730 results on '"Ziade, N."'
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2. POS0879 EXPLORING DIAGNOSTIC TIMELINES: A CROSS-SECTIONAL STUDY OF REFERRAL AND DIAGNOSTIC DELAYS OF PATIENTS WITH CHRONIC INFLAMMATORY RHEUMATIC DISEASES
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Ziade, N., primary, Al-Ani, N. A., additional, Maroof, A., additional, Ridha Adnan, A., additional, EL Rakaawi, M., additional, Haouichet, C., additional, Elzorkany, B., additional, Gamal, S., additional, Erraoui, M., additional, Mashaleh, M., additional, Alnaimat, F., additional, Masri, B., additional, Baron, F., additional, El Kibbi, L., additional, Aouad, K., additional, Mechleb, K., additional, and Hmamouchi, I., additional
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- 2024
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3. AB1333 SOCIAL MEDIA STRATEGIES TO ENGAGE PATIENTS WITH RHEUMATIC AND MUSCULOSKELETAL DISEASES: A CROSS-SECTIONAL INFODEMIOLOGY STUDY
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Hmamouchi, I., primary, Ziade, N., additional, Al-Ani, N. A., additional, Abutiban, F., additional, Rakaawi, M. EL, additional, Ghogho, M., additional, Hajjaj-Hassouni, N., additional, Masri, B., additional, Halabi, H., additional, and El Kibbi, L., additional
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- 2024
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4. COVID-19 vaccination-related delayed adverse events among people with rheumatoid arthritis: results from the international COVAD survey.
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Dey M, Doskaliuk B, Parodis I, Lindblom J, Wincup C, Joshi M, Dey D, Katchamart W, Kadam E, Sen P, Shinjo SK, Nune A, Goo PA, Ziade N, Chen YM, Traboco LS, Gutiérrez CET, Vaidya B, Agarwal V, Gupta L, and Nikiphorou E
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This study aimed to assess COVID-19 vaccination-related AEs in patients with rheumatoid arthritis (RA), in the COVID-19 Vaccination in Autoimmune Diseases (COVAD)-2 study. An online international cross-sectional survey captured self-reported data on COVID-19 vaccination-related adverse events (AEs) in people with RA, autoimmune diseases (AIDs; rheumatic [r] and non-rheumatic [nr]) and healthy controls (HCs). The survey was circulated by the COVAD study group, comprising 157 collaborators across 106 countries, from February to June 2022. Delayed AEs among RA were compared with other rAIDs, nrAIDs and HCs using multivariable binary regression. A total of 7203 participants were included (1423 [19.7%] RA, 2620 [36.4%] rAIDs, 426 [5.9%] nrAIDs, 2734 [38%] HCs), with 75% female. Compared to HCs, individuals with RA reported higher overall major AEs [OR 1.3 (1.0-1.7)], and an increased number of several minor AEs. Compared to nrAIDs, people with RA had several increased reported minor AEs including myalgia and joint pain. People with active RA had increased major AEs [OR 1.8 (1.1-3.0)] and hospitalisation [OR 4.1 (1.3 - 13.3)] compared to inactive RA. RA patients without autoimmune comorbidities had significantly fewer major and minor AEs than those with other rAIDs. A decreased incidence of hospitalisation was seen in patients taking methotrexate or TNF inhibitors compared to patients not taking these medications. COVID-19 vaccination is associated with minimal to no risks of delayed AEs in patients with RA compared to HCs, and fewer compared to other rAIDs. Active RA and presence of co-existing rAIDs were associated with an increased risk of delayed AEs., (© 2024. The Author(s).)
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- 2024
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5. The impact of multimorbidity on QoL in inflammatory myopathies: COVAD cluster analysis.
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Fornaro M, Venerito V, Pellico MR, Iannone F, Joshi M, Chen YM, Tan AL, Saha S, Chatterjee T, Agarwal V, Shinjo SK, Hoff LS, Kadam E, Ziade N, Velikova T, Hasan ATMT, Shumnalieva R, Milchert M, Tan CL, Edgar Gracia-Ramos A, Cavagna L, Vaidya B, Kuwana M, Sazliyana Shaharir S, Knitza J, Makol A, Zamora Tehozol EA, Rojas Serrano J, Halabi H, Dey D, Toro Gutierrez CE, Akawatcharangura Goo P, Caballero Uribe CV, Distler O, Katchamart W, Day J, Parodis I, Nikiphorou E, Chinoy H, Agarwal V, and Gupta L
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Objective: The presence of comorbidities can substantially affect patients' quality of life, but data regarding their impact on idiopathic inflammatory myopathies (IIMs) are limited., Methods: We examined the prevalence of comorbidities in IIM patients, other autoimmune rheumatic diseases (oAIRDs), and healthy controls (HCs), using data from the self-reported COVAD-2 survey. We defined Basic Multimorbidity (BM) as the presence of ≥ 2 non-rheumatic chronic conditions and Complex Multimorbidity (CM) as the presence of ≥ 3 non-rheumatic chronic conditions affecting ≥3 organ systems. Hierarchical Clustering on Principal Components was performed for grouping., Results: Among the COVAD respondents, 1558 IIMs, 4591 oAIRDs, and 3652 HCs were analysed. IIMs exhibited a high burden of comorbidities (OR: 1.62 vs oAIRDs and 2.95 vs HCs, p< 0.01), BM (OR 1.66 vs oAIRDs and 3.52 vs HCs, p< 0.01), CM (OR: 1.69 vs AIRDs and 6.23 vs HCs, p< 0.01), and mental health disorders (MHDs) (OR 1.33 vs oAIRDs and 2.63 vs HCs, p< 0.01). Among the IIM patients, those with comorbidities or MHDs had lower PROMIS Global Physical (PGP), PROMIS Global Mental (PGM), and PROMIS Physical Function (SF10) scores, and higher fatigue (F4a) scores (all p< 0.001). PGP, PGM, SF10a and F4a were influenced by age, active disease, BM, and MHDs. Four distinct clusters were identified among the IIMs according to comorbidities and PROMIS scores., Conclusion: Patients with IIMs have a higher burden of comorbidities that influence physical and mental health, identifiable as clinical clusters for optimized and holistic management approaches., (© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology.)
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- 2024
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6. Drug persistence in patients with rheumatic and musculoskeletal diseases during a major economic crisis: results from a nationwide cross-sectional online survey.
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Asmar S, Messaykeh J, Hilal N, Rida MA, Mroue K, Aouad K, Minkara F, Hajjar A, and Ziade N
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- Female, Humans, Middle Aged, Male, Cross-Sectional Studies, Economic Recession, Arthritis, Rheumatoid drug therapy, Biological Products therapeutic use, Antirheumatic Agents therapeutic use, Musculoskeletal Diseases drug therapy, Musculoskeletal Diseases epidemiology, Muscular Diseases
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To evaluate the drug persistence in patients with rheumatic and musculoskeletal diseases (RMDs) during the current economic crisis in Lebanon and to estimate predictors of persistence. A nationwide multicentric cross-sectional study using an online questionnaire was conducted in Lebanon with patients with chronic inflammatory rheumatic diseases (CIRDs) and non-inflammatory RMDs controls between July and October 2022. Disease-modifying antirheumatic drugs (DMARDs) were categorized as conventional synthetic (cs), biological (b), subcutaneous (SC) or intravenous (IV), and targeted synthetic (ts). Persistence was defined as "number of tablets or injections taken during the past month versus prescribed". The percentage of patients who discontinued or changed treatment due to cost or non-availability was reported. Factors associated with persistence were identified using multivariable linear regression. The study included 317 patients with RMDs (286 CIRDs); mean age 49.5 years, 68% females, 58% reporting currently low economic level. Persistence at one month was low for tsDMARDs (36%) and bDMARDs (SC55%, IV63%), and acceptable for csDMARDs (88%). A persistence ≥80% was found in 23.3% of patients on tsDMARDs, 42.9% on SC bDMARDs, 45.0% on IV bDMARDs, and 74.7% on csDMARDs. During the past 6 months, 55.8% of CIRD patients discontinued or changed treatment due to non-availability (45.3%) or cost (21.2%). Persistence was positively associated with finding alternative sources such as buying abroad (36%), depending on friends or families abroad (20%), charities (10%), and negatively associated with unemployment and low financial status. Persistence was significantly compromised for essential antirheumatic drugs and was mostly driven by treatment unavailability and cost., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
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7. Épuisement professionnel chez 445 rhumatologues pratiquant dans les pays arabes : évaluation de la prévalence et identification des facteurs prédictifs
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Naim, R., primary, Ziade, N., additional, Haouichat, C., additional, Baron, F., additional, Al-Mayouf, S., additional, Abdullateef, N., additional, Masri, B., additional, Elrakawi, M., additional, El Kibbi, L., additional, Al Mashaleh, M., additional, Abutiban, F., additional, and Hmamouchi, I., additional
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- 2023
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8. Chevauchement significatif de caractéristiques inflammatoires et dégénératives à l’imagerie chez les patients atteints de pathologie dégénérative du rachis, d’hyperostose squelettique idiopathique diffuse et de spondylarthrite axiale radiographique
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Ziade, N., primary, Kougkas, N., additional, Udod, M., additional, Tsiami, S., additional, and Baraliakos, X., additional
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- 2023
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9. Significant overlap of inflammatory and degenerative features on imaging among patients with degenerative disc disease, diffuse idiopathic skeletal hyperostosis and axial spondyloarthritis: a real-life cohort study.
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Ziade N, Udod M, Kougkas N, Tsiami S, and Baraliakos X
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- Humans, Male, Female, Middle Aged, Retrospective Studies, Cross-Sectional Studies, Cohort Studies, Adult, Aged, Low Back Pain diagnostic imaging, Low Back Pain etiology, Radiography methods, Inflammation diagnostic imaging, Diagnosis, Differential, Spondylarthritis diagnostic imaging, Hyperostosis, Diffuse Idiopathic Skeletal diagnostic imaging, Magnetic Resonance Imaging methods, Intervertebral Disc Degeneration diagnostic imaging, Axial Spondyloarthritis diagnostic imaging
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Background: Differentiating between degenerative disc disease (DDD), diffuse idiopathic skeletal hyperostosis (DISH), and axial spondyloarthritis (axSpA) represents a diagnostic challenge in patients with low back pain (LBP). We aimed to evaluate the distribution of inflammatory and degenerative imaging features in a real-life cohort of LBP patients referred to a tertiary university rheumatology center., Methods: In a retrospective cross-sectional analysis of patients referred for LBP, demographics, symptom information, and available imaging were collected. SpA-like changes were considered in the spine in the presence of one of the following lesions typically related to SpA: erosions, sclerosis, squaring, and syndesmophytes on conventional radiographs (CR) and bone marrow oedema (BMO), erosions, sclerosis, and fat lesions (FL) on MRI. SIJ CR were graded per New York criteria; on MRIs, SIJs were evaluated by quadrant for BMO, erosions, FL, sclerosis and ankylosis, similar to the approach used by the Berlin SIJ MRI scoring system. The final diagnosis made by the rheumatologist was the gold standard. Data were presented descriptively, by patient and by quadrant, and compared among the three diagnosis groups., Results: Among 136 referred patients, 71 had DDD, 38 DISH, and 27 axSpA; median age 62 years [IQR55-73], 63% males. On CR, SpA-like changes were significantly higher in axSpA in the lumbar (50%, vs. DDD 23%, DISH 22%), in DISH in the thoracic (28%, vs. DDD 8%, axSpA 12%), and in DDD in the cervical spine (67% vs. DISH 0%, axSpA 33%). On MRI, BMO was significantly higher in DISH in the thoracic (37%, vs. DDD 22%, axSpA 5%) and equally distributed in the lumbar spine (35-42%). FL were significantly more frequently identified in DISH and axSpA in the thoracic (56% and 52%) and DDD and axSpA in the lumbar spine (65% and 74%, respectively). Degenerative changes were frequent in the three groups. Sacroiliitis (NY criteria) was identified in 49% (axSpA 76%, DDD 48%, DISH 29%)., Conclusion: A significant overlap was found among DDD, DISH, and axSpA for inflammatory and degenerative imaging features. Particularly, SpA-like spine CR features were found in one-fourth of patients with DISH, and MRI BMO was found in one-third of those patients., (© 2024. The Author(s).)
