Full Papers
Adherence of Italian rheumatologists to the EULAR recommendations and outcomes in early rheumatoid arthritis patients after starting conventional DMARDs: Methotrexate in Italian patients wiTh Rheumatoid Arthritis (the MITRA study). A cohort study of the I
M. Fornaro1, F. Benaglio2, C. Montecucco3, B. Raffeiner4, M. Di Franco5, C. Iannuccelli6, P. Conigliaro7, C. Lomater8, M. Govoni9, E. Silvagni10, A. Zanetti11, S. Parisi12, G. Carrara13, C.A. Scirè14, R. Caporali15, F. Iannone16
- Rheumatology Unit, Department of Emergency and Organ Transplantation (DETO), University of Bari, Italy.
- Division of Rheumatology, IRCCS Policlinico San Matteo Foundation, University of Pavia, Italy.
- Division of Rheumatology, IRCCS Policlinico San Matteo Foundation, University of Pavia, Italy.
- Rheumatology, Central Hospital of Bolzano, Italy.
- Rheumatology Unit, Dipartimento di Scienze Cliniche, Internistiche, Anestesiologiche e Cardiovascolari, Sapienza University of Rome, AOU Policlinico Umberto I, Rome, Italy.
- Rheumatology Unit, Dipartimento di Scienze Cliniche, Internistiche, Anestesiologiche e Cardiovascolari, Sapienza University of Rome, AOU Policlinico Umberto I, Rome, Italy.
- Rheumatology Unit, Allergology and Clinical Immunology, University of Rome Tor Vergata, Rome, Italy.
- Rheumatology Unit, Mauriziano Hospital, Turin, Italy.
- Rheumatology Unit, Department of Medical Sciences, University of Ferrara and Azienda Ospedaliero-Universitaria di Ferrara, Cona, Italy.
- Rheumatology Unit, Department of Medical Sciences, University of Ferrara and Azienda Ospedaliero-Universitaria di Ferrara, Cona, Italy.
- Epidemiology Unit, Italian Society for Rheumatology (SIR), Milan, and Department of Statistics and Quantitative Methods, Division of Biostatistics, Epidemiology and Public Health, University of Milano-Bicocca, Milan, Italy.
- Epidemiology Unit, Italian Society for Rheumatology (SIR), Milan, and Rheumatology Unit, AOU Città della Salute e della Scienza di Torino, Turin, Italy.
- Epidemiology Unit, Italian Society for Rheumatology (SIR), Milan, Italy.
- Rheumatology Unit, Department of Medical Sciences, University of Ferrara and Azienda Ospedaliero-Universitaria di Ferrara, Cona, and Epidemiology Unit, Italian Society for Rheumatology (SIR), Milan, Italy.
- Division of Clinical Rheumatology, ASST Gaetano Pini-CTO Institute, Milan, and Department of Clinical Sciences and Community Health, Research Center for Adult and Paediatric Rheumatic Diseases, Università degli Studi di Milano, Italy.
- Rheumatology Unit, Department of Emergency and Organ Transplantation (DETO), University of Bari, Italy. florenzo.iannone@uniba.it
CER15009
2022 Vol.40, N°9
PI 1693, PF 1700
Full Papers
PMID: 35084309 [PubMed]
Received: 18/07/2021
Accepted : 18/10/2021
In Press: 12/01/2022
Published: 20/09/2022
Abstract
OBJECTIVES:
The aim of this study was to assess the real-life adherence of Italian rheumatologist to the 2013 EULAR recommendations and treatment outcome in rheumatoid arthritis (RA) patients who started a conventional synthetic disease-modifying anti-rheumatic drug (csDMARD).
METHODS:
The MITRA study is an Italian multicentre observational cohort focused on treatment naïve RA patients with early diagnosis recruited in an 18-month period starting from 2015. The data related to treatment with csDMARDs during the following 12 months follow-up were presented in this paper.
RESULTS:
Two-hundred and fifty-nine RA patients from MITRA cohort who had a follow-up visit and started a csDMARD were included in the prospective analysis. Methotrexate was started as first conventional DMARD in 224 (86.4%) patients. During the first year after starting conventional DMARDs, 175 (67.6%) RA patients reached the pre-specified target, which was DAS28 remission (<2.6) for 112 (43.2%) patients and LDA (<3.2) for 63 (24.3%) patients. Factors that negatively impacted the target achievement were fibromyalgia (HR: 0.2 [0.05–0.81]), HAQ-DI (HR: 0.72 [0.56–0.93]) and ESR (HR: 0.99 [0.99–1]). Globally, 33 (12.7%) patients started a biologic DMARD, while 61 out of 84 (72.6%) patients who had never reached the target remained on conventional DMARD. One-hundred and ninety-three adverse events (AEs) were recorded, the majority classified as mild (91 cases, 51%).
CONCLUSIONS:
A high proportion of RA patients achieved the target during the first-year follow-up. However, a considerable portion of RA patients did not start a biological drug although the target was never reached. AEs remain frequent with conventional DMARDs, but the majority were mild.