Pediatric sepsis resident survival guide: Difference between revisions

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| style="text-align: center; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5); font-size: 120%;" | [[#Top|{{fontcolor|#F8F8FF|Sepsis in Pediatric Patients}}]]
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! style="padding: 0 5px; font-size: 100%; background: #A8A8A8;" align=center| {{fontcolor|#2B3B44|Neonatal Sepsis<BR>Resident Survival Guide}}
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[[{{PAGENAME}}#Diagnostic Criteria|{{fontcolor|#F8F8FF|Diagnostic Criteria}}]]
<li>[[{{PAGENAME}}#Systemic Inflammatory Response Syndrome|{{fontcolor|#F8F8FF|Systemic Inflammatory Response Syndrome}}]]</li>
<li>[[{{PAGENAME}}#Sepsis|{{fontcolor|#F8F8FF|Sepsis}}]]</li>
<li>[[{{PAGENAME}}#Severe Sepsis|{{fontcolor|#F8F8FF|Severe Sepsis}}]]</li>
<li>[[{{PAGENAME}}#Septic Shock|{{fontcolor|#F8F8FF|Septic Shock}}]]</li>
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! style="font-size: 90%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Diagnostic Criteria|Diagnostic Criteria]]
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[[{{PAGENAME}}#Causes|{{fontcolor|#F8F8FF|Causes}}]]
<li>[[{{PAGENAME}}#Children > 1 Month|{{fontcolor|#F8F8FF|Children > 1 Month}}]]</li>
<li>[[{{PAGENAME}}#Children < 1 Month|{{fontcolor|#F8F8FF|Children < 1 Month}}]]</li>
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! style="font-size: 90%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Causes|Causes]]
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[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation (Infants and Children)|{{fontcolor|#F8F8FF|Focused Initial Rapid Evaluation}}]]
<li>[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation (Infants and Children)|{{fontcolor|#F8F8FF|Infants and Children}}]]</li>
<li>[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation (Newborns)|{{fontcolor|#F8F8FF|Newborns}}]]</li>
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! style="font-size: 90%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|Focused Initial Rapid Evaluation]]
| style="padding: 2px 10px; background: #4479BA; border-radius: 5px 5px 5px 5px; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5); box-shadow: 0 1px 1px rgba(0, 0, 0, 0.5);" |
[[{{PAGENAME}}#Empiric Antibiotic Therapy|{{fontcolor|#F8F8FF|Empiric Antibiotic Therapy}}]]
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! style="font-size: 90%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Empiric Antibiotic Therapy|Empiric Therapy]]
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|-
[[{{PAGENAME}}#Dos and Don'ts|{{fontcolor|#F8F8FF|Dos and Don'ts}}]]
! style="font-size: 90%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Dos|Dos]]
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! style="font-size: 90%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Don'ts|Don'ts]]
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__NOTOC____NOEDITSECTION__
__NOTOC____NOEDITSECTION__
{{Main|Sepsis}}
{{Main|Sepsis}}
{{Seealso|Sepsis resident survival guide}}
{{See also|Sepsis resident survival guide}}
{{CMG}}; {{AE}} {{AZ}}; {{VB}}
{{CMG}}
 
==Diagnostic Criteria==


==Diagnostic Criteria==
===Systemic Inflammatory Response Syndrome===
===Systemic Inflammatory Response Syndrome===
Systemic inflammatory response syndrome (SIRS) represents the complex findings resulting from systemic activation of the innate immune response triggered by localized or generalized infection, trauma, thermal injury, or sterile inflammatory processes. However, criteria for SIRS are considered to be too nonspecific to be of utility in diagnosing a cause for the syndrome or in identifying a distinct pattern of host response.<ref>{{Cite journal| doi = 10.1097/CCM.0b013e31827e83af| issn = 1530-0293| volume = 41| issue = 2| pages = 580–637| last1 = Dellinger| first1 = R. Phillip| last2 = Levy| first2 = Mitchell M.| last3 = Rhodes| first3 = Andrew| last4 = Annane| first4 = Djillali| last5 = Gerlach| first5 = Herwig| last6 = Opal| first6 = Steven M.| last7 = Sevransky| first7 = Jonathan E.| last8 = Sprung| first8 = Charles L.| last9 = Douglas| first9 = Ivor S.| last10 = Jaeschke| first10 = Roman| last11 = Osborn| first11 = Tiffany M.| last12 = Nunnally| first12 = Mark E.| last13 = Townsend| first13 = Sean R.| last14 = Reinhart| first14 = Konrad| last15 = Kleinpell| first15 = Ruth M.| last16 = Angus| first16 = Derek C.| last17 = Deutschman| first17 = Clifford S.| last18 = Machado| first18 = Flavia R.| last19 = Rubenfeld| first19 = Gordon D.| last20 = Webb| first20 = Steven A.| last21 = Beale| first21 = Richard J.| last22 = Vincent| first22 = Jean-Louis| last23 = Moreno| first23 = Rui| last24 = Surviving Sepsis Campaign Guidelines Committee including the Pediatric Subgroup| title = Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2012| journal = Critical Care Medicine| date = 2013-02| pmid = 23353941}}</ref>
Systemic inflammatory response syndrome (SIRS) represents the complex findings resulting from systemic activation of the innate immune response triggered by localized or generalized infection, trauma, thermal injury, or sterile inflammatory processes. However, criteria for SIRS are considered to be too nonspecific to be of utility in diagnosing a cause for the syndrome or in identifying a distinct pattern of host response.<ref>{{Cite journal| doi = 10.1097/CCM.0b013e31827e83af| issn = 1530-0293| volume = 41| issue = 2| pages = 580–637| last1 = Dellinger| first1 = R. Phillip| last2 = Levy| first2 = Mitchell M.| last3 = Rhodes| first3 = Andrew| last4 = Annane| first4 = Djillali| last5 = Gerlach| first5 = Herwig| last6 = Opal| first6 = Steven M.| last7 = Sevransky| first7 = Jonathan E.| last8 = Sprung| first8 = Charles L.| last9 = Douglas| first9 = Ivor S.| last10 = Jaeschke| first10 = Roman| last11 = Osborn| first11 = Tiffany M.| last12 = Nunnally| first12 = Mark E.| last13 = Townsend| first13 = Sean R.| last14 = Reinhart| first14 = Konrad| last15 = Kleinpell| first15 = Ruth M.| last16 = Angus| first16 = Derek C.| last17 = Deutschman| first17 = Clifford S.| last18 = Machado| first18 = Flavia R.| last19 = Rubenfeld| first19 = Gordon D.| last20 = Webb| first20 = Steven A.| last21 = Beale| first21 = Richard J.| last22 = Vincent| first22 = Jean-Louis| last23 = Moreno| first23 = Rui| last24 = Surviving Sepsis Campaign Guidelines Committee including the Pediatric Subgroup| title = Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2012| journal = Critical Care Medicine| date = 2013-02| pmid = 23353941}}</ref><ref>{{Cite journal| doi = 10.1097/CCM.0b013e31819323c6| issn = 1530-0293| volume = 37| issue = 2| pages = 666–688| last1 = Brierley| first1 = Joe| last2 = Carcillo| first2 = Joseph A.| last3 = Choong| first3 = Karen| last4 = Cornell| first4 = Tim| last5 = Decaen| first5 = Allan| last6 = Deymann| first6 = Andreas| last7 = Doctor| first7 = Allan| last8 = Davis| first8 = Alan| last9 = Duff| first9 = John| last10 = Dugas| first10 = Marc-Andre| last11 = Duncan| first11 = Alan| last12 = Evans| first12 = Barry| last13 = Feldman| first13 = Jonathan| last14 = Felmet| first14 = Kathryn| last15 = Fisher| first15 = Gene| last16 = Frankel| first16 = Lorry| last17 = Jeffries| first17 = Howard| last18 = Greenwald| first18 = Bruce| last19 = Gutierrez| first19 = Juan| last20 = Hall| first20 = Mark| last21 = Han| first21 = Yong Y.| last22 = Hanson| first22 = James| last23 = Hazelzet| first23 = Jan| last24 = Hernan| first24 = Lynn| last25 = Kiff| first25 = Jane| last26 = Kissoon| first26 = Niranjan| last27 = Kon| first27 = Alexander| last28 = Irazuzta| first28 = Jose| last29 = Irazusta| first29 = Jose| last30 = Lin| first30 = John| last31 = Lorts| first31 = Angie| last32 = Mariscalco| first32 = Michelle| last33 = Mehta| first33 = Renuka| last34 = Nadel| first34 = Simon| last35 = Nguyen| first35 = Trung| last36 = Nicholson| first36 = Carol| last37 = Peters| first37 = Mark| last38 = Okhuysen-Cawley| first38 = Regina| last39 = Poulton| first39 = Tom| last40 = Relves| first40 = Monica| last41 = Rodriguez| first41 = Agustin| last42 = Rozenfeld| first42 = Ranna| last43 = Schnitzler| first43 = Eduardo| last44 = Shanley| first44 = Tom| last45 = Kache| first45 = Saraswati| last46 = Skache| first46 = Sara| last47 = Skippen| first47 = Peter| last48 = Torres| first48 = Adalberto| last49 = von Dessauer| first49 = Bettina| last50 = Weingarten| first50 = Jacki| last51 = Yeh| first51 = Timothy| last52 = Zaritsky| first52 = Arno| last53 = Stojadinovic| first53 = Bonnie| last54 = Zimmerman| first54 = Jerry| last55 = Zuckerberg| first55 = Aaron| title = Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock: 2007 update from the American College of Critical Care Medicine| journal = Critical Care Medicine| date = 2009-02| pmid = 19325359}}</ref>


