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在接受有创机械通气或体外膜肺氧合治疗的 COVID-19 患者中,加用巴瑞替尼联合常规治疗降低了全因死亡率。

In patients with COVID-19 receiving IMV or ECMO, adding baricitinib to usual care reduced all-cause mortality.

机构信息

Mayo Clinic, Rochester, Minnesota, USA (A.S., J.C.O.).

出版信息

Ann Intern Med. 2022 Jun;175(6):JC64. doi: 10.7326/J22-0033. Epub 2022 Jun 7.

DOI:10.7326/J22-0033
PMID:35667076
Abstract

Ely EW, Ramanan AV, Kartman CE, et al. Lancet Respir Med. 2022;10:327-36. 35123660.

摘要

埃利·E·W、拉马南·A·V、卡特曼·C·E 等人。柳叶刀呼吸医学。2022;10:327-36. 35123660.

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In patients with COVID-19 receiving IMV or ECMO, adding baricitinib to usual care reduced all-cause mortality.在接受有创机械通气或体外膜肺氧合治疗的 COVID-19 患者中,加用巴瑞替尼联合常规治疗降低了全因死亡率。
Ann Intern Med. 2022 Jun;175(6):JC64. doi: 10.7326/J22-0033. Epub 2022 Jun 7.
2
Efficacy and safety of baricitinib plus standard of care for the treatment of critically ill hospitalised adults with COVID-19 on invasive mechanical ventilation or extracorporeal membrane oxygenation: an exploratory, randomised, placebo-controlled trial.巴瑞替尼联合标准治疗对接受有创机械通气或体外膜肺氧合治疗的 COVID-19 重症住院成年患者的疗效和安全性:一项探索性、随机、安慰剂对照试验。
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A Phase I/II Clinical Trial to evaluate the efficacy of baricitinib to prevent respiratory insufficiency progression in onco-hematological patients affected with COVID19: A structured summary of a study protocol for a randomised controlled trial.一项评估巴瑞替尼预防 COVID19 相关血液肿瘤患者呼吸功能不全进展的疗效的 I/II 期临床试验:一项随机对照试验研究方案的结构化总结。
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Efficacy and safety of baricitinib for the treatment of hospitalised adults with COVID-19 (COV-BARRIER): a randomised, double-blind, parallel-group, placebo-controlled phase 3 trial.巴瑞替尼治疗住院 COVID-19 成人患者的疗效和安全性(COV-BARRIER):一项随机、双盲、平行分组、安慰剂对照的 3 期临床试验。
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In adults hospitalized with COVID-19, adding baricitinib vs. dexamethasone to remdesivir did not differ for MV-free survival.在因 COVID-19 住院的成年人中,与地塞米松相比,将巴瑞替尼加用至瑞德西韦并未改善有创机械通气生存。
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Baricitinib in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial and updated meta-analysis.巴瑞替尼治疗 COVID-19 住院患者的疗效(RECOVERY 研究):一项随机、对照、开放标签、平台试验及更新的荟萃分析。
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Anti-C5a antibody (vilobelimab) therapy for critically ill, invasively mechanically ventilated patients with COVID-19 (PANAMO): a multicentre, double-blind, randomised, placebo-controlled, phase 3 trial.抗 C5a 抗体(vilobelimab)治疗 COVID-19 危重症、有创机械通气患者(PANAMO):一项多中心、双盲、随机、安慰剂对照、3 期临床试验。
Lancet Respir Med. 2022 Dec;10(12):1137-1146. doi: 10.1016/S2213-2600(22)00297-1. Epub 2022 Sep 7.