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    Arterialbasedcontinuouscardiacoutputmeasurement

    factorfiction

    HermannGilly,PhD

    DepartmentofAnaesthesia,GeneralIntensiveCareMedicineandPain

    Therapy

    MedicalUniversityVienna,Vienna,Austria

    Arterial based, less invasive techniques for cardiac output

    measurementThe long road from bolus dilution to continuous cardiac outputNowadays: Fact or Fiction?Methods

    PAC Thermodilution thegoldenstandard

    (Quasi)ContinuousCOmeasurement

    PICCO

    PRAM

    LiDCo

    APCOcomparedwithGoldstandard

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    Whyhemodynamicmonitoring?

    Why

    Cardiac

    output

    (CO)

    measurement?

    Oxygenhastobecontinuouslydeliveredtothetissuesforsustainablecellularfunction

    Determinantsofoxygendelivery

    Oxygenatedhemoglobin

    Cardiacoutput

    Manipulationofcardiacoutput

    Fluidmanagement Pharmacologicinterventions

    Resultinginin ordecreasingvesselresistance,heartrateetc.

    Invasiveversuslessinvasivehemodynamicmonitoring

    Mostinvasivecontinuous Em/USflowprobearoundaortaorpulmonaryartery

    Invasive(quasicontinuous) u monaryarterycat eter , wan anz

    Continuous(lessinvasive) Arterialpressurebased(APCOetc)

    TransesophagealDoppler CO2 rebreathing

    Lessinvasive,intermittent

    Noninvasive,continuous Transthoracicbioimpedance

    AIM:minimally(=less) orevennon invasive continuousCOmeasurement

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    Methods

    for

    Cardiac

    Output

    measurement

    FickprincipleInputoutputbalance

    Indicatordilution

    Ultrasound

    Dopplervelocity

    Ventricledimensions/volumes

    Directmeasurement

    mpe ancecar ograp yPulsecontour

    Modelbasedmethods

    Ficksprinciple

    oxygenuptake

    Intermittent atbest,slowresponseassteadystateisrequired,invasiveca

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    Thermodilution Bolustechnique

    Calculationof

    areaunder

    curve(AUC)pulmonaryTD transpulmonaryDD

    thedecayofthe

    dilutioncurve

    normalcardiacoutput

    PACGoldstandard Bolusthermodilution

    Primaryparameter:timecourseoftemperatureinpulmonaryarteryorinaperipheralarteryafterinjectinganamountofcold

    Influencedby: temperaturechangesduetosimultaneousinfusions

    appropriatemixing ventilation,phase

    injection

    T

    siteofmeasurement nofinaloffset propertiesofcatheter

    possible

    loss

    of

    indicator

    (extravasal) high/lowflowsituation (softwarerelease)

    primaryendpoint:CardiacOutput(CO)

    t

    secondary: ejectionfraction,(central)bloodvolume

    oxygensaturation,oxygendelivery

    whencombinedwithDD:EVLW

    requiresinvasiveinstrumentation:PAC

    34singledeterminations(averaging)

    Overallaccuracy:1015%

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    Continuouspulmonarythermal(heat)dilutionclinicalvalidationincomparisontocoldbolusTD

    FrombolusTDtocontinuousTD (vigilancemonitor)

    IntelliCath OptiQ

    /min)

    min)

    CCOTD(

    C

    COTD(L

    (CCO+TD)/2(L/min) (CCO+TD)/2(L/min)

    acceptable

    C Zllner, et al: Continuous cardiac output measurements do not agree with conventional bolus thermodilution

    cardiac output determination. CAN J ANESTH 2001 48: 11 ; 11431147

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    F Mielck, W Buhre, G Hanekop, T Tirilomis, R Hilgers, H Sonntag. Comparison of Continuous CardiacOutput Measurements in Patients After Cardiac Surgery. Journal of Cardiothoracic and Vascular Anesthesia,Vol 17, No 2 (April), 2003: pp 211216

    FeaturesofPAC (TD,DD,bolus&cont)

    EnsureenoughoxygenisdeliveredtomeetmetabolicdemandbyCOandScvO2

    Provideinsightfor augmentingoxygendelivery, fluidsvsvasoactingdrugsbyCVP,PAP,PAWP

