Can we obtain a noninvasive and continuous estimation of cardiac output? Comparison between three noninvasive methods

Zainab Raissuni1, Florian Zores, Odile Henriet

  • 1Pôle d'Activité Médico-Chirurgicale Cardiovasculaire, Unité de prise en charge de I'insuffisance cardiaque et des cardiomyopathies Nouvel Hôpital Civil.

Insights

This study compared three noninvasive methods for measuring cardiac output (CO) in cardiac patients. While estimated continuous cardiac output (esCCO) showed good reproducibility, its agreement with other methods was less precise, suggesting potential for screening.

Area of Science:

  • Cardiology
  • Hemodynamics
  • Medical Devices

Background:

  • Assessing cardiac output (CO) is crucial for managing critically ill cardiac patients.
  • Noninvasive methods like inert gas rebreathing (IGR) and 2D-Doppler echocardiography are validated for CO measurement.
  • Estimated continuous cardiac output (esCCO) offers a novel approach using electrocardiogram, pulse oximetry, and arterial blood pressure.

Purpose of the Study:

  • To evaluate the agreement and reproducibility of esCCO compared to IGR and 2D-Doppler echocardiography for noninvasive CO calculation.
  • To assess the clinical utility of esCCO in critically ill cardiac patients.

Main Methods:

  • A comparative study involving 34 cardiac patients.
  • Simultaneous CO measurements using esCCO, IGR, and 2D-Doppler echocardiography.
  • Statistical analysis using Bland and Altman plots and intraclass correlation coefficients.

Main Results:

  • Good agreement observed between IGR and 2D-Doppler echocardiography (bias = 0.31 L/minute).
  • esCCO showed a larger bias compared to IGR (1.18 L/minute) and 2D-Doppler echocardiography (1.51 L/minute).
  • Intraclass correlation was poor across all methods, but esCCO demonstrated satisfactory reproducibility and accuracy.

Conclusions:

  • esCCO exhibits satisfactory reproducibility and accuracy, comparable to established methods.
  • The larger bias suggests esCCO may be more suitable for patient screening and monitoring rather than precise individual CO assessment.
  • Further validation is warranted for widespread clinical adoption in critical care settings.

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