ABSTRACT BACKGROUND AND OBJECTIVES: The barriers of scientific knowledge and adequate training can influence the skills of health professionals in the management of chronic pain in non-specialized environments. The aim of this study was to assess the beliefs and attitudes of the Brazilian public health care system's (Sistema Único de Saúde - SUS) professionals who work in the care of patients with chronic pain in the clinical routine. METHODS: This is a cross-sectional study carried out with non-specialized pain professionals from primary and medium-complexity care, assessed by the Inventory of Attitudes towards Pain. Participants were grouped by place of work and length of training for comparison analysis using the t-test for independent samples. Effect sizes were calculated (η² generalized), and the level of statistical significance was set at p<0.05. RESULTS: Seventy health professionals took part in this study. They presented undesirable beliefs about curing pain and caring behaviors. They also had desirable beliefs about the influence of emotions, the relationship between pain and tissue damage and the possibility of control by those who feel it. An effect of place of practice was also observed, with undesirable beliefs among primary care professionals about pain-related disability, and also an effect on length of training for the control domain, with less desirable beliefs among those with less than ten years of training. CONCLUSION: The undesirable beliefs presented by the health professionals allow for a situational diagnosis that indicates the need for continuing education in chronic pain in order to implement training with evidence-based practices in the SUS care routine. OBJECTIVES nonspecialized non specialized environments systems system s Sistema routine METHODS crosssectional cross sectional mediumcomplexity medium complexity Pain ttest t test samples η² η (η generalized, generalized , generalized) p005 p 0 05 p<0.05 RESULTS behaviors emotions it observed painrelated related disability domain CONCLUSION evidencebased evidence based p00 p<0.0 p0 p<0. p<0 p<

RESUMO JUSTIFICATIVA E OBJETIVOS: As barreiras do conhecimento científico e do treinamento adequado podem influenciar as competências dos profissionais de saúde no manejo da dor crônica em ambientes não especializados. O objetivo deste estudo foi avaliar as crenças e atitudes de profissionais do Sistema Único de Saúde (SUS) que atuam no cuidado de pacientes com dor crônica na rotina clínica. MÉTODOS: Trata-se de estudo transversal realizado com profissionais não especialistas em dor da atenção primária e média complexidade, avaliados pelo Inventário de Atitudes frente à dor. Os participantes foram agrupados por local de atuação e tempo de formação para a análise de comparação através do teste t para amostras independentes. Foram calculados os tamanhos de efeito (η² generalizado) e o nível de significância estatística foi definido em p<0,05. RESULTADOS: Participaram deste estudo 70 profissionais de saúde, que apresentaram crenças indesejáveis a respeito da cura da dor e de comportamentos de solicitude. Esses profissionais também apresentaram crenças desejáveis quanto a influência das emoções, relação da dor com lesão tecidual e possibilidade de controle por quem a sente. Foi observado um efeito do local de atuação, com crenças indesejáveis dos profissionais da atenção primária sobre incapacidade relativa à dor, além de um efeito sobre o tempo de formação para o domínio controle, com crenças menos desejáveis entre aqueles com menos de 10 anos de formação. CONCLUSÃO: As crenças indesejáveis apresentadas pelos profissionais permitem um diagnóstico situacional que indica a necessidade de educação continuada em dor crônica para implementar treinamentos com práticas baseadas em evidências na rotina de cuidado do SUS. OBJETIVOS especializados SUS (SUS clínica MÉTODOS Tratase Trata se complexidade independentes η² η (η generalizado p005 p 0 05 p<0,05 RESULTADOS 7 solicitude emoções sente 1 CONCLUSÃO p00 p<0,0 p0 p<0, p<0 p<

Abstract Sjogren’s disease (SjD) is an autoimmune disease that is characterized not only by the sicca symptoms it causes but also by its systemic nature, which is capable of several and not yet fully understood extraglandular manifestations. To gain a clearer understanding of these manifestations as well as a better practical approach, a panel of experts from the Brazilian Society of Rheumatology conducted a systematic review and meta-analysis on the identification of epidemiologic and clinical features of the extraglandular manifestations present in ESSDAI (EULAR Sjogren´s syndrome disease activity index), followed by a voting panel with recommendations for clinical practice. This publication is complementary to others already published and covers cutaneous and hematological manifestations, with prevalence data generated by a meta-analysis of 13 clinical or laboratory manifestations and 6 clinical management recommendations. Sjogrens Sjogren s SjD (SjD nature approach metaanalysis meta analysis EULAR index, index , index) practice 1

