动静脉二氧化碳清除术(AVCO/sub 2/R)治疗严重呼吸衰竭

J. Zwischenberger, Dongfong Wang, S. Alpard, C. Savage, D. Deyo, F. Schmalstieg, A. Bidani
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引用次数: 0

摘要

在急性呼吸窘迫综合征(ARDS)期间,通过简单的动静脉分流器中的低阻力气体交换器去除动静脉二氧化碳(AVCO/sub - 2/R)能够实现接近全部的CO/sub - 2/去除和肺休息。在一项前瞻性、随机、对照、非盲的7天无呼吸机天数和生存率研究中,我们评估了AVCO/sub 2/R对LD/sub 50/ smoke/burn(36次呼吸,40% III/spl度/ TBSA) ARDS模型的影响。所有的AVCO/sub 2/R羊存活,而只有2只SHAM动物存活。AVCO/ sub2 /R患者依赖呼吸机时间为2.4天,SHAM患者为6.5天。在我们的初步患者经验中,5名无反应的严重ARDS患者在床边成功插管AVCO/sub 2/R,并完成72小时的试验,其中3/5患者出院。AVCO/sub 2/R去除约70%的CO/sub 2/。从基线到48 h呼吸机参数的变化包括潮气量、峰值吸气压、分钟通气量和呼吸速率的下降。然后对8例ARDS患者进行AVCO/sub 2/R的前后对比研究。尽管每分钟通气量较基线降低,且ph值正常化,但PaCO/sub 2/仍显著降低。我们建议CO/sub 2/的正常化和每分钟通气量的减少可改善ARDS的病理生理。
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Arterio venous carbon dioxide removal (AVCO/sub 2/R) for severe respiratory failure
Arteriovenous carbon dioxide removal (AVCO/sub 2/R) by a low-resistance gas exchanger in a simple arteriovenous shunt is capable of achieving near total CO/sub 2/ removal and lung rest during acute respiratory distress syndrome (ARDS). We evaluated AVCO/sub 2/R effect on a LD/sub 50/ smoke/burn (36 breath, 40% III/spl deg/ TBSA) ARDS model in a prospective, randomized, controlled, unblinded 7-day outcomes study of ventilator free days and survival. All AVCO/sub 2/R sheep survived, while only 2 SHAM animals survived the 7-day study. AVCO/sub 2/R had 2.4 ventilator dependent days versus 6.5 days with SHAM. For our initial patient experience, 5 adults in unresponsive, severe ARDS were successfully cannulated for AVCO/sub 2/R at bedside and completed the 72-h trial and 3/5 patients were discharged. AVCO/sub 2/R removed approximately 70% of CO/sub 2/. Changes in ventilator parameters from baseline to 48 h included a decrease in tidal volume, peak inspiratory pressure, minute ventilation, and respiratory rate. Next, a before-after study of AVCO/sub 2/R was performed on 8 subjects with ARDS. PaCO/sub 2/ decreased significantly despite a decrease in minute ventilation from baseline and normalization of pH. We propose the normalization of CO/sub 2/ and decreased minute ventilation allows amelioration of the pathophysiology of ARDS.
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