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Shock in the Pediatric Patient:Shock in the Pediatric Patient:
oror
Oxygen Don’t GoOxygen Don’t Go
Where the Blood Won’t Flow!Where the Blood Won’t Flow!
Dr. Virendra Kumar GuptaDr. Virendra Kumar Gupta
MD PediatricsMD Pediatrics
Fellowship In pediatric Gastroentero-Hepatology & LiverFellowship In pediatric Gastroentero-Hepatology & Liver
TransplantationTransplantation
Assistant ProfessorAssistant Professor
Institute of Paediatric GastroenterologyInstitute of Paediatric Gastroenterology
Nims University Jaipur Nims University Jaipur 
ObjectivesObjectives
Define shock and its different categoriesDefine shock and its different categories
Review basic physiologic aspects of shockReview basic physiologic aspects of shock
Describe management of shock including:Describe management of shock including:
 oxygen supply and demandoxygen supply and demand
 fluid resuscitationfluid resuscitation
 crystalloid vs. colloid controversycrystalloid vs. colloid controversy
 vasopressor supportvasopressor support
IntroductionIntroduction
Shock is a syndrome that results fromShock is a syndrome that results from
inadequate oxygen delivery to meetinadequate oxygen delivery to meet
metabolic demandsmetabolic demands
Oxygen delivery (DOOxygen delivery (DO22 ) is less than) is less than
Oxygen Consumption (< VOOxygen Consumption (< VO22))
Untreated this leads to metabolicUntreated this leads to metabolic
acidosis, organ dysfunction and deathacidosis, organ dysfunction and death
Oxygen DeliveryOxygen Delivery
Oxygen delivery = Cardiac Output x ArterialOxygen delivery = Cardiac Output x Arterial
Oxygen ContentOxygen Content
(DO(DO22 = CO x CaO= CO x CaO22))
Cardiac Output = Heart Rate x Stroke VolumeCardiac Output = Heart Rate x Stroke Volume
((CO = HR x SV)CO = HR x SV)
– SV determined by preload, afterload andSV determined by preload, afterload and
contractilitycontractility
Art Oxygen Content = Oxygen content of theArt Oxygen Content = Oxygen content of the
RBC + the oxygen dissolved in plasmaRBC + the oxygen dissolved in plasma
(CaO(CaO22 = Hb X SaO= Hb X SaO22 X 1.34 + (.003 X PaOX 1.34 + (.003 X PaO22))
Figure 1. FACTORS AFFECTING OXYGEN DELIVERY
DO2
CaO2
CO
SV
HR
Oxygenation
Hgb
A-a gradient
DPG
Acid-Base Balance
Blockers
Competitors
Temperature
Drugs
Conduction System
Ventricular
Compliance
EDV
ESV Contractility
CVP
Venous Volume
Venous Tone
Afterload Blockers
Temperature Competitors
Drugs Autonomic Tone
Metabolic Milieu
Ions
Acid Base
Temperature
Drugs
Toxins
Influenced By
Influenced By
Influenced By
Influenced By
SUPPLYSUPPLY << DEMANDDEMAND
Definition of ShockDefinition of Shock
Inadequate tissue perfusion to meetInadequate tissue perfusion to meet
tissue demandstissue demands
Usually result of inadequate blood flowUsually result of inadequate blood flow
and/or oxygen deliveryand/or oxygen delivery
Shock is not a blood pressure diagnosis!!Shock is not a blood pressure diagnosis!!
Characteristics of ShockCharacteristics of Shock
End organ dysfunction:End organ dysfunction:
 reduced urine outputreduced urine output
 altered mental statusaltered mental status
 poor peripheral perfusionpoor peripheral perfusion
Metabolic dysfunction:Metabolic dysfunction:
 acidosisacidosis
 altered metabolic demandsaltered metabolic demands
Essentials of LifeEssentials of Life
Gas exchange capability of lungsGas exchange capability of lungs
HemoglobinHemoglobin
Oxygen contentOxygen content
Cardiac outputCardiac output
Tissues to utilize substrateTissues to utilize substrate
PreloadPreload
AfterloadAfterload
ContractilityContractility
ResistanceResistance
Stroke VolumeStroke Volume Heart RateHeart Rate
Arterial BloodArterial Blood
PressurePressure
OO22 DeliveryDelivery
OO22 ContentContent Cardiac OutputCardiac Output
xx
xx xx
Classification of ShockClassification of Shock
HypovolemicHypovolemic
 dehydration,burns,dehydration,burns,
hemorrhagehemorrhage
DistributiveDistributive
 septic, anaphylactic, spinalseptic, anaphylactic, spinal
CardiogenicCardiogenic
 myocarditis,dysrhythmiamyocarditis,dysrhythmia
ObstructiveObstructive
 tamponade,pneumothoraxtamponade,pneumothorax
CompensatedCompensated
 organ perfusion isorgan perfusion is
maintainedmaintained
UncompensatedUncompensated
 Circulatory failureCirculatory failure
with end organwith end organ
dysfunctiondysfunction
IrreversibleIrreversible
 Irreparable loss ofIrreparable loss of
essential organsessential organs
Hypovolemic Shock
Most common form of shock world-wide
Results in decreased circulating blood
volume, decrease in preload, decreased
stroke volume and resultant decrease in
cardiac output.
