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重症监护病房中脉搏血氧饱和度床边测量准确性需求的证据。

Evidence for the need of bedside accuracy of pulse oximetry in an intensive care unit.

作者信息

Seguin P, Le Rouzo A, Tanguy M, Guillou Y M, Feuillu A, Mallédant Y

机构信息

Service de Réanimation Chirurgicale, CHRU de Pontchaillou, Rennes, France.

出版信息

Crit Care Med. 2000 Mar;28(3):703-6. doi: 10.1097/00003246-200003000-00017.

Abstract

OBJECTIVE

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.

DESIGN

Prospective clinical study.

SETTING

Surgical intensive care unit in a university hospital.

PATIENTS

Thirty-three patients with a pulse oximeter probe in whom arterial blood gas was measured with a radial artery line.

INTERVENTIONS

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.

MEASUREMENTS AND MAIN RESULTS

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%.

CONCLUSIONS

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%.

摘要

目的

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。

设计

前瞻性临床研究。

地点

大学医院的外科重症监护病房。

患者

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。

干预措施

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)。

测量指标及主要结果

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%。

结论

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。

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