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Septic shock is defined as sepsis-induced hypotension persisting despite adequate fluid resuscitation, in the absence of other causes for hypotension.
Septic shock is defined as sepsis-induced hypotension persisting despite adequate fluid resuscitation, in the absence of other causes for hypotension.
* '''Septic shock in adult patients''' refers to a state of acute circulatory failure characterized by persistent arterial hypotension unexplained by other causes.
* '''Septic shock in adult patients''' refers to a state of acute circulatory failure characterized by persistent arterial hypotension unexplained by other causes.
* '''Septic shock in pediatric patients''' is defined as a tachycardia (may be absent in the hypothermic patient) with signs of decreased perfusion including decreased peripheral pulses compared with central pulses, altered alertness, flash capillary refill or capillary refill 􏰀2 seconds, mottled or cool extremities, or decreased urine output.
* '''Septic shock in pediatric patients''' is defined as 1) a suspected infection manifested by hypothermia or hyperthermia, and 2) clinical signs of inadequate tissue perfusion including any of the following:<ref>{{Cite journal| doi = 10.1097/CCM.0b013e31819323c6| issn = 1530-0293| volume = 37| issue = 2| pages = 666–688| last1 = Brierley| first1 = Joe| last2 = Carcillo| first2 = Joseph A.| last3 = Choong| first3 = Karen| last4 = Cornell| first4 = Tim| last5 = Decaen| first5 = Allan| last6 = Deymann| first6 = Andreas| last7 = Doctor| first7 = Allan| last8 = Davis| first8 = Alan| last9 = Duff| first9 = John| last10 = Dugas| first10 = Marc-Andre| last11 = Duncan| first11 = Alan| last12 = Evans| first12 = Barry| last13 = Feldman| first13 = Jonathan| last14 = Felmet| first14 = Kathryn| last15 = Fisher| first15 = Gene| last16 = Frankel| first16 = Lorry| last17 = Jeffries| first17 = Howard| last18 = Greenwald| first18 = Bruce| last19 = Gutierrez| first19 = Juan| last20 = Hall| first20 = Mark| last21 = Han| first21 = Yong Y.| last22 = Hanson| first22 = James| last23 = Hazelzet| first23 = Jan| last24 = Hernan| first24 = Lynn| last25 = Kiff| first25 = Jane| last26 = Kissoon| first26 = Niranjan| last27 = Kon| first27 = Alexander| last28 = Irazuzta| first28 = Jose| last29 = Irazusta| first29 = Jose| last30 = Lin| first30 = John| last31 = Lorts| first31 = Angie| last32 = Mariscalco| first32 = Michelle| last33 = Mehta| first33 = Renuka| last34 = Nadel| first34 = Simon| last35 = Nguyen| first35 = Trung| last36 = Nicholson| first36 = Carol| last37 = Peters| first37 = Mark| last38 = Okhuysen-Cawley| first38 = Regina| last39 = Poulton| first39 = Tom| last40 = Relves| first40 = Monica| last41 = Rodriguez| first41 = Agustin| last42 = Rozenfeld| first42 = Ranna| last43 = Schnitzler| first43 = Eduardo| last44 = Shanley| first44 = Tom| last45 = Kache| first45 = Saraswati| last46 = Skache| first46 = Sara| last47 = Skippen| first47 = Peter| last48 = Torres| first48 = Adalberto| last49 = von Dessauer| first49 = Bettina| last50 = Weingarten| first50 = Jacki| last51 = Yeh| first51 = Timothy| last52 = Zaritsky| first52 = Arno| last53 = Stojadinovic| first53 = Bonnie| last54 = Zimmerman| first54 = Jerry| last55 = Zuckerberg| first55 = Aaron| title = Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock: 2007 update from the American College of Critical Care Medicine| journal = Critical Care Medicine| date = 2009-02| pmid = 19325359}}</ref>
:* Decreased or altered mental status
:* Decreased urine output 􏰁&lt;1 ml/kg/h
:* Bounding peripheral pulses (warm shock)
:* Diminished peripheral pulses compared with central pulses (cold shock)
:* Wide pulse pressure (warm shock)
:* Prolonged capillary refill &gt;􏰃2 seconds (cold shock)
:* Flash capillary refill (warm shock)
:* Mottled or cool extremities (cold shock)
* '''Septic shock in newborns''' manifests as tachycardia, respiratory distress, poor feeding, poor tone, poor color, tachypnea, diarrhea, or reduced perfusion, particularly in the presence of a maternal history of chorioamnionitis or prolonged rupture of membranes.


==Causes==
==Causes==
''Sepsis is a life-threatening condition and must be treated immediately irrespective of the underlying cause.''
''Sepsis is a life-threatening condition and must be treated immediately irrespective of the underlying cause.''
* If associated with [[community-acquired pneumonia]]
:* ''[[Streptococcus pneumoniae]]''
:* ''[[Staphylococcus aureus]]'' and [[MRSA]]
:* ''[[Legionella]]''
:* [[Gram-negative bacilli]]
* If associated with [[urinary tract infection]]
:* [[Aerobic]] [[gram-negative bacilli]]
:* ''[[Enterococcus]]''
* If associated with [[intra-abdominal infection]]
:* [[Aerobic]] [[gram-negative bacilli]]
:* [[Anaerobic]] [[gram-negative bacilli]]
* If associated with [[intravenous drug use]]
:* ''[[Staphylococcus]]''
:* ''[[Nocardia]]''
* If associated with [[petechiae]]
:* ''[[Neisseria meningitidis]]''
:* [[Rocky Mountain spotted fever]]


==FIRE: Focused Initial Rapid Evaluation==
===Children > 1 Month===
* ''[[Streptococcus pneumoniae]]''
* ''[[Neisseria meningitidis]]''
* ''[[Staphylococcus aureus]]''
* ''[[Haemophilus influenzae]]''
 
===Children < 1 Month===
* ''[[Streptococcus agalactiae]]''
* ''[[Escherichia coli]]''
* ''[[Klebsiella]]''
* ''[[Enterobacter]]''
* ''[[Staphylococcus aureus]]''
* ''[[Listeria]]''
* ''[[Salmonella]]''
* ''[[Haemophilus influenzae]]''
* ''[[Staphylococcus epidermidis]]''
 
==FIRE: Focused Initial Rapid Evaluation (Infants and Children)==
<span style="background: #FFF0F5; font-weight: bold; font-style: italic;">Focused Initial Rapid Evaluation (FIRE)</span> should be undertaken to identify patients requiring urgent intervention.
<span style="background: #FFF0F5; font-weight: bold; font-style: italic;">Focused Initial Rapid Evaluation (FIRE)</span> should be undertaken to identify patients requiring urgent intervention.


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CVP, central venous pressure;
CVP, central venous pressure;
DC, differential count;
DC, differential count;
ECMO, extracorporeal membrane oxygenation;
FATD, femoral arterial thermodilution;
HMG, hepatomegaly;
IAP, intra-abdominal pressure;
ICU, intensive care unit;
ICU, intensive care unit;
INR, international normalized ratio;
INR, international normalized ratio;
IO, intraosseous;
IV, intravenous;
LFT, liver function test;
LFT, liver function test;
MAP, mean arterial pressure;
MAP, mean arterial pressure;
PA, pulmonary artery;
PCWP, pulmonary capillary wedge pressure;
PCWP, pulmonary capillary wedge pressure;
PDA, patent ductus arteriosus;
PT, prothrombin time;
PT, prothrombin time;
PTT, partial prothrombin time;
PTT, partial prothrombin time;
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SBP, systolic blood pressure;
SBP, systolic blood pressure;
ScvO2, central venous oxygen saturation;
ScvO2, central venous oxygen saturation;
SMA-7, sequential multiple analysis-7;
SvO2, mixed venous oxygen saturation;
SvO2, mixed venous oxygen saturation;
SMA-7, sequential multiple analysis-7.
VLBW, very low birth weight.
</span>
</span>


