Four different methods of measuring cardiac index during cytoreductive surgery and hyperthermic intraperitoneal

Amon Heijne1, Piet Krijtenburg1, Andre Bremers2

  • 1Department of Anesthesiology, Pain and Palliative Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.

Insights

Less invasive cardiac index (CI) monitoring methods like ClearSight, FloTrac, and ProAQT are unreliable during high-risk cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). These systems failed to accurately track CI compared to transpulmonary thermodilution (TPTD).

Area of Science:

  • Anesthesiology and Critical Care Medicine
  • Cardiovascular Hemodynamics
  • Surgical Oncology

Background:

  • Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) represent extensive, high-risk abdominal procedures.
  • Accurate cardiac index (CI) monitoring is crucial during high-risk surgeries, with a growing trend towards less invasive methods.
  • Existing less invasive CI monitoring techniques require validation in complex surgical settings like CRS-HIPEC.

Purpose of the Study:

  • To evaluate the accuracy and reliability of various less invasive cardiac index (CI) monitoring systems.
  • To compare CI measurements from ClearSight, FloTrac, ProAQT, and arterial pressure waveform analysis (APWA) against transpulmonary thermodilution (TPTD).
  • To assess the performance of these devices during cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in both the operating room and intensive care unit (ICU).

Main Methods:

  • Twenty-five patients undergoing CRS-HIPEC were enrolled in the study.
  • Simultaneous hemodynamic measurements, including cardiac index (CI), were collected at nine predefined time points.
  • Data analysis involved Bland-Altman plots, four-quadrant plots, and interchangeability assessments to compare CI measurements from TPTD with ClearSight, FloTrac, ProAQT, and APWA.

Main Results:

  • All tested devices (ClearSight, FloTrac, ProAQT, APWA) demonstrated significant bias and wide limits of agreement compared to transpulmonary thermodilution (TPTD).
  • Percentage errors and interchangeability rates were high across all devices, indicating poor agreement.
  • Trending capabilities, assessed by concordance and angular bias, were unsatisfactory for all less invasive methods, with low percentages of interchangeable data pairs.

Conclusions:

  • ClearSight, FloTrac, and ProAQT systems are not reliable for accurate cardiac index (CI) measurement during CRS-HIPEC when compared to TPTD.
  • The reproducibility of CI changes over time, evaluated through concordance, angular bias, and interchangeability, was insufficient for all tested devices.
  • These findings suggest caution when using less invasive CI monitoring in this specific high-risk surgical population.
Abstract