    Responsetimenotimmediatebecauseofaveragingseveralcardiaccycles

    Invasive,relativelypronetocomplications

    CurrentstatusofPAC

    over CVC

    Probably reserved for patients with significant cardiacpathology/major morbidities (septic shock, large fluid shifts)

    TDCO:Overallaccuracy1015%

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    Basisforarterialpressurebasedpulsecontourcardiacoutput:

    describingthe

    (left)

    ventricular

    pump

    Q(t)Flow

    Frank's Windkessel - describes the hemodynamic of the arterial systemin terms of resistance and compliance

    WINDKESSSELMODEL

    Peripheral resistance is calculated according to

    R=(pao,mean pven,mean)CO pao,mean CO pao,mean - mean aortic pressure

    pven,mean -mean venous pressure CO- Cardiac Output

    Total arterial compliance is calculated as;

    C=V

    14

    C Total arterial compliance

    V- Volume change

    p Presure change

    Nico Westerhof.ThearterialWindkessel.SpecialIssueReview. MedBioEngComput.

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    methods

    accountingformoredetails

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    TheWindkesselmodel

    FirstmodelbyWesseling AddingtheCompliance

    R:totalsystemicperipheralresistance(SVR);Z:characteristic impedanceoftheproximal

    aorta;C:Windkesselcomplianceoftheaorta

    Lessinvasivepresasurepulsebasedquasicontinuous

    COmethods

    , ,

    Modelflow(Finapres Medical Systems, Amsterdam, NL)

    PRAM(Mostcare FIAB SpA, Florence, IT)

    LiDCOplus/PulseCO system (LiDCO Ltd, Cambridge, UK)

    Howtoaccountforthecharacteristicimpedance?

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    Q(t)

    Howtoaccountforthecharacteristicimpedance?

    PiCCOplus Aufbau

    Centralvenousaccess

    Injectate

    temperature

    PCCI

    AP13.0316.28 TB37.0

    A P 1 40

    117 92

    (CVP) 5

    SVRI 2762

    PC

    C I 3 .2 4

    HR 78

    SVI 4 2

    PiCCO: combines transpulmonary thermodilution for calibration and arterialpulse contour analysis 2nd sw-version: adapted algorithm: analyzes shape of the pressure wave-

    form, accounting for individual compliance and systemic vascular resistance

    S VV 5 %

    dPmx1140

    (GEDI) 625

    Arterialtemperature

    stroke volume computed byintegrating the systolic area under

    the arterial pressure waveform

    20

    PULSIOCATH

    thermodilution catheter

    PULSIONpressuretransducer

    For calibration the specific aortic impedance isrequired: calculated by comparison of the systolicarea and thermodilution CO measured

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    Irlbeck et al. 20 / 165 -0.09 0.85 0.93 1.x patients on ICU

    Buhre et al 12 / 36 1.6 - 9.2 0.003 0.63 0.88 1.x patients on ICU

    Rdig et al. 26 / 308 2.3 - 12.6 0.18 1.24 1.xduring coronarybypass surgery

    after cardiothoracic

    PiCCO vsPA-TD Cardiac Output / Cardiac Index *

    References # n Mean SD Range Bias SD PE r ** Software Condition of

    (l/min) (l/min) (l/min) Version the participants

    ner e a . . - . . . . surgery

    Rauch et al. 25 / 380 1.95 - 11.6 -0.14 1.16 1.xpatients undergoingHCPB

    Mielck et al. 22 / 96

    6.6

    1.7 0.40 1.30 39 post cardiac surgery

    Gdje et al. 24 / 517 2.7 - 14.1 -0.20 1.15 0.88 4.1after cardiothoracicsurgery

    Della Rocca et al. 62 / 186 3.0 - 13.0 0.04 0.84 0.94 4.1undergoing livertransplantation

