| Term 
 
        | Biofilm-associated infections |  | Definition 
 
        | intravenous catheter infections urinary catheter infections
 Device/implant infections
 **Pacemakers/VADs
 **prosthetic joints
 |  | 
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        | Term 
 | Definition 
 
        | sophisticated communities of matrix-encased surface attached bacteria |  | 
        |  | 
        
        | Term 
 
        | What do hydrated structyres with water channels allow. |  | Definition 
 
        | Allow nutrients and o2 difussions |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-microbial host-derived componenets- platlets cell-to-cell communication of molecules
 dense matrix of polysccharides
 bacterial proteins (adhesins) and virulence factors
 |  | 
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        | Term 
 | Definition 
 
        | Nope, they are rough in nature |  | 
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        | Term 
 
        | How are ways that you can deliver antimicrobials to the site of infection? |  | Definition 
 
        | oral therapy intravenous therapy
 material design: embedding/coating device with antimicrobials
 localized therapy
 **topical antiseptics
 **antimicrobial beads, spacers, and cements
 |  | 
        |  | 
        
        | Term 
 
        | What is the infectious diseases society of america 10X 20 initiative? |  | Definition 
 
        | Pursuing a gloabl commitment to develop 10 new antimicrobial drugs by 2020 
 * this isn't going too well, only 2 new antibiotics are going to be approved
 |  | 
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        | Term 
 
        | Limited targets for antimicrobials |  | Definition 
 
        | cell wall synthesis protein synthesis
 DNA synthesis
 anti-metabolites
 |  | 
        |  | 
        
        | Term 
 
        | Clinical implications of bacterial biofilms |  | Definition 
 
        | Attachment and growth of bacterial communities 
 involved in prosthetic and catheter relation infections
 
 common staphylococci pseudomonas spp, many others
 
 biofilm microbes are 10-1000 X less susceptible to antimicrobials
 |  | 
        |  | 
        
        | Term 
 
        | Which organisms can form biofilms? |  | Definition 
 
        | almost any organism will form biofilms under the right condition! 
 epidemiology is based on access/patient
 |  | 
        |  | 
        
        | Term 
 
        | Why are US hospitals now mandated to report Catheter related infections? |  | Definition 
 
        | the big idea is to prevent these events from occuring! |  | 
        |  | 
        
        | Term 
 
        | What are the two foci of preventative strategies for intravascular catheter-related infections? |  | Definition 
 
        | catheter insertion site 
 catheter hub
 |  | 
        |  | 
        
        | Term 
 
        | CDC's steps to prevent resistance |  | Definition 
 
        | 1. vaccinate 2. remove vatheters
 3. target pathogen
 4. access experts
 5. animicrobial control
 6. use local data
 7. treat infection not contamination/colonization
 8. know when to say no
 9. stop treatment
 10. Isolate pathogen
 11. break chain of contagion
 |  | 
        |  | 
        
        | Term 
 
        | What are treatment approaches of CRBSI?? |  | Definition 
 
        | 1) prevention- infection control practices, topical antiseptics, antibiotics coated devices 2) systemic and local therapy- intravenous therapy, antibiotic locks and washes.
 |  | 
        |  | 
        
        | Term 
 
        | what are the 2011 guidelines for the prevention of intravascular catheter-related infections |  | Definition 
 
        | 1) education and training health-care providers who insert and maintain catheters. 2) using maximal sterile barrier precautions during central venous catheter insertion 3) using a 2% chlorhedine preparation for skin antisepsis 4) avoiding routine replacement of central venous catheters as a strategy to prevent infection 5) using antiseptic/antibiotic impregnated short-term central venous catheters if the rate of infection is high despite adherence to other strategies (education and training, max sterile barrier precauations, and 2% chlorhexidine for skin antisepsis) |  | 
        |  | 
        
        | Term 
 
        | what are 2009 guidelines for the treatment of invascular catheter-related infections |  | Definition 
 
        | 1) when denoting duration of antimicrobial therapy day 1 is the first day on which negative blood culture results are obtained 2) vancomycin is recommended of empirical therapy in health care settings which is an elevated prevalence of methicillin-resistant staphylococcus aureus (MRSA) for institutions in which the preponderance of MRSA isolates have vancomycin minimum inhibitory concentration(MIC) values > 2micrograms/ml alternative agents, such as daptomycin, should be used
 