Etiology: Hemorrhage, renal and/or GI
fluid losses, capillary leak syndromes
Distributive Shock
Due to an abnormality in vascular tone leading
to peripheral pooling of blood with a relative
hypovolemia.
Etiology
– Anaphylaxis
– Drug toxicity
– Neurologic injury
– Early sepsis
Management
– Fluid
– Treat underlying cause
Obstructive Shock
Mechanical obstruction to ventricular
outflow
Etiology: Congenital heart disease, massive
pulmonary embolism, tension pneumothorax,
cardiac tamponade
Inadequate C.O. in the face of adequate
preload and contractility
Treat underlying cause.
Dissociative Shock
Inability of Hemoglobin molecule to give up
the oxygen to tissues
Etiology: Carbon Monoxide poisoning,
methemoglobinemia, dyshemoglobinemias
Tissue perfusion is adequate, but oxygen
release to tissue is abnormal
Early recognition and treatment of the cause
is main therapy
Cardiogenic ShockCardiogenic Shock
Cardiogenic shock is commonly describedCardiogenic shock is commonly described
as “pump failure” (decreased contractility)as “pump failure” (decreased contractility)
The common causes areThe common causes are
myocarditis, dysrhythmias,and drugsmyocarditis, dysrhythmias,and drugs
with a myocardial depressant action,with a myocardial depressant action,
acidosis, congenital heart lesions andacidosis, congenital heart lesions and
sepsis.sepsis.
SIRS/Sepsis/Septic shock
Mediator release:
exogenous & endogenous
Decreased blood
flow
Cardiac
dysfunction
Imbalance of
oxygen
supply and
demand
Alterations in
metabolism
SEPTIC SHOCKSEPTIC SHOCK
Decreased Volume / Decreased Pump Function/Abnormal Vessel
Tone
Mechanical Requirements forMechanical Requirements for
Adequate Tissue PerfusionAdequate Tissue Perfusion
FluidFluid
PumpPump
VesselsVessels
FlowFlow
Clinical AssessmentClinical Assessment
Heart rateHeart rate
Peripheral circulationPeripheral circulation
 capillary refillcapillary refill
 pulsespulses
 extremity temperatureextremity temperature
PulmonaryPulmonary
End organ perfusionEnd organ perfusion
 brainbrain
 kidneykidney
Improving Stroke Volume:Improving Stroke Volume:
Therapy for Cardiovascular SupportTherapy for Cardiovascular Support
Preload Volume
Contractility Inotropes
Afterload Vasodilators
Septic ShockSeptic Shock
Early (“Warm”)Early (“Warm”)
Decreased peripheral vascular resistanceDecreased peripheral vascular resistance
Increased cardiac outputIncreased cardiac output
Late (“Cold”)Late (“Cold”)
Increased peripheral vascular resistanceIncreased peripheral vascular resistance
Decreased cardiac outputDecreased cardiac output
Assessment of CirculationAssessment of Circulation
Early Late
Heart rate Tachycardia Tachycardia/
Bradycardia
Blood
pressure
Normal Decreased
Peripheral
circulation
Warm/Cool
Decreased/
Increased
pulses
Cool
Decreased
pulses
Assessment of CirculationAssessment of Circulation
Early Late
End-organ:
Skin
Decreased
cap refill
Very decreased
cap refill
Brain Irritable,
restless
Lethargic,
unresponsive
Kidneys Oliguria Oliguria, anuria
Heart Rate and Perfusion PressureHeart Rate and Perfusion Pressure
(MAP-CVP) Parameters by Age(MAP-CVP) Parameters by Age
Age Heart Rate MAP-CVP
Term
newborn
120-180 55
< 1 120-180 60
< 2 120-160 65
< 7 120-160 65
< 15 90-140 65
Hemodynamic Assessment of ShockHemodynamic Assessment of Shock
Type of Shock Preload Afterload Contractility Cardiac
Output
Cardiogenic ⇑ ⇑ ⇓ ⇓
Hypovolemic ⇓ ⇑ ⇔ ⇓
Septic
Early
Late
⇓
⇑
⇓
⇑
⇔
⇓
⇑
⇓
Obstructive ⇓ ⇑ ⇓ ⇓
Distributive ⇓ ⇓ ⇑ ⇔
Goals of ResuscitationGoals of Resuscitation
Overall goal:Overall goal:
 increase Oincrease O22 deliverydelivery
 decrease demanddecrease demand
TreatmentTreatment
OO22 contentcontent CardiacCardiac
outputoutput
BloodBlood
pressurepressure
Sedation/analgesiaSedation/analgesia
Principles of ManagementPrinciples of Management
A: AirwayA: Airway
 patent upper airwaypatent upper airway
B: BreathingB: Breathing
 adequate ventilation and oxygenationadequate ventilation and oxygenation
C: CirculationC: Circulation
 optimizeoptimize
 cardiac functioncardiac function
 oxygenationoxygenation
Act quickly,
Think slowly.
