COVID-19与系统性硬化症相关间质性肺病患者的疫苗接种保护

IF 1.4 Q3 RHEUMATOLOGY
Stylianos Panopoulos, Vasilios Tzilas, Vasiliki-Kalliopi Bournia, Anastasios Karamanakos, Katerina Laskari, Demosthenes Bouros, Maria Tektonidou, Petros P Sfikakis
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引用次数: 1

摘要

目的:关于COVID-19在间质性肺病患者中的数据很少,SARS-CoV-2是否会引发间质性肺病进展尚不清楚。我们的目的是分析COVID-19在系统性硬化症相关间质性肺病患者中的结局,包括可能的胸片进展。患者和方法:对本中心截至2022年9月1日确诊为SARS-CoV2感染的43例系统性硬化症相关间质性肺疾病患者(平均±SD, 55.2±11.6岁,36例女性)进行分析。比较新冠肺炎前(3个月)和后(2-5个月)个体间质性肺疾病的高分辨率CT (HRCT)程度。结果:在SARS-CoV-2感染病例中,9/43例患者未接种疫苗,5、26和3例分别接种了2、3和4剂mRNA疫苗。31例患者接受免疫抑制剂单药治疗(霉酚酸酯,n = 7;环磷酰胺,n = 2;甲氨蝶呤,n = 10;托珠单抗,n = 7;利妥昔单抗,n = 1;依那西普,n = 1),或它们的组合(n = 3)。8名患者(20%)(其中4名未接种疫苗)因肺炎需要住院治疗,3名患者(7%)死于急性呼吸衰竭(n = 2,均未接种疫苗)或心脏骤停。缺乏疫苗接种是住院的唯一独立预测因子(OR = 7.98, 95% CI: 1.25-51.09)和死亡的唯一独立预测因子(OR = 32.7, 95% CI: 0.97-1110.98),无论是否存在弥漫性系统性硬化症、间质性肺疾病程度大于20%或免疫抑制治疗。在22例可获得HRCT对的患者(接种疫苗= 20例)中,除1例患者外,其余患者在COVID-19之前的间质性肺疾病程度(20.4%±17.8%)保持不变(22.4%±18.5%)。结论:对所有系统性硬化症合并间质性肺疾病患者,接种SARS-CoV-2疫苗至关重要。在接种疫苗的患者中,COVID-19似乎不会促进系统性硬化症相关间质性肺病的进展,但需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 and protection of vaccination in patients with systemic sclerosis-associated interstitial lung disease.

Objectives: Data on COVID-19 in patients with interstitial lung disease are scarce and whether SARS-CoV-2 may trigger interstitial lung disease progression remains unknown. We aimed to analyze outcomes of COVID-19 in patients with systemic sclerosis-associated interstitial lung disease, including possible thoracic radiographic progression.

Patients and methods: All 43 patients with systemic sclerosis-associated interstitial lung disease followed in our center (mean ± SD, 55.2 ± 11.6 years, 36 female) with confirmed SARS-CoV2 infection up to 1 September 2022 were analyzed. Individual interstitial lung disease extent on high resolution CT (HRCT) performed before (up to 3 months) and after COVID-19 (2-5 months) was compared.

Results: At SARS-CoV-2 infection, 9/43 patients were unvaccinated, whereas 5, 26, and 3 had received 2, 3, or 4 doses of an mRNA vaccine, respectively. Thirty-one patients were either on monotherapy with immunosuppressives (mycophenolate, n = 7; cyclophosphamide, n = 2; methotrexate, n = 10; tocilizumab, n = 7; rituximab, n = 1; etanercept, n = 1), or their combinations (n = 3). Eight patients (20%), of whom four unvaccinated, required hospitalization for pneumonia and three (7%) died of acute respiratory failure (n = 2, both unvaccinated) or cardiac arrest. Lack of vaccination was the only independent predictor for hospitalization (OR = 7.98, 95% CI: 1.25-51.09) and marginally for death (OR = 32.7, 95% CI: 0.97-1110.98), regardless of the presence of diffuse systemic sclerosis, interstitial lung disease extent greater than 20% or immunosuppressive treatment. In 22 patients with available HRCT pairs (vaccinated = 20), the interstitial lung disease extent before COVID-19 (20.4%± 17.8%) remained unchanged (22.4% ± 18.5%) in all but one patient.

Conclusion: SARS-CoV-2 vaccination is of outmost importance for every systemic sclerosis patient with interstitial lung disease. COVID-19 does not seem to promote progression of systemic sclerosis-associated interstitial lung disease in vaccinated patients, but further studies are warranted.

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