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Effects of continuous tracheal gas insufflation during pressure limited ventilation on pulmonary surfactant in rabbits with acute lung injury

机译:限压通气中连续气管充气对急性肺损伤家兔肺表面活性物质的影响

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Background Pulmonary surfactant dysfunction may contribute to the development of ventilator induced lung injury (VILI). Tracheal gas insufflation (TGI) is a technique in which fresh gas is introduced into the trachea and augment ventilation by reducing the dead space of ventilatory system, reducing ventilatory pressures and tidal volume (V_T) while maintaining constant partial arterial CO_2 pressure (PaCO_2). We hypothesised that TGI limited peak inspiratory pressure (PIP) and V_T and would minimize conventional mechanical ventilation (CMV) induced pulmonary surfactant dysfunction and thereby attenuate VILI in rabbits with acute lung injury (ALI). Methods ALI was induced by intratracheal administration of lipopolysaccharide in anaesthetized, ventilated healthy adult rabbits randomly assigned to continuous TGI at 0.5 L/min (TGI group) or CMV group (n=8 for each group), and subsequently ventilated with limited PIP and V_T to maintain PaCO_2 within 35 to 45 mmHg for 4 hours. Physiological dead space to V_T ratio (V_D/V_T), dynamic respiratory compliance (Cdyn) and partial arterial O_2 pressure (PaO_2) were monitored. After ventilation, lungs were analysed for total phospholipids (TPL), total proteins (TP), pulmonary surfactant small to large aggregates ratio (SA/LA) in bronchoalveolar lavage fluid (BALF) and for determination of alveolar volume density (V_V), myeloperoxidase and interleukin (IL)-8. Results TGI resulted in significant (P < 0.05 or P < 0.01) decrease in PIP [(22.4+1.8) cmH_2O vs (29.5±1.1) cmH_2O], V_T [(6.9±1.3) ml/kg vs (9.8±1.11) ml/kg], V_D/V_T [(32±5)% vs (46±2)%], TP [(109±22) mg/kg vs (187±25) mg/kg], SA/LA (2.5±0.4 vs 5.4±0.7), myeloperoxidase [(6.2±0.5) U/g tissue vs (12.3±0.8) U/g tissue] and IL-8 [(987±106) ng/g tissue vs (24±3) mN/m] of BALF, and significant (P < 0.05) increase in Cdyn [(0.47±0.02) ml •cmH_2O~(-1)•kg~(-1) vs (0.31±0.02) ml •cmH_2O~(-1) •kg~(-1)], PaO_2 [(175±24) mmHg vs (135±26) mmHg], TPL/TP (52±8 vs 33±11) and V_V (0.65±0.05 vs 0.44±0.07) as compared with CMV. Conclusions In this animal model of ALI, TGI decreased ventilatory requirements (PIP, V_T and V_D/V_T), resulted in more favourable alveolar pulmonary surfactant composition and function and less severity of lung injury than CMV. TGI in combination with pressure limited ventilation may be a lung protective strategy for ALI.
机译:背景技术肺表面活性物质功能障碍可能会导致呼吸机诱发的肺损伤(VILI)的发展。气管内注气(TGI)是一种将新鲜气体引入气管并通过减少通气系统的死腔,降低通气压力和潮气量(V_T)并同时保持恒定的局部动脉CO_2压力(PaCO_2)来增强通气的技术。我们假设TGI限制了峰值吸气压力(PIP)和V_T,并且将使传统的机械通气(CMV)引起的肺表面活性剂功能障碍减至最小,从而减轻了急性肺损伤(ALI)家兔的VILI。方法通过气管内脂多糖经气管内给予麻醉的,通气的健康成年兔,以0.5 L / min(TGI组)或CMV组(每组n = 8)随机分配为连续TGI,然后用有限的PIP和V_T通气,从而诱发ALI将PaCO_2维持在35至45 mmHg之间4小时。监测生理性死腔与V_T之比(V_D / V_T),动态呼吸顺应性(Cdyn)和动脉局部O_2压力(PaO_2)。通气后,分析肺中的总磷脂(TPL),总蛋白(TP),支气管肺泡灌洗液(BALF)中肺表面活性剂小到大聚集比(SA / LA),并测定肺泡体积密度(V_V),髓过氧化物酶和白介素(IL)-8。结果TGI导致PIP显着降低(P <0.05或P <0.01)[(22.4 + 1.8)cmH_2O与(29.5±1.1)cmH_2O],V_T [(6.9±1.3)ml / kg与(9.8±1.11)ml / kg],V_D / V_T [(32±5)%与(46±2)%],TP [(109±22)mg / kg与(187±25)mg / kg],SA / LA(2.5± 0.4 vs 5.4±0.7),髓过氧化物酶[(6.2±0.5)U / g组织vs(12.3±0.8)U / g组织]和IL-8 [(987±106)ng / g组织vs(24±3)mN / m],而Cdyn [(0.47±0.02)ml•cmH_2O〜(-1)•kg〜(-1)与(0.31±0.02)ml•cmH_2O〜(-1)显着(P <0.05)增加)•kg〜(-1)],PaO_2 [(175±24)mmHg对(135±26)mmHg],TPL / TP(52±8对33±11)和V_V(0.65±0.05对0.44±0.07)与CMV相比。结论在这种ALI动物模型中,与CMV相比,TGI降低了通气需求(PIP,V_T和V_D / V_T),导致肺泡肺表面活性物质组成和功能更有利,肺部损伤的严重程度降低。 TGI结合压力受限通气可能是ALI的肺保护策略。

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