Masimo总血红蛋白SpHb®连续无创血红蛋白监测设备与使用静脉样本的实验室全血细胞计数测量的比较:妊娠风险和婴儿监测与测量联盟母婴健康(PRISMA MNH)研究的观察性亚研究方案。

Gates Open Research Pub Date : 2024-02-05 eCollection Date: 2023-01-01 DOI:10.12688/gatesopenres.14499.1
Fouzia Farooq, Emily R Smith, Qing Pan, Sasha Glass Baumann, Victor Akelo, Fyezah Jehan, Margaret Kasaro, Imran Nisar, Gregory Ouma, Bellington Vwalika, M Bridget Spelke, Joan T Price, Zahra Hoodbhoy
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引用次数: 0

摘要

背景:Masimo Total Hemoglobin SpHb®是一种用于测量血红蛋白水平的连续无创手持设备。先前的研究发现,SpHb能够准确检测成年患者的血红蛋白水平,其偏差和标准偏差与护理点侵入性方法测量的偏差和标准差相似。一般来说,临床证据有限,Masimo在高于和低于血红蛋白阈值时缺乏验证,以及支持使用Masimo进行准确的血红蛋白检测以诊断妊娠期贫血的科学共识,都需要进一步研究。方法和分析:拟议的前瞻性队列将嵌套在正在进行的妊娠风险和婴儿监测与测量联盟(PRISMA)母婴健康(MNH)研究中。三个研究地点(位于赞比亚、肯尼亚和巴基斯坦)将参与并收集五个时间点的血红蛋白数据(结论:本研究的主要目的是评估无创Masimo设备与妊娠期和产后有创血红蛋白测量金标准方法相比诊断贫血的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of Masimo Total Hemoglobin SpHb® continuous non-invasive hemoglobin monitoring device with laboratory complete blood count measurement using venous sample: Protocol for an observational substudy of the Pregnancy Risk and Infant Surveillance and Measurement Alliance Maternal and Newborn Health (PRISMA MNH) study.

Comparison of Masimo Total Hemoglobin SpHb® continuous non-invasive hemoglobin monitoring device with laboratory complete blood count measurement using venous sample: Protocol for an observational substudy of the Pregnancy Risk and Infant Surveillance and Measurement Alliance Maternal and Newborn Health (PRISMA MNH) study.

Comparison of Masimo Total Hemoglobin SpHb® continuous non-invasive hemoglobin monitoring device with laboratory complete blood count measurement using venous sample: Protocol for an observational substudy of the Pregnancy Risk and Infant Surveillance and Measurement Alliance Maternal and Newborn Health (PRISMA MNH) study.

Background: The Masimo Total Hemoglobin SpHb® is a continuous and non-invasive handheld device to measure hemoglobin levels. Previous research has found that SpHb is able to accurately detect hemoglobin levels in adult patients with a similar degree of bias and standard deviation to point-of-care invasive method measurements. Generally, limited clinical evidence, lack of validation of Masimo at higher than and lower than hemoglobin threshold values, and scientific consensus supporting the use of Masimo for accurate hemoglobin testing for the diagnosis of anemia during pregnancy calls for further research.

Methods and analysis: The proposed prospective cohort will be nested within the ongoing Pregnancy Risk and Infant Surveillance and Measurement Alliance (PRISMA) Maternal and Newborn Health (MNH) study. Three study sites (located in Zambia, Kenya, and Pakistan) will participate and collect hemoglobin data at five time points (<20 weeks, 20 weeks, 28 weeks, 36 weeks' gestation, and six weeks postpartum). We will measure hemoglobin using a venous blood sample via hematology auto-analyzer complete blood count (gold standard) and the non-invasive device. The primary objective is to assess agreement between Masimo total hemoglobin and complete blood count and on a continuous scale using Intraclass Correlation Coefficient and Bland-Altman Analysis. The second objective is to assess agreement between the two measures on a binary scale using Positive Percentage Agreement and Negative Percentage Agreement, Cohen's Kappa, and McNemar Test. On an ordinal scale, agreement will be measured using Weighted Cohen's Kappa and Harrel's Concordance Index. Lastly, we will assess factors that might affect the accuracy of Masimo total hemoglobin using linear mixed models.

Conclusions: The primary aim of this study is to assess the validity of the non-invasive Masimo device compared to the gold standard method of invasive hemoglobin measurements during pregnancy and postpartum periods for the diagnosis of anemia.

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来源期刊
Gates Open Research
Gates Open Research Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
3.60
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90
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