TY - JOUR
T1 - Clinical validation of a computerized algorithm to determine mean systemic filling pressure
AU - Meijs, Loek P. B.
AU - van Houte, Joris
AU - Conjaerts, Bente C. M.
AU - Bindels, Alexander J. G. H.
AU - Bouwman, Arthur
AU - Houterman, Saskia
AU - Bakker, Jan
N1 - Funding Information:
This study was funded by the Catharina Hospital Intensive Care Research Fund.
Publisher Copyright:
© 2021, The Author(s).
PY - 2022/2
Y1 - 2022/2
N2 - Mean systemic filling pressure (Pms) is a promising parameter in determining intravascular fluid status. Pms derived from venous return curves during inspiratory holds with incremental airway pressures (Pms-Insp) estimates Pms reliably but is labor-intensive. A computerized algorithm to calculate Pms (Pmsa) at the bedside has been proposed. In previous studies Pmsa and Pms-Insp correlated well but with considerable bias. This observational study was performed to validate Pmsa with Pms-Insp in cardiac surgery patients. Cardiac output, right atrial pressure and mean arterial pressure were prospectively recorded to calculate Pmsa using a bedside monitor. Pms-Insp was calculated offline after performing inspiratory holds. Intraclass-correlation coefficient (ICC) and assessment of agreement were used to compare Pmsa with Pms-Insp. Bias, coefficient of variance (COV), precision and limits of agreement (LOA) were calculated. Proportional bias was assessed with linear regression. A high degree of inter-method reliability was found between Pmsa and Pms-Insp (ICC 0.89; 95%CI 0.72–0.96, p = 0.01) in 18 patients. Pmsa and Pms-Insp differed not significantly (11.9 mmHg, IQR 9.8–13.4 vs. 12.7 mmHg, IQR 10.5–14.4, p = 0.38). Bias was −0.502 ± 1.90 mmHg (p = 0.277). COV was 4% with LOA –4.22 − 3.22 mmHg without proportional bias. Conversion coefficient Pmsa ➔ Pms-Insp was 0.94. This assessment of agreement demonstrates that the measures Pms-Insp and the computerized Pmsa-algorithm are interchangeable (bias −0.502 ± 1.90 mmHg with conversion coefficient 0.94). The choice of Pmsa is straightforward, it is non-interventional and available continuously at the bedside in contrast to Pms-Insp which is interventional and calculated off-line. Further studies should be performed to determine the place of Pmsa in the circulatory management of critically ill patients. (www.clinicaltrials.gov; TRN NCT04202432, release date 16-12-2019; retrospectively registered). Clinical Trial Registrationwww.ClinicalTrials.gov, TRN: NCT04202432, initial release date 16-12-2019 (retrospectively registered).
AB - Mean systemic filling pressure (Pms) is a promising parameter in determining intravascular fluid status. Pms derived from venous return curves during inspiratory holds with incremental airway pressures (Pms-Insp) estimates Pms reliably but is labor-intensive. A computerized algorithm to calculate Pms (Pmsa) at the bedside has been proposed. In previous studies Pmsa and Pms-Insp correlated well but with considerable bias. This observational study was performed to validate Pmsa with Pms-Insp in cardiac surgery patients. Cardiac output, right atrial pressure and mean arterial pressure were prospectively recorded to calculate Pmsa using a bedside monitor. Pms-Insp was calculated offline after performing inspiratory holds. Intraclass-correlation coefficient (ICC) and assessment of agreement were used to compare Pmsa with Pms-Insp. Bias, coefficient of variance (COV), precision and limits of agreement (LOA) were calculated. Proportional bias was assessed with linear regression. A high degree of inter-method reliability was found between Pmsa and Pms-Insp (ICC 0.89; 95%CI 0.72–0.96, p = 0.01) in 18 patients. Pmsa and Pms-Insp differed not significantly (11.9 mmHg, IQR 9.8–13.4 vs. 12.7 mmHg, IQR 10.5–14.4, p = 0.38). Bias was −0.502 ± 1.90 mmHg (p = 0.277). COV was 4% with LOA –4.22 − 3.22 mmHg without proportional bias. Conversion coefficient Pmsa ➔ Pms-Insp was 0.94. This assessment of agreement demonstrates that the measures Pms-Insp and the computerized Pmsa-algorithm are interchangeable (bias −0.502 ± 1.90 mmHg with conversion coefficient 0.94). The choice of Pmsa is straightforward, it is non-interventional and available continuously at the bedside in contrast to Pms-Insp which is interventional and calculated off-line. Further studies should be performed to determine the place of Pmsa in the circulatory management of critically ill patients. (www.clinicaltrials.gov; TRN NCT04202432, release date 16-12-2019; retrospectively registered). Clinical Trial Registrationwww.ClinicalTrials.gov, TRN: NCT04202432, initial release date 16-12-2019 (retrospectively registered).
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U2 - 10.1007/s10877-020-00636-2
DO - 10.1007/s10877-020-00636-2
M3 - Article
C2 - 33791920
SN - 1387-1307
VL - 36
SP - 191
EP - 198
JO - Journal of Clinical Monitoring and Computing
JF - Journal of Clinical Monitoring and Computing
IS - 1
ER -