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17 Cards in this Set
- Front
- Back
what are 2 broad classes of anti-infectives?
p126 |
antiseptics - on tissue, inhibits w/o killing, bacteriostatic/fungistatic
Disinfectants - on inanimate objects, kills, bactriocidal,fungicidal,virucidal,sporicidal |
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t/f disinfecting is sterilization b/c of limitation of our commercial products all can be safely autoclaved. who regulates disinfection?
p126 |
disinfection is ont sterilization
EPA (environmental protection agency) |
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minor oral infections are treated how?
p126 |
with antiseptics, often used for 2nd-ary infections of superficial oral ulcerations, topical
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antiseptics used preventatively?
p126 |
ADA guidelines test to establish efficacy (if better than placebo) - used to prevent plaque and gingivitis
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what are mechanisms of action for anti-infectives?
p127 |
denaturing proteins, bind covalently with sulfhydryls and disulfide bonds in key enzymes
osmotic disruption (pore formation) interferes with specific metabolic processes - altring enzymatic processes all bacteriocidal |
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effectiveness of anti-infectives depends on preparation, avoid what? what else is important with preparation/use?
p127 |
avoid ritualism
measure accurately shelf life - read instructions contacting time (w/ organisms) read |
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why scrub instruments before anti-infectives used?
p128 |
many agents have reduced efficacy to organic materials, bind tightly and don't go after the microbes they should. so scrub debris away first
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3 facts about sodium hypochlorite, first, what is sodium hypochlorite?
(mech, mj clinical application, mj disadvantage) p128 |
bleach 1. releases chlorine denaturing key enzymes
2. effective surface disinfctant, needs 10 min contact time 3 corrosive to metals (incl. instruments) and plastics, irritates skin |
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iodine
mech, mj. clinical application, mj disadvantage p129 |
1. release of iodine denatures
2. complexes o polymers (or glycols) to form IODOPHORS) which are surface disinfectants. less discoloring, odor, pain (open wounds) 3. corrosive o some metals, discolors some, inactive w/ hard water |
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glutaraldehyde
mech, mj. clinical application, mj disadvantage p129 |
1. cross-links to denature enzymes
2. used as immersion disinfectant (instruments) 10 hrs, overnight 3. irritation to lungs, mucous membranes, never spray, ventilation, short shelf life |
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triclosan
mech, mj. clinical application, mj disadvantage p129 |
1. nonionic molecule, dissolves into lipid memB., and disrupts transport mech's
2. antiplaque/antigingivitis, less than chx 3. doesn't bind oral structures so complexed to a copolymer for effectiveness |
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essential oils (thymol, clorothymol, menthol, hexylresorcinol) listerine
mech, mj. clinical application, mj disadvantage p130 |
1. phenolic compounds related to triclosan, denaturing proteins
2. ADA approvedfor mouthrinse (supragingival plaque/gingivitis) 3. discoloration, objectionable taste, high alcolol, allergic, poor h2o solubility |
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Sanquinarine (in Viadent)
mech, mj. clinical application, mj disadvantage p130 |
denatures enzymes by binding sulfhydryl
2. antiplaque, not ADA ok, too substantive (binds tissue) 3. tastes bad, poor clinical efficacy |
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quaternary ammoniums (cetylpyridinium)
mech, mj. clinical application, mj disadvantage p130 |
1. cationic detergent (like triclosan), memB's & memB enzymes
2. in mouthrinses as antiplaue, moderately effective good substantivity 3. poor activty w/ gm -. inactivated by organic stuff, low pH, soaap, metal ions, taste bad |
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hydrogen peroxide
mech, mj. clinical application, mj disadvantage p131 |
oxidizing agent. 1. hydroxyl radical, attacks bacteria components
2. used as antiseptic (3%) perio, O2 toxic to anaerobes. effervescent O release 3. lot of peroxidase enzymes, carcinogenic at high doses. little proof |
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Chlorhexidine (bis-biquanides)
mech, mj. clinical application, mj disadvantage p131 |
1. binds bacterial memB = leakage
2. .12% chlorhexidine mouthrinse (peridex) "gold standard antiplaque", good for immunocompromised 3. stains, incrased calculus formation, changes taste perception |
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Chlorhexidine (periochip)
mech, mj. clinical application, mj disadvantage p131 |
chlorhexidine gelatin matrix, resorbable, 6-9 day. placed after SRP, in pocket that's been resistant to previous PT, destroys disruptive bacteria, localized, improved PD and CAL
3. less likely = resistance/allergy |