1. Efficacy and tolerability of abatacept treatment: results of 12 months observation
- Author
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E L Luchihina, M A Borisova, Nasonov El, S V Glukhova, Ya A Sigidin, Dmitry Karateev, Galina Lukina, and E. S. Aronova
- Subjects
musculoskeletal diseases ,rheumatoid arthritis ,History ,medicine.medical_specialty ,abatacept ,“biologic-naive” pts ,Endocrinology, Diabetes and Metabolism ,retention rate ,Population ,lcsh:Medicine ,Arthritis, Rheumatoid ,Internal medicine ,medicine ,Humans ,biologics ,Adverse effect ,education ,skin and connective tissue diseases ,education.field_of_study ,Biological Products ,Intention-to-treat analysis ,business.industry ,Abatacept ,lcsh:R ,General Medicine ,Retention rate ,Middle Aged ,medicine.disease ,Methotrexate ,Treatment Outcome ,Tolerability ,Rheumatoid arthritis ,Antirheumatic Agents ,Female ,Family Practice ,business ,medicine.drug - Abstract
Objectives: This article reports 1-year clinical outcomes of patients with rheumatoid arthritis (RA) receiving abatacept (ABA) therapy. Materials and methods: Patients (n=91) with high RA activity (DAS28 = 5.1 ± 1.0) and an inadequate response on synthetic DMARDs (mainly methotrexate, 70.3%) and biologics (mainly TNF-α inhibitors, 93%) were included in the study. The majority of patients were middle-aged (49 ± 13.5) womens, RF (72.5%) and ACPA (77%) positive, with moderate functional impairment - HAQ = 1.4 (0.9-2). ABA were administered IV, 10 mg/kg according to the standard scheme. The evaluation of the effectiveness of the therapy was carried out according to the EULAR / ACR 2011 criteria using SDAI, CDAI, HAQ and the intention to treat approach. Results: ABA led to a significant (p
- Published
- 2018