Agathe Papelard
Paris Descartes University
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Featured researches published by Agathe Papelard.
PLOS ONE | 2011
Christelle Nguyen; Alice Bérezné; Thierry Baubet; Caroline Mestre-Stanislas; François Rannou; Agathe Papelard; S. Morell-Dubois; M. Revel; Loïc Guillevin; Serge Poiraudeau; Luc Mouthon
Objectives To assess the association of gender with clinical expression, health-related quality of life (HRQoL), disability, and self-reported symptoms of depression and anxiety in patients with systemic sclerosis (SSc). Methods SSc patients fulfilling the American College of Rheumatology and/or the Leroy and Medsger criteria were assessed for clinical symptoms, disability, HRQoL, self-reported symptoms of depression and anxiety by specific measurement scales. Results Overall, 381 SSc patients (62 males) were included. Mean age and disease duration at the time of evaluation were 55.9 (13.3) and 9.5 (7.8) years, respectively. One-hundred-and-forty-nine (40.4%) patients had diffuse cutaneous SSc (dcSSc). On bivariate analysis, differences were observed between males and females for clinical symptoms and self-reported symptoms of depression and anxiety, however without reaching statistical significance. Indeed, a trend was found for higher body mass index (BMI) (25.0 [4.1] vs 23.0 [4.5], p = 0.013), more frequent dcSSc, echocardiography systolic pulmonary artery pressure >35 mmHg and interstitial lung disease in males than females (54.8% vs 37.2%, p = 0.010; 24.2% vs 10.5%, p = 0.003; and 54.8% vs 41.2%, p = 0.048, respectively), whereas calcinosis and self-reported anxiety symptoms tended to be more frequent in females than males (36.0% vs 21.4%, p = 0.036, and 62.3% vs 43.5%, p = 0.006, respectively). On multivariate analysis, BMI, echocardiography PAP>35 mmHg, and anxiety were the variables most closely associated with gender. Conclusions In SSc patients, male gender tends to be associated with diffuse disease and female gender with calcinosis and self-reported symptoms of anxiety. Disease-associated disability and HRQoL were similar in both groups.
Rheumatology | 2010
Christelle Nguyen; Serge Poiraudeau; Caroline Mestre-Stanislas; François Rannou; Alice Bérezné; Agathe Papelard; D. Choudat; M. Revel; Loïc Guillevin; Luc Mouthon
OBJECTIVE To assess employment status and socio-economic burden in SSc patients. METHODS Eighty-seven SSc patients (72 females), fulfilling the ACR or the Leroy and Medsger criteria, or both, were evaluated for employment status, socio-economic burden and handicap. Statistical analysis involved Mann-Whitney U-test and Fishers exact test and backward stepwise regression analysis. RESULTS In total, 60.9% of the SSc patients were on full-time sick leave and 35.6% were receiving a disability pension. On univariate analysis, myalgia was the only clinical manifestation more frequently encountered in sick-leave patients than others (73.6 vs 47.1%; P = 0.012). Karnofsky performance status (KPS) was lower in SSc patients who were on sick leave or were receiving a disability pension than others [78.5 (10.6) vs 85.8 (9.0); P = 0.004 and 78.1 (8.7) vs 83.1 (11.2); P = 0.016, respectively]. In addition, greater global, hand and mouth handicaps and depression were observed in patients on sick leave [HAQ 0.9 (0.7) vs 0.6 (0.5); P = 0.021; Cochin Hand Function Scale 21.7 (18.9) vs 10.7 (12.1); P = 0.003; mouth handicap scale 20.2 (10.8) vs 14.6 (10.0); P = 0.014; and depression dimension of the hospital anxiety and depression scale 7.1 (3.9) vs 4.8 (3.4); P = 0.003]. On multivariate analysis, factors associated with sick leave were KPS [odds ratio (OR) 0.92; 95%CI 0.88, 0.98] and myalgias (OR 3.19; 95% CI 1.19, 8.58), and the factor associated with receiving a disability pension was decreased income (OR 8.19; 95% CI 2.67, 25.12). CONCLUSIONS SSc patients commonly have to take full-time sick leave from work. Despite such patients receiving disability pensions, the socio-economic burden is considerable.
