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A Single Center Experience in Biological Therapy for the Treatment of Rheumatoid Arthritis in Saudi Arabia

机译:沙特阿拉伯类风湿关节炎生物治疗的单一中心经验

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Background: Biological therapy is indicated in the treatment of RA (Rheumatoid Arthritis) after failure of disease-modifying anti-rheumatic drugs (DMARDS) by the ACR/EULAR recommendations. The objective of the study is to describe the characteristics of Saudi patients at the initiation of biological therapy and to evaluate clinical effectiveness of this therapy measured by the disease activity score DAS 28. Methods: This was a retrospective cohort study of RA (rheumatoid arthritis) patients in King Fahad Hospital in Jeddah, Saudi Arabia from January 2005-July 2011. Data were collected from the medical records of all RA patients on biological therapy including: demographics, disease characteristics, comorbid illnesses and DAS 28 score over a period of 1 year. Results: 139 patients were studied (mean age 46 ± 13 years), of which 118 (84%) were females; mean duration of affliction with RA was 7.2 years ranging 1-45 years. Rheumatoid factor (RF) was positive in 88 patients (63.3%) and one or more comorbidities were present in 102 patients (73.3%). First choice of biological drug was ADA (Adalimumab) 44 patients (31.7%) and RTX (Rituximab) was the 2nd frequently prescribed biological drug. Mean DAS 28 activity at baseline was in ADA 41 patients (6.10 ± 1.62), ETA (Etarnercept) 29 patients (6.64 ± 1.42) and RTX 50 patients (6.7 ± 1.32). Moderate to good EULAR response was obtained in 74%, 85.7% and 53.3% at 6 months in ADA, ETA and RTX patients respectively. Moderate to good EULAR response was obtained in 61.8%, 86.6% and 72% in ADA, ETA AND RTX patients respectively at 1 year of treatment. Therapeutic effectiveness was comparable with the response rates in published observational trials. Conclusion: Our data demonstrate daily clinical practice in management of RA. The pattern of prescription is in agreement with the ACR/EULAR recommendations for initiation of biologicals in the treatment of RA.
机译:背景:根据ACR / EULAR的建议,在疾病缓解型抗风湿药(DMARDS)失败后,在RA(类风湿关节炎)的治疗中应采用生物疗法。这项研究的目的是描述沙特阿拉伯患者在开始生物疗法时的特征,并通过疾病活动评分DAS 28评估该疗法的临床有效性。方法:这是对RA(类风湿关节炎)的一项回顾性队列研究。 2005年1月至2011年7月在沙特阿拉伯吉达的法哈德国王医院接受治疗的患者。数据从所有RA患者的生物治疗医疗记录中收集,包括:人口统计学,疾病特征,合并症和DAS 28评分,为期1年。结果:研究了139例患者(平均年龄46±13岁),其中118例(84%)为女性。 RA的平均病程为7.2年,范围为1至45年。类风湿因子(RF)阳性88例(63.3%),一种或多种合并症存在102例(73.3%)。生物药物的首选是ADA(阿达木单抗)44例(31.7%),而RTX(利妥昔单抗)是第二种经常开处方的生物药物。基线时平均DAS 28活动为ADA 41例患者(6.10±1.62),ETA(Etarnercept)29例患者(6.64±1.42)和RTX 50例患者(6.7±1.32)。 ADA,ETA和RTX患者在6个月时分别获得74%,85.7%和53.3%的中度至良好EULAR反应。治疗1年后,ADA,ETA和RTX患者分别获得61.8%,86.6%和72%的中度至良好EULAR反应。治疗效果与已发表的观察性试验的缓解率相当。结论:我们的数据证明了RA治疗的日常临床实践。处方模式与ACR / EULAR有关在RA治疗中启动生物制剂的建议一致。

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