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Volume Optimization in Severe Sepsis
Dr. Yasser Sakr Dept. of Anesthesiology and Intensive Care
Uniklinikum Jena, Germany
Antalya/ 2016
The ultimate goal of the cardiovascular system – Supply
Energy substrates (O2/Nutrition) Hormones Mediatores (e.g. cytokines)
– Elimination Metabolic products
i.e to ensure adequate tissue perfusion
Physiologic backgrounds
Supply
Demand
DO2 = Hb% x SaO2 x CI x 10
ü SvO2 ü ScO2 ü Lactate VO2
Physiologic backgrounds
Microcirculation
Global
Regional
Physiologic backgrounds
Global hemodynamic parameters do not correlate with microvascular perfusion
Dellinger, Crit Care Med 2003 , 31(3): 946-55
Septic shock
2
-- DO2
++ VO2 Myocardial dysfunction
Vascular derangements Relative hypovolemia
Organ dysfunction
Severe sepsis
Pathophysiology
VO2 DO2
optimal = normal
Therapeutic target
?? Medikament
Benefit Risk
++ DO2 Primum non nocere ! Florence Nightingale Notes on hospitals / London 1859
Therapeutic targets
Pres
sures
Flow
Resistence
Target vs. Indices
SV
Target vs. indices
3
SV
Preload Afterload
Contractility Heart rate
Therapeutic targets
Fluids
Frank Starling Law
Preload assessment Static parameters – CVP/PCWP (Neither reflect ventricular volumes or
track preload-responsiveness) – LVEDV/LVEDP – GEDV/ITBV
Kumar et al. Crit Care Med 32:691-9, 2004
Predicting Fluid Responsiveness in ICU Patients
Responders / Non-responders % Responders
Calvin (Surgery 81) 20 / 8 71%
Schneider (Am Heart J 88) 13 / 5 72%
Reuse (Chest 90) 26 / 15 63%
Magder (J Crit Care 92) 17 / 16 52%
Diebel (Arch Surgery 92) 13 / 9 59%
Diebel (J Trauma 94) 26 / 39 40%
Wagner (Chest 98) 20 / 16 56%
Tavernier (Anesthesio 98) 21 / 14 60%
Magder (J Crit Care 99) 13 / 16 45%
Tousignant (A Analg 00) 16 / 24 40%
Michard (AJRCCM 00) 16 / 24 40%
Feissel (Chest 01) 10 / 9 53%
Mean 211 / 195 52%
Michard & Teboul. Chest 121:2000-8, 2002
V
V
SV
SV
SV
Preload
Frank-Starling revisited
High contractility
Normal Contractility
target area volume responsive volume overloaded
Poor contractility
Preload assessment
Dynamic parameters – SVV – PPV – PLR – dRAP during inspiration – dAP with valsalva – dVC
4
SV
Target vs. indices
PPV/SVV/PLR GEDV/ITBV
EDV CVP/PAOP
Fluid challenge
Principle Method Advantages Disadvantages Fick Calorimetry Accurate Require MVO2, error when ETT leak, PTX,
FiO2>0.5
NICO Accurate, non-invasive
>20kg, hypercapnea
Dilution PA Accurate, semi-continuous
Affect by respiration, difficult for children, complications, R≠L CO
Trans-pulmonary
Easy for small p’t, continuous
Require dedicated A line, safe duration?
Dye Accurate Sequential measurement limited by dye clearance,
Lithium Accurate, use pre-existing CV/A line
Toxicity, blood sampling
Doppler Echo Structural and function Expertise, users variations
Trans-esophageal
Continuous, rapid insertion, less invasive
Probe fixation, individual errors, tracked accurately
Bio-impedance
Non-invasive Doubtful accuracy in critical illness
Monitoring, Toy or Tool?
