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letter
. 2020 May 6;34(12):3488–3490. doi: 10.1053/j.jvca.2020.04.050

Table 1.

Technologies Available for Hemodynamic Monitoring in COVID-19 Patients

Monitoring Device Measurement Method Parameters Major Advantages Major Disadvantages
PAC Thermodilution Measurements: right atrial and ventricular pressures, PAP, PCWP, SvO2 (continuously with specialized PACs)
Calculations: CO, SVR, PVR, RVEF
Provides numerous variables to gauge volume status and cardiac function; minimizes expenditure of hospital resources; reliable in ARDS management High PEEP could lead to overestimation of LV volume by increasing PADP; invasive monitor with risk of PA perforation; equivocal effectiveness in altering clinical outcomes
PiCCO TPTD, pulse wave analysis CO, SV, SVV, PPV
Volumetric assessments: GEDV, EVLW, PVPI
Continuous, accurate CO relative to PAC; provides volumetric measures of preload (GEDV) and pulmonary edema (EVLW, PVPI); associated with favorable ARDS outcomes Invasive monitor that requires CVC and arterial catheter*
LiDCO Transpulmonary lithium dye dilution, pulse wave analysis CO, SV, SVV, PPV Continuous, accurate CO relative to PAC; requires arterial catheter without the need for CVC Unreliable with use of muscle relaxants; not yet examined in ARDS management*
FloTrac Pulse wave analysis CO, SV, SVV, PPV Easy-to-use, operator-independent system Accuracy of CO remains equivocal, especially in the setting of low SVR; SVV is poorly predictive of volume responsiveness*
NICOM Thoracic bioreactance CO, SV, SVV Continuous, accurate CO that correlates with fluid responsiveness, irrespective of hemodynamic instability or arrhythmias; noninvasive device that uses electrodes Not yet examined in ARDS management
Esophageal Doppler Doppler ultrasound in the esophagus at 45° relative to the descending aorta CO, SV Accurate assessment of CO and fluid responsiveness; provides invaluable information about preload, afterload, and contractility Expertise required because improper positioning of the esophageal probe can underestimate CO
Echocardiography (transthoracic, transesophageal) 2D and 3D imaging; pulsed wave Doppler CO; dynamic parameters of volume responsiveness, ie, respiratory variations in venocaval size, as well as changes in ventricular size, LVOT, VTI, and LV filling pressure Detects numerous pathophysiological states, such as wall motion abnormalities, LV diastolic dysfunction, and pericardial effusions No continuous monitoring; expertise required

Abbreviations: CO, cardiac output; CVC, central venous catheter; EVLW, extravascular lung water; GEDV, global end-diastolic volume; LiDCO, lithium dilution cardiac output; LV, left ventricle; LVOT, left ventricular outflow tract; NICOM, noninvasive cardiac output monitoring; PAC, pulmonary artery catheter; PADP, pulmonary artery diastolic pressure; PAP, pulmonary arterial pressure; PCWP, pulmonary capillary wedge pressure; PEEP, positive end-expiratory pressure; PiCCO, pulse index contour cardiac output; PPV, pulse pressure variation; PVPI, pulmonary vascular permeability index; PVR, pulmonary vascular resistance; RVEF, right ventricular ejection fraction; SvO2, mixed venous oxygen saturation; SV, stroke volume; SVV, stroke volume variation; SVR, systemic vascular resistance; TPTD, transpulmonary thermodilution; VTI, velocity-time integral.

Pulse contour analysis may be less accurate in the setting of arrhythmias, valve pathology, intracardiac shunts, and extracorporeal circulation.