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- 2024
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10. Prevalence and characteristics of, and knowledge related to, photosensitivity in patients with lupus erythematosus: the international PHOTOLUP study.
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Battesti G, Felten R, Piga M, Sarmiento-Monroy JC, Ziade N, El Kibbi L, Ugarte-Gil M, Arnaud L, and Chasset F
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- Humans, Female, Adult, Male, Cross-Sectional Studies, Middle Aged, Prevalence, Sunscreening Agents therapeutic use, Surveys and Questionnaires, Photosensitivity Disorders epidemiology, Photosensitivity Disorders etiology, Lupus Erythematosus, Systemic epidemiology, Lupus Erythematosus, Cutaneous epidemiology, Health Knowledge, Attitudes, Practice
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Objective: The objective of this study was to assess the prevalence and characteristics of, and knowledge about, photosensitivity and the use of photoprotective measures in an international cohort of cutaneous lupus erythematosus and SLE patients., Methods: We conducted an international, cross-sectional study based on a 46-question web-based survey, including patients with medically confirmed lupus erythematosus, conducted between November 2021 and April 2022., Results: A total of 600 patients with lupus erythematosus [94% female, median age: 41 years, interquartile range (IQR): 33-51] from 50 countries were included. A history of photosensitivity was reported by 389/600 (64.8%) patients. Photosensitivity was associated with the presence of other cutaneous involvement [odds ratio (OR) = 3.8; 95% CI 2.5-5.7; P < 0.001] and differed according to the area of residence and level of education (P < 0.001, for all). Photosensitivity was characterized by a wide range of clinical manifestations (both cutaneous and systemic symptoms in 56.1% and systemic symptoms only in 29.8% of patients). Fatigue was the most frequently reported systemic manifestation (82.3%). Overall, 559/600 (93%) patients were aware of the detrimental role of ultraviolet radiation exposure in lupus erythematosus, but 160/480 (33.3%) were unaware of the importance of photoprotective measures, including 90/310 (29%) among those with photosensitivity., Conclusion: A high rate of self-reported photosensitivity characterizes lupus erythematosus patients. Photosensitivity frequently includes subjective features, which makes it difficult to evaluate in clinical practice. As fatigue is frequent in lupus erythematosus, further study is needed to clarify the causal link with ultraviolet radiation exposure. About one-third of lupus erythematosus patients are unaware of the importance of photoprotective measures. This should be improved through more frequent and targeted awareness interventions., (© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
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- 2024
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11. HLA-B5 prevalence in patients with spondyloarthritis and impact on disease phenotype: a multicentric case-control study.
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Ziade N, Jaoude SB, Nacouzi R, Mroue' K, Merheb G, Klayme S, and Ghorra P
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Objective: The study aimed to estimate the prevalence of HLA-B51 and HLA-B52 in Lebanese patients with spondyloarthritis (SpA) compared to healthy controls (HC). We further aimed to evaluate the impact of HLA-B51 on phenotype and identify the distribution of the alleles in the HLA-B locus., Methods: A case-control study enrolled consecutive SpA patients from three rheumatology clinics in Lebanon, including axial (axSpA), peripheral SpA (pSpA), and psoriatic arthritis (PsA) and HC from blood donors. Demographic and disease data were collected through interviews and file reviews, with testing of the entire HLA-B locus using molecular techniques. The prevalence of HLA-B51 and B52 was estimated in SpA patients versus controls. Prevalence comparisons were made, and logistic regression identified factors associated with HLA-B51 in patients., Results: Data from 120 HC and 86 SpA patients (65 axSpA, 15 pSpA, 6 PsA), mean age 25.6 and 46.4 years, respectively, showed a higher HLA-B51 prevalence in SpA (25.6%), especially axSpA (29.2%) versus HC (12.5%), p = 0.016, and a numerically higher HLA-B52 prevalence (8.1% versus 4.2%, p = 0.230). HLA-B51 correlated with recurrent oral ulcerations (OR 7.99(95%CI 2.14-29.84) and radiographic juxta-articular erosions (OR 7.65(95%CI 1.14-38.03)). HLA-B35 was the most dominant allele in both groups (18.7%), followed by HLA-B27 (15.7%) and HLA-B51 (13.4%) in SpA., Conclusion: HLA-B51 was identified more frequently in patients with SpA compared to HC and was associated with recurrent oral ulcerations and juxta-articular radiographic erosions. Longitudinal studies are needed to determine whether this association indicates a disease overlap or might correlate with a specific SpA phenotype., (© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology.)
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- 2024
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12. Gender differences in patient experience in idiopathic inflammatory myopathies: Subanalysis from the COVAD dataset.
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Yoshida A, Kim M, Kuwana M, Ravichandran N, Makol A, Sen P, Lilleker JB, Agarwal V, Kardes S, Day J, Milchert M, Joshi M, Gheita T, Salim B, Velikova T, Gracia-Ramos AE, Parodis I, Nikiphorou E, Chatterjee T, Tan AL, Nune A, Cavagna L, Saavedra MA, Shinjo SK, Ziade N, Knitza J, Distler O, Chinoy H, Agarwal V, Aggarwal R, and Gupta L
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- Humans, Female, Male, Middle Aged, Aged, Sex Factors, Patient Reported Outcome Measures, SARS-CoV-2, Fatigue, Myositis epidemiology, Myositis immunology, COVID-19 epidemiology
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Objectives: We aimed to investigate the gender-based differences in idiopathic inflammatory myopathies (IIMs), with a particular focus on patient-reported outcomes, utilizing the data obtained through the international COVID-19 vaccination in autoimmune disease e-survey., Methods: Patient-reported outcomes including fatigue, pain, and physical function were extracted from the COVID-19 vaccination in autoimmune disease database and compared between genders, adjusting for demographics and IIM subgroups by multivariable analysis. Inclusion body myositis (IBM) was analysed separately because of the substantial differences in outcomes., Results: A total of 1197 complete responses from patients with IIMs as of 31 August 2021 were analysed. Seventy percent were women. Women were younger (58 [48-68] vs. 69 [58-75] years old, median [interquartile range], P < .001) and were more likely to suffer from autoimmune multimorbidity, defined as three or more autoimmune diseases in an individual patient (11.4% vs. 2.8%, P < .001). In non-IBM IIMs, fatigue visual analogue scale scores were higher in women (5 [3-7] vs. 4 [2-6], median [interquartile range], P = .004), whereas no significant gender-based differences were noted in IBM. Multivariable analysis in non-IBM IIMs revealed that women, residence in high-income countries, overlap myositis, and autoimmune multimorbidity were independently associated with increased fatigue., Conclusions: Women with IIMs suffer from autoimmune multimorbidity and experience increased fatigue compared to men., (© Japan College of Rheumatology 2023. Published by Oxford University Press.)
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- 2024
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13. Collating the voice of people with autoimmune diseases: Methodology for the Third Phase of the COVAD Studies.
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Kadam E, Javaid M, Sen P, Saha S, Ziade N, Day J, Wincup C, Andreoli L, Parodis I, Tan AL, Shinjo SK, Dey D, Cavagna L, Chatterjee T, Knitza J, Wang G, Dalbeth N, Velikova T, Battista S, Cheng K, Boyd P, Kobert L, Gracia-Ramos AE, Mittal S, Makol A, Gutiérrez CET, Uribe CVC, Kuwana M, Burmester GR, Guillemin F, Nikiphorou E, Chinoy H, Aggarwal V, and Gupta L
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- Humans, Cross-Sectional Studies, Rheumatic Diseases psychology, Self Report, Medication Adherence, Mental Health, Social Determinants of Health, Research Design, Surveys and Questionnaires, Autoimmune Diseases psychology, Quality of Life
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Introduction: The growing recognition of holistic patient care highlights the various factors shaping the quality of life of individuals with autoimmune and rheumatic diseases (AIRDs). Beyond the traditional disease measures, there is an emerging acknowledgment of the less-explored aspects, including subjective well-being, social determinants of health, comorbidities, mental health, and medication adherence. Moreover, digital health services have empowered patients to engage actively in decision-making alongside clinicians. To explore these domains within the context of AIRDs, the "Collating the Voice of People with Autoimmune Diseases" COVAD survey was conceived, a successor of the previous two COVAD surveys. In this document, we present the study protocol in comprehensive detail., Methods: The COVAD-3 survey is a cross-sectional patient self-reported e-survey incorporating multiple widely accepted scales/scores to assess various aspects of patients' lifestyles objectively. To ensure the survey's accuracy and usability across diverse regions, it will be translated into multiple languages and subjected to rigorous vetting and pilot testing. It will be distributed by collaborators via online platforms and data will be collected from patients with AIRDs, and healthy individuals over eight months. Data analysis will focus on outcome measures related to various social, demographic, economic, and psychological factors., Conclusion: With the increasing awareness to adopt a holistic treatment approach encompassing all avenues of life, the COVAD-3 survey aims to gain valuable insights into the impact of social, demographic, economic, and psychological determinants of health on the subjective well-being in patients with AIRDs, which will contribute to a better understanding of their overall health and well-being., (© 2024. The Author(s).)
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- 2024
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14. The rheumatology workforce in the Arab countries: current status, challenges, opportunities, and future needs from an ArLAR cross-sectional survey.
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Ziade N, Hmamouchi I, Haouichat C, Baron F, Al Mayouf S, Abdulateef N, Masri B, El Rakawi M, El Kibbi L, El Mashaleh M, Elzorkany B, Al Saleh J, Dejaco C, and Abutiban F
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The Arab League of Associations for Rheumatology (ArLAR) Research Group (ARCH) conducted this study to investigate the number of current practicing rheumatologists in the Arab countries, to estimate the projected number of rheumatologists in 10 years, and to evaluate the current workload, practice profile, consultation waiting time, and geographical mobilities of these rheumatologists. This cross-sectional survey study was conducted in 16 Arab countries in two parts. The first survey was addressed nominally to national societies to estimate the current and projected workforce. The second was an anonymous e-survey elaborated by the study steering committee on the Google Forms platform and distributed to Arab rheumatologists using social media, WhatsApp, and mass e-mails to evaluate their practice. The mean number of rheumatologists in Arab countries was 0.84 per 100,000 inhabitants (mean age 47.5 years, 55% females), ranging from 0.06 (Sudan) to 1.86 (Tunisia). The number of rheumatologists is expected to increase by 50% in 2032. Nevertheless, a 20% increase in population associated with an increase in demand is also expected. Data from 446 rheumatologists (mean age 43.9 years, 60.5% females) revealed that 72% worked full-time, and 53% were employed in the public sector only. The average waiting time for a rheumatology consultation was 19.9 days. Of 394 rheumatologists, 19% obtained their rheumatology diplomas from non-Arab countries, and 47% of Gulf rheumatologists were non-citizen physicians. Considering local demographic disparities, healthcare system differences, and geographical mobilities, national authorities are advised to implement effective intervention plans to optimize the rheumatology workforce., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2023
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15. COVID-19 vaccine safety during pregnancy and breastfeeding in women with autoimmune diseases: results from the COVAD study.
