Section of Rheumatology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Clinical Epidemiology Unit, Orthopedics, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Ann Rheum Dis. 2017 Jul;76(7):1245-1252. doi: 10.1136/annrheumdis-2016-210239. Epub 2017 Jan 10.
To examine predictors of work ability gain and loss after anti-tumour necrosis factor (TNF) start, respectively, in working-age patients with rheumatoid arthritis (RA) with a special focus on disease duration.
Patients with RA, aged 19-62 years, starting their first TNF inhibitor 2006-2009 with full work ability (0 sick leave/disability pension days during 3 months before bio-start; n=1048) or no work ability (90 days; n=753) were identified in the Swedish biologics register (Anti-Rheumatic Treatment In Sweden, ARTIS) and sick leave/disability pension days retrieved from the Social Insurance Agency. Outcome was defined as work ability gain ≥50% for patients without work ability at bio-start and work ability loss ≥50% for patients with full work ability, and survival analyses conducted. Baseline predictors including disease duration, age, sex, education level, employment, Health Assessment Questionnaire, Disease Activity Score 28 and relevant comorbidities were estimated using Cox regression.
During 3 years after anti-TNF start, the probability of regaining work ability for totally work-disabled patients was 35% for those with disease duration <5 years and 14% for disease duration ≥5 years (adjusted HR 2.1 (95% CI 1.4 to 3.2)). For patients with full work ability at bio-start, disease duration did not predict work ability loss. Baseline disability pension was also a strong predictor of work ability gain after treatment start.
A substantial proportion of work-disabled patients with RA who start anti-TNF therapy regain work ability. Those initiating treatment within 5 years of symptom onset have a more than doubled 3-year probability of regaining work ability compared with later treatment starts. This effect seems largely due to the impact of disease duration on disability pension status.
分别研究抗肿瘤坏死因子(TNF)治疗后工作能力改善和丧失的预测因素,重点关注疾病持续时间。
在瑞典生物制剂登记处(Anti-Rheumatic Treatment In Sweden,ARTIS)中确定了年龄在 19-62 岁之间、2006-2009 年首次使用 TNF 抑制剂且具有完全工作能力(生物治疗前 3 个月内无病假/残疾抚恤金天数;n=1048)或无工作能力(90 天;n=753)的类风湿关节炎(RA)患者,并从社会保险局检索病假/残疾抚恤金天数。无生物治疗前无工作能力的患者工作能力改善≥50%,具有完全工作能力的患者工作能力丧失≥50%定义为结局,并进行生存分析。使用 Cox 回归估计基线预测因素,包括疾病持续时间、年龄、性别、教育程度、就业状况、健康评估问卷、疾病活动评分 28 以及相关合并症。
在抗 TNF 治疗后 3 年内,完全丧失工作能力的患者中,病程<5 年的患者恢复工作能力的概率为 35%,病程≥5 年的患者为 14%(调整后的 HR 2.1(95%CI 1.4 至 3.2))。对于生物治疗时具有完全工作能力的患者,疾病持续时间并不预测工作能力丧失。基线残疾抚恤金也是治疗开始后工作能力改善的有力预测因素。
相当一部分开始接受抗 TNF 治疗的 RA 残疾患者恢复了工作能力。与晚期治疗开始相比,发病后 5 年内开始治疗的患者,3 年内恢复工作能力的概率增加了一倍以上。这种效果似乎主要归因于疾病持续时间对残疾抚恤金状况的影响。