Fluid responsiveness Fluid responsiveness Monitoring in Surgical - - PowerPoint PPT Presentation

fluid responsiveness fluid responsiveness monitoring in
SMART_READER_LITE
LIVE PREVIEW

Fluid responsiveness Fluid responsiveness Monitoring in Surgical - - PowerPoint PPT Presentation

Fluid responsiveness Fluid responsiveness Monitoring in Surgical Monitoring in Surgical and Critically Ill Patients and Critically Ill Patients Impact clinique de la Goal-directed-therapy Goal-directed-therapy Impact clinique de la Patrice


slide-1
SLIDE 1

Fluid responsiveness Fluid responsiveness Monitoring in Surgical Monitoring in Surgical and Critically Ill Patients and Critically Ill Patients

Cliniques universitaires Saint Luc Université catholique de Louvain, Brussels, Belgium.

Patrice FORGET, M.D

Impact clinique de la Impact clinique de la Goal-directed-therapy Goal-directed-therapy

slide-2
SLIDE 2

Introduction Introduction

 Expansion volémique

Expansion volémique

Intervention fréquente et importante But: augmenter le stroke volume pour

améliorer l’outcome

 Individualiser le remplissage reste un

Individualiser le remplissage reste un challenge challenge

Prédire la réponse au remplissage Eviter l’hypo- comme l’hypervolémie

slide-3
SLIDE 3

Why do I need to fill my patient? Why do I need to fill my patient?

 To rise his CO

To rise his CO

 To improve clinical parameters

To improve clinical parameters

 To improve oxygen delivery

To improve oxygen delivery

 To correct lactic acidosis

To correct lactic acidosis

 …

Rapidity is determinant! Rapidity is determinant!

slide-4
SLIDE 4

But fluid loading may be insufficient But fluid loading may be insufficient

 Only 40 to 72% “responders”

Only 40 to 72% “responders”

 Cardiac failure, organic pathologies,

Cardiac failure, organic pathologies, renal tubulopathy renal tubulopathy And potentially harmful… And potentially harmful…

slide-5
SLIDE 5

Fluids may be harmful! Fluids may be harmful!

Kehlet et al, BJA 2002

slide-6
SLIDE 6

Fluids may be harmful! Fluids may be harmful!

 To fear hypo- as hypervolemia

To fear hypo- as hypervolemia

 Liberal vs Restrictive?

Liberal vs Restrictive?

Interest of the fluid restriction in major

abdominal surgery but…

Debate still open

 Holte et al, B J Anaesth 2007

Tailoring the fluid management

 Poeze et al, Crit Care 2005

slide-7
SLIDE 7

Fluids may be harmful! Fluids may be harmful!

Optimization of perioperative fluid Optimization of perioperative fluid management may include a management may include a combination of limited crystalloid combination of limited crystalloid administration together with administration together with individualized goal-directed colloid individualized goal-directed colloid administration to maintain a maximal administration to maintain a maximal stroke volume stroke volume

Bungaard-Nielsen, Secher and Kehlet et al, Acta Anaesthesiol Scand 2009

slide-8
SLIDE 8

Goal directed fluid management Goal directed fluid management

Fluid volume Complications Optimal CO

slide-9
SLIDE 9

Goal directed fluid management Goal directed fluid management

Fluid volume Complications

slide-10
SLIDE 10

Goal directed fluid management Goal directed fluid management

Fluid volume Complications

slide-11
SLIDE 11

Goal directed fluid management Goal directed fluid management

 To fill before the clinical signs of

To fill before the clinical signs of hypovolemia hypovolemia

To optimise the CO To improve the morbi- mortality To improve the quality of care and accelerate the

rehabilitation

To shorten the hospital stay To limit the costs

slide-12
SLIDE 12

Goal directed therapy Goal directed therapy Well defined parameters Well defined parameters Which parameters Which parameters?

?

slide-13
SLIDE 13

Preload Stroke Volume

slide-14
SLIDE 14

Preload Stroke Volume

slide-15
SLIDE 15

Goal directed fluid management Goal directed fluid management

 Clinical signs and context

Clinical signs and context

 Evolution of static “classical”

Evolution of static “classical” parameters (CVP, PAOP, CF) parameters (CVP, PAOP, CF)

 Dynamic tests (Passive leg raising,

Dynamic tests (Passive leg raising, fluid challenge) fluid challenge)

 Biological parameters

Biological parameters

Helpful but insufficient! Helpful but insufficient!

slide-16
SLIDE 16

Goal directed fluid management Goal directed fluid management

 Dynamic parameters

Dynamic parameters

Cyclic variations of cardiac preload Preload-dependency analysis

 PPV (deltaPP), SVV, SPV, dDown, PVI

slide-17
SLIDE 17

Pulse Pressure Variation Pulse Pressure Variation

Michard et al, Am J Resp Crit C Med 2000.

slide-18
SLIDE 18

Pulse Pressure Variation Pulse Pressure Variation

Inspiratory positive pressure Inspiratory positive pressure

 ↓

↓ venous return venous return

 ↓

↓ right ventricular output right ventricular output

 ↓

↓ left ventricular preload left ventricular preload

 ↑

↑ transmural pressures transmural pressures

 ↑

↑ ANS ANS

slide-19
SLIDE 19

Physiology Background Physiology Background

Boulain et al, Chest 2002

slide-20
SLIDE 20

Goal directed fluid management Goal directed fluid management

Michard et al, Am J Resp Crit C Med 2000.