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Andreoli L, Lini D, Schreiber K, Parodis I, Sen P, Ravichandran N, Day J, Joshi M, Jagtap K, Nune A, Nikiphorou E, Agarwal V, Saha S, Tan AL, Shinjo SK, Ziade N, Velikova T, Milchert M, Gracia-Ramos AE, Cavagna L, Kuwana M, Knitza J, Makol A, Patel A, Pauling JD, Wincup C, Barman B, Zamora Tehozol EA, Serrano JR, De La Torre IG, Colunga-Pedraza IJ, Merayo-Chalico J, Chibuzo OC, Katchamart W, Akarawatcharangura Goo P, Shumnalieva R, Chen YM, Hoff LS, El Kibbi L, Halabi H, Vaidya B, Shaharir SS, Hasan ATMT, Dey D, Toro Gutiérrez CE, Caballero-Uribe CV, Lilleker JB, Salim B, Gheita T, Chatterjee T, Saavedra MA, Distler O, Chinoy H, Agarwal V, Aggarwal R, and Gupta L
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- Humans, Female, Pregnancy, Adult, SARS-CoV-2 immunology, Vaccination adverse effects, Breast Feeding, Autoimmune Diseases, COVID-19 Vaccines adverse effects, COVID-19 prevention & control
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Objectives: We investigated coronavirus disease 2019 (COVID-19) vaccine safety in pregnant and breastfeeding women with autoimmune diseases (AID) in the COVID-19 Vaccination in Autoimmune Diseases (COVAD) study., Methods: Delayed-onset (>7 days) vaccine-related adverse events (AE), disease flares and AID-related treatment modifications were analysed upon diagnosis of AID vs healthy controls (HC) and the pregnancy/breastfeeding status at the time of at least one dose of vaccine., Results: Among the 9201 participants to the self-administered online survey, 6787 (73.8%) were women. Forty pregnant and 52 breastfeeding patients with AID were identified, of whom the majority had received at least one dose of COVID-19 vaccine (100% and 96.2%, respectively). AE were reported significantly more frequently in pregnant than in non-pregnant patients (overall AE 45% vs 26%, P = 0.01; minor AE 40% vs 25.9%, P = 0.03; major AE 17.5% vs 4.6%, P < 0.01), but no difference was found in comparison with pregnant HC. No difference was observed between breastfeeding patients and HC with respect to AE. Post-vaccination disease flares were reported by 17.5% of pregnant and 20% of breastfeeding patients, and by 18.3% of age- and disease-matched non-pregnant and non-breastfeeding patients (n = 262). All pregnant/breastfeeding patients who experienced a disease flare were managed with glucocorticoids; 28.6% and 20% of them required initiation or change in immunosuppressants, respectively., Conclusion: This study provides reassuring insights into the safety of COVID-19 vaccines administered to women with AID during the gestational and post-partum periods, helping overcome hesitant attitudes, as the benefits for the mother and for the fetus by passive immunization appear to outweigh potential risks., (© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
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- 2024
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16. Characteristics of emerging new autoimmune diseases after COVID-19 vaccination: A sub-study by the COVAD group.
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Shumnalieva R, Ravichandran N, Hannah J, Javaid M, Darooka N, Roy D, Gonzalez DE, Velikova T, Milchert M, Kuwana M, Joshi M, Gracia-Ramos AE, Boyd P, Yaadav P, Cheng K, Kobert L, Cavagna L, Sen P, Day J, Makol A, Gutiérrez CET, Caballero-Uribe CV, Saha S, Parodis I, Dey D, Nikiphorou E, Distler O, Kadam E, Tan AL, Shinjo SK, Ziade N, Knitza J, Chinoy H, Aggarwal R, Agarwal V, and Gupta L
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- Humans, Male, Female, Middle Aged, Cross-Sectional Studies, Aged, Adult, Vaccination adverse effects, Risk Factors, SARS-CoV-2 immunology, COVID-19 Vaccines adverse effects, Autoimmune Diseases epidemiology, Autoimmune Diseases diagnosis, COVID-19 prevention & control, COVID-19 epidemiology
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Background: Despite the overall safety and efficacy of COVID-19 vaccinations, rare cases of systemic autoimmune diseases (SAIDs) have been reported post-vaccination. This study used a global survey to analyze SAIDs in susceptible individuals' post-vaccination., Methods: A cross-sectional study was conducted among participants with self-reported new-onset SAIDs using the COVID-19 Vaccination in Autoimmune Diseases (COVAD) 2 study dataset-a validated, patient-reported e-survey-to analyze the long-term safety of COVID-19 vaccines. Baseline characteristics of patients with new-onset SAIDs and vaccinated healthy controls (HCs) were compared after propensity score matching based on age and sex in a 1:4 ratio., Results: Of 16 750 individuals, 74 (median age 52 years, 79.9% females, and 76.7% Caucasians) had new-onset SAID post-vaccination, mainly idiopathic inflammatory myopathies (IIMs) (n = 23, 31.51%), arthritis (n = 15; 20.53%), and polymyalgia rheumatica (PMR) (n = 12, 16.40%). Higher odds of new-onset SAIDs were noted among Caucasians (OR = 5.3; 95% CI = 2.9-9.7; p < .001) and Moderna vaccine recipients (OR = 2.7; 95% CI = 1.3-5.3; p = .004). New-onset SAIDs were associated with AID multimorbidity (OR = 1.4; 95% CI = 1.1-1.7; p < .001), mental health disorders (OR = 1.6; 95% CI = 1.3-1.9; p < .001), and mixed race (OR = 2.2; 95% CI = 1.2-4.2; p = .010), where those aged >60 years (OR = 0.6; 95% CI = 0.4-0.8; p = .007) and from high/medium human development index (HDI) countries (compared to very high HDI) reported fewer events than HCs., Conclusion: This study reports a low occurrence of new-onset SAIDs following COVID-19 vaccination, primarily IIMs, PMR, and inflammatory arthritis. Identified risk factors included pre-existing AID multimorbidity, mental health diseases, and mixed race. Revaccination was well tolerated by most patients; therefore, we recommend continuing COVID-19 vaccination in the general population. However, long-term studies are needed to understand the autoimmune phenomena arising post-vaccination., (© 2024 The Authors. International Journal of Rheumatic Diseases published by Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.)
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- 2024
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17. Listening to patients, for the patients: The COVAD Study-Vision, organizational structure, and challenges.
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Joshi M, Darooka N, Saha S, Dyball S, Sen P, Yaadav P, Javaid M, Kadam E, Shinjo SK, Dey D, Cavagna L, Makol A, Gutiérrez CET, Caballero Uribe CV, Kuwana M, Burmester GR, Ziade N, Wincup C, Andreoli L, Parodis I, Tan AL, Guillemin F, Knitza J, Wang G, Dalbeth N, Velikova T, Gracia-Ramos AE, Nikiphorou E, Day J, Chinoy H, Aggarwal R, Agarwal V, and Gupta L
- Subjects
- Humans, Social Media, SARS-CoV-2, Vaccination, COVID-19 epidemiology, Rheumatic Diseases therapy, Rheumatic Diseases epidemiology, Patient Reported Outcome Measures
- Abstract
Background: The pandemic presented unique challenges for individuals with autoimmune and rheumatic diseases (AIRDs) due to their underlying condition, the effects of immunosuppressive treatments, and increased vaccine hesitancy., Objectives: The COVID-19 vaccination in autoimmune diseases (COVAD) study, a series of ongoing, patient self-reported surveys were conceived with the vision of being a unique tool to gather patient perspectives on AIRDs. It involved a multinational, multicenter collaborative effort amidst a global lockdown., Methods: Leveraging social media as a research tool, COVAD collected data using validated patient-reported outcomes (PROs). The study, comprising a core team, steering committee, and global collaborators, facilitated data collection and analysis. A pilot-tested, validated survey, featuring questions regarding COVID-19 infection, vaccination and outcomes, patient demographics, and PROs was circulated to patients with AIRDs and healthy controls (HCs)., Discussion: We present the challenges encountered during this international collaborative project, including coordination, data management, funding constraints, language barriers, and authorship concerns, while highlighting the measures taken to address them., Conclusion: Collaborative virtual models offer a dynamic new frontier in medical research and are vital to studying rare diseases. The COVAD study demonstrates the potential of online platforms for conducting large-scale, patient-focused research and underscores the importance of integrating patient perspective into clinical care. Care of patients is our central motivation, and it is essential to recognize their voices as equal stakeholders and valued partners in the study of the conditions that affect them., (© 2024 The Authors. International Journal of Rheumatic Diseases published by Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.)
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- 2024
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18. Impaired health-related quality of life in idiopathic inflammatory myopathies: a cross-sectional analysis from the COVAD-2 e-survey.
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Yoshida A, Li Y, Maroufy V, Kuwana M, Sazliyana Shaharir S, Makol A, Sen P, Lilleker JB, Agarwal V, Kadam E, Akawatcharangura Goo P, Day J, Milchert M, Chen YM, Dey D, Velikova T, Saha S, Edgar Gracia-Ramos A, Parodis I, Nikiphorou E, Tan AL, Nune A, Cavagna L, Toro Gutiérrez CE, Caballero-Uribe CV, Saavedra MA, Shinjo SK, Ziade N, El Kibbi L, Knitza J, Distler O, Chinoy H, Agarwal V, Aggarwal R, and Gupta L
- Abstract
Objectives: To investigate health-related quality of life in patients with idiopathic inflammatory myopathies (IIMs) compared with those with non-IIM autoimmune rheumatic diseases (AIRDs), non-rheumatic autoimmune diseases (nrAIDs) and without autoimmune diseases (controls) using Patient-Reported Outcome Measurement Information System (PROMIS) instrument data obtained from the second COVID-19 vaccination in autoimmune disease (COVAD-2) e-survey database., Methods: Demographics, diagnosis, comorbidities, disease activity, treatments and PROMIS instrument data were analysed. Primary outcomes were PROMIS Global Physical Health (GPH) and Global Mental Health (GMH) scores. Factors affecting GPH and GMH scores in IIMs were identified using multivariable regression analysis., Results: We analysed responses from 1582 IIM, 4700 non-IIM AIRD and 545 nrAID patients and 3675 controls gathered through 23 May 2022. The median GPH scores were the lowest in IIM and non-IIM AIRD patients {13 [interquartile range (IQR) 10-15] IIMs vs 13 [11-15] non-IIM AIRDs vs 15 [13-17] nrAIDs vs 17 [15-18] controls, P < 0.001}. The median GMH scores in IIM patients were also significantly lower compared with those without autoimmune diseases [13 (IQR 10-15) IIMs vs 15 (13-17) controls, P < 0.001]. Inclusion body myositis, comorbidities, active disease and glucocorticoid use were the determinants of lower GPH scores, whereas overlap myositis, interstitial lung disease, depression, active disease, lower PROMIS Physical Function 10a and higher PROMIS Fatigue 4a scores were associated with lower GMH scores in IIM patients., Conclusion: Both physical and mental health are significantly impaired in IIM patients, particularly in those with comorbidities and increased fatigue, emphasizing the importance of patient-reported experiences and optimized multidisciplinary care to enhance well-being in people with IIMs., (© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology.)
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- 2024
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19. Characteristics and risk factors of COVID-19 breakthrough infections in Idiopathic Inflammatory Myopathies: Results from the COVAD study.
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Hoff LS, Naveen R, Sen P, Day J, Joshi M, Nune A, Nikiphorou E, Saha S, Tan AL, Shinjo SK, Ziade N, Velikova T, Milchert M, Jagtap K, Parodis I, Edgar Gracia-Ramos A, Cavagna L, Kuwana M, Knitza J, Chen YM, Makol A, Agarwal V, Patel A, Pauling JD, Wincup C, Barman B, Zamora Tehozol EA, Rojas Serrano J, García-De La Torre I, Colunga-Pedraza IJ, Merayo-Chalico J, Chibuzo OC, Katchamart W, Akarawatcharangura Goo P, Shumnalieva R, El Kibbi L, Halabi H, Vaidya B, Shaharir SS, Hasan ATMT, Dey D, Toro Gutiérrez CE, Caballero-Uribe CV, Lilleker JB, Salim B, Gheita T, Chatterjee T, Distler O, Saavedra MA, Chinoy H, Agarwal V, Aggarwal R, and Gupta L
- Abstract
Objectives: To explore prevalence, characteristics and risk factors of COVID-19 breakthrough infections (BIs) in idiopathic inflammatory myopathies (IIM) using data from the COVID-19 Vaccination in Autoimmune Diseases (COVAD) study., Methods: A validated patient self-reporting e-survey was circulated by the COVAD study group to collect data on COVID-19 infection and vaccination in 2022. BIs were defined as COVID-19 occurring ≥14 days after 2 vaccine doses. We compared BIs characteristics and severity among IIMs, other autoimmune rheumatic and non-rheumatic diseases (AIRD, nrAID), and healthy controls (HC). Multivariable Cox regression models assessed the risk factors for BI, severe BI and hospitalisations among IIMs., Results: Among 9449 included response, BIs occurred in 1447 (15.3%) respondents, median age 44 years (IQR 21), 77.4% female, and 182 BIs (12.9%) occurred among 1406 IIMs. Multivariable Cox regression among IIMs showed age as a protective factor for BIs [Hazard Ratio (HR)=0.98, 95%CI = 0.97-0.99], hydroxychloroquine and sulfasalazine use were risk factors (HR = 1.81, 95%CI = 1.24-2.64, and HR = 3.79, 95%CI = 1.69-8.42, respectively). Glucocorticoid use was a risk factor for severe BI (HR = 3.61, 95%CI = 1.09-11.8). Non-White ethnicity (HR = 2.61, 95%CI = 1.03-6.59) was a risk factor for hospitalisation. Compared with other groups, patients with IIMs required more supplemental oxygen therapy (IIM = 6.0% vs AIRD = 1.8%, nrAID = 2.2%, and HC = 0.9%), intensive care unit admission (IIM = 2.2% vs AIRD = 0.6%, nrAID, and HC = 0%), advanced treatment with antiviral or monoclonal antibodies (IIM = 34.1% vs AIRD = 25.8%, nrAID = 14.6%, and HC = 12.8%), and had more hospitalisation (IIM = 7.7% vs AIRD = 4.6%, nrAID = 1.1%, and HC = 1.5%)., Conclusion: Patients with IIMs are susceptible to severe COVID-19 BI. Age and immunosuppressive treatments were related to the risk of BIs., (© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
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- 2024
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20. Global disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study.
