Salton Francesco, Confalonieri Paola, Meduri G Umberto, Santus Pierachille, Harari Sergio, Scala Raffaele, Lanini Simone, Vertui Valentina, Oggionni Tiberio, Caminati Antonella, Patruno Vincenzo, Tamburrini Mario, Scartabellati Alessandro, Parati Mara, Villani Massimiliano, Radovanovic Dejan, Tomassetti Sara, Ravaglia Claudia, Poletti Venerino, Vianello Andrea, Gaccione Anna Talia, Guidelli Luca, Raccanelli Rita, Lucernoni Paolo, Lacedonia Donato, Foschino Barbaro Maria Pia, Centanni Stefano, Mondoni Michele, Davì Matteo, Fantin Alberto, Cao Xueyuan, Torelli Lucio, Zucchetto Antonella, Montico Marcella, Casarin Annalisa, Romagnoli Micaela, Gasparini Stefano, Bonifazi Martina, D'Agaro Pierlanfranco, Marcello Alessandro, Licastro Danilo, Ruaro Barbara, Volpe Maria Concetta, Umberger Reba, Confalonieri Marco
Department of Pulmonology, University Hospital of Cattinara, Trieste, Italy.
Pulmonary, Critical Care, and Sleep Medicine Service and Research Service, Memphis VA Medical Center and Department of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Open Forum Infect Dis. 2020 Sep 12;7(10):ofaa421. doi: 10.1093/ofid/ofaa421. eCollection 2020 Oct.
In hospitalized patients with coronavirus disease 2019 (COVID-19) pneumonia, progression to acute respiratory failure requiring invasive mechanical ventilation (MV) is associated with significant morbidity and mortality. Severe dysregulated systemic inflammation is the putative mechanism. We hypothesize that early prolonged methylprednisolone (MP) treatment could accelerate disease resolution, decreasing the need for intensive care unit (ICU) admission and mortality.
We conducted a multicenter observational study to explore the association between exposure to prolonged, low-dose MP treatment and need for ICU referral, intubation, or death within 28 days (composite primary end point) in patients with severe COVID-19 pneumonia admitted to Italian respiratory high-dependency units. Secondary outcomes were invasive MV-free days and changes in C-reactive protein (CRP) levels.
Findings are reported as MP (n = 83) vs control (n = 90). The composite primary end point was met by 19 vs 40 (adjusted hazard ratio [aHR], 0.41; 95% CI, 0.24-0.72). Transfer to ICU and invasive MV were necessary in 15 vs 27 ( = .07) and 14 vs 26 ( = .10), respectively. By day 28, the MP group had fewer deaths (6 vs 21; aHR, 0.29; 95% CI, 0.12-0.73) and more days off invasive MV (24.0 ± 9.0 vs 17.5 ± 12.8; = .001). Study treatment was associated with rapid improvement in PaO:FiO and CRP levels. The complication rate was similar for the 2 groups ( = .84).
In patients with severe COVID-19 pneumonia, early administration of prolonged MP treatment was associated with a significantly lower hazard of death (71%) and decreased ventilator dependence. Treatment was safe and did not impact viral clearance. A large randomized controlled trial (RECOVERY trial) has been performed that validates these findings. ClinicalTrials.gov NCT04323592.
在2019冠状病毒病(COVID-19)肺炎住院患者中,进展为需要有创机械通气(MV)的急性呼吸衰竭与显著的发病率和死亡率相关。严重的全身炎症失调是推测的机制。我们假设早期延长甲基强的松龙(MP)治疗可加速疾病缓解,减少重症监护病房(ICU)收治需求和死亡率。
我们进行了一项多中心观察性研究,以探讨在入住意大利呼吸高依赖病房的重症COVID-19肺炎患者中,延长低剂量MP治疗暴露与28天内ICU转诊、插管或死亡需求(复合主要终点)之间的关联。次要结局为无有创MV天数和C反应蛋白(CRP)水平变化。
报告的结果为MP组(n = 83)与对照组(n = 90)。复合主要终点在MP组和对照组中分别有19例和40例达到(调整后风险比[aHR],0.41;95%置信区间[CI],0.24 - 0.72)。分别有15例和27例(P = 0.07)需要转入ICU,14例和26例(P = 0.10)需要进行有创MV。到第28天时,MP组死亡病例较少(6例 vs 21例;aHR,0.29;95% CI,0.12 - 0.73),无有创MV天数更多(24.0 ± 9.0天 vs 17.5 ± 12.8天;P = 0.001)。研究治疗与动脉血氧分压与吸入氧浓度比值(PaO:FiO)和CRP水平的快速改善相关。两组并发症发生率相似(P = 0.84)。
在重症COVID-19肺炎患者中,早期给予延长的MP治疗与显著更低的死亡风险(71%)和降低的呼吸机依赖相关。治疗是安全的,且不影响病毒清除。一项大型随机对照试验(RECOVERY试验)已进行,验证了这些发现。ClinicalTrials.gov标识符:NCT04323592。