Impedance cardiography


Impedance cardiography is a noninvasive technology measuring total electrical conductivity of the thorax and its changes in time to process continuously a number of cardiodynamic parameters, such as Stroke Volume, SV, Heart Rate, HR, Cardiac Output, CO, Ventricular Ejection Time, VET, Pre-ejection Period and used to detect the impedance changes caused by a high-frequency, low magnitude current flowing through the thorax between additional two pairs of electrodes located outside of the measured segment. The sensing electrodes also detect the ECG signal, which is used as a timing clock of the system.

Introduction

Impedance cardiography, also referred to as electrical impedance plethysmography or Thoracic Electrical Bioimpedance has been researched since the 1940s. NASA helped develop the technology in the 1960s. The use of impedance cardiography in psychophysiological research was pioneered by the publication of an article by Miller and Horvath in 1978. Subsequently, the recommendations of Miller and Horvath were confirmed by a standards group in 1990. A comprehensive list of references is available at . With ICG, the placement of four dual disposable sensors on the neck and chest are used to transmit and detect electrical and impedance changes in the thorax, which are used to measure and calculate cardiodynamic parameters.

How ICG Works

Hemodynamics is a subchapter of cardiovascular physiology, which is concerned with the forces generated by the heart and the resulting motion of blood through the cardiovascular system. These forces demonstrate themselves to the clinician as paired values of blood flow and blood pressure measured simultaneously at the output node of the left heart.
Hemodynamics is a fluidic counterpart to the Ohm's Law in electronics: pressure is equivalent to voltage, flow to current, vascular resistance to electrical resistance and myocardial work to power.
The relationship between the instantaneous values of aortic blood pressure and blood flow through the aortic valve over one heartbeat interval and their mean values are depicted in Fig.1. Their instantaneous values may be used in research; in clinical practice, their mean values, MAP and SV, are adequate.

Blood Flow Parameters

Systemic blood flow parameters are ' the blood flow per heartbeat, the Stroke Volume, SV , and ' the blood flow per minute, the Cardiac Output, CO .
There is clear relationship between these blood flow parameters:
CO = /1000
where HR is the Heart Rate frequency.
Since the normal value of CO is proportional to body mass it has to perfuse, one "normal" value of SV and CO for all adults cannot exist. All blood flow parameters have to be indexed. The accepted convention is to index them by the Body Surface Area, BSA , by DuBois & DuBois Formula, a function of height and weight:
BSA = W0.425 × H0.725 × 0.007184
The resulting indexed parameters are Stroke Index, SI defined as
SI = SV/BSA
and Cardiac Index, CI, defined as
CI = CO/BSA
These indexed blood flow parameters exhibit typical ranges:
For the Stroke Index: 35 < SItypical < 65 ml/beat/m²; for the Cardiac Index: 2.8 < CItypical < 4.2 l/min/m².
Eq.1 for indexed parameters then changes to
CI = /1000

Hemodynamics: The Dynamic Modulator of Oxygen Transport

The primary function of the cardiovascular system is transport of oxygen: blood is the vehicle, oxygen is the cargo. The task of the healthy cardiovascular system is to provide adequate perfusion to all organs and to maintain a dynamic equilibrium between oxygen demand and oxygen delivery. In a healthy patient, his or her cardiovascular system always increases blood flow in response to increased oxygen demand. However, in a hemodynamically compromised patient, when the system is unable to satisfy increased oxygen demand, the blood flow to organs lower on the oxygen delivery priority list is reduced and these organs may, eventually, fail. Digestive disorders, male impotence, tiredness, sleepwalking, environmental temperature intolerance, etc. are classical examples of a low-flow-state, resulting in reduced blood flow to the gut, sexual organs, skeletal muscles, skin, etc.