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Ziade N, Aoude M, Hmamouchi I, R N, Lilleker JB, Sen P, Joshi M, Agarwal V, Kardes S, Day J, Makol A, Milchert M, Gheita T, Salim B, Velikova T, Edgar Gracia-Ramos A, Parodis I, Nikiphorou E, Chatterjee T, Tan AL, Saavedra MA, Shinjo SK, Knitza J, Kuwana M, Nune A, Cavagna L, Distler O, Chinoy H, Agarwal V, Aggarwal R, and Gupta L
- Subjects
- Female, Humans, Middle Aged, Male, COVID-19 Vaccines, Cross-Sectional Studies, Immunoglobulins, Intravenous therapeutic use, Immunosuppressive Agents therapeutic use, Adjuvants, Immunologic, Myositis drug therapy, Autoimmune Diseases
- Abstract
Objectives: We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' gross national income (GNI), disease subtypes, and symptoms using patient-reported information., Methods: A cross-sectional ancillary analysis of the 'COVID-19 vaccination in auto-immune disease' (COVAD) e-survey containing demographic characteristics, IIM subtypes (DM, PM, IBM, anti-synthetase syndrome [ASSD], immune-mediated necrotizing myopathy [IMNM], overlap myopathies [OM]), current symptoms (surrogate for organ involvement) and treatments (corticosteroids [CS], immunomodulators [IM], i.e. antimalarials, immunosuppressants [IS], IVIG, biologic treatments and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM and organ involvement, and associated factors were analysed using multivariable binary logistic regressions., Results: Of 18 851 respondents from 94 countries, 1418 with IIM were analysed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%) and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%) and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biologic treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnoea). Most inter-regional treatment disparities persisted after multivariable analysis., Conclusion: We identified marked regional treatment disparities in a global cohort of IIM. These observations highlight the need for international consensus-driven management guidelines considering patient-centred care and available resources., (© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
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- 2024
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21. COVAD survey 2 long-term outcomes: unmet need and protocol
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Fazal, Z.Z., Sen, P., Joshi, M., Ravichandran, N., Lilleker, J.B., Agarwal, V., Kardes, S., Kim, M., Day, J., Makol, A., Milchert, M., Gheita, T., Salim, B., Velikova, T., Gracia-Ramos, A.E., Parodis, I., Nikiphorou, E., Tan, A.L., Chatterjee, T., Cavagna, L., Saavedra, M.A., Shinjo, S.K., Ziade, N., Selva-O’Callaghan, A., Nune, A., Knitza, J., Kuwana, M., Gutiérrez, C-E.T., Caballero-Uribe, C.V., Dey, D., Distler, O., Chinoy, H., Aggarwal, R., Gupta, L., Barman, B., Singh, Y.P., Ranjan, R., Jain, A., Pandya, S.C., Pilania, R.K., Sharma, A., Manoj, M.M., Gupta, V., Kavadichanda, C.G., Patro, Pr.S., Ajmani, S., Phatak, S., Goswami, R.P., Chowdhury, A.C., Mathew, A.J., Shenoy, P., Asranna, A., Bommakanti, K.T., Shukla, A., Pandey, A.K.R., Gaur, P.S., Mamadapur, M., Ghodke, A., Chandwar, K., Jagtap, K., Cansu, D.Ü., Yıldırım, R., Patel, A., Pauling, J.D., Wincup, C., Giannini, M., Maurier, F., Campagne, J., Meyer, A., Del Papa, N., Sambataro, G., Fabiola, A., Govoni, M., Parisi, S., Bocci, E.B., Sebastiani, G.D., Fusaro, E., Sebastiani, M., Quartuccio, L., Franceschini, F., Sainaghi, P.P., Orsolini, G., De Angelis, R., Danielli, M.G., Venerito, V., Grignaschi, S., Giollo, A., Traboco, L.S., Shaharir, S.S., Wibowo, S.A.K., Tehozol, E.A.Z., Serrano, J.R., De La Torre, I.G., Colunga‑Pedraza, I.J., Merayo-Chalico, J., Loarce-Martos, J., Prieto-González, S., Gil-Vila, A., Aranega, R., Hoff, L.S., Nakashima, R., Sato, S., Kimura, N., Kaneko, Y., Tomaras, S., Proft, F.N., Holzer, M-T, Gromova, M.A., Aharonov, O., Nagy-Vincze, M., Griger, Z., Hmamouchi, I., El bouchti, P.I., Baba, Z., Ima-Edomwonyi, U., Dedeke, I., Airenakho, E., Madu, N.H., Yerima, A., Olaosebikan, H., Chibuzo, O.C., Becky, A., Koussougbo, O.D., Palalane, E., Langguth, D., Limaye, V., Needham, M., Srivastava, N., Hudson, M., Landon-Cardinal, O., Zuleta, W.G.R., Arbeláez, Á., Cajas, J., Silva, J.A.P., Fonseca, J.E., Zimba, O., Bohdana, D., So, H., Ugarte-Gil, M.F., Chinchay, L., Bernaola, J.P., Pimentel, V., Tanveer Hasan, A.T.M., Saha, S., Vaidya, B., Fathi, H.M., Mohammed, R.H.A., Chen, Y-M, Harifi, G., El Kibbi, L., Halabi, H.M., Akawatcharangura, P., Katchamart, W., Fuentes-Silva, Y., Cabriza, K., Losanto, J., Colaman, N., Cachafeiro-Vilar, A., Bautista, G.G., Ho, E.J.G., González, R.A., Nunez, L.S., Vergara, C.M., Báez, J.T., Alonzo, H., Pastelin, C.B.S., Salinas, R.G., Obiols, A.Q., Chávez, N., Ordóñez, A.B., Argueta, S., Quijivix, D., Llerena, G.A.R., Sierra-Zorita, R., Arrieta, D., Hidalgo, E.R., Saenz, R., M., I.E., Morales, R., Calapaqui, W., Quezada, I., Arredondo, G., Fazal, Z.Z., Sen, P., Joshi, M., Ravichandran, N., Lilleker, J.B., Agarwal, V., Kardes, S., Kim, M., Day, J., Makol, A., Milchert, M., Gheita, T., Salim, B., Velikova, T., Gracia-Ramos, A.E., Parodis, I., Nikiphorou, E., Tan, A.L., Chatterjee, T., Cavagna, L., Saavedra, M.A., Shinjo, S.K., Ziade, N., Selva-O’Callaghan, A., Nune, A., Knitza, J., Kuwana, M., Gutiérrez, C-E.T., Caballero-Uribe, C.V., Dey, D., Distler, O., Chinoy, H., Aggarwal, R., Gupta, L., Barman, B., Singh, Y.P., Ranjan, R., Jain, A., Pandya, S.C., Pilania, R.K., Sharma, A., Manoj, M.M., Gupta, V., Kavadichanda, C.G., Patro, Pr.S., Ajmani, S., Phatak, S., Goswami, R.P., Chowdhury, A.C., Mathew, A.J., Shenoy, P., Asranna, A., Bommakanti, K.T., Shukla, A., Pandey, A.K.R., Gaur, P.S., Mamadapur, M., Ghodke, A., Chandwar, K., Jagtap, K., Cansu, D.Ü., Yıldırım, R., Patel, A., Pauling, J.D., Wincup, C., Giannini, M., Maurier, F., Campagne, J., Meyer, A., Del Papa, N., Sambataro, G., Fabiola, A., Govoni, M., Parisi, S., Bocci, E.B., Sebastiani, G.D., Fusaro, E., Sebastiani, M., Quartuccio, L., Franceschini, F., Sainaghi, P.P., Orsolini, G., De Angelis, R., Danielli, M.G., Venerito, V., Grignaschi, S., Giollo, A., Traboco, L.S., Shaharir, S.S., Wibowo, S.A.K., Tehozol, E.A.Z., Serrano, J.R., De La Torre, I.G., Colunga‑Pedraza, I.J., Merayo-Chalico, J., Loarce-Martos, J., Prieto-González, S., Gil-Vila, A., Aranega, R., Hoff, L.S., Nakashima, R., Sato, S., Kimura, N., Kaneko, Y., Tomaras, S., Proft, F.N., Holzer, M-T, Gromova, M.A., Aharonov, O., Nagy-Vincze, M., Griger, Z., Hmamouchi, I., El bouchti, P.I., Baba, Z., Ima-Edomwonyi, U., Dedeke, I., Airenakho, E., Madu, N.H., Yerima, A., Olaosebikan, H., Chibuzo, O.C., Becky, A., Koussougbo, O.D., Palalane, E., Langguth, D., Limaye, V., Needham, M., Srivastava, N., Hudson, M., Landon-Cardinal, O., Zuleta, W.G.R., Arbeláez, Á., Cajas, J., Silva, J.A.P., Fonseca, J.E., Zimba, O., Bohdana, D., So, H., Ugarte-Gil, M.F., Chinchay, L., Bernaola, J.P., Pimentel, V., Tanveer Hasan, A.T.M., Saha, S., Vaidya, B., Fathi, H.M., Mohammed, R.H.A., Chen, Y-M, Harifi, G., El Kibbi, L., Halabi, H.M., Akawatcharangura, P., Katchamart, W., Fuentes-Silva, Y., Cabriza, K., Losanto, J., Colaman, N., Cachafeiro-Vilar, A., Bautista, G.G., Ho, E.J.G., González, R.A., Nunez, L.S., Vergara, C.M., Báez, J.T., Alonzo, H., Pastelin, C.B.S., Salinas, R.G., Obiols, A.Q., Chávez, N., Ordóñez, A.B., Argueta, S., Quijivix, D., Llerena, G.A.R., Sierra-Zorita, R., Arrieta, D., Hidalgo, E.R., Saenz, R., M., I.E., Morales, R., Calapaqui, W., Quezada, I., and Arredondo, G.
- Abstract
Vaccine hesitancy is considered a major barrier to achieving herd immunity against COVID-19. While multiple alternative and synergistic approaches including heterologous vaccination, booster doses, and antiviral drugs have been developed, equitable vaccine uptake remains the foremost strategy to manage pandemic. Although none of the currently approved vaccines are live-attenuated, several reports of disease flares, waning protection, and acute-onset syndromes have emerged as short-term adverse events after vaccination. Hence, scientific literature falls short when discussing potential long-term effects in vulnerable cohorts. The COVAD-2 survey follows on from the baseline COVAD-1 survey with the aim to collect patient-reported data on the long-term safety and tolerability of COVID-19 vaccines in immune modulation. The e-survey has been extensively pilot-tested and validated with translations into multiple languages. Anticipated results will help improve vaccination efforts and reduce the imminent risks of COVID-19 infection, especially in understudied vulnerable groups.
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- 2022
22. POS0558 FLARES OF AUTOIMMUNE RHEUMATIC DISEASE FOLLOWING COVID-19 INFECTION: OBSERVATIONS FROM THE COVAD STUDY
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Ravichandran, N., primary, Sandhu, N., additional, Nune, A., additional, Day, J., additional, Sen, P., additional, Nikiphorou, E., additional, Tan, A. L., additional, Joshi, M., additional, Saha, S., additional, Katsuyuki Shinjo, S., additional, Jagtap, K., additional, Agarwal, V., additional, Ziade, N., additional, Velikova, T., additional, Milchert, M., additional, Kuwana, M., additional, Makol, A., additional, Chinoy, H., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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23. AB1586 THE RHEUMATOLOGY WORKFORCE IN THE ARAB COUNTRIES: WHAT IS THE CURRENT STATUS AND WHAT ARE THE PROJECTED UNMET NEEDS?
