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Measurement of cardiac output

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Title: Measurement of cardiac output


1
Measurement of cardiac output
  • Dr Kavitha Lakshman

University College of Medical Sciences GTB
Hospital, Delhi
2
Methods used for measurement of Cardiac Output
  • Invasive
  • PA catheter
  • - Ficks cardiac output measurement
  • - Thermodilution Technique
  • - Mixed venous oximetry pulmonary catheter
  • Minimally invasive
  • Doppler Ultrasound
  • Lithium dilution cardiac output monitoring
  • Pulse contour cardiac output monitoring
  • Transpulmonary thermodilution
  • Non-invasive
  • Bio impedence cardiac output monitoring
  • Partial carbon dioxide re breathing cardiac
    output monitoring

3
INVASIVE METHODS OF CARDIAC OUTPUT MEASUREMENT
(PAC)
4
  • PULMONARY ARTERY CATHETERISATION
  • First used by Swan, Ganz for hemodymamic
    monitoring of patients
  • PAC can be placed from any central venous
    cannulation sites, but right internal jugular
    vein is most commonly used.
  • Standard PAC is 7.0 to 9.0 Fr in circumference,
    110 cm long, has 4 internal lumens

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PHYSIOLOGICAL CONCEPTS OF CARDIAC OUTPUT
MEASUREMENT
7
  • INDICATOR DILUTION TECHNIQUE
  • Tracer substance is injected into the bloodstream
    concentration change measured at a
    downstream site
  • Indocyanin green most commonly used dye
  • Stewart Hamilton Equation
  • I
  • Q
  • ? CI dt
  • Where
  • Q CO
  • I Amount of indicator
  • ? CI dt Integral of indicator concentration
    over time
  • Drawbacks of indicator dilution method
  • Limited to cardiac catheterization laboratories
  • Continuous withdrawal of arterial blood to plot
    the dye concentration curve
  • Dye needs regular injections (can accumulate)

8
  • Other guidelines for placement waveforms
    were already discussed

9
  • Complication of PA catheterisation-
  • Infection, endocarditis
  • Thrombo embolism
  • Endocardial damage, valve injury
  • PA infarction
  • PA rupture
  • Catheter knotting
  • Ventricular fibrillation, arrhythmia, RBBB

10
Bolus - Thermodilution Cardiac Output Monitoring
  • Variant of indicator dilution technique
  • Iced indicator/ room temperature indicator
    (bolus)- 10 ml or 0.15ml/kg in children
  • Advantages
  • Performed quickly, repeatedly
  • Does not require advanced diagnostic or technical
    skills
  • Uses non-toxic, non-accumulative indicator

11
Stewart Hamilton equation is modified
  • (TB TI) x K
  • Q
  • ? ? TB (t) dt
  • Where
  • Q CO
  • TB Blood temp.
  • TI Injectate temp.
  • K Computational constant
  • ? ? TB (t) dt Integral of temp. change over
    time

12
  • Method
  • Volume of ice cold or room temperature fluid is
    injected as bolus
  • ?
  • Change in pulmonary artery blood temperature is
    recorded
  • Source of error
  • Intra or extra-cardiac shunt
  • Tricuspid or pulmonary valve regurgitation
  • Inadequate delivery of indicator
  • Thermister malfunction
  • Unrecognised blood temperature fluctuation
  • Respiratory cycle influence

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Continuous - Thermodilution CO monitoring
  • Warm or cold thermal indicator
  • Methods
  • Release of small quantity of heat from a 10 cm
    thermal filament incorporated into right
    ventricular portion of a PAC approx. 15-20 cm
    from catheter tip
  • ?
  • Heating filament is cycled on off
  • ?
  • Thermal signal measured
  • ?
  • CO derived from cross-correlation of measured
    pulmonary artery temp.
  • ?
  • Displayed value of CO is updated every 30-60 sec
    represents the average value for cardiac output
    measured over 3-6 min

15
  • Advantages
  • External system for cold fluid injection is not
    required
  • Fewer measurement error
  • Less risk of fluid overload and infection
  • Measures average CO value - derived over several
    mins
  • Beat-to-beat variation in SV that occur during
    single respiratory cycle are equally represented
  • In contrast bolus technique measures cardiac
    output values depending on phase of respiration

16
MINIMALLY INVASIVE METHODS OF CARDIAC OUTPUT
MEASUREMENT
17
Doppler Ultrasound
  • Doppler principle
  • When USG waves strike moving objects, these waves
    are reflected back to their source at a different
    frequency, termed the Doppler shift frequency
    that is directly related to the velocity of
    moving object and the angle at which the USG beam
    strikes these objects
  • Red blood cells serve as moving object target

