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Uncomplicated Sepsis, Severe Sepsis,

          & Septic Shock

        Susie Brishaber, RN
           August, 2012
   All Sepsis categories hold    Tachycardia (HR > 90)
    the same general clinical     Warm skin, possibly
    manifestations                 rash
       Hyperthermia (>38         Generalized Weakness
        degrees Celsius)          High WBC count
       Hypothermia (<36           (>12,000 µL-1)
        degrees Celsius)          Low WBC count
       Difficulty Breathing       (<4,0000 µL-1)
        (Tachypnea, >20 BPM)      Coagulation Imbalance
   Severe Sepsis – in addition to general clinical
    manifestations
   Is categorized by having one or more vital organs affected
    ◦ Lungs
    ◦ Heart
    ◦ Kidney
    ◦ Liver
    ◦ Central Nervous System
   Severe Sepsis –
      RENAL SYSTEM:
      Serum Creatinine level > /= 177 µ mol/L
      Oliguria (Output of < 0.5 ml/Kg/ hr., if adequate fluid resuscitation)


      CARDIOVASCULAR:
      Hypotension (Systolic < 90 mm Hg, Diastolic < 60mm Hg)
      Atria or Ventricular Rhythms
      MAP < 65
   LIVER
    ◦ Jaundice
    ◦ Increased levels of Hepatic Enzymes
        AST > 48 U/L
        ALT > 55 U/L
        PT > 10.8 seconds
        INR > 1.5
        PTT > 60 seconds
   IMMUNILOGICAL
    ◦ Nosocomial Infection development
    ◦ Increase Leukocytosis
    ◦ Fever (>100.0)
   NEUROLOGICAL
    ◦ Altered LOC
    ◦ Altered CNS function
    ◦ Encelopathy

   ENDOCRINE
    ◦ Hyperglycemia (in absence of Diabetes, >140)
    ◦ Weight loss
    ◦ Cachexia (Muscle atrophy)
 Skin

 ◦ Poor tissue perfusion
   Lactic Acid Level (>5 mmol/L)
   Edema (With fluid management)
   Activity Intolerance
   Acute Pain
   Anxiety
   Chronic Pain
   Decreased Cardiac Output
   Impaired Gas Exchange
   Process of PES
   P = Problem statement/diagnostic label/definition
   E = Etiology/related factors/causes
   S = Defining characteristics/signs and symptoms
Etiology/Related
      Factors/Causes


   Sepsis can be caused
    from many different
  infections in different
areas of the body. With
              each body
  system, bacteria has a
  place to grow if given
             the chance.
   The lungs are the
    major source of
    infection in severe
    sepsis (especially
    with hospital-
    acquired
    infections), with
    sepsis usually
    associated with
    pneumonia.
   Infection in the
    abdomen, eg, appendicitis,
     bowel
    problems, gallbladder
    infections. When the outer
    surface of the abdominal
    organs (called the
    peritoneum) is involved in
    the infection, it is called
    "peritonitis.“
   Diabetic patients are also
    at increased risk of urinary
    infections leading to
    sepsis. Sometimes this is
    referred to as "urosepsis"
    which just refers to sepsis
    related to a urinary tract
    infection.
   (Surviving Sepsis
    Campaign)
   Bacteria enter the skin
    through wounds and skin
    inflammations; they also
    enter the skin and blood
    through an opening
    provided by intravenous
    ("IV") catheters (small
    tubes for dripping fluids),
    which are required for the
    administration of fluids
    and/or medicines.
   Surviving Sepsis Campaign
    ◦   Setting Aims
    ◦   Establishing Measures
    ◦   Creating a Protocol
    ◦   Enhancing Reliability
    ◦   Testing Changes
   The goal is to perform all indicated tasks 100%of the
    time within the first 6 hours of identification of severe
    sepsis.
   The tasks are:
   1. Measure serum lactate
   2. Obtain blood cultures prior to antibiotic
    administration
   3. Administer broad-spectrum antibiotic, within 3 hrs.
    of ED admission and within 1 hour of non-ED
    admission
   4. In the event of hypotension and/or a serum lactate > 4
    mmol/L
    ◦ a. Deliver an initial minimum of 20 ml/kg of crystalloid or an
      equivalent
    ◦ b. Apply vasopressors for hypotension not responding to initial fluid
      resuscitation to maintain mean arterial pressure (MAP) > 65 mm Hg
   5. In the event of persistent hypotension despite fluid
    resuscitation (septic shock) and/or lactate > 4mmol/L
    ◦ a. Achieve a central venous pressure (CVP) of > 8 mm Hg
    ◦ b. Achieve a central venous oxygen saturation (ScvO2) > 70 % or
      mixed venous oxygen saturation (SvO2) > 65 %
                                  (Surviving Sepsis Campaign)
   Efforts to accomplish these goals should begin
    immediately, but these items may be completed within 24
   hours of presentation for patients with severe sepsis or septic
    shock.
   1. Administer low-dose steroids for septic shock in accordance
    with a standardized ICU policy. If not administered, document
    why the patient did not qualify for low-dose steroids based
    upon the standardized protocol.
   2. Administer drotrecogin alfa (activated) in accordance
    with a standardized ICU policy. If not
    administered, document why the patient did not qualify
    for drotrecogin alfa (activated).
   3. Maintain glucose control > 70, but < 150 mg/dl
   4. Maintain a median inspiratory plateau pressure (IPP)* <
    30 cm H2O for mechanically ventilated patients
   Apache II Score
   Measure Serum Lactate Levels
   Blood cultures
   Initiate IV Antibiotic Therapy
   Treatment of Hypotension
   Keep oxygen saturation stable/Ventilator
 Broad  Spectrum Antibiotics should
  be administered within 3 hours of
  suspected Severe Sepsis or Septic
  Shock
 Blood cultures need to be drawn
  before antibiotics are started
   Treat Hypotension
   If presenting with hypotension and/or lactate level of
    >4 mmol/L give 20mL/kg of crystalloid solution
    ◦ Lactated Ringer’s
    ◦ Normal saline