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Ziade, N., primary, Hmamouchi, I., additional, Haouichet, C., additional, Baron, F., additional, Al-Mayouf, S. M., additional, Al-Ani, N. A., additional, Masri, B., additional, EL Rakaawi, M., additional, Kibbi, L., additional, Mashaleh, M., additional, Zorkany, B., additional, El Saleh, J., additional, Dejaco, C., additional, and Abutiban, F., additional
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- 2023
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24. POS1216 MULTIMORBIDITY AND PROMIS HEALTH OUTCOMES IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES: DATA FROM A LARGE, GLOBAL E-SURVEY (COVAD STUDY)
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Fornaro, M., primary, Venerito, V., additional, Iannone, F., additional, Ravichandran, N., additional, Nikiphorou, E., additional, Joshi, M., additional, Tan, A. L., additional, Saha, S., additional, Katsuyuki Shinjo, S., additional, Agarwal, V., additional, Ziade, N., additional, Velikova, T., additional, Jagtap, K., additional, Milchert, M., additional, Parodis, I., additional, Gracia-Ramos, A. E., additional, Cavagna, L., additional, Kuwana, M., additional, Knitza, J., additional, Makol, A., additional, Dzifa, D., additional, Toro Gutierrez, C. E., additional, Vinicio Caballero, C., additional, Distler, O., additional, Day, J., additional, Study, C., additional, Chinoy, H., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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25. POS0893 SIGNIFICANT OVERLAP OF INFLAMMATORY AND DEGENERATIVE FEATURES ON SPINAL IMAGING AMONG PATIENTS WITH DEGENERATIVE SPINAL DISEASE, DIFFUSE IDIOPATHIC SKELETAL HYPEROSTOSIS AND RADIOGRAPHIC AXIAL SPONDYLOARTHRITIS
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Ziade, N., primary, Kougkas, N., additional, Udod, M., additional, Tsiami, S., additional, and Baraliakos, X., additional
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- 2023
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26. AB1295 SAFETY AND TOLERANCE OF ANTI-SARS-CoV-2 VACCINES IN SJÖGREN’S SYNDROME: RESULTS FROM THE COVAD STUDY
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Alunno, A., primary, Carubbi, F., additional, Gracia-Ramos, A. E., additional, Ziade, N., additional, Agarwal, V., additional, Velikova, T., additional, Kuwana, M., additional, Makol, A., additional, Chatterjee, T., additional, Joshi, M., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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27. OP0081 PREVALENCE, CHARACTERISTICS, AND PREDICTORS OF BREAKTHROUGH COVID-19 INFECTIONS IN PATIENTS WITH RHEUMATOID ARTHRITIS: DATA FROM THE COVID-19 VACCINATION IN AUTOIMMUNE DISEASE (COVAD) STUDY
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Ravichandran, N., primary, Parodis, I., additional, Gupta, L., additional, Katsuyuki Shinjo, S., additional, Ziade, N., additional, Milchert, M., additional, Cavagna, L., additional, Tan, A. L., additional, Lilleker, J. B., additional, Nune, A., additional, Pauling, J., additional, Wincup, C., additional, Katchamart, W., additional, Goo, P. A., additional, Study, C., additional, Chinoy, H., additional, Aggarwal, R., additional, Agarwal, V., additional, and Nikiphorou, E., additional
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- 2023
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28. POS1506 IDENTIFYING DETERMINANTS OF FAVOURABLE AND POOR PHYSICAL FUNCTION IN SYSTEMIC LUPUS ERYTHEMATOSUS: RESULTS FROM AN INTERNATIONAL COLLABORATIVE STUDY
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Lee, S. Y., primary, Holloway, A., additional, Nikiphorou, E., additional, Parodis, I., additional, Ravichandran, N., additional, Day, J., additional, Joshi, M., additional, Saha, S., additional, Jagtap, K., additional, Katchamart, W., additional, Goo, P. A., additional, Vaidya, B., additional, Velikova, T., additional, Sen, P., additional, Katsuyuki Shinjo, S., additional, Agarwal, V., additional, Tan, A. L., additional, Ziade, N., additional, Milchert, M., additional, Gracia-Ramos, A. E., additional, Vinicio Caballero, C., additional, Chinoy, H., additional, Aggarwal, R., additional, Gupta, L., additional, and Wincup, C., additional
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- 2023
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29. POS0573 COMORBIDITIES, COMPLEX MULTIMORBIDITY AND PROMIS HEALTH OUTCOMES AMONGAUTOIMMUNE RHEUMATIC DISEASES: DATA FROM THE COVAD STUDY
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Gupta, L., primary, Ravichandran, N., additional, Venerito, V., additional, Dey, M., additional, Sen, P., additional, Saha, S., additional, Tan, A. L., additional, Katsuyuki Shinjo, S., additional, Agarwal, V., additional, Joshi, M., additional, Ziade, N., additional, Velikova, T., additional, Jagtap, K., additional, Milchert, M., additional, Parodis, I., additional, Gracia-Ramos, A. E., additional, Cavagna, L., additional, Kuwana, M., additional, Knitza, J., additional, Makol, A., additional, Dzifa, D., additional, Toro Gutierrez, C. E., additional, Vinicio Caballero, C., additional, Distler, O., additional, Day, J., additional, Chinoy, H., additional, Aggarwal, R., additional, and Nikiphorou, E., additional
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- 2023
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30. POS0273 POST COVID-19 SYNDROME IN PATIENTS WITH AUTOIMMUNE RHEUMATIC DISEASES: RESULTS FROM THE COVAD STUDY
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Sen, P., primary, Ravichandran, N., additional, Joshi, M., additional, Saha, S., additional, Jagtap, K., additional, Agarwal, V., additional, Distler, O., additional, Nikiphorou, E., additional, Tan, A. L., additional, Katsuyuki Shinjo, S., additional, Ziade, N., additional, Velikova, T., additional, Milchert, M., additional, Parodis, I., additional, Gracia-Ramos, A. E., additional, Cavagna, L., additional, Kuwana, M., additional, Knitza, J., additional, Makol, A., additional, Patel, A., additional, Pauling, J., additional, Wincup, C., additional, Barman, B., additional, Zamora-Tehozol, E. A., additional, Rojas-Serrano, J., additional, Garcia-De La Torre, I., additional, Colunga-Pedraza, I. J., additional, Merayo-Chalico, J., additional, Katchamart, W., additional, Goo, P. A., additional, Chen, Y. M., additional, Hoff, L. S., additional, Kibbi, L., additional, Halabi, H., additional, Vaidya, B., additional, Shaharir, S. S., additional, Shumnalieva, R., additional, Hasan, A. T. M. T., additional, Dzifa, D., additional, Toro Gutierrez, C. E., additional, Vinicio Caballero, C., additional, Lilleker, J. B., additional, Salim, B., additional, Gheita, T. A., additional, Chatterjee, T., additional, Nune, A., additional, Saavedra, M. A., additional, Day, J., additional, Chinoy, H., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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31. AB1593 SEVERE IMPACT OF THE ECONOMIC CRISIS ON TREATMENT PERSISTENCE IN PATIENTS WITH RHEUMATIC AND MUSCULOSKELETAL DISEASES: A MULTICENTRIC CROSS-SECTIONAL STUDY IN LEBANON
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Asmar, S., primary, Messaykeh, J., additional, Hilal, N., additional, Rida, M. A., additional, Mroue’, K., additional, Aouad, K., additional, Minkara, F., additional, Hajjar, A., additional, and Ziade, N., additional
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- 2023
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32. POS1542 THE PSORIATIC ARTHRITIS IMPACT OF DISEASE (PSAID-12) QUESTIONNAIRE IS VALID IN ARABIC AND STRONGLY LINKED TO DISEASE ACTIVITY AND PATIENT-REPORTED OUTCOMES IN ARAB-SPEAKING COUNTRIES: AN ARLAR INITIATIVE
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Ziade, N., primary, Abbas, N., additional, Hmamouchi, I., additional, Kibbi, L., additional, Maroof, A., additional, Zorkany, B., additional, Al-Ani, N. A., additional, Ridha, A., additional, Ihsan, N., additional, Isho Gorial, F., additional, Al Chama, N., additional, Haouichet, C., additional, Alnaimat, F., additional, Hannawi, S., additional, Atawina, S., additional, Halabi, H., additional, Mashaleh, M., additional, Aljazwi, L., additional, Abogamal, A., additional, Ayoub, L., additional, Bouajina, E., additional, Bahiri, R., additional, Saad, S., additional, Sabkar, M., additional, Aouad, K., additional, and Gossec, L., additional
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- 2023
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33. AB1581 HIGH PREVALENCE OF BURNOUT SYNDROME AMONG RHEUMATOLOGISTS PRACTICING IN ARAB COUNTRIES: AN ARLAR MULTINATIONAL STUDY IN 394 RHEUMATOLOGISTS
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Naim, R., primary, Hmamouchi, I., additional, Haouichet, C., additional, Baron, F., additional, Al-Mayouf, S. M., additional, Al-Ani, N. A., additional, Masri, B., additional, EL Rakaawi, M., additional, Kibbi, L., additional, Mashaleh, M., additional, Abutiban, F., additional, and Ziade, N., additional
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- 2023
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34. POS1231 IMPAIRED HEALTH-RELATED QUALITY OF LIFE IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES: A CROSS-SECTIONAL ANALYSIS FROM AN INTERNATIONAL E-SURVEY
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Yoshida, A., primary, LI, Y., additional, Maroufy, V., additional, Kuwana, M., additional, Ravichandran, N., additional, Makol, A., additional, Sen, P., additional, Lilleker, J. B., additional, Agarwal, V., additional, Kardes, S., additional, Day, J., additional, Milchert, M., additional, Joshi, M., additional, Gheita, T. A., additional, Salim, B., additional, Velikova, T., additional, Gracia-Ramos, A. E., additional, Parodis, I., additional, Nikiphorou, E., additional, Tan, A. L., additional, Nune, A., additional, Cavagna, L., additional, Saavedra, M. A., additional, Katsuyuki Shinjo, S., additional, Ziade, N., additional, Knitza, J., additional, Distler, O., additional, Chinoy, H., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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35. AB1148 PATIENT AND PHYSICIAN GLOBAL ASSESSMENT OF PSORIATIC ARTHRITIS APPEAR MORE IN AGREEMENT IN ARAB COUNTRIES THAN PREVIOUSLY REPORTED ELSEWHERE – AN INTERNATIONAL STUDY UNDER THE AEGIS OF ARLAR
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Ziade, N., primary, Abbas, N., additional, Kibbi, L., additional, Maroof, A., additional, Zorkany, B., additional, Al-Ani, N. A., additional, Ridha, A., additional, Ihsan, N., additional, Isho Gorial, F., additional, Al Chama, N., additional, Haouichet, C., additional, Alnaimat, F., additional, Hannawi, S., additional, Atawina, S., additional, Halabi, H., additional, Mashaleh, M., additional, Aljazwi, L., additional, Abogamal, A., additional, Ayoub, L., additional, Bouajina, E., additional, Bahiri, R., additional, Saad, S., additional, Sabkar, M., additional, Aouad, K., additional, Gossec, L., additional, and Hmamouchi, I., additional
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- 2023
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36. POS0880 COMPARATIVE DISEASE BURDEN IN PATIENTS WITH RHEUMATOID ARTHRITIS, PSORIATIC ARTHRITIS OR ANKYLOSING SPONDYLITIS: DATA FROM COVAD PATIENT-REPORTED E-SURVEY
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Venerito, V., primary, Fornaro, M., additional, Iannone, F., additional, Cavagna, L., additional, Kuwana, M., additional, Agarwal, V., additional, Ravichandran, N., additional, Day, J., additional, Joshi, M., additional, Saha, S., additional, Shaharir, S. S., additional, Katchamart, W., additional, Goo, P. A., additional, Traboco, L., additional, Chen, Y. M., additional, Sen, P., additional, Lilleker, J. B., additional, Nune, A., additional, Pauling, J., additional, Wincup, C., additional, Tan, A. L., additional, Ziade, N., additional, Milchert, M., additional, Gracia-Ramos, A. E., additional, Vinicio Caballero, C., additional, Study, C., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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37. AB1312 MYOSITIS PATIENTS WITHOUT AUTOIMMUNE MULTIMORBIDITY AT LOWER RISK OF DELAYED ONSET COVID-19 VACCINE ADVERSE EVENTS THAN OTHER AUTOIMMUNE DISEASES: RESULTS FROM THE COVAD STUDY
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Shaharir, S. S., primary, Doskaliuk, B., additional, Ravichandran, N., additional, Day, J., additional, Sen, P., additional, Katsuyuki Shinjo, S., additional, Joshi, M., additional, Ziade, N., additional, Velikova, T., additional, Milchert, M., additional, Saha, S., additional, Knitza, J., additional, Makol, A., additional, Jagtap, K., additional, Agarwal, V., additional, Dey, D., additional, Toro Gutierrez, C. E., additional, Vinicio Caballero, C., additional, Aggarwal, R., additional, and Gupta, L., additional
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- 2023
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38. Significant overlap of inflammatory and degenerative features on spinal imaging among patients with Degenerativ spinal diease, diffuse idiopathic skeletal hyperostosis and radiographic axial spondyloarthritis
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Ziade, N, Tsiami, S, Kougkas, N, Udod, M, Baraliakos, X, Ziade, N, Tsiami, S, Kougkas, N, Udod, M, and Baraliakos, X
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- 2023
39. PREVALENCE, CHARACTERISTICS, AND PREDICTORS OF BREAKTHROUGH COVID-19 INFECTIONS IN PATIENTS WITH RHEUMATOID ARTHRITIS : DATA FROM THE COVID-19 VACCINATION IN AUTOIMMUNE DISEASE (COVAD) STUDY
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Ravichandran, N., Parodis, Ioannis, Gupta, L., Katsuyuki Shinjo, S., Ziade, N., Milchert, M., Cavagna, L., Tan, A. L., Lilleker, J. B., Nune, A., Pauling, J., Wincup, C., Katchamart, W., Goo, P. A., Study, C., Chinoy, H., Aggarwal, R., Agarwal, V., Nikiphorou, E., Ravichandran, N., Parodis, Ioannis, Gupta, L., Katsuyuki Shinjo, S., Ziade, N., Milchert, M., Cavagna, L., Tan, A. L., Lilleker, J. B., Nune, A., Pauling, J., Wincup, C., Katchamart, W., Goo, P. A., Study, C., Chinoy, H., Aggarwal, R., Agarwal, V., and Nikiphorou, E.