    Felbinger et al. 20 / 360 2.05 - 6.3 * 0.14 0.33 * 0.93 post cardiac surgery

    Sujatha et al. 60 / 480 0.23 0.50 20

    surgery

    Halvorsen et al. 31 / 252 5.0 - 7.1 -0.76 1.17 43 5.1undergoing OPCABsurgery

    Chakravarthy et al 15 / 438 -0.13 1.12undergoing OPCABsurgery

    de Wilde et al. 24 / 199

    4.7

    ? 2.1 - 9.7 -0.14 0.87 47 undergoing OPCABsurgery

    Button et al. 31 / 185 2.4 - 9.3 0.28 1.30 6.0 perioperative period

    PEpercentageerror;accordingtoCritchley&Critchley

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    LiDCOTMplus/PulseCOTMsystem

    minimally invasive lithium dilution technique for calibrationcentral or peripheral venous access for indicator injection (0.002-0.004mmol/kg; upper limit of 3mmol/day).Cardiac output the arterial concentration time curve obtained by an ion-selective electrode located in ablood flow-through-cell

    beat-to-beat estimate of the cardiac output continuously analyzing the arterialblood pressure waveform. The algorithm is supposed to be independent of the arterialmeasurement site.

    For the analysis of the pressure trace a 3-step transformation by Jonas is used.

    1) the transformation of the arterial pressure signal into a standardized volume-time waveform (done by an algorithm compliance with a lookup table).

    2) in order to obtain cardiac output, the duration of the cardiac cycle and thes ro e vo ume s ca cu a e y au ocorre a on

    3) this result is calibrated by comparison with a LIDCO-measured value, whichthe manufacturer recommends to be done every 4 to 6 hours. This calibrationfactor corrects for the arterial compliance for a given arterial blood pressure and for variations betweenindividuals. Further details for the exact calculation are not provided

    LiDCO-technique

    The secret of LiDCOLinton et al: BJA (2001) 86: 486-496

    ZA aortic impedance, A cross section phase difference flow=velocityf frequency

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    Cardiac Output / Cardiac Index *

    PulseCO/LiDCO References # n Mean SD Range Bias SD PE r ** Condition ofPA-TD (l/min) (l/min) (l/min) the participants

    Linton et al. 40 / 160 -0.25 0.5 0.97 patients after surgery

    Garcia-Rodr iguez et a l. 31 / 93 5.55 ? 2.4 -11.5 -0.5 0.7 24 after major surgery

    Hamilton et al 20 / 100 3.4 - 8.5 0.05 0.6 0.86 post CABG surgery

    Yamashita et al 23 / ? 0.76 1.93 0.74undergoing OPCABsurgery

    Costa et al 23 / 151 3.4 - 13.2 -0.29 1.09 16.8 0.852 hours after liver

    transplantation

    de Wilde et al 24 / 199 5.0 ? 2.5 - 8.9 0.17 0.69 28 undergoing CABG

    PRAM/Mostcare

    standard arterial radial or femoral catheter, Calibration with other techniques not required

    beat-to-beat values of cardiac output based on the mathematical analysis ofthe arterial pressure profile changes

    The algorithm is based on the principle of perturbations performing a beat-to-beatanalyis of the whole arterial pressure wave morphology (instead of just the pulsatile

    . , ,points of perturbance are evaluated.

    PRAM claims to consider aortic impedance, compliance and systemic vascularresistance, which are affecting the pressure signal, further details undisclosed.

    Cardiac Output / Cardiac Index *

    PA-TDvs References # n Mean SD Range Bias SD PE r ** Condition of

    the participantsPRAM

    (l/min) (l/min) (l/min)

    Romano&Pistolesi 18 / ? 2.6 0.6 *1.7 - 4.0

    *-0.15 0.35

    * 27 0.88undergoing heartcatherization

    Giomarelli et al. 28 / 112 2.3 - 7.4 0.03 0.89 0.88 undergoing CABG

    Romano et al. 50 / ? 2.7 0.6 *1.6 - 4.2

    *-0.03 0.42

    * 31 0.85undergoing heartcatherization

    Romano et al. 32 / 128 4.0 0.7 0.07 0.40 20 0.87 undergoing CABG

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    Slidetakenfrom:EdwardsLifesciencesWebsite,modified

    Patentapplication:EdwardsLifesciences

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    Slidetakenfrom:EdwardsLifesciencesWebsite,modified

    Slidetakenfrom:EdwardsLifesciencesWebsite

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    Slidetakenfrom:EdwardsLifesciencesWebsite

    Slidetakenfrom:EdwardsLifesciencesWebsite

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    ThesecretofthecalculationofAPCO(Vigileo)(takenfromthepatentsdescription)