 3) linezolid should not be used for empirical therapy (ie for patients suspected but not proven to be CRBSI)
 |  | 
        |  | 
        
        | Term 
 
        | 2009 guidelines: non gram-positive isolates |  | Definition 
 
        | 1) empirical coverage for gram-negative bacilli should be based on local antimicrobial susceptibility data and the severity of disease (eg a fourth generation cephalosporin, carbapenem or beta lactam beta lactamase combination, with or without aminoglycoside) 
 2) in addition to coverage for gram-positive pathogens, empirical therapy for suspected CRBSI involving femoral catheters in critically ill patients should include coverage for gram-negative bacilli and candida species) fa
 |  | 
        |  | 
        
        | Term 
 
        | Why should an antibiotic lock therapy should be used? |  | Definition 
 
        | for cather salvage(B-LL);however if antibiotitc lock therapy cannot be used in this situation, systemic antibiotics should be administered through the colonized catheter. |  | 
        |  | 
        
        | Term 
 
        | Formulations of antibiotic lock solutions |  | Definition 
 
        | 1)ethanol, 2)anticoagulants (compatitbility vs biofilm proliferation- heparin, sodium citrate, ethylenediaminetertraacetate- EDTA)3) dose- often multiple times the level of organism susceptibility, 4) dwell time and stability, 5) preparation praticality for pharmacy. |  | 
        |  | 
        
        | Term 
 
        | Antimicrobial-coated catheters (Pros vs cons) |  | Definition 
 
        | Pros- reduced risk of infection, short term bridge for treatment. Cons- increased costs, local reactions, lack of long term success, resistance potential (chlorhexidine/silver sulfadiazine, minocycline/rifampin, platinum/silver, silver cuffs) |  | 
        |  | 
        
        | Term 
 
        | What are the 3 most common organisms in a urinary catheter infection? |  | Definition 
 
        | candida albicans, ecoli, entercoccus spp |  | 
        |  | 
        
        | Term 
 
        | What is the most common type of healthcare associated infection? |  | Definition 
 
        | Catheter administrated UTI |  | 
        |  | 
        
        | Term 
 
        | what is the hospital impact of CAUTI? |  | Definition 
 
        | increased morbidity and mortality excess length of stay (2-4 days)
 increased cost
 uncessary antimicrobial use
 |  | 
        |  | 
        
        | Term 
 
        | is routine use of systemic antimicrobial recommended? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | For recurrent disease, what kind of catheter should you use? |  | Definition 
 
        | antimicrobial coated catheter |  | 
        |  | 
        
        | Term 
 
        | What is CAU-ti prophylaxis? |  | Definition 
 
        | it is a comprehensive strategy, high priority recommendations for urinary catheter use, aseptic insertion, and maintenance |  | 
        |  | 
        
        | Term 
 
        | what kind of cathethers may prevent adhesions and proliferation? |  | Definition 
 
        | silicone/hydrophobic catheters. |  | 
        |  | 
        
        | Term 
 
        | How do you treat a prosthetic join infection? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Risk factors of prosethetic joint infection? |  | Definition 
 
        | 1) prior surgery @ site of prosthesis, 2) Rheumatoid arthritis 3)immunocompromised states 4) diabetes mellitus 5) poor  nutritional status 6) obesity 7) psoriasis 8) extremely advanced age |  | 
        |  | 
        
        | Term 
 
        | What are the three prosethetic joint infections  pathogens that are most common? |  | Definition 
 
        | Coagulase-negative staphylococci staphylococcus aureus
 gram negative aerobic bacilli
 |  | 
        |  | 
        
        | Term 
 
        | what are three other device associated infections? 
 how effective is this?
 
 What are the uses?
 
 what are the advantages?
 |  | Definition 
 
        | antibiotic spacers/beads/cement use: to treat/prevent local infection of bone and soft tissue.
 
 Data for effectiveness is limited
 
 advantages: delivery direct local therapy @ high concentrations, fill dead space from debridement, low systemic effects
 |  | 
        |  | 
        
        | Term 
 
        | Common materials for delievery of antibiotic spacers/beads/cement |  | Definition 
 
        | PMMA, hydroxyapatite, ca2+ phosphate, microspheres, nanoparticles |  | 
        |  | 
        
        | Term 
 
        | antibiotics used in local therapy |  | Definition 
 
        | vancomycin, gentamicin, daptomycin, silver and SSD, rifampin, amikacin, amphotericin |  | 
        |  |