Antimicrobial Drugs Flashcards

1
Q

How Antibiotic Resistance Happens

A
  • Antibiotics were discovered and first really used in the 20s
  • Every decade there is resistance that has started to appear
  • We have companies that want drugs to be used a lot (this is their product!), but we HAVE to limit our use of antibiotics
  • note: dont use the word germs
  • there is always resistant bacteria around, but we need to keep some competition present!
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2
Q

Examples of how Antibiotic Resistance Spreads

A
  • eating meat with antibiotic resistant bacteria
  • hard to know the exact role of pets in all this but they are part of it and can get resistant bacteria from owner!
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3
Q

Goal of Antibacterial Therapy

A
  • not every infection needs antibiotics
  • when we use them appropriately, they are to HELP the host rid of the infectious organism
  • bacterial cells are different to the mammalian cell
  • where as: it is hard to treat cancer cells as they are similar to the host and the drug is therefore somewhat toxic
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4
Q

Antibiotic therapy is most effective when…

A
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5
Q

Natural Defence Mechs of Patient

A
  • If M.E. is damaged, they are very prone to building respiratory tract infections
  • UTIs can occur for people with renal issues
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6
Q

Bacterial Resistance and Antibacterial Agents

A
  • bacterial resistance existed well before antibiotics were invented!
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7
Q

Bacterial resistance

A
  • Bacteria have been killing eachother with “antibiotics” for ages to kill other bacteria!
  • A good amount of the antibiotics come from fungi (e.g. penicillin)
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8
Q

Resistance and Antibiotic selection

A
  • resistance does not just emerge at the site of infection but the normal flora in the gut and the skin
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9
Q

The Gut Microbe- What does it do and why do we care?

A
  • what happens if the gut/skin microbiome are altered by antibiotics
  • both (esp. gut) is very important for the immune system and body function
  • basically signals to the immune system what is ok to have in body and what isnt
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10
Q

Immune system and cohabiting microbiota

A
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11
Q
A
  • Dysbiosis= when microbiome of the gut/skin become disordered and arent at the amount they should be
  • loss of control by the gut and immune system
  • often a mix of all these
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12
Q

Bigger Picture: increased prevelance in people

A
  • Increasing in prevelance despite the fact of knowing more and more about these diseases
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13
Q

People with Immune Mediated Diseases

A
  • Diseases we didnt think were immune mediated did start as immune mediated in many cases
  • start with a different microbiota
  • meaning antibiotics can have an effect in these situations
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14
Q

Antibiotics and the microbiome

A
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15
Q

Whether an antibiotic is used appropriately or not…

A
  • we will cause resistance either way
  • is the benefit going to outweigh the fact that you are going to change the microbiota
  • use of antibiotics in the early stages of life seem to have the largest impact on the immune system and functionality of animal/human
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16
Q

Responsibility of Veterinarian

A
  • antibiotics dont cause many side effects as they are aimed at bacterial cells, not mammalian cells (different to anti-cancer drugs, NSAIDS)
  • Vets have used lightly before as there arent really any side effects to mammalian cells
  • disease prevention: worming suggestions, diet, etc.
  • conservatively: treat with the right dose at the right time only when needed!
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17
Q

Issues for food animals

A
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18
Q

Horses

A
  • MUST be signed out or it has to be treated as a food animal
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19
Q

Food animals and Drug Residues

A
  • Drugs have a calculated withdrawal time: time where drug administration has stopped and when the animal is able to be slaughtered
  • REALLY try to avoid the use of antibiotics in food animals, or be very strict about it!
  • even the smallest bit of antibiotics (ex: penicillin) can cause an allergic reaction in people who consume products
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20
Q

Food Animals and Withdrawal times

A
  • times are stated for all registered drugs
  • the criteria MUST be followed for that withdrawal period to work
  • If you are giving antibiotics for an animal destined for slaughter and production, you MUST look at data sheet
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21
Q

If not licensed: The Cascade

A
  • There are a lot of times where the drugs may not be licensed for a certain condition or species
  • you as a vet need to make a risk based clinical judgement: happens all the time!
  • need to get owner consent
  • for food animals: need to have an MRL and need to be able to specify the MINIMUM withdrawal time
  • also keep records of treatment
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22
Q

If not licensed in food animals?

