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Champigneulle, Benoit; Reinhard, Lukas; Mademilov, Maamed; Marillier, Mathieu; Ulrich, Tanja; Carta, Arcangelo F.; Scheiwiller, Philipp; Shabykeeva, Saltanat B.; Sheraliev, Ulan U.; Abdraeva, Ainura K.; Magdieva, Kamila M.; Mirzalieva, Gulzada; Taalaibekova, Aijan T.; Ozonova, Aigul K.; Erkinbaeva, Aidai O.; Shakiev, Nurdin U.; Azizbekov, Syimyk A.; Ainslie, Philip N.; Sooronbaev, Talant M.; Ulrich, Silvia; Bloch, Konrad E.; Verges, Samuel; Furian, Michael

Multidisciplinary Digital Publishing Institute

Investigation of pulmonary gas exchange efficacy usually requires arterial blood gas analysis (aBGA) to determine arterial partial pressure of oxygen (mPaO₂) and compute the Riley alveolar-to-arterial oxygen difference (A-aDO₂); that is a demanding and invasive procedure. A noninvasive approach (AGM100), allowing the calculation of PaO₂ (cPaO₂) derived from pulse oximetry (SpO₂), has been developed, but this has not been validated in a large cohort of chronic obstructive pulmonary disease (COPD) patients. Our aim was to conduct a validation study of the AG100 in hypoxemic moderate-to-severe COPD. Concurrent measurements of cPaO₂ (AGM100) and mPaO₂ (EPOC, portable aBGA device) were performed in 131 moderate-to-severe COPD patients (mean ±SD FEV₁: 60 ± 10% of predicted value) and low-altitude residents, becoming hypoxemic (i.e., SpO₂ < 94%) during a short stay at 3100 m (Too-Ashu, Kyrgyzstan). Agreements between cPaO₂ (AGM100) and mPaO₂ (EPOC) and between the O₂-deficit (calculated as the difference between end-tidal pressure of O₂ and cPaO₂ by the AGM100) and Riley A-aDO₂ were assessed. Mean bias (±SD) between cPaO₂ and mPaO₂ was 2.0 ± 4.6 mmHg (95% Confidence Interval (CI): 1.2 to 2.8 mmHg) with 95% limits of agreement (LoA): −7.1 to 11.1 mmHg. In multivariable analysis, larger body mass index (p = 0.046), an increase in SpO₂ (p < 0.001), and an increase in PaCO₂-PETCO₂ difference (p < 0.001) were associated with imprecision (i.e., the discrepancy between cPaO₂ and mPaO₂). The positive predictive value of cPaO₂ to detect severe hypoxemia (i.e., PaO₂ ≤ 55 mmHg) was 0.94 (95% CI: 0.87 to 0.98) with a positive likelihood ratio of 3.77 (95% CI: 1.71 to 8.33). The mean bias between O₂-deficit and A-aDO₂ was 6.2 ± 5.5 mmHg (95% CI: 5.3 to 7.2 mmHg; 95%LoA: −4.5 to 17.0 mmHg). AGM100 provided an accurate estimate of PaO₂ in hypoxemic patients with COPD, but the precision for individual values was modest. This device is promising for noninvasive assessment of pulmonary gas exchange efficacy in COPD patients.

Article

eng

Vancouver : University of British Columbia Library

10.14288/1.0448050

Health and Social Development, Faculty of (Okanagan); Non UBC; Health and Exercise Sciences, School of (Okanagan)

10.3390/jcm12030795

Faculty; Researcher

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