Greek Proverb
Airway ManagementAirway Management
Patients in shock have:Patients in shock have:
 OO22 deliverydelivery
 progressive respiratory fatigue/failureprogressive respiratory fatigue/failure
 energy shunted from vital organsenergy shunted from vital organs
 afterloadafterload
Airway ManagementAirway Management
Early intubation provides:Early intubation provides:
 OO22 delivery and contentdelivery and content
 controlled ventilation which:controlled ventilation which:
 reduces metabolic demandreduces metabolic demand
 allows C.O. to vital organsallows C.O. to vital organs
TherapyTherapy
Vagolysis
Chromotropy
V o lu m e
C V P
P re lo a d
V a s o d ila to rs
V a s o c o n s tric to rs
A fte rlo a d
C o rre c t
a c id o s is
h y p o x ia
h y p o g ly c e m ia
In o tro p ic
a g e n ts
C o n tra c tility
S tro k e V o lu m e
Heart
Rate 
Fluid ChoicesFluid Choices
Less Filling
Less Filling
Tastes Great !
Tastes Great !
Colloid Crystalloid
CrystalloidsCrystalloids
Hypotonic Fluids (DHypotonic Fluids (D55 1/4 NS)1/4 NS)
No role in resuscitationNo role in resuscitation
Maintenance fluids onlyMaintenance fluids only
Fluids, Fluids, FluidsFluids, Fluids, Fluids
Key to most resuscitativeKey to most resuscitative
effortsefforts
Give generously and reassessGive generously and reassess
CrystalloidsCrystalloids
Isotonic FluidsIsotonic Fluids
Intravascular volume expansionIntravascular volume expansion
Hauser:Hauser:
 crystalloids rapidly redistributecrystalloids rapidly redistribute
Lethal animal modelLethal animal model
 NS = good resuscitative fluidNS = good resuscitative fluid
 4x blood volume to restore hemodynamics4x blood volume to restore hemodynamics
CrystalloidsCrystalloids
Isotonic FluidsIsotonic Fluids
2 trauma studies2 trauma studies
crystalloids = colloids but:crystalloids = colloids but:
 4x amount4x amount
 longer time to resuscitationlonger time to resuscitation
CrystalloidsCrystalloids
ComplicationsComplications
Under-resuscitationUnder-resuscitation
 renal failurerenal failure
Over-resuscitationOver-resuscitation
 pulmonary edemapulmonary edema
 peripheral edemaperipheral edema
CrystalloidsCrystalloids
SummarySummary
Crystalloids less effective than equalCrystalloids less effective than equal
volume of colloidsvolume of colloids
Preferred when 1Preferred when 1oo
deficit is waterdeficit is water
and/or electrolytesand/or electrolytes
Good in initial resuscitation to restoreGood in initial resuscitation to restore
extracellular volumeextracellular volume
Hypertonic solutions however, may actHypertonic solutions however, may act
as plasma volume expandersas plasma volume expanders
Oncotic pressure
(tendency to pull unit)
CapillaryCapillary
Hydrostatic pressure
(tendency to drive unit)
FluidFluid
TransportTransport
ColloidsColloids
AlbuminAlbumin
Hepatic productionHepatic production
MW = 69,000MW = 69,000
80% of COP80% of COP
Serum tSerum t1/21/2::
18 hours endogenous18 hours endogenous
16 hours16 hours exogenousexogenous
ColloidsColloids
Hydroxyethyl Starch (Hespan)Hydroxyethyl Starch (Hespan)
SyntheticSynthetic
Derived from corn starchDerived from corn starch
AverageAverage MW = 69,000MW = 69,000
Stable, nonantigenicStable, nonantigenic
Used for volume expansionUsed for volume expansion
Renal excretionRenal excretion
 tt 1/21/2 2-67 hours2-67 hours
 90% gone in 42 days90% gone in 42 days
Greater in COP than albuminGreater in COP than albumin
Longer duration of actionLonger duration of action
0.006% adverse reactions0.006% adverse reactions
No effect on blood typingNo effect on blood typing
Prolongs PT, PTT and clotting timesProlongs PT, PTT and clotting times
DosageDosage
 20 ml/Kg/day20 ml/Kg/day
 max 1500 ml/daymax 1500 ml/day
ColloidsColloids
Hydroxyethyl Starch (Hespan)Hydroxyethyl Starch (Hespan)
Fluid ChoicesFluid Choices
Based on:Based on:
 type of deficittype of deficit
 urgency of repletionurgency of repletion
 pathophysiology of conditionpathophysiology of condition
 plasma COPplasma COP
Tastes Great !
Tastes Great !