Abstract Introduction The Strengthening and Stretching for Rheumatoid Arthritis of the Hand (SARAH) program is a personalized, progressive 12-week exercise program for people with hand problems due to rheumatoid arthritis (RA). Patients are provided with two guidance documents, the ‘Patient Exercise Booklet’ and the ‘Personal Exercise Guide’, to continue the exercises independently at home. Objective This study aimed to translate and culturally adapt the SARAH protocol into Brazilian Portuguese and validate its content. Methods The guidance documents ‘Patient Exercise Booklet’ and ‘Personal Exercise Guide’ of the SARAH program were translated and culturally adapted to Brazilian Portuguese. The content validity was obtained by calculating the content validity index (CVI). Results The Brazilian version of the SARAH protocol reached semantic, idiomatic, conceptual, and cultural equivalences. The CVI was greater than 0.8, corresponding to a satisfactory index. The verbal comprehension was 4.9, showing good verbal comprehension ofthe target population. Conclusion The Brazilian Portuguese version of the SARAH protocol is available to Brazilian people with compromised hands due to RA with satisfactory content validity. (SARAH personalized 12week week 12 RA. . (RA) Patient Booklet Personal Guide, Guide , home CVI. (CVI) semantic idiomatic conceptual equivalences 08 0 8 0.8 49 4 9 4.9 population 1 (RA (CVI 0. 4.

Abstract Background Diagnosis of SS is a complex task, as no symptom or test is unique to this syndrome. The American-European Consensus Group (AECG 2002) and the American-European classification criteria of 2016 (ACR/EULAR 2016) emerged through a search for consensus. This study aims to assess the prevalence of Sjögren’s Syndrome (SS) in patients with Systemic Lupus Erythematosus (SLE), according to AECG 2002 and ACR-EULAR 2016 classifications, as well as clinical and histopathological features in this overlap. To date, there is no study that has evaluated SS in SLE, using the two current criteria. Methods This cross-sectional study evaluated 237 SLE patients at the outpatient rheumatology clinic between 2016 and 2018. Patients were submitted to a dryness questionnaire, whole unstimulated salivary flow (WUSF), “Ocular Staining Score” (OSS), Schirmer’s test I (ST-I), and labial salivary gland biopsy (LSGB). Results After verifying inclusion and exclusion criteria, a total of 117 patients were evaluated, with predominance of females (94%) and mixed ethnicity (49.6%). The prevalence of SS was 23% according to AECG 2002 and 35% to ACR- EULAR 2016. Kappa agreement between AECG 2002 and ACR-EULAR 2016 were 0.7 (p < 0.0001). After logistic regression, predictors for SS were: anti/Ro (OR = 17.86, p < 0.05), focal lymphocytic sialadenitis (OR = 3.69, p < 0.05), OSS ≥ 5 (OR = 7.50, p < 0.05), ST I positive (OR = 2.67, p < 0.05), and WUSF ≤ 0.1 mL/min (OR = 4.13, p < 0.05). Conclusion The prevalence of SS in SLE was 23% (AECG 2002) and 35% (ACR-EULAR 2016). The presence of glandular dysfunction, focal lymphocytic sialadenitis, and anti/Ro were predictors of SS in SLE. The greatest advantage of the new ACR-EULAR 2016 criteria is to enable an early diagnosis and identify the overlapping of these two diseases. ACR- EULAR 2016 criteria is not yet validated for secondary SS and this study is a pioneer in investigating prevalence based on the new criteria. task syndrome AmericanEuropean American European 201 ACR/EULAR ACREULAR ACR consensus Sjögrens Sjögren s (SS , (SLE) 200 classifications overlap date crosssectional cross sectional 23 2018 questionnaire WUSF, (WUSF) Ocular Score OSS, (OSS) Schirmers Schirmer STI, STI (ST-I) LSGB. LSGB . (LSGB) 11 94% 94 (94% 49.6%. 496 49.6% 49 6 (49.6%) 35 07 0 7 0. 0.0001. 00001 0.0001 0001 0.0001) regression antiRo anti Ro OR 1786 17 86 17.86 0.05, 005 0.05 05 0.05) 369 3 69 3.69 750 50 7.50 267 2 67 2.67 01 1 mLmin mL min 413 4 13 4.13 0.05. dysfunction diseases 20 (SLE (WUSF (OSS (ST-I (LSGB 9 (94 49.6 (49.6% 0000 0.000 000 178 8 17.8 00 0.0 36 3.6 75 7.5 26 2.6 41 4.1 (9 49. (49.6 0.00 17. 3. 7. 2. 4. ( (49. (49 (4