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<BIG>'''Suspected sepsis'''</BIG> [[Sepsis resident survival guide#Diagnostic Criteria|(details)]]
<BIG>'''Suspected Septic Shock'''</BIG> [[Pediatric sepsis resident survival guide#Diagnostic Criteria|(details)]]
----
----
'''Signs and Symptoms'''
* Suspected infection manifested by hypothermia or hyperthermia
* Fever (&gt;38.3°C)
* Clinical signs of inadequate tissue perfusion
* Hypothermia (core temperature &lt;36°C)
:* Altered mental status
* Heart rate &gt;90/min–1 or more than two SD above the normal value for age
:* Decreased urine output 􏰁&lt;1 ml/kg/h
* Tachypnea
:* Diminished peripheral pulses compared with central pulses (cold shock)
* Altered mental status
:* Prolonged capillary refill &gt;􏰃2 seconds (cold shock)
* Significant edema or positive fluid balance (&gt;20 mL/kg over 24 hr)
:* Mottled or cool extremities (cold shock)
* Hypotension (SBP &lt;90 mm Hg, MAP &lt;70 mm Hg, or an SBP decrease &gt;40 mm Hg)
:* Bounding peripheral pulses (warm shock)
* Hypoxemia (PaO2/FiO2 &lt;300)
:* Flash capillary refill (warm shock)
* Acute oliguria (urine output &lt;0.5 mL/kg/hr for at least 2 hrs despite adequate fluid resuscitation)
:* Wide pulse pressure (warm shock)
* Ileus (absent bowel sounds)
</div>}}
* Diminished capillary refill or mottling
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'''Laboratory Findings'''
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* Hyperglycemia (plasma glucose &gt;140mg/dL or 7.7 mmol/L) in the absence of diabetes
<BIG>'''The First Hour of Resuscitation'''</BIG>
* Leukocytosis (WBC count &gt;12,000 μL–1)
----
* Leukopenia (WBC count &lt;4000 μL–1)
* Secure airway ± intubation (atropine / ketamine / benzodiazepine if indicated)
* Bandemia &gt;10% immature forms
* Administer high-flow oxygen supplementation
* C-reactive protein more than two SD above the normal value
* Administer IV boluses of 20 ml/kg saline until perfusion restores or rales/HMG develop
* Procalcitonin greater than two SD above the normal value
* Administer empiric antibiotics [[Pediatric sepsis resident survival guide#Empiric Antibiotic Therapy|(details)]]
* Creatinine increase &gt;0.5mg/dL or 44.2 μmol/L
* ± Correct hypoglycemia and hypocalcemia
* Coagulation abnormalities (INR &gt;1.5 or aPTT &gt;60 s)
<BIG>'''For Fluid Refractory Shock'''</BIG>
* Thrombocytopenia (platelet count &lt;100,000 μL–1)
----
* Hyperbilirubinemia (plasma total bilirubin &gt;4 mg/dL or 70 μmol/L)
* Place central venous line and monitor CVP
* Hyperlactatemia (&gt;1 mmol/L)
* Reverse cold shock by titrating dopamine or epinephrine
* Reverse warm shock by titrating norepinephrine
* Administer hydrocortisone if at risk for adrenal insufficiency
<BIG>'''Therapeutic End Points'''</BIG>
----
* Normal mental status
* Urine output 􏰃&gt;1 mL/kg/h
* Warm extremities
* Capillary refill 􏰉≤2 seconds
* Normal peripheral and central pulses
* Normal blood pressure for age
* Normal glucose concentration
* Normal ionized calcium concentration
</div>}}
</div>}}
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<BIG>'''Early Goal-Directed Therapy'''</BIG>
<BIG>'''Beyond the First Hour of Resuscitation'''</BIG>
----
----
* Supplemental oxygen ± intubation / ventilatory support ± sedation to maintain SaO2 ≥93%
* ± Transfuse RBC if Hb &lt;􏰁10 g/dL
* Arterial and central venous line placement
* ± Infuse FFP if prolonged INR
<BIG>'''Rivers Protocol'''</BIG>
* ± Diuretics/dialysis if fluid overloaded
* Adjust D10%-containing isotonic fluid to maintain normoglycemia
<BIG>'''Therapeutic End Points'''</BIG>
----
* Normal mental status
* Urine output 􏰃&gt;1 mL/kg/h
* Capillary refill 􏰉≤2 seconds
* Warm extremities
* Threshold heart rates
* Normal peripheral and central pulses
* Perfusion pressure appropriate for age
* CI 􏰃&gt;3.3 L/min/m2 and &lt;􏰁6.0 L/min/m2
* ScvO2 &gt;􏰃70%
</div>}}
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<BIG>'''For Cold Shock with Normal Blood Pressure'''</BIG>
----
----
* Infuse a 500 ml bolus of crystalloid q 30 minutes to maintain CVP at 8–12 mm Hg.
* Titrate fluid and epinephrine
* If MAP &lt;65 mm Hg, administer vasopressors to maintain MAP at ≥65 mm Hg.
* Maintain ScvO2 &gt;70% and Hb &gt;10 g/dL
* If MAP &gt;90 mm Hg, administer vasodilators until MAP ≤90 mm Hg.
* Add nitroprusside / nitroglycerin / milrinone with volume loading if ScvO2 &lt;70%
* If ScvO2 <70%, transfuse RBC to maintain Hct at ≥30%.
* Consider levosimendan / enoximone in recalcitrant low CO syndrome
* Once CVP/MAP/Hct are optimized, if ScvO2 is still <70%, load dobutamine 2.5 μg/kg/min.
* ± Thyroid hormone replacement
* Titrate dobutamine by 2.5 μg/kg/min q 30 minutes until 20 μg/kg/min or ScvO2 ≥70%.
* ± Hydrocortisone replacement
* Taper or discontinue dobutamine if MAP &lt;65 mm Hg or HR &gt;120 bpm.<ref>{{Cite journal| doi = 10.1056/NEJMoa010307| issn = 0028-4793| volume = 345| issue = 19| pages = 1368–1377| last1 = Rivers| first1 = E.| last2 = Nguyen| first2 = B.| last3 = Havstad| first3 = S.| last4 = Ressler| first4 = J.| last5 = Muzzin| first5 = A.| last6 = Knoblich| first6 = B.| last7 = Peterson| first7 = E.| last8 = Tomlanovich| first8 = M.| last9 = Early Goal-Directed Therapy Collaborative Group| title = Early goal-directed therapy in the treatment of severe sepsis and septic shock| journal = The New England Journal of Medicine| date = 2001-11-08| pmid = 11794169}}</ref>
<BIG>'''For Cold Shock with Low Blood Pressure'''</BIG>
<BIG>'''Surviving Sepsis Campaign Care Bundles'''</BIG>
----
----
'''To Be Completed Within 3 Hours:'''
* Titrate fluid and epinephrine
* Measure lactate level
* Maintain ScvO2 &gt;70% and Hb &gt;10 g/dL
* Obtain ≥2 sets of blood cultures prior to administration of antibiotics
* Add norepinephrine if hypotensive
* Administer 30 mL/kg crystalloid for hypotension or lactate ≥4 mmol/L
* Consider dobutamine / milrinone / levosimendan / enoximone if ScvO2 &lt;70%
* Administer empiric antibiotics [[Sepsis resident survival guide#Empiric Antibiotic Therapy|(details)]]
<BIG>'''For Warm Shock with Normal Blood Pressure'''</BIG>
'''To Be Completed Within 6 Hours:'''
* Administer vasopressors for persistent hypotension to maintain MAP ≥65 mm Hg
* For septic shock or initial lactate ≥4 mmol/L (36 mg/dL):
: — Measure CVP
: — Measure ScvO2
* Remeasure lactate if initial lactate was elevated
<BIG>'''Goals of Initial Resuscitation'''</BIG>
----
----
* CVP 8–12 mm Hg
* Titrate fluid and norepinephrine
* MAP ≥65 mm Hg
* Maintain ScvO2 &gt;70%
* Urine output ≥0.5 mL/kg/hr
* Consider vasopressin / terripressin / angiotensin with volume if hypotensive
* ScvO2 ≥70% or MvO2 ≥65%
* Consider low-dose epinephrine if ScvO2 &lt;70%
* Normalization of lactate
</div>}}
</div>}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| | |!| | | |}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| |!| | | |}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| | C01 | | |C01=<div style="padding: 15px;">
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| A01 | | |A01=<div style="padding: 15px;">
<BIG>'''Antimicrobial Therapy'''</BIG> [[Sepsis resident survival guide#Antimicrobial Therapy|(details)]]
<BIG>'''For Cateocholamine Resistant Shock'''</BIG>
----
----
* Reassess antimicrobial regimen daily for potential deescalation
* Rule out and correct occult comorbidities
<BIG>'''Source Control'''</BIG> [[Sepsis resident survival guide#Source Control|(details)]]
:* Pericardial effusion
:* Pneumothorax
:* Hypoadrenalism
:* Hypothyroidism
:* Active hemorrhage
:* Increased IAP (&gt;12 mm Hg)
:* Necrotic tissue
:* Inappropriate control of infection source
:* Immunocompromised / immunosuppressive state
* Consider PA / PiCCO / FATD catheter placement
* Target CI 􏰃&gt;3.3 L/min/m2 and &lt;􏰁6.0 L/min/m2
* ± Doppler ultrasound to guide fluid therapy
* Consider ECMO
</div>}}
{{Familytree/end}}
</div>
 
==FIRE: Focused Initial Rapid Evaluation (Newborns)==
<span style="background: #FFF0F5; font-weight: bold; font-style: italic;">Focused Initial Rapid Evaluation (FIRE)</span> should be undertaken to identify patients requiring urgent intervention.
 