Less Filling
Less Filling
Fluid ChoicesFluid Choices
Crystalloids for initial resuscitationCrystalloids for initial resuscitation
PRBC’s to replace blood lossPRBC’s to replace blood loss
Fluid Management in PediatricFluid Management in Pediatric
Septic ShockSeptic Shock
Emphasis on the golden hourEmphasis on the golden hour
Early aggressive use of fluids mayEarly aggressive use of fluids may
improve outcomeimprove outcome
Titrate-Reassess!Titrate-Reassess!
Clinical Practice Parameters,
Carcillo et al., CCM, 2002
Alpha-Beta MeterAlpha-Beta Meter
ααßßDopamineDopamine
EpinephrineEpinephrine
Norepinephrine
Norepinephrine
Dobutam
ine
Dobutam
ine
Neosynephrine
Neosynephrine
InotropesInotropes
Agent Site of action Dose
(µg/kg/min)
Effects
Dopamine Dopaminergic
β
α > β
1-3
5-10
11-20
Renal vasodilator
Inotrope
Vasoconstriction
Increase PVR
Dobutamine β1 and β2 1-20 Inotrope
Vasodilation
Epinephrine β > α 0.05-1.0 Inotrope
Tachycardia
Norepinephrine α > β 0.05-1.0 Profound
vasoconstriction
Inotrope
Nitroprusside Vasodilator
Arterial >
venous
0.5-1.0 Vasodilation
Milrinone PDE inhibitor 0.5-0.75 Inotrope
Vasodilator
Dopamine ActivityDopamine Activity
0.5-5.0 mcg/kg/min - dopaminergic receptors0.5-5.0 mcg/kg/min - dopaminergic receptors
2.0-10 mcg/kg/min - beta receptors (inotrope)2.0-10 mcg/kg/min - beta receptors (inotrope)
10-20 mcg/kg/min - alpha and beta receptors10-20 mcg/kg/min - alpha and beta receptors
Over 20 mcg/kg/min - alpha receptors (pressors)Over 20 mcg/kg/min - alpha receptors (pressors)
A Rational Approach to Shock in theA Rational Approach to Shock in the
Pediatric PatientPediatric Patient
Shock / HypotensionShock / Hypotension
Volume ResuscitationVolume Resuscitation
Signs of adequate circulationSigns of adequate circulation
Adequate MAPAdequate MAP
NONO
NONO
pressorspressors
YesYes
A Rational Approach to PressorA Rational Approach to Pressor
Use in the PICUUse in the PICU
NONO
DopamineDopamine
Inadequate MAPInadequate MAP
Dopamine and/orDopamine and/or
NorepinephrineNorepinephrine
Signs of adequate circulationSigns of adequate circulation
Adequate MAPAdequate MAP
A Rational Approach to PressorA Rational Approach to Pressor
Use in the PICUUse in the PICU
Dopamine and/orDopamine and/or
norepinephrinenorepinephrine
Inadequate MAPInadequate MAP
low C.O.low C.O.
epinephrineepinephrine
adequateadequate
MAPMAP
DobutamineDobutamine
oror
MilrinoneMilrinone
tachycardiatachycardia
phenylephrine??phenylephrine??
COCO
““New” Therapies in SepticNew” Therapies in Septic
ShockShock
SteroidsSteroids
VasopressinVasopressin
Activated Protein C (Xigris) in septicActivated Protein C (Xigris) in septic
shockshock
Management of Pediatric SepticManagement of Pediatric Septic
Shock: The Golden HourShock: The Golden Hour
First 15 minutesFirst 15 minutes
Emphasis on response to volumeEmphasis on response to volume
Clinical Practice Parameters,
Carcillo et al., CCM, 2002
Early Goal directed therapy in treatment of sepsis and septic shock- Rivers et al., NEJM, Nov 2001
Community-Acquired SepsisCommunity-Acquired Sepsis
 Pneumonia-Quinolone PLUS B-lactamPneumonia-Quinolone PLUS B-lactam
 Abdominal-Carbapenem OR Pip-TazoAbdominal-Carbapenem OR Pip-Tazo
 Skin/Soft Tissue-Vanco PLUS Carbapenem or Pip-TazoSkin/Soft Tissue-Vanco PLUS Carbapenem or Pip-Tazo
 Urinary Tract-Quinolone PLUS Amp/VancoUrinary Tract-Quinolone PLUS Amp/Vanco
 Unknown-Vanco PLUS B-lactamUnknown-Vanco PLUS B-lactam
Health-Care Associated SepsisHealth-Care Associated Sepsis
 Lung-B-lactam PLUS VancoLung-B-lactam PLUS Vanco
 BloodstreamBloodstream -B-lactam PLUS Vanco +/- Antifungal-B-lactam PLUS Vanco +/- Antifungal
 Surgical SiteSurgical Site -B-lactam PLUS Vanco +/- Anaerobic coverage-B-lactam PLUS Vanco +/- Anaerobic coverage
 Suspected Candida-CaspofunginSuspected Candida-Caspofungin
 Unknown-B-lactam PLUS VancoUnknown-B-lactam PLUS Vanco
Antibiotic Guidelines in Sepsis by Suspected SiteAntibiotic Guidelines in Sepsis by Suspected Site
Patients don’t suddenlyPatients don’t suddenly
deteriorate, healthcaredeteriorate, healthcare
professionals suddenlyprofessionals suddenly
notice!notice!
