Hashim Zia, Ghatak Tanmoy, Nath Alok, Singh Ratender Kumar
Department of Pulmonary Medicine, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Emergency Medicine, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Lung India. 2022 May-Jun;39(3):286-291. doi: 10.4103/lungindia.lungindia_530_21.
Severe hypoxia due to coronavirus disease 2019 (COVID-19) is challenging in the intensive care unit (ICU). It is often unresponsive to mechanical ventilation at high positive end-expiratory pressure and the fraction of inspired oxygen combination. The cause of such worsening hypoxia may be microvascular thrombosis in the pulmonary vascular system because of the procoagulant nature of COVID-19 infection. Confirming the diagnosis with computed tomographic pulmonary angiography is not always possible, as the patients are too sick to be shifted. Tissue plasminogen activator (tPA) is recommended for pulmonary thromboembolism with hypotension and worsening hypoxia, as confirmed by computed tomography pulmonary angiography. However, its role in worsening hypoxia because of presumed microthrombi in the pulmonary vasculature in COVID-19 is unclear. We present six cases from our ICU where we used low-dose tPA in COVID-19 refractory hypoxia with presumed microthrombi in the pulmonary vasculature (oligemic lung field, refractory hypoxia, increased D dimer, electrocardiographic features of pulmonary embolism, and right ventricular strain on echocardiography). Oxygenation improved within 6 h and was maintained for up to 48 h in all patients. Therefore, there is a possible role of microthrombi in the mechanism of hypoxia in this setting. An early decision to start low-dose tPA may improve the outcome. However, all patients finally succumbed to sepsis and multiorgan failure later in their course. A systematic review of the literature has also been performed on the mechanism of thrombosis and the use of tPA in hypoxia due to COVID-19.
2019冠状病毒病(COVID-19)导致的严重缺氧在重症监护病房(ICU)中是一项挑战。它通常对高呼气末正压通气和吸入氧分数联合治疗无反应。这种缺氧恶化的原因可能是由于COVID-19感染的促凝性质导致肺血管系统微血管血栓形成。由于患者病情太重无法转运,通过计算机断层扫描肺血管造影来确诊并不总是可行的。对于经计算机断层扫描肺血管造影确诊的伴有低血压和缺氧恶化的肺血栓栓塞症,推荐使用组织纤溶酶原激活剂(tPA)。然而,其在COVID-19中因肺血管系统中推测的微血栓导致缺氧恶化方面的作用尚不清楚。我们展示了来自我们ICU的6例病例,在这些病例中,我们对COVID-19难治性缺氧且推测肺血管系统存在微血栓(肺野血流减少、难治性缺氧、D-二聚体升高、肺栓塞的心电图特征以及超声心动图显示右心室应变)的患者使用了低剂量tPA。所有患者的氧合在6小时内得到改善,并维持长达48小时。因此,在这种情况下,微血栓可能在缺氧机制中起作用。尽早决定开始使用低剂量tPA可能会改善预后。然而,所有患者最终在病程后期均死于脓毒症和多器官功能衰竭。我们还对COVID-19导致的血栓形成机制和tPA在缺氧中的应用进行了文献系统综述。