intro to antibiotic Flashcards

(35 cards)

1
Q

—- substance that, in small amounts, kills or inhibits the growth of bacteria
—- substance that, in small amounts, kills or inhibits
the growth of micro-organisms (includes antibiotics, antivirals, antifungals)

A

antibiotic
anti microbial

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2
Q

why do we prescribe antimicrobials:
1- to — infection ( prophlyxis) as:
a) — prophylaxis – clean-implant, contaminated surgical procedures
b) — prophylaxis – chemotherapy, transplant immunosuppression, post splenectomy
2- to — suspected infection
a) Start smart by – therapy: antibiotic treatment before specific culture results reported or confirmed
b) Then focus by — therapy: Treatment focused to known pathogen & its susceptibility
3- — reasons which is less common as anti-inflammatory properties (azithromycin), prokinetic properties(erythromycin)

A

prevent
surgical
medical
treat
empiric
targeted
non infection

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3
Q

the ideal antimicrobial drug ( there’s no perfect drug ) :
1. selective — : against pathogen but not host
2. — rather than –
3. Favorable — : reach target site in body with effective concentration (good — )
4. Spectrum: – if required, or — as required
5. Lack of —
– High Therapeutic Index: difference between effective & toxic dose is –
6. Little — developing – can withstand bacterial resistance mechanisms

A

toxicity
bactericidal
bacterstatic
pharmokinetics
bioavailability
broad
narrow
side effects
high
little resistance

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4
Q

antibacterials can be classified by:

A
  1. Anti-bacterial family
  2. Mechanism of action (See relevant
    lecture)
  3. Spectrum: broad or narrow-
    spectrum
  4. Activity: bactericidal or
    bacteriostatic
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5
Q

1- antibiotic families as
: * b-lactams
* Glycopeptides
* Aminoglycosides
* Quinolones
* Macrolides
* Tetracyclines
2- antimicrobial spectrum can be:
— anti-bacterials active against a limited range of bacteria e.g. —
—- anti-bacterials active against a wide range of different bacteria e.g.
3- —- antibiotics prevents bacteria from multiplying while — antibiotics kill the bacteria

A

narrow
benzylpencilin
broad
co-amoxiclav
bacteriostatic
bacterocicidal

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6
Q

1- bactericidal activity:
* The level of antimicrobial activity that – the organism.
* Determined in –
* Minimum bactericidal
concentration (MBC) refers to the – concentration of antibiotic that kills — of the population
2- bacteriostatic :
* The level of antimicrobial
activity that inhibits the — of an organism.
* Determined in – .
* Minimum inhibitory
concentration (MIC) refers to the – concentration that inhibits the growth of the organisms

A

kills
vitro
lowest
99.9%
growth
vitro
lowest

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7
Q

How do we know which antimicrobial will work against which organism?
1- in — testing:
* Individual bacterium incubated with antimicrobial in lab to determine inhibition of growth
* The bacterium is “susceptible” or “sensitive” if its growth is inhibited by an antibiotic & “resistant” if it
is not
* There are several methods of susceptibility testing

A

in vitro suspectibility

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8
Q

2- disk diffusion testing ( multiple antibiotics) which is a — test :
- bacteria in broth spread over —
- — disks impregnated with standard amount of antimicrobial
applied to agar (each disk with different antimicrobial)
- — diffuses into the agar & inhibits growth of organism (if — )
- The — the zone of inhibition, the more susceptible the organism
- There are internationally-agreed ‘ —- ’, relating to the diameter of these zones of inhibition classifying ‘resistance’ or ‘susceptibility’ to each agent

A

qualitative
agar surface
cellulose disks
antimicrobial
susceptible
larger
breakpoints

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9
Q

minimum inhibtory contectration MIC is a — testing:
* The MIC doesn’t always — with how well the antimicrobial works in real life (in vivo)
* Variable concentrations of antibiotic
– in broth or in agar (next slide)
* Concentrations chosen for testing reflect — concentration
* Detects changes in — ; a — test
* Useful for predicting —
– e.g. —- , —
* Determination important in the — of certain
infections e.g. —

A

quantitive
correlate
tissue
susceptibility
quantitive test
clinical response
s penumomiea n pencilin
management
endocarditis

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10
Q

true or false
broth micodiluation is a gold standard

A

true

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11
Q

ETEST an agar based quantitive suspectibiltiy test can be used by –
* Utilizes a — strip
–> impregnated with an – concentration of antibiotic
–> a numerical scale corresponds to — concentration
* MIC = where the elliptical zone of clearing intersects with the strip
* A separate strip is needed for each antibiotic

A

MIC
plastic test
increasing
anitibitoc

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12
Q

MIC by ETEST :
1- solutions of bacteria in – both spread over agar surface
2- Strip with – antimicrobial at – concentrations
applied to agar
3- .Antimicrobial diffuses into
agar & inhibits bacterial
growth
( check slide 21 sooo important for pic )