The Journal of Rheumatology | 2010
Christelle Nguyen; Luc Mouthon; Caroline Mestre-Stanislas; François Rannou; Alice Bérezné; Katherine Sanchez; Agathe Papelard; Michel Revel; Loïc Guillevin; Serge Poiraudeau
Objective. To assess the sensitivity to change of the McMaster-Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR) in systemic sclerosis (SSc) and a shift in patient priorities over time. Methods. We assessed 49 patients with SSc (8 men) using the MACTAR in a prospective longitudinal study twice or more during annual meetings of the French patient association from 2004 to 2007. Patient-perceived improvement or worsening regarding health status was recorded. Sensitivity to change was assessed by the effect size (ES) and the standardized response mean (SRM) of the MACTAR. Results. The MACTAR global score was significantly increased at followup in the whole group of patients, and the ES and SRM values were −0.37 and −0.34, respectively. These values were similar to those observed for widely used outcome measures for SSc such as the Health Assessment Questionnaire. As defined by the International Classification of Functioning, Disability and Health, the 3 disability domains most often cited at baseline were mobility (7 activities, cited 17 times; 33.3% of patients), domestic life (4 activities, cited 17 times; 33.3% of patients), and community, social and civic life (3 activities, cited 10 times; 19.6% of patients). At followup, 40 patients had changed their first priority and 34 changed 3 priorities. Conclusion. The evolution in MACTAR global score over time for patients with SSc reflects longterm general feelings of deterioration. However, shifts in patient priorities are common and may influence the sensitivity to change of the instrument.
The Journal of Rheumatology | 2010
Christelle Nguyen; Imad Bendeddouche; Katherine Sanchez; Marylène Jousse; Agathe Papelard; A. Feydy; Michel Revel; Serge Poiraudeau; François Rannou
Objective. Patients with chronic low back pain (cLBP) and vertebral endplate Modic I signal changes on lumbar magnetic resonance imaging (MRI) have clinical features that could mimic inflammatory back pain related to spondyloarthritis (SpA) and/or ankylosing spondylitis (AS). We aimed to assess whether such patients fulfilled criteria for SpA and/or AS. Methods. For 5 months in 2008, all patients (n = 314) referred to a tertiary care physical medicine and rehabilitation facility in France were consecutively screened. A total of 185 hospitalized for non-specific cLBP were prospectively assessed. Forty patients fulfilling inclusion criteria were consecutively enrolled and included in 2 groups according to MRI findings: Modic I (n = 15) and non-Modic I (n = 25). MRI findings were assessed independently by 2 spine specialists and a radiologist. HLA-B27 status was determined. Data were collected on clinical measurements and fulfillment of Amor criteria (AC) and modified New York criteria (mNYC). All assessors were blinded to HLA-B27 status. Results. Whatever the Modic group, no patient fulfilled AC or mNYC, and mean total scores were comparable [3 ± 2 (range 0–22; p = 0.977), 1 ± 1 (range 0–3; p = 1.000), and 0 ± 0 (range 0–1; p = 1.000) for AC and clinical and radiological mNYC, respectively]. HLA-B27 status was similar in both groups [n = 2 (13%) vs n = 0 (0%); p = 0.135]. Conclusion. Patients with cLBP and Modic I vertebral endplate signal changes on lumbar MRI do not fulfill widely used and validated criteria for SpA and/or AS. Such cases are clinically distinct from SpA and AS.
Spine | 2009
Katherine Sanchez; Agathe Papelard; Christelle Nguyen; Marylène Jousse; François Rannou; Michel Revel; Serge Poiraudeau
Study Design. A cross sectional survey. Objective. To assess patient priorities in disability and restriction in participation with disabling chronic low back pain (CLBP) by use of the McMaster-Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR) and to compare this questionnaire with other outcome measures widely used in this situation. Summary of Background Data. Disability and participation restriction are widely assessed in CLBP but do not account for patient priorities. Knowing what is important to patients could be useful to help form treatment goals and plans. Methods. A total of 150 patients hospitalized in a tertiary care teaching hospital for the management of CLBP were enrolled in the study. Evaluation was by the MACTAR, the Quebec Back Pain Disability Questionnaire (QUEBEC), the Hospital Anxiety and Depression scale, the Fear-Avoidance Beliefs Questionnaire, the Coping Strategies Questionnaire, and pain and handicap visual analog scales. Correlations between the MACTAR score and scores for other scales were analyzed by the Spearman coefficient. Results. On the MACTAR, patients with CLBP cited as most important 3 disability domains classified by the International Classification of Functioning, Disability, and Health: mobility (n = 23 activities, 165 times, 33% of the patients); community, social, and civic life (n = 7 activities, 138 times, 27.6% of the patients); and domestic life (n = 10 activities, 123 times, 24.6% of the patients). Patients ranked first in importance 37 different activities, especially sport (n = 29 times; 19.3% of the patients), shopping (n = 14; 9.3% of the patients), and walking (n = 13; 8.7% of the patients). The MACTAR score was correlated moderately with visual analog scale handicap (r = 0.51), weakly with the QUEBEC score (r = 0.40), and not at all with Hospital Anxiety and Depression scale, Fear-Avoidance Beliefs Questionnaire, and Coping Strategies Questionnaire scores. Conclusion. For assessing priorities in disability and participation restriction among patients with CLBP, the MACTAR has acceptable construct validity. The weak correlation between QUEBEC and MACTAR scores suggests that the latter scale adds useful information for assessing the health priorities of disabled CLBP patients.
