| Term 
 
        | How is successful patient outcomes determined for IAIs? |  | Definition 
 
        | - Early diagnosis - Rapid surgical intervention
 - Selection of appropriate antibiotic
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        | Term 
 
        | What areas are IAIs located? |  | Definition 
 
        | - Peritoneal cavity - base of diaphragm to pelvis - Retroperitoneal cavity - pancreas, kidneys, adrenals, duodenum, aorta/vena cava
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        | Term 
 
        | What are the 3 types of peritonitis? |  | Definition 
 
        | - Primary - Intact GI, no barrier disruption. Caused by cirrhosis, dialysis, nephrotic syndrome - 2ndary - inflammation and barrier disruption. Caused by diverticulitis, appendix, neoplasms, OPERATIONS
 - tertiary - persistent infection
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        | Term 
 
        | What is an abscess in IAI? |  | Definition 
 
        | purulent collection of fluid - walls off necrotic debris, bacteria, and inflammatory cells |  | 
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        | Term 
 
        | What are the 2 types of IAIs? |  | Definition 
 
        | - Uncomplicated - inflammatory process in a SINGLE organ. May progress to complicated. Appendicitis, cholecyst - Complicated - Inflammatory process in the peritoneal or other sterile region. Need source control!
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        | Term 
 
        | What 3 components determine therapy in IAIs? |  | Definition 
 
        | - Presence of barrier disruption - Severity of disease expression
 - Likelihood of resistance
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        |  | 
        
        | Term 
 | Definition 
 
        | Systemic inflammatory response syndrome: 2+ of: - Temp > 38 or < 36
 - WBC >12 or < 4
 - HR > 90, RR > 20
 **Sepsis - Infection + SIRS
 ** Severe Sepsis - Sepsis + organ dysfunction
 ** Septic shock - Sepsis + hypotension
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        | Term 
 
        | What is Source control for IAIs? |  | Definition 
 
        | In a stabilized patient - drain infected foci, control contamination, and restore function **Failure the more sick the person is, Incr age, low albumin
 |  | 
        |  | 
        
        | Term 
 
        | When are fluids indicated for IAIs? |  | Definition 
 
        | Even in the absence of severe sepsis - an early goal |  | 
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        | Term 
 
        | What kind of coverage is needed in IAIs? |  | Definition 
 
        | Gram(+), gram(-) and anaerobes Special considerations for:
 - Resistant enterobactereciae
 - MRSA
 - Enterococci
 - Candida
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        | Term 
 
        | What is the difference between community and hospital acquired IAIs? |  | Definition 
 
        | - Community - no hospital or hospital < 7 days - Hospital - Hospital > 7 days
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        | Term 
 
        | What are special considerations for IAIs? |  | Definition 
 
        | - Resistant gram(-) - FQN resistant or ESBL - Enterococci - source control not achieved.  Vanc, Zosyn, Penems
 - E. faecium - Tigecyclin, linezolid. VRE or liver transplant
 - MRSA - Vanc for known colonization, treatment failure,
 - Candida - Fluconazole, Echocandin - Immunosuppression, transplant, recurrent IAI
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        | Term 
 
        | How do you cover classification #'s in IAIs? |  | Definition 
 
        | 1 - baseline coverage - Augmentin, or a Cef + metronidazole 2 - everything but candida - Zosyn or carbipenem/ +/- Vanc
 3 - EVERYTHING. In severe septic shock and severe sepsis of HA-diffuse peritonitis. Never just one agent. Zosyn + Vanc + AG + fluconazole/echocandin
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