-Hsing University, Taiwan, and Division of Chest Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

Correspondence to:
Dr J-L Lan, Taichung Veterans General Hospital, No 160, Section 3, Taichung-Kang Road, Taichung City 40705, Taiwan; jllan@mail.vghtc.gov.tw

Accepted 22 August 2008

The first 150 words of the full text of this article appear below.

Adult-onset Still’s disease (AOSD) has been recognised as an important cause of fever of unknown origin. Over 99% of AOSD patients displayed fever during their disease course.1 The diagnosis of bacterial infection in febrile AOSD patients is challenging because traditional markers of infection are often misleading. This prompted us to search for a reliable marker that allows early discrimination between non-infectious inflammation and bacterial infection in febrile AOSD patients.

Procalcitonin, a novel marker that can distinguish disease activity from infection, has been investigated in febrile patients with systemic lupus erythematosus (SLE).2 3 Procalcitonin has proved to be a diagnostic marker of infection in critically ill patients compared with other inflammatory parameters.4 Serum procalcitonin is normally undetectable (<0.05 ng/ml) and procalcitonin levels of 0.5 ng/ml or greater can distinguish infection from non-infectious inflammation.3 5 Contradictory results for procalcitonin have recently been reported in AOSD because of the investigation of only small sample groups.5 6

. . . [Full text of this article]


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