| Literature DB >> 22472929 |
João Eurico Fonseca1, Miguel Bernardes, Helena Canhão, Maria José Santos, Alberto Quintal, Armando Malcata, Adriano Neto, Ana Cordeiro, Ana Rodrigues, Ana Filipa Mourão, Ana Sofia Ribeiro, Ana Rita Cravo, Anabela Barcelos, Anabela Cardoso, António Vilar, Arecili Braña, Augusto Faustino, Candida Silva, Cátia Duarte, Domingos Araújo, Dolores Nour, Elsa Sousa, Eugénia Simões, Fátima Godinho, Filipe Brandão, Francisco Ventura, Graça Sequeira, Guilherme Figueiredo, Inês Cunha, J Alves Matos, Jaime Branco, João Ramos, José António Costa, José António Gomes, José Pinto, José Canas Silva, J A Silva, José Vaz Patto, Lúcia Costa, Luís Cunha Miranda, Luís Inês, Luís Maurício Santos, Margarida Cruz, Maria João Salvador, Maria Júlia Ferreira, Maria Rial, Mário Viana Queiroz, Mónica Bogas, Paula Araújo, Paulo Reis, Pedro Abreu, Pedro Machado, Patrícia Pinto, Rui André, Rui Melo, Sandra Garcês, Sara Cortes, Sérgio Alcino, Sofia Ramiro, Susana Capela.
Abstract
The authors present the revised version of the Portuguese Society of Rheumatology (SPR) guidelines for the treatment of Rheumatoid Arthritis (RA) with biological therapies. In these guidelines the criteria for introduction and maintenance of biological agents are discussed as well as the contraindications and procedures in the case of nonresponders. Biological treatment (with a tumour necrosis factor antagonist, abatacept or tocilizumab) should be considered in RA patients with a disease activity score 28 (DAS 28) equal to or greater than 3.2 despite treatment with at least 20mg-weekly-dose of methotrexate (MTX) for at least 3 months or, if such treatment is not possible, after 3 months of other conventional disease modifying drug or combination therapy. A DAS 28 score between 2.6 and 3.2 with a significant functional or radiological deterioration under treatment with conventional regimens could also constitute an indication for biological treatment. The treatment goal should be remission or, if that is not achievable, at least a low disease activity, defined by a DAS28 lower than 3.2, without significative functional or radiological worsening. The response criteria, at the end of the first 3 months of treatment, are a decrease of at least 0.6 in the DAS28 score. After 6 months of treatment response criteria is defined as a decrease greater than 1.2 in the DAS28 score. Non-responders, in accordance to the Rheumatologist’s clinical opinion, should try a switch to another biological agent (tumour necrosis factor antagonist, abatacept, rituximab or tocilizumab).Entities:
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Year: 2011 PMID: 22472929
Source DB: PubMed Journal: Acta Reumatol Port ISSN: 0303-464X Impact factor: 1.290