Division of Rheumatology, Allergy and Immunology, Department of Medicine, Stony Brook University Renaissance School of Medicine, USA.
Division of Rheumatology, Allergy and Immunology, Department of Medicine, Stony Brook University Renaissance School of Medicine, USA.
Semin Arthritis Rheum. 2020 Aug;50(4):680-686. doi: 10.1016/j.semarthrit.2020.05.010. Epub 2020 May 23.
To analyze clinical characteristics and outcome of COVID-19 patients with underlying rheumatic diseases (RD) on immunosuppressive agents.
A case series of COVID-19 patients with RD on disease modifying anti-rheumatic drugs (DMARDs) were studied by a retrospective chart review. A literature search identified 9 similar studies of single cases and case series, which were also included.
There were 4 COVID-19 inpatients with RD from our hospital, and the mean age was 57 ± 21 years. Two patients had a mild infection, and 2 developed severe COVID-19 related respiratory complications, including 1 patient on secukinumab requiring mechanical ventilation and 1 patient on rituximab developing viral pneumonia requiring supplemental oxygenation. All 4 patients had elevated acute phase reactants, 2 patients had mild COVID-19 with lymphopenia, and 2 patients had severe COVID-19 with normal lymphocyte counts, and high levels of IL-6. None of the patients exhibited an exacerbation of their underlying RD. In the literature, there were 9 studies of COVID-19 involving 197 cases of various inflammatory RD. Most patients were on DMARDs or biologics, of which TNFα inhibitors were most frequently used. Two tocilizumab users had a mild infection. Two patients were on rituximab with 1 severe COVID-19 requiring mechanical ventilation. Six patients were on secukinumab with 1 hospitalization. Of the total 201 cases, 12 died, with an estimated mortality of 5.9% CONCLUSION: Patients with RD are susceptible to COVID-19. Various DMARDs or biologics may affect the viral disease course differently. Patients on hydroxychloroquine, TNFα antagonists or tocilizumab may have a mild viral illness. Rituximab or secukinumab could worsen the viral disease. Further study is warranted.
分析 COVID-19 合并风湿免疫病(RD)患者的临床特征及结局。
通过回顾性病历分析,研究了我院 COVID-19 合并 RD 且正在使用改善病情抗风湿药物(DMARDs)的病例系列。通过文献检索,确定了 9 项关于单例和病例系列的类似研究,也将这些研究纳入分析。
我院有 4 例 COVID-19 合并 RD 的住院患者,平均年龄为 57±21 岁。2 例患者感染较轻,2 例患者出现严重 COVID-19 相关呼吸系统并发症,其中 1 例使用司库奇尤单抗的患者需要机械通气,1 例使用利妥昔单抗的患者出现病毒性肺炎需要补充氧气。所有 4 例患者均有急性期反应物升高,2 例患者出现 COVID-19 伴淋巴细胞减少症,2 例患者出现 COVID-19 伴正常淋巴细胞计数和高水平 IL-6。无患者出现基础 RD 恶化。文献中共有 9 项 COVID-19 研究,涉及 197 例不同的炎症性 RD 患者。大多数患者正在使用 DMARDs 或生物制剂,其中 TNFα 抑制剂最常使用。2 例使用托珠单抗的患者感染较轻。2 例使用利妥昔单抗的患者中有 1 例 COVID-19 严重,需要机械通气。6 例使用司库奇尤单抗的患者中有 1 例住院。在总共 201 例患者中,有 12 例死亡,死亡率估计为 5.9%。
RD 患者易感染 COVID-19。各种 DMARDs 或生物制剂可能对病毒疾病进程有不同影响。使用羟氯喹、TNFα 拮抗剂或托珠单抗的患者可能患有轻度病毒性疾病。利妥昔单抗或司库奇尤单抗可能会使病毒疾病恶化。需要进一步研究。