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在大型美国理赔数据库中,免疫抑制药物与非感染性葡萄膜炎患者 2019 冠状病毒病结局的相关性。

Association between Immunosuppressive Drugs and Coronavirus Disease 2019 Outcomes in Patients with Noninfectious Uveitis in a Large US Claims Database.

机构信息

F.I. Proctor Foundation, University of California, San Francisco, California.

F.I. Proctor Foundation, University of California, San Francisco, California; Department of Ophthalmology, University of California, San Francisco, California.

出版信息

Ophthalmology. 2022 Oct;129(10):1096-1106. doi: 10.1016/j.ophtha.2022.05.008. Epub 2022 May 17.

Abstract

PURPOSE

To determine the dose-dependent risk of systemic corticosteroids (SCs) and the risk of other immunosuppressive therapies on coronavirus disease 2019 (COVID-19) infection, hospitalization, and death in patients with noninfectious uveitis (NIU).

DESIGN

A retrospective cohort study from January 20, 2020, to December 31, 2020 (an era before widespread COVID-19 vaccination), using the Optum Labs Data Warehouse, a US national de-identified claims database.

PARTICIPANTS

Patients who had at least 1 NIU diagnosis from January 1, 2017.

METHODS

Unadjusted and adjusted hazard ratios (HRs) were estimated for each variable and COVID-19 outcome using Cox proportional hazards models, with time-updated dichotomous indicators for outpatient immunosuppressive medication exposure. To assess the dose-dependent effect of SC exposure, the average daily dose of prednisone over the exposed interval was included in the adjusted models as a continuous variable, in addition to the dichotomous variable.

MAIN OUTCOME MEASURES

Incidence rates of COVID-19 infection, COVID-19-related hospitalization, and COVID-19-related in-hospital death.

RESULTS

This study included 52 286 NIU patients of whom 12 000 (23.0%) were exposed to immunosuppressive medications during the risk period. In adjusted models, exposure to SCs was associated with increased risk of COVID-19 infection (HR, 2.66; 95% confidence interval [CI], 2.19-3.24; P < 0.001), hospitalization (HR, 3.26; 95% CI, 2.46-4.33; P < 0.001), and in-hospital death (HR, 1.99; 95% CI, 0.93-4.27; P = 0.08). Furthermore, incremental increases in the dosage of SCs were associated with a greater risk for these outcomes. Although tumor necrosis factor-α (TNF-α) inhibitors were associated with an increased risk of infection (HR, 1.48; 95% CI, 1.08-2.04; P = 0.02), other immunosuppressive treatments did not increase the risk of COVID-19 infection, hospitalization, or death.

CONCLUSIONS

This study from an era before widespread COVID-19 vaccination demonstrates that outpatient SC exposure is associated with greater risk of COVID-19 infection and severe outcomes in patients with NIU. Future studies should evaluate the impact of immunosuppression in vaccinated NIU patients. Limiting exposure to SCs and use of alternative therapies may be warranted.

摘要

目的

确定全身皮质类固醇(SCs)的剂量依赖性风险以及其他免疫抑制疗法对非感染性葡萄膜炎(NIU)患者 2019 年冠状病毒病(COVID-19)感染、住院和死亡的风险。

设计

这是一项回顾性队列研究,研究对象为 2020 年 1 月 20 日至 2020 年 12 月 31 日(COVID-19 疫苗广泛接种前的一个时期)期间在 Optum Labs 数据仓库(美国全国去识别索赔数据库)就诊的至少有 1 次 NIU 诊断的患者。

参与者

至少有 1 次 NIU 诊断的患者,来自 2017 年 1 月 1 日。

方法

使用 Cox 比例风险模型,根据门诊免疫抑制药物暴露情况,对每个变量和 COVID-19 结果进行未调整和调整后的风险比(HR)估计。为了评估 SC 暴露的剂量依赖性效应,在调整后的模型中,将暴露间隔内泼尼松的平均日剂量作为连续变量,而不是二分类变量,包括在内。

主要观察指标

COVID-19 感染、COVID-19 相关住院和 COVID-19 相关院内死亡的发生率。

结果

本研究共纳入 52286 例 NIU 患者,其中 12000 例(23.0%)在风险期内接受免疫抑制药物治疗。在调整后的模型中,SC 暴露与 COVID-19 感染风险增加相关(HR,2.66;95%置信区间[CI],2.19-3.24;P<0.001)、住院(HR,3.26;95%CI,2.46-4.33;P<0.001)和院内死亡(HR,1.99;95%CI,0.93-4.27;P=0.08)。此外,SC 剂量的增量增加与这些结果的风险增加相关。虽然肿瘤坏死因子-α(TNF-α)抑制剂与感染风险增加相关(HR,1.48;95%CI,1.08-2.04;P=0.02),但其他免疫抑制治疗并未增加 COVID-19 感染、住院或死亡的风险。

结论

本研究来自 COVID-19 疫苗广泛接种前的一个时期,表明门诊 SC 暴露与 NIU 患者 COVID-19 感染和严重结局风险增加相关。未来的研究应评估免疫抑制对接种 NIU 患者的影响。限制 SC 暴露和使用替代疗法可能是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45c/9110065/756d0e0d8b08/gr1_lrg.jpg

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