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Sepsis
Objectives
 Define SIRS / sepsis / severe sepsis / septic shock
 Early recognition of Sepsis
 Early Goal Directed Therapy
CASE
 64yr Samoan male
 24 hr Fever, productive cough, SOB and delirium
 Initial Obs
 HR 162, RR 40, sats 90% on 15l, BP 85/50 (60), T 103
 History
 24 hr Fever, productive cough, SOB and delirium. Last few
hours with altered mental status and progressively less
responsive to wife and inability to complete sentences 2/2
SOB. Wife called 911
Definitions
 A continuum of severity describing the host systemic
inflammatory response
SIRS
 SIRS – systemic inflammatory response syndrome
 Must have at least 2 of the following:
 Temperature >38.5ºC or <36ºC
 Heart rate >90 beats/min
 Respiratory rate >20 breaths/min or PaCO2 <32
mmHg
 WBC >12,000 cells/mm3, <4000 cells/mm3, or >10 %
immature (band) forms
 SIRS is the body’s response to infection,
inflammation, stress.
Sepsis and Severe Sepsis
 Sepsis – SIRS + suspected or confirmed infection
(documented via cultures or visualized via physical
exam/imaging)
 Severe Sepsis – Sepsis + at least one sign of organ
hypo-perfusion or dysfunction
Areas of mottled skin Disseminated intravascular coagulation
Capillary refill > 3 secs AKI
UOP < 0.5cc/kg /hr ARDS or acute lung injury (ALI)
Lactate > 2mmol /L Cardiac dysfunction on echo
Altered mental status Plt < 100
Abnormal EEG Troponin Leak
Septic Shock
 Septic Shock - Severe sepsis plus one of the following
conditions:
 MAP <60 mm Hg (<80 mm Hg if previous hypertension) after
adequate fluid resuscitation
 Need for pressors to maintain BP after fluid resuscitation
 Adequate fluid resuscitation = 40 to 60 mL/kg saline solution
(NS 5L-10L)
 Lactate > 4mmol /L
SURVIVING SEPSIS CAMPAIGN
 STEP 1: Identify SEPSIS
 STEP 2: Categorize SEPSIS
 STEP 3: Initiate TREATMENT
Antibiotics
 Cultures / Antibiotics / Labs
 Cultures PRIOR to Antibiotics ( 2 Sets, one peripheral and one
from any line older than 48hrs)
 IV Abx within 3 hrs in the ED, within 1 hr in the ICU
 Broad Spectrum, combination therapy for neutropenic and
patients with pseudomonas risk factors
 Vancomycin PLUS Zosyn
 Consider need for Source Control !
 Drainage of abscess or cholangitis, removal of infected catheters,
debridement or amputation of osteomyelitis
Fluid therapy
 Central Line Access (Fluid hydration +/- pressor)
 1st line therapy – fluids, fluids, fluids!
 Crystalloid equivalent to colloid
 Initial 1-2 Liters (20mg /kg) crystalloid or 500 ml
colloid
 Careful in CHF patients !!
Pressors
 See separate lecture on vasopressors
 Start with Levophed (norepinephrine) as first line therapy +/-
Vasopressin
 Consider Dopamine peripherally on floor
 ** This is available in crash cart ** If not responding to fluids,
don’t want for pharmacy to send levophed.
Corticosteroids
 Use in Septic Shock, if NO response to vasopressors
and fluids
 HYDROCORTISONE 200mg -300mg / day Divided doses
(Q6hrs)
 Initial Dose 100mg IV x1
 Consider for patients who received etomidate
 No need for cosyntropin stim test
 Wean Steroids QUICKLY once off pressors
KEY TAKE HOME POINTS
 Recongnize Sepsis EARLY and determine
SEVERITY
 EARLY Antibiotics are critical to resolution of shock
 RESUSCITATE severe sepsis and septic shock ASAP
 EARLY GOAL DIRECTED THERAPY

