Antibiotics Part 2 Flashcards
Describe features of Vancomycin
- It is a glycopeptide antibiotic which is ultrabroad spectrum for gram positive bacteria.
- Delivered IV but has difficult pharmacodynamics
- Less effective than fluclox for MSSA but used in patients who have MRSA or can’t take fluclox.
- Active against MRSA, streptococci, MSSA,
- Main issue in clinical use is underdosing
Not active against coliforms, difficult gram negatives or anaerobes
What are the diffierent toxic effects seen with vancomycin
- Nephrotoxicity (with high doses)
- Red-man syndrome if injected rapidly (anaphylactoid syndrome)
- Ototoxicity
- Therefore theraputic drug monitoring is undertaken due to its narrow theraputic range
What gene gave rise to S.aurus resistance and what drug can be used in MRSA
- MecA gene inherited from S. fleurettii
- Vancomycin is used
Describe features of Gentamicin
- It is an aminoglycoside antibiotic with very broad spectrum which can only be delivered IV
- Principally useful against gram negatives so useful with intra-abdominal infections and UTI
- Low rates of resistance in community but not uncommon
Active against most gram negatives
Explain the mechanism of action of aminoglycosides
- Reversibly binds to the 30S ribosome which causes a bacteriostatic action, prolonging the post-antibiotic effect.
- It has a bactericidal action by acting on the cell membrane. Results in rapid lysis early in dosing intervals with high doses
What are the toxic side effects of aminoglycosides
- Nephrotoxicity
- Ototoxicity (hearing loss, loss of balance, oscillopsia)
- Neuromuscular blockage (usually only significant in patients with myasthenia gravis - AVOID in these patients)
What is the dosing regimen for aminoglycosides
- Once daily dosing. High initial dose to take advantage of rapid killing.
- Leave long dosing interval (24-48hrs) to minimuse toxicity
- Make sure to measure trough level between doses to ensure drug is not accumulating
- Give for 3 days only
What are personal risk factors for resistance?
- Antibiotic consumption within the last 6 months
- Overnight stays in hospitals
- Visiting countries with high incidence of drug resistance
- This resistence may occur for many months after acquired
Describe features of Macrolides
- Class of antibiotics with a good spectrum of activity against gram positives and respiratory gram negatives
- Active against atypicals such as legionella, mycoplasm or chlamydia
- Ecellent oral absorption
- Examples include erythromycin, azithromycin and clarithromycin
What are the main targets of antibiotics
- Cell wall biosynthesis (targeted by betalactams and vancomycin)
- Protein biosynthesis (argeted by macrolides, aminoglycosides and tetracyclines)
- DNA and RNS synthesis (Rifampin and quinolones)
- Folate metabolism (trimethoprim)
What are the main side effects and drug interactions of macrolides
- Side effects are diarrhoea and vomiting, QT prolongations and hearing loss with long term use.
- Resistance among typical pathogens is common but in atypical pathogens is rare.
- Interacts with simvastatin so avoid co-prescription, atorvastatin and warfarin.
Describe features of clindamycin
- Similar to macrolides as it has same mechanism, good oral absorptions and principally active against gram positives
- However no action against aerobic gram negatives or atypicals but does have excellent activity against anerobes so often used in abscesses
- It is highly effectice at stopping exotoxin production so added alongside other antibiotics in toxic shock syndrome and necrotising fasciitis
Name and describe the C.differgic antibiotics
- These are antibiotics that dramatically disturb the colonic flora. C.diff forms spores which are difficult to erradicate from hospitals
- 4Cs are the common causes but all antibiotics can cause C.diff:
- Clindamycin
- Co-amoxiclav
- Cephalosporins
- Ciprofloxacin
Describe features of tetracyclines
- Active against MSSA, streptococci and atypical organisms
- Relatively non doxic but avoid in children and pregnant women as it can cause bone abnormalities and tooth discolouration
Describe features of Quinolones
- Broad spectrum, bactericidal antibiotics which targert Dna/RNS synthesis
- Excellent oral bioavailability
- Agtive gainst many atypical pathogens
Explain side effects of quinolones
- Toxic side effects include: GI toxicity, QT prolongation and tendonitis which can cause tendon rupture.
- Resistance is emerging and is prone to causing C.diff esp. in N.America
Name examples of quinolones and their uses
- Ciprofloxacin. Mainly used against gram negative pathogens, can be used against pseudomonas.
- Levofloxacin. It is an extended spectrum quinolone with increased activity against gram positive (MRSA). Used for LRTI/pneumonia
What are the indications and interactions of rifampicin
- Used for tuberculosis (combination therapy) or in addition to another antibiotic in serious gram positive infections.
- Rifampicin is a potent CYP450 enzyme inducer so affect most drugs that undergo hepatic metabolism
NEVER prescribe rifampicin as a monotherapy.
Explain the methanism of action of trimethorprim and other folate metabolism antibiotics
- Inhibition of folate metabolism pathway leads to impaired nucleotide synthesis and therefore impaired DNA replication
Describe the uses and side effects of trimethoprim
- Good range against gram positive and negative but due to resistance is limited to uncompensated UTIs
- Toxic effects: Cause elevation of serum creatinine, elevation of serum potassium, Rash and Gi distrubances (uncommone)
What is co-trimoxazole and its side effects
- Combination of trimethoprim and sulphamethoxazole
- Can cause bone marrow suppression and steven johnson syndrome
- Tends to only be used by specalists
Describe features of metronidazole
- Enters the cell by passive diffusion and produces free redicles.
- More effective against anaerobic bacteria
- Often added to therapy for intra-abdominal infections
- Causes unpleasant reaction with alcohol and peripheral neuropathy