   Fluid administration to reach a CVP of >8mm Hg
   When patients do not respond to initial fluid
    resuscitation, use vasopressor therapy to maintain a
    MAP > 65mm Hg
    ◦ Dopamine
    ◦ Norepinephrine

    ◦ Titrate according to protocol
   Blood cultures should be re-evaluated in 48
    hours to determine specific antibiotic therapy
   Continue monitoring patient’s vital signs till
    hemodynamically stable
   Follow protocols for PICC dressing, hand
    washing, dressing changes, and peri care
   http://www.survivingsepsis.org/What_You_Should_Kn
    ow/Pages/default.aspx
   http://www.nigms.nih.gov/Education/factsheet_sepsis.h
    tm
   http://www.merckmanuals.com/professional/critical_ca
    re_medicine/sepsis_and_septic_shock/sepsis_and_septi
    c_shock.html
   http://www.merckmanuals.com/home/infections/bacter
    emia_sepsis_and_septic_shock/sepsis_and_septic_shoc
    k.html
   http://www.survivingsepsis.org/SiteCollectionDocumen
    ts/Pathophysiology%20of%20Sepsis%20Phil(2).pdf
   Surviving Sepsis Campaign, 2010
   Dellinger, P., Levy, M., Carlet, J., Bion, J., Parker, M.,
    Jaeschke, R.,et al (2008). Surviving Sepsis Campaign:
    International guidelines for management of severe
    sepsis and septic shock. Critical Care Medicine, 1-33,
    DOI: 10.1097/01.CCM.0000298158.12101.41.
   Wesley, E., Kleinpell, R., Goyette, R., (2003).
    Advances in the understanding of clinical
    manifestations and therapy of severe sepsis: An update
    for critical care nurses. American Journal of Critical
    Care, 12(2),120-133. Retrieved from
    http://ajcc.aacnjournals.org/content/12/2/1
    20.full