    11parameters 1 11

    Slidetakenfrom:EdwardsLifesciencesWebsite

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    FlowtracversusICO FlowtracversusCCO

    Slidetakenfrom:EdwardsLifesciencesWebsite

    CCOvsICO

    Slidetakenfrom:EdwardsLifesciencesWebsite

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    ChangesinCOduetolinedamping

    Slidetakenfrom:EdwardsLifesciencesWebsite

    Art.Radialis(original;ProbandH.L.) Art.Radialis

    smoothed

    1 2 3 4 5 6 7 98 10 11

    Harmonicfrequencies

    26.April2007 Druckmessung

    XAchse:ArbitrreEinheit

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    Setkonfiguration

    Eigen

    frequenz

    Dmpfungs

    faktor

    Flowtrac 38,8 0,188

    39,5 0,170

    mit 10l Luftblasetransducerseitig

    38,4 0,175

    38,9 0,175

    mit BD-Kanle24,2 0,236

    25,0 0,241

    mit BD-Kanleund 10l Luft

    22,5 0,261

    21,8 0,262

    Manecke,2005

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    ClinicalvalidationofcontinuousAPCO(FCI)

    comparisontocontinuouspulmonarythermaldilution(Vigilance)

    Chakravarthy M,RajeevS,JawaliV.Cardiacindexvaluemeasurementbyinvasive,semiinvasiveandnon

    invasivetechniques:aprospectivestudyinpostoperativeoffpumpcoronaryarterybypasssurgerypatients.J

    ClinMonitComput2009;23:175180

    FCIandBCI 0.18 0.08

    OAPCO

    Difference

    inHI(PiC

    (L/min/m2)

    Mean(L/min/m2)

    BZukunft:EvaluierungdesminimalinvasivenFloTrac/VigileoMonitoringsystemsankritisch

    krankenPatienten.ThesisCharit UniversittsmedizinBerlin.2008

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    BZukunft:EvaluierungdesminimalinvasivenFloTrac/Vigileo

    MonitoringsystemsankritischkrankenPatienten.Thesis

    Charit UniversittsmedizinBerlin.2008

    ComparisonofFloTrac/Vigileo anda.femoralis(PiCCO)calculatedHIdata

    and FloTrac/Vigileo anda.radialis calculatedHIdata.SpearmanRhoKorrelation

    BlandAltmannAnalysis:biasundlimitsofagreement0.35 0.38l/min/m2,PE 38.3%

    ComparisonofchangesinindividualconsecutivelymeasuredHIdata,

    obtainedfromFloTrac/VigileoandtranspulmonaryTD/PCA(PiCCO)

    BZukunft:EvaluierungdesminimalinvasivenFloTrac/VigileoMonitoringsystemsankritischkranken

    Patienten.ThesisCharit UniversittsmedizinBerlin.2008

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    Vigileo versus

    PulmArt TD Cardiac Output / Cardiac Index *

    References # n Mean SD Range Bias SD PE r ** Software Condition of

    (l/min) (l/min) (l/min) Version the participants

    Sander et al 30 / 120 0.60 1.40 54 0.53 undergoing CABG

    Button et al. 31 / 185 2.4 - 9.3 0.25 1.13 1.07 perioperative period

    Mayer et al 40 / 244 2.8 0 .65 * 1.6 - 4 .9 * 0.46 0 .58 * 46 0.53 1.0 cardiac surgical patients

    Manecke and

    Auger 50 / 295 2.8 - 9.6 0.55 0.98 post cardiac surgery

    Opdam et al. 6 / 218 0.21 1.02 * 0.35 post cardiac surgery

    Prasser e t al . 20 / 164 5.9 1 .15 3 .4 - 9.8 0.02 1 .49 49.3 0.58 1.03 critically ill in a neurosurgical ICU

    Breukers et al. 20 / 56 5.5 0.85 3.3 - 8.8 -0.14 1.00 36 0.74 post cardiac surgery

    Chakravarthy et

    al 15 / 438 -0.15 0.33 undergoing OPCAB surgery

    Cannesson et al. 11 / 166 4.7 0.95 1.9 - 8.2 0.26 0.87 37 0.66 undergoing CABGMcGee et al 84 / ? 5.9 ? 3.1 - 9.2 0.20 1.28 43 critically ill patients on ICU

