Jumble Flashcards
Drugs only effective against gram positive bacteria
Penicillinase resistant penicillins (cloxacillin)
Vancomycin
Linezolid
Trimethoprim
Drugs only effective against gram negative bacteria
Aztreonam
Ciprofloxacin (mostly)
What drugs are effective against atypicals
Tetracyclines, macrolides
Levofloxacin
What drugs are effective against MRSA
Ceftaroline, ceftobiprole
Vancomycin
Macrolides, clindamycin, linezolid
Sulfonamides, trimethoprim, cotrimoxazole
Fluoroquinolones not used due to resistance
Drugs with oral bioavailability
NP V, PRP, aminopenicillins, 1st and 2nd gen cephalosporins
Vancomycin (CDAD)
Tetracyclines
Macrolides esp azithromycin
Clindamycin, linezolid
Neomycin for bowel prep
Fluoroquinolones, sulfonamides, trimethoprim, cotrimoxazole, nitrofurantoin
Amphotericin B, 5-flucytosine, metronidazole
NRTI, NNRTI, integrase inhibitors
Acyclovir, valacyclovir, ganciclovir, valganciclovir
Drugs that can be administered for pregnancy
Penicillins, cephalosporins, carbapenems, aztreonam
Oral vancomycin for CDAD
Azithromycin, erythromycin
Amphotericin B, itraconazole, voriconazole, terbinafine
Metronidazole (Avoid first trimester)
PEP - Tenofovir + emtricitabine
Integrase inhibitors (with folic acid)
Acyclovir, valacyclovir
Drugs effective against anaerobes
Aminopenicillins, piperacillin + tazobactam, carbapenems
Clindamycin
Levofloxacin, moxifloxacin
Metronidazole (first line)
Simple UTI drugs
Nitrofurantoin, cotrimoxazole are first line
Amoxicillin, cephalexin
Fluoroquinolones (but may have resistance)
Good CSF penetration
Penicillins
3-5th gen cephalosporins
Meropenem
Aztreonam
Vancomycin
Linezolid
Aminoglycosides
Fluconazole, voriconazole
MRSA orally
Clindamycin, linezolid, doxycycline
Sulfonamides, trimethoprim, cotrimoxazole
Pregnancy orally
NPV, PRP, aminopenicillins, 1-2 gen cephalosporins
Oral vancomycin for CDAD
Azithromycin, erythromycin
Amphotericin B, metronidazole (Avoid first trimester)
Tenofovir, emtricitabine, integrase inhibitors (with folic acid)
Acyclovir, valacyclovir
Anaerobes orally
Aminopenicillins
Clindamycin
Levofloxacin, moxifloxacin
Metronidazole (first line)
Atypicals pregnant
Azithromycin, erythromycin
MRSA pregnant
Ceftaroline, ceftobiprole
Anaerobes pregnant
Aminopenicillins, piperacillin + tazobactam, carbapenems
Metronidazole (AVoid first trimester)
UTI pregnant
Amoxicillin, cephalexin
Endocarditis
Gentamicin + penicillin first line
Streptomycin + penicilin
LA administered for procaine allergy
Bupivacaine
Lidocaine
Etidocaine
Mepivacaine
Prilocaine
Mechanisms of LAs
Bind to sodium channels to prevent opening and influx of Na+ causing depolarization
Prevents AP generation
Binds preferentially to small unmyelinated rapidly-firing and peripheral nerves
Binds more to nociceptive fibers to block noxious stimuli from generating pain signals
What local factors can affect LA action
Fiber positioning in nerve bundle, size and myelination, frequency of firing
Dosage
Site of injection (acidity, blood supply)
Acidity
What is a potential adverse effect when administering LA? How to prevent?