A
  • these withdrawal periods are set by LAW
  • use in food animals still applies the needed use of antibiotics in general, but the added layer of withdrawal times
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23
Q

Gram Staining

A
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24
Q

Microbial Spectrum

A
  • 4 quadrants
  • gram (-) aerobe: like E.Coli
  • Penicillinase producing staph is really important!
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25
Q
A
  • gram + aerobic bacteria - STREP
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26
Q
A
  • Gram Negative aerobic bacteria
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27
Q
A
  • Staph aureus
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28
Q

Atypical Bacteria Species

(6)

A
  • they don’t gram stain!
    enormously important as a causes of a variety of diseases depend on which area you are practicing in
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29
Q

Antimicrobial classes: Inhibition of Cell Wall Synthesis

(3)

A
  • knowing the mech of action doesnt reallyyy change how much we use them, but it is important in our clinical reasoning
  • bacitracin: in ear drops
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30
Q

Antimicrobial Classes: Inhibition of Cell Membrane Function

(4)

A
  • most of these are anti-fungal drugs and not antibiotics!
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31
Q

Classes: Inhibition of Protein Synthesis

(5)

A
  • chloramphenicol
  • macrolides
  • lincosamides
  • tetracyclines -commonly used
  • aminoglycosides
  • these do have the capacity to change mammalian protein synthesis but much lower affinity for mammalian cells!
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32
Q

Classes: Inhibition of Nucleic Acid Synthesis

(5)

A
  • chunking them doesnt matter a lot of the time, but helps to put them into groups to remember them!
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33
Q

When to use antimicrobials?

A
  • only when you definitely diagnose a bacterial infection that needs treatment
  • would cause critical illness and would progress if we do not treat it
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34
Q

Key Q’s and Clues: bacterial infection

A
  • what are you looking for in clues? - signs of bacterial infection!
  • increased body temp can ALSO occur in situations of cancer, or other illnesses (not a hard fast sign)
  • neutrophil increase can happen in non-bacterial inflammation, stress, cancer
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35
Q

Antibiotics not indicated for….

A
  • vomiting/no diarrhea: likely do not have a bacterial disease even if they ingested most disgusting items
  • urine in cats is very hostile to bacteria (echo) - often environmental/stress. OVER ten years, urine becomes more dilute and then they are more prone to bacterial infections
  • huge misconception: blood in feces needs antibiotics. not necessarily a bacterial infection causing blood to be in feces
  • peridontal disease: commonly given AB’s before, during, after–> mechanically clean teeth!! don’t use the AB’s- biofilms
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36
Q

Choosing the right antibacterial drug

A
  • can use guidelines, but you need to understand why those drugs are appropriate
  • prescribe based on what is the most likely bacteria you are going to run into in the area of issue
  • culture and sensitivity? is it recurrent?
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37
Q

Key Questions to Ask

(8)

A

*

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38
Q
A
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39
Q

Factors Affecting the Success of Antibacterial Therapy

A
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40
Q

Where do infections come from?

A
  • A lot of the time the bacteria comes from within and gets to a place where it shouldnt be or they are in same area but the is not enough restriction placed by the body–> become a pathogen
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41
Q

Infection based on location

A
  • gram (-) aerobes and anaerobes in large bowel?
  • liver: coming from up the biliary tract or systemically (which would be staph)
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42
Q

What groups of bacteria live in the gut?

A
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43
Q

What Bacteria live on the skin?