Abstract Sjogren's syndrome (SS) is an autoimmune disease characterized by lymphocytic infiltration of the exocrine glands and other organs, associated with sicca syndrome but also with systemic involvement with varying degrees of severity. Despite their importance, some systemic manifestations, mainly liver, gastrointestinal, and pancreatic are not routinely evaluated. To address these manifestations, the Sjögren's Syndrome Committee of the Brazilian Society of Rheumatology conducted a broad systematic review of the literature on studies investigating prevalence and diagnosis of these symptoms in Sjogren´s patients and made recommendations based on the findings. Agreement between the experts was achieved using the Delphi method. This is the second part of this guideline, providing 6 recommendations for liver, gastrointestinal, and pancreatic care of SS patients.

Abstract Sjogren’s Syndrome (SS) is an autoimmune disease characterized by lymphocytic infiltration of the exocrine glands and other organs, associated with sicca syndrome but also with systemic involvement with varying degrees of severity. Despite their importance, these systemic manifestations are not routinely evaluated and there is no homogenous approach to their diagnosis or evaluation. To close this gap, a panel of experts from the Brazilian Society of Rheumatology conducted a systematic review and meta-analysis on the identification of epidemiologic and clinical features of these manifestations and made recommendations based on the findings. Agreement between the experts was achieved using the Delphi method. The first part of this guideline summarizes the most important topics, and 11 recommendations are provided for the articular, pulmonary, and renal care of SS patients.

Abstract Background: Few studies have evaluated the relation of quality of life (QoL) with symptoms and disease activity in primary Sjögren’s syndrome (pSS). There is also scant information on the predictors of QoL in this population. The aim of this study was to assess QoL in patients with pSS and to investigate their possible predictors. Methods: In a cross-sectional study, 77 patients with pSS were evaluated using the following questionnaires: Functional Assessment of Chronic Illness Therapy Fatigue Subscale (FACIT-Fatigue), EULAR Sjögren’s Syndrome Patient Reported Index (ESSPRI), EULAR Sjögren’s Syndrome Disease Activity Index (ESSDAI), Short Form-36 Health Survey (SF-36) and World Health Organization Quality of Life Assessment (WHOQOL-BREF). Seventy-seven healthy controls responded to the SF-36 and WHOQOL-BREF. The Mann-Whitney test, t-test, Pearson and Spearman correlation, and multiple regression analysis were used in the statistical analysis. Results: Patients with pSS and healthy controls were matched by gender and age. The mean scores for the ESSDAI, ESSPRI and FACIT-Fatigue were 3.34 ±4.61, 6.58 ± 2.29 and 26.17 ± 11.02, respectively. Patients had a lower employment rate (36.4% versus 62.3%, p < 0.01) and higher work disability (10.4% versus 1.3%, p < 0.01). SF-36 and WHOQOL-BREF values were lower in patients with pSS (p < 0.001), except in the WHOQOL-BREF environment domain. Pain (ESSPRI), fatigue (FACIT-Fatigue), antinuclear antibody (ANA), anti-Ro-SSA and economic class (Brazilian Economic Classification Criteria - CCEB) were independent predictors of QoL. Conclusions: The main predictors of poor QoL in patients with pSS were pain and fatigue, and these symptoms had an impact regardless of disease activity, age, schooling, marital status, work disability and fibromyalgia.

