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1.
Int J Infect Dis ; 84: 1-4, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30930186

ABSTRACT

OBJECTIVE: Chikungunya (CHIKV) is an arbovirus that causes acute, debilitating polyarthritis. Its diagnosis can be difficult for clinicians not used to managing joint diseases or detecting synovitis. Joint Doppler ultrasonography (DUS) is a simple, non-invasive examination, able to visualize synovitis. Its diagnostic and prognostic value in rheumatoid arthritis is well-established. METHODS: Patients with serologically proven acute arbovirosis where included. Clinical examination and joint count were performed (DAS score). Ultrasound examination was performed by another clinician - experienced in joint DUS - who also performed ultrasound joint score. Joints were examined by DUS in B-mode looking for: subcutaneous infiltration, effusion, tenosynovitis, erosion and Doppler signal. RESULTS: In our experience, joint DUS is able to detect effusions in 92.8% of painful joints, with 28.3% of the effusions emitting a high-power Doppler signal. No erosion was observed. Subcutaneous inflammatory infiltration of the ankles (aseptic cellulitis) was found in 28.6% of patients. CONCLUSION: Joint DUS is able to detect objective signs responsible for joint pain, which can be useful for practitioners not accustomed to this type of pathology. It also makes possible distinction between articular and periarticular manifestations.


Subject(s)
Chikungunya Fever/therapy , Ultrasonography, Doppler , Acute Disease , Adult , Chikungunya Fever/complications , Chikungunya Fever/diagnostic imaging , Female , Humans , Joints/diagnostic imaging , Male , Middle Aged
2.
Joint Bone Spine ; 84(4): 455-461, 2017 Jul.
Article in English | MEDLINE | ID: mdl-27825567

ABSTRACT

OBJECTIVES: Studies suggest that rheumatoid arthritis (RA) is less frequent in African populations. However, no recent precise data exists for Afro-Caribbeans. The EPPPRA project is a prospective epidemiological survey to describe prevalence and clinical aspects of RA in the French West Indies (Martinique, Guadeloupe, French Guiana). METHODS: EPPPRA involved all rheumatologists from the French West Indies who included all patients with a known clinical diagnosis of RA, during a one-year period. We outline here results for Martinique. RESULTS: EPPPRA estimated an overall world age-standardized prevalence of RA at 0.10% [95% CI 0.09% to 0.11%] in Martinique, with a high female predominance (88.1%) and 93.1% of self-reported Afro-Caribbeans. Mean age at diagnosis was 49.6±16.0 years. A majority of subjects presented at least 4 criteria points from the 1987 American College of Rheumatology (ACR) classification (94.4%) and at least 6 points (78.2%) from the 2010 ACR/European League Against Rheumatism (EULAR) classification. A high immune seropositivity rate was highlighted (84.2%). Despite functional impact observed in 40.5% of patients, 71.4% presented a low disease activity level. Methotrexate was the most common ongoing treatment (73%), followed by biotherapies (24.4%). Numerous patients (68.6%) received a steroid regimen. Cardiovascular risk factors were very frequent, contrasting with a very low tobacco use (8.7%), CONCLUSION: This work outlines low standardized prevalence of RA in a French Afro-Caribbean population with specific characteristics (high female predominance, high immune seropositivity, low tobacco use). Despite easy access to care and biotherapies, approximately half of RA patients still present destructive disease with functional impact.


Subject(s)
Arthritis, Rheumatoid/epidemiology , Adolescent , Adult , Aged , Aged, 80 and over , Arthritis, Rheumatoid/diagnosis , Female , Humans , Male , Martinique/epidemiology , Middle Aged , Prevalence , Young Adult
3.
Arthritis Rheumatol ; 68(11): 2817-2824, 2016 11.
Article in English | MEDLINE | ID: mdl-27273928

ABSTRACT

OBJECTIVE: To describe chronic chikungunya manifestations seen during the outbreak in the Caribbean from December 2013 to January 2015. METHODS: Patients were seen at our center, the only rheumatology department in Martinique Island, and were examined by a senior rheumatologist using a standard care report form. Chikungunya was diagnosed collectively based on consensus among all clinicians. The median time from onset of acute chikungunya to the first rheumatology consultation was calculated, severity was evaluated based on clinical scales and the degree of joint destruction, and each patient's treatment was recorded. RESULTS: For the 147 patients analyzed, the median time between onset of acute chikungunya and the first rheumatology consultation was 8 months. After review of each patient's medical record, 19 (12.9%) were diagnosed as having epidemic-influenced chikungunya. Four distinct rheumatologic patterns were observed in the remaining patients (those with compatible history and positive serologic findings): 47 patients (32%) had reactivation of painful chronic mechanical manifestations, 9 patients (6.1%) had fibromyalgia, 45 patients (30.6%) met criteria for spondyloarthritis (as evaluated before the chikungunya virus infection in all patients) and experienced a flare, and 27 patients (18.4%), with no history of joint disease, developed de novo bilateral symmetric chronic inflammatory joint disease in response to chikungunya virus infection. For inflammatory arthritis, most patients were treated with methotrexate (up to 25 mg/week), with good response and tolerance. Thirteen patients were treated with conventional doses of anti-tumor necrosis factor agents, with good tolerance and efficacy as expected. CONCLUSION: The term "chronic chikungunya syndrome" covers multiple etiologies. Compliance with the French Society of Rheumatology recommendations, careful recording of patient histories, and serologic verification help prevent errors inherent to the epidemic context and ensure early therapeutic intervention for these patients. To avoid late initiation of treatment, patients should receive rheumatologic consultation as early as possible.