A
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44
Q

Examples of gram (-) bacteria that cause disease in animals

A
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45
Q

Examples of anaerobic bacteria that cause disease in animals

A
46
Q

Examples of gram + aerobic bacteria that cause disease in animals

A
47
Q

Examples of atypical bacteria that cause disease in animals

A
48
Q

Bacterial Susceptibility

A
  • Strep is dumb - hasnt developed much
  • gram negatives can be very unpredictable on the other hand in their sensitivity patterns
49
Q

MIC

A
  • helps us determine sensitivity pattern
  • lowest effective dose!
  • Drug brands have to name the bacteria that show sensitivity to that drug
  • also need to be aware which slow growth and which kill
  • issues: really only applies in lab settings and is inconsistent
50
Q

Bacteriostatic vs bactericidal?

A
  • can really tell if bacteriacidal is better than bacteriostatic drugs: especially in terms of gram (+) infections
51
Q

Bacteriostatic Drugs

A
  • For these drugs to be clinically effective, the drug concentration needs to be above the MIC for the duration of treatment or else the bacterial population will continue to grow
  • need to stress the importance of timing of these doses!
52
Q

Bacteriostatic

(5)

A
  • These are what they are broadly
53
Q

Bactericidal

A
  • don’t need ideal conditions?
  • Good if we are concerned that these animals are immunocompromised or the infection is at a specific site
54
Q

Bactericidal

(6)

A
  • when all is working well, they are bactericidal
55
Q

Bactericidal Killing

A
  • How do these drugs kill the bacteria?
  • can be done in a time dependent manner or dose (concentration) dependent manner
56
Q

Time Dependent

A
  • want that drug to be above the MIC throughout the dosing period
  • 3 bactericidals by time dependent killing mechanisms
  • cant give with a drug that slows down growth because they are only effective against a growing population of bacteria!
  • Can’t give one dose as the concentration decreases too much before the end of the 24hr period - thus we want to give this dose twice in 12 hour periods! (graph)
  • Don’t say give twice a day –> need to say EVERY 12 hours
57
Q

Concentration Dependent

A
  • determined by the peak concentration achieved- can combine with bacteriostatic drugs!
  • don’t depend on bacteria growing
  • needs to be 8-10 times more than the MIC to be effective
  • doesn’t matter that it is gone before 24 hours, but main thing is that their effec tis through concentration!
  • Hamsters/rabbits: tend to give it twice a day in really small animals as they have very high metabolisms and time of action is much faster
58
Q

Red Antibacterial Activity

A
59
Q

Spectrum - Red Drugs

A
  • all the dots represent bacteria
  • if they are mostly in red as you are talking about a drug, wont be affective against those bacteria species
  • REMEMBER THIS MOST OF ALL
  • Fluoroquinolones and aminoglycosides have no effect against obligate anaerobes
  • Penicillin/aminopenicillins don’t work against pen. producing staph and metranidazole does not work in anaerobic conditions? (echo)
60
Q

Green and Blue Antibacterial

A
  • Once they have had multiple courses of antibiotics, this won’t work as the pattern of resistance has changed
61
Q

Spectrum- Green Drugs

A
  • The more that a drug is used, the more you will see red dots appear
62
Q

Brown Antibacterials

A
63
Q

Brown Drugs

A
  • there is a mixture
  • don’t memorize
  • but they are not red/not green
64
Q

Brown Drugs and the Empirical Choice

A
  • don’t use if you aren’tsure what the bacterial infection is!!
65
Q

Structure of the microbiota community can be influenced by…

(4)

A
  • genetics
  • diet (supersize me)
  • infection
  • antibiotics - which we have control over!
66
Q

Atypical Bacteria

A
67
Q

What if I know the likely bacterial species causing the infection?

A
  • Bordatella becoming an issue because so many dogs are getting treated by AB’s
68
Q

Factors Affecting the Success of AB therapy

(5)

A
  • What bugs live where?
  • Bacterial susceptibility
  • Distribution to site of infection (pharmacokinetic phase)
  • Local Conditions (pharamacodynamic phase)
  • Client Compliance
69
Q

Pharmacokinetic Factors

A
70
Q

Difficult to Access Areas

A
71
Q

Intracellular bacteria

A
  • need to be lipid soluble to get in the cell!!
72
Q

How well do they penetrate?

