评估两种脉搏血氧仪在患有紫绀型和无紫绀型先天性心脏病婴儿中的准确性。

IF 1.7 4区 医学 Q2 ANESTHESIOLOGY Pediatric Anesthesia Pub Date : 2024-12-01 Epub Date: 2024-10-04 DOI:10.1111/pan.15017
Yordan Hristov Georgiev, Felix Neunhoeffer, Michael Hofbeck, Jörg Michel
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引用次数: 0

摘要

背景:通过外周测量的血氧饱和度(SpO2)与通过联合血氧饱和度测量的动脉血氧饱和度(SaO2)经常会有差异,尤其是在较低的血氧饱和度范围内。这可能会影响先天性心脏病患儿的临床决策和治疗,因为严重的低氧血症可能会被忽视。目的:我们的目的是研究两种不同的脉搏血氧仪与 SaO2 相比在先天性心脏病婴儿中的准确性:方法:将两种不同脉搏血氧仪(飞利浦 IntelliVue X3 监护仪和 Nellcor™ OxiMax™)同时记录的 SpO2 与动脉血气分析获得的 SaO2 进行比较:共对 44 名动脉血氧饱和度在 70% 到 100% 之间的婴儿进行了 153 次测量。我们将测量结果分为 3 个亚组:第 1 组--SaO2 70.0%-85.0%;第 2 组--SaO2 85.1%-94.0%;第 3 组--SaO2 >94.1%。对于 Philipps,第 1、2 和 3 组的中位偏差分别为 5.3(IQR:2.6-8.7)%、2.3(IQR:0.9-6.0)% 和 1.1(IQR:-0.8-2.4)%。对于 OxiMax™,第 1、2 和 3 组的偏差中值分别为 2.7 (IQR:0.5-5.1)%、0.2 (IQR:-0.9-2.6) % 和 -0.5 (IQR:-1.3-0.6)%。关于这些血氧仪的准确性,根据准确性均方根指数(Arms)评估,Philipps 和 OxiMax™ 的准确性分别为:第 1 组 9.8% 对 4.5%,第 2 组 4.5% 对 2.9%,第 3 组 2.4% 对 1.9%:在饱和度介于 70% 和 85% 之间的较低范围内,两种脉搏血氧仪的准确度都超过了美国食品药品管理局 (FDA) 建议的≤3% 的阈值。因此,考虑到外周脉搏血氧仪的局限性,对于患有先天性心脏病的婴儿,应谨慎解释较低血氧饱和度范围内的外周脉搏血氧仪。对于患有紫绀型先天性心脏病的儿童,应首选直接辅助血氧饱和度测量法来支持临床决策。
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Assessment of accuracy of two pulse oximeters in infants with cyanotic and acyanotic congenital heart diseases.

Background: Peripherally measured oxygen saturation (SpO2) may often differ from arterial oxygen saturation (SaO2), measured by co-oximetry, especially within the lower range of oxygen saturations. This can potentially impact clinical decisions and therapy in children with congenital heart disease, as critical hypoxemia might remain unnoticed.

Aims: Our aim was to investigate the accuracy of two different pulse oximeters compared to SaO2 in infants with congenital heart diseases.

Methods: Simultaneous recordings of SpO2, measured by two different pulse oximeters (Philips IntelliVue X3 Monitor and Nellcor™ OxiMax™), were compared to SaO2 obtained by arterial blood gas analysis.

Results: A total of 153 measurements were performed in 44 infants with arterial oxygen saturation between 70 and 100%. We divided the measurements into 3 subgroups: group 1-SaO2 70.0%-85.0%, group 2-SaO2 85.1%-94.0%, group 3-SaO2 >94.1%. For Philipps, the median bias was 5.3 (IQR: 2.6-8.7) %, 2.3 (IQR: 0.9-6.0) % and 1.1 (IQR: -0.8-2.4) % in group 1, 2 and 3, respectively. For OxiMax™, the median bias was 2.7 (IQR: 0.5-5.1) %, 0.2 (IQR: -0.9-2.6) % and -0.5 (IQR: -1.3-0.6) % in group 1, 2 and 3, respectively. Regarding the accuracy of these oximeters, as evaluated with the Accuracy root mean squared index (Arms), it was 9.8 versus 4.5% in group 1, 4.5 versus 2.9% in group 2 and 2.4 versus 1.9% in group 3 for Philipps and OxiMax™, respectively.

Conclusions: In lower range saturations between 70% and 85% the accuracy of both pulse oximeters exceeded the threshold of ≤3% recommended by the Food and Drug Administration (FDA). Therefore, peripheral pulse oximetry within the lower range of oxygen saturations should be interpreted with caution in infants with congenital heart diseases, taking into consideration its limitations. Direct co-oximetry should be the preferred method to support clinical decisions in children with cyanotic congenital heart diseases.

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来源期刊
Pediatric Anesthesia
Pediatric Anesthesia 医学-麻醉学
CiteScore
3.20
自引率
11.80%
发文量
222
审稿时长
3-8 weeks
期刊介绍: Devoted to the dissemination of research of interest and importance to practising anesthetists everywhere, the scientific and clinical content of Pediatric Anesthesia covers a wide selection of medical disciplines in all areas relevant to paediatric anaesthesia, pain management and peri-operative medicine. The International Editorial Board is supported by the Editorial Advisory Board and a team of Senior Advisors, to ensure that the journal is publishing the best work from the front line of research in the field. The journal publishes high-quality, relevant scientific and clinical research papers, reviews, commentaries, pro-con debates, historical vignettes, correspondence, case presentations and book reviews.
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