<span style="font-size: 85%;">
'''Abbreviations''':
CBC, complete blood count;
CI, cardiac index;
CK-MB, creatine kinase MB isoform;
CVP, central venous pressure;
DC, differential count;
ECMO, extracorporeal membrane oxygenation;
FATD, femoral arterial thermodilution;
HMG, hepatomegaly;
IAP, intra-abdominal pressure;
ICU, intensive care unit;
INR, international normalized ratio;
IO, intraosseous;
IV, intravenous;
LFT, liver function test;
MAP, mean arterial pressure;
PA, pulmonary artery;
PCWP, pulmonary capillary wedge pressure;
PDA, patent ductus arteriosus;
PT, prothrombin time;
PTT, partial prothrombin time;
SaO2, arterial oxygen saturation;
SBP, systolic blood pressure;
ScvO2, central venous oxygen saturation;
SMA-7, sequential multiple analysis-7;
SvO2, mixed venous oxygen saturation;
VLBW, very low birth weight.
</span>
 
<div style="font-size: 90%;">
{{Familytree/start}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| A01 | | |A01=<div style="padding: 15px;">
<BIG>'''Suspected Septic Shock'''</BIG> [[Pediatric sepsis resident survival guide#Diagnostic Criteria|(details)]]
----
----
* Remove potentially infected intravascular devices after establishing another accesss
* Suspected infection manifested by hypothermia or hyperthermia
<BIG>'''Infection Prevention'''</BIG> [[Sepsis resident survival guide#Infection Prevention|(details)]]
* Inadequate tissue perfusion
* Poor feeding
* Diarrhea
* Poor tone
* Poor color
* Tachycardia
* Tachypnea
* Respiratory distress
* Maternal history of chorioamnionitis or prolonged rupture of membranes
</div>}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| |!| | | |}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| A01 | | |A01=<div style="padding: 15px;">
<BIG>'''The First Hour of Resuscitation'''</BIG>
----
----
* Use oral chlorhexidine gluconate in ICU patients with severe sepsis
* Secure airway and maintain oxygenation / ventilation
<BIG>'''Corticosteroids'''</BIG> [[Sepsis resident survival guide#Corticosteroids|(details)]]
* Administer IV boluses of 10 ml/kg saline until perfusion restores or HMG develops
* Administer prostaglandin until ductal-dependent lesion is excluded
* Administer empiric antibiotics [[Pediatric sepsis resident survival guide#Empiric Antibiotic Therapy|(details)]]
* ± Correct hypoglycemia and hypocalcemia
<BIG>'''For Fluid Refractory Shock'''</BIG>
----
----
* Continuous infusion of low-dose hydrocortisone if indicated
* Titrate dopamine 5-9 mcg/kg/min
* Taper steroid therapy once vasopressors are no longer required
* Administer dobutamine up to 10 mcg/kg/min
<BIG>'''Blood Product Administration'''</BIG> [[Sepsis resident survival guide#Blood Product Administration|(details)]]
* Consider epinephrine (0.05-0.3 􏰄g/kg/min) to restore blood pressure and perfusion
<BIG>'''For Persistent Pulmonary Hypertension'''</BIG>
----
----
* RBC transfusion if Hb <7.0 g/dL (target: 7.0–9.0 g/dL)
* Administer 100% oxygen
* Prophylactic platelets if indicated
* Institute NaHCO3 / tromethamine until up to pH 7.50 and inhaled NO is available
<BIG>'''Mechanical Ventilation of Sepsis-Induced ARDS'''</BIG> [[Sepsis resident survival guide#Mechanical Ventilation of Sepsis-Induced ARDS|(details)]]
* Hyperventilate to achieve 􏰁&lt;5% difference in preductal and postductal SaO2 and 100% SaO2
<BIG>'''Therapeutic End Points'''</BIG>
----
----
* Tidal volume at 6 mL/kg predicted body weight
* Normal mental status
* Plateau pressures ≤30 cm H2O
* Urine output 􏰃&gt;1 mL/kg/h
* PEEP >5 cm H2O
* Warm extremities
* Head of the bed elevated to 30–45 degrees
* Capillary refill 􏰉≤2 seconds
* Prone positioning if indicated
* Normal peripheral and central pulses
<BIG>'''Sedation, Analgesia, and Neuromuscular blockade'''</BIG> [[Sepsis resident survival guide#Sedation, Analgesia, and Neuromuscular blockade|(details)]]
* Normal blood pressure for age
* Normal glucose concentration
* Normal ionized calcium concentration
* Difference in preductal and postductal O2 saturation 􏰁&lt;5%
* SaO2 ≥95%
</div>}}
{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| |!| | | |}}
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<BIG>'''Beyond the First Hour of Resuscitation'''</BIG>
----
----
* Avoid undue sedation in mechanically ventilated sepsis patients
* ± Transfuse RBC if Hb &lt;􏰁10 g/dL
<BIG>'''Glucose Control'''</BIG> [[Sepsis resident survival guide#Glucose Control|(details)]]
* ± Infuse FFP if prolonged INR
* ± Diuretics/dialysis if fluid overloaded
* Adjust D10%-containing isotonic fluid to maintain normoglycemia
<BIG>'''Therapeutic End Points'''</BIG>
----
----
* Target an upper blood glucose ≤180 mg/dL
* Normal mental status
* Monitor q 1–2 hrs until glucose levels / insulin infusion rates are stable, then q 4 hrs thereafter
* Urine output 􏰃&gt;1 mL/kg/h
<BIG>'''Deep Vein Thrombosis Prophylaxis'''</BIG> [[Sepsis resident survival guide#Deep Vein Thrombosis Prophylaxis|(details)]]
* Capillary refill 􏰉≤2 seconds
* Warm extremities
* Normal peripheral and central pulses
* Normal blood pressure for age
* CI 􏰃&gt;3.3 L/min/m2
* SaO2 &gt;95%
* ScvO2 &gt;􏰃70%
* Difference in preductal and postductal O2 saturation 􏰁&lt;5%
* Absence of right-to-left shunt, tricuspid regurgitation, or right ventricular failure
* Normal glucose concentration
* Normal ionized calcium concentration
* SVC flow &gt;40 mL/kg/min
* Normal INR
* Normal anion gap
* Normal lactate
* Fluid overload &lt;10%
</div>}}
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<BIG>'''For Cold Shock with LV Dysfunction'''</BIG>
----
----
* LMWH / dalteparin / UFH if indicated
* Add nitroprusside / nitroglycerin / milrinone with volume loading if:
* Compression stockings or intermittent pneumatic compression devices
:* ScvO2 &lt;70%
<BIG>'''Stress Ulcer Prophylaxis'''</BIG> [[Sepsis resident survival guide#Stress Ulcer Prophylaxis|(details)]]
:* SVC flow &lt;40 mL/kg/min
:* CI &lt;3.3 L/min/m2
<BIG>'''For Cold Shock with Low Blood Pressure and RV Dysfunction'''</BIG>
----
----
* H2 blocker or PPI in patients with bleeding risks
* Administer inhaled NO if persistent pulmonary hypertension with:
<BIG>'''Nutrition'''</BIG> [[Sepsis resident survival guide#Nutrition |(details)]]
:* ScvO2 &lt;70%
:* SVC flow &lt;40 mL/kg/min
:* CI &lt;3.3 L/min/m2
* Consider milrinone / inhaled iloprost / adenosine
<BIG>'''For Warm Shock with Low Blood Pressure'''</BIG>
----
----
* Administer oral or enteral feedings as tolerated within the first 48 hours
* Titrate fluid and norepinephrine
 
* Administer inotropes to maintain ScvO2 &gt;70%, SVC flow &gt;40 mL/kg/min, and CI &gt;3.3 L/min/m2
* Administer intravenous glucose and enteral nutrition within the first 7 days
* Consider vasopressin / terripressin / angiotensin with volume if hypotensive
<BIG>'''Setting Goals of Care'''</BIG> [[Sepsis resident survival guide#Setting Goals of Care|(details)]]
</div>}}
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{{Familytree|boxstyle=width: 600px; text-align: left; font-size: 100%; padding: 0px;| A01 | | |A01=<div style="padding: 15px;">
<BIG>'''For Cateocholamine Resistant Shock'''</BIG>
----
----
* Discuss goals of care and prognosis with patients and families within 72 hours of ICU admission</div>}}
* Rule out and correct occult comorbidities
:* Pericardial effusion
:* Pneumothorax
:* Hypoadrenalism
:* Hypothyroidism
:* Active hemorrhage
:* Increased IAP (&gt;12 mm Hg)
:* Necrotic tissue
:* Inappropriate control of infection source
:* Immunocompromised / immunosuppressive state
* ± Thyroid hormone replacement
* ± Hydrocortisone replacement
* Administer pentoxifylline if VLBW newborn
* Consider closing PDA if hemodynamically significant
* Consider ECMO
</div>}}
{{Familytree/end}}
{{Familytree/end}}
</div>
</div>
Line 261: Line 433:
==Empiric Antibiotic Therapy==
==Empiric Antibiotic Therapy==


===History of intravenous drug use with high prevalence of MRSA===
===Children aged >1 month===
{{abx|Vancomycin 1 gm IV q12h}}
{{rx|Preferred Regimen}}
* [[Cefotaxime]] 50 mg/kg IV q8h {{or}} [[Ceftriaxone]] 100 mg/kg IV q24h {{and}}
* [[Vancomycin]] 15 mg/kg IV q6h
</li>
{{rx|Alternative Regimen}}
* [[Aztreonam]] 7.5 mg/kg IV q6h {{and}}
* [[Linezolid]] 10 mg/kg IV q8h
</li>


===Sepsis associated with petechiae===
===Children aged <1 month===
{{abx|Ceftriaxone 2 gm IV q12h}}
{{rx|Preferred Regime}}
* [[Ampicillin]] 25 mg/kg IV q8h {{and}}
* [[Cefotaxime]] 50 mg/kg q12h {{and}}
* [[Vancomycin]] 15 mg/kg IV q12h (if suspecting [[MRSA]])
</li>
{{rx|Alternative Regimen}}
* [[Ampicillin]] 25 mg/kg IV q6h {{and}}
* [[Ceftriaxone]] 75 mg/kg IV q24h {{and}}
* [[Vancomycin]] 15 mg/kg IV q12h (if suspecting [[MRSA]])
</li>


===Biliary source===
==Dos and Don'ts==
{{abx|Ampicillin-Sulbactam 3 gm IV q6h|Piperacillin-Tazobactam 3.375 gm IV q4h|Ticarcillin-Clavulanate 3.1 gm IV q4h}}
 
===Community-acquired pneumonia===
{{abx|Levofloxacin 750 mg IV q24h|Moxifloxacin 400 mg IV q24h}}
 
