Antimicrobial resistance Flashcards

1
Q

AMR consequences on animal and public health

A

Increased patient mortality and morbidity

Risk of zoonotic transmission

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2
Q

AMR Economic consequences

A

More visits, laboratory test and therapies
Prolonged hospitalization (companion animals)
Reduced weight gain (food animals)
Loss of customers/reputation by veterinarians
Costs for hospital/farm decontamination
Costs for surveillance and intervention program

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3
Q

Microbiological definition AMR

A

Resistance is the property of bacterial strains to survive at higher antibiotic concentration compared with the wild type population (bacterial population that does not contain any resistance gene or mutation conferring resistance within the species)
The ability of microbes to grow in the presence of a drug that would normally kill them or limit their growth

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4
Q

Clinical definition AMR

A

Resistance is the bacterial ability to survive antimicrobial therapy and cause therapeutic failure

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5
Q

One health dimension of AMR

A

Spread between animals
Spread between animals and humans including via food
Spread between humans
Spread in environment, including via contaminated water and fertilizer

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6
Q

Different antimicrobial resistance strategies

A

To stop the antibiotic from reaching its target at high enough concentration
To modify or bypass the target that the antibiotic inhibits

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7
Q

To stop the antibiotic from reaching target

A

Efflux pumps
Decrease permeability of the membrane that surrounds the bacterial cell
Destroy the antibiotic: production of bacterial enzymes (B-lactamase)
Modify the antibiotic by adding different chemical groups to antibiotics

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8
Q

To modify/bypass the target

A

Camouflage the target
Express alternative proteins
Reprogram target: some bacteria can produce a different variant of a structure it needs
-vancomycin-resistant bacteria make a different cell wall compared to susceptible bacteria

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9
Q

Intrinsic resistance

A

Naturally acquired trait

Species or genus specific

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10
Q

Acquired resistance

A

By mutation in the existing DNA of the organism

By acquisition of new DNA via transformation, transduction or conjugation

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11
Q

Antibiotic selection

A

Bacteria that have acquired resistance keep passing it to other bacteria. At the same time, antimicrobials keep killing bacteria that have no resistance, increasing the share of resistant bacteria

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12
Q

Methicillin Resistant- Staphylococcus aureus, MRSA

A

Gram + skin commensal of many animals and humans (S. aureus)
Acquired resistance gene (mecA) encoding for new penicillin-binding proteins with low affinity to most B-lactams (penicillins and cephalosporins)
Major role in nosocomial infections
-community-acquired MRSA
- Hospital-acquired MRSA
-Livestock-acquired MRSA

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13
Q

Methicillin Resistant- Staphylococcus pseudintermedius, MRSP

A

Gram + skin commensal of dogs
Acquired resistance gene (mecA), similar to MRSA
Approximately 70% of cases are skin and wound postsurgical infections acquired in the clinic (nosocomial infections)
Some MRSP strains are multi-drug resistant bacteria (MDR) and may be resistant to all antibiotics licensed for veterinary use

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14
Q

Extended Spectrum Beta Lactamase producing enterobacteriaceae, ESBL

A

Gram - bacteria producing an enzyme that can hydrolyze/inactivate most B-lactams, except Carbapenems
Risk of foodborne transmission is higher for ESBL-producing E coli
-gut commensal
-may transfer from animals to humans via consumption of meat
-Upon ingestion, may colonize the gut and transfer ESBL-encoding plasmids to resident e. coli

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15
Q

Antimicrobial dilemma

A

Antimicrobials are essential in the cure of infectious diseases in humans and animals
Antibiotic selection leads to reduced efficacy over time
AMR cannot be eradicated but only controlled through rational animicrobial use

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16
Q

Critical questions for implementing rational antimicrobial use in vet practice

A
Antimicrobial?
-reducing overall antimicrobial consumption
Culture?
-improving use of diagnostic testing
Choice of drug
-prudent use of second line, critically important antimicrobials
Which drug dosage
-optimizing dosage regimes
17
Q

Reduce overall antimicrobial consumption

A

Disease prevention: hygiene, management, vaccination

Avoid unnecessary, routine prophylaxis

  • growth promotion
  • clean sterile surgery doesnt always need post-operative prophylaxis

Avoid unnecessary therapy

  • viral infections (upper respiratory tract infections)
  • self-limiting infections (acute diarrhea)
  • disease conditions which require solely topical products (superficial pyoderma and wounds)
18
Q

Improvising use of diagnostic testing

A

Maximize use of cytology to guide antimicrobial choice for relevant disease conditions (UTI, otitis externa)
Increase the use of culture and susceptibility testing
Use a good diagnostic laboratory providing following services
-guidance for optimal specimen management (selection, collections, storage)
State of the art methods for identification and susceptibility testing
Implementation of transparent and ongoing quality assurance measures, preferably by accredited laboratories
Availability of skilled microbiologists for case-based report advice and data interpretation

19
Q

To culture or not to culture

A
Bacterial culturing is amost never contraindicated
Strongly recommended in following:
-no response to therapy
-previous antibiotic treatment
-relapse or re-infection
-immunocompromised patients
-life-threatening infections
-patients at risk of MDR carriage or infection
-high prevalence of AMR
-long treatment
20
Q

Criteria for empiric therapy

A

Use of first choice drugs are defined by national or international animal and disease specific guidelines
Hold disease-specific antibiotics formularies indicating first choice drugs for each disease condition
National guidelines in general better than international ones
-take into account local patterns of antibiotic use
-local AMR trends
-Availability of antimicrobials on market
-National regulations on antimicrobial use
-Cultural differences

21
Q

Prudent use of second line CIA

A

Minimize empiric use of CIAs, especially those that have broad-spectrum, are known to select for MDR bacteria and should be preserved for treatment of difficult infections

  • 3rd and 4th generation cephalosporins
  • Macrolides (limited to livestock and horses)
  • Fluoroquinolones
22
Q

Shoot high

A

Use the highest possible dose
For concentration-dependent drugs
To enhance therapeutic efficacy
To prevent selection of resistant mutants

23
Q

Shoot regular

A

Administer the drug at regular intervals
For time-dependent drugs
To enhance therapeutic efficacy
Inform owner of the importance of compliance

24
Q

Shoot fast

A

Treat the earliest and for the shortest time possible

25
Q

Control of antimicrobial use

A
Legal interventions
-limiting profit of prescriber
-penalties for high use
-ban and restriction
Preventative vet med
Antimicrobial stewardship
26
Q

Control of AMR transmission

A

Farm biosecurity
Hospital infection control
Improved slaughterhouse hygiene
Education of consumers and owners

27
Q

Antimicrobial stewardship

A

Antimicrobial Stewardship Programs are dedicated to improving antibiotic use, to optimize treatment and patient safety, and reduce adverse events associated with AMR
ASPs comprise education, clinical guidelines, pre-prescription approval, post-prescription review and computer-based decision support
Usually underdeveloped in vet clinics
Establishment of ASPs requires coordination by specialist, commitment by clinical staff, and collaboration with microbiology lab

28
Q

Hospital infection control

A

Every vet clinic should have a formal infection control program, a written manual, and an infection control practitioner to coordinate program
Routine practices (hand hygiene, PPE, cleaning and disinfection)
Hospital surveillance of pathogens and AMR