A tiny current

Four sensors on the left side, two at the base of the neck and two at and below the lower ribs, pass a 50 kHz current of at most 2 mA through the thorax and measure its conductivity.

Isolate the beat

Breathing and tissue change conductivity slowly. Filtering keeps the fast, heartbeat-synchronous part of the signal; the method models its peak rate of change on accelerating aortic flow.

Cells line up

The model behind the method: in diastole, red cells in the aorta lie randomly; when the aortic valve opens, pulsatile flow aligns them with the flow and conductivity rises sharply.

From speed to volume

How fast the alignment happens gives peak aortic acceleration and left-ventricular ejection time. A patented algorithm converts them into stroke volume, beat by beat.

Watch one heartbeat, slowed down

The aorta on the left and the signals on the right run on the same clock. Step between diastole and systole to see the cells turn, and conductivity rise as they line up.

Diastoleaortic valve closed · cells lie randomly

Red blood cells in a segment of the aorta With the aortic valve closed the cells lie in random orientations. When the valve opens, flow lines them up along the vessel and the conductivity bar rises. Aortic valve Flow Red blood cells, schematic: not to scale
Conductivity at baseline
ECG, conductivity change and its rate of change over one beat A cursor sweeps across one heartbeat. After the R wave of the ECG, the aortic valve opens at point B; conductivity rises (impedance falls) while the valve is open, and its rate of change peaks early, at point C, before the valve closes at point X. ECG Conductivity change (−ΔZ) Its rate of change (dZ/dt) R C B X aortic valve open
  • B: valve opens · X: valve closes
  • C: peak rate of change
A teaching model of the principle Electrical Cardiometry is based on, running about three times slower than a heart at 75 beats per minute. Cell shapes, numbers and timing are schematic. Conductivity change is drawn upwards: as conductivity rises, impedance (Z) falls.

Placing the sensors

Four sensors, one side, placed in minutes

All four sensors go on the patient's left side. The outer pair carries the small current; the inner pair measures the voltage it produces, from which the monitor reads the conductivity of the thorax.

Sensor placement on an adult, front view Patient's left is on your right. Sensor 1 on the left side of the neck and sensor 2 at the base of the neck, about 5 cm apart. Sensor 3 on the lower left thorax at the level of the xiphoid, sensor 4 10 to 15 cm below it. Current flows between sensors 1 and 4; sensors 2 and 3 measure voltage. xiphoid level V 10–15 cm ≈ 5 cm current path L R 1 2 3 4
Front view: the patient's left is on your right. Schematic positions; follow the manufacturer's current instructions for use for exact placement.
  1. 1 · 2
    Base of the neck, left. Two sensors about 5 cm apart.
  2. 3 · 4
    Lower left thorax. One at the level of the xiphoid, one 10–15 cm below it.
  3. 1 + 4
    Outer pair: current. The 50 kHz current of at most 2 mA runs between them, through the thorax.
  4. 2 + 3
    Inner pair: voltage. Measures the voltage between them, from which the monitor reads the conductivity of the thorax.
Neonatal placement: outer sensors on the forehead and the thigh 1 2 3 4

Neonates and small children. In neonates and small children the outer two sensors can go on the forehead and the thigh.

What the monitor needs

WeightHeightAgeSex
Stroke volume and output
+ Blood pressure+ CVP+ Haemoglobin+ SpO₂
SVR and oxygen delivery

Stroke volume and output need only the patient's weight, height, age and sex; SVR and oxygen delivery also need blood pressure, CVP, haemoglobin and SpO₂. The patient should lie still and quiet, and values appear within seconds.

The heart and the aorta, front view Blood leaves the left ventricle through the aortic valve into the ascending aorta, over the aortic arch and down the descending thoracic aorta. The aorta is highlighted because the method models its signal on accelerating flow there. LV Ascendingaorta Pulmonaryartery Aortic valve Aortic arch Descendingthoracic aorta
Schematic, not to scale. Heart icon used elsewhere on this page: Health Icons, healthicons.org (MIT licence).
Where the signal is modelled

From the aortic valve to the thoracic aorta

Breathing and tissue change conductivity slowly. Filtering keeps the fast, heartbeat-synchronous part of the signal; the method models its peak rate of change on accelerating aortic flow, from the valve through the ascending aorta and arch to the thoracic aorta, which runs along the path of the current.

How it differs from older thoracic bioimpedance: classic impedance cardiography read the beat-to-beat signal as a change in blood volume in the chest. Electrical Cardiometry reads it as a velocity signal from aligning red cells, which is meant to hold up better across body sizes, from preterm babies to obese patients.

