Jirak Peter, van Almsick Vincent, Dimitroulis Dimitrios, Mirna Moritz, Seelmaier Clemens, Shomanova Zornitsa, Wernly Bernhard, Semo Dilvin, Dankl Daniel, Mahringer Magdalena, Lichtenauer Michael, Hoppe Uta C, Reinecke Holger, Pistulli Rudin, Larbig Robert, Motloch Lukas J
Clinic II for Internal Medicine, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Department of Cardiology I - Coronary and Peripheral Vascular Disease, Heart Failure, University Hospital Münster, Münster, Germany.
Front Med (Lausanne). 2022 Feb 2;9:808221. doi: 10.3389/fmed.2022.808221. eCollection 2022.
Severe COVID-19 pneumonia requiring intensive care treatment remains a clinical challenge to date. Dexamethasone was reported as a promising treatment option, leading to a reduction of mortality rates in severe COVID-19 disease. However, the effect of dexamethasone treatment on cardiac injury and pulmonary embolism remains largely elusive.
In total 178 critically ill COVID-19 patients requiring intensive care treatment and mechanical ventilation were recruited in three European medical centres and included in the present retrospective study. One hundred thirteen patients (63.5%) were treated with dexamethasone for a median duration of 10 days (IQR 9-10). Sixty five patients (36.5%) constituted the non-dexamethasone control group.
While peak inflammatory markers were reduced by dexamethasone treatment, the therapy also led to a significant reduction in peak troponin levels (231 vs. 700% indicated as relative to cut off value, = 0.001). Similar, dexamethasone resulted in significantly decreased peak D-Dimer levels (2.16 mg/l vs. 6.14 mg/l, = 0.002) reflected by a significant reduction in pulmonary embolism rate (4.4 vs. 20.0%, = 0.001). The antithrombotic effect of dexamethasone treatment was also evident in the presence of therapeutic anticoagulation (pulmonary embolism rate: 6 vs. 34.4%, < 0.001). Of note, no significant changes in baseline characteristics were observed between the dexamethasone and non-dexamethasone group.
In severe COVID-19, anti-inflammatory effects of dexamethasone treatment seem to be associated with a significant reduction in myocardial injury. Similar, a significant decrease in pulmonary embolism, independent of anticoagulation, was evident, emphasizing the beneficial effect of dexamethasone treatment in severe COVID-19.
迄今为止,需要重症监护治疗的重症新型冠状病毒肺炎(COVID-19)仍是一项临床挑战。据报道,地塞米松是一种有前景的治疗选择,可降低重症COVID-19疾病的死亡率。然而,地塞米松治疗对心脏损伤和肺栓塞的影响在很大程度上仍不清楚。
在三个欧洲医疗中心招募了总共178例需要重症监护治疗和机械通气的重症COVID-19患者,并纳入本回顾性研究。113例患者(63.5%)接受地塞米松治疗,中位疗程为10天(四分位间距9-10天)。65例患者(36.5%)构成非地塞米松对照组。
虽然地塞米松治疗降低了炎症标志物峰值,但该疗法也导致肌钙蛋白峰值水平显著降低(相对于临界值,分别为231%对700%,P = 0.001)。类似地,地塞米松导致D-二聚体峰值水平显著降低(2.16 mg/l对6.14 mg/l,P = 0.002),这反映在肺栓塞发生率显著降低(4.4%对20.0%,P = 0.001)。在地塞米松治疗联合抗凝治疗时,其抗血栓形成作用也很明显(肺栓塞发生率:6%对34.4%,P < 0.001)。值得注意的是,地塞米松组和非地塞米松组之间的基线特征未观察到显著变化。
在重症COVID-19中,地塞米松治疗的抗炎作用似乎与心肌损伤的显著减轻有关。类似地,肺栓塞显著减少,且与抗凝无关,这突出了地塞米松治疗在重症COVID-19中的有益作用。