Systemic adverse effects like vasovagal syndrome, depressed CNS syndrome, restlessness, lightheadedness, dizziness, cyanosis, hypersensitivity, nausea, vomiting, liver damage
Administer with vasoconstrictor
Inhaled vs IV GA
Inhaled
- Maintenance, sometimes induction in children
- Surgical anesthesia, loss of consciousness
- Slower onset and offset
- Most excretion via lungs
- Can cause respiratory and cardiac depression (variable effect on heart rate but SV and systemic resistance typically fall)
IV
- Induction, adjunct to inhaled
- Cannot achieve surgical anesthesia (except ketamine) or loss of consciousness
- Faster onset and offset
- Dose controlled more accurately
- Does not require expensive vaporizer equipment or disposal equipment
- Most metabolism via liver and excretion via kidneys
- Respiratory and cardiac depression
Ester LAs
Procaine
Cocaine
Chloroprocaine
Tetracaine
PK of LA
PK does not affect onset
PK affects offset
- A and D into systemic bloodstream causes drop in [LA] to below MEC
- A and D into tissues slows excretion
- A depends on acidity –> more acidic = more charged, less penetration
- A and D depends on vasoconstrictor usage
- M via liver or butyrylcholinesterases
- E renally
Isoflurane VS Nitrous oxide
Isoflurane
- Inhaled GA
- Liquid, has to be vapourized
- Anxiolysis, amnesia, analgesia, sedation
- Loss of consciousness, surgical anesthesia
- Used for maintenance of GA
- Metab in body
- Excreted primarily via lungs
- Higher solubility, slower onset and offset
- Dose dependent respiratory depression
- MOA via increasing brain Cl- opening times, hyperpolarization
Nitrous oxide
- Inhaled GA
- Gaseous
- Anxiolysis, amnesia, analgesia, sedation
- Loss of consciousness, surgical anesthesia
- Used as adjunct to labour pain and adjunct to other inhaled GAs
- Metab in GI bacteria
- Excreted primarily via lungs
- Lower solubility, faster onset and offset
- Lowest risk of increasing ICP
- MOA via increasing brain Cl- opening times, hyperpolarization
LA for 1h long procedure
Procaine
LA administration
Infiltrative plexus block
Topical
Advantages of using LA with adrenaline
Longer duration of action
Lower risk of systemic side effects
MOA of IV GAs
Bind to GABA receptors and potentiate GABA in the brain
Prolongs Cl- opening time and increases frequency of opening, hyperpolarizing the cell
Prevents AP generation, block motor and autonomic responses to noxious stimuli
Analgesic, amnesic, anxiolytic, sedative
Adverse effects of IV GAs
Generally decrease respiration, cardiac output and can cause hypotension, anterograde amnesia, increased ICP
Excitement phase associated with amnesia but not delirium, vomiting + retching upon stimulation
Ketamine causes post-op disorientation, illusions, dreams
Post-op nausea
Malignant hyperthermia (hyperthermia, muscle rigidity, tachycardia, hypertension, acidosis, death)
Balanced anesthesia?
IV induction
Inhaled maintenance
LA pre- and perioperative analgesia
Muscle relaxants for tracheal intubation and efficiency of surgery
CVS drugs to control transient autonomic responses to noxious stimuli
NSAID mechanism of action
COX enzyme inhibition
COX1 constitutive, COX2 inducible (except kidneys, female repro tract, CNS, joints)
COX1 produces TXA2, PGE2, PGI2
COX1 inhibition causes antiplatelet effect, cardioprotection, hypernatremia, hypertension, easy bruising, increased risk of hyperkalemia and acute liver failure, nausea, vomiting, abdominal discomfort, gastric ulcers, exacerbate existing wounds, contraindicated in pregnancy
COX2 produces PGE2, PGI2
COX2 inhibition causes increased thrombosis, decreases inflammation and pain, hypernatremia, hypertension, increased risk of hyperkalemia and acute renal failure
Inhibition of prostanoids reduces sensitization of nociceptive fibers, analgesic effect with analgesic ceiling
Inhibition of COX2 prostaglandins reduces inflammation
NSAIDs also associated with hypersensitivity, SJS, TEN