Subject(s)
Chikungunya Fever/physiopathology , Rheumatic Diseases/physiopathology , Acute Disease , Adult , Aged , Aged, 80 and over , Antirheumatic Agents/therapeutic use , Arthritis/drug therapy , Arthritis/etiology , Arthritis/physiopathology , Bursitis/etiology , Bursitis/physiopathology , Carpal Tunnel Syndrome/etiology , Carpal Tunnel Syndrome/physiopathology , Chikungunya Fever/complications , Chikungunya Fever/drug therapy , Chikungunya Fever/epidemiology , Chronic Disease , Epidemics , Female , Fibromyalgia/etiology , Fibromyalgia/physiopathology , Humans , Low Back Pain/etiology , Low Back Pain/physiopathology , Male , Martinique/epidemiology , Methotrexate/therapeutic use , Middle Aged , Osteoarthritis/etiology , Osteoarthritis/physiopathology , Rheumatic Diseases/drug therapy , Rheumatic Diseases/etiology , Spondylarthritis/drug therapy , Spondylarthritis/etiology , Spondylarthritis/physiopathology , Tendinopathy/etiology , Tendinopathy/physiopathology , Tumor Necrosis Factor-alpha/antagonists & inhibitors
5.
Joint Bone Spine ; 80(2): 178-82, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23022422

ABSTRACT

OBJECTIVES: Calcium pyrophosphate (CPP) crystal-induced arthritis occurs particularly in elderly people. This population has frequently associated comorbidities and treatments, which could limit the use of conventional therapies (colchicine, non-steroidal anti-inflammatory drugs and corticosteroids). The aim of the study was to evaluate the efficacy and tolerance of anakinra in patients with CPP crystal-induced arthritis. METHODS: We performed a multicentric retrospective chart review of patients who received anakinra for CPP crystal-induced arthritis. Demographic information, comorbidities, co-prescription, short-term treatment outcomes, adverse event, complication and subsequent flares were reviewed. RESULTS: A total of 16 patients (12 females, mean age: 80.2±11.1 years) received anakinra (100 mg subcutaneously per day). The mean number of anakinra injection was 15.5±42.9 per patient (median: 3). All patients had contraindication and/or failure to conventional therapies. The majority (14 [87.5%]) of patients with CPP crystal-induced arthritis demonstrated a beneficial response to anakinra therapy: 10 good responses and four partial responses. A relapse occurred in six (37.5%) patients (mean time to relapse: 3.4±4.9 months). One patient had an acute bacterial pneumonitis. CONCLUSION: Our results suggest that anakinra is relatively well tolerated and could be a good option in the treatment of CPP crystal-induced arthritis, illustrating that IL-1ß blockade may be helpful to control flares in patients having CPP crystal-induced arthritis for which conventional therapies are ineffective or contra-indicated.


Subject(s)
Antirheumatic Agents/administration & dosage , Calcium Pyrophosphate/metabolism , Chondrocalcinosis/drug therapy , Interleukin 1 Receptor Antagonist Protein/administration & dosage , Adrenal Cortex Hormones/administration & dosage , Aged , Aged, 80 and over , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Antirheumatic Agents/adverse effects , Calcium Pyrophosphate/chemistry , Chondrocalcinosis/metabolism , Crystallization , Female , Humans , Interleukin 1 Receptor Antagonist Protein/adverse effects , Male , Retrospective Studies
6.
Arthritis Res Ther ; 15(5): R123, 2013.
Article in English | MEDLINE | ID: mdl-24432362

ABSTRACT

INTRODUCTION: Gout is a common arthritis that occurs particularly in patients who frequently have associated comorbidities that limit the use of conventional therapies. The main mechanism of crystal-induced inflammation is interleukin-1 production by activation of the inflammasome. We aimed to evaluate the efficacy and tolerance of anakinra in gouty patients. METHODS: We conducted a multicenter retrospective review of patients receiving anakinra for gouty arthritis. We reviewed the response to treatment, adverse events and relapses. RESULTS: We examined data for 40 gouty patients (32 men; mean age 60.0 ± 13.9 years) receiving anakinra. Mean disease duration was 8.7 ± 8.7 years. All patients showed contraindications to and/or failure of at least two conventional therapies. Most (36; 90%) demonstrated good response to anakinra. Median pain on a 100-mm visual analog scale was rapidly decreased (73.5 (70.0 to 80.0) to 25.0 (20.0 to 32.5) mm, P < 0.0001), as was median C-reactive protein (CRP) level (130.5 (55.8 to 238.8) to 16.0 (5.0 to 29.5) mg/l, P < 0.0001). After a median follow-up of 7.0 (2.0 to 13.0) months, relapse occurred in 13 patients after a median delay of 15.0 (10.0 to 70.0) days. Seven infectious events, mainly with long-term use of anakinra, were noted. CONCLUSIONS: Anakinra may be efficient in gouty arthritis, is relatively well tolerated with short-term use, and could be a relevant option in managing gouty arthritis when conventional therapies are ineffective or contraindicated. Its long-term use could be limited by infectious complications.


Subject(s)
Arthritis, Gouty/drug therapy , Interleukin 1 Receptor Antagonist Protein/therapeutic use , Aged , Antirheumatic Agents/adverse effects , Antirheumatic Agents/therapeutic use , Arthritis, Gouty/pathology , C-Reactive Protein/metabolism , Female , Follow-Up Studies , Humans , Interleukin 1 Receptor Antagonist Protein/adverse effects , Male , Middle Aged , Pain Measurement/methods , Recurrence , Retrospective Studies , Staphylococcal Infections/chemically induced , Time Factors , Treatment Outcome
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