THANK YOUTHANK YOU

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Shock

  • 1. Shock in the Pediatric Patient:Shock in the Pediatric Patient: oror Oxygen Don’t GoOxygen Don’t Go Where the Blood Won’t Flow!Where the Blood Won’t Flow! Dr. Virendra Kumar GuptaDr. Virendra Kumar Gupta MD PediatricsMD Pediatrics Fellowship In pediatric Gastroentero-Hepatology & LiverFellowship In pediatric Gastroentero-Hepatology & Liver TransplantationTransplantation Assistant ProfessorAssistant Professor Institute of Paediatric GastroenterologyInstitute of Paediatric Gastroenterology Nims University Jaipur Nims University Jaipur 
  • 2. ObjectivesObjectives Define shock and its different categoriesDefine shock and its different categories Review basic physiologic aspects of shockReview basic physiologic aspects of shock Describe management of shock including:Describe management of shock including:  oxygen supply and demandoxygen supply and demand  fluid resuscitationfluid resuscitation  crystalloid vs. colloid controversycrystalloid vs. colloid controversy  vasopressor supportvasopressor support
  • 3. IntroductionIntroduction Shock is a syndrome that results fromShock is a syndrome that results from inadequate oxygen delivery to meetinadequate oxygen delivery to meet metabolic demandsmetabolic demands Oxygen delivery (DOOxygen delivery (DO22 ) is less than) is less than Oxygen Consumption (< VOOxygen Consumption (< VO22)) Untreated this leads to metabolicUntreated this leads to metabolic acidosis, organ dysfunction and deathacidosis, organ dysfunction and death
  • 4. Oxygen DeliveryOxygen Delivery Oxygen delivery = Cardiac Output x ArterialOxygen delivery = Cardiac Output x Arterial Oxygen ContentOxygen Content (DO(DO22 = CO x CaO= CO x CaO22)) Cardiac Output = Heart Rate x Stroke VolumeCardiac Output = Heart Rate x Stroke Volume ((CO = HR x SV)CO = HR x SV) – SV determined by preload, afterload andSV determined by preload, afterload and contractilitycontractility Art Oxygen Content = Oxygen content of theArt Oxygen Content = Oxygen content of the RBC + the oxygen dissolved in plasmaRBC + the oxygen dissolved in plasma (CaO(CaO22 = Hb X SaO= Hb X SaO22 X 1.34 + (.003 X PaOX 1.34 + (.003 X PaO22))
  • 5. Figure 1. FACTORS AFFECTING OXYGEN DELIVERY DO2 CaO2 CO SV HR Oxygenation Hgb A-a gradient DPG Acid-Base Balance Blockers Competitors Temperature Drugs Conduction System Ventricular Compliance EDV ESV Contractility CVP Venous Volume Venous Tone Afterload Blockers Temperature Competitors Drugs Autonomic Tone Metabolic Milieu Ions Acid Base Temperature Drugs Toxins Influenced By Influenced By Influenced By Influenced By
  • 7. Definition of ShockDefinition of Shock Inadequate tissue perfusion to meetInadequate tissue perfusion to meet tissue demandstissue demands Usually result of inadequate blood flowUsually result of inadequate blood flow and/or oxygen deliveryand/or oxygen delivery Shock is not a blood pressure diagnosis!!Shock is not a blood pressure diagnosis!!
  • 8. Characteristics of ShockCharacteristics of Shock End organ dysfunction:End organ dysfunction:  reduced urine outputreduced urine output  altered mental statusaltered mental status  poor peripheral perfusionpoor peripheral perfusion Metabolic dysfunction:Metabolic dysfunction:  acidosisacidosis  altered metabolic demandsaltered metabolic demands
  • 9. Essentials of LifeEssentials of Life Gas exchange capability of lungsGas exchange capability of lungs HemoglobinHemoglobin Oxygen contentOxygen content Cardiac outputCardiac output Tissues to utilize substrateTissues to utilize substrate
  • 10. PreloadPreload AfterloadAfterload ContractilityContractility ResistanceResistance Stroke VolumeStroke Volume Heart RateHeart Rate Arterial BloodArterial Blood PressurePressure OO22 DeliveryDelivery OO22 ContentContent Cardiac OutputCardiac Output xx xx xx
  • 11. Classification of ShockClassification of Shock HypovolemicHypovolemic  dehydration,burns,dehydration,burns, hemorrhagehemorrhage DistributiveDistributive  septic, anaphylactic, spinalseptic, anaphylactic, spinal CardiogenicCardiogenic  myocarditis,dysrhythmiamyocarditis,dysrhythmia ObstructiveObstructive  tamponade,pneumothoraxtamponade,pneumothorax CompensatedCompensated  organ perfusion isorgan perfusion is maintainedmaintained UncompensatedUncompensated  Circulatory failureCirculatory failure with end organwith end organ dysfunctiondysfunction IrreversibleIrreversible  Irreparable loss ofIrreparable loss of essential organsessential organs
  • 12. Hypovolemic Shock Most common form of shock world-wide Results in decreased circulating blood volume, decrease in preload, decreased stroke volume and resultant decrease in cardiac output. Etiology: Hemorrhage, renal and/or GI fluid losses, capillary leak syndromes
  • 13. Distributive Shock Due to an abnormality in vascular tone leading to peripheral pooling of blood with a relative hypovolemia. Etiology – Anaphylaxis – Drug toxicity – Neurologic injury – Early sepsis Management – Fluid – Treat underlying cause
  • 14. Obstructive Shock Mechanical obstruction to ventricular outflow Etiology: Congenital heart disease, massive pulmonary embolism, tension pneumothorax, cardiac tamponade Inadequate C.O. in the face of adequate preload and contractility Treat underlying cause.