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Background: Global data on COVID-19 breakthrough infections (BI) following COVID-19 vaccination among autoimmune rheumatic diseases (AIRDs) and especially rheumatoid arthritis (RA) is scarce. Objectives: This study aimed to examine the characteristics of COVID-19 BI among patients with RA and compare them with AIRDs and healthy controls (HCs). Methods: A global e-survey, January-May 2022, collected data on COVID-19 vaccination, and BI in patients with RA, AIRDs, non-rheumatic autoimmune disease (nrAIDs), and HCs. BI was defined as infection after both primary or booster vaccine doses. Severe BI was defined as the need for hospitalization, including intensive unit care, oxygen therapy, or advanced treatment in the form of monoclonal antibodies. Results: Of the 9595 vaccinated respondents of the e-survey, 3224 (33.6%) reported COVID-19. One BI was reported in 323/1802 (17.9%) patients with RA, 584/3869 (15.0%) patients with other AIRDs, and 467/3435 (13.5%) HCs. Similarly, second BI was reported by 280 (8.6%); 42 (2.3%) among RA, 90 (2.3%) among other AIRDs, and 124 (3.6%) among HCs. The prevalence of first BI in patients with RA was higher than that in those with AIRDs (OR=1.2; 95%CI=1.1-1.4; p=0.001) and HCs (OR=1.4; 95%CI=1.2-1.6; p<0.001), but similar to nrAIDs (p=0.783). The prevalence of second BI was lower in patients with RA than in HCs (OR=0.6; 95%CI=0.4-0.9; p=0.012) and nrAIDs (OR=0.4; 95%CI=0.2-0.7; p=0.004), but similar to AIRDs (p=0.991). When compared with HCs, patients with RA reported significantly higher joint pain, hospitalizations, and need for advanced treatment at first BI. Patients with RA from very high HDI countries had lower hazard of first BI than those from high HDI countries (HR=0.026; 95%CI=0.001-0.6; p=0.027). Rituximab use predicted more frequent hospitalization (OR=3.4; 95%CI=1.3-11.4; p=0.045) and severe BI (OR=3.0; 95%CI=1.2-7.3; p=0.014). Conclusion: Nearly one in five patients with RA reported BI. BI prevalence was higher in pat
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40. IMPAIRED HEALTH-RELATED QUALITY OF LIFE IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES : A CROSS-SECTIONAL ANALYSIS FROM AN INTERNATIONAL SURVEY
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Yoshida, A., Li, Y., Maroufy, V., Kuwana, M., Ravichandran, N., Makol, A., Sen, P., Lilleker, J. B., Agarwal, V., Kardes, S., Day, J., Milchert, M., Joshi, M., Gheita, T. A., Salim, B., Velikova, T., Gracia-Ramos, A. E., Parodis, Ioannis, Nikiphorou, E., Tan, A. L., Nune, A., Cavagna, L., Saavedra, M. A., Katsuyuki Shinjo, S., Ziade, N., Knitza, J., Distler, O., Chinoy, H., Aggarwal, R., Gupta, L., Yoshida, A., Li, Y., Maroufy, V., Kuwana, M., Ravichandran, N., Makol, A., Sen, P., Lilleker, J. B., Agarwal, V., Kardes, S., Day, J., Milchert, M., Joshi, M., Gheita, T. A., Salim, B., Velikova, T., Gracia-Ramos, A. E., Parodis, Ioannis, Nikiphorou, E., Tan, A. L., Nune, A., Cavagna, L., Saavedra, M. A., Katsuyuki Shinjo, S., Ziade, N., Knitza, J., Distler, O., Chinoy, H., Aggarwal, R., and Gupta, L.
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Background: Comprehensive and large-scale assessment of health-related quality of life in patients with idiopathic inflammatory myopathies (IIMs) worldwide is lacking. The second COVID-19 vaccination in autoimmune disease (COVAD-2) study [1] is an international, multicentre, self-reported e-survey assessing several aspects of COVID-19 infection and vaccination as well as validated patient-reported outcome measures (PROMs) to outline patient experience in various autoimmune diseases (AIDs), with a particular focus on IIMs. Objectives: To investigate physical and mental health in a global cohort of IIM patients compared to those with non-IIM autoimmune inflammatory rheumatic diseases (AIRDs), non-rheumatic AIDs (NRAIDs), and those without AIDs (controls), using Patient-Reported Outcome Measurement Information System (PROMIS) global health data obtained from the COVAD-2 survey. Methods: Demographics, AID diagnoses, comorbidities, disease activity, treatments, and PROMs were extracted from the COVAD-2 database. The primary outcomes were PROMIS Global Physical Health (GPH) and Global Mental Health (GMH) scores. Secondary outcomes included PROMIS physical function short form-10a (PROMIS PF-10a), pain visual analogue scale (VAS), and PROMIS Fatigue-4a scores. Each outcome was compared between IIMs, non-IIM AIRDs, NRAIDs, and controls. Factors affecting GPH and GMH scores in IIMs were identified using multivariable regression analysis. Results: A total of 10,502 complete responses from 1582 IIMs, 4700 non-IIM AIRDs, 545 NRAIDs, and 3675 controls, which accrued as of May 2022, were analysed. Patients with IIMs were older [59±14 (IIMs) vs. 48±14 (non-IIM AIRDs) vs. 45±14 (NRAIDs) vs. 40±14 (controls) years, p<0.001] and more likely to be Caucasian [82.7% (IIMs) vs. 53.2% (non-IIM AIRDs) vs. 62.4% (NRAIDs) vs. 34.5% (controls), p<0.001]. Among IIMs, dermatomyositis (DM) and juvenile DM were the most common (31.4%), followed by inclusion body myositis (IBM) (24.9%). Patie
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41. EVALUATING GLOBAL PATTERNS IN TREATMENT AND PREVALENCE OF COMORBIDITIES IN SYSTEMIC LUPUS ERYTHEMATOSUS
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Holloway, A., Lee, S. Y., Nikiphorou, E., Parodis, Ioannis, Ravichandran, N., Day, J., Joshi, M., Saha, S., Shaharir, S. S., Katchamart, W., Goo, P. A., Traboco, L., Chen, Y. M., Sen, P., Lilleker, J. B., Nune, A., Pauling, J., Tan, A. L., Ziade, N., Milchert, M., Gracia-Ramos, A. E., Vinicio Caballero, C., Agarwal, V., Aggarwal, R., Gupta, L., Wincup, C., Holloway, A., Lee, S. Y., Nikiphorou, E., Parodis, Ioannis, Ravichandran, N., Day, J., Joshi, M., Saha, S., Shaharir, S. S., Katchamart, W., Goo, P. A., Traboco, L., Chen, Y. M., Sen, P., Lilleker, J. B., Nune, A., Pauling, J., Tan, A. L., Ziade, N., Milchert, M., Gracia-Ramos, A. E., Vinicio Caballero, C., Agarwal, V., Aggarwal, R., Gupta, L., and Wincup, C.
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Background: Regional disparities in the management of systemic lupus erythematosus (SLE) are frequently described. Governance, funding, logistic barriers, and physician choice may be important determinants though scarce data from underrepresented regions limits our understanding. Objectives: To evaluate global patterns in treatment of SLE and identify the prevalence of comorbidities. Methods: We identified SLE patients from the COVAD 2 database, consisting of over 20,000 respondents worldwide. Healthy controls (HC) were included to assess population comorbidity levels. Demographics, treatment i.e., corticosteroids (CS), antimalarials, immunosuppressants (IS), cyclophosphamide and biologics plus comorbidity data was recorded. Country Human Development Index (HDI) classification, a composite index formulated by the United Nations to rank countries into tiers of development, was utilised. Results: 3323 HCs and 1167 SLE patients were included in analysis. Patients from low/medium HDI (lmHDI) countries were younger than those from high/very high HDI (hvhHDI) countries (median age 32, IQR 27-41 vs 41, IQR 32-52 years, p<0.0001). Disease duration was shorter in lmHDI countries (median 5, IQR 3-10 vs 10, IQR 5-19 years, p<0.0001). A higher proportion of SLE patients from lmHDI countries were on CS (73% vs 59%, p=0.0002), antimalarials (81% vs 68%, p=0.0002) and IS (66% vs 53%, p=0.0009) compared with patients from hvhHDI countries. Choice of IS varied with azathioprine prescribed more frequently in lmHDI countries (p=0.049). Biologics use was more common in hvhHDI countries (7% vs 2%, p=0.0055). Comorbidity prevalence was similar between groups, however when adjusted for age, patients with chronic kidney disease were significantly younger in lmHDI countries (36.67 vs 44.64 years, p=0.015), as were patients with coronary artery disease (35.7 vs. 44.6 years, p=0.015) and hypertension (41.5 vs 49.8 years, p=0.003). Results are detailed in Table 1. Conclusion: To our know
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42. COMORBIDITIES, COMPLEX MULTIMORBIDITY AND PROMIS HEALTH OUTCOMES AMONGAUTOIMMUNE RHEUMATIC DISEASES : DATA FROM THE COVAD STUDY
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Gupta, L., Ravichandran, N., Venerito, V., Dey, M., Sen, P., Saha, S., Tan, A. L., Shinjo, S. Katsuyuki, Agarwal, V., Joshi, M., Ziade, N., Velikova, T., Jagtap, K., Milchert, M., Parodis, Ioannis, Gracia-Ramos, A. E., Cavagna, L., Kuwana, M., Knitza, J., Makol, A., Dzifa, D., Gutierrez, C. E. Toro, Caballero, C. Vinicio, Distler, O., Day, J., Chinoy, H., Aggarwal, R., Nikiphorou, E., Gupta, L., Ravichandran, N., Venerito, V., Dey, M., Sen, P., Saha, S., Tan, A. L., Shinjo, S. Katsuyuki, Agarwal, V., Joshi, M., Ziade, N., Velikova, T., Jagtap, K., Milchert, M., Parodis, Ioannis, Gracia-Ramos, A. E., Cavagna, L., Kuwana, M., Knitza, J., Makol, A., Dzifa, D., Gutierrez, C. E. Toro, Caballero, C. Vinicio, Distler, O., Day, J., Chinoy, H., Aggarwal, R., and Nikiphorou, E.
