首页> 外文期刊>Anesthesiology >Accuracy of postoperative end-tidal Pco2 measurements with mainstream and sidestream capnography in non-obese patients and in obese patients with and without obstructive sleep apnea.
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Accuracy of postoperative end-tidal Pco2 measurements with mainstream and sidestream capnography in non-obese patients and in obese patients with and without obstructive sleep apnea.

机译:非肥胖患者和有无阻塞性睡眠呼吸暂停的肥胖患者,采用主流和旁流二氧化碳描记术进行潮气末Pco2测量的准确性。

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BACKGROUND: Obtaining accurate end-tidal carbon dioxide pressure measurements via nasal cannula poses difficulties in postanesthesia patients who are mouth breathers, including those who are obese and those with obstructive sleep apnea (OSA); a nasal cannula with an oral guide may improve measurement accuracy in these patients. The authors evaluated the accuracy of a mainstream capnometer with an oral guide nasal cannula and a sidestream capnometer with a nasal cannula that did or did not incorporate an oral guide in spontaneously breathing non-obese patients and obese patients with and without OSA during recovery from general anesthesia. METHODS: The study enrolled 20 non-obese patients (body mass index less than 30 kg/m) without OSA, 20 obese patients (body mass index greater than 35 kg/m) without OSA, and 20 obese patients with OSA. End-tidal carbon dioxide pressure was measured by using three capnometer/cannula combinations (oxygen at 4 l/min): (1) a mainstream capnometer with oral guide nasal cannula, (2) a sidestream capnometer with a nasal cannula that included an oral guide, and (3) a sidestream capnometer with a standard nasal cannula. Arterial carbon dioxide partial pressure was determined simultaneously. The major outcome was the arterial-to-end-tidal partial pressure difference with each combination. RESULTS: In non-obese patients, arterial-to-end-tidal pressure difference was 3.0 +/- 2.6 (mean +/- SD) mmHg with the mainstream capnometer, 4.9 +/- 2.3 mmHg with the sidestream capnometer and oral guide cannula, and 7.1 +/- 3.5 mmHg with the sidestream capnometer and a standard cannula (P < 0.05). In obese non-OSA patients, it was 3.9 +/- 2.6 mmHg, 6.4 +/- 3.1 mmHg, and 8.1 +/- 5.0 mmHg, respectively (P < 0.05). In obese OSA patients, it was 4.0 +/- 3.1 mmHg, 6.3 +/- 3.2 mmHg, and 8.3 +/- 4.6 mmHg, respectively (P < 0.05). CONCLUSIONS: Mainstream capnometry performed best, and an oral guide improved the performance of sidestream capnometry. Accuracy in non-obese and obese patients, with and without OSA, was similar.
机译:背景:通过鼻插管获得准确的潮气末二氧化碳压测量值对呼吸困难的麻醉后患者(包括肥胖和阻塞性睡眠呼吸暂停(OSA)患者)造成了困难;带有鼻导管的鼻插管可以提高这些患者的测量准确性。作者评估了在从一般情况下恢复期间自发呼吸的非肥胖患者和肥胖患者(无论是否患有OSA)中,带口引导鼻导管的主流型二氧化碳监测仪和带或不带口引导的鼻导管侧向流二氧化碳监测仪的准确性。麻醉。方法:该研究招募了20例无OSA的非肥胖患者(体重指数小于30 kg / m),20例无OSA的肥胖患者(体重指数大于35 kg / m)和20例有OSA的肥胖患者。潮气末二氧化碳压力的测量是通过使用三种吹气仪/插管组合(氧气流量为4 l / min)进行的:(1)带有口腔引导鼻插管的主流吹气计,(2)带有鼻插管的侧流式吹气计(包括一个口腔)指南,以及(3)带有标准鼻插管的侧向流式二氧化碳监测仪。同时测定动脉二氧化碳分压。主要结果是每种组合的动脉到潮气分压差。结果:在非肥胖患者中,主流监护仪的潮气端到端潮气压差为3.0 +/- 2.6(平均+/- SD)mmHg,侧流监护仪和口腔导流管为4.9 +/- 2.3 mmHg ,并使用侧流二氧化碳分析仪和标准插管进行7.1 +/- 3.5 mmHg(P <0.05)。肥胖的非OSA患者分别为3.9 +/- 2.6 mmHg,6.4 +/- 3.1 mmHg和8.1 +/- 5.0 mmHg(P <0.05)。在肥胖的OSA患者中,分别为4.0 +/- 3.1 mmHg,6.3 +/- 3.2 mmHg和8.3 +/- 4.6 mmHg(P <0.05)。结论:主流二氧化碳分析法效果最好,口服指南改善了旁流二氧化碳分析法的性能。有和没有OSA的非肥胖和肥胖患者的准确性相似。

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