  • 15. Dissociative Shock Inability of Hemoglobin molecule to give up the oxygen to tissues Etiology: Carbon Monoxide poisoning, methemoglobinemia, dyshemoglobinemias Tissue perfusion is adequate, but oxygen release to tissue is abnormal Early recognition and treatment of the cause is main therapy
  • 16. Cardiogenic ShockCardiogenic Shock Cardiogenic shock is commonly describedCardiogenic shock is commonly described as “pump failure” (decreased contractility)as “pump failure” (decreased contractility) The common causes areThe common causes are myocarditis, dysrhythmias,and drugsmyocarditis, dysrhythmias,and drugs with a myocardial depressant action,with a myocardial depressant action, acidosis, congenital heart lesions andacidosis, congenital heart lesions and sepsis.sepsis.
  • 17. SIRS/Sepsis/Septic shock Mediator release: exogenous & endogenous Decreased blood flow Cardiac dysfunction Imbalance of oxygen supply and demand Alterations in metabolism SEPTIC SHOCKSEPTIC SHOCK Decreased Volume / Decreased Pump Function/Abnormal Vessel Tone
  • 18.
  • 19. Mechanical Requirements forMechanical Requirements for Adequate Tissue PerfusionAdequate Tissue Perfusion FluidFluid PumpPump VesselsVessels FlowFlow
  • 20. Clinical AssessmentClinical Assessment Heart rateHeart rate Peripheral circulationPeripheral circulation  capillary refillcapillary refill  pulsespulses  extremity temperatureextremity temperature PulmonaryPulmonary End organ perfusionEnd organ perfusion  brainbrain  kidneykidney
  • 21. Improving Stroke Volume:Improving Stroke Volume: Therapy for Cardiovascular SupportTherapy for Cardiovascular Support Preload Volume Contractility Inotropes Afterload Vasodilators
  • 22. Septic ShockSeptic Shock Early (“Warm”)Early (“Warm”) Decreased peripheral vascular resistanceDecreased peripheral vascular resistance Increased cardiac outputIncreased cardiac output Late (“Cold”)Late (“Cold”) Increased peripheral vascular resistanceIncreased peripheral vascular resistance Decreased cardiac outputDecreased cardiac output
  • 23. Assessment of CirculationAssessment of Circulation Early Late Heart rate Tachycardia Tachycardia/ Bradycardia Blood pressure Normal Decreased Peripheral circulation Warm/Cool Decreased/ Increased pulses Cool Decreased pulses
  • 24. Assessment of CirculationAssessment of Circulation Early Late End-organ: Skin Decreased cap refill Very decreased cap refill Brain Irritable, restless Lethargic, unresponsive Kidneys Oliguria Oliguria, anuria
  • 25. Heart Rate and Perfusion PressureHeart Rate and Perfusion Pressure (MAP-CVP) Parameters by Age(MAP-CVP) Parameters by Age Age Heart Rate MAP-CVP Term newborn 120-180 55 < 1 120-180 60 < 2 120-160 65 < 7 120-160 65 < 15 90-140 65
  • 26. Hemodynamic Assessment of ShockHemodynamic Assessment of Shock Type of Shock Preload Afterload Contractility Cardiac Output Cardiogenic ⇑ ⇑ ⇓ ⇓ Hypovolemic ⇓ ⇑ ⇔ ⇓ Septic Early Late ⇓ ⇑ ⇓ ⇑ ⇔ ⇓ ⇑ ⇓ Obstructive ⇓ ⇑ ⇓ ⇓ Distributive ⇓ ⇓ ⇑ ⇔
  • 27. Goals of ResuscitationGoals of Resuscitation Overall goal:Overall goal:  increase Oincrease O22 deliverydelivery  decrease demanddecrease demand TreatmentTreatment OO22 contentcontent CardiacCardiac outputoutput BloodBlood pressurepressure Sedation/analgesiaSedation/analgesia
  • 28. Principles of ManagementPrinciples of Management A: AirwayA: Airway  patent upper airwaypatent upper airway B: BreathingB: Breathing  adequate ventilation and oxygenationadequate ventilation and oxygenation C: CirculationC: Circulation  optimizeoptimize  cardiac functioncardiac function  oxygenationoxygenation
  • 30. Airway ManagementAirway Management Patients in shock have:Patients in shock have:  OO22 deliverydelivery  progressive respiratory fatigue/failureprogressive respiratory fatigue/failure  energy shunted from vital organsenergy shunted from vital organs  afterloadafterload