A

broth
single
reducing

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13
Q

in automated MIC systems:
* Several commercial systems available
* Conveniently prepared & formatted
microdilution panels, inoculated with
the test bacteria, with instrumentation
& automated reading
* These methods are intended to
reduce — & lengthy preparation –

A

reduce technical errors
times

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14
Q

molecular testing for antimicrobial resistance:
* Increasing use in recent years
* – results
* Doesn’t tell you if the antimicrobial will inhibit growth of the bacterium
or not…..allows you to —
resistance by detecting a certain –
* e.g. – tests available for genes for multi-drug-resistant tuberculosis (MDR-TB),(MRSA)

A

rapid
allows u to predict
gene
pcr

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15
Q

mechanism of action of anti bacterials :
1- —- Beta lactams (e.g. penicillins, cephalosporins, carbapenems)
Glycopeptides (e.g. vancomycin)
Polymixin (e.g. colistin)
2- — daptomycin
3- —- quinlones , metrandazole
4- —- trimethoprim , sulphonamide
5- —- Aminoglycosides (e.g.
gentamicin) , Tetracyclin
6- — rifampicin
7- —-
—- (e.g. clarithromycin )
— (e.g. clindamycin)
— (e.g. linezolid)

A

cell wall inhibitors
calcium channels
dna sythesis
antimetabolites
protein sythesis (30s)
protein sythesis ( 50s)
macrolide
lincosamides
oxazolidioones

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16
Q

b lactams antitonic defined by the presence of b lacram ring and the four types are: — , — , — , —
* Standard penicillin
e.g. benzylpenicillin/Penicillin G- (intravenous only) or acid-
stable Penicillin V (used orally)
Use examples: —-
* Anti-staphylococcal
e.g.— not inhibited by —
* Aminopenicillins
Contain an amino group. Not effective against —
but enhanced activity against – infections
e.g. ampicillin, amoxicillin
Use examples: H. influenza, E. coli, Salmonella & Shigella
* Anti-pseudomonal penicillins
Similar to aminopenicillins (no Staphylococci activity) with enhanced activity against Pseudomonas aeruginosa e.g.
piperacillin, a — ; and ticarcillin, a —

A

Penicillins( first used in treatment of human infection ) , Cephalosporins, Carbapenems, Monobactams
streptococci , meiignicocci , syphlilitis
flucloxicillin
beta lactamase ( resistant to degradation )
staphylococci
gram -ve
ureidopencilin
carboxypenciliin

17
Q

examples of pencilin antibiotics:
1- benzylpeniclin which is — penicillin
- — spectrum used for :
- limited for — as :
- used for treatment of :
2- ampicillin , amoxilin are–
- — sprecum including —- but resistance increasing in – , —
- not effective against —
- good oral absorption
- used treatment of:

A

standard
narrow
Gram positive cocci e.g.
Streptococci & Staphylococci.
Gram negative cover e.g. Neisseria spp. (Gram negative cocci)
meningitis, endocarditis, cellulitis
broad
Gram negative bacilli
e coli h influenza
staphylococci
respiratory tract infection, urinary tract infection (only as targeted therapy for UTI because of resistance)

18
Q

examples of cephalosporins
1st generation cephalosporins
* Good anti-Gram – activity
* Orally active e.g. cephalexin
* — & — infections (e.g. Streptococci, Staphylococci, E. coli)
2nd generation cephalosporins
* Retain anti-Gram positive activity with anti-Gram negative activity
* Oral & IV, e.g. cefuroxime for — prophylaxis
* Activity against H. influenzae and B. fragilis
3rd generation cephalosporins
* Good anti-Gram— activity, less anti-Gram – activity
* Most IV, e.g. cefotaxime, to treat —

A

positive
respiratory n urinary infections
surgical
-ve
+ve
meningitis

19
Q
  • Not inactivated by staphylococcal b- lactamase
  • Narrow spectrum
  • Used for susceptible S. aureus infections – not
    MRSA
    known as
A

fluloxacillin ( PENICILLINASE-STABLE PENICILLINS)

20
Q

carbpanes are example of b lactams :
* Very – spectrum – active against Gram-negative & Gram- positive organisms
* Stable to — (active against ESBL producers)
* Meropenem, ertapenem
* Some cross reactivity in
penicillin allergy but less than —
* Critically important antimicrobial

A

broad
beta lactamase
cephalosporins

21
Q
  • Active against Gram-negative
    organisms only – no activity
    against Gram-positive organisms
    or anaerobes
  • Suitable for patients with
    penicillin allergy
A

azteronam ( exmaple of monobactam which is a b lactam )

22
Q

glycopeptides are used for gram – only and used to treat — by — and treats — by —
main examples of glycopeptide are:

