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35 Cards in this Set

  • Front
  • Back
infx
-localized process
bacteremia
-bacteria in the blood
systemic inflammatory response syndrome (SIRS)
-An inflammatory response to a variety of clinical insults.
SEPSIS
-SIRS CAUSED BY A KNOWN OR SUSPECTED INFX
-Does not require positive blood cultures!
severe sepsis
-sepsis plus hypotension OR hypoperfusion OR organ dysfunction
shock
-A syndrome of impaired tissue oxygenation and perfusion
septic shock
-A progression of severe sepsis with hypotension despite adequate fluid resuscitation and perfusion abnormalities.
MODS/MOSF/MSOF
-Multiple Organ Dysfunction Syndrome/Multiple Organ System Failure/Multisystem Organ Failure
SIRS criteri
-at least 2:
1. temp >38 degrees C or <36
2. HR >90bpm
3. Respiratory rate >20 bpm or PaCO2 <32 mmHg
4. WBC >12,000 or <4,000 OR >10% bands
-may seen tachypnea, clammy skin, pul edema, tissue edema, cyanotic fingers, clotting disorders
slide 8
slide 8
sepsis
-the most common cause of SIRS
-~750,000 cases/yr
-15% mortality!!!
-Criteria:
1. at least 2 SIRS criteria met
2. known or suspected infx
-initially you may see non-specific clinical signs: tachypnea, AMS
severe sepsis
-sepsis + 1 of the following
hypotension: SBP <90, if pt is normally hypertensive, a dec in SBP >40 from baseline is sig
hypoperfusion: abml peripheral circulation, organ dysfunction
shock
-a condition in which oxygen supply does not meet demand
-4 types:
1. hypovolemic - low bl vol --> hemorrhagic or not
2. Cardiogenic - hearts not pumping; ischemic, valvular, arrithymic
3. Distributive - septic*, adrenal crisis, neurogenic, anaphylactic
4. Obstructive - pum embolism, tension PTX, cardiac tamponade, constrictive pericarditis
hemodynamic profiles of shock
slide 12
Septic shock
-a type of distributive shock
-a progression of severe sepsis with: hypotension despite adequate fluid resuscitation, the presence of perfusion abnormalities
-40% of pts with sepsis will progress to septic shock
-pts with septic shock have a 40-70% mortality
whos at risk?
1. elderly
2. co-mobidities: DM, COPD< vavlular disease, HIV/neutropenia, malignancy, malnourished
3. surgery or instrumentation
4. prior abc therapy
5. recent or current hospitalization
6. genetics
common sites of infection
1. lungs
2. urinary tract
3. intra-abd
4. IV catheter -staph
5. skin
6. heart valves (endocarditis)
7. sinuses/meninges
HPI
-fever?
-constitutional sx
-localized ssx
PMH
-previous surgery or dental procedures
-hospitalizations
-recent travel
-medications including abx, immunosuppresants, NSAIDs, bblockers (HR may not be inc even though they are septic)
-gyn
-ETOH, IVDU
PE
-ABCs
-general appearance
-VS: rectal temp, pulse (quality), resp rate, BP
-skin: warm and flushed then becomes cool and clammy
-HEENT
-pulmonary
-CV
-abd: scars, ascites, tenderness
-Pelvic/GU/rectal
-MS: pain due to septic joint?
-neuro
SERIAL EXAMS
Labs
1. CBC with diff
2. SMA20
3. coag profile
4. blood cultures: 2 sets from 2 different sites, 10 ml per cx, take from noninfected sites
5. ABG
6. Lactate! -> follow these serially!
7. CRP
8. procalcitonin -> marker for severe sepsis
diagnostic studies
1. UA
2. gram stain
3. LP
4. wound cxs
5. Radiographs: CXR,
6. Head/chest. abd CT
7. US
mgmt
#1 You must intervene early!
#2 Constant re-evaluation is necessary
-Patients will require a monitored setting
#3 Therapy should be goal directed
-What are you trying to accomplish?
-Keep O2 saturation >90%
-SBP >90
-Urine output 30-60ml/hr (0.5ml/kg/hr)***
-Clear the infection
mgmt- the first 6 hours - initial resuscitation
1. Initial resuscitation:
1. begin immediately in pts who are hypotensive or have lactate >4mmol
2. start with 500-1000ml crystalloid or 300-500ml colloid over 30 min
3. Resuscitation goals:
-CVP 8-12 mmHg
-MAP (mean arterial BP) >/= mmHg
-U/O >/= 0.5 ml/kg/hr
-ScvO2 >/= 70% (central venous oxygenation)
4. constantly evaluate and monitor pts response
first 6 hours- diagnosis
1. obtain appropriate bl cultures BEFORe starting abx
-2+ cltures
-get one from each vascular site placed within 48hrs
-cx other sites
2. do NOT delay starting abc if you cnanot obtain bl cultures
3. get appropriate imaging studies
first 6 hours- abx therapy
1. ALWAYS within 1st hr of recognizing severe sepsis or septic shock
2. start with broach spectrum coverage with good penetration into the likely source
-re-eval abx daily
3. stop antimicrobial therapy if the cause is noninfectious
first 6 hours- source identification and control
A specific site of infection should be established as rapidly as possible within the first six hours of presentation.
Formally evaluate a patient to see if their infection can be treated with a source control measure (ie: tissue debridement, abscess drainage).
Implement the source control measure as soon as possible after initial resuscitation (unless it’s pancreatic necrosis).
Remove intravascular devices if potentially infected.
mgmt- respiratory
-continuous pulse ox
-keep SpO2 >90%
-use supplemental O2
-intubate
-mechanical ventilation in sepsis-induced ALI/ARDS
1. tidal vol: 6 ml/kg
2. place pt in semirecumbant position
Vasopressors
-used ot keep MAP >/= 65 mHg
-NE and dopamine are the first line choice (must be administered through central venous catheter)
-add vasopressin if needed
-insert an arterial line
Inotropes
-used to inc CO by increasing contractility
-dobutamine should be the first choice
Steroids
-controversial!
-only consider if sepsis is causing a shock state or if the pts pmhx warrants corticosteroid therapy
-hydrocortisone dose should be <300mg/day
glucose mgmt
-Goal: gluc </= 150 mg/dl
-when using IV insulin, monitor every 1-2 hrs
-tight glucose control (80-110) has been associated with increased rates of hypoglycemia, thus the guidelines now recommend against IV insulin therapy titrated to the "nml" range
other mgmt
1. DVT prophylaxis
2. stress ulcer prophylaxis
3. nutrition
4. prevention of nosocomial infxs
5. blood transfusions: consider if heme is <7
6. discuss advanced care plannign with pts families
Recombinant Human Activated protein C (Xigris)
-Antithrombotic, profibrinolytic, and anti-inflammatory properties
-shown to reduce mortality
-ONLY considered for pts who are extremely sick with multi-organ dysfunction (APACHE II score >/=25)
-most common AE: BLEEDING
Etiology
1. gram positive sepsis: Staph ,strep, enterococcus
-at risk: IVDU, burn pts, indwelling IVs, mechanical devices
2. gram neg sepsis: e.coli, klebsiella, proteus, pseudomonas
-DM, Etoh, cirrhosis, burns, CA, chemo, steroids, TPN, elderly, COPD, GI/GU infections, neutropenic
3. fungal sepsis: Candida
-Immunosuppressed, neutropenic, steroid use, TPN, prolonged use of broad spectrum abx
-splenectomy pts are at inc risk for S.pneumo, H. flu, and N.meningitidis