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Auteur de référence en rhumatologie
25 articles scientifiques publiés — un praticien à la pointe de la recherche
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Délais de RDV courts dans la région
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✨ Génération du profil synthétique IA en cours…
LE PIN
93 RUE DE LA LIBERATION, 38300 BOURGOIN JALLIEU
LE PIN
CENTRE HOSPITALIER PIERRE OUDOT 30 AVENUE DU MEDIPOLE, 38300 BOURGOIN JALLIEU
LE PIN
20 AVENUE ALSACE LORRAINE, 38110 LA TOUR DU PIN
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
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CLINIQUE ST VINCENT DE PAUL 70 AVENUE DU MEDIPOLE, 38300 BOURGOIN JALLIEU
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
Joint bone spine · 2013
Arthritis care & research · 2016
ObjectiveIn this randomized controlled trial, we compared the effect of celecoxib and acetaminophen on pain and magnetic resonance imaging (MRI) scores in patients with chronic nonspecific low back pain.MethodsA total of 50 patients with chronic nonspecific low back pain were blindly randomized into 2 groups treated with celecoxib (200 mg twice daily) or acetaminophen (500 mg twice daily). Outcome measures included total back pain, nocturnal back pain, Oswestry Disability Index (ODI) scores, the Short Form 36 health survey to assess physical and mental status, and patient global assessment. Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Bath Ankylosing Spondylitis Functional Index, and Bath Ankylosing Spondylitis Metrology Index scores were also assessed before and after the therapy. The Spondyloarthritis Research Consortium of Canada scoring method was used to evaluate spinal MRI changes.ResultsCelecoxib showed a superior effect on total back pain, ODI, BASDAI, nocturnal back pain, and patient global assessment, compared to acetaminophen (P < 0.05). The number of patients with a significant change in back pain scales was higher in the celecoxib arm (ODI 34.8% versus 4.5%, nocturnal back pain 41.7% versus 9.1%, total back pain 33.3% versus 9.1%, and BASDAI 30.4% versus 9.1%; P < 0.01 for all). The responsiveness to celecoxib, calculated by Guyatt's Responsiveness Index, was 1.62, 1.28, 1.27, and 0.58 for the ODI, total back pain, BASDAI, and nocturnal back pain, respectively. The MRI scores for sacroiliac joints and spine showed no significant change with either treatment when compared with baseline values (P > 0.05).ConclusionThere was superior efficacy of celecoxib compared with acetaminophen in chronic nonspecific low back pain. Inflammatory lesions of sacroiliac joints and spine are commonly seen in nonspecific low back pain, but these lesions did not change with either celecoxib or acetaminophen treatments and were not associated with clinical response to either agent.
Lupus science & medicine · 2021
Background SLE is an independent risk factor for cardiovascular disease (CVD). This study aimed to determine which among QRISK2, QRISK3, Framingham Risk Score (FRS), modified Framingham Risk Score (mFRS) and SLE Cardiovascular Risk Equation (SLECRE) best predicts CVD. Methods This is a single-centre analysis on 1887 patients with SLE followed prospectively according to a standard protocol. Tools’ scores were evaluated against CVD development at/within 10 years for patients with CVD and without CVD. For patients with CVD, the index date for risk score calculation was chosen as close to 10 years prior to CVD event. For patients without CVD, risk scores were calculated as close to 10 years prior to the most recent clinic appointment. Proportions of low-risk (<10%), intermediate-risk (10%–20%) and high-risk (>20%) patients for developing CVD according to each tool were determined, allowing sensitivity, specificity, positive/negative predictive value and concordance (c) statistics analysis. Results Among 1887 patients, 232 CVD events occurred. QRISK2 and FRS, and QRISK3 and mFRS, performed similarly. SLECRE classified the highest number of patients as intermediate and high risk. Sensitivities and specificities were 19% and 93% for QRISK2, 22% and 93% for FRS, 46% and 83% for mFRS, 47% and 78% for QRISK3, and 61% and 64% for SLECRE. Tools were similar in negative predictive value, ranging from 89% (QRISK2) to 92% (SLECRE). FRS and mFRS had the greatest c-statistics (0.73), while QRISK3 and SLECRE had the lowest (0. 67). Conclusion mFRS was superior to FRS and was not outperformed by the QRISK tools. SLECRE had the highest sensitivity but the lowest specificity. mFRS is an SLE-adjusted practical tool with a simple, intuitive scoring system reasonably appropriate for ambulatory settings, with more research needed to develop more accurate CVD risk prediction tools in this population.
