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通过 LPS 诱导的急性呼吸窘迫综合征大猪模型经腹腔内和胸腔内途径测试富氧微泡。

Testing oxygenated microbubbles via intraperitoneal and intrathoracic routes on a large pig model of LPS-induced acute respiratory distress syndrome.

机构信息

Biomedical Engineering Program, Department of Mechanical and Material Engineering, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.

Institutional Animal Care Program, Office of Research & Economic Development, University of Nebraska - Lincoln, Lincoln, Nebraska, USA.

出版信息

Physiol Rep. 2022 Sep;10(17):e15451. doi: 10.14814/phy2.15451.

Abstract

With a mortality rate of 46% before the onset of COVID-19, acute respiratory distress syndrome (ARDS) affected 200,000 people in the US, causing 75,000 deaths. Mortality rates in COVID-19 ARDS patients are currently at 39%. Extrapulmonary support for ARDS aims to supplement mechanical ventilation by providing life-sustaining oxygen to the patient. A new rapid-onset, human-sized pig ARDS model in a porcine intensive care unit (ICU) was developed. The pigs were nebulized intratracheally with a high dose (4 mg/kg) of the endotoxin lipopolysaccharide (LPS) over a 2 h duration to induce rapid-onset moderate-to-severe ARDS. They were then catheterized to monitor vitals and to evaluate the therapeutic effect of oxygenated microbubble (OMB) therapy delivered by intrathoracic (IT) or intraperitoneal (IP) administration. Post-LPS administration, the PaO value dropped below 70 mmHg, the PaO /FiO ratio dropped below 200 mmHg, and the heart rate increased, indicating rapidly developing (within 4 h) moderate-to-severe ARDS with tachycardia. The SpO and PaO of these LPS-injured pigs did not show significant improvement after OMB administration, as they did in our previous studies of the therapy on small animal models of ARDS injury. Furthermore, pigs receiving OMB or saline infusions had slightly lower survival than their ARDS counterparts. The OMB administration did not induce a statistically significant or clinically relevant therapeutic effect in this model; instead, both saline and OMB infusion appeared to lower survival rates slightly. This result is significant because it contradicts positive results from our previous small animal studies and places a limit on the efficacy of such treatments for larger animals under more severe respiratory distress. While OMB did not prove efficacious in this rapid-onset ARDS pig model, it may retain potential as a novel therapy for the usual presentation of ARDS in humans, which develops and progresses over days to weeks.

摘要

在 COVID-19 爆发之前,急性呼吸窘迫综合征(ARDS)的死亡率为 46%,在美国影响了 20 万人,导致 7.5 万人死亡。目前 COVID-19 ARDS 患者的死亡率为 39%。ARDS 的肺外支持旨在通过向患者提供维持生命的氧气来补充机械通气。在猪重症监护病房(ICU)中开发了一种新的快速发作、人体大小的猪 ARDS 模型。这些猪通过气管内雾化吸入高剂量(4mg/kg)内毒素脂多糖(LPS)2 小时,以诱导快速发作的中度至重度 ARDS。然后对它们进行导管插入术以监测生命体征,并评估通过胸腔内(IT)或腹腔内(IP)给药的含氧微泡(OMB)治疗的治疗效果。LPS 给药后,PaO 值降至 70mmHg 以下,PaO/FiO 比值降至 200mmHg 以下,心率增加,表明中度至重度 ARDS 伴有心动过速迅速发展(在 4 小时内)。与我们之前关于 ARDS 损伤小动物模型的治疗的研究一样,接受 LPS 损伤的猪在接受 OMB 治疗后,SpO 和 PaO 并没有显著改善。此外,接受 OMB 或盐水输注的猪的存活率略低于其 ARDS 对应物。在该模型中,OMB 给药没有引起统计学上显著或临床上相关的治疗效果;相反,盐水和 OMB 输注似乎都略微降低了生存率。这一结果很重要,因为它与我们之前的小动物研究的阳性结果相矛盾,并限制了此类治疗方法在更严重呼吸窘迫的较大动物中的疗效。虽然 OMB 在这种快速发作的 ARDS 猪模型中没有证明有效,但它可能作为一种新的治疗方法保留在人类中 ARDS 的常见表现,其在数天至数周内发展和进展。

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