Abstract Sjogren’s syndrome (SS) is an autoimmune disease characterized by lymphocytic infiltration of the exocrine glands and other organs. Women with SS often experience gynecological symptoms due to the disease and need extra care regarding their sexual activity, reproductive health and during pregnancy, conditions that are not properly conducted in the clinical practice. To cover this gap, a panel of experts from the Brazilian Society of Rheumatology conducted a systematic review and meta-analysis on the identification of symptoms, diagnosis, monitoring, prognosis, and treatment of these manifestations. A Focus Group meeting was held and included experts in the field and methodologists, based on a previously developed script, with themes related to the objective of the study. The most important topics were summarized and 11 recommendations were provided.

Abstract Background: Primary Sjögren's syndrome (pSS) is a systemic immune-mediated disease whose main characteristic is exocrine gland inflammation and, subsequent reduction in tear and saliva production. A delayed diagnosis is common due to the nonspecific clinical manifestations of disease. The aim of the present study was to develop recommendations for the diagnosis of glandular manifestations of pSS based on evidence and expert opinion. Main body of the abstract: We conducted a systematic literature review to retrieve the best evidence available on the accuracy of diagnostic tests for pSS. We also held two in-person meetings with experts (rheumatologists, pathologists, ophthalmologists and dentists) to establish their level of agreement using the Delphi method. Ultimately, we generated 18 recommendations that aim to facilitate the diagnosis of the glandular manifestations of pSS. Conclusion: The diagnosis of glandular manifestations of pSS is complex and multidisciplinary. It requires specific knowledge in the field of ophthalmology, immunology, pathology and imaging, making it compulsory for the rheumatologist to work with professionals from these different areas in order to improve accuracy and early diagnosis. Glandular dysfunction tests, ANA, RF, Anti-Ro, protein electrophoresis, urinalysis, blood count, C-Reactive protein, complement, testing for syphilis and viruses (HCV, HIV) and SGUS should be investigated when dryness or systemic manifestation are present. Minor salivary gland biopsy is recommended for all anti-Ro negative or incomplete criteria cases.

RESUMOObjetivo:Fazer a adaptação transcultural do Eular Sjögren's Syndrome Patient Reported Index (ESSPRI) para a língua portuguesa e avaliar as suas propriedades psicométricas.Método:Estudo transversal de pacientes com síndrome de Sjögren primária (SS). Foram estudadas as propriedades psicométricas (reprodutibilidade intraobservador e a validade de construto). Na validade de construto, o ESSPRI foi comparado com o Patient's Global Assessment (PaGA), Profile of Fatigue and Discomfort (Profad), Sicca Symptoms Inventory (SSI) e Functional Assessment of Chronic Illness Therapy (Facit-fatigue). Os testes estatísticos usados foram o α-Cronbach, coeficiente de correlação intraclasse (CCI), método de Bland-Altman e coeficiente de Spearman. Foi considerado significativo o p ≤ 0,05.Resultados:Não houve diferença entre as versões nas duas línguas e obteve-se, assim, a versão consensual brasileira. Todos os indivíduos foram mulheres de 49,4 ± 11,6 anos, com início dos sintomas de 7,2 ± 5,4 anos e tempo de diagnóstico de 3 ± 3,3 anos. A média do ESSPRI foi de 6,87 ± 1,97. A reprodutibilidade intraobservador foi alta e significativa (0,911) e, no método de Bland-Altman, não houve viés sistemático na concordância das medidas entre as avaliações. Houve correlação moderada do ESSPRI com todos os instrumentos testados.Conclusão:A versão do ESSPRI em português é válida e reprodutível.