Impedance cardiography

Reads the beat as a change in blood volume in the chest.

Electrical Cardiometry

Reads it as a velocity signal from aligning red cells.

The heart, illustrated

The pump behind every number

On the left, the heart from the front, with the aortic arch and its three branches above it. On the right, the heart cut open in systole: the aortic valve is open and red cells stream into the aorta, lined up with the flow. That alignment is the change in conductivity the sensors pick up.

AI-generated teaching illustrations (Magnific), checked for the structures named here; artistic, not an anatomical reference.

Reading the waveform

Where the timing numbers come from

The monitor times every beat against the ECG. The points on the rate-of-change curve (dZ/dt) mark when the aortic valve opens and closes and when flow accelerates fastest; the intervals between them give several of the parameters below.

Annotated ECG and dZ/dt waveform The ECG R wave is followed by point B on the dZ/dt curve, where the aortic valve opens. The pre-ejection period runs from the start of the Q wave to B. The curve peaks at C, read as peak aortic acceleration, the basis of ICON. Point X, the trough, marks aortic valve closure. Left-ventricular ejection time runs from B to X. The RR interval is the time between two R waves. RR interval ECG dZ/dt R Q B C peak → ICON X valve closes valve opens PEP LVET STR = PEP ÷ LVET FTc = LVET ÷ √RR
Schematic waveforms for teaching, not a recording. The shaded band is ejection, with the aortic valve open.
R
The ECG R wave: the electrical start of the beat that the monitor times everything against.
B
Aortic valve opening: blood starts to leave the ventricle and the dZ/dt curve turns upward.
C
The peak of dZ/dt, read as peak acceleration of aortic blood flow: the basis of ICON.
X
Aortic valve closure: the trough that ends ejection.
PEP
Pre-ejection period: from the start of the Q wave to valve opening (B).
LVET
Left-ventricular ejection time: from valve opening (B) to closure (X).
STR
Systolic time ratio, PEP/LVET.
FTc
Corrected flow time: ejection time corrected for heart rate, LVET / √RR interval.
Osypka Medical monitors: the hand-held ICON in front, with a larger bedside monitor and a module behind it
ICON® monitor (Osypka Medical)
The method and the monitors

In clinical use since 2002

2002Osypka Medical launched the method
≈ 200clinical studies listed by the manufacturer
4skin sensors, no line, any age
Secondsuntil the first values appear

Osypka Medical launched the method in 2002 and lists close to 200 clinical studies, including comparisons with thermodilution, Fick and echocardiography. It is available on Osypka Medical's ICON® (hand-held) and ICONCORE® (PC-based) monitors.

Agreement for absolute values is moderate; changes over time are more reliable than single readings.

Trending holds best for routine changes (a leg raise, a fluid challenge, drug titration) and is weaker with large fluid shifts, vasoplegia after bypass, movement and shivering.

Measuring cardiac output

Electrical Cardiometry among the other methods

Every way of measuring cardiac output trades accuracy against invasiveness, cost and skill. Knowing the alternatives tells you when a non-invasive trend is enough and when it is not.

Catheter through the heart

Pulmonary artery catheter

Thermodilution through a right-heart catheter. The historical reference, with pressures and mixed venous saturation, but invasive and with its own risks.

Central line + arterial line

Transpulmonary thermodilution

Cold indicator through a central line, read at an arterial catheter; usually combined with pulse-contour analysis for continuous values.

Arterial line

Pulse-contour analysis

Stroke volume estimated from the arterial waveform, calibrated or not. Needs an arterial line; less reliable when vascular tone changes fast.

Probe in the oesophagus

Oesophageal Doppler

Descending aortic flow from a probe in the oesophagus. Used in theatre for goal-directed fluid therapy; needs a sedated patient.

Ultrasound probe

Echocardiography

Stroke volume from the LV outflow tract area and VTI, plus structure, valves and function. Operator-dependent and intermittent, but irreplaceable for the cause.

Four skin sensors

Electrical Cardiometry™

Four skin sensors, any age, continuous, no line. Moderate agreement for absolute values; strongest for trends and responses to treatment. Available on Osypka Medical's ICON® (hand-held) and ICONCORE® (PC-based) monitors.

