DMARD disruption, rheumatic disease flare, and prolonged COVID-19 symptom duration after acute COVID-19 among patients with rheumatic disease: A prospective study.

DMARD disruption, rheumatic disease flare, and prolonged COVID-19 symptom duration after acute COVID-19 among patients with rheumatic disease: A prospective study.
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DOI:
10.1016/j.semarthrit.2022.152025
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发表时间:
2022-08
影响因子:
5
通讯作者:
Sparks, Jeffrey A.
Sparks, Jeffrey A.
中科院分区:
医学2区
文献类型:
--
作者:
Di Iorio, Michael;Cook, Claire E.;Vanni, Kathleen M. M.;Patel, Naomi J.;D'Silva, Kristin M.;Fu, Xiaoqing;Wang, Jiaqi;Prisco, Lauren C.;Kowalski, Emily;Zaccardelli, Alessandra;Martin, Lily W.;Qian, Grace;Hsu, Tiffany Y-T;Wallace, Zachary S.;Sparks, Jeffrey A.

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描述患有全身性自身免疫性风湿病(SARD)的COVID-19幸存者中的疾病缓解抗风湿药(DMARD)中断、风湿病发作/活动和COVID-19症状持续时间延长。我们调查了在马萨诸塞州布里格姆将军医院确诊COVID-19的既存SARD患者,以调查COVID-19的急性后遗症。我们获得了人口统计学、临床特征、COVID-19症状/病程和患者报告指标的数据。我们使用logistic回归分析了COVID-19症状持续时间延长(定义为持续≥28天)的基线预测因素。我们分析了2021年3月至2022年1月期间174名COVID-19幸存者(平均年龄52岁,81%为女性,80%为白色,50%为类风湿性关节炎)的调查。在接受DMARD治疗的127名受访者中,有51%的人报告称,在COVID-19发病后,他们的治疗方案受到了干扰。对于个体DMARD,56-77%有任何变化,除了羟氯喹(23%)和利妥昔单抗(46%)。COVID-19后的SARD发作报告率为41%。在调查时,全球患者报告的疾病活动度比COVID-19之前更差(平均值6.6±2.9 vs. 7.6±2.3,p<0.001)。COVID-19症状缓解的中位时间为25天(IQR 11,160)。45%的患者症状持续时间延长≥28天。因COVID-19住院(OR 3.54,95%CI 1.27-9.87)和初始COVID-19症状计数(每种症状OR 1.38,95%CI 1.17-1.63)与症状持续时间延长相关。与没有长期症状的人相比,经历长期症状持续时间的受访者有更高的RAPID 3评分(p=0.007)和更多的疼痛(p<0.001)和疲劳(p=0.03)。在这项针对COVID-19幸存者的前瞻性研究中,DMARD中断、SARD发作和COVID-19症状持续时间延长是常见的,这表明急性COVID-19后对SARD产生了重大影响。
To describe disease-modifying antirheumatic drug (DMARD) disruption, rheumatic disease flare/activity, and prolonged COVID-19 symptom duration among COVID-19 survivors with systemic autoimmune rheumatic diseases (SARDs). We surveyed people with pre-existing SARDs who had confirmed COVID-19 at Mass General Brigham to investigate post-acute sequelae of COVID-19. We obtained data on demographics, clinical characteristics, COVID-19 symptoms/course, and patient-reported measures. We examined baseline predictors of prolonged COVID-19 symptom duration (defined as lasting ≥28 days) using logistic regression. We analyzed surveys from 174 COVID-19 survivors (mean age 52 years, 81% female, 80% White, 50% rheumatoid arthritis) between March 2021 and January 2022. Fifty-one percent of 127 respondents on any DMARD reported a disruption to their regimen after COVID-19 onset. For individual DMARDs, 56-77% had any change, except for hydroxychloroquine (23%) and rituximab (46%). SARD flare after COVID-19 was reported by 41%. Global patient-reported disease activity was worse at the time of survey than before COVID-19 (mean 6.6±2.9 vs. 7.6±2.3, p<0.001). Median time to COVID-19 symptom resolution was 25 days (IQR 11, 160). Prolonged symptom duration of ≥28 days occurred in 45%. Hospitalization for COVID-19 (OR 3.54, 95%CI 1.27-9.87) and initial COVID-19 symptom count (OR 1.38 per symptom, 95%CI 1.17-1.63) were associated with prolonged symptom duration. Respondents experiencing prolonged symptom duration had higher RAPID3 scores (p=0.007) and more pain (p<0.001) and fatigue (p=0.03) compared to those without prolonged symptoms. DMARD disruption, SARD flare, and prolonged COVID-19 symptom duration were common in this prospective study of COVID-19 survivors, suggesting substantial impact on SARDs after acute COVID-19.
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