Non-arterial line cardiac output calculation misclassifies exercise pulmonary hypertension and increases risk of data

Luiz Campedelli1, S Mehdi Nouraie1,2, Michael G Risbano3,2

  • 1Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Pittsburgh School of Medicine and UPMC, Pittsburgh, PA, USA.

Insights

Using peripheral oxygen saturation (SpO2) instead of arterial oxygen saturation (SaO2) during invasive exercise testing can misclassify exercise pulmonary hypertension (ePH). This method also leads to significant data loss, especially in Black patients and those with scleroderma or Raynaud's.

Area of Science:

  • Cardiopulmonary physiology
  • Clinical exercise testing
  • Medical diagnostics

Background:

  • The direct Fick principle is standard for cardiac output (CO) calculation, crucial for detecting CO-dependent conditions like exercise pulmonary hypertension (ePH).
  • Fick CO calculations can utilize arterial (Hba, SaO2) or non-arterial (Hbmv, SpO2) values, with the latter used when arterial lines are absent.
  • Discrepancies in oxygen saturation and hemoglobin between arterial and non-arterial measurements may impact Fick CO calculations and ePH classification during exercise.

Purpose of the Study:

  • To compare SpO2 and SaO2, Hba and Hbmv, and COarterial vs. COnon-arterial in invasive cardiopulmonary exercise testing (iCPET).
  • To assess the risk of misclassifying pre- and post-capillary ePH using non-arterial measurements.
  • To evaluate data loss associated with inaccurate SpO2 during iCPET.

Main Methods:

  • Retrospective analysis of 296 iCPET studies.
  • Comparison of SpO2 (pulse oximetry) and SaO2 (radial arterial).
  • Assessment of Hba, Hbmv, COarterial, and COnon-arterial, and analysis of data loss and ePH misclassification.

Main Results:

  • Low correlation was observed between SpO2 and SaO2, and between COarterial and COnon-arterial.
  • Significantly higher data loss occurred with SpO2 (18%) compared to SaO2 (0.88%).
  • ePH was misclassified in 17.1% of pre-capillary and 8.7% of post-capillary cases using COnon-arterial. SpO2 data loss was higher in Black patients (31.6%) and those with scleroderma/Raynaud's (33.3%).

Conclusions:

  • Reliance on SpO2 during iCPET leads to misclassification of ePH.
  • Unmeasurable SpO2 in certain patient groups (Black, scleroderma, Raynaud's) limits diagnostic accuracy.
  • Invasive exercise testing without an arterial line may compromise diagnostic and prognostic value due to unreliable SpO2 measurements.
Abstract

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