antimicrobials - emergencypedia · a: differs greatly for different penicillins dicloxacillin,...
TRANSCRIPT
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Antimicrobials PHARMACOLOGY
DR HUNG DIEP
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Mechanisms of Action
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Definitions
Bacteriostatic: slow or stop bacterial growth Needs a competent immune system to eliminate the microbe
Bactericidal: results in bacterial death
Concentration-dependent killing: concentration of the drug must reach a threshold before it is efficacious Leads to post-antibiotic effects
Time-dependent killing: requires microbes to be exposed to the drug for a period of time before it is efficacious
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Mechanisms of Resistance
Potential methods of developing antibiotic resistance include: Decreased cell permeability
Enzymatic inactivation of the drug
Alteration of the target binding site
Active transport out of the cell (efflux pump)
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β-Lactams
Bacterial cell wall synthesis inhibitors
Bactericidal
Only kills cells that are actively developing
Classes include: Penicillins
Cephalosporins
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Penicillins
All have a β-lactam ring that binds to D-ala-D-ala of a Penicillin-binding protein Interferes with transpeptidsiation of the bacterial cell wall
This process is unique to bacteria
Results in cell lysis, however only in cells actively dividing
Mechanisms of resistance include; Formation of β-lactamases
Modification of target binding site
Development of efflux pump
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Classification
Penicillins (e.g. Benzylpenicillin) Greatest activity against Gram-positive, Gram-negative cocci and non-β-lactamase
producing anaerobes
Susceptible to hydrolysis by β-lactamases
Anti-Staphylococcal Penicillins (Methicillins e.g. Flucloxacillin/Dicloxacillin) Resistant to staphylococcal β-lactamases
Active against staphylocci and streptococci, but ineffective against Gram-negative and anaerobic bacteria (narrow-spectrum)
Extended-Spectrum Penicillins (Aminopenicillins e.g. Ampicillin/Amoxicillin; Carboxypenicllins e.g. Ticarcillin) Improved activity against Gram-negative organisms, but susceptible to β-lactamases
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Pharmacokinetics
A: differs greatly for different penicillins Dicloxacillin, Ampicillin and Amoxicillin are acid stable and well absorbed
Absorption of most oral penicillins are impaired by food
D: widely distributed in body fluids and tissues Concentration in most tissues is equal to serum with poor penetration into the
eye, central nervous system With active meningeal infections, the BBB is disrupted
M: mostly excreted in tact, some inactivation facilitated by the liver
E: rapid renal clearance (generally requires frequent dosing)
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Indications
Penicillins: streptococcal, meningococcal, enterococcal, staphylococcal
Methicillins: Gram-positive infections with β-lactamase activity
Aminopenicillins and Carboxypenicillins: greater activity against Gram-negative bacteria
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Adverse Effects
Generally non-toxic
Most serious reaction is hypersensitivity All are cross-sensitising and cross reacting
<1% of people who have had a penicillin in the past develop a new allergy
Anaphylaxis occurs in 0.05%
Serum sickness reactions can occur
High doses (especially in renal failure) can precipitate seizures
Desensitisation processes can be used if necessary
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Cephalosporins
Similar to Penicillins, but are more stable to β-lactamase activity
Generally have a broader spectrum of action
Not effective against enterococci or listeria species
Currently, there are four generations
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Adverse Effects
Allergic reactions 5-10% cross reactivity with Penicillins
Do NOT give if anaphylaxis with Penicillins
Local irritation and pain after intramuscular and intravenous injection
Renal toxicity with acute interstitial nephritis and acute tubular necrosis
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First-Generation Cephalosporins
Mostly Gram-positive activity, with little Gram-negative activity
No CSF bioavailability
Inactivated by β-lactamases
Includes Cefalothin, Cephazolin
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Pharmacokinetics
Oral (e.g. Cephalexin) A: absorbed in the gut to varying degrees D: varying tissue penetration M: little hepatic metabolism (10%) E: urinary excretion via tubules of unchanged drug (90%)
Probenecid blocks tubular secretion and may increase serum levels
Parenteral (e.g. Cephazolin) A: 100% bioavailability D: low Vd M: minimal E: urinary excretion of unchanged drug
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Indications
Urinary tract infections
Cellulitis with Staphylococcal and Streptococcal species
Surgical prophylaxis
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Second-Generation Cephalosporins
Active against organisms resistant to first-generation cephalosporins
