Dosing of Propofol, Etomidate and Lidocaine

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Propofol (induction dose)
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1-2.5 mg/kg
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Propofol (maintenance)
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100-200 mcg/kg/min
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Propofol (conscious sedation)
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25-75 mcg/kg/min
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Propofol (onset)
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30 seconds
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Propofol (duration)
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3-8 minutes
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Etomidate (induction dose)
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0.2-0.6 mg/kg
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Etomidate (onset)
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30-60 seconds
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Etomidate (duration)
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3-5 minutes
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Lidocaine (induction dose)
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1.5 mg/kg
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Lidocaine (max LA dose w/out Epi)
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4 mg/kg
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Lidocaine (max LA dose w/ Epi)
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7 mg/kg
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Ketamine (IV dose induction)
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2-4 mg/kg
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Ketamine (PO)
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10mg/kg
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Ketamine (IV infusion or iv push)
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15-45 mcg/kg/min (1-3 mg/min infusion) 0.5-1.0 mg/kg iv
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Ketamine (IM dose)
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4-6 mg/kg
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Ketamine (IV onset)
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1-2 minutes
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Ketamine (IM onset)
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3-8 minutes
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Ketamine (IV duration)
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6-15 minutes
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Ketamine (IM duration)
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15-20 minutes
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Ketamine (conscious sedation)
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0.25-0.5 mg/kg IV
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Succinylcholine (IV onset)
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30-60 seconds
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Succinylcholine (IM onset)
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2-3 minutes
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Succinylcholine (IV duration)
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3-5 minutes
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Succinylcholine (IM duration)
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10-30 minutes
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Succinylcholine (IV induction)
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1-1.5 mg/kg
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Succinylcholine (IM dose)
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3 mg/kg
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Succinylcholine (laryngospasm dose)
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20 mg IV
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Vecuronium (IV induction)
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0.1 mg/kg
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Vecuronium (Maintenance gtt)
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1 mcg/kg/min
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Vecuronium (onset)
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2-4 minutes
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Vecuronium (duration)
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30-60 minutes
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Cisatracurium (duration)
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30-60 minutes
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Cisatracurium (onset)
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2-4 minutes
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Cisastracurium (IV induction)
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0.1 mg/kg
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Cisastracurium (maintenance)
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1-3 mcg/kg/min
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Rocuronium (induction dose)
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0.6-1.2 mg/kg
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Rocuronium (maintenance)
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5-12 mcg/kg/min
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Rocuronium (duration)
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30-60 minutes
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Rocuronium (onset)
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60-90 seconds
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Atracurium (induction)
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0.5 mg/kg
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Atracurium (duration)
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30-60 minutes
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Atracurium (maintenance)
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3-5 mcg/kg/min
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Atracurium (onset)
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2-4 minutes
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Ofirmev (dose)
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1000mg q6 or 650mg q4 infused over 15 minutes. Max daily dose 4000mg
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Ofirmev (onset/peak/duration)
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10 minutes/ 1hr/ 4-6 hours
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Hydrocortisone (dose)
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250mg IV
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Scopolamine (IV/IM dose)
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0.3- 0.6 IV/IM
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Scopolamine Patch (dose/onset/ duration)
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1.5mg total dosage for patch; 4 hours/ 3 days
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Scopolamine (onset IV)
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8-10 minutes
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Scopolamine (onset IM)
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30 minutes
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Scopolamine (duration IV)
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2 hours
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Scopolamine (duration IM)
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4 hours
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Dopamine (onset)
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5 minutes
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Dopamine (duration)
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minutes after discontinuing
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Dopamine (dosing)
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1-70 mcg/kg/min (Only dopaminergic receptors stimulated at less than 2 mcg/kg/min, Beta at 2-5 mcg/kg/min, Alpha at rates greater than 10 mcg/kg/min)
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Phenylephrine (bolus dose)
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50-100 mcg/dose (do not exceed 0.5mg in adults)
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Phenylephrine (duration)
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10-15 minutes
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Phenylephrine (onset)
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immediate
