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Quantitative analysis of changes in blood concentrations and ‘presumed effect-site concentration’ of sevoflurane during one-lung ventilation

机译:定量分析单肺通气期间七氟醚的血药浓度和“估计作用部位浓度”的变化

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摘要

During one-lung ventilation, ventilation-perfusion mismatch decreases the arterial concentration of inhaled anaesthetics due to the arterial-to-venous concentration difference. This study tested the hypothesis that in humans, the ‘presumed effect-site concentration’ (taken as the mid-point between the arterial and superior jugular venous concentrations) of inhaled anaesthetic falls during one-lung (vs two-lung) ventilation. Four patients scheduled for elective prostatectomy (two-lung ventilation) and four patients for elective thoracotomy (one-lung ventilation) were randomly selected and assigned to receive sevoflurane (vaporiser-dial setting, 1.5%). Sevoflurane concentrations were measured periodically from radial artery and superior jugular vein (via a catheter advanced cephalad from the jugular vein). During one-lung ventilation, the end-expiratory sevoflurane concentration was stable at ~1.3% but the mean (SD) presumed effect-site concentration declined initially from 58 (6.7) to 43 (4.7) μg.ml?1 (p?=?0.011) before slowly recovering. A period of insufficient depth of anaesthesia is thus a risk during one-lung ventilation.
机译:在单肺通气期间,由于动脉与静脉之间的浓度差异,通气-灌注不匹配会降低吸入麻醉剂的动脉浓度。这项研究检验了以下假设:在人类中,单肺通气(相对于两肺)通气时,吸入麻醉药的“假定的作用部位浓度”(作为动脉和颈上静脉血药浓度之间的中点)。随机选择四名计划进行前列腺切除术(两肺通气)的患者和四名择期开胸手术(一肺通气)的患者,并分配其接受七氟醚的治疗(气化器拨盘设置,为1.5%)。定期测量radial动脉和颈上静脉的七氟醚浓度(通过颈静脉导管前移头)。在单肺通气期间,呼气末七氟醚浓度稳定在〜1.3%,但假定的效应部位平均浓度(SD)最初从58(6.7)降至43(4.7)μg.ml 1 < / sup>(p≥0.011),然后慢慢恢复。因此,在单肺通气期间存在麻醉深度不足的时期。

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  • 来源
    《Anaesthesia》 |2012年第10期|1125-1131|共7页
  • 作者单位

    Staff Physician Department of Anaesthesia Kasukabe-chuo General Hospital Saitama Japan and Graduate Student Department of Emergency and Critical Care Medicine Graduate School of Medicine The University of Tokyo Tokyo Japan;

    Department Chief Department of Anaesthesia Kasukabe-chuo General Hospital Saitama Japan;

    Executive Scientist Department of Clinical Development Maruishi Pharmaceutical Co. Ltd. Osaka Japan;

    Professor and Department Chair Department of Emergency and Critical Care Medicine Graduate School of Medicine The University of Tokyo Tokyo Japan;

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