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sepsis.ppt

  • 2. Objectives  Define SIRS / sepsis / severe sepsis / septic shock  Early recognition of Sepsis  Early Goal Directed Therapy
  • 3. CASE  64yr Samoan male  24 hr Fever, productive cough, SOB and delirium  Initial Obs  HR 162, RR 40, sats 90% on 15l, BP 85/50 (60), T 103  History  24 hr Fever, productive cough, SOB and delirium. Last few hours with altered mental status and progressively less responsive to wife and inability to complete sentences 2/2 SOB. Wife called 911
  • 4. Definitions  A continuum of severity describing the host systemic inflammatory response
  • 5. SIRS  SIRS – systemic inflammatory response syndrome  Must have at least 2 of the following:  Temperature >38.5ºC or <36ºC  Heart rate >90 beats/min  Respiratory rate >20 breaths/min or PaCO2 <32 mmHg  WBC >12,000 cells/mm3, <4000 cells/mm3, or >10 % immature (band) forms  SIRS is the body’s response to infection, inflammation, stress.
  • 6. Sepsis and Severe Sepsis  Sepsis – SIRS + suspected or confirmed infection (documented via cultures or visualized via physical exam/imaging)  Severe Sepsis – Sepsis + at least one sign of organ hypo-perfusion or dysfunction Areas of mottled skin Disseminated intravascular coagulation Capillary refill > 3 secs AKI UOP < 0.5cc/kg /hr ARDS or acute lung injury (ALI) Lactate > 2mmol /L Cardiac dysfunction on echo Altered mental status Plt < 100 Abnormal EEG Troponin Leak
  • 7. Septic Shock  Septic Shock - Severe sepsis plus one of the following conditions:  MAP <60 mm Hg (<80 mm Hg if previous hypertension) after adequate fluid resuscitation  Need for pressors to maintain BP after fluid resuscitation  Adequate fluid resuscitation = 40 to 60 mL/kg saline solution (NS 5L-10L)  Lactate > 4mmol /L
  • 8. SURVIVING SEPSIS CAMPAIGN  STEP 1: Identify SEPSIS  STEP 2: Categorize SEPSIS  STEP 3: Initiate TREATMENT
  • 9.
  • 10. Antibiotics  Cultures / Antibiotics / Labs  Cultures PRIOR to Antibiotics ( 2 Sets, one peripheral and one from any line older than 48hrs)  IV Abx within 3 hrs in the ED, within 1 hr in the ICU  Broad Spectrum, combination therapy for neutropenic and patients with pseudomonas risk factors  Vancomycin PLUS Zosyn  Consider need for Source Control !  Drainage of abscess or cholangitis, removal of infected catheters, debridement or amputation of osteomyelitis
  • 11. Fluid therapy  Central Line Access (Fluid hydration +/- pressor)  1st line therapy – fluids, fluids, fluids!  Crystalloid equivalent to colloid  Initial 1-2 Liters (20mg /kg) crystalloid or 500 ml colloid  Careful in CHF patients !!
  • 12. Pressors  See separate lecture on vasopressors  Start with Levophed (norepinephrine) as first line therapy +/- Vasopressin  Consider Dopamine peripherally on floor  ** This is available in crash cart ** If not responding to fluids, don’t want for pharmacy to send levophed.
  • 13. Corticosteroids  Use in Septic Shock, if NO response to vasopressors and fluids  HYDROCORTISONE 200mg -300mg / day Divided doses (Q6hrs)  Initial Dose 100mg IV x1  Consider for patients who received etomidate  No need for cosyntropin stim test  Wean Steroids QUICKLY once off pressors
  • 14. KEY TAKE HOME POINTS  Recongnize Sepsis EARLY and determine SEVERITY  EARLY Antibiotics are critical to resolution of shock  RESUSCITATE severe sepsis and septic shock ASAP  EARLY GOAL DIRECTED THERAPY

Notas del editor

  1. KEY POINTS what is important in this patient to recognize ? (Vitals / Hx) Things to look for on physical examination What to order for labs/ diagnostic tests Do you want to start therapy ? IF so, what ? Does this patient need to be admitted ? If so, to where ?
  2. Stress that this is a spectrum of syndromes from SIRS progressing to Septic Shock, importance of identifying which step in this spectrum a patient is in to predict outcomes as well as decide on therapies.
  3. Definitions according to the American College of Chest Physicians (ACCP) and Society of Critical Care Medicine (SCCM) in 1992
  4. HIGHEST RISK OF MORTALITY
  5. Surviving Sepsis Campaign is important to know as specific at UCI we are taking an aggressive approach to septic patients from admission to ICU. Key Steps
  6. Run through chart so they are familiar with it Top Left, this is the nursing screening This progresses down to identifying sepsis VS Severe Sepsis / Shock Treatment of Sepsis VS Severe Sepsis/ Shock Box to right focus of EARLY GOAL DIRECTED THERAPY ( CVP/ MAP / SvO2 Goals)
  7. Stress importance of early cultures and IV antibiotics (BROAD). Think Source control if relevant for your patient and possible need for surgery evaluation.
  8. Short discussion on Levophed (peripheral vasoconstriction ideal for septic shock as distributive shock) ** Think dopamine on floor if patient is not responding to wide open fluids **
  9. 2 Trials Annane et al, JAMA 2002; 228: 862-871 Corticus Trial, NEJM 2008; 358: 111-124