  • 31. Airway ManagementAirway Management Early intubation provides:Early intubation provides:  OO22 delivery and contentdelivery and content  controlled ventilation which:controlled ventilation which:  reduces metabolic demandreduces metabolic demand  allows C.O. to vital organsallows C.O. to vital organs
  • 32. TherapyTherapy Vagolysis Chromotropy V o lu m e C V P P re lo a d V a s o d ila to rs V a s o c o n s tric to rs A fte rlo a d C o rre c t a c id o s is h y p o x ia h y p o g ly c e m ia In o tro p ic a g e n ts C o n tra c tility S tro k e V o lu m e Heart Rate 
  • 33. Fluid ChoicesFluid Choices Less Filling Less Filling Tastes Great ! Tastes Great ! Colloid Crystalloid
  • 34. CrystalloidsCrystalloids Hypotonic Fluids (DHypotonic Fluids (D55 1/4 NS)1/4 NS) No role in resuscitationNo role in resuscitation Maintenance fluids onlyMaintenance fluids only
  • 35. Fluids, Fluids, FluidsFluids, Fluids, Fluids Key to most resuscitativeKey to most resuscitative effortsefforts Give generously and reassessGive generously and reassess
  • 36. CrystalloidsCrystalloids Isotonic FluidsIsotonic Fluids Intravascular volume expansionIntravascular volume expansion Hauser:Hauser:  crystalloids rapidly redistributecrystalloids rapidly redistribute Lethal animal modelLethal animal model  NS = good resuscitative fluidNS = good resuscitative fluid  4x blood volume to restore hemodynamics4x blood volume to restore hemodynamics
  • 37. CrystalloidsCrystalloids Isotonic FluidsIsotonic Fluids 2 trauma studies2 trauma studies crystalloids = colloids but:crystalloids = colloids but:  4x amount4x amount  longer time to resuscitationlonger time to resuscitation
  • 38. CrystalloidsCrystalloids ComplicationsComplications Under-resuscitationUnder-resuscitation  renal failurerenal failure Over-resuscitationOver-resuscitation  pulmonary edemapulmonary edema  peripheral edemaperipheral edema
  • 39. CrystalloidsCrystalloids SummarySummary Crystalloids less effective than equalCrystalloids less effective than equal volume of colloidsvolume of colloids Preferred when 1Preferred when 1oo deficit is waterdeficit is water and/or electrolytesand/or electrolytes Good in initial resuscitation to restoreGood in initial resuscitation to restore extracellular volumeextracellular volume Hypertonic solutions however, may actHypertonic solutions however, may act as plasma volume expandersas plasma volume expanders
  • 40. Oncotic pressure (tendency to pull unit) CapillaryCapillary Hydrostatic pressure (tendency to drive unit) FluidFluid TransportTransport
  • 41. ColloidsColloids AlbuminAlbumin Hepatic productionHepatic production MW = 69,000MW = 69,000 80% of COP80% of COP Serum tSerum t1/21/2:: 18 hours endogenous18 hours endogenous 16 hours16 hours exogenousexogenous
  • 42. ColloidsColloids Hydroxyethyl Starch (Hespan)Hydroxyethyl Starch (Hespan) SyntheticSynthetic Derived from corn starchDerived from corn starch AverageAverage MW = 69,000MW = 69,000 Stable, nonantigenicStable, nonantigenic Used for volume expansionUsed for volume expansion Renal excretionRenal excretion  tt 1/21/2 2-67 hours2-67 hours  90% gone in 42 days90% gone in 42 days
  • 43. Greater in COP than albuminGreater in COP than albumin Longer duration of actionLonger duration of action 0.006% adverse reactions0.006% adverse reactions No effect on blood typingNo effect on blood typing Prolongs PT, PTT and clotting timesProlongs PT, PTT and clotting times DosageDosage  20 ml/Kg/day20 ml/Kg/day  max 1500 ml/daymax 1500 ml/day ColloidsColloids Hydroxyethyl Starch (Hespan)Hydroxyethyl Starch (Hespan)
  • 44. Fluid ChoicesFluid Choices Based on:Based on:  type of deficittype of deficit  urgency of repletionurgency of repletion  pathophysiology of conditionpathophysiology of condition  plasma COPplasma COP Tastes Great ! Tastes Great ! Less Filling Less Filling
  • 45. Fluid ChoicesFluid Choices Crystalloids for initial resuscitationCrystalloids for initial resuscitation PRBC’s to replace blood lossPRBC’s to replace blood loss
