New technologyNon-Invasive Cardiac Output Determination by Two-Dimensional Independent Doppler During and After Cardiac Surgery
Section snippets
Technology
After written consent, we prospectively studied 36 consecutive patients (26 males; mean age 67.2 ± 10 years; height 170 ± 8 cm; weight 79 ± 14 kg; New York Heart Association functional class 3.1 ± 0.3) undergoing surgical coronary revascularization, with a preoperative electrocardiogram demonstrating sinus rhythm without any higher grade supraventricular or ventricular arrhythmia.
The USCOM system is based on a 300 MHz National Semiconductor GEODE GX1 CPU with 64 MB SDRAM based on Microsoft
Technique
Intraoperatively 6 patients were studied after median sternotomy and revascularization, with CO simultaneously determined by PAC and the USCOM system with the transducer placed directly on the pulmonary artery after cessation of extracorporeal circulation. Postoperatively, all patients were monitored invasively with the PAC using the Baxter thermodilution system (Baxter Healthcare Corp, Irvine, CA), with simultaneous CO, stroke volume (SV), and central venous saturations (CVS) percentage
Hemodynamic Data
The mean heart rate was 103 ± 11 bpm, and the mean invasive systolic and diastolic blood pressures were 121 ± 21 mm Hg and 62 ± 13 mm Hg, respectively. Mean right atrial pressure was 9 ± 3 mm Hg, direct left atrial pressure was 13 ± 5 mm Hg, and CVS percentage was 72 ± 9%.
Invasive and Noninvasive Cardiac Output Data
Invasive CO measured by the PAC was 4.92 ± 2 L/min (95% confidence intervals, 4.63 to 5.22 L/min). The noninvasive Doppler device determined CO by the USCOM system was 5.15 ± 1.98 L/min (95% confidence intervals, 4.86 to 5.44
Comment
This study confirmed that it is feasible, using the transcutaneous USCOM device, to determine beat-to-beat CO in critically ill patients in the postcardiac surgical intensive care noninvasively. Measurements demonstrated a high correlation to invasively determined CO with a PAC as both correlated well with SV and CVS percentage. These findings confirm the reliability of the USCOM device and suggest that it may have multiple clinical applications in which the immediate and noninvasive assessment
Disclosures and Freedom of Investigation
The authors independently determined the design, method, outcome, data analysis, and writing of this article without influence from any external party.
Disclaimer
The Society of Thoracic Surgeons, the Southern Thoracic Surgical Association, and The Annals of Thoracic Surgery neither endorse nor discourage use of the new technology described in this article.
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The first two authors contributed equally to this work.