Seguin P, Le Rouzo A, Tanguy M, Guillou Y M, Feuillu A, Mallédant Y
Service de Réanimation Chirurgicale, CHRU de Pontchaillou, Rennes, France.
Crit Care Med. 2000 Mar;28(3):703-6. doi: 10.1097/00003246-200003000-00017.
To compare pulse oximetry saturation (Spo2 with arterial blood gas saturation (SaO2) obtained during clinical routine to determine the optimal lowest reliable value of SpO2 in ventilator-dependent patients before setting up a nurse-directed protocol of FIO2 titration.
Prospective clinical study.
Surgical intensive care unit in a university hospital.
Thirty-three patients with a pulse oximeter probe in whom arterial blood gas was measured with a radial artery line.
SPO2 was recorded by the nurses and compared with SaO2 obtained by blood gas analysis with a co-oximeter. Two sensors currently used in our surgical intensive care unit and connected to a monitor (HP OmniCare M1165/66A; Hewett Packard, Andover, MA) were tested. In group I, the Durensor DS 100A (Nellcor Puritan Bennett, Pleasanton, CA), a reusable sensor, was used. In group II, the Oxisensor D25L (Nellcor Puritan Bennett), a nonreusable sensor, was used.
In group 1, 64 data pairs were obtained. In this group, SaO2 ranged from 87 to 98% and SpO2 ranged from 92 to 100%. The bias was -1.90% and the limits of agreement ranged from -5.56 to 1.76%. In group 11, 47 data pairs were obtained. In this group, SaO2 ranged from 87 to 99% and SpO2 ranged from 92 to 100%. The bias was -2.49% and the limits of agreement ranged from -6.62 to 1.64%.
In the range of SaO2 tested, regardless of the sensor used, SpO2 overestimated SaO2. Large limits of agreement were found. Based on this result, the authors concluded that before defining a nurse-directed protocol of FIO2 titration with SpO2, the material used daily must be evaluated. A minimum threshold SpO2 value of 96% in both groups I and II is more reliable to ensure SaO2 > or = 90%.
比较临床常规操作中测得的脉搏血氧饱和度(Spo2)与动脉血气饱和度(SaO2),以确定在建立由护士指导的FiO2滴定方案之前,依赖呼吸机患者Spo2的最佳最低可靠值。
前瞻性临床研究。
大学医院的外科重症监护病房。
33例使用脉搏血氧仪探头且通过桡动脉穿刺测量动脉血气的患者。
护士记录Spo2,并与通过血气分析仪和血氧计测得的SaO2进行比较。对目前在我们外科重症监护病房使用并连接到监护仪(惠普OmniCare M1165/66A;惠普公司,马萨诸塞州安多弗)的两种传感器进行了测试。在第一组中,使用了可重复使用的Durensor DS 100A传感器(Nellcor Puritan Bennett公司,加利福尼亚州普莱森顿)。在第二组中,使用了不可重复使用的Oxisensor D25L传感器(Nellcor Puritan Bennett公司)。
在第一组中,获得了64对数据。在该组中,SaO2范围为87%至98%,Spo2范围为92%至100%。偏差为-1.90%,一致性界限范围为-5.56%至1.76%。在第二组中,获得了47对数据。在该组中,SaO2范围为87%至99%,Spo2范围为92%至100%。偏差为-2.49%,一致性界限范围为-6.62%至1.64%。
在所测试的SaO2范围内,无论使用哪种传感器,Spo2均高估了SaO2。发现一致性界限范围较大。基于该结果,作者得出结论,在定义由护士指导的基于Spo2的FiO2滴定方案之前,必须评估日常使用的材料。为确保SaO2≥90%,第一组和第二组中Spo2的最低阈值96%更为可靠。