A
  • good= good enough at passing the membrane
  • Great= VERY LIPID SOLUBLE
  • If we are choosing to treat a brain infection, bronchiole infection, iron infection systemically –> needs to come from blues and greens!
73
Q

Environmental Conditions

A
  • What has happened at the site of infection to prevent a drug from working properly
  • need to drain an abcess before giving AB
  • foreign material : stone, devitalized part of bone, splinter
74
Q

Foreign Material (pharmacodynamics)

A
  • body has to fight two battles
75
Q

Effects of Env’t Conditions

A
76
Q

Surgical Prophylaxis

A
  • Use of antimicrobials pre and post surgery to prevent infection
  • Need to think about what bacteria may be present in a surgical procedure
  • ALSO, which surgeries require prophylaxis
77
Q

Post Operative Infection Risk

A
  • health of the tissue involves the effect of the surgery itself as well
  • there is a gradation of asepsis
78
Q

When should I use perioperative antibiotics?

A
79
Q

Justification for surgical prophylaxis

A
80
Q

Post Op Risk: Surgeon and Implants

A
81
Q

Wound Classification

A
  • Contaminated - e.g. penetrating abdominal cavity injury. might not yet have peritonitis, but the fact that there is a penetrating wound, infection is extremely likely
  • Dirty - e.g. septic peritonitis. wound breakdown, ulcer into cavity, etc.
  • Clean: no inflammation, GIT or Resp tract are not affected (ex: a spay)
82
Q

Post Operative Infection risk factors

A
  • patients are shocked/emaciated have a higher risk
83
Q

Post Op Infection risk: Anaesthesia and propofol

A
84
Q

Post Op Infection Risk Factors: clipping, etc

A
  • Just can’t clip as well when you they are awake
  • Abnormal skin will lead to staph possibly populating and invading the area
85
Q
  • Indications for Surgical Prophylaxis
A
  • In places where the aseptic technique is not as great, it is BETTER and CHEAPER to fix the aseptic technique before just giving them ABs
  • dentals? - (diseases where they are more at risk to develop infection after dental) –> hypoadrenocorticism patients maybe, mitral valve disease
  • patients with a low WBC
  • ortho procedures usually get pre and then repeated if it goes longer than 90 min (surgery time) and after? - consequences would be disastrous
86
Q

Timing of Surgical Prophylaxis

A
  • depending on what drug is given, you ideally give it at the time of induction as there is no delay
  • if it is given SQ or IM then it can take about 1-2 hours to take effect
  • Has to be present in the wound at the time of contamination!
87
Q

Best Drug for Surgical Prophylaxis?

A
  • 2nd gen cephalosporin- not licensed vet med, owner will have to give consent, but it has a lot of benefits
  • formulaitons may be different in different regions of the world - need to adapt
  • IV induction IF possible (can take an hour and half for amoxycillin caluvulanate to reach therapeutic level)
88
Q

Surgical continuation therapy

A
  • supposed to act like a security guard checking for any intruders, but don’t continue giving afterwards
  • We are treating an infection, we are preventing the infection from occurring
89
Q

What are clear situations when antimicrobials are inappropriate?

A

*

90
Q

Consideration if some WHO defined critically imp. antimicrobials of highest priority are really needed

A
  • Some of the ABs that are clinically important are also important for our animals
  • Only use carbapenems if necessary- ONLY if indicated as only solution
  • 3rd gen cephalosporins –> very good against nasty gram (-)s
  • fluoroquinolones: really important in human health and therefore we need to be very careful when using them, we can use it, but just NEED to be careful
91
Q

Major Factors influencing postop infection risk:

A
92
Q

Where would these pathogens be coming from?

(surgical Prophylaxis)

A

Skin is a big one! (surgeon and animal!)

  • also depends on what surgery it is
  • need to think about the likely contaminating pathogens
93
Q

What is the most useless drug to use for surgical prophylaxis in most SA cases?

A
  • Amoxycillin (at least in 70% of cases- penicillinase producing)
  • It is no good against staph!
  • staph is one of the main concerns of surgical prophylaxis
  • never use penicillin G in a SA practice
  • clamoxyl is even worse - in addition will not be in the wound at the time needed
94
Q

Which are the best?