Reading the screen

Every parameter, in plain words

Indexed values (the ones ending in “I”) adjust for body size so patients of different size can be compared: flows are divided by body surface area (CI = CO / BSA, SI = SV / BSA), while resistance is multiplied by it (SVRI = SVR × BSA, or 80 × (MAP − CVP) / CI). Children and neonates still have their own normal ranges, and neonatal output is often expressed per kilogram. Reference values below are typical for an adult; the monitor calculates its own range for each patient's age and size, as a visual guide only.

Blood flowHow much blood is the heart moving?

HR

Heart rate

Beats per minute, taken from an ECG-like signal between two of the sensors (not a diagnostic ECG). Together with stroke volume it sets cardiac output.

bpm · adult ≈ 55–90
SV / SI

Stroke volume / stroke index

Blood ejected by the left ventricle with each beat. The first number to look at in shock.

mL · mL/m² · adult SV ≈ 60–130 mL
CO / CI

Cardiac output / cardiac index

Blood pumped per minute: heart rate × stroke volume. The flow that delivers oxygen.

L/min · L/min/m² · adult CI ≈ 2.5–4.0

Vascular resistanceHow hard do the vessels push back?

SVR / SVRI

Systemic vascular resistance

How hard the vessels push back. Calculated from mean arterial pressure, central venous pressure and cardiac output, so it is only as good as the entered or default CVP and the latest cuff pressure. Without a central line, CVP is entered by hand or left at a default, so SVR is an estimate: an unrecognised CVP of 18 mmHg, for example, makes it read too high. Low in sepsis; high in hypovolaemic and cardiogenic shock and in hypertension.

dyn·s·cm⁻⁵ · SVR = 80 × (MAP − CVP) / CO · adult ≈ 900–1500

ContractilityHow strongly does the heart eject?

ICON™

Index of contractility

Peak acceleration of aortic blood flow: how forcefully the ventricle ejects. It is load-dependent, changing with preload and afterload as well as contractility, and it can fall before blood pressure does.

no unit · adult ≈ 40–60
VIC™

Variation of index of contractility

Respiratory variation of the ICON value. Like SVV, it mostly reflects changes in filling with ventilation, not true changes in contractility.

%
STR

Systolic time ratio

Pre-ejection period divided by LV ejection time (PEP/LVET). A rough, qualitative pointer to ejection fraction: it rises as the ventricle weakens, but also with low preload and with conduction delay such as bundle-branch block or pacing.

ratio · adult ≈ 0.3–0.5
CPI

Cardiac power index

The heart's hydraulic power output indexed to body size: MAP × CI / 451. A strong marker of prognosis in cardiogenic shock. (Some brochures call it the cardiac performance index.)

W/m²

Fluid statusToo little fluid, or too much?

TFC

Thoracic fluid content

The baseline conductivity of the chest, which rises with fluid inside and outside the vessels, in the lungs and chest wall. It cannot separate intravascular volume, lung water, effusions, ascites and chest-wall oedema, so use it as a trend: follow its trend in heart failure, fluid therapy and weaning.

1/kΩ · adult ≈ 25–35
SVV

Stroke volume variation

Swing in stroke volume with breathing. High values (roughly above 10–13%, with a grey zone) suggest fluid responsiveness, but only with controlled ventilation and no spontaneous breaths, sinus rhythm, a tidal volume of about 8 mL/kg or more, and a closed chest. Not valid with spontaneous breathing, arrhythmia, low-tidal-volume ventilation or most neonatal ventilation. In adults, use a passive leg raise instead; in children and neonates, leg-raise methods and thresholds are less established, so use a small fluid challenge with close reassessment and echocardiography.

% · ≈ 5–15
FTc

Corrected flow time

Ejection time corrected for heart rate (LVET / √RR interval). Short values point to low preload or high afterload. Low specificity: not a fluid-responsiveness test on its own.

ms · ≈ 300–500

Oxygen and pressureIs enough oxygen reaching the tissues, at what pressure?

DO₂ / DO₂I

Oxygen delivery

Oxygen carried to the tissues per minute, from cardiac output, haemoglobin and SpO₂ (entered or imported).

mL/min · mL/min/m²
MAP

Mean arterial pressure

Calculated from the entered systolic and diastolic pressures.

mmHg

Bars show the typical adult range on a fixed scale, as a visual guide only. Heart icon: Health Icons, healthicons.org (MIT licence).