PLOS ONE | 2014
Christelle Nguyen; Brigitte Ranque; Thierry Baubet; Alice Bérezné; Caroline Mestre-Stanislas; François Rannou; Agathe Papelard; S. Morell-Dubois; M. Revel; Marie Rose Moro; Loïc Guillevin; Serge Poiraudeau; Luc Mouthon
Objectives To identify clinical, functional and health-related quality of life (HRQoL) correlates of clinically significant symptoms of anxiety and depression in patients with systemic sclerosis (SSc). Methods Three-hundred-and-eighty-one patients fulfilling the American College of Rheumatology and/or the Leroy and Medsger criteria for SSc were assessed for visceral involvement, disability and HRQoL (assessed by SF-36). Clinically significant symptoms of anxiety and depression were evaluated with the Hospital Anxiety Depression Scale (HAD) (defined cut-off≥8). Results 9.2% the patients had limited SSc, 50.5% limited cutaneous SSc (lcSSc), and 40.3% diffuse cutaneous SSc (dcSSc). Overall, 40.4% and 58.8% of the patients had clinically significant symptoms of depression and anxiety, respectively. Compared to patients without clinically significant symptoms of depression, patients with clinically significant symptoms of depression had poorer health status, HRQoL mental and physical component, and greater global disability, hand disability and aesthetic impairment. Compared to patients without clinically significant symptoms of anxiety, patients with clinically significant symptoms of anxiety had poorer SF-36 mental and physical component scores. On multivariable analysis, excluding mental component score of SF-36, variables independently associated with clinically significant symptoms of depression and anxiety were global disability and physical component of SF-36, plus female gender for clinically significant symptoms of anxiety only. Remarkably, patients with and without clinically significant psychiatric symptoms were comparable for all disease-related clinical features assessed. Conclusion High levels of clinically significant symptoms of anxiety and depression are observed among SSc patients. Clinically significant psychiatric symptoms are rather associated with increased disability and altered HRQoL, than with disease-specific organ manifestations.
Jcr-journal of Clinical Rheumatology | 2009
Christelle Nguyen; Blandine Briquel Jean-Luc; Agathe Papelard; Serge Poiraudeau; Michel Revel; François Rannou
A 50-year-old man had experienced chronic left knee effusion for 5 years. He had psoriatic skin lesions since the age of 19 and reported axial and intermittent peripheral joint tenderness and swelling since 2003, consistent with psoriatic arthritis. Physical examination revealed sacroiliac joint pain and swelling involving the left knee and right metatarsophalangeal joints associated with spreading psoriatic skin lesions. Detailed history revealed that he had persistent effusion of the left knee for 5 years with discomfort rather than pain, whereas the effusion of the metatarsophalangeal joints was only intermittent and very painful. Laboratory test and radiography results were unremarkable. Arthrocentesis revealed inflammatory aseptic fluid, with leukocyte count of 6900/ L. Magnetic resonance imaging (MRI) T1-weighted (Fig. 1) and T2-weighted fat-saturated (Fig. 2) images of the knee showed a synovial mass with signal intensity similar to that with subcutaneous fat. Synovial biopsy confirmed diffuse articular lipomatosis associated with nonspecific chronic synovitis. Lipoma arborescens is a rare primary benign tumor of the synovium, predominantly affecting the knee joint. Its etiology is unknown. Most commonly associated conditions include osteoarthritis and joint trauma. Conversely, association with inflammatory arthritis has rarely been described. Thus, only a few cases of lipoma arborescens associated with rheumatoid arthritis, and only 3 cases with psoriatic arthritis, have been reported. However, because the presence of chronic joint effusion may be attributed wrongly to the natural course of the underlying rheumatic disease, the frequency of this association may be underestimated. With chronic effusion involving a single joint in patients with known inflammatory rheumatic diseases, MRI could help detect a concomitant local disease such as lipoma arborescens. The role of chronic local inflammatory conditions in the development of such fatty tumors is questionable. Finally, MRI typically demonstrates villous lipomatous proliferation with signal intensity similar to that of fat, mass-like subsynovial fat deposition, as well as joint effusion, as seen in our patient, which allows for a definitive diagnosis.
Joint Bone Spine | 2012
Christelle Nguyen; Agathe Papelard; A. Schnitzler; Paolo Mangione; Serge Poiraudeau; François Rannou
Joint Bone Spine - In Press.Proof corrected by the author Available online since vendredi 30 septembre 2011
Joint Bone Spine | 2011
Imad Bendeddouche; Agathe Papelard; François Rannou; M. Revel
Joint Bone Spine - In Press.Proof corrected by the author Available online since samedi 21 mai 2011
PLOS ONE | 2011
Katherine Sanchez; Agathe Papelard; Christelle Nguyen; Imad Bendeddouche; Marylène Jousse; François Rannou; M. Revel; Serge Poiraudeau