A
  • Def want something that can treat Staph
  • FLuoroquinolones are really good against gram negative and can be very potent around humans- try not to use!
95
Q

Questions that need to be answered in order to use ABs

A
  • quinolones are the most abuse in vet med!
96
Q

Do we use Antibiotics?

A
  • Pierre was given amoxicillin but it reoccured
  • need to think about staph infection, gram (-)
  • he is intact: need to think about prostate - need to think about drugs that can penetrate this
  • could be stones since it is recurrent meaning that it could be an uncomplicated urinary infection
  • amoxycillin cannot penetrate the prostate, therefore was a bit better but it returned
97
Q

questions we need to think about when prescribing AB’s

A
98
Q

What Determines what Antibiotics are used?

A
  • # 1: If it is not legal, don’t use it! - you can lose vet license if you use certain drugs
  • Drugs behave very differently in different species (goat v. sheep v. cow… etc.)
  • micro-env’t: what will stop AB’s from working? - debris, fluids
99
Q

AB’s: Inhibition of Cell Wall Synthesis

A
  • Penicillins
  • Cephalosporins
  • Bacitracin
100
Q

AB’s: Inhibition of cell membrane function

A
  • Polymyxins
  • amphotericin B
  • imidazoles
  • nystatin - Nystatin is an antifungal that works by stopping the growth of fungus
101
Q

AB’s: Inhibition of Protein Synthesis

A
  • Chloramphenicol
  • Macrolides
  • Lincosamides
  • Tetracyclines
  • Aminoglycosides
102
Q

AB’s: Inhibition of NA synthesis

A
  • Sulphonamides
  • Trimethoprim
  • Quinolones
  • Metronidazole
  • Rifampin
103
Q

Bacteriostatic Drugs

A
  • Tetracyclines
  • chloramphenicol & florphenicol
  • non-potentiated sulphonamides
  • macrolides
  • lincosamides
104
Q

Bactericidal Drugs

A
  • aminoglycosides
  • cephalosporins
  • fluoroquinolones
  • metronidazole
  • penicillins
  • potentiated sulphonamides
105
Q

Batericidal Drugs

Time Dependent Drugs

A
  • should be above MIC for as long as possible each day
  • Recommened >80% of the day
  • No advantage of high Cmax
  • Correct Dose Timings are Important
  • BACTERIA NEED TO BE MULTIPLYING TO HAVE EFFECT- Do not give with Bacteriostatics
  • penicillins, cephalosporins, TMPS (Trimethoprim/sulfamethoxazole)
106
Q

Bactericidal:

Concentration Dependent Drugs

A
  • peak concentration achieved and/or area under plasma concentration vs. time curve predicts antibacterial success
  • higher peak plasma concentration = greater proportion of target bacteria killed & longer post-antibiotic effect
  • Cmax/MIC ratio = predictive of success of treatment
  • optimal: achieve > 8:1
  • Dont need to be multiplying! - can give with bacteriostatics
  • aminoglycosides, fluoroquinolones, metranidazole
107
Q

Most common treatment for atypical bacteria

(ex: Mycoplasma & Chlamydia)

A
  • Tetracyclines
  • Chloramphenicol or Florphenicol
  • Fluoroquinolones
  • Macrolides
108
Q

Pus inactivates…

(pharmacodynamic phase)

A

TMPS

109
Q

Low PH–>

(Pharmacodynamic phase)

A

marked loss of activity

  • erythromycin
  • clindamycin
  • fluoroquinolones
110
Q

What Drugs must you never use in FA species (FPA’s)

*Some horses exempt due to Section 9 of passports

A
  • Metronidazole (carcinogenic)
  • Benzyl-penicillin (Crystapen)
  • Metaclopramide
  • Chloramphenicol -> aplastic anemia in humans after oral consumption
  • Lidocaine
  • Gentamicin/amikacin
  • Phenylbutazone (–>A. anaemia)
  • Enrofloxacin (Baytril) - Do not use in birds producing eggs for human consumption