AND
 
{{abx|Piperacillin-Tazobactam 3.375 gm IV q4h}}
 
AND
 
{{abx|Vancomycin 1 gm IV q12h}}
 
===Unclear infection source===
{{abx|Doripenem 500 mg IV q8h|Ertapenem 1 gm IV q24h|Imipenem 0.5 gm IV q6h|Meropenem 1 gm IV q8h}}
 
AND
 
{{abx|Vancomycin 1 gm IV q12h}}
 
===Low prevalence of ESBL and/or carbapenemase-producing aerobic GNB===
{{abx|Piperacillin-Tazobactam 3.375 gm IV q4h}}
 
AND
 
{{abx|Vancomycin 1 gm IV q12h}}
 
===High prevalence of ESBL and/or carbapenemase-producing aerobic GNB===
{{abx|Colistin 2.5 mg/kg then 1.5 mg/kg IV q12h}}
 
AND
 
{{abx|Meropenem 1 gm IV q8h}}
 
AND
 
{{abx|Vancomycin 1 gm IV q12h}}
 
==Dos==
====<span style="background: #FFFFF0;">Initial Resuscitation</span>====
====<span style="background: #FFFFF0;">Initial Resuscitation</span>====
1. For respiratory distress and hypoxemia start with face mask oxygen or if needed and available, high flow nasal cannula oxygen or nasopharyngeal CPAP (NP CPAP). For improved circulation, peripheral intravenous access or intraosseus access can be used for fluid resuscitation and inotrope infusion when a central line is not available. If mechanical ventilation is required then cardiovascular instability during intubation is less likely after appropriate cardiovascular resuscitation. {{GRADE2|C}}
* For respiratory distress and hypoxemia, start with face mask oxygen or if needed and available, high flow nasal cannula oxygen or nasopharyngeal CPAP (NP CPAP). For improved circulation, peripheral intravenous access or intraosseus access can be used for fluid resuscitation and inotrope infusion when a central line is not available. If mechanical ventilation is required then cardiovascular instability during intubation is less likely after appropriate cardiovascular resuscitation. {{GRADE2|C}}


2. Initial therapeutic end points of resuscitation of septic shock: capillary refill of ≤2 secs, normal blood pressure for age, normal pulses with no differential between peripheral and central pulses, warm extremities, urine output >1 mL·kg-1·hr-1, and normal mental status. Scvo2 saturation ≥70% and cardiac index between 3.3 and 6.0 L/min/m2 should be targeted thereafter. {{GRADE2|C}}
* Initial therapeutic end points of resuscitation of septic shock: capillary refill of ≤2 secs, normal blood pressure for age, normal pulses with no differential between peripheral and central pulses, warm extremities, urine output >1 mL·kg-1·hr-1, and normal mental status. Scvo2 saturation ≥70% and cardiac index between 3.3 and 6.0 L/min/m2 should be targeted thereafter. {{GRADE2|C}}


3. Follow American College of Critical Care Medicine-Pediatric Life Support (ACCM-PALS) guidelines for the management of septic shock. {{GRADE1|C}}
* Follow American College of Critical Care Medicine-Pediatric Life Support (ACCM-PALS) guidelines for the management of septic shock. {{GRADE1|C}}


4. Evaluate for and reverse pneumothorax, pericardial tamponade, or endocrine emergencies in patients with refractory shock. {{GRADE1|C}}
* Evaluate for and reverse pneumothorax, pericardial tamponade, or endocrine emergencies in patients with refractory shock. {{GRADE1|C}}


====<span style="background: #FFFFF0;">Antibiotics and Source Control</span>====
====<span style="background: #FFFFF0;">Antibiotics and Source Control</span>====
1. Empiric antibiotics be administered within 1 hr of the identification of severe sepsis. Blood cultures should be obtained before administering antibiotics when possible but this should not delay administration of antibiotics. The empiric drug choice should be changed as epidemic and endemic ecologies dictate (eg H1N1, MRSA, chloroquine resistant malaria, penicillin-resistant pneumococci, recent ICU stay, neutropenia). {{GRADE1|D}}
* Empiric antibiotics be administered within 1 hr of the identification of severe sepsis. Blood cultures should be obtained before administering antibiotics when possible but this should not delay administration of antibiotics. The empiric drug choice should be changed as epidemic and endemic ecologies dictate (eg H1N1, MRSA, chloroquine resistant malaria, penicillin-resistant pneumococci, recent ICU stay, neutropenia). {{GRADE1|D}}


2. Clindamycin and anti-toxin therapies for toxic shock syndromes with refractory hypotension. {{GRADE2|D}}
* Clindamycin and anti-toxin therapies for toxic shock syndromes with refractory hypotension. {{GRADE2|D}}


3. Early and aggressive source control. {{GRADE1|D}}
* Early and aggressive source control. {{GRADE1|D}}


4. Clostridium difficile colitis should be treated with enteral antibiotics if tolerated. Oral vancomycin is preferred for severe disease. {{GRADE1|A}}
* Clostridium difficile colitis should be treated with enteral antibiotics if tolerated. Oral vancomycin is preferred for severe disease. {{GRADE1|A}}


====<span style="background: #FFFFF0;">Fluid Resuscitation</span>====
====<span style="background: #FFFFF0;">Fluid Resuscitation</span>====
1. In the industrialized world with access to inotropes and mechanical ventilation, initial resuscitation of hypovolemic shock begins with infusion of isotonic crystalloids or albumin with boluses of up to 20 mL/kg crystalloids (or albumin equivalent ) over 5–10 minutes, titrated to reversing hypotension, increasing urine output, and attaining normal capillary refill, peripheral pulses, and level of consciousness without inducing hepatomegaly or rales. If hepatomegaly or rales exist then inotropic support should be implemented, not fluid resuscitation. In non-hypotensive children with severe hemolytic anemia (severe malaria or sickle cell crises) blood transfusion is considered superior to crystalloid or albumin bolusing. {{GRADE2|C}}
* In the industrialized world with access to inotropes and mechanical ventilation, initial resuscitation of hypovolemic shock begins with infusion of isotonic crystalloids or albumin with boluses of up to 20 mL/kg crystalloids (or albumin equivalent) over 5–10 minutes, titrated to reversing hypotension, increasing urine output, and attaining normal capillary refill, peripheral pulses, and level of consciousness without inducing hepatomegaly or rales. If hepatomegaly or rales exist then inotropic support should be implemented, not fluid resuscitation. In non-hypotensive children with severe hemolytic anemia (severe malaria or sickle cell crises) blood transfusion is considered superior to crystalloid or albumin bolusing. {{GRADE2|C}}


====<span style="background: #FFFFF0;">Inotropes/Vasopressors/Vasodilators</span>====
====<span style="background: #FFFFF0;">Inotropes/Vasopressors/Vasodilators</span>====
1. Begin peripheral inotropic support until central venous access can be attained in children who are not responsive to fluid resuscitation. {{GRADE2|C}}
* Begin peripheral inotropic support until central venous access can be attained in children who are not responsive to fluid resuscitation. {{GRADE2|C}}


2. Patients with low cardiac output and elevated systemic vascular resistance states with normal blood pressure be given vasodilator therapies in addition to inotropes. {{GRADE2|C}}
* Patients with low cardiac output and elevated systemic vascular resistance states with normal blood pressure be given vasodilator therapies in addition to inotropes. {{GRADE2|C}}


====<span style="background: #FFFFF0;">Extracorporeal Membrane Oxygenation (ECMO)</span>====
====<span style="background: #FFFFF0;">Extracorporeal Membrane Oxygenation (ECMO)</span>====
1. Consider ECMO for refractory pediatric septic shock and respiratory failure. {{GRADE2|C}}
* Consider ECMO for refractory pediatric septic shock and respiratory failure. {{GRADE2|C}}


====<span style="background: #FFFFF0;">Corticosteroids</span>====
====<span style="background: #FFFFF0;">Corticosteroids</span>====
1. Timely hydrocortisone therapy in children with fluid refractory, catecholamine resistant shock and suspected or proven absolute (classic) adrenal insufficiency. {{GRADE1|A}}
* Timely hydrocortisone therapy in children with fluid refractory, catecholamine resistant shock and suspected or proven absolute (classic) adrenal insufficiency. {{GRADE1|A}}
 
====<span style="background: #FFFFF0;">Protein C and Activated Protein Concentrate</span>====
No recommendation as no longer available.