Extended Gram-negative coverage, including Haemophilus and Proteus species
NO activity against Pseudomonas
No CSF bioavailability
Inactivated by β-lactamases
Includes: Cefaclor
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Pharmacokinetics
Cefaclor A: well absorbed orally (90%), has sustained release preparations
D: unknown
M: no metabolism
E: renally excreted
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Indications
Effective against β-lactamase producing Haemophilus influenzae or Moraxella catarrhalis
Primarily used to treat sinusitis, otitis media or lower respiratory tract infections
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Third-Generation Cephalosporins
Reversed spectrum – covers Gram-negative organisms, including Pseudomonas species
Have CSF bioavailability
Resistant to β-lactamases
Includes: Ceftriaxone, Cefotaxime
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Pharmacokinetics
Ceftriaxone A: intravenous administration
D: large Vd, penetrate body tissues well, all penetrate to the CSF
M: moderate hepatic metabolism into inactive form
E: metabolites excreted into the bile, proportion also excreted via urine as unchanged (33-67%) – does not require renal adjustment Other Third-Generations are more dependent on renal excretion – require adjustment
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Indications
Ceftriaxone and Cefotaxime are used for meningitis
Fever of unknown origin in immunocompetent hosts
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Fourth-Generation Cephalosporins
Similar spectrum to Third-Generation Cephalosporins
Has CSF bioavailabiliy
More resistant to β-lactamases compared to Third-Generation
Includes: Cefepime
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Pharmacokinetics
Cefepime A: intravenous administration
D: high Vd, penetrates into CSF well
M: little
E: predominantly excreted unchanged in the urine (85%)
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Monobactams
Synthetic monocyclic β-lactam
Well tolerated in penicillin allergic individuals
Relatively resistant to β-lactamases
Active against Gram-negative rods
Includes: Aztreonam
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Pharmacokinetics
Aztreonam A: intravenous infusion or intramuscular injection
D: moderate Vd (12.6L approx. equivalent to ECV)
M: little hepatic metabolism
E: urinary excretion of predominantly unchanged drug
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β-Lactamase Inhibitors
Inhibitors of many, but not all bacterial β-lactamases Can protect Penicillins that would otherwise be hydrolysed from these enzymes
Activity against staphylococcal, haemophilus, neisseria, gonorrhoea, salmonella, shigella, echerichia, klebsiella species
Includes: Clavulanate, Sulbactam, Tazobactam
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Carbapenems
Structurally related to β-lactam antibiotics
Prevents bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Bactericidal
Includes: Meropenem, Ertapenem
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Pharmacokinetics
Meropenem A: intravenous administration
D: high Vd, penetrates tissues well including CSF
M: small hepatic metabolism
D: predominantly excreted unchanged in the urine (70%)
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Indications
Enterobacter infections
Extended-Spectrum β-Lactamase producing Gram-positive, Gram-negative and anaerobic organisms
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Adverse Effects
Nausea and vomiting
Diarrhoea
Rash
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Glycopeptides
Inhibits cell wall synthesis by binding to the D-Ala-D-Ala terminus of newly formed peptidoglycans
Exclusive Gram-positive activity
Bactericidal
Slower killing effect compared to β-lactam antibiotics as only works on new peptidoglycans
Includes: Vancomycin
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Pharmacokinetics
Vancomycin A: poor oral absorption
Intravenous administration for systemic effects
Oral administration for Clostridium difficile infections
D: low Vd, moderate protein binding (55%), CSF levels are approx. 30% of serum levels
M: none
E: renal excretion as unchanged drug
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Indications
Infections caused by Gram-positive bacteria resistant to Methicillins, including: Sepsis
Endocarditis
Meningitis
Clostridium difficile infections
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Adverse Effects
Red man syndrome – flushing of the upper body, may be followed by hypotension, angioedema and pruritis
Nephrotoxicity is rare More common when used with aminoglycosides
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome can develop – potentially life threatening Severe drug eruption, erythematous rash, inflammation of internal organs
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Aminoglycosides
Reversible inhibitors of protein synthesis Initially passively diffuses into bacterial cells via porin channels, then is actively
transported Transport is enhanced by cell wall synthesis inhibitors, including penicillins,
vancomycin
Binds to the 30S ribosomal subunits, which inhibits protein synthesis by: Interfering with peptide formation Misreading mRNA, which causes incorporation of incorrect amino acids Formation of non-functional monosomes
