首页> 外文期刊>Rheumatology >The treatment of inflammatory arthritis with methotrexate in clinical practice: treatment duration and incidence of adverse drug reactions.
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The treatment of inflammatory arthritis with methotrexate in clinical practice: treatment duration and incidence of adverse drug reactions.

机译:在临床实践中用甲氨蝶呤治疗炎性关节炎:治疗时间和药物不良反应的发生率。

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OBJECTIVE: To identify the proportion of patients with inflammatory arthritis who remain on methotrexate in the medium to long term and the incidence of side-effects in clinical practice. METHOD: The study population comprised all patients with inflammatory arthritis treated with methotrexate and monitored in clinics under the auspices of Staffordshire Rheumatology Centre. Two clinical auditors collected data retrospectively from the computer database used to support monitoring of patients on disease-modifying anti-rheumatic drugs. Information was collected on duration of treatments and reasons for stopping treatment. For patients identified as having potentially serious side-effects or who died whilst taking methotrexate, further information on their outcome was collected from patients' medical notes and where applicable post mortem reports and death registers. RESULTS: Between 1986 and 1999, 673 patients were treated with methotrexate, of whom 551 had a diagnosis of rheumatoid arthritis. From the Kaplan-Meier analysis, the probability of patients remaining on treatment 5 yr after starting methotrexate was 0.74. Three hundred and sixteen patients stopped methotrexate between 1986 and 1999. In 117 patients, the methotrexate was restarted. Seventy-two patients (10.7% of all patients) stopped because of inefficacy or patient choice or situation. Thirty-seven patients (5.5%) stopped methotrexate due to abnormal haematology (usually low neutrophils). Thirty-seven patients (5.5%) stopped methotrexate due to abnormalities in liver function tests. Life-threatening side-effects were identified in 12 patients (1.8%). These included six pneumonitis, five cytopenias and one disseminated varicella zoster. Two of these patients (0.3%) died, one from pneumonitis and one from disseminated varicella zoster. A total of 25 patients (3.7%) died while taking methotrexate and four died (0.6%) within 3 months of stopping methotrexate. One death (0.15%) was directly attributable to methotrexate (methotrexate pneumonitis). CONCLUSION: This study has shown that methotrexate is well tolerated in clinical practice in the medium to long term. It has produced accurate data on the incidence of adverse effects of methotrexate in a local population in a non-research setting. It has identified the incidence of life-threatening side-effects to be 1.7% with one death (0.15%) directly due to methotrexate. This information should prove useful when recommending such treatment to patients with inflammatory arthritis.
机译:目的:确定在中长期内仍使用甲氨蝶呤的炎性关节炎患者的比例以及临床实践中的副作用发生率。方法:研究人群包括所有接受甲氨蝶呤治疗并在斯塔福德郡风湿病学中心主持下的诊所进行监测的炎性关节炎患者。两名临床审核员从计算机数据库中回顾性收集了数据,该数据用于支持对患者的疾病改良抗风湿药的监测。收集有关治疗时间和停止治疗原因的信息。对于被确定具有潜在严重副作用或在服用甲氨蝶呤时死亡的患者,其结果的进一步信息从患者的医疗记录中收集,并在尸检报告和死亡登记簿中适用。结果:在1986年至1999年之间,有673例患者接受了甲氨蝶呤治疗,其中551例被诊断为类风湿关节炎。根据Kaplan-Meier分析,开始使用甲氨蝶呤5年后患者继续接受治疗的可能性为0.74。 1986年至1999年之间,共有316例患者停止使用甲氨蝶呤。在117例患者中,甲氨蝶呤重新开始使用。 72名患者(占所有患者的10.7%)由于无效或患者选择或情况而停下来。三十七名患者(5.5%)由于血液学异常(通常是中性粒细胞低)而停用甲氨蝶呤。三十七名患者(5.5%)由于肝功能检查异常而停用甲氨蝶呤。在12例患者中发现了威胁生命的副作用(1.8%)。其中包括6例肺炎,5例血细胞减少和1例弥漫性水痘带状疱疹。其中两名患者(0.3%)死亡,一名死于肺炎,另一名死于弥散性水痘带状疱疹。服用甲氨蝶呤时,共有25例患者(3.7%)死亡,而在停用甲氨蝶呤的3个月内有4例患者死亡(0.6%)。一例死亡(0.15%)直接归因于甲氨蝶呤(甲氨蝶呤肺炎)。结论:这项研究表明,甲氨蝶呤在中长期临床实践中耐受性良好。在非研究背景下,它已经产生了关于甲氨蝶呤在当地人群中不良反应发生率的准确数据。它已确认威胁生命的副作用的发生率为1.7%,其中甲氨蝶呤直接导致1例死亡(0.15%)。当向炎症性关节炎患者推荐这种治疗方法时,该信息应被证明是有用的。

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