====<span style="background: #FFFFF0;">Blood Products and Plasma Therapies</span>====
====<span style="background: #FFFFF0;">Blood Products and Plasma Therapies</span>====
1. Similar hemoglobin targets in children as in adults. During resuscitation of low superior vena cava oxygen saturation shock (< 70%), hemoglobin levels of 10 g/dL are targeted. After stabilization and recovery from shock and hypoxemia then a lower target > 7.0 g/dL can be considered reasonable. {{GRADE1|B}}
* Similar hemoglobin targets in children as in adults. During resuscitation of low superior vena cava oxygen saturation shock (< 70%), hemoglobin levels of 10 g/dL are targeted. After stabilization and recovery from shock and hypoxemia then a lower target > 7.0 g/dL can be considered reasonable. {{GRADE1|B}}


2. Similar platelet transfusion targets in children as in adults. {{GRADE2|C}}
* Similar platelet transfusion targets in children as in adults. {{GRADE2|C}}


3. Use plasma therapies in children to correct sepsis-induced thrombotic purpura disorders, including progressive disseminated intravascular coagulation, secondary thrombotic microangiopathy, and thrombotic thrombocytopenic purpura. {{GRADE2|C}}
* Use plasma therapies in children to correct sepsis-induced thrombotic purpura disorders, including progressive disseminated intravascular coagulation, secondary thrombotic microangiopathy, and thrombotic thrombocytopenic purpura. {{GRADE2|C}}


====<span style="background: #FFFFF0;">Mechanical Ventilation</span>====
====<span style="background: #FFFFF0;">Mechanical Ventilation</span>====
1. Lung-protective strategies during mechanical ventilation. {{GRADE2|C}}
* Lung-protective strategies during mechanical ventilation. {{GRADE2|C}}


====<span style="background: #FFFFF0;">Sedation/Analgesia/Drug Toxicities</span>====
====<span style="background: #FFFFF0;">Sedation/Analgesia/Drug Toxicities</span>====
1. We recommend use of sedation with a sedation goal in critically ill mechanically ventilated patients with sepsis. {{GRADE1|D}}
* We recommend use of sedation with a sedation goal in critically ill mechanically ventilated patients with sepsis. {{GRADE1|D}}


2. Monitor drug toxicity labs because drug metabolism is reduced during severe sepsis, putting children at greater risk of adverse drug-related events. {{GRADE1|C}}
* Monitor drug toxicity labs because drug metabolism is reduced during severe sepsis, putting children at greater risk of adverse drug-related events. {{GRADE1|C}}


====<span style="background: #FFFFF0;">Glycemic Control</span>====
====<span style="background: #FFFFF0;">Glycemic Control</span>====
1. Control hyperglycemia using a similar target as in adults ≤ 180 mg/dL. Glucose infusion should accompany insulin therapy in newborns and children because some hyperglycemic children make no insulin whereas others are insulin resistant. {{GRADE2|C}}
* Control hyperglycemia using a similar target as in adults ≤ 180 mg/dL. Glucose infusion should accompany insulin therapy in newborns and children because some hyperglycemic children make no insulin whereas others are insulin resistant. {{GRADE2|C}}


====<span style="background: #FFFFF0;">Diuretics and Renal Replacement Therapy</span>====
====<span style="background: #FFFFF0;">Diuretics and Renal Replacement Therapy</span>====
1. Use diuretics to reverse fluid overload when shock has resolved, and if unsuccessful then continuous venovenous hemofiltration (CVVH) or intermittent dialysis to prevent > 10% total body weight fluid overload. {{GRADE2|C}}
* Use diuretics to reverse fluid overload when shock has resolved, and if unsuccessful then continuous venovenous hemofiltration (CVVH) or intermittent dialysis to prevent > 10% total body weight fluid overload. {{GRADE2|C}}
 
====<span style="background: #FFFFF0;">Deep Vein Thrombosis (DVT) Prophylaxis</span>====
No recommendation on the use of DVT prophylaxis in prepubertal children with severe sepsis.
 
====<span style="background: #FFFFF0;">Stress Ulcer (SU) Prophylaxis</span>====
No recommendation on the use of SU prophylaxis in prepubertal children with severe sepsis.


====<span style="background: #FFFFF0;">Nutrition</span>====
====<span style="background: #FFFFF0;">Nutrition</span>====
1. Enteral nutrition given to children who can be fed enterally, and parenteral feeding in those who cannot. {{GRADE2|C}}
* Enteral nutrition given to children who can be fed enterally, and parenteral feeding in those who cannot. {{GRADE2|C}}
 


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


</div></div>
[[Category:Resident survival guide]]
[[Category:Resident survival guide]]

Latest revision as of 01:58, 26 August 2020

Sepsis in Pediatric Patients

Diagnostic Criteria

  • Systemic Inflammatory Response Syndrome
  • Sepsis
  • Severe Sepsis
  • Septic Shock
  • Causes

  • Children > 1 Month
  • Children < 1 Month
  • Focused Initial Rapid Evaluation

  • Infants and Children
  • Newborns
  • Empiric Antibiotic Therapy

    Dos and Don'ts

    Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

    Diagnostic Criteria

    Systemic Inflammatory Response Syndrome

    Systemic inflammatory response syndrome (SIRS) represents the complex findings resulting from systemic activation of the innate immune response triggered by localized or generalized infection, trauma, thermal injury, or sterile inflammatory processes. However, criteria for SIRS are considered to be too nonspecific to be of utility in diagnosing a cause for the syndrome or in identifying a distinct pattern of host response.[1][2]

    SIRS is considered to be present when patients have two or more of the following clinical findings:
    • Body temperature >38 °C (100.4 °F) or <36 °C (96.8 °F)
    • Heart rate >90 beats per minute
    • Hyperventilation evidenced by a respiratory rate of >20 breaths per minute or a PaCO2 <32 mm Hg
    • White blood cell count of >12000 cells/mm³ or <4000 cells/mm³ (>12 x 109 cells/L or <4 x 109 cells/L) or bandemia (>10% band forms)

    Sepsis

    Sepsis is defined as the presence (probable or documented) of infection together with systemic manifestations of infection. Diagnostic criteria for sepsis are as follows:

    Sepsis = infection (documented or suspected) and some of the following:
    General variables
    • Fever (>38.3°C)
    • Hypothermia (core temperature <36°C)
    • Heart rate >90/min–1 or more than two SD above the normal value for age
    • Tachypnea
    • Altered mental status
    • Significant edema or positive fluid balance (>20 mL/kg over 24 hr)
    • Hyperglycemia (plasma glucose >140mg/dL or 7.7 mmol/L) in the absence of diabetes
    Inflammatory variables
    • Leukocytosis (WBC count >12,000 μL–1)
    • Leukopenia (WBC count <4000 μL–1)
    • Normal WBC count with greater than 10% immature forms
    • Plasma C-reactive protein more than two SD above the normal value
    • Plasma procalcitonin more than two SD above the normal value
    Hemodynamic variables
    • Arterial hypotension (SBP <90mm Hg, MAP <70mm Hg, or an SBP decrease >40mm Hg in adults or less than two SD below normal for age)
    Organ dysfunction variables
    • Arterial hypoxemia (Pao2/Fio2 <300)
    • Acute oliguria (urine output <0.5 mL/kg/hr for at least 2 hrs despite adequate fluid resuscitation)
    • Creatinine increase >0.5mg/dL or 44.2 μmol/L
    • Coagulation abnormalities (INR >1.5 or aPTT >60 s)
    • Ileus (absent bowel sounds)
    • Thrombocytopenia (platelet count <100,000 μL–1)
    • Hyperbilirubinemia (plasma total bilirubin >4mg/dL or 70 μmol/L)
    Tissue perfusion variables
    • Hyperlactatemia (>1 mmol/L)
    • Decreased capillary refill or mottling

    Severe Sepsis

    Severe sepsis is defined as sepsis plus sepsis-induced organ dysfunction or tissue hypoperfusion.

    Severe sepsis = sepsis-induced tissue hypoperfusion or organ dysfunction (any of the following thought to be due to the infection)
    • Sepsis-induced hypotension (SBP of <90 mm Hg or MAP <70 mm Hg or a SBP decrease >40 mm Hg or <2 SD below normal for age in the absence of other causes of hypotension)
    • Lactate above upper limits laboratory normal
    • Urine output <0.5 mL/kg/hr for more than 2 hrs despite adequate fluid resuscitation
    • Acute lung injury with PaO2/FIO2 <250 in the absence of pneumonia as infection source
    • Acute lung injury with PaO2/FIO2 <200 in the presence of pneumonia as infection source
    • Creatinine >2.0 mg/dL (176.8 μmol/L)
    • Bilirubin >2 mg/dL (34.2 μmol/L)
    • Platelet count <100,000 μL
    • Coagulopathy (international normalized ratio >1.5)

    Septic Shock

    Septic shock is defined as sepsis-induced hypotension persisting despite adequate fluid resuscitation, in the absence of other causes for hypotension.

    • Septic shock in adult patients refers to a state of acute circulatory failure characterized by persistent arterial hypotension unexplained by other causes.
    • Septic shock in pediatric patients is defined as 1) a suspected infection manifested by hypothermia or hyperthermia, and 2) clinical signs of inadequate tissue perfusion including any of the following:[3]
    • Decreased or altered mental status
    • Decreased urine output 􏰁<1 ml/kg/h
    • Bounding peripheral pulses (warm shock)
    • Diminished peripheral pulses compared with central pulses (cold shock)
    • Wide pulse pressure (warm shock)
    • Prolonged capillary refill >􏰃2 seconds (cold shock)
    • Flash capillary refill (warm shock)
    • Mottled or cool extremities (cold shock)
    • Septic shock in newborns manifests as tachycardia, respiratory distress, poor feeding, poor tone, poor color, tachypnea, diarrhea, or reduced perfusion, particularly in the presence of a maternal history of chorioamnionitis or prolonged rupture of membranes.

    Causes

    Sepsis is a life-threatening condition and must be treated immediately irrespective of the underlying cause.

    Children > 1 Month

    Children < 1 Month

    FIRE: Focused Initial Rapid Evaluation (Infants and Children)

    Focused Initial Rapid Evaluation (FIRE) should be undertaken to identify patients requiring urgent intervention.