Concentration-dependent killing Includes: Gentamicin, Streptomycin, Amikacin
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Aminoglycosides
Resistance occurs via three mechanisms: 1. Inactivation by phosphorylation of the aminoglycoside
2. Impaired intracellular transport
3. Receptor on 30S subunit may be deleted
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Pharmacokinetics
Gentamicin A: poor oral absorption
D: small Vd, highly polar compound that does not readily enter cells; in presence of inflammation, have higher rate of CSF bioavailability
M: not metabolised
E: renal clearance
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Indications
Sepsis caused by aerobic Gram-negative bacteria
Synergistic activity in endocarditis caused by streptococci, staphylococci and enterococci
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Adverse Effects
Most likely to occur when dosing is continued for 5 days Toxicity is both concentration- and time-dependent
Nephrotoxicity (reversible)
Ototoxicity (irreversible) Results in tinnitus and high frequency hearing loss
Vestibular damage can result in vertigo and ataxia
Neuromuscular blockade may occur in very high doses
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Tetracyclines
Inhibitors of the 30S ribosomal subunit
Broad spectrum – covers Gram-positive, Gram-negative, protozoa
Bacteriostatic
Resistance occurs via: Impaired influx or increased efflux
Production of proteins that interfere with ribosomal binding
Enzymatic inactivation
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Pharmacokinetics
Doxycycline A: well-absorbed orally, although varies between different types
Portion remains intraluminal and alters gut flora
D: distributes widely into tissues, except CSF; able to cross the placenta
M: susceptible to enzyme induction when also taking anticonvulsants, and chronic alcohol consumption leading to a shortened half-life
E: mixed clearance – bile and urine Doxycycline in particular has non-renal mechanisms of elimination
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Indications
Infections caused by mycoplasma, chlamydiae, rickettsiae, some spirochetes
Malaria
Helicobacter pylori
Acne
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Adverse Effects
Photosensitivity
Gastrointestinal upset
Hepatotoxicity
Deposition in bone and teeth, particularly during foetal development
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Macrolides
Inhibitors of the 50S ribosomal subunit Activity is enhanced by alkaline pH
Bacteriostatic
Effective against Gram-positive (pneumococci, streptococci, staphylococci) and Gram-negative (neisseria, bordetella, treponema)
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Pharmacokinetics
Erythromycin A: IV, oral – enteric coated as gastric acid interferes with absorption
D: widely distributed, except the CNS
M: half-life of 1.5h, metabolised by liver
E: excreted in biliary system
Azithromycin has a higher Vd thus has once daily dosing
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Indications
Community acquired pneumonia Penicillin substitute in allergic patients
Drug of choice in Coryneabacterium
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Adverse Effects
Nausea, vomiting, diarrhoea
Cholestatic hepatitis
Interacts with anticoagulants, theophylline, cyclosporin, methylprednisolone
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Lincosamide
Binds to ribosomal 50S subunits to interfere with protein synthesis
Effective against Streptococci, Staphylococci and Pneumococci Enterococci and Gram-negative organisms are resistant
Includes: Clindamycin
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Pharmacokinetics
Clindamycin A: well absorbed orally
D: well-distributed except CNS Penetrates well into abscesses
M: metabolised by liver, half-life of 2-2.5h
E: cleared by liver
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Indications
Skin and soft tissue infections
Anaerobic infections
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Adverse Effects
GI upset
Impaired LFTs
Clostridium difficile colitis
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Folate Antagonists
Synergistic combination of folate antagonists blocks purine production and nucleic acid synthesis Interferes with folate production and therefore DNA synthesis
Mammalian cells use exogenous folate
Active against Gram-positive, Gram-negative, nocardia, chlamydia and some protozoa
Includes: Trimethoprim which inhibits dihydrofolate reductase
Sulphonamides antagonise dihydropteroate synthase as a PABA analogue
Trimethoprim + Sulphonamides in combination are bactericidal In isolation, they are each bacteriostatic
Synergistic as trimethoprim acts on the sequential step of folate synthesis
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Folate Antagonists
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Pharmacokinetics
Trimethoprim + Sulfamethoxazole A: oral, IV
D: reasonable distribution
M: little metabolism
E: renal clearance
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Indications
Urinary tract infections
Pneumocystis jiroveci pneumonia
Toxoplasmosis
Nocardiosis