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Background: Comorbidities have a profound impact on the QoL of patients living with autoimmune rheumatic diseases (AIRDs). Unfortunately, global data on the burden of comorbidities and its impact on health outcomes in this vulnerable group is scarce. Objectives: We studied the prevalence, distribution and clustering of comorbidities and multimorbidity among patients with AIRDs and healthy controls (HCs) and its impact on health outcomes, utilizing data from the ongoing 2nd COVAD study. Methods: The COVAD study is a global e-survey that embodies patient voice while empowering collaborators and young researchers. The study group of 157 physicians across 106 countries from February-June 2022 captured details of AIRDs, autoimmune and non-autoimmune comorbidities, and validated patient reported outcomes. Human Development Index (UNDP 2021-22) of country of residence was taken as a surrogate marker for socioeconomic status (SES). Basic multimorbidity (BM), Complex multimorbidity (CM), Autoimmune multimorbidity (AM) are defined as the co-occurrence of ≥2 non-rheumatic comorbidities, ≥3 non-rheumatic chronic conditions affecting ≥3 different organ systems [1] and ≥3 autoimmune diseases (AIDs) in an individual respectively. PROMIS global physical health (PGP), mental health (PGM), fatigue 4a (F4a) and physical function short form (SF10) scores were calculated for the different groups and compared using descriptive statistics, linear regression and cluster analysis (hierarchical followed by K means). Results: Of 17,612 total respondents, 6149 (62.7%) had underlying AIRDs and 3652 (37.3%) were HCs, with female (80.8%) and Caucasian (53.9%) predominance in the former. All types of multimorbidity were more frequent in AIRDs than HCs, including any comorbidity (77.1% versus 25.0%; OR: 2.9; 2.7-3.2), BM (21.0% vs 6.2%; 4.0; 3.4-4.6), and CM (3.1% vs 0.5%; 6.4; 3.9-10.4), and with prevalence increasing with age (p<0.001) (Figure 1A, B). Comorbidity prevalence was the highest amo
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43. IDENTIFYING DETERMINANTS OF FAVOURABLE AND POOR PHYSICAL FUNCTION IN SYSTEMIC LUPUS ERYTHEMATOSUS : RESULTS FROM AN INTERNATIONAL COLLABORATIVE STUDY
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Lee, S. Y., Holloway, A., Nikiphorou, E., Parodis, Ioannis, Ravichandran, N., Day, J., Joshi, M., Saha, S., Jagtap, K., Katchamart, W., Goo, P. A., Vaidya, B., Velikova, T., Sen, P., Katsuyuki Shinjo, S., Agarwal, V., Tan, A. L., Ziade, N., Milchert, M., Gracia-Ramos, A. E., Vinicio Caballero, C., Chinoy, H., Aggarwal, R., Gupta, L., Wincup, C., Lee, S. Y., Holloway, A., Nikiphorou, E., Parodis, Ioannis, Ravichandran, N., Day, J., Joshi, M., Saha, S., Jagtap, K., Katchamart, W., Goo, P. A., Vaidya, B., Velikova, T., Sen, P., Katsuyuki Shinjo, S., Agarwal, V., Tan, A. L., Ziade, N., Milchert, M., Gracia-Ramos, A. E., Vinicio Caballero, C., Chinoy, H., Aggarwal, R., Gupta, L., and Wincup, C.
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Background: Systemic lupus erythematosus (SLE) can result in impaired daily physical function through various mechanisms including active disease, chronic damage, and mental health symptoms that are common in the disease. However, the key drivers of reduced physical function are poorly understood, and no large-scale global studies investigating this have been conducted to date. Objectives: To investigate key factors that contribute to impaired physical function in SLE globally. Methods: SLE patients were identified from the COVAD 2 database, a global register of more than 20,000 respondents. Healthy controls (HC) were included to compare differences in physical function using the Patient Reported Outcome Measurement Information System (PROMIS) questionnaire. Demographics, medication, comorbidities, disease activity, Global Physical Health (GPH) and Global Mental Health (GMH) were collected. Multivariable regression analysis was used to identify contributing factors to favourable or poor physical function (measured by PROMIS Physical Function shortform PF-10a score). Results: 979 SLE patients and 3358 HCs were included in analysis. Patients with SLE had significantly lower PF-10a score as compared to HCs (median 42, IQR 36-47 vs median 49, IQR 45-50, p<0.0001). Determinants of physical function status in patients with SLE are summarised in Table 1. Briefly, factors associated with poor physical function included increasing age (-0.042, 95% CI -0.069 to -0.015, p=0.002) and methotrexate use (-0.928, 95% CI -1.844 to -0.012, p=0.047). Diabetes (-1.862, 95% CI -3.481 to -0.243, p=0.024) and interstitial lung disease (ILD) (-2.441, 95% CI -4.366 to -0.517, p=0.013), but not asthma or COPD, also contributed to lower PF-10a score. From a mental health perspective, anxiety (-0.970, 95% CI -1.853 to -0.087, p=0.031) but not depression contributed to a lower physical function score. Higher Pain Visual Analogue Scales (VAS) (-2.889, 95% CI -3.107 to -2.671, p<0.001) and
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- 2023
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44. MULTIMORBIDITY AND PROMIS HEALTH OUTCOMES IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES : DATA FROM A LARGE, GLOBAL E-SURVEY (COVAD STUDY)
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Fornaro, M., Venerito, V., Iannone, F., Ravichandran, N., Nikiphorou, E., Joshi, M., Tan, A. L., Saha, S., Shinjo, S. Katsuyuki, Agarwal, V., Ziade, N., Velikova, T., Jagtap, K., Milchert, M., Parodis, Ioannis, Gracia-Ramos, A. E., Cavagna, L., Kuwana, M., Knitza, J., Makol, A., Dzifa, D., Toro Gutierrez, C. E., Vinicio Caballero, C., Distler, O., Day, J., Chinoy, H., Aggarwal, R., Gupta, L., Fornaro, M., Venerito, V., Iannone, F., Ravichandran, N., Nikiphorou, E., Joshi, M., Tan, A. L., Saha, S., Shinjo, S. Katsuyuki, Agarwal, V., Ziade, N., Velikova, T., Jagtap, K., Milchert, M., Parodis, Ioannis, Gracia-Ramos, A. E., Cavagna, L., Kuwana, M., Knitza, J., Makol, A., Dzifa, D., Toro Gutierrez, C. E., Vinicio Caballero, C., Distler, O., Day, J., Chinoy, H., Aggarwal, R., and Gupta, L.
- Abstract
Background: Prevalence of comorbidities and their impact on health outcomes in Idiopathic inflammatory myopathies (IIMs) is limited. Objectives: This study aimed to explore the prevalence of multimorbidity in patients with IIMs, other autoimmune rheumatic diseases (AIRDs) and Healthy controls (HCs). We further explore the impact of comorbidities on patients’ physical, mental, and social health assessed by the Patient-Reported Outcome Measurement Information System (PROMIS instruments). Methods: Data for this study were acquired from the COVAD 2 e-survey hosted by a study group consisting of 167 collaborators in 110 countries. Basic multimorbidity (BM) was defined as the co-occurrence of two or more comorbidities in an individual, while complex multimorbidity (CM) signified the co-occurrence of 3 or more chronic conditions affecting 3 or more different organ systems. PROMIS global physical health (PGP), mental health (PGM), fatigue 4a (F4a) and physical function short form (SF10) were analysed using descriptive statistics and linear regression models. Hierarchical Clustering on Principal Components was performed to outline the grouping. Results: Of 10740 complete respondents, 1558 IIMs, 4591 AIRDs and 3652 HCs were analysed. Individuals with IIMs exhibited high burden of any comorbidity (OR: 1.62 vs AIRDs and 2.95 vs HCs,p<0.01), BM (OR 1.66 vs AIRDs and 3.52 vs HCs,p<0.01), CM (OR: 1.69 vs AIRDs and 6.23 vs HCs,p<0.01), and mental health disorders (MHDs) (OR 1.33 vs AIRDs and 2.63 vs HCs,p<0.01). IIM patients with comorbidities (and MHDs) had worse physical function (low PGP, PGM, SF10 and higher F4a scores, all p<0.001). Worse physical function (PGP) was predicted by age (0.35; 0.030), active disease (-1.51; <0.001), BM (-1.11; <0.001), and MHDs (-1.47; <0.001). PGM was impacted by age (0.51; 0.004), active disease (-1.34, <0.001), BM (-0.75; 0.001) and MHDs (-2.22; <0.001). Determinants of SF10a were age (-3.86; <0.001), active dis
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- 2023
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45. Quelle est la meilleure stratégie de référence pour la spondylarthrite axiale ? Étude multicentrique prospective de 515 patients souffrant de lombalgie chronique suspecte
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Ziade, N., primary, Maroof, A., additional, Elzorkany, B., additional, Abdullateef, N., additional, Adnan, A., additional, Abogamal, A., additional, Saad, S., additional, El Kibbi, L., additional, Alemadi, S., additional, Ansari, A., additional, Abi Najm, A., additional, Younan, T., additional, Kharrat, K., additional, Maarawi, J., additional, Sebaaly, A., additional, Rachkidi, R., additional, Witte, T., additional, and Baraliakos, X., additional
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- 2022
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46. Intérêt des anticorps anti-CD74 pour le diagnostic de la spondylolarthrite axiale : résultats d’une étude prospective chez des patients référés en rhumatologie pour lombalgie suspecte
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Ziade, N., primary, Maroof, A., additional, Abi Najm, A., additional, Witte, T., additional, and Baraliakos, X., additional
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- 2022
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47. Systemic sclerosis and COVID-19 vaccine safety: short-term insights from the global COVID-19 vaccination in autoimmune disease (COVAD) survey
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Naveen, R., Thakare, D. R., Kuwana, M., Pauling, J. D., Day, J., Joshi, M., Parodis, I., Sen, P., Jagtap, K., Nikiphorou, E., Saha, S., Agarwal, V., Chatterjee, T., Lilleker, J. B., Kardes, S., Milchert, M., Gheita, T., Salim, B., Velikova, T., Gracia-Ramos, A. E., Tan, A. L., Nune, A., Cavagna, L., Saavedra, M. A., Shinjo, S. K., Ziade, N., Knitza, J., Distler, O., Chinoy, H., Barman, B., Singh, Y. P., Ranjan, R., Jain, A., Pandya, S. C., Pilania, R. K., Sharma, A., Manesh Manoj, M., Gupta, V., Kavadichanda, C. G., Patro, P. S., Ajmani, S., Phatak, S., Goswami, R. P., Chowdhury, A. C., Mathew, A. J., Shenoy, P., Asranna, A., Bommakanti, K. T., Shukla, A., Pande, A. R., Chandwar, K., Cansu, D. U., Wincup, C., Makol, A., Del Papa, N., Sambataro, G., Fabiola, A., Govoni, M., Parisi, S., Bocci, E. B., Sebastiani, G. D., Fusaro, E., Sebastiani, M., Quartuccio, L., Franceschini, F., Sainaghi, P. P., Orsolini, G., De Angelis, R., Danielli, M. G., Venerito, V., Traboco, L. S., Wibowo, S. A. K., Serrano, J. R., La Torre, I. G. -D., Tehozol, E. A. Z., Loarce-Martos, J., Prieto-Gonzalez, S., Gonzalez, R. A., Yoshida, A., Nakashima, R., Sato, S., Kimura, N., Kaneko, Y., Tomaras, S., Gromova, M. A., Aharonov, O., Hmamouchi, I., Hoff, L. S., Giannini, M., Maurier, F., Campagne, J., Meyer, A., Nagy-Vincze, M., Langguth, D., Limaye, V., Needham, M., Srivastav, N., Hudson, M., Landon-Cardinal, O., Shaharir, S. S., Zuleta, W. G. R., Silva, J. A. P., Fonseca, J. E., Zimba, O., Aggarwal, R., and Gupta, L.