    Abbreviations: CBC, complete blood count; CI, cardiac index; CK-MB, creatine kinase MB isoform; CVP, central venous pressure; DC, differential count; ECMO, extracorporeal membrane oxygenation; FATD, femoral arterial thermodilution; HMG, hepatomegaly; IAP, intra-abdominal pressure; ICU, intensive care unit; INR, international normalized ratio; IO, intraosseous; IV, intravenous; LFT, liver function test; MAP, mean arterial pressure; PA, pulmonary artery; PCWP, pulmonary capillary wedge pressure; PDA, patent ductus arteriosus; PT, prothrombin time; PTT, partial prothrombin time; SaO2, arterial oxygen saturation; SBP, systolic blood pressure; ScvO2, central venous oxygen saturation; SMA-7, sequential multiple analysis-7; SvO2, mixed venous oxygen saturation; VLBW, very low birth weight.

    Suspected Septic Shock (details)


    • Suspected infection manifested by hypothermia or hyperthermia
    • Clinical signs of inadequate tissue perfusion
    • Altered mental status
    • Decreased urine output 􏰁<1 ml/kg/h
    • Diminished peripheral pulses compared with central pulses (cold shock)
    • Prolonged capillary refill >􏰃2 seconds (cold shock)
    • Mottled or cool extremities (cold shock)
    • Bounding peripheral pulses (warm shock)
    • Flash capillary refill (warm shock)
    • Wide pulse pressure (warm shock)
     
     
     
     
     
     
     
     

    The First Hour of Resuscitation


    • Secure airway ± intubation (atropine / ketamine / benzodiazepine if indicated)
    • Administer high-flow oxygen supplementation
    • Administer IV boluses of 20 ml/kg saline until perfusion restores or rales/HMG develop
    • Administer empiric antibiotics (details)
    • ± Correct hypoglycemia and hypocalcemia

    For Fluid Refractory Shock


    • Place central venous line and monitor CVP
    • Reverse cold shock by titrating dopamine or epinephrine
    • Reverse warm shock by titrating norepinephrine
    • Administer hydrocortisone if at risk for adrenal insufficiency

    Therapeutic End Points


    • Normal mental status
    • Urine output 􏰃>1 mL/kg/h
    • Warm extremities
    • Capillary refill 􏰉≤2 seconds
    • Normal peripheral and central pulses
    • Normal blood pressure for age
    • Normal glucose concentration
    • Normal ionized calcium concentration
     
     
     
     
     
     
     
     

    Beyond the First Hour of Resuscitation


    • ± Transfuse RBC if Hb <􏰁10 g/dL
    • ± Infuse FFP if prolonged INR
    • ± Diuretics/dialysis if fluid overloaded
    • Adjust D10%-containing isotonic fluid to maintain normoglycemia

    Therapeutic End Points


    • Normal mental status
    • Urine output 􏰃>1 mL/kg/h
    • Capillary refill 􏰉≤2 seconds
    • Warm extremities
    • Threshold heart rates
    • Normal peripheral and central pulses
    • Perfusion pressure appropriate for age
    • CI 􏰃>3.3 L/min/m2 and <􏰁6.0 L/min/m2
    • ScvO2 >􏰃70%
     
     
     
     
     
     
     
     

    For Cold Shock with Normal Blood Pressure


    • Titrate fluid and epinephrine
    • Maintain ScvO2 >70% and Hb >10 g/dL
    • Add nitroprusside / nitroglycerin / milrinone with volume loading if ScvO2 <70%
    • Consider levosimendan / enoximone in recalcitrant low CO syndrome
    • ± Thyroid hormone replacement
    • ± Hydrocortisone replacement

    For Cold Shock with Low Blood Pressure


    • Titrate fluid and epinephrine
    • Maintain ScvO2 >70% and Hb >10 g/dL
    • Add norepinephrine if hypotensive
    • Consider dobutamine / milrinone / levosimendan / enoximone if ScvO2 <70%

    For Warm Shock with Normal Blood Pressure


    • Titrate fluid and norepinephrine
    • Maintain ScvO2 >70%
    • Consider vasopressin / terripressin / angiotensin with volume if hypotensive
    • Consider low-dose epinephrine if ScvO2 <70%
     
     
     
     
     
     
     
     

    For Cateocholamine Resistant Shock


    • Rule out and correct occult comorbidities
    • Pericardial effusion
    • Pneumothorax
    • Hypoadrenalism
    • Hypothyroidism
    • Active hemorrhage
    • Increased IAP (>12 mm Hg)
    • Necrotic tissue
    • Inappropriate control of infection source
    • Immunocompromised / immunosuppressive state
    • Consider PA / PiCCO / FATD catheter placement
    • Target CI 􏰃>3.3 L/min/m2 and <􏰁6.0 L/min/m2
    • ± Doppler ultrasound to guide fluid therapy
    • Consider ECMO
     
     

    FIRE: Focused Initial Rapid Evaluation (Newborns)

    Focused Initial Rapid Evaluation (FIRE) should be undertaken to identify patients requiring urgent intervention.

    Abbreviations: CBC, complete blood count; CI, cardiac index; CK-MB, creatine kinase MB isoform; CVP, central venous pressure; DC, differential count; ECMO, extracorporeal membrane oxygenation; FATD, femoral arterial thermodilution; HMG, hepatomegaly; IAP, intra-abdominal pressure; ICU, intensive care unit; INR, international normalized ratio; IO, intraosseous; IV, intravenous; LFT, liver function test; MAP, mean arterial pressure; PA, pulmonary artery; PCWP, pulmonary capillary wedge pressure; PDA, patent ductus arteriosus; PT, prothrombin time; PTT, partial prothrombin time; SaO2, arterial oxygen saturation; SBP, systolic blood pressure; ScvO2, central venous oxygen saturation; SMA-7, sequential multiple analysis-7; SvO2, mixed venous oxygen saturation; VLBW, very low birth weight.

    Suspected Septic Shock (details)


    • Suspected infection manifested by hypothermia or hyperthermia
    • Inadequate tissue perfusion
    • Poor feeding
    • Diarrhea
    • Poor tone
    • Poor color
    • Tachycardia
    • Tachypnea
    • Respiratory distress
    • Maternal history of chorioamnionitis or prolonged rupture of membranes
     
     
     
     
     
     
     
     

    The First Hour of Resuscitation


    • Secure airway and maintain oxygenation / ventilation
    • Administer IV boluses of 10 ml/kg saline until perfusion restores or HMG develops
    • Administer prostaglandin until ductal-dependent lesion is excluded
    • Administer empiric antibiotics (details)
    • ± Correct hypoglycemia and hypocalcemia

    For Fluid Refractory Shock


    • Titrate dopamine 5-9 mcg/kg/min
    • Administer dobutamine up to 10 mcg/kg/min
    • Consider epinephrine (0.05-0.3 􏰄g/kg/min) to restore blood pressure and perfusion

    For Persistent Pulmonary Hypertension


    • Administer 100% oxygen
    • Institute NaHCO3 / tromethamine until up to pH 7.50 and inhaled NO is available
    • Hyperventilate to achieve 􏰁<5% difference in preductal and postductal SaO2 and 100% SaO2

    Therapeutic End Points


    • Normal mental status
    • Urine output 􏰃>1 mL/kg/h
    • Warm extremities
    • Capillary refill 􏰉≤2 seconds
    • Normal peripheral and central pulses
    • Normal blood pressure for age
    • Normal glucose concentration
    • Normal ionized calcium concentration
    • Difference in preductal and postductal O2 saturation 􏰁<5%
    • SaO2 ≥95%
     
     
     
     
     
     
     
     

    Beyond the First Hour of Resuscitation


    • ± Transfuse RBC if Hb <􏰁10 g/dL
    • ± Infuse FFP if prolonged INR
    • ± Diuretics/dialysis if fluid overloaded
    • Adjust D10%-containing isotonic fluid to maintain normoglycemia

    Therapeutic End Points


    • Normal mental status
    • Urine output 􏰃>1 mL/kg/h
    • Capillary refill 􏰉≤2 seconds
    • Warm extremities
    • Normal peripheral and central pulses
    • Normal blood pressure for age
    • CI 􏰃>3.3 L/min/m2
    • SaO2 >95%
    • ScvO2 >􏰃70%
    • Difference in preductal and postductal O2 saturation 􏰁<5%
    • Absence of right-to-left shunt, tricuspid regurgitation, or right ventricular failure
    • Normal glucose concentration
    • Normal ionized calcium concentration
    • SVC flow >40 mL/kg/min
    • Normal INR
    • Normal anion gap
    • Normal lactate
    • Fluid overload <10%
     
     
     
     
     
     
     
     

    For Cold Shock with LV Dysfunction


    • Add nitroprusside / nitroglycerin / milrinone with volume loading if:
    • ScvO2 <70%
    • SVC flow <40 mL/kg/min
    • CI <3.3 L/min/m2

    For Cold Shock with Low Blood Pressure and RV Dysfunction


    • Administer inhaled NO if persistent pulmonary hypertension with:
    • ScvO2 <70%
    • SVC flow <40 mL/kg/min
    • CI <3.3 L/min/m2
    • Consider milrinone / inhaled iloprost / adenosine

    For Warm Shock with Low Blood Pressure


    • Titrate fluid and norepinephrine
    • Administer inotropes to maintain ScvO2 >70%, SVC flow >40 mL/kg/min, and CI >3.3 L/min/m2
    • Consider vasopressin / terripressin / angiotensin with volume if hypotensive
     
     
     
     
     
     
     
     

    For Cateocholamine Resistant Shock


    • Rule out and correct occult comorbidities
    • Pericardial effusion
    • Pneumothorax
    • Hypoadrenalism
    • Hypothyroidism
    • Active hemorrhage
    • Increased IAP (>12 mm Hg)
    • Necrotic tissue
    • Inappropriate control of infection source
    • Immunocompromised / immunosuppressive state
    • ± Thyroid hormone replacement
    • ± Hydrocortisone replacement
    • Administer pentoxifylline if VLBW newborn
    • Consider closing PDA if hemodynamically significant
    • Consider ECMO
     