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
The Journal of rheumatology · 2026 · Letter
Aboulenain S, Koppikar S, McDonald-Blumer H, Powell MF, et al.
Georgian medical news · 2025 · Journal Article
Omer S, Abdrabo A, Omar A, Osman E
Journal of ISAKOS : joint disorders & orthopaedic sports medicine · 2024 · Journal Article
McEwen P, Omar A, Hiranaka T
The Journal of rheumatology · 2023 · Journal Article
Kwok TSH, Omar A
Journal of immunology (Baltimore, Md. : 1950) · 2019 · Journal Article
Khor B, Conway KL, Omar AS, Biton M, et al.
The Medical journal of Malaysia · 1995 · Journal Article
Omar A
The British journal of clinical practice · 1975 · Clinical Trial
Haslock I, Omar AS, Wright V
International medical case reports journal · 2025 · Case Reports
Balla Y, Dimbil AH, Jalei AA, Omar AI, et al.
Case reports in medicine · 2025 · Case Reports
Omar A, Salameh R, Karam K, Khoury C, et al.
Medicine · 2022 · Case Reports
Al-Mashdali AF, Gul M, Umer W, Omar A, et al.
Arthritis research & therapy · 2021 · Journal Article
Kudsi M, Nahas LD, Alsawah R, Hamsho A, et al.
Lupus science & medicine · 2021 · Journal Article
Sivakumaran J, Harvey P, Omar A, Tayer-Shifman O, et al.
The Egyptian journal of immunology · 2005 · Journal Article
Fathy A, Mohamed RW, Tawfik GA, Omar AS
Journal of medical case reports · 2021 · Case Reports
Omar AA, Ahmed S, Rodrigues JC, Kayiza A, et al.
Joint bone spine · 2013 · Clinical Trial
Omar A, Abo-Elyoun I, Hussein H, Nabih M, et al.
Optometry and vision science : official publication of the American Academy of Optometry · 2018 · Case Reports
Eldeeb M, Chan EW, Omar A
Pharmacogenomics · 2014 · Journal Article
Morgan MD, Al-Shaarawy N, Martin S, Robinson JI, et al.
Cureus · 2023 · Journal Article
Ahmed A, Omar A, Ghattas M, Ghaly M, et al.
International journal of rheumatic diseases · 2013 · Journal Article
Ahmed AZ, El-Shahaly HA, Omar AS, Ghattas MH
Academic radiology · 2022 · Journal Article
Malécot N, Chrusciel J, Sanchez S, Sellès P, et al.
Arthritis care & research · 2021 · Journal Article
Lawson DO, Eraso M, Mbuagbaw L, Joanes M, et al.
La Clinica terapeutica · 2026 · Journal Article
Mohammed M, Alsayed H, Omar A, Mohamed A, et al.
Arthritis care & research · 2016 · Journal Article
Bedaiwi MK, Sari I, Wallis D, O'shea FD, et al.
Skeletal radiology · 2016 · Journal Article
Adib O, Berthier E, Loisel D, Aubé C
Lupus · 2020 · Journal Article
Elkaraly NE, Nasef SI, Omar AS, Fouad AM, et al.
Arthritis care & research · 2021 · Journal Article
Lawson DO, Eraso M, Mbuagbaw L, Joanes M, et al.
Arthritis care & research · 2021 · Journal Article
Lawson DO, Eraso M, Mbuagbaw L, Joanes M, et al.
Lupus science & medicine · 2021 · Journal Article
Sivakumaran J, Harvey P, Omar A, Tayer-Shifman O, et al.
La Clinica terapeutica · 2026 · Journal Article
Mohammed M, Alsayed H, Omar A, Mohamed A, et al.