rheumatological diseases
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Acta Medica ◽  
2021 ◽  
pp. 1-8
Author(s):  
Berkan Armağan ◽  
Bayram Farisoğulları ◽  
Hakan Oral ◽  
Levent Kılıç ◽  
Şule Apraş Bilgen ◽  
...  

Objective: Intravenous immunoglobulin is an alternative therapeutic agent that can be used off-label in many autoimmune rheumatological diseases. The aim of this study is to evaluate the autoimmune rheumatological diseases characteristics in which intravenous immunoglobulin therapy is used and the efficacy and safety of this therapy. Methods and Methods: We performed a retrospective review of 133 patients with autoimmune rheumatological disease who received at least 1 course of intravenous immunoglobulin treatment at Hacettepe University Rheumatology Outpatient Clinic between January 2013 and December 2020. The autoimmune rheumatological disease demographic and clinical features, organ involvements, treatment phases (primary-secondary or infection), treatment responses and adverse effects were evaluated. Results: A total of 79% (n=105) patients were female and the mean±SD age was 45.5±16.9 years. The most common underlying rheumatic diseases were systemic lupus erythematosus (35%, n=47) and dermatomyositis/polymyositis (35%, n=47). Intravenous immunoglobulin therapy was most commonly used for resistant/relapsed myositis and haematological involvement. The median (IQR) intravenous immunoglobulin treatment course was 6.5 (13) and the duration of intravenous immunoglobulin treatment was 10.8 (24) months. Although it is used as second-line therapy in 77% of patients, complete clinical response was observed in 32% and partial response in 47%. There was a significant reduction in the median (IQR) steroid doses (methylprednisolone or equivalent dose) patients received from baseline after intravenous immunoglobulin treatment [30 (33) vs 8 (12), p<0.0001]. It was observed that the use of conventional disease-modifying antirheumatic drugs decreased after intravenous immunoglobulin treatment and the use of rituximab increased. Adverse effects associated with intravenous immunoglobulin treatment (10%) and discontinuation (4%) were found to be very low. Conclusion: Intravenous immunoglobulin treatment was commonly given in systemic lupus erythematosus and dermatomyositis/polymyositis patients because of hematological involvement and resistant/relapsed myositis in our study, respectively. Although it is mainly the second-line treatment, two-thirds of the patients achieved a complete/partial response. Side effects and related discontinuation due to intravenous immunoglobulin treatment are very few.


Author(s):  
Daniela Juárez-Melchor ◽  
Pamela Munguía-Realpozo ◽  
Claudia Mendoza-Pinto ◽  
Ivet Etchegaray-Morales ◽  
Jorge Ayón-Aguilar ◽  
...  

2021 ◽  
pp. 483-512
Author(s):  
Nilson Ramires de Jesús ◽  
Marcela Ignacchiti Lacerda ◽  
Flavia Cunha dos Santos ◽  
Roger Abramino Levy ◽  
Guilherme Ramires de Jesús

2021 ◽  
Vol 21 (02) ◽  
pp. 70-77
Author(s):  
Chloe Kwong Yee Cheung ◽  
Mandy Oi Man Wong ◽  
Carmen Kar Mun Chan ◽  
Ho Yin Chung

Uveitis is the most common ophthalmological disorder in the field of rheumatology, accounting for a significant proportion of visual morbidity, both locally and internationally. Causative factors can be divided into infectious and noninfectious etiologies. The diagnosis of uveitis is a major challenge due to heterogeneity in presentation. The disease course may be acute monophasic, recurrent, or chronic relapsing. Complications include posterior synechiae, secondary cataract, ocular hypertension or glaucoma, macular edema, retinal vascular occlusion, epiretinal membrane, and so on, and ultimately visual loss. Antimicrobial therapy is indicated for infection, whereas noninfectious uveitis warrants a combination of steroids, immunosuppressives, and anti-inflammatory agents. With the advancement of biologics, treatment strategies in chronic, noninfectious uveitis have had multiple breakthroughs, particularly in treatment-resistant cases. This article provides a review of the diagnostic approach to uveitis based on symptomatology and ophthalmological findings, and discussion of relevant treatment modalities and strategies.


Author(s):  
I. V. Fridman ◽  
N. A. Lyubimova ◽  
M. M. Kostik ◽  
S. M. Kharit ◽  
Yu. E. Konstantinova

Background. Vaccination is the most effective method for reducing morbidity, disability, mortality from of various infections. However, there was a view for a long time that vaccines are ineffective and unsafe to use in people with rheumatological diseases, including juvenile idiopathic arthritis (JIA). Objective.The aim of the study is to analyze literature data on safety and efficacy of vaccination for JIA patients with live and non-live vaccines.Methods: literature analysis was based on data from medical databases PubMed and Google Scholar.Results. Both live and non-live vaccines are safe and immunogenic enough for children with JIA. Most studies confirm vaccination efficacy in patients with JIA when using glucocorticosteroids (GCS) and methotrexate, while therapy with disease-modifying antirheumatic drugs (DMARD) can reduce antibody titers over time. In general, antibodies levels preservation in previously vaccinated children with JIA is less than in global population. This indicates the need to administer booster doses for such patients. No adverse effects on the course of primary disease after vaccination and no post-vaccine complications were revealed.Conclusion. Vaccination of patients with JIA should be performed with reference to the therapy that the patient already receives, under the control of antibodies level. Booster doses should be implemented in case of titers decrease below the protective levels.


2021 ◽  
Author(s):  
Masaaki Mori ◽  
Shinji Akioka ◽  
Toru Igarashi ◽  
Yuzaburo Inoue ◽  
Hiroaki Umebayashi ◽  
...  

ABSTRACT Issues related to transitioning from paediatric to adult healthcare are currently receiving international attention. In Japan, 1000 patients with childhood-onset chronic rheumatological diseases reach adulthood every year and require transition from care by paediatric to care by adult rheumatologists. Here, we propose a guide for the latter, wherein the adult caregiver poses the clinical questions about transitional support that they need to have answered, and the paediatric caregiver mainly compiles the plans for the transition. To formulate the guide, we sought comments from both the Japan College of Rheumatology and the Pediatric Rheumatology Association of Japan and obtained their approval. Here, we present the outcome of this consultation in the form of a Guide for Supporting Transitional Care, aiming to provide essential knowledge to physicians in the fields of adult internal medicine and orthopaedics who may be involved in treating patients with rheumatic disease during the transition from paediatric to adult care. The features of transitional support that are common for patients with various different rheumatic diseases are presented in this guide, with the aim of informing policy and strategies to deliver optimal outcomes in transitional care by non-paediatric rheumatologists.


Author(s):  
Haitov Abdulaziz Haydar O'g'li ◽  

This literature review describes an analysis of the epidemic process associated with COVID-19 and presents possible scenarios. The most common anamnestic findings, symptoms of infection, clinical presentation, and possible complications are described in sufficient detail. The features of the course of COVID-19 in risk groups and algorithms of administrative and medical actions, which should form the basis of medical care for patients with cardiovascular, oncological, rheumatological diseases, pregnant women, etc., are highlighted.


Author(s):  
Pelin Asfuroglu ◽  
Tugba Sismanlar Eyuboglu ◽  
Ayse Tana Aslan ◽  
Sevcan Bakkaloğlu Ezgu ◽  
Oguz Soylemezoglu

2021 ◽  
Author(s):  
Irvin J. Huang ◽  
Jenna L. Thomason ◽  
Alison M. Bays

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