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托珠单抗治疗 COVID-19 相关急性呼吸窘迫综合征行无创通气患者的疗效。

Efficacy of tocilizumab in patients with COVID-19 ARDS undergoing noninvasive ventilation.

机构信息

Pneumology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS di Reggio Emilia, 42123, Reggio Emilia, Italy.

Division of Rheumatology, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

出版信息

Crit Care. 2020 Sep 29;24(1):589. doi: 10.1186/s13054-020-03306-6.

Abstract

BACKGROUND

The severity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is extremely variable, ranging from asymptomatic patients to those who develop severe acute respiratory distress syndrome (ARDS). As for now, there are still no really effective therapies for coronavirus disease 2019 (COVID-19). Some evidences suggest that tocilizumab (TCZ) may avoid the progression of severe COVID-19. The aim of this retrospective case-control study was to analyze the efficacy and safety of TCZ in patients with COVID-19 ARDS undergoing noninvasive mechanical ventilation (NIV).

METHODS

Seventy-nine consecutive patients with severe COVID-19 pneumonia and worsening acute respiratory failure (ARF) were admitted to the Pulmonology Unit of Azienda USL of Reggio Emilia-IRCCS. All patients were inflamed (elevated CRP and IL-6 levels) and received NIV at admission according to the presence of a pO/FiO ratio ≤ 200 mmHg. The possibility of being treated with TCZ depended on the drug availability. The primary outcome was the in-hospital mortality rate. A secondary composite outcome of worsening was represented by the patients who died in the pulmonology unit or were intubated.

RESULTS

Out of 79 patients, 41 were treated with TCZ. Twenty-eight patients received intravenous (IV) TCZ and 13 patients received subcutaneous (SC) TCZ. In-hospital overall mortality rate was 38% (30/79 patients). The probabilities of dying and being intubated during the follow-up using Kaplan-Meier method were significantly lower in total patients treated with TCZ compared to those of patients not treated with TCZ (log-rank p value = 0.006 and 0.036, respectively). However, using Cox multivariate analyses adjusted for age and Charlson comorbidity index only the association with the reduced risk of being intubated or dying maintained the significance (HR 0.44, 95%CI 0.22-0.89, p = 0.022). Two patients treated with TCZ developed cavitating lung lesions during the follow-up.

CONCLUSIONS

This study shows that TCZ treatment may be effective in COVID-19 patients with severe respiratory impairment receiving NIV. More data on safety are required. Randomized controlled trials are needed to confirm these results.

摘要

背景

严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)感染的严重程度差异极大,从无症状患者到发生严重急性呼吸窘迫综合征(ARDS)的患者不等。目前,对于 2019 年冠状病毒病(COVID-19)还没有真正有效的治疗方法。一些证据表明,托珠单抗(TCZ)可能避免严重 COVID-19 的进展。本回顾性病例对照研究的目的是分析 TCZ 治疗接受无创机械通气(NIV)的 COVID-19 合并 ARDS 患者的疗效和安全性。

方法

79 例连续患有严重 COVID-19 肺炎和急性呼吸衰竭(ARF)恶化的患者被收入雷焦艾米利亚 Azienda USL-IRCCS 的肺病科。所有患者均有炎症(CRP 和 IL-6 水平升高),并根据存在 pO/FiO 比≤200mmHg 而入院时接受 NIV。是否接受 TCZ 治疗取决于药物的可用性。主要结局是住院死亡率。恶化的次要复合结局由肺病科死亡或插管的患者代表。

结果

79 例患者中,41 例接受 TCZ 治疗。28 例患者接受静脉 TCZ 治疗,13 例患者接受皮下 TCZ 治疗。住院总体死亡率为 38%(79 例患者中有 30 例死亡)。使用 Kaplan-Meier 方法的总 TCZ 治疗患者与未接受 TCZ 治疗的患者相比,死亡和随访期间插管的概率明显较低(对数秩 p 值分别为 0.006 和 0.036)。然而,使用 Cox 多变量分析调整年龄和 Charlson 合并症指数后,仅与降低插管或死亡风险相关的关联仍然具有统计学意义(HR 0.44,95%CI 0.22-0.89,p=0.022)。两名接受 TCZ 治疗的患者在随访期间出现有空洞的肺部病变。

结论

本研究表明,TCZ 治疗可能对接受 NIV 的严重呼吸功能障碍的 COVID-19 患者有效。需要更多关于安全性的数据。需要随机对照试验来证实这些结果。

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