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秋水仙碱用于近期住院的新冠肺炎患者:一项随机对照试验(COL-COVID)

Colchicine in Recently Hospitalized Patients with COVID-19: A Randomized Controlled Trial (COL-COVID).

作者信息

Pascual-Figal Domingo A, Roura-Piloto Aychel E, Moral-Escudero Encarnación, Bernal Enrique, Albendín-Iglesias Helena, Pérez-Martínez M Teresa, Noguera-Velasco Jose Antonio, Cebreiros-López Iria, Hernández-Vicente Álvaro, Vázquez-Andrés David, Sánchez-Pérez Carmen, Khan Amjad, Sánchez-Cabo Fátima, García-Vázquez Elisa

机构信息

Cardiology Department, Hospital Universitario Virgen de la Arrixaca, IMIB-Arrixaca, Universidad de Murcia, Murcia, Spain.

Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares, (CIBERCV), Madrid, Spain.

出版信息

Int J Gen Med. 2021 Sep 11;14:5517-5526. doi: 10.2147/IJGM.S329810. eCollection 2021.

Abstract

BACKGROUND

Colchicine has been proposed as a potential therapy in coronavirus disease 2019 (COVID-19) due to their anti-inflammatory actions.

METHODS

The COL-COVID study was a prospective, randomized, controlled and open-label clinical trial that compared colchicine added to standard treatment vs standard treatment in hospitalized COVID-19 patients that do not need mechanical ventilatory support. Colchicine was initiated within the first 48 hours of admission at a 1.5 mg loading dose, followed by 0.5 mg b.i.d. for one week and 0.5 mg per day for 28 days. The study endpoints were clinical status (7-points WHO ordinal scale) and inflammatory biomarkers (IL-6 and CRP).

RESULTS

A total of 103 patients (51±12 years, 52% male) were randomly allocated to colchicine arm (n=52) and control arm (n=51). At day 28, all patients in the colchicine group were alive and discharged, whereas in the control group, two patients died in-hospital and one patient remained hospitalized. Clinical improvement in terms of changes on WHO scale at day 14 and 28 and time to 1-point clinical improvement did not differ between the two groups. Clinical deterioration (increase of at least 1-point in WHO scale) was observed in a higher proportion of cases in colchicine group (13.8%) vs control group (5.8%) (p=0.303); after adjustment by baseline risk factors and concomitant therapies, colchicine therapy was associated with a lower risk of clinical deterioration (p=0.030). Inflammatory biomarkers CRP and IL-6 concentrations course did not differ between the two arms.

CONCLUSION

In hospitalized COVID-19 patients, colchicine treatment neither improved the clinical status, nor the inflammatory response, over the standard treatment. Nevertheless, a preventive effect for further clinical deterioration might be possible.

TRIAL REGISTRATION

NCT04350320.

摘要

背景

秋水仙碱因其抗炎作用,已被提议作为2019冠状病毒病(COVID-19)的一种潜在治疗方法。

方法

COL-COVID研究是一项前瞻性、随机、对照、开放标签的临床试验,比较了在不需要机械通气支持的住院COVID-19患者中,标准治疗加用秋水仙碱与单纯标准治疗的效果。秋水仙碱在入院后48小时内开始使用,负荷剂量为1.5毫克,随后一周每日两次,每次0.5毫克,共28天,每日0.5毫克。研究终点为临床状态(世界卫生组织7分序贯量表)和炎症生物标志物(白细胞介素-6和C反应蛋白)。

结果

共有103例患者(年龄51±12岁,52%为男性)被随机分配至秋水仙碱组(n=52)和对照组(n=51)。在第28天,秋水仙碱组所有患者均存活并出院,而对照组有2例患者在住院期间死亡,1例患者仍住院。两组在第14天和28天世界卫生组织量表变化及达到1分临床改善时间方面的临床改善情况无差异。秋水仙碱组临床恶化(世界卫生组织量表至少增加1分)的病例比例高于对照组(13.8%对5.8%)(p=0.303);在对基线风险因素和伴随治疗进行调整后,秋水仙碱治疗与较低的临床恶化风险相关(p=0.030)。两组炎症生物标志物C反应蛋白和白细胞介素-6浓度变化过程无差异。

结论

在住院的COVID-19患者中,与标准治疗相比,秋水仙碱治疗既未改善临床状态,也未改善炎症反应。然而,秋水仙碱可能对预防进一步临床恶化有作用。

试验注册号

NCT04350320。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7880/8445096/4da180f6191c/IJGM-14-5517-g0001.jpg

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