slide-21
SLIDE 21

Pulse Pressure Variation Pulse Pressure Variation

 Colorectal (Haifang

Colorectal (Haifang et al, et al, Chin Med J 2002) Chin Med J 2002)

 Pheo (Mallat

Pheo (Mallat et al, et al, C J Anesth 2003) C J Anesth 2003)

 CABG (Cannesson

CABG (Cannesson et al, et al, A&A 2008) A&A 2008)

 PO CABG (Rex

PO CABG (Rex et al, et al, B J Anaesth 2004) B J Anaesth 2004)

 Hepatectomy (Solus

Hepatectomy (Solus et al, et al, B J Anaesth B J Anaesth 2006) 2006)

 High-risk (Lopes

High-risk (Lopes et al, et al, Crit Care 2007) Crit Care 2007)

slide-22
SLIDE 22

Dynamic parameters Dynamic parameters

slide-23
SLIDE 23

Dynamic parameters Dynamic parameters

slide-24
SLIDE 24

Dynamic parameters Dynamic parameters

slide-25
SLIDE 25

Dynamic parameters Dynamic parameters

slide-26
SLIDE 26

Pulse Pressure Variation Pulse Pressure Variation

 But…

But…

Actually limited to controlled ventilation In the absence of arrhythmia Importance of the clinical context!

 Orthopic liver transplantation (Gouvêa et al, B J

Anaesth 2009)

In the case of automated calculation, importance

  • f the validation of the software!

 Vigileo? (Lahner et al, B J Anaesth 2009)

Dynamic invasive methods are often impractical,

complex and costly.

slide-27
SLIDE 27

Dynamic parameters Dynamic parameters

slide-28
SLIDE 28

PPV and deltaPOP PPV and deltaPOP

Cannesson et al, Crit Care 2005.

slide-29
SLIDE 29

deltaPOP and PVI deltaPOP and PVI

 Haifang

Haifang et al, et al, Chin Med J 2002 Chin Med J 2002

 Cannesson

Cannesson et al, et al, Crit Care 2005 Crit Care 2005

 Natalini

Natalini et al, et al, Anesthesiology 2006 Anesthesiology 2006

 Solus

Solus et al, et al, B J Anaesth 2006 B J Anaesth 2006

 Cannesson

Cannesson et al, et al, B J Anaesth 2008 B J Anaesth 2008

PVI >14% predicts fluid responsiveness.

slide-30
SLIDE 30

Pleth Variability Index Pleth Variability Index

slide-31
SLIDE 31

Pleth Variability Index Pleth Variability Index

slide-32
SLIDE 32

Pleth Variability Index Pleth Variability Index

 43 mechanically-ventilated septic shock patients

43 mechanically-ventilated septic shock patients

 500 ml saline fluid challenge, passive leg raising

500 ml saline fluid challenge, passive leg raising

 Results

Results

 Correlation of 0.90 for PVI vs. ΔPP  PVI >20 vs. ΔPP >15%

 Sensitivity 84%, specificity 90%

 PVI >20 was 100% accurate in discriminating fluid

responders from non-responders

Feissel et al. ISICEM 2009.

slide-33
SLIDE 33

Optimisation of the PVI? Optimisation of the PVI?

 To guide fluid management and to optimise

To guide fluid management and to optimise circulatory status during the surgery? circulatory status during the surgery?

 Randomised Clinical Trial

Randomised Clinical Trial

to compare the intraoperative PVI-directed fluid

management vs standard care

 Clinicaltrials.gov Number NCT00816153

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-34
SLIDE 34

Optimisation by the PVI Optimisation by the PVI

 Group PVI (P)

Group PVI (P)

 500 mL of cristalloids followed by 2 mL.kg-1.h-1  Colloids 250 mL added for a PVI value of 10 to 13%  If required, vasoactive support to maintain the mean

arterial pressure above 65 mmHg

 Group Control (C)

Group Control (C)

 500 mL of cristalloids followed by fluid management based

  • n fluid challenges and CVP

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-35
SLIDE 35

Optimisation by the PVI Optimisation by the PVI

 Primary outcome

Primary outcome

Perioperative lactate levels

 Secondary outcomes

Secondary outcomes

Hemodynamic data Postoperative complications

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-36
SLIDE 36

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-37
SLIDE 37

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-38
SLIDE 38

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-39
SLIDE 39

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-40
SLIDE 40

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-41
SLIDE 41

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-42
SLIDE 42

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-43
SLIDE 43

Optimisation by the PVI Optimisation by the PVI

Forget P, Lois F and De Kock M, Anesth Analg 2010.

slide-44
SLIDE 44

Conclusion

 Tailored fluid administration is associated

Tailored fluid administration is associated with improved morbidity and hospital with improved morbidity and hospital length of stay length of stay

 Focusing on optimization of CO help in the

Focusing on optimization of CO help in the choice of monitoring methods choice of monitoring methods

 More studies are needed to confirm the

More studies are needed to confirm the clinical value and the limits of available clinical value and the limits of available fluid responsiveness monitoring methods fluid responsiveness monitoring methods

slide-45
SLIDE 45

Conclusion (2)

 The PVI allows for noninvasive,

The PVI allows for noninvasive, automated, continuous of fluid automated, continuous of fluid responsiveness monitoring responsiveness monitoring

 Our study add evidence to the concept of

Our study add evidence to the concept of Goal-Directed fluid management Goal-Directed fluid management