18
2
  • Where
  • f Doppler shift frequency
  • v Velocity of red blood cell targets
  • f0 Transmitted USG beam frequency
  • 0 Angle b/w the USG beam and the vector of
    RBC flow
  • C Velocity of USG in blood (approx. 1570
    m/sec)
  • Cosine 0 1 as long as angle of insonation
    is small

19
SV v x ET x CSA
  • Where
  • SV Stroke volume
  • v Spatial average velocity of blood
    flow (cm/sec)
  • ET Systolic ejection time
  • CSA Cross-sectional area of vessel
  • -Estimated CSA close to the mean value during
    systole obtained from a nomogram stored in the
    computer
  • -Measured CSA using an M mode echo transducer
    incorporated in the probe

20
  • Types of probe-Suprasternal(Ascending aorta)

  • Esophageal(Descending aorta)
  • Suprasternal probe position instability limited
    their use for extended period of time
  • Esophageal probes have 2 advantage over the
    suprasternal probe
  • Smooth muscle tone of the oesophagus maintains
    the probe position
  • Its in close proximity to the aorta thereby
    minimizing signal interference

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22
The shape of the waveform allows Assessment of
the venticular preload, afterload and
contractility
23
PULSE CONTOUR CARDIAC OUTPUT MONITORING
  • Cardiac output is determined through analysis of
    arterial pressure wave form obtained from an
    arterial catheter or from a non invasive finger
    blood pressure waveform
  • CO is measured on a beat to beat basis
  • Wesseling and colleagues devised an algorithm
    for the calculation of SV from aortic impedence
    and changes in arterial pressure during systole
  • SV ? dP/dt
  • Z

24
  • Advantage-
  • It has the potential for continuous, beat to beat
    monitoring of cardiac output
  • Disadvantage-
  • Baseline calibration with known cardiac output is
    required
  • Recalibration is required every 8 to 12 hrs
    Require calibration to compensate for the
    algorithms inability to independently assess the
    ever changing effects of vascular tone
  • A well defined arterial pressure waveform is
    needed

25
  • Pulse contour cardiac output estimation without
    external calibration(Flo Trac)
  • Doesnt require external calibration
  • The algorithm works on the principle that SV is
    directly proportional to pulse pressure and
    inversely proportional to aortic compliance
  • The aortic pressure is sampled at 100Hz analysed
    and updated every 20 sec
  • SV K(SdAP)
  • The standard deviation-SdAP is proportional to
    the pulse pressure, which is proportional to SV.
    K is the constant derived from patient
    characteristics as described by Langewouler and
    co workers

26
NON INVASIVE CARDIAC OUTPUT MEASUREMENT
27
BIOIMPEDENCE CARDIAC OUTPUT MONITORING
  • Developed by Kubiceck and NASA researchers in
    1960s
  • Based on changes in electrical resistance of the
    thoracic cavity occurring with change in aortic
    blood volume during systole diastole
  • 4Pairs -Each pair of electrode consists of a
    transmitting and a sensing electrode
  • Two pairs are applied to the base of the neck on
    opposite sides, two pairs are applied to the
    lateral aspect of the thorax at the level of the
    xiphoid process on opposite sides

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  • The electrodes mark the upper and lower
    boundaries of the thorax
  • An alternating current of low amplitude and high
    frequency is applied which is sensed by
    electrodes placed over the neck lateral aspect
    of the chest.
  • Volume of thorax is calculated according to the
    height, weight and gender

30
  • Advantage-
  • Non invasive, continuous monitoring
  • Measures thoracic fluid content, left ventricular
    ejection time, cardiac index
  • Disadvantage-
  • Susceptibility to electrical interference
  • Relies on correct placement of the electrodes

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32
References
  • Lailu M, Kalyan RK. Cardiac output monitoring.
    Annals of Cardiac monitoring.2008 1156-61
  • Jhanji S, Dawson J and Pearse R M. Cardiac output
    monitoringbasic science and clinical
    application. Anaesthesia .2008 172-78
  • Rebecca A, Schroeder, Atilio B, Shahar B and
    Jonathan B. Cardiovascular Monitoring. Millers
    Anaesthesia 7th edition 1314-21
  • William F Ganong, Review of medical physiology
    22nd edition 819
  • Kaplan JA. Hemodynamic monitoring. Kaplans
    Cardiac Anaesthesia 5th edition 283-86
  • Edward Morgan.Patient monitors. Clinical
    Anaesthesiology 4th edition 137-139

33
  • THANK YOU
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