ABSTRACTObjective:To carry out the cross-cultural adaptation of EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI) for Portuguese language and evaluate its psychometric properties.Method:Cross-secal study of patients with primary Sjögren's syndrome (SS). The psychometric properties (intraobserver reproducibility and construct validity) were studied. In construct validity, ESSPRI was compared with the Patient's Global Assessment (PGA), Profile of Fatigue and Discomfort (Profad), Sicca Symptoms Inventory (SSI) and Functional Assessment of Chronic Illness Therapy (Facit-F). Statistical tests used were: Cronbach's alpha, intraclass correlation coefficient (ICC), Bland-Altman method and Spearman coefficient. A value of p ≤ 0.05 was considered significant.Results:There was no difference between versions in both languages; thus, a Brazilian consensual version was obtained. All subjects were women aged 49.4 ± 11.6 years, with onset of symptoms of 7.2 ± 5.4 years, and time of diagnosis of 3.0 ± 3.3 years. The mean ESSPRI was 6.87 ± 1.97. The intraobserver reproducibility was high and significant (0.911) and, with Bland-Altman method, there was no systematic bias in the agreement of measures among evaluations. A moderate correlation of ESSPRI with all tested instruments was observed.Conclusion:The Brazilian Portuguese version of ESSPRI is a valid and reproducible version.

RESUMOAs recomendações propostas pela Comissão de Síndrome de Sjögren da Sociedade Brasileira de Reumatologia para tratamento da síndrome de Sjögren foram baseadas em uma revisão sistemática da literatura nas bases de dados Medline (PubMed) e Cochrane até outubro de 2014 e opinião de especialistas na ausência de artigos sobre o assunto. Foram incluídos 131 artigos classificados de acordo com Oxford & Grade. Essas recomendações foram elaboradas com o objetivo de orientar o manejo adequado e facilitar o acesso aos tratamentos para aqueles pacientes com adequada indicação de recebê-los, considerando o contexto socioeconômico brasileiro e os medicamentos disponíveis no país.

ABSTRACTThe recommendations proposed by the Sjögren's Syndrome Committee of the Brazilian Society of Rheumatology for the treatment of Sjögren's syndrome were based on a systematic review of literature in Medline (PubMed) and the Cochrane databases until October 2014 and on expert opinion in the absence of studies on the subject. 131 articles classified according to Oxford & Grade were included. These recommendations were developed in order to guide the management and facilitate the access to treatment for those patients with an appropriate indication, considering the Brazilian socioeconomic context and pharmacological agents available in this country.

Objetivo: Fazer a adaptação transcultural e a validação do Profile of Fatigue and Discomfort – Sicca Symptoms Inventory (short form) (Profad-SSI-SF), questionário que avalia os aspectos subjetivos dos sintomas da síndrome de Sjögren primária (SSp), para a língua portuguesa brasileira. Método: Foi avaliada a equivalência conceitual, de item, semântica e operacional. A versão brasileira do Profad-SSI-SF foi aplicada a 62 mulheres com SSp conforme consenso europeu-americano de 2002 para avaliar a equivalência de mensuração. Foi usado o α-Cronbach para consistência interna; coeficiente de correlação intraclasse (ICC) para reprodutibilidade intraobservador; e coeficiente de correlação de Spearman para validade em comparação com o Patient Global Assessment (PaGA), Eular Sjögren’s Syndrome Patient Reported Index (ESS-PRI), Functional Assessment of Chronic Illness Therapy Fatigue Subscale (Facit-F) e EuroQOL(EQ-5D). Resultados: A consistência interna do Profad, do SSI e da pontuação total foi de 0,80, 0,78 e 0,87, respectivamente. A reprodutibilidade intraobservador do Profad total foi de 0,89; do SSI total de 0,86 e da pontuação total de 0,89. Na validade, o Profad apresentou correlação significativa com o PaGA (r = 0,50), Facit-F (r = 0,59), Esspri (r = 0,58) e todos os domínios do EQ-5D, com exceção da mobilidade. Já o SSI apresentou correlação significativa com o PaGA (r = 0,43), Facit-F (r = 0,57), Esspri (r = 0,55) e a maioria dos domínios do EQ-5D. A pontuação total do Profad-SSI-SF só não obteve correlação estatisticamente significante com o domínio mobilidade e escala 1 a 100 do EQ-D5.

