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Fluid Responsiveness Dr. Daniel Rankmore JHH ICU Junior Doctor Teaching 7 th March 2012

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Fluid Responsiveness. Dr. Daniel Rankmore JHH ICU Junior Doctor Teaching 7 th March 2012. Today’s Topic. Why give fluids “Fluid responsive” What fluids are avalible. Why g ive fluids. the air goes in and out and the blood goes round and round. Oxygen Delivery (DO 2 ). - PowerPoint PPT Presentation

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Page 1: Fluid Responsiveness

Fluid ResponsivenessDr. Daniel Rankmore

JHH ICU Junior Doctor Teaching 7th March 2012

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Today’s TopicWhy give fluids“Fluid responsive”What fluids are avalible

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Why give fluidsOxygen Delivery (DO2)the air goes in and out and the blood goes round and round

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Why give fluids

Intra-venous fluid

Intra-vascular volume

Cardiac Output

Tissue Perfusion

Oxygen Delivery

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DO2 VO2> = Shock= Bad

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DO2

Oxygenation

Cardiac Output+

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DO2

Oxygenation

Cardiac Output+

(Bersten & Soni, 2009, pp. 317-318):

FiO2

Airway

Gas Movem

entHeam

Hb

TissueDiffusio

nCytochro

meMitochon

rial

Alveolar

Diffusion

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DO2Cardiac Output

SV HR x

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DO2Cardiac Output

SV HR x

PreloadContractilityAfterloadFilling Time

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Frank StarlingSt

roke

Vol

ume

‘Preload’

A ‘normal’ heart

A heart ‘failing’

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Frank StarlingSt

roke

Vol

ume

‘Preload’

500mlBolus

SVCO

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Frank Starling CurveSt

roke

Vol

ume

‘Preload’

500mlBolus

SVCO

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Frank Starling CurveSt

roke

Vol

ume

‘Preload’

500mlBolus

SVCO

EVLWPulmonary Oedema

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Liberal Fluid Therapy compared with either Goal Directed Therapy or Restrictive Fluid Therapy3861 patients in 35 RCTsLiberal vs Restrictive

Pneumonia RR 2.2 95% CI 1-4.5Pulmonary Oedema RR 2.8 95% CI 1.1-13Longer Hospital Stay Mean 2 Days 95% CI 0.5-3.4

Goal Directed vs Not Goal DirectedPneumonia RR 0.7 (CI 0.6-0.9)Renal Complications RR 0.7 (CI 0.5-0.9)Reduced Hospital Stay Mean 2 Days (CI 1-3)

LiberalProlonged Hospital Stay Mean 4 Days (CI 3.4-4.4)Time to first bowel movement 2 Days (CI 1.3-2.3)

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RCT 1000 patients with ALI 60 day follow upPrimary end point – mortality.Secondary end points – lung physiology, vent free days, organ failure free days7 day fluid balance 136ml vs. 6992mls.

Conserve

Liberal

p

Mortality

25.5%

28.4%

0.3

Vent Free Days

14.6 12.1 <0.001

ICU free days

13.4 11.2 <0.001

Shock & RRT

10% 14% 0.6

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Three studies of colorectal surgeryReduced incidence of cardiorespiratory and fewer post operative problems.

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88 patients undergoing major abdo surgery.PVI group – 500ml crystalloid bolus then 2ml/kg/hr if PVI <13% then 250ml colloid given, MAP maintained with vassopressors.Control group – 500ml crystalloid then fluid management per CVP and MAP.PVI group – improved intra-op and post op lactate and reduced total fluid input.

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Retrospective review of IV fluids in the first 4 days of 778 patients in the VASST (Vasopressin in Septic Shock Trial)Conclusion:

A more positive fluid balance at 12 hours and 4 days was associated with increased mortality.CVP correlated with IV Fluid given for the first 12 hours.

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When to give fluids

Fluid ResponsivenessGiving what the patient needs when the patient needs it

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Fluid Responsiveness>15% increase in Cardiac Output following 500-1000ml fluid bolus

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Static MeasurementsBP (MAP)UOCVPPAOP – ‘the wedge’ ITBVMVSaO2

IVC DiameterLVEDA

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Central Venous PressureThe number that keeps getting measured…

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Studies includedCVP & Blood volume (5 studies)CVP or ΔCVP cf: SI and CI pre & post boluses

(24 studies heterogeneous patient cohort including vascular surg, CABG, Sepsis, Health, 803 patients)

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Central Venous Pressure

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Central Venous PressureCVP & blood volume: 0.16 (95% CI: 0.03-0.28) CVP & SVI/CI: 0.18 (95% CI: 0.08-0.28) ROC 0.56∆CVP & SVI/CI: 0.11 (95% CI: 0.015-0.25)

ROC 0.5 true-positive = false positiveROC 0.9+ an adequate testConclusion

In none of the included studies was CVP able to predict fluid responsive or blood volume.

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Central Venous Pressure

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Hea32 healthy people given 3L saline over 3 hoursCVP PAOP useless..

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Mixed Venous Saturations

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Dynamic MeasurementsThe Fluid ChallengePassive Leg RaiseWaveform Analysis

Systolic Pressure VariationPulse Pressure VariationStroke Volume Variation

EchocardiographyPleth Variability IndexBioimpedance & Bioreactance

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Fluid ResponsiveGive some fluid… see what happens…

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Passive Leg RaisePLR. Free. Reversible. Effective.

