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首页> 外文期刊>Anesthesia and Analgesia: Journal of the International Anesthesia Research Society >High-Flow Nasal Oxygen Improves Safe Apnea Time in Morbidly Obese Patients Undergoing General Anesthesia: A Randomized Controlled Trial
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High-Flow Nasal Oxygen Improves Safe Apnea Time in Morbidly Obese Patients Undergoing General Anesthesia: A Randomized Controlled Trial

机译:高流量的鼻氧气在经过一般麻醉的病态肥胖患者中改善了安全的呼吸暂停时间:随机对照试验

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BACKGROUND: Morbidly obese patients undergoing general anesthesia are at risk of hypoxemia during anesthesia induction. High-flow nasal oxygenation use during anesthesia induction prolongs safe apnea time in nonobese surgical patients. The primary objective of our study was to compare safe apnea time, between patients given high-flow nasal oxygenation or conventional facemask oxygenation during anesthesia induction, in morbidly obese surgical patients. METHODS: Research ethics board approval was obtained. Elective surgical patients >= 18 years with body mass index >= 40 kg center dot m(-2) were included. Patients with severe comorbidity, gastric reflux disease, known difficult airway, or nasal obstruction were excluded. After obtaining informed consent patients were randomized. In the intervention (high-flow nasal oxygenation) group, preoxygenation was provided by 100% nasal oxygen for 3 minutes at 40 L center dot minute(-1); in the control group, preoxygenation was delivered using a facemask with 100% oxygen, targeting end-tidal O-2 >85%. Anesthesia was induced with propofol, remifentanil, and rocuronium. Bag-mask ventilation was not performed. At 2 minutes after rocuronium, videolaryngoscopy was performed. If the laryngoscopy grade was I or II, laryngoscope was left in place and the study was continued; if grade III or IV was observed, the patient was excluded from the study. During the apnea period, high-flow nasal oxygenation patients received nasal oxygen at 60 L center dot minute(-1); control group patients received no supplemental oxygen. The primary outcome, safe apnea time, was reached when oxygen saturation measured by pulse oximetry (Spo(2)) fell to 95% or maximum 6 minutes of apnea. The patient was then intubated. T tests and chi(2) analyses were used to compare groups. P < .05 was considered significant. RESULTS: Forty patients completed the study. Baseline parameters were comparable between groups. Safe apnea time was significantly longer (261.4 +/- 77.7 vs 185.5 +/- 52.9 seconds; mean difference [95% CI], 75.9 [33.3-118.5]; P = .001) and the minimum peri-intubation Spo(2) was higher (91.0 +/- 3.5 vs 88.0 +/- 4.8; mean difference [95% CI], 3.1 [0.4-5.7]; P = .026) in the high-flow nasal oxygenation group compared to the control group. CONCLUSIONS: High-flow nasal oxygenation, compared to conventional oxygenation, provided a longer safe apnea time by 76 seconds (40%) and higher minimum Spo(2) in morbidly obese patients during anesthesia induction. High-flow oxygenation use should be considered in morbidly obese surgical patients.
机译:背景:经过一般麻醉的病态肥胖患者在麻醉诱导期间存在缺氧血症的风险。麻醉期间的高流量鼻氧合用途延长了非同一手术患者的安全呼吸暂停时间。我们研究的主要目的是比较安全的呼吸暂停时间,患者在麻醉诱导期间给予高流量的鼻氧合或常规面罩氧合,在病态肥胖的手术患者中。方法:研究伦理委员会批准。选修外科患者> = 18岁,体重指数> = 40kg中心点M(-2)。患有严重合并症,胃回流疾病,已知困难气道或鼻塞的患者被排除在外。获得知情同意后,患者随机化。在干预(高流量鼻氧化)基团中,在40L中心点分钟(-1)下通过100%鼻氧提供预氧化3分钟。在对照组中,使用具有100%氧的面罩递送预氧化,靶向潮端O-2> 85%。用异丙酚,雷芬菊酯和罗孔诱导麻醉。没有进行袋掩模通风。在罗科尼鎓后2分钟,进行录像镜检查。如果喉镜镜等级是I或II,则喉镜留下,继续研究;如果观察到III级或IV级,则从研究中排除患者。在呼吸暂停期间,高流量的鼻氧化患者在60L中心点分钟(-1)接受鼻氧;对照组患者没有补充氧气。当通过脉冲血氧血管测量(SPO(2))降至呼吸暂停的95%或最大6分钟时,达到主要结果,达到安全呼吸暂停时间。然后插管患者。 T测试和CHI(2)分析用于比较群体。 P <.05被认为是显着的。结果:四十名患者完成了研究。基线参数在组之间是可比的。安全的呼吸暂停时间明显更长(261.4 +/- 77.7 vs 185.5 +/- 52.9秒;平均差异[95%ci],75.9 [33.3-118.5]; p = .001)和最小的Peri-Intubation Spo(2)更高(91.0 +/- 3.5 Vs 88.0 +/- 4.8;与对照组相比,高流量鼻氧化合物中的平均差异[95%CI],3.1 [0.4-5.7]; p = .026)。结论:与常规氧合相比,高流量的鼻氧合,在麻醉诱导期间,在病态肥胖患者中提供了更长的安全呼吸暂停时间(40%)和较高的最小孢子(2)。在病态肥胖的手术患者中应考虑高流量氧合用途。

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