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Clonidine (dose)
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0.1-0.6 mg (in 2 or 3 dose orally)
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Precedex (loading dose)
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1 mcg/kg IV over 10 minutes
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Precedex (Maintenance Drip)
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0.2-1.4 mcg/kg/hr
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Precedex (fiberoptic intubation)
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0.7 mcg/kg/hr
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Precedex (procedural sedation)
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start 0.6 mcg/kg/hr and titrate
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Precedex (duration)
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10-30 min after infusion stops
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Precedex (onset)
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10-20 minutes
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Nitroglycerine (dose)
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25-50 mcg IV bolus 5-200 mcg/min IV infusion (200= max dose) 0.4 mg SL q5 x 3 doses
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Nitroglycerine (duration)
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3-5 minutes
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Nitroglycerine (onset)
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1 minute
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Hydralazine (dose)
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2.5- 20mg IV (5-10mg q20 with a max dose of 40mg)
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Hydralazine (duration)
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4-8 hours
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Hydralazine (onset)
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15-20 minutes
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Labetalol/ Trandate (non-selective) IV intermittent dose
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0.25mg/kg
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Labetalol/ Trandate (non-selective) Infusion dose
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up to 2 mg/min
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Labetalol/ Trandate (non-selective) IV bolus dose
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20mg-80mg q10 (start with 20 and work up 300mg max)
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Labetalol (duration)
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2-4 hours
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Labetalol/Trandate (onset)
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immediately
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Metoprolol/Lopressor (dose)
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(selective) 2.5 to 5mg q5 max dose 15mg
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Metoprolol/Lopressor (duration)
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(selective) 5-8 hours
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Metoprolol/ Lopressor (onset)
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immediately
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Esmolol/ Brevibloc (onset)
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(selective) 1-2 minutes
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Esmolol/ Brevibloc (duration)
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(selective) 5-10 minutes
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Esmolol/ Brevibloc (bolus and infusion dose)
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(selective) Bolus 10-15 mg Infusion: 25-350 mcg/kg/min (loading dose of 500mcg/kg/min for 1 min then titrate)
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Propanolol/ Inderal (dose)
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(non selective) IV 1mg q5 minutes up to 5mg
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Propanolol/Inderal (onset)
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(non selective) 15 minutes
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Propanolol/Inderal (duration)
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6 hours
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Epinephrine (onset)
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less than a minute
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Epinephrine (duration)
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5-10 minutes
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Epinephrine (peak)
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1-2 minutes
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Epinephrine (iv push)
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10-100mcg
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Epinephrine (Infusion)
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0.01-0.03 mcg/kg/min (Beta) 0.03-0.15 mcg/kg/min (alpha and beta) 0.15-0.3 mcg/kg/min (alpha
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Norepinephrine (infusion dose)
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0.01-0.2 mcg/kg/min
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Norepinephrine (onset)
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less than 1 minute
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Norepinephrine (duration)
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2-10 minutes
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Norepinephrine (peak)
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1-2 minutes
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Albuterol/ Proventil/ Ventolin (dose)
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90 mcg/inhalation 2 puff MDI q4-6 hours 2.5mg neb q4-6 hours
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Albuterol/ Proventil/ Ventolin (duration)
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6-12 hours
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Albuterol/ Proventil/ Ventolin (onset)
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15-30 minutes
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Zofran (dose)
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4-8mg IV (0.15mg/kg)
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Zofran (duration)
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4-8 hours
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Zofran (onset)
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rapid
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Granisetron (Kytril; IV and PO dose)
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1 mg IV 2 mg PO
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Promethazine (dose)
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12.5-25 mg IV 6.25mg/5ml PO
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Promethazine (duration)
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4-12 hours
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Promethazine (onset)
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3-5 minutes
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Metoclopramide (dose)
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10-20mg IV
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Metoclopramide (duration)
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1-2 hours
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Metoclopramide (onset)
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1-3 minutes
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Ranitidine (dose)
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50-100 mg IV (1-2.5 mg/kg) 150-300 PO
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Flumazenil (dose)
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0.2 mg/kg (slow titration max 3mg)
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Flumazenil (onset)
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1-2 minutes
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Flumazenil (duration)
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45-90 minutes
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Benadryl (dose)
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25-50mg (PO/IV/IM) (0.5-1.5mg/kg)
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Benadryl (duration)
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3-6 hours
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Dexamethasone