gram positive organisms Flashcards

(48 cards)

1
Q

start smart

A

Take history of relevant allergies
 Initiate prompt effective antibiotic treatment within 1 hour of diagnosis (or as soon as possible) in patients with life- threatening infections
 Comply with local prescribing guidance
 Document clinical indication and dose on
drug chart and in clinical notes
 Include review / stop date or duration- all bloods back by 48 hours
 Ensure relevant microbiological specimens taken

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2
Q

clinical review at 48 hours:

A

clinical review, check microbiology, make and document decision:

  1. STOP
  2. IV/oral switch
  3. change to arrow spectrum
  4. continue and review again after a further 24 hours
  5. OPAT
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3
Q

gram positive bacteria can be

A

cocci or bacilli

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4
Q

gram positive cocci can be further divided into?

A

staphylococci, streptococci, enterococci

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5
Q

gram positive bacilli can be further divided into?

A

listeria monocytogenes
clostridia
corynebacterium

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6
Q

what is more common cocci or bacilli?

A

cocci

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7
Q

common staphylococci

A

Staph, aureus (MSSA and MRSA)

staph. epidermidis and other coagulase neg staphylococci

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8
Q

common enterocci

A

E. faecalis and E. Faecium

VRE

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9
Q

common clostridia

A

clostridioides difficile

clostridium perfringens

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10
Q

common corneybacterium

A

aka diphtheroids

not the same as diphtheria

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11
Q

B Lactams

A

Arguably most important drug class
• Multiple modifications over time have increased spectrum of
activity
• Allergy is due to a degradation product of the beta lactams
• True beta lactam anaphylaxis is <0.05 %

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12
Q

what are B lactam antibiotics?

A
  • Penicillin
  • Flucloxacillin
  • Amoxicillin
  • Cephalosporins
  • Piperacillin/tazobactam
  • carbepenems
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13
Q

true anaphylaxis with penicillins is

A

in less than 5% of cases

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14
Q

what causes the allergy in penicillins?

A

Beta-lactam ring

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15
Q

what is bioavailability?

A
  • Mild infections are often treated in the outpatients , orally
  • Some drugs taken orally are almost completely absorbed and achieve high levels in the serum
  • Sepsis usually requires intravenous antibiotics

over time, depending on the route of the drug, will determine the amount of drug remaining in the blood

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16
Q

what is minimum inhibitory concentration?

A

how much drug you need to kill the pathogen

concentration of drug required for kill of 99.9% of organisms during 18 to 24 hours
• the concentration of drug that allows a tube (or well) containing the pathogen to remain clear by visual examination after 18 to 24 hours.
• Useful for guiding endocarditis, meningitis antimicrobial choi

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17
Q

general roles?

A

• More difficult for antibiotics to get into areas with tight junctions • Central nervous system, eyes, prostate
• Antibiotic penetration usually be site dependant
• Within the same class of antibiotic, agaents may have a different
spectrum and site penetration
• Biofilms require special thought ( CF, bronchiectasis, prosthetic material)

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18
Q

gram positive streptococci shape

A

pairs or chains

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19
Q

gram positive streptococci features

A

Gram positive cocci occur in pairs or chains
• Catalase positive , need particular nutrients
• Nutritionally fastidious, require complex media, preferably supplemented with blood
• ‘Facultative anaerobes’

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20
Q

what are facultative anaerobes?

A

‘Facultative anaerobes’ (grow aerobically and anaerobically – technically though they do not use oxygen in metabolism, some are capnophilic, some prefer anaerobic conditions for growth

21
Q

beta hemolytic strep

A

complete lysis next to growth

clear zone

22
Q

alpha hemolytic streptococci

A

partial hemolysis

greenish color to the blood agar

23
Q

hamma haemolytic streptococci

A

non-haemolytic

24
Q

lance field antigen

A
20 antigens in cell wall
• Differences in carbohydrate
• A to U ( without the letter I or J)
• Not useful for all streptococci
• Usefulness of classification changed with pcr and other molecular methods
• Nomenclature remains
25
2 types of lance field strep
strep. pneumonia and beat hemolysis strep
26
strep. pyogenes
Group A beta haemolytic strep • Pharyngitis, skin • Immunologic sequelae
27
strep. agalactaiae
aka Group B (beta) haemolytic strep | • Pregnancy and neonates
28
viridian's strep group
many members of this group, see | Streptococcus anginosus entry)
29
strep.bovis
Streptococcus bovis renamed Streptococcus gallollyticus subsp. gallolyticus • Typical endocarditis pathogen - requires colonoscopy because of link with carcinoma
30
strep pneumoniae causes
otitis, pneumonia, meningitis
31
what does penicillin do in strep. pneumonia?
Penicillin inhibits S. | pneumoniae by binding enzymes ( penicillin binding proteins/ PBPs) needed to synthesize peptidoglycan
32
what do you do if a person has traveled to a country with high rates of penicillin resistant pneumococci?
add vancomycin IV (aim for prepose level 15-20mg/L) or rifampicin IV/PO 600mg bd
33
countries with high rates of pneumococcal resistance?
canada | pakistan
34
strep. pneumonia vaccination
More than 90 strains( serotypes) • 2 types of vaccine • Varying immunogenicity • Game changer
35
what is the most common enterocci
E. faecalis
36
where of you see enterococci?
GI tract, UTI, endocarditis, bacteraemia
37
what is the 1st line treatment of enterococci?
amoxicillin
38
what is used if amoxicillin resistance in treating enterococci?
vancomycin, teicoplanin
39
VRE:
Linezolid • Daptomycin • Tigecycline • Quinupristine/Dalfopristin
40
intrinsic antibiotic resistance to enterococci?
Penicillin, Flucloxacillin, cephalosporin • aminoglycosides
41
1st line treatment in S. aureus in sepsis?
flucloxacillin IV
42
treatment of S. aureus in allergy or MRSA?
vancomycin IV
43
other active drugs in treating S. aureus if not sepsis?
Oral doxycycline, Cotrimoxazole, clindamycin
44
coagulase negative
* E.g. Staph epidermidis * Many are flucloxacillin resistant • Not as virulent as staph aureus * Clinical story and multiple good quality cultures matter.
45
determining the right drug and right dose?
pharmacodynamics pharmacokinetics MIC protein binding of drug matters because active drug is non bound drug animal models and trials human models and trials to account for inter patient variability specific to site and given sensitivity of an organism
46
pharmacodynamics?
Relationship between infection outcome and drug outcome
47
pharmacokinetics?
is the effect of the body’s processes on the drug
48
pharmacokinetics?
is the effect of the body’s processes on the drug