A

postive
mrsa iv NOT oral
C. difficile oral NOT iv
vancomycin , teicoplannin

23
Q

— as gentamicin
* IV only - not absorbed orally
* Active against Gram-negative bacilli, S. aureus,
mycobacteria, brucella – inactive against
anaerobes
* In combination to treat — infection (mixed flora) / infective — (synergy)
* Must monitor blood levels to minimise —

A

ahminoglycosides
intra abdominal
endocarditis
toxicity ( nerphtoxic , ototoxic for hearing n balance )

24
Q

clarithromycin, erythromycin &
azithromycin are examples of:
they are — but – in some species
used for — “atypical” pathogens (e.g. Mycoplasma spp., Coxiella spp., Chlamydia spp.);
b-lactams ineffective
– Mycoplasma spp. have no cell wall
– Coxiella/ Chlamydia spp. replicate intracellularly
* Associated with prolonged QTc– avoid if history of —

A

macrolide
bacteriostatic
bactericidal
respiratory infection
arthrymia

25
quinlones inhibit --- * Ciprofloxacin, levofloxacin, moxifloxacin, etc. * Good oral bioavailability * Mainly against Gram -- bacilli * Urinary & intra-abdominal infections, but not -- choice agents * Newer quinolones e.g. levofloxacin also have anti-Gram positive activity & used to treat respiratory infections * Significant side-effect profile, e.g. ---
dna gyrase -ve first bone/joints
26
tetracycline inhibits --- subunit as doxyclincs - used to treat infections caused by Chlamydia, Rickettsia, Coxiella, Mycoplasma - caused growing teeth to become --- - Contraindicated in children & pregnant women
30s ribosomal yellow brown
27
--- is an Anti-anaerobic & anti-protozoal * For known or suspected anaerobic infections, e.g. intra-abdominal infections * Bacteroides spp., Fusobacterium spp. & Clostridium spp. * In combination for prophylaxis in bowel surgery & to treat abdominal infection * Inactive against staphylococci & aerobic GNBs such as E. coli
metronidazole
28
summary : - b lactams n glycopeptides inhibits --- synthesis and have --- activity - FQ as ciprofloxacin is inhibitor of --- with --- activity - amino glycoside inhibits --- with --- and macrolide inhibits --- without --- - tetracycline inhibit ---- without ---
cell wall bactericidal dna replciation bactericidal protein sytheis bactericidal protein sytheuss noooo bactericidal protein sythesis not bactericidal
29
reasons to use more than 1 antimicrobial : 1. To broaden the antimicrobial spectrum for-- therapy, e.g. anti-bacterial & anti-fungal for abdominal infection 2. To prevent the emergence of --- organisms during therapy, e.g. four drugs initially for TB 3. To achieve a -- killing effect, e.g. bacterial endocarditis.
empiric resistant synergic
30
1- If two antimicrobials given together achieve a better effect than the sum of their individual effects, they are -- 2- If two antimicrobials are given together & one interferes with the action of the other, they are ---
synergic antagonistic
31
when should we NOT use anti bacterials : 1. Infections not caused by bacteria e.g. --- 2. To “treat” -- i.e. if bacteria grow from specimens, e.g. surgical site (wound) but no clinical evidence of infection 3. “Prophylaxis” when not -- e.g. after a surgical procedure (too late)
viral infection colonisation indicated
32
principles when choosing anti microbial : 1- --- assessment : what's likely site of infection 2- --- where do we think the patient got the infection is it by community/hopsitals or by local factors as antibiotic resistance rates 3- previous including from gp n other hospitals 4- previous --- result 5- history of --
clinical acquisition antibiotic microbiology allergy
33
factors to consider after starting anti microbial : 1.Revision of --- when culture results available – empiric to targeted 2. --- of therapy, e.g. six weeks for acuteosteomyelitis, 3-5 days for cystitis
antimicrobial therapy duration
34
5 prescribing options at 24-48 hours: 1. --- antimicrobial(s) – no evidence of bacterial infection, or infection resolved 2. -- from intravenous to oral antimicrobial(s) – if patient meets criteria for oral switch 3. --- antimicrobial(s) – narrower spectrum, if possible – broader spectrum, if indicated 4. -- current antimicrobial(s) – review again after further 24 hours 5. Outpatient parenteral antimicrobial therapy (OPAT) – consult with local OPAT team
stop switch change continue
35
start -- : 1. Start antibiotics only if there is clinical evidence of bacterial infection – Check local antibiotic guidelines 2. Obtain appropriate cultures beforehand 3. When writing up the prescription, specify the Route, Indication & Duration 4. Give antibiotics within 4h of prescription – within 1 hour for sepsis focus : At 24-48 hours after starting antibiotics, make an Antimicrobial Prescribing Decision: – Review the clinical diagnosis – Review laboratory/ radiology results – Choose one of the five prescribing decision options ( aka the stop switch etc)
smart