Hemodynamic Modulators

SI variability and MAP variability are accomplished through activity of hemodynamic modulators.
The conventional cardiovascular physiology terms for the hemodynamic modulators are preload, contractility and afterload. They deal with ' the inertial filling forces of blood return into the atrium, which stretch the myocardial fibers, thus storing energy in them, ' the force by which the heart muscle fibers shorten thus releasing the energy stored in them in order to expel part of blood in the ventricle into the vasculature, and the forces the pump has to overcome in order to deliver a bolus of blood into the aorta per each contraction.
The level of preload is currently assessed either from the PAOP in a catheterized patient, or from EDI by use of ultrasound. Contractility is not routinely assessed; quite often inotropy and contractility are interchanged as equal terms. Afterload is assessed from the SVRI value.
Rather than using the terms preload, contractility and afterload, the preferential terminology and methodology in per-beat hemodynamics is to use the terms for actual hemodynamic modulating tools, which either the body utilizes or the clinician has in his toolbox to control the hemodynamic state:
The preload and the Frank-Starling -induced level of contractility is modulated by variation of intravascular volume.
Pharmacological modulation of contractility is performed with cardioactive inotropic agents being present in the blood stream and affecting the rate of contraction of myocardial fibers.
The afterload is modulated by varying the caliber of sphincters at the input and output of each organ, thus the vascular resistance, with the vasoactive pharmacological agents. Afterload also increases with increasing blood viscosity, however, with the exception of extremely hemodiluted or hemoconcentrated patients, this parameter is not routinely considered in clinical practice.
Please note that with the exception of volume expansion, which can be accomplished only by physical means, all other hemodynamic modulating tools are pharmacological, cardioactive or vasoactive agents.
The measurement of CI and its derivatives allow clinicians to make timely patient assessment, diagnosis, prognosis, and treatment decisions. It has been well established that both trained and untrained physicians alike are unable to estimate cardiac output through physical assessment alone.

Invasive Hemodynamic Monitoring

Clinical measurement of cardiac output has been available since the 1970s. However, this blood flow measurement is highly invasive, utilizing a flow-directed, thermodilution catheter, which represents significant risks to the patient. In addition, this technique is costly and requires a skilled physician and a sterile environment for catheter insertion. As a result, it has been used only in very narrow strata of critically ill and high-risk patients in whom the knowledge of blood flow and oxygen transport outweighed the risks of the method. In the United States, it is estimated that at least two million pulmonary artery catheter monitoring procedures are performed annually, most often in peri-operative cardiac and vascular surgical patients, decompensated heart failure, multi-organ failure, and trauma.

Noninvasive Hemodynamic Monitoring

In theory, a noninvasive way to monitor hemodynamics would provide exceptional clinical value because data similar to invasive hemodynamic monitoring methods could be obtained with much lower cost and no risk. While noninvasive hemodynamic monitoring can be used in patients who previously required an invasive procedure, the largest impact can be made in patients and care environments where invasive hemodynamic monitoring was neither possible nor worth the risk or cost. Because of its safety and low cost, the applicability of vital hemodynamic measurements could be extended to significantly more patients, including outpatients with chronic diseases. ICG has even been used in extreme conditions such as outer space and a Mt. Everest expedition. Heart failure, hypertension, pacemaker, and dyspnea patients are four conditions in which outpatient noninvasive hemodynamic monitoring can play an important role in the assessment, diagnosis, prognosis, and treatment. Some studies have shown ICG cardiac output is accurate, while other studies have shown it is inaccurate. Use of ICG has been shown to improve blood pressure control in resistant hypertension when used by both specialists and general practitioners. ICG has also been shown to predict worsening status in heart failure.

ICG Parameters

The electrical and impedance signals are processed to determine fiducial points, which are then utilized to measure and calculate hemodynamic parameters, such as cardiac output, stroke volume, systemic vascular resistance, thoracic fluid content, acceleration index, and systolic time ratio.
ParameterDefinition
Heart RateNumber of heart beats each minute
Cardiac OutputAmount of blood pumped by the left ventricle each minute
Cardiac IndexCardiac output normalized for body surface area
Stroke VolumeAmount of blood pumped by the left ventricle each heartbeat
Stroke IndexStroke volume normalized for body surface area
Systemic Vascular ResistanceThe resistance to the flow of blood in the vasculature
Systemic Vascular Resistance IndexSystemic vascular resistance normalized for body surface area
Acceleration IndexPeak acceleration of blood flow in the aorta
Velocity IndexPeak velocity of blood flow in the aorta
Thoracic Fluid ContentThe electrical conductivity of the chest cavity, which is primarily determined by the intravascular, intraalveolar, and interstitial fluids in the thorax
Left Cardiac WorkAn indicator of the amount of work the left ventricle must perform to pump blood each minute
Left Cardiac Work IndexLeft cardiac work normalized for body surface area
Systolic Time RatioThe ratio of the electrical and mechanical systole
Pre Ejection PeriodThe time interval from the beginning of electrical stimulation of the ventricles to the opening of the aortic valve
Left Ventricular Ejection TimeThe time interval from the opening to the closing of the aortic valve