PAWP/PACP RAP/RVP/PAP CO SvO2 RVEF
1) Fick method/principle
2) Indicator dilution technique
-dye dilution
CO measurement
Pulmonary artery catheter
Tranosophageal Doppler (TOD) Lithium indicator dilution (LiDCO) Minimally invasive/simple/reliable
CVC/AC Lithium Chlorid (150 mM) as Indicator 0.15 -0.30 mmol (adult) BW > 40kg, good renal function
Simple Reliable
CO = (Li Dose x 60)/ (Area x (1-PCV))
5
PiCCO
Pulse contour analysis
Continuous pulse contour cardiac analysis (PCCO) Arterial blood pressure (AP) Heart rate (HR) Stroke volume (SV) Stroke volume variation (SVV) Systemic vascular resistance (SVR) Index of left ventricular contractility
Intermittent transpulmonary thermodilution
Transpulmonary cardiac output (CO) Intrathoracic blood volume (ITBV) Extravascular lung water (EVLW) Cardiac function index (CFI)
Microcirculation
Global
Regional
Physiologic backgrounds
§ Physical Exam – Hypoperfused state
• Cool extremities • Low urine output • Increasing HR • Confusion • Nausea/Vomiting • SOB
Labs – Increasing BUN/CR
ratio – Lactate – Coagulation
abnormalities – BNP – Hyponatremia – Acidosis
SSC-Guidelines
We recommend that initial fluid challenge in patients with sepsis-induced tissue hypoperfusion with suspicion of hypovolemnic be started with ≥ 1000 mL of crystalloids (to achieve a minimum of 30ml/kg of crystalloids in the first 4 to 6 hours). (Grade 1B).
1. Identify the problem
2. Choose monitoring 3. Measure indices
4. Assess the target
Therapeutic optimization Early Goal-Directed Therapy
Rivers et al. N Engl J Med 2001;345:1368-77
0
10
20
30
40
50
60
Hosp mortality
Hosp (sev sep)
Hosp (sep shock)
Hosp (sep)
28d mortality
60d mortality
Standard EGDT
6
PAC; the right patients, the appropriate indication, the right way ….
31 Pinsky M and Vincent JL. Crit Care Med 2005; 33:1119–1122
Cardiac output
High Low
SvO2 SvO2
High Low High Low SEPSIS EXCESSIVE BLOOD FLOW (hypervolemia, excessive vasoactive therapy)
ANEMIA HYPOXIA HIGH VO2 (Inadequate cardiac output?)
LOW VO2 (anesthesia, hypothermia, ...) (Adequate cardiac output?)
LOW OUTPUT SYNDROME (hypervolemia, heart failure pulmonary embolism ...)
Vincent Critical Care 2003, 7:276-278
PAC; the right patients, the appropriate indication, the right way ….
LiDCO Decision tree for hemodynamic / volumetric monitoring**
*not available in USA **without guarantee
*
+
+
CI (l/min/m 2 )
GEDI (ml/m 2 ) or ITBI ( ml/m 2 )
ELWI (ml/kg) (slowly responding)
>3.0 <3.0
>700 >850
<700 <850
>700 >850
<700 <850
ELWI (ml/kg)
GEDI (ml/m 2 ) or ITBI (ml/m 2 )
CFI (1/min) or GEF (%)
<10 >10 <10 <10 <10 >10 >10 >10
V+ V+! V+! V+ Cat Cat
OK!
V -
>700 >850
700 - 800 850 - 1000
>4.5 >25
>5.5 >30
>4.5 >25
700 - 800 850 - 1000
Cat
>5.5 >30
>700 >850
700 - 800 850 - 1000
700 - 800 850 - 1000
≤ 10 ≤ 10 ≤ 10 ≤ 10
V -
V + = volume loading (! = cautiously) V - = volume contraction Cat = catecholamine / cardiovascular agents SVV only applicable in ventilated patients without cardiac arrh ythmia
>700 >850
<10 Optimise to SVV (%) <10 <10 <10
R E S U L T S
T A R G E T
T H E R A P Y
1.
2. <10 <10 <10 <10
Take home message Physiologic knowledge is essential Consider global but do not forget microvascular perfusion Target SV preferably using dynamic assessment of volume responsiveness Use whichever monitor you want but understand the meaning what you are measuring Hemodynamic monitorng do not replace medical sense, choose the right patient, the time, and the right approach