Wolfson Marla R, Enkhbaatar Perenlei, Fukuda Satoshi, Nelson Christina L, Williams Robert O, Surasarang Soraya Hengsawas, Sahakijpijarn Sawittree, Calendo Gennaro, Komissarov Andrey A, Florova Galina, Sarva Krishna, Idell Steven I, Shaffer Thomas H
Department of Thoracic Medicine & Surgery, Physiology & Pediatrics, and Temple Lung Center, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, USA.
Department of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, USA.
Clin Transl Med. 2020 Jan;10(1):258-274. doi: 10.1002/ctm2.26.
Effective clinical management of airway clot and fibrinous cast formation of severe inhalational smoke-induced acute lung injury (ISALI) is lacking. Aerosolized delivery of tissue plasminogen activator (tPA) is confounded by airway bleeding; single-chain urokinase plasminogen activator (scuPA) moderated this adverse effect and supported transient improvement in gas exchange and lung mechanics. However, neither aerosolized plasminogen activator (PA) yielded durable improvements in physiologic responses or reduction in cast burden. Here, we hypothesized that perfluorochemical (PFC) liquids would facilitate PA distribution and sustain improvements in physiologic outcomes in ISALI.
Spontaneously breathing adult sheep (n = 36) received anesthesia and analgesia and were instrumented, exposed to cotton smoke inhalation, and supported by mechanical ventilation for 48 h. Groups (n = 6/group) were studied without supplemental treatment, or, starting 4 h post injury, they received intratracheal low volume (8 mL) PFC liquid alone or a dose range of tPA/PFC or scuPA/PFC suspensions (4 or 8 mg in 8 mL PFC) every 8 h. Outcomes were evaluated by sequential measurements of cardiopulmonary parameters, lung histomorphology, and biochemical analyses of bronchoalveolar lavage fluid.
Dose-response and PA-type comparisons of outcomes demonstrated sustained superiority with low-volume PFC suspensions of scuPA over tPA or PFC alone, favoring the highest dose of scuPA/PFC suspension over lower doses, without airway bleeding.
We propose that this improved profile over previously reported aerosolized delivery is likely related to improved dose distribution. Sustained salutary responses to scuPA/PFC suspension delivery in this translational model are encouraging and support the possibility that the observed outcomes could be of clinical importance.
对于严重吸入性烟雾所致急性肺损伤(ISALI)的气道血凝块和纤维蛋白铸型形成,目前缺乏有效的临床管理方法。组织纤溶酶原激活剂(tPA)雾化给药会因气道出血而受到干扰;单链尿激酶型纤溶酶原激活剂(scuPA)可减轻这种不良反应,并支持气体交换和肺力学的短暂改善。然而,两种雾化的纤溶酶原激活剂(PA)均未在生理反应上产生持久改善,也未减轻铸型负荷。在此,我们假设全氟化合物(PFC)液体将促进PA的分布,并维持ISALI生理结局的改善。
36只自主呼吸的成年绵羊接受麻醉和镇痛处理,进行仪器植入,吸入棉烟,并接受机械通气支持48小时。研究分组(每组n = 6)为:不进行补充治疗,或在受伤后4小时开始,每隔8小时给予气管内低容量(8 mL)PFC液体,或不同剂量范围的tPA/PFC或scuPA/PFC混悬液(8 mL PFC中含4或8 mg)。通过连续测量心肺参数、肺组织形态学以及支气管肺泡灌洗的生化分析来评估结局。
结局的剂量反应和PA类型比较表明,scuPA低容量PFC混悬液比单独的tPA或PFC具有持续优势,最高剂量的scuPA/PFC混悬液优于较低剂量,且无气道出血。
我们认为,与先前报道的雾化给药相比,这种改善可能与剂量分布改善有关。在这个转化模型中,scuPA/PFC混悬液给药产生的持续有益反应令人鼓舞,并支持所观察到的结局可能具有临床意义的可能性。