    Staier et al. 30 / 120 0.02 1.04 44.3 aortic valve replacement

    Mayer et a l. 40 / 282 2.5 0.55 * 1.2 - 4.1 * 0.19 0.30 * 24.6 1.10 undergoing CABG

    Metha et al 12 / ? 4.5 1.33 2.8 - 7.7 0.26 0.66 29 1.07 undergoing OPCAB surgery

    Matth ieu et al. 20 / 400 5.5 1 .0 2 .1 - 9.5 -0.8 ? 43 1.07 undergoing liver transplantation

    All currently available noninvasive arterial pressure based CO

    monitors have advantages and limitations.With an increasing number of clinical studies being published on the

    applicability, suitability, and clinical utility of these monitors their use should

    continue to gain popularity. However, evaluation of changes and direction of

    Conclusion

    changes essential (!)

    When using these monitors in conjunction with the

    administration of fluids and vasopressors to specific therapeuticend points (goal directed therapy) there limitations should be

    kept in mind.

    less invasive state of the art devices presently available remains

    questionable.

    True continuous cardiac output : no end in sight yet at present more fiction than fact in dynamic conditions##personalview

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    ThankYouforYourattention!

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    MBiais,KNouetteGaulain,AQuinart,SRoullet, PRevel,Fsztark. Uncalibrated StrokeVolumeVariationsAre

    AbletoPredicttheHemodynamicEffectsofPositiveEndExpiratoryPressureinPatientswithAcuteLungInjury

    orAcuteRespiratoryDistressSyndromeafterLiverTransplantationAnesthesiology2009;111:85562

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    DLahner,BKabon,CMarschalek,AChiari,GPestel,AKaider,E Fleischmann,HHetz.Evaluation

    responsivenessintraoperatively .BritishJournalofAnaesthesia doi:10.1093/bja/aep200

    Results. Twenty patients received 67 fluid boluses. Fiftytwo of the 67 fluidboluses administered resulted in fluid responsiveness. SVV achieved an area

    under the ROC curve of 0.512 [CI 0.320.70].

    Conclusions.Thisprospective,interventionalobserverblindedstudydemonstrates

    thatSVVobtainedbyAPCO,usingtheFloTrac/Vigileo system,cannotserveasa

    surgery.

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    TranspulmonaleThermodilution:

    HerzzeitvolumenNach zentralvenser Injektion desIndikators misst ein Thermistor inder Spitze

    des arteriellen Katheter dieTemperaturvernderungen stromabwrts.

    DasHerzzeitvolumenwirddurchdieAnalysederThermodilutionskurve nach

    einem modifiziertenStewartHamiltonAlgorithmusberechnet.

    Temperaturverdnnungskurve Bolusverfahren

    Tb Injektion

    t

    dtT

    KV)T(THZV

    b

    iibTD

    Tb =Bluttemperatur

    Ti =Injektattemperatur

    Vi =Injektatvolumen

    T . dt =Flche unter der Thermodilutionskurve

    BerechnungdesHZV:

    Flcheunterder

    Thermodilutionskurve

    dtT

    KV)T(THZV

    b

    iibTD

    78

    K =Korrekturfaktor,aus spezifischem Gewichtundspezifischer Wrmekapazitt vonBlut undInjektat

    Thermodilution Bolustechnique

    Calculationof

    areaunder

    mittels

    Extrapolation

    des

    abfallenden

    Kurventeils,

    Fitting

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    AJPHeartCircPhysiol VOL281SEPTEMBER

    2001

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    PiCCO

    PiCCO-Technology combines transpulmonary thermodilution forcalibration and arterial pulse contour analysis.

    inline injectate temperature sensor in a central vene4-French thermistor-tipped arterial pressure catheter (peripheral artery: femoral, axillary,brachial)

    PiCCO algorithm for continuous cardiac output determination as described byWesseling et al.stroke volume computed by integrating the systolic area under thearterial pressure waveform.For calibration the specific aortic impedance is required: calculated bycomparison of the systolic area and thermodilution CO measured.2nd software generation: adapted algorithm: analyzes the shape of thepressure waveform, taking into account the individual compliance andsystemic vascular resistance