Children are not small adults

What “normal” looks like in newborns

Newborns pump about 200–270 mL of blood per kilogram per minute, three to four times the adult figure. Their unindexed vascular resistance looks enormous (around 10,000 dyn·s·cm⁻⁵) simply because the body is tiny; indexed values and age-specific ranges are what matter. Never compare unindexed values across ages. Measured by Electrical Cardiometry in these studies:

PopulationValueStudy
Healthy term newborns, day 1–2Left-ventricular output 534 ± 105 mL/minNoori et al., 2012
Low and very-low-birth-weight infantsCardiac output 265 ± 49 mL/kg/minGrollmuss and Gonzalez, 2014
Preterm infantsCardiac output about 200 mL/kg/minSong et al., 2014
Stable preterm infantsStroke volume 3.1 ± 1.5 mL (echo 1.9 mL: EC reads higher)Boet et al., 2016
Very-low-birth-weight infants with a ductus (mean 929 g)HR 163 ± 12 · CI 2.82 ± 0.56 L/min/m² · SVR about 10,500 dyn·s·cm⁻⁵Lien et al., Eur J Pediatr 2014

Values are study means and spreads, not cut-offs. Electrical Cardiometry tends to read higher than echocardiography in preterm infants, so follow each baby's own trend.

Patterns at a glance

Four mechanisms of shock, four fingerprints

The same low blood pressure can come from an empty tank (hypovolemic), a weak pump (cardiogenic), open vessels (distributive: sepsis, anaphylaxis) or a blocked circuit (obstructive: tamponade, pulmonary embolism, tension pneumothorax). The flow numbers help tell them apart. Typical patterns, not rules: mixed pictures are common, and obstructive shock needs bedside imaging to confirm.

Typical hemodynamic pattern by type of shock
ShockSVCOHRSVRICONSTRTFC
Hypovolemic↓↓ / =↑↑↓ / =↑↓
Cardiogenic↓↓↑= / ↑↓↑= / ↑
Distributive: septic (after fluid)=↑↑↓↑ / ↓==
Distributive: anaphylactic↓ (early = / ↑)↓ (early = / ↑)↑↓↓=== / ↓
Obstructive↓↓↑↑== / ↑=

↑ high · ↓ low · = normal. Adapted from Osypka Medical teaching material, which lists thoracic fluid in cardiogenic shock as normal or low; it is shown here as possibly raised because pulmonary congestion is common. Late septic shock can turn low-output when the heart tires. STR rises in hypovolaemia because ejection time shortens; septic ICON can be high (hyperdynamic) or low (septic cardiomyopathy); established anaphylaxis is a low-preload, low-flow state, although flow can be normal or high early on.

Know its limits

When to be careful with the numbers

Like every monitor, Electrical Cardiometry has situations where it should not be used or should be read with caution. In comparison studies, percentage errors against reference methods are often 30–40%, so it is not interchangeable with them for absolute values: trends and responses to treatment are more reliable than any single value. Trending holds best for routine changes (a leg raise, a fluid challenge, drug titration) and is weaker with large fluid shifts, vasoplegia after bypass, movement and shivering.

Not suitable

  • Open chest: thoracotomy or open-heart surgery
  • Ventricular assist devices or an artificial heart
  • High-frequency ventilation
  • Rate-responsive pacemakers that use impedance-based minute ventilation
  • During external defibrillation

Read with caution

  • Moderate to severe aortic regurgitation; intracardiac shunts and a large patent ductus
  • Arrhythmia such as atrial fibrillation, and frequent ectopics (SVV in particular)
  • Marked obesity, massive chest-wall oedema, pleural effusions or chest drains
  • Intra-aortic balloon pump or ECMO
  • Movement, talking, shivering; electrosurgery nearby
  • Sensors moved off their standard positions

Summarised from the ICON instructions for use and Osypka training material. Always check the waveforms and the signal-quality indicator before acting on a value, and follow the manufacturer's current instructions for use.

Where it is used

From the NICU to the dialysis unit

Intensive care

Shock assessment, fluid and vasopressor guidance in adult and paediatric ICUs.

Neonatology

Studied in preterm and term neonates, where invasive lines carry the most risk. Best used for trends, paired with echocardiography.

Anaesthesia and surgery

Goal-directed therapy in liver transplant, neuro, orthopaedic and cardiac surgery.

Emergency and transport

Helping to distinguish cardiogenic, septic and hypovolemic shock early.

Cardiology

Heart failure, hypertension, the cath lab and pacemaker optimisation.

Obstetrics and nephrology

Preeclampsia and postpartum bleeding; dry weight in haemodialysis.

Application areas as listed by Osypka Medical. Indications and local registration vary by country.