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39 patient. 4min PLR. 300ml bolus. Circ insufficiency and Mech Ventilation.Measurements: PP (rad artline), HR, PAOP, CO.Correlation between PLR and SV – 0.77 P < 000.1Correlation between PLR and Bolus – 0.84 P <000.1

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Question: Can PLR induced ΔCardiac Output ΔPulse Pressure predict fluid responsiveness9 articles 353 patientsPLR-cCO – sensitivity 89.4% specificity 91.4%Not altered by ventilation mode or cardiac rhythm. PLR-cCO – ROC 0.95 cf. PLR-cPP – ROC 0.76 P<0.001

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Thermodilution

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How much water is in my bucket?

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Thermodilution• Like the bucket analogy• Add to this concentration change over time

and • You can calculate flow

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Waveform AnalysisNumerous. Complex. Useful.

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Stroke Volume VarianceInvasive: pulse contour analysis (PICCO, LIDCO, Flotrac, Vigileo)Noninvasive: echo, pulse ox waveform,

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Pulse Pressure Variance

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Broad inclusion criteria: SVV, PVV, CVP, GEDI, ΔSV, & ΔCI compared with PEEP challenge or fluid challenge.29 studies 685 patientsBaseline and ΔCI

PPV (threshold 12.5%) – ROC 0.94 Sens 0.89 Spec 0.88 OR 59SVV (threshold 11.6%) – ROC 0.84 Sens 0.82 Spec 0.88 OR 27SBPV – ROC 0.86 CVP – ROC 0.55GEDI – ROC 0.56LVEDI – ROC 0.64

LimitationMandatory ventilation

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PiccoThermodilutionWaveform analysis

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Vigileo

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EchocardiographyPretty. Skilled. Detailed. .

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EchoSV = VTI x CSAVTI – AUC of dopplerCSA – valve area

Changes in resp cycle20% VTI12% peak flow

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Bioreactance

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110 Patients. PAC-CCO (thermodilution) cf. NICOMStable CO – correlation coefficient R = 0.82Increasing CO – correlation increased to 96%Decreasing CO – correlation decreased to 84-90%Changes seen on NICOM 3 +/- 3 minutes faster

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75 Adult patients post cardiac surgeryCorrelation between PLR FR and NICOM and FRBut I couldn’t get the article in time…

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Which fluids to give

Choice of IV therapyThink contentsThink compartmentsThink volume

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Compartments

(Ganong’s Review of Medical Physiology, 23e)

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The SalinesFluid Na Cl K Glucos

eOsmola

itypH

Plasma0.18% NaCl4% Glucose

30 30 - 40g/L637kJ

282 3.5-6.5

0.45% NaCl 76 76 - - 150 4.0-7.00.9% NaCl

“Normal Saline”154 154 - - 300 4.0-7.0

3%“Hypertonic”

513 513 - - 1000 4.5-7.0

23.4% 4000 4000 - - 80000.9% Saline + 30mmol KCL

154 184 30 - 368 3.5-7.0

0.9% NaCl + 40mmol KCL

100 140 40 - 280 4.0-7.0

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The SugarsFluid Na Cl Glucose Osmolali

typH

PlasmaWater - - - -

0.18% NaCl + 4% Glucose

30 30 40g/L637kJ

282 3.5-6.5

0.45% NaCl + 2.5% Glucose

77 77 25g/L398kJ

292 3.5-6.5

5% Glucose - - 55g/L835kJ

278 3.5-5.5

10% Glucose - - 100g/L796kJ

556 3.5-6.5

50% Glucose - - 500g/L~4000kJ

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Pre-mixed drinks and other concoctions

Fluid Na Cl Lactate

Ca K Bicarb

Mg Glucose

Osmality

pH

PlasmaCompou

nd Sodium Lactate“Hartma

n’s”

129 109

29 2 5 - - - 274 5.0-7.0

Plasma-lyte

140 98 - - 5 27Acetate

1.5 23 gluconat

e66kJ

294 4.0-6.0

Sodium Bicarb 8.4%

1000

- - - - 1000 - - 2000 7.2-8.7

Voluven 6%

154 154

- - - - - - 304 4.0-5.5

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Blood ProductsFluid Na Cl Octonat

eAlbumin pH Osmol

Plasma4% Albumex 140 128 Octonate

6.440g/L 250

20% Albumex 48-100 Octonate 32

200g/L

pRBC

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The Colloids

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Double Blinded, RCT, 0.9% saline vs. 4% Albumin.6997 pt critically ill patientsPrimary Outcome: 28 day mortality.Secondary Outcomes: length of stay (ICU & Hosp), days on vent, days on RRT, new onset organ dysfucntion.Result: No difference.

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Severe Sepsis subset analysis of SAFE Trial1218 patients AlbuminHR and CVP day 1-3 (p 0.002, 0.03)No diff Sequential Organ Failure Assessment (p. 0.98)Improved mortality 0.87 (CI 0.74-1.02, p 0.06)Multiriant logistic regression anaylsis mortality 0.71 (Ci 0.52-097, p 0.03)

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460 patients, GCS 3-8.Post hoc subgroup analysis with 2 year follow upEnd point mortalityTotal Alb 71 of 214 0.9% 42 of 206 (RR 1.63 p 0.003)GCS 3-8 Alb 61 of 146 0.9% of 32 of 144 (RR 1.88 p <0.001)

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Final ThoughtsConclusion

Understand the question you are asking.Think of fluids as you would a drug – dose, kinetics, dynamics, side effectsThink of alternatives – pressors or inotropes.Remember there are many tools in the toolbox.ABCD and repeat.

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