Objective: To perform a cross-cultural adaptation and validation of the Profile of Fatigue and Discomfort – Sicca Symptoms Inventory (short form) (PROFAD-SSI-SF) questionnaire assessing the subjective aspects of the symptoms of primary Sjögren syndrome (pSS), for the Brazilian Portuguese language. Method: Conceptual, of the item, semantic and operational equivalences were evaluated. The Brazilian version of PROFAD-SSI-SF was administered to 62 women with pSS according to the European-American consensus 2002 to assess measurement equivalence. α-Cronbach was used for internal consistency; intraclass correlation coefficient (ICC) for intraobserver reproducibility; and Spearman correlation coefficient for validity by comparing with Patient Global Assessment (PaGA), EULAR Sjögren’s Syndrome Patient Reported Index (ESSPRI), Functional Assessment of Chronic Illness Therapy Fatigue Subscale (FACIT-F) and EuroQOL(EQ-5D). Results: The internal consistency of PROFAD, SSI and total score was 0.80; 0.78; and 0.87, respectively. The intraobserver reproducibility of total PROFAD was 0.89; of total SSI was 0.86; and total score was 0.89. In terms of validity, PROFAD correlated significantly with PaGA (r = 0.50), FACIT-F (r = 0.59), ESSPRI (r = 0.58) and all domains of EQ-5D, with the exception of Mobility. On the other hand, SSI correlated significantly with PaGA (r = 0.43), FACIT-F (r = 0.57), ESSPRI (r = 0.55) and most domains of EQ-5D. The total score of PROFAD-SSI-SF had a nonstatistically significant correlation only with Mobility domain and with 1–100 range of EQ-5D.

INTRODUÇÃO: O EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) é um índice de atividade sistêmica da síndrome de Sjögren primária (SSP). OBJETIVO: Realizar a adaptação transcultural do ESSDAI para a língua portuguesa. MÉTODO: Estudo transversal com 62 pacientes com SSP de acordo com consenso europeu-americano de 2002. Foram realizadas seis etapas: equivalência conceitual, de item, semântica, operacional, funcional e de mensuração (reprodutibilidade interobservador e a validade de constructo). Para a validade, o ESSDAI foi comparado com a avaliação global do médico (PhGA), o Sjögren's Syndrome Disease Activity Index (SSDAI) e o Sjögren's Systemic Clinical Activity Index (SCAI). Os pacientes foram classificados por um médico especialista conforme a atividade da doença em dois grupos, "ativo" e "inativo", e conforme a intenção de tratar nos grupos "aumento de terapia" e "sem aumento de terapia". O ESSDAI foi testado nesses grupos. Utilizou-se os testes estatísticos: coeficiente de correlação intraclasse (CCI) e método de Bland Altman para a reprodutibilidade; e coeficiente de Spearman (r s) e teste de Mann-Whitney para a validade (P < 0,05 e IC 95%). RESULTADOS: A média do ESSDAI foi de 4,95 ± 6,73. A reprodutibilidade obteve um forte CCI de 0,89 e boa concordância. Na comparação com outros índices, apresentou forte coeficiente de Spearman com o PhGA (r s = 0,83; P < 0,000), moderado com o SSDAI (r s = 0,658 ; P < 0,000) e fraco com o SCAI (r s = 0,411; P = 0,001). O grupo "ativo" e o grupo "com aumento de terapia" obtiveram maiores valores de ESSDAI (P = 0,000). CONCLUSÃO: a versão em português do ESSDAI mostrou ser adaptável, reprodutível e válida para a língua portuguesa.