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Adverse events ,Autoimmune diseases ,Vaccination ,COVID-19 ,Systemic sclerosis - Published
- 2023
48. Vaccine hesitancy decreases in rheumatic diseases, long-term concerns remain in myositis: a comparative analysis of the COVAD surveys
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Sen, P, Naveen, R, Houshmand, N, Kia, Sm, Joshi, M, Saha, S, Jagtap, K, Agarwal, V, Nune, A, Nikiphorou, E, Tan, Al, Shinjo, Sk, Ziade, N, Velikova, T, Milchert, M, Parodis, I, Gracia-Ramos, Ae, Cavagna, L, Kuwana, M, Knitza, J, Makol, A, Patel, A, Pauling, Jd, Wincup, C, Barman, B, Tehozol, Eaz, Serrano, Jr, de la Torre, I, Colunga-Pedraza, Ij, Merayo-Chalico, J, Chibuzo, Oc, Katchamart, W, Goo, Pa, Shumnalieva, R, Chen, Ym, Hoff, Ls, El Kibbi, L, Halabi, H, Vaidya, B, Shaharir, Ss, Hasan, Atmt, Dey, D, Gutierrez, Cet, Caballero-Uribe, Cv, Lilleker, Jb, Salim, B, Gheita, T, Chatterjee, T, Distler, O, Saavedra, Ma, Day, J, Chinoy, H, COVAD Study Grp, Kardes, S, Kardes, Sa, Andreoli, L, Lini, D, Screiber, K, Vince, Mn, Singh, Yp, Ranjan, R, Jain, A, Pandya, Sc, Pilania, Rk, Sharma, A, Manoj, Mm, Gupta, V, Kavadichanda, Cg, Patro, Ps, Ajmani, S, Phatak, S, Goswami, Rp, Chowdhury, Ac, Mathew, Aj, Shenoy, P, Asranna, A, Bommakanti, Kt, Shukla, A, Pande, Ar, Chandwar, K, Ghodke, A, Boro, H, Fazal, Zz, Cansu, Du, Yildirim, R, Gasparyan, Ay, Del Papa, N, Sambataro, G, Fabiola, A, Govoni, M, Parisi, S, Bocci, Eb, Sebastiani, Gd, Fusaro, E, Sebastiani, M, Quartuccio, L, Franceschini, F, Sainaghi, Pp, Orsolini, G, De Angelis, R, Danielli, Mg, Venerito, V, Grignaschi, S, Giollo, A, Alluno, A, Ioannone, F, Fornaro, M, Traboco, Ls, Wibowo, Sak, Loarce-Martos, J, Prieto-Gonzalez, S, Gonzalez, Ra, Yoshida, A, Nakashima, R, Sato, S, Kimura, N, Kaneko, Y, Gono, T, Tomaras, S, Proft, Fn, Holzer, Mt, Gromova, Ma, Aharonov, O, Griger, Z, Hmamouchi, I, El Bouchti, I, Baba, Z, Giannini, M, Maurier, F, Campagne, J, Meyer, A, Langguth, D, Limaye, V, Needham, M, Srivastav, N, Hudson, M, Landon-Cardinal, O, Zuleta, Wgr, Arbelaez, A, Cajas, J, Silva, Jap, Fonseca, Je, Zimba, O, Bohdana, D, Ima-Edomwonyi, U, Dedeke, I, Airenakho, E, Madu, Nh, Yerima, A, Olaosebikan, H, Becky, A, Koussougbo, Od, Palalane, E, So, H, Ugarte-Gil, Mf, Chinchay, L, Bernaola, Jp, Pimentel, V, Fathi, Hm, Mohammed, Rha, Harifi, G, Fuentes-Silva, Y, Cabriza, K, Losanto, J, Colaman, N, Cachafeiro-Vilar, A, Bautista, Gg, Ejg, Ho, Gonzalez, R, Nunez, Ls, Vergara, Mc, Baez, Jt, Alonzo, H, Pastelin, Cbs, Salinas, Rg, Obiols, Aq, Chavez, N, Ordonez, Ab, Argueta, S, Llerena, Gar, Sierra-Zorita, R, Arrieta, D, Hidalgo, Er, Saenz, R, Escalante, Mi, Morales, R, Calapaqui, W, Quezada, I, Arredondo, G, Aggarwal, R, and Gupta, L
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Rheumatology ,idiopathic inflammatory myopathies ,COVID-19 vaccines ,vaccine hesitancy ,registries ,Pharmacology (medical) ,autoimmune disease - Abstract
ObjectiveCOVID-19 vaccines have a favorable safety profile in patients with autoimmune rheumatic diseases (AIRDs) such as idiopathic inflammatory myopathies (IIMs); however, hesitancy continues to persist among these patients. Therefore, we studied the prevalence, predictors and reasons for hesitancy in patients with IIMs, other AIRDs, non-rheumatic autoimmune diseases (nrAIDs) and healthy controls (HCs), using data from the two international COVID-19 Vaccination in Autoimmune Diseases (COVAD) e-surveys.MethodsThe first and second COVAD patient self-reported e-surveys were circulated from March to December 2021, and February to June 2022 (ongoing). We collected data on demographics, comorbidities, COVID-19 infection and vaccination history, reasons for hesitancy, and patient reported outcomes. Predictors of hesitancy were analysed using regression models in different groups.ResultsWe analysed data from 18 882 (COVAD-1) and 7666 (COVAD-2) respondents. Reassuringly, hesitancy decreased from 2021 (16.5%) to 2022 (5.1%) (OR: 0.26; 95% CI: 0.24, 0.30, P ConclusionVaccine hesitancy has decreased from 2021 to 2022, long-term safety concerns remain among patients with IIMs, particularly in Caucasians and those with poor physical function.
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- 2023
49. Flares in IIMs and the timeline following COVID-19 vaccination: a combined analysis of the COVAD-1 and -2 surveys.
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R N, Sen P, Griger Z, Day J, Joshi M, Nune A, Nikiphorou E, Saha S, Tan AL, Shinjo SK, Ziade N, Velikova T, Milchert M, Jagtap K, Parodis I, Gracia-Ramos AE, Cavagna L, Kuwana M, Knitza J, Chen YM, Makol A, Agarwal V, Patel A, Pauling JD, Wincup C, Barman B, Zamora Tehozol EA, Rojas Serrano J, García-De La Torre I, Colunga-Pedraza IJ, Merayo-Chalico J, Chibuzo OC, Katchamart W, Akarawatcharangura Goo P, Shumnalieva R, Hoff LS, El Kibbi L, Halabi H, Vaidya B, Shaharir SS, Hasan ATMT, Dey D, Toro Gutiérrez CE, Caballero-Uribe CV, Lilleker JB, Salim B, Gheita T, Chatterjee T, Distler O, Saavedra MA, Chinoy H, Agarwal V, Aggarwal R, and Gupta L
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- Female, Humans, Male, Middle Aged, Surveys and Questionnaires, Vaccination adverse effects, Disease Progression, Autoimmune Diseases physiopathology, COVID-19 prevention & control, COVID-19 Vaccines adverse effects, Myositis physiopathology, Rheumatic Diseases physiopathology
- Abstract
Objectives: Disease flares in the post-coronavirus disease 2019 (COVID-19) vaccination period represent a prominent concern, though risk factors are poorly understood. We studied these flares among patients with idiopathic inflammatory myopathies (IIMs) and other autoimmune rheumatic diseases (AIRDs)., Methods: The COVAD-1 and -2 global surveys were circulated in early 2021 and 2022, respectively, and we captured demographics, comorbidities, AIRDs details, COVID-19 infection history and vaccination details. Flares of IIMs were defined as (a) patient self-reported, (b) immunosuppression (IS) denoted, (c) clinical sign directed and (d) with >7.9-point minimal clinically significant improvement difference worsening of Patient-Reported Outcomes Measurement Information System (PROMIS) PROMISPF10a score. Risk factors of flares were analysed using regression models., Results: Of 15 165 total respondents, 1278 IIMs (age 63 years, 70.3% female, 80.8% Caucasians) and 3453 AIRDs were included. Flares of IIM were seen in 9.6%, 12.7%, 8.7% and 19.6% patients by definitions (a) to (d), respectively, with a median time to flare of 71.5 (10.7-235) days, similar to AIRDs. Patients with active IIMs pre-vaccination (OR 1.2; 95% CI 1.03, 1.6, P = 0.025) were prone to flares, while those receiving rituximab (OR 0.3; 95% CI 0.1, 0.7, P = 0.010) and AZA (OR 0.3, 95% CI 0.1, 0.8, P = 0.016) were at lower risk. Female gender and comorbidities predisposed to flares requiring changes in IS. Asthma (OR 1.62; 95% CI 1.05, 2.50, P = 0.028) and higher pain visual analogue score (OR 1.19; 95% CI 1.11, 1.27, P < 0.001) were associated with disparity between self-reported and IS-denoted flares., Conclusion: A diagnosis of IIMs confers an equal risk of flares in the post-COVID-19 vaccination period to AIRDs, with active disease, female gender and comorbidities conferring a higher risk. Disparity between patient- and physician-reported outcomes represents a future avenue for exploration., (© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
- Published
- 2024
- Full Text
- View/download PDF
50. Correlates of breakthrough COVID-19 in vaccinated patients with systemic sclerosis: survival analysis from a multicentre international patient-reported survey.
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Ahmed S, Gupta L, Kuwana M, Pauling JD, Day J, Ravichandran N, Joshi M, Parodis I, Sen P, Jagtap K, Nikiphorou E, Saha S, Agarwal V, Chatterjee T, Lilleker JB, Kardes S, Milchert M, Gheita T, Salim B, Velikova T, Gracia-Ramos AE, Tan AL, Nune A, Cavagna L, Saavedra MA, Shinjo SK, Ziade N, Knitza J, Distler O, Wibowo SAK, Chinoy H, Aggarwal R, Agarwal V, and Makol A
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- Humans, Cross-Sectional Studies, Survival Analysis, Surveys and Questionnaires, Patient Reported Outcome Measures, COVID-19 epidemiology, COVID-19 prevention & control, COVID-19 complications, Rheumatic Diseases complications, Scleroderma, Systemic complications
- Abstract
This study aimed to assess the incidence, predictors, and outcomes of breakthrough infection (BI) following coronavirus disease (COVID-19) vaccination in patients with systemic sclerosis (SSc), a risk group associated with an immune-suppressed state and high cardiopulmonary disease burden. Cross-sectional data from fully vaccinated respondents with SSc, non-SSc autoimmune rheumatic diseases (AIRDs), and healthy controls (HCs) were extracted from the COVAD database, an international self-reported online survey. BI was defined according to the Centre for Disease Control definition. Infection-free survival was compared between the groups using Kaplan-Meier curves with log-rank tests. Cox proportional regression was used to assess the association between BI and age, sex, ethnicity, and immunosuppressive drugs at the time of vaccination. The severity of BI in terms of hospitalization and requirement for oxygen supplementation was compared between groups. Of 10,900 respondents, 6836 fulfilled the following inclusion criteria: 427 SSc, 2934 other AIRDs, and 3475 HCs. BI were reported in 6.3% of SSc, 6.9% of non-SSc AIRD, and 16.1% of HCs during a median follow-up of 100 (IQR: 60-137) days. SSc had a lower risk for BI than HC [hazard ratio (HR): 0.56 (95% CI 0.46-0.74)]. BIs were associated with age [HR: 0.98 (0.97-0.98)] but not ethnicity or immunosuppressive drugs at the time of vaccination. Patients with SSc were more likely to have asymptomatic COVID-19, but symptomatic patients reported more breathlessness. Hospitalization [SSc: 4 (14.8%), HCs: 37 (6.6%), non-SSc AIRDs: 32(15.8%)] and the need for oxygenation [SSc: 1 (25%); HC: 17 (45.9%); non-SSc AIRD: 13 (40.6%)] were similar between the groups. The incidence of BI in SSc was lower than that in HCs but comparable to that in non-SSc AIRDs. The severity of BI did not differ between the groups. Advancing age, but not ethnicity or immunosuppressive medication use, was associated with BIs., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
- Full Text
- View/download PDF
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