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Sepsis powerpoints

  • 1. Uncomplicated Sepsis, Severe Sepsis, & Septic Shock Susie Brishaber, RN August, 2012
  • 2. All Sepsis categories hold  Tachycardia (HR > 90) the same general clinical  Warm skin, possibly manifestations rash  Hyperthermia (>38  Generalized Weakness degrees Celsius)  High WBC count  Hypothermia (<36 (>12,000 µL-1) degrees Celsius)  Low WBC count  Difficulty Breathing (<4,0000 µL-1) (Tachypnea, >20 BPM)  Coagulation Imbalance
  • 3. Severe Sepsis – in addition to general clinical manifestations  Is categorized by having one or more vital organs affected ◦ Lungs ◦ Heart ◦ Kidney ◦ Liver ◦ Central Nervous System
  • 4. Severe Sepsis –  RENAL SYSTEM:  Serum Creatinine level > /= 177 µ mol/L  Oliguria (Output of < 0.5 ml/Kg/ hr., if adequate fluid resuscitation)  CARDIOVASCULAR:  Hypotension (Systolic < 90 mm Hg, Diastolic < 60mm Hg)  Atria or Ventricular Rhythms  MAP < 65
  • 5. LIVER ◦ Jaundice ◦ Increased levels of Hepatic Enzymes  AST > 48 U/L  ALT > 55 U/L  PT > 10.8 seconds  INR > 1.5  PTT > 60 seconds  IMMUNILOGICAL ◦ Nosocomial Infection development ◦ Increase Leukocytosis ◦ Fever (>100.0)
  • 6. NEUROLOGICAL ◦ Altered LOC ◦ Altered CNS function ◦ Encelopathy  ENDOCRINE ◦ Hyperglycemia (in absence of Diabetes, >140) ◦ Weight loss ◦ Cachexia (Muscle atrophy)
  • 7.  Skin ◦ Poor tissue perfusion  Lactic Acid Level (>5 mmol/L)  Edema (With fluid management)
  • 8. Activity Intolerance  Acute Pain  Anxiety  Chronic Pain  Decreased Cardiac Output  Impaired Gas Exchange
  • 9. Process of PES  P = Problem statement/diagnostic label/definition  E = Etiology/related factors/causes  S = Defining characteristics/signs and symptoms
  • 10. Etiology/Related Factors/Causes Sepsis can be caused from many different infections in different areas of the body. With each body system, bacteria has a place to grow if given the chance.
  • 11. The lungs are the major source of infection in severe sepsis (especially with hospital- acquired infections), with sepsis usually associated with pneumonia.
  • 12. Infection in the abdomen, eg, appendicitis, bowel problems, gallbladder infections. When the outer surface of the abdominal organs (called the peritoneum) is involved in the infection, it is called "peritonitis.“  Diabetic patients are also at increased risk of urinary infections leading to sepsis. Sometimes this is referred to as "urosepsis" which just refers to sepsis related to a urinary tract infection.  (Surviving Sepsis Campaign)
  • 13. Bacteria enter the skin through wounds and skin inflammations; they also enter the skin and blood through an opening provided by intravenous ("IV") catheters (small tubes for dripping fluids), which are required for the administration of fluids and/or medicines.
  • 14. Surviving Sepsis Campaign ◦ Setting Aims ◦ Establishing Measures ◦ Creating a Protocol ◦ Enhancing Reliability ◦ Testing Changes
  • 15.
  • 16. The goal is to perform all indicated tasks 100%of the time within the first 6 hours of identification of severe sepsis.  The tasks are:  1. Measure serum lactate  2. Obtain blood cultures prior to antibiotic administration  3. Administer broad-spectrum antibiotic, within 3 hrs. of ED admission and within 1 hour of non-ED admission
  • 17. 4. In the event of hypotension and/or a serum lactate > 4 mmol/L ◦ a. Deliver an initial minimum of 20 ml/kg of crystalloid or an equivalent ◦ b. Apply vasopressors for hypotension not responding to initial fluid resuscitation to maintain mean arterial pressure (MAP) > 65 mm Hg  5. In the event of persistent hypotension despite fluid resuscitation (septic shock) and/or lactate > 4mmol/L ◦ a. Achieve a central venous pressure (CVP) of > 8 mm Hg ◦ b. Achieve a central venous oxygen saturation (ScvO2) > 70 % or mixed venous oxygen saturation (SvO2) > 65 % (Surviving Sepsis Campaign)
  • 18. Efforts to accomplish these goals should begin immediately, but these items may be completed within 24  hours of presentation for patients with severe sepsis or septic shock.  1. Administer low-dose steroids for septic shock in accordance with a standardized ICU policy. If not administered, document why the patient did not qualify for low-dose steroids based upon the standardized protocol.
  • 19. 2. Administer drotrecogin alfa (activated) in accordance with a standardized ICU policy. If not administered, document why the patient did not qualify for drotrecogin alfa (activated).  3. Maintain glucose control > 70, but < 150 mg/dl  4. Maintain a median inspiratory plateau pressure (IPP)* < 30 cm H2O for mechanically ventilated patients
  • 20. Apache II Score  Measure Serum Lactate Levels  Blood cultures  Initiate IV Antibiotic Therapy  Treatment of Hypotension  Keep oxygen saturation stable/Ventilator
  • 21.  Broad Spectrum Antibiotics should be administered within 3 hours of suspected Severe Sepsis or Septic Shock  Blood cultures need to be drawn before antibiotics are started
  • 22. Treat Hypotension  If presenting with hypotension and/or lactate level of >4 mmol/L give 20mL/kg of crystalloid solution ◦ Lactated Ringer’s ◦ Normal saline  Fluid administration to reach a CVP of >8mm Hg
  • 23. When patients do not respond to initial fluid resuscitation, use vasopressor therapy to maintain a MAP > 65mm Hg ◦ Dopamine ◦ Norepinephrine ◦ Titrate according to protocol
  • 24. Blood cultures should be re-evaluated in 48 hours to determine specific antibiotic therapy  Continue monitoring patient’s vital signs till hemodynamically stable  Follow protocols for PICC dressing, hand washing, dressing changes, and peri care
  • 25. http://www.survivingsepsis.org/What_You_Should_Kn ow/Pages/default.aspx  http://www.nigms.nih.gov/Education/factsheet_sepsis.h tm  http://www.merckmanuals.com/professional/critical_ca re_medicine/sepsis_and_septic_shock/sepsis_and_septi c_shock.html  http://www.merckmanuals.com/home/infections/bacter emia_sepsis_and_septic_shock/sepsis_and_septic_shoc k.html
  • 26. http://www.survivingsepsis.org/SiteCollectionDocumen ts/Pathophysiology%20of%20Sepsis%20Phil(2).pdf  Surviving Sepsis Campaign, 2010  Dellinger, P., Levy, M., Carlet, J., Bion, J., Parker, M., Jaeschke, R.,et al (2008). Surviving Sepsis Campaign: International guidelines for management of severe sepsis and septic shock. Critical Care Medicine, 1-33, DOI: 10.1097/01.CCM.0000298158.12101.41.
  • 27. Wesley, E., Kleinpell, R., Goyette, R., (2003). Advances in the understanding of clinical manifestations and therapy of severe sepsis: An update for critical care nurses. American Journal of Critical Care, 12(2),120-133. Retrieved from http://ajcc.aacnjournals.org/content/12/2/1 20.full