     

    Empiric Antibiotic Therapy

    Children aged >1 month

  • Children aged <1 month

  • Dos and Don'ts

    Initial Resuscitation

    • For respiratory distress and hypoxemia, start with face mask oxygen or if needed and available, high flow nasal cannula oxygen or nasopharyngeal CPAP (NP CPAP). For improved circulation, peripheral intravenous access or intraosseus access can be used for fluid resuscitation and inotrope infusion when a central line is not available. If mechanical ventilation is required then cardiovascular instability during intubation is less likely after appropriate cardiovascular resuscitation. (Grade 2C)
    • Initial therapeutic end points of resuscitation of septic shock: capillary refill of ≤2 secs, normal blood pressure for age, normal pulses with no differential between peripheral and central pulses, warm extremities, urine output >1 mL·kg-1·hr-1, and normal mental status. Scvo2 saturation ≥70% and cardiac index between 3.3 and 6.0 L/min/m2 should be targeted thereafter. (Grade 2C)
    • Follow American College of Critical Care Medicine-Pediatric Life Support (ACCM-PALS) guidelines for the management of septic shock. (Grade 1C)
    • Evaluate for and reverse pneumothorax, pericardial tamponade, or endocrine emergencies in patients with refractory shock. (Grade 1C)

    Antibiotics and Source Control

    • Empiric antibiotics be administered within 1 hr of the identification of severe sepsis. Blood cultures should be obtained before administering antibiotics when possible but this should not delay administration of antibiotics. The empiric drug choice should be changed as epidemic and endemic ecologies dictate (eg H1N1, MRSA, chloroquine resistant malaria, penicillin-resistant pneumococci, recent ICU stay, neutropenia). (Grade 1D)
    • Clindamycin and anti-toxin therapies for toxic shock syndromes with refractory hypotension. (Grade 2D)
    • Clostridium difficile colitis should be treated with enteral antibiotics if tolerated. Oral vancomycin is preferred for severe disease. (Grade 1A)

    Fluid Resuscitation

    • In the industrialized world with access to inotropes and mechanical ventilation, initial resuscitation of hypovolemic shock begins with infusion of isotonic crystalloids or albumin with boluses of up to 20 mL/kg crystalloids (or albumin equivalent) over 5–10 minutes, titrated to reversing hypotension, increasing urine output, and attaining normal capillary refill, peripheral pulses, and level of consciousness without inducing hepatomegaly or rales. If hepatomegaly or rales exist then inotropic support should be implemented, not fluid resuscitation. In non-hypotensive children with severe hemolytic anemia (severe malaria or sickle cell crises) blood transfusion is considered superior to crystalloid or albumin bolusing. (Grade 2C)

    Inotropes/Vasopressors/Vasodilators

    • Begin peripheral inotropic support until central venous access can be attained in children who are not responsive to fluid resuscitation. (Grade 2C)
    • Patients with low cardiac output and elevated systemic vascular resistance states with normal blood pressure be given vasodilator therapies in addition to inotropes. (Grade 2C)

    Extracorporeal Membrane Oxygenation (ECMO)

    • Consider ECMO for refractory pediatric septic shock and respiratory failure. (Grade 2C)

    Corticosteroids

    • Timely hydrocortisone therapy in children with fluid refractory, catecholamine resistant shock and suspected or proven absolute (classic) adrenal insufficiency. (Grade 1A)

    Blood Products and Plasma Therapies

    • Similar hemoglobin targets in children as in adults. During resuscitation of low superior vena cava oxygen saturation shock (< 70%), hemoglobin levels of 10 g/dL are targeted. After stabilization and recovery from shock and hypoxemia then a lower target > 7.0 g/dL can be considered reasonable. (Grade 1B)
    • Similar platelet transfusion targets in children as in adults. (Grade 2C)
    • Use plasma therapies in children to correct sepsis-induced thrombotic purpura disorders, including progressive disseminated intravascular coagulation, secondary thrombotic microangiopathy, and thrombotic thrombocytopenic purpura. (Grade 2C)

    Mechanical Ventilation

    • Lung-protective strategies during mechanical ventilation. (Grade 2C)

    Sedation/Analgesia/Drug Toxicities

    • We recommend use of sedation with a sedation goal in critically ill mechanically ventilated patients with sepsis. (Grade 1D)
    • Monitor drug toxicity labs because drug metabolism is reduced during severe sepsis, putting children at greater risk of adverse drug-related events. (Grade 1C)

    Glycemic Control

    • Control hyperglycemia using a similar target as in adults ≤ 180 mg/dL. Glucose infusion should accompany insulin therapy in newborns and children because some hyperglycemic children make no insulin whereas others are insulin resistant. (Grade 2C)

    Diuretics and Renal Replacement Therapy

    • Use diuretics to reverse fluid overload when shock has resolved, and if unsuccessful then continuous venovenous hemofiltration (CVVH) or intermittent dialysis to prevent > 10% total body weight fluid overload. (Grade 2C)

    Nutrition

    • Enteral nutrition given to children who can be fed enterally, and parenteral feeding in those who cannot. (Grade 2C)

    References

    1. Dellinger, R. Phillip; Levy, Mitchell M.; Rhodes, Andrew; Annane, Djillali; Gerlach, Herwig; Opal, Steven M.; Sevransky, Jonathan E.; Sprung, Charles L.; Douglas, Ivor S.; Jaeschke, Roman; Osborn, Tiffany M.; Nunnally, Mark E.; Townsend, Sean R.; Reinhart, Konrad; Kleinpell, Ruth M.; Angus, Derek C.; Deutschman, Clifford S.; Machado, Flavia R.; Rubenfeld, Gordon D.; Webb, Steven A.; Beale, Richard J.; Vincent, Jean-Louis; Moreno, Rui; Surviving Sepsis Campaign Guidelines Committee including the Pediatric Subgroup (2013-02). "Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2012". Critical Care Medicine. 41 (2): 580–637. doi:10.1097/CCM.0b013e31827e83af. ISSN 1530-0293. PMID 23353941. Check date values in: |date= (help)
    2. Brierley, Joe; Carcillo, Joseph A.; Choong, Karen; Cornell, Tim; Decaen, Allan; Deymann, Andreas; Doctor, Allan; Davis, Alan; Duff, John; Dugas, Marc-Andre; Duncan, Alan; Evans, Barry; Feldman, Jonathan; Felmet, Kathryn; Fisher, Gene; Frankel, Lorry; Jeffries, Howard; Greenwald, Bruce; Gutierrez, Juan; Hall, Mark; Han, Yong Y.; Hanson, James; Hazelzet, Jan; Hernan, Lynn; Kiff, Jane; Kissoon, Niranjan; Kon, Alexander; Irazuzta, Jose; Irazusta, Jose; Lin, John; Lorts, Angie; Mariscalco, Michelle; Mehta, Renuka; Nadel, Simon; Nguyen, Trung; Nicholson, Carol; Peters, Mark; Okhuysen-Cawley, Regina; Poulton, Tom; Relves, Monica; Rodriguez, Agustin; Rozenfeld, Ranna; Schnitzler, Eduardo; Shanley, Tom; Kache, Saraswati; Skache, Sara; Skippen, Peter; Torres, Adalberto; von Dessauer, Bettina; Weingarten, Jacki; Yeh, Timothy; Zaritsky, Arno; Stojadinovic, Bonnie; Zimmerman, Jerry; Zuckerberg, Aaron (2009-02). "Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock: 2007 update from the American College of Critical Care Medicine". Critical Care Medicine. 37 (2): 666–688. doi:10.1097/CCM.0b013e31819323c6. ISSN 1530-0293. PMID 19325359. Check date values in: |date= (help)
    3. Brierley, Joe; Carcillo, Joseph A.; Choong, Karen; Cornell, Tim; Decaen, Allan; Deymann, Andreas; Doctor, Allan; Davis, Alan; Duff, John; Dugas, Marc-Andre; Duncan, Alan; Evans, Barry; Feldman, Jonathan; Felmet, Kathryn; Fisher, Gene; Frankel, Lorry; Jeffries, Howard; Greenwald, Bruce; Gutierrez, Juan; Hall, Mark; Han, Yong Y.; Hanson, James; Hazelzet, Jan; Hernan, Lynn; Kiff, Jane; Kissoon, Niranjan; Kon, Alexander; Irazuzta, Jose; Irazusta, Jose; Lin, John; Lorts, Angie; Mariscalco, Michelle; Mehta, Renuka; Nadel, Simon; Nguyen, Trung; Nicholson, Carol; Peters, Mark; Okhuysen-Cawley, Regina; Poulton, Tom; Relves, Monica; Rodriguez, Agustin; Rozenfeld, Ranna; Schnitzler, Eduardo; Shanley, Tom; Kache, Saraswati; Skache, Sara; Skippen, Peter; Torres, Adalberto; von Dessauer, Bettina; Weingarten, Jacki; Yeh, Timothy; Zaritsky, Arno; Stojadinovic, Bonnie; Zimmerman, Jerry; Zuckerberg, Aaron (2009-02). "Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock: 2007 update from the American College of Critical Care Medicine". Critical Care Medicine. 37 (2): 666–688. doi:10.1097/CCM.0b013e31819323c6. ISSN 1530-0293. PMID 19325359. Check date values in: |date= (help)