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Adverse Effects
Bone marrow suppression
Hyperkalaemia
Rash
Fever
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Chloramphenicol
Prevents bacterial protein synthesis by binding to the 50S ribosomal subunit
Bacteriostatic against susceptible bacteria
Broad spectrum antibiotic
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Pharmacokinetics
A: rapidly absorbed orally
D: widely distributed to virtually all tissues, including CSF
M: mostly inactivated by conjugation in the liver
E: metabolites renally excreted
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Indications
Rarely used in the developed world due to serious toxicities
Can be used against Haemophilus influenzae, Neisseria meningiditis, and bactericides
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Adverse Effects
Red cell suppression
Aplastic anaemia
Grey-Baby syndrome
Nausea/vomiting/diarrhoea
Interacts with phenytoin and warfarin to increase serum concentrations
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Quinolones
Inhibits DNA replication by binding to DNA gyrase and topoisomerase IV
Bactericidal activity against susceptible bacteria
Active against Gram-positive, Gram-negative and pseudomonas
Includes: Ciprofloxacin, Moxifloxacin
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Pharmacokinetics
Ciprofloxacin A: oral bioavailability 80-95%
D: large Vd
M: some hepatic metabolism
E: mixed clearance, predominantly renally excreted
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Indications
Urinary tract infections
Gastroenteritis
Osteomyelitis
Anthrax
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Adverse Effects
Gastrointestinal upset
Neurotoxicity
QT prolongation
Tendonitis
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Nitroimidazole
Disrupts electron chain transport
Bactericidal
Activity against anaerobic bacteria and protozoa
Includes: Metronidazole, Tinidazole
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Pharmacokinetics
Metronidazole A: oral or IV administration
D: widely distributed
M: some hepatic metabolism
E: excreted in urine both unchanged and as metabolites
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Indications
Anaerobic infections
Vaginitis
Clostridium difficile colitis
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Adverse Effects
Gastrointestinal upset
Metallic taste
Neuropathy
Seizures
Interacts with alcohol resulting in a disulfiram-like reactio0n
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Anti-Malarials (Chloroquine)
Various anti-malarial drugs with differing mechanisms of action
Chloroquine is thought to be a rapidly acting schizonticide with some gametocytocidal activity Increases intravacuolar pH and affects the parasite’s ability to metabolism
haemoglobin
Interferes with DNA or RNA synthesis
Also has anti-inflammatory activity and may also have immunosuppressive effects
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Pharmacokinetics
Chloroquine A: rapid and complete
D: large Vd
M: unknown
E: urinary excretion
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Indications
Considered in non-falciparum malaria
Considered in sensitive falciparum cases
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Adverse Effects
Generally well tolerated
Haemolysis in those with G6PD deficiency
Pruritis
Gastrointestinal symptoms
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Antivirals
Viral replication occurs via several steps: Attachment and entry through cell membrane
Uncaring of nucleic acid
Synthesis of regulatory proteins
Synthesis of late proteins
Assembly of viral particles
Release
Antivirals interfere with these steps
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Antivirals
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Nucleic Acid Synthesis Inhibitors
Aciclovir is a guanine analogue (produg) that is phosphorylated by viral and cellular enzymes Conversion to its active form is limited in normal cells
Inhibits viral DNA polymerase and DNA synthesis
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Pharmacokinetics
A: IV, oral (low oral bioavailability)
D: low protein binding
M: partial metabolism by liver
E: urine (60% unchanged)
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Indications
Treatment and prevention of HSV, shingles
Acute varicella zoster in immunocompromised patients
HSV encephalitis
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Adverse Effects
Gastrointestinal upset
Diarrhoea
Headache
Encephalopathy
Neurotoxicity
Seizures
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Neuraminidase Inhibitors
Oseltamivir is a produg that is activated by hepatic esterases Inhibits the viral surface enzyme neuraminidase
Prevents release of new virus from infected cells
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Pharmacokinetics
A: oral (75% oral bioavailability)
D: low protein binding, moderate Vd
M: liver activates produg
E: urinary excretion of active metabolite (99%)
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Indications
Treatment and prevention of influenza A and B
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Adverse Effects
Gastrointestinal upset
Headache
Gastrointestinal bleeding
Hepatitis