Infectious Disease Flashcards
Gram positive cocci in clusters likely organism?
Staphylococcus spp. including MRSA and MSSA
Gram positive cocci in pairs or chains likely organisms? 3 specifically
- Strep pneumoniae (diplococci)
- Streptococcus spp. (including Strep. Pyrogenes)
- Enterococcus spp (including VRE)
Gram positive rods likley organisms?
Lester was a positive nimRod
- Listeria monocytogenes
Gram positive spores anaerobes?
PAC
- Peptostreptococcus
- Actinomyces spp
- Clostridium spp
Atypicals which dont stain well
4
- Chlamydia
- Legionella
- Mycoplasma pneumoniae
- Mycobacterium tuberculosis
Gram negative (pink)
Cocci
- Neisseria spp
Gram negative rods
enteric colonization
PEKSEC
- Proteus mirabilis
- E. Coli
- Klebsiella
- Serratia
- Enterobacter cloace
- Citrobacter spp
G (-) rods that do not colonize in the gut
PHP
- Pseudomonas aerogenosa
- Haemophilus influenzae
- Providencia spp
G - rods curved or spiral shaped
5
- H. pylori
- Campylobacter spp
- Treponema
- Borrelia
- Leptospira
Gram - coccibacilli ABM
- Acinetobacter baum
- Bordetella pertussis
- Moraxella catarrhalis
Gram - anaerobes
Baby Penguins are Mean and dont breathe
- Bacteroides fragilis
- prevetella
What two classes can sometimes be used synergistically to treat gram positive endocarditis?
AGs and beta-lactams
Beta-lactam opens the cell up so the AG can get to the ribosome and be effective
Antibiograms
Provide susceptibility patterns usually over one year
Aid in selecting empiric therapy and track resistance over time
Mechanisms of Resistance
Intrinsic resistance: natural to the organism
Selection pressure: susceptible bacteria are killed leaving only resistant bacteria
Enzyme Inactivation: Beta lactamases, extended spectrum beta lactamases (treated with carbapenems or newer cephalosporin beta lactamase inhbitors)
Carbapenem-resistant enterobactericae (MDR gram negative organisms): produce carbapenemase: combination treatment with polymyxins
Common Resistant Pathogens 7
Kill Each and Every Strong Pathogen
- Klebsiella pneumonae (ESBL, CRE)
- Eschericha Coli (ESLB, CRE
- Acinetobacter baumannii
- Enterococcus faecalis, Enterococcus faecium (VRE)
- Staph aureus (MRSA)
- Pseudomonas Aeroginosa
Folic Acid Synthesis Inhibitors
- Sulfonamides
- Trimethoprim
- Dapsone
Cell wall inhibitors:
BMVDTO
- Beta-lactams (penicillins, cephalosporins, carbapenems)
- Monobactams (aztreonam)
- Vanc, dalbavancin, televancin, oritavancin
Protein synthesis inhibitors: 7
AMTCLTQ/D
- AGs
- Macrolides
- Tetracyclines
- Clindamycin
- Linezolid, tedilozid
- Quinu/Dalfo
Cell membrane inhibitors:
PDTO
- Polymyxins
- Daptomycin
- Televancin
- Oritavancin
DNA/RNA Inhibitors
- Quinolones (DNA gyrase, topoisomerase IV)
- Metronidazole, tinidazole
- Rifampin
Hydrophilic agents 5 and attributes
- Beta lactams
- AGs
- Glycopeptides
- Dapto
- Polymyxins
- Small Vd: Poor tissue penetration
- Renal elimination: nephrotoxicity
- Low intracellular concentrations: Not active against atypicals
- Increased clearances or distribution in sepsis: consider loading dose and aggresive dosing in sepsis
- Poor-moderate bioavailability Not used PO or IV PO ratio is not 1:1
Lipophilic Agents 6 and attributes
QMRLTC
- Quinolones
- Macrolides
- Rifampin
- Linezolid
- Tetracyclines
- Chloramphenicol
- Large Vd: great tissue penetration
- Hepatic metabolism: hepatotoxic and DDI
- Achieve intracellular concentrations: active against atypicals
- Clearance and distribution is not changed by sepsis
- Great bioavailability: IV:PO is usually 1:1
Concentration dependent killing
AGs, quinolones, dapto
can be dosed less frequently and at higher doses to maximize concentration above the MIC
Time dependent killing
Beta lactams
Dose more frequently to maximize time above MIC
if obese use adjusted BW