  • 46. Fluid Management in PediatricFluid Management in Pediatric Septic ShockSeptic Shock Emphasis on the golden hourEmphasis on the golden hour Early aggressive use of fluids mayEarly aggressive use of fluids may improve outcomeimprove outcome Titrate-Reassess!Titrate-Reassess! Clinical Practice Parameters, Carcillo et al., CCM, 2002
  • 48. InotropesInotropes Agent Site of action Dose (µg/kg/min) Effects Dopamine Dopaminergic β α > β 1-3 5-10 11-20 Renal vasodilator Inotrope Vasoconstriction Increase PVR Dobutamine β1 and β2 1-20 Inotrope Vasodilation Epinephrine β > α 0.05-1.0 Inotrope Tachycardia Norepinephrine α > β 0.05-1.0 Profound vasoconstriction Inotrope Nitroprusside Vasodilator Arterial > venous 0.5-1.0 Vasodilation Milrinone PDE inhibitor 0.5-0.75 Inotrope Vasodilator
  • 49. Dopamine ActivityDopamine Activity 0.5-5.0 mcg/kg/min - dopaminergic receptors0.5-5.0 mcg/kg/min - dopaminergic receptors 2.0-10 mcg/kg/min - beta receptors (inotrope)2.0-10 mcg/kg/min - beta receptors (inotrope) 10-20 mcg/kg/min - alpha and beta receptors10-20 mcg/kg/min - alpha and beta receptors Over 20 mcg/kg/min - alpha receptors (pressors)Over 20 mcg/kg/min - alpha receptors (pressors)
  • 50. A Rational Approach to Shock in theA Rational Approach to Shock in the Pediatric PatientPediatric Patient Shock / HypotensionShock / Hypotension Volume ResuscitationVolume Resuscitation Signs of adequate circulationSigns of adequate circulation Adequate MAPAdequate MAP NONO NONO pressorspressors YesYes
  • 51. A Rational Approach to PressorA Rational Approach to Pressor Use in the PICUUse in the PICU NONO DopamineDopamine Inadequate MAPInadequate MAP Dopamine and/orDopamine and/or NorepinephrineNorepinephrine Signs of adequate circulationSigns of adequate circulation Adequate MAPAdequate MAP
  • 52. A Rational Approach to PressorA Rational Approach to Pressor Use in the PICUUse in the PICU Dopamine and/orDopamine and/or norepinephrinenorepinephrine Inadequate MAPInadequate MAP low C.O.low C.O. epinephrineepinephrine adequateadequate MAPMAP DobutamineDobutamine oror MilrinoneMilrinone tachycardiatachycardia phenylephrine??phenylephrine?? COCO
  • 53. ““New” Therapies in SepticNew” Therapies in Septic ShockShock SteroidsSteroids VasopressinVasopressin Activated Protein C (Xigris) in septicActivated Protein C (Xigris) in septic shockshock
  • 54. Management of Pediatric SepticManagement of Pediatric Septic Shock: The Golden HourShock: The Golden Hour First 15 minutesFirst 15 minutes Emphasis on response to volumeEmphasis on response to volume Clinical Practice Parameters, Carcillo et al., CCM, 2002
  • 55.
  • 56. Early Goal directed therapy in treatment of sepsis and septic shock- Rivers et al., NEJM, Nov 2001
  • 57. Community-Acquired SepsisCommunity-Acquired Sepsis  Pneumonia-Quinolone PLUS B-lactamPneumonia-Quinolone PLUS B-lactam  Abdominal-Carbapenem OR Pip-TazoAbdominal-Carbapenem OR Pip-Tazo  Skin/Soft Tissue-Vanco PLUS Carbapenem or Pip-TazoSkin/Soft Tissue-Vanco PLUS Carbapenem or Pip-Tazo  Urinary Tract-Quinolone PLUS Amp/VancoUrinary Tract-Quinolone PLUS Amp/Vanco  Unknown-Vanco PLUS B-lactamUnknown-Vanco PLUS B-lactam Health-Care Associated SepsisHealth-Care Associated Sepsis  Lung-B-lactam PLUS VancoLung-B-lactam PLUS Vanco  BloodstreamBloodstream -B-lactam PLUS Vanco +/- Antifungal-B-lactam PLUS Vanco +/- Antifungal  Surgical SiteSurgical Site -B-lactam PLUS Vanco +/- Anaerobic coverage-B-lactam PLUS Vanco +/- Anaerobic coverage  Suspected Candida-CaspofunginSuspected Candida-Caspofungin  Unknown-B-lactam PLUS VancoUnknown-B-lactam PLUS Vanco Antibiotic Guidelines in Sepsis by Suspected SiteAntibiotic Guidelines in Sepsis by Suspected Site
  • 58. Patients don’t suddenlyPatients don’t suddenly deteriorate, healthcaredeteriorate, healthcare professionals suddenlyprofessionals suddenly notice!notice! THANK YOUTHANK YOU