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Intratracheal Heparin Improves Plastic Bronchitis Due to Sulfur Mustard Analog

机译:气管内肝素可改善芥子气类似物导致的塑性支气管炎

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Background: Inhalation of sulfur mustard (SM) and SM analog, 2-chloroethyl ethyl sulfide (CEES), cause fibrinous cast formation that occludes the conducting airways, similar to children with Fontan physiology-induced plastic bronchitis. These airway casts cause significant mortality and morbidity, including hypoxemia and respiratory distress. Our hypothesis was that intratracheal heparin, a highly cost effective and easily preserved rescue therapy, could reverse morbidity and mortality induced by bronchial cast formation. Methods: Sprague-Dawley rats were exposed to 7.5% CEES via nose-only aerosol inhalation to produce extensive cast formation and mortality. The rats were distributed into three groups: non-treated, phosphate-buffered saline (PBS)-treated, and heparin-treated groups. Morbidity was assessed with oxygen saturations and clinical distress. Blood and bronchoalveolar lavage fluid (BALF) were obtained for analysis, and lungs were fixed for airway microdissection to quantify the extent of airway cast formation. Results: Heparin, given intratracheally, improved survival (100%) when compared to non-treated (75%) and PBS-treated (90%) controls. Heparin-treated rats also had improved oxygen saturations, clinical distress and airway cast scores. Heparin-treated rats had increased thrombin clotting times, factor Xa inhibition and activated partial thromboplastin times, indicating systemic absorption of heparin. There were also increased red blood cells (RBCs) in the BALF in 2/6 heparin-treated rats compared to PBS-treated control rats. Conclusions: Intratracheal heparin 1hr after CEES inhalation improved survival, oxygenation, airway obstruction, and clinical distress. There was systemic absorption of heparin in rats treated intratracheally. Some rats had increased RBCs in BALF, suggesting a potential for intrapulmonary bleeding if used chronically after SM inhalation. Pediatr Pulmonol. 2015; 50:118-126. (c) 2014 Wiley Periodicals, Inc.
机译:背景:吸入硫芥子油(SM)和SM类似物2-氯乙基乙基硫化物(CEES)会导致纤维状铸型形成,从而阻塞传导气道,这类似于患有Fontan生理学诱发的塑料性支气管炎的儿童。这些气道铸型会导致严重的死亡率和发病率,包括低氧血症和呼吸窘迫。我们的假设是,气管内肝素是一种高成本效益且易于保存的抢救疗法,可逆转由支气管铸型形成引起的发病率和死亡率。方法:通过仅鼻喷雾吸入使Sprague-Dawley大鼠暴露于7.5%CEES,以产生大量的铸型和死亡率。将大鼠分为三组:未治疗组,磷酸盐缓冲盐水(PBS)治疗组和肝素治疗组。通过氧饱和度和临床困扰评估发病率。获得血液和支气管肺泡灌洗液(BALF)进行分析,并固定肺以进行气道显微解剖,以量化气道铸型形成的程度。结果:与未治疗(75%)和PBS治疗(90%)对照相比,气管内给予肝素可提高生存率(100%)。肝素治疗的大鼠还具有改善的血氧饱和度,临床窘迫和气道石膏得分。肝素治疗的大鼠凝血酶凝血时间增加,Xa因子抑制作用和部分凝血活酶激活时间增加,表明肝素被全身吸收。与用PBS治疗的对照大鼠相比,用2/6肝素治疗的大鼠的BALF中的红细胞(RBC)也增加。结论:CEES吸入后1小时气管内肝素可改善生存率,氧合作用,气道阻塞和临床困扰。气管内处理的大鼠肝素有全身吸收。一些大鼠的BALF中的RBC增加,表明如果在SM吸入后长期使用,可能会引起肺内出血。小儿科薄荷油。 2015; 50:118-126。 (c)2014年威利期刊有限公司

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