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Mena-Vázquez Natalia Jimenez-Núñez Francisco Gabriel Godoy-Navarrete Francisco Javier Manrique-Arija Sara Aguilar-Hurtado María Carmen Romero-Barco Carmen María Ureña-Garnica Inmaculada Espildora F. Padin-Martín María Isabel Fernández-Nebro Antonio 《Clinical rheumatology》2021,40(6):2377-2385
Clinical Rheumatology - To analyze the diagnostic utility of lung ultrasound (US) to detect interstitial lung disease (ILD) in rheumatoid arthritis (RA) patients comparing with high-resolution... 相似文献
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Pilar Espiño-Lorenzo Sara Manrique-Arija Inmaculada Ureña Francisco Gabriel Jiménez-Núñez María López-Lasanta Carmen María Romero-Barco María Angeles Belmonte-López María Victoria Irigoyen Antonio Fernández-Nebro 《Reumatología clinica》2013,9(1):18-23
AimTo determine whether rheumatoid arthritis (RA) patients who have been prescribed biological agents exhibit a different comorbidity burden than RA patients who take disease-modifying antirheumatic drugs (DMARDs) alone, and to understand the association between comorbidity and other variables, as well as the association between comorbidity and multimorbidity.MethodsThis observational case–control study included 114 RA patients treated with biological agents and a control group comprising 163 sex- and age-matched RA patients treated with DMARDs only. Current and previous data regarding the patients’ disease activity, comorbidities, and treatments were collected. The data were analysed using bivariate and multivariate regression models.ResultsThe patients who were prescribed biological agents exhibited poorer disease control, received more DMARDs and steroids, and underwent more total joint arthroplasties compared with the patients in the control group. However, the risk factors for cardiovascular disease and the comorbidity frequency were similar between cases and controls. The most prevalent comorbidities were hypertension, obesity, and respiratory, thyroid, and upper gastrointestinal disorders. The incidence of cardiovascular disease was low, and only 29% of the patients exhibited multimorbidities. A bivariate association of age, late diagnosis, joint replacements and a high score on the health assessment questionnaire score (HAQ) with comorbidity was observed. There were also correlations between the Charlson index and age, joint reconstructive surgery, disease activity (DAS28), and HAQ score. However, when binary logarithmic regression models were applied, only patient age remained significantly associated with comorbidity and multimorbidity [hazard ratio, 1.08; 95% confidence interval, 1.05–1.12; p < 0.0005].ConclusionRA patients taking biological drugs have a comorbidity burden equivalent to those treated with DMARDs alone. Age is the main predictive factor of comorbidity in these patients. 相似文献
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Mena-Vázquez Natalia Godoy-Navarrete Francisco Javier Manrique-Arija Sara Aguilar-Hurtado María Carmen Romero-Barco Carmen María Ureña-Garnica Inmaculada Espildora F Añón-Oñate Isabel Pérez-Albaladejo Lorena Gomez-Cano Carmen Jimenez-Núñez Francisco Gabriel Padin-Martín María Isabel Fernández-Nebro Antonio 《Clinical rheumatology》2021,40(1):133-142
Clinical Rheumatology - To analyze the effect of disease-modifying antirheumatic drugs (DMARDs) on the outcome of interstitial lung disease secondary to rheumatoid arthritis (RA-ILD). We performed... 相似文献
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Francisco Gabriel Jiménez-Núñez Sara Manrique-Arija Inmaculada Ureña-Garnica Carmen María Romero-Barco Blanca Panero-Lamothe Miguel Ángel Descalzo Loreto Carmona Manuel Rodríguez-Pérez Antonio Fernández-Nebro 《Calcified tissue international》2013,93(1):62-68
We evaluated the efficacy of a triage approach based on a combination of osteoporosis risk-assessment tools plus peripheral densitometry to identify low bone density accurately enough to be useful for clinical decision making in postmenopausal women. We conducted a cross-sectional diagnostic study in postmenopausal Caucasian women from primary and tertiary care. All women underwent dual-energy X-ray absorptiometric (DXA) measurement at the hip and lumbar spine and were categorized as osteoporotic or not. Additionally, patients had a nondominant heel densitometry performed with a PIXI densitometer. Four osteoporosis risk scores were tested: SCORE, ORAI, OST, and OSIRIS. All measurements were cross-blinded. We estimated the area under the curve (AUC) to predict the DXA results of 16 combinations of PIXI plus risk scores. A formula including the best combination was derived from a regression model and its predictability estimated. We included 505 women, in whom the prevalence of osteoporosis was 20 %, similar in both settings. The best algorithm was a combination of PIXI + OST + SCORE with an AUC of 0.826 (95 % CI 0.782–0.869). The proposed formula is Risk = (–12) × [PIXI + (?5)] × [OST + (?2)] × SCORE and showed little bias in the estimation (0.0016). If the formula had been implemented and the intermediate risk cutoff set at ?5 to 20, the system would have saved €4,606.34 in the study year. The formula proposed, derived from previously validated risk scores plus a peripheral bone density measurement, can be used reliably in primary care to avoid unnecessary central DXA measurements in postmenopausal women. 相似文献
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