INTRODUCTION: The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) is an index of primary Sjögren's syndrome (PSS) systemic activity. OBJECTIVE: To perform the ESSDAI transcultural adaptation into Brazilian Portuguese. METHOD: This was a cross-sectional study with 62 patients with PSS according to the criteria of the 2002 American-European Consensus. Six stages were conducted: conceptual, item, semantic, operational, functional, and measurement equivalences (interobserver reproducibility and construct validity). For the validity assessment, the ESSDAI was compared with the Physician's Global Assessment (PhGA), the Sjögren's Syndrome Disease Activity Index (SSDAI), and the Sjögren's Systemic Clinical Activity Index (SCAI). Patients were classified by a specialist physician into two groups according to disease activity (active and inactive), and according to the intention-to-treat (increase in therapy and no increase in therapy). The ESSDAI was tested in these groups. The following statistical tests were used: intraclass correlation coefficient (ICC), Bland-Altman plot for reproducibility, and Spearman's correlation coefficient (r s) and Mann-Whitney's test for validity (P < 0.05 and 95% CI). RESULTS: The mean ESSDAI score was 4.95 ± 6.73. The reproducibility obtained a strong ICC of 0.89 and good agreement. When compared with other indices, it showed a strong r s with PhGA (0.83; P < 0.000), a moderate r s with SSDAI (0.658; P < 0.000) and a weak r s with the SCAI (0.411; P = 0.001). The group "active" and the group " increase in therapy" had higher ESSDAI values (P = 0.000). CONCLUSION: The Brazilian Portuguese version of ESSDAI was shown to be adaptable, reproducible, and valid for this language.

OBJETIVO: correlacionar o instrumento de avaliação de qualidade de vida específico para osteoporose, o Osteoporosis Assessment Questionnaire (OPAQ), com o instrumento genérico, o The Medical Outcomes Study 36 - Item Short Form Health Survery (SF-36). PACIENTES E MÉTODOS: estudo observacional de corte transversal que incluiu 40 mulheres acima de 60 anos, diagnosticadas com osteoporose. Houve um momento para avaliação e um único examinador. Para a análise estatística foram utilizados coeficiente correlação de Pearson e análise fatorial do OPAQ. RESUTADOS: houve correlação entre os domínios e componentes finais do SF-36 com os domínios do OPAQ. Evidenciou-se que os coeficientes mais altos foram entre o OPAQ Sintomas e os seguintes domínios do SF-36: dor (r=-0,6), aspectos sociais (r=-0,6%) e saúde mental (r=-0,5). Quase todos os aspectos do SF-36 se correlacionaram com o OPAQ Sintomas. E, ainda, por análise fatorial do OPAQ, observa-se que os seus 18 componentes representaram 63% de carga fatorial, ou seja, eles explicaram o valor total de impacto da osteoporose na qualidade de vida e agruparam-se em cinco fatores: fator 1 (mobilidade, cuidados próprios, independência e trabalho doméstico), fator 2 (flexibilidade, movimentação e sono), fator 3 (dor nas costas, dor relacionada à osteoporose, fadiga e humor), fator 4 (medo de cair, atividades sociais, apoio familiar e tensão) e fator 5 (andar-inclinar, imagem corporal e trabalho). CONCLUSÃO: foi encontrada a correlação esperada entre SF-36 e OPAQ, que é um instrumento de avaliação específico com capacidade para avaliar aspectos específicos e gerais da qualidade de vida nesta população.

OBJECTIVE: to correlate the quality of life assessment instrument, specific to osteoporosis, OPAQ (Osteoporosis Assessment Questionnaire), with the generic instrument SF-36 (Item Short Form Health Survey). PATIENTS AND METHODS: the cross sectional observational study included 40 female patients older than 60 years with osteoporosis. A single assessment was always conducted by the same evaluator. For the statistics analisys the Pearson’s coefficient and the factor analysis to OPAQ were used. RESULTS: there was a correlation between the domains and final components of SF-36 with the domains of OPAQ. The higher coefficients were between the OPAQ Symptoms and some domains of SF-36: pain (r=-0,6), social aspects (r=-0,6) and mental health (r=-0,5). Almost every aspect of SF-36 was correlated with the OPAQ Symptoms. By factor analysis of OPAQ it was observed that the 18 components of OPAQ represented 63% of factor load, and they explained the total account of osteoporosis’s impact in the quality of life and were grouped in five factors: factor 1 (mobility, self-care, independence and household tasks), factor 2 (flexibility, transfers and sleep), factor 3 (backache, pain related to osteoporosis, fatigue and mood), factor 4 (fear of fall, social activity, family support and tension) and factor 5 (walking and bending, body image and work). CONCLUSION: the expected correlation was achieved between SF-36 and OPAQ, wich is a specific assessment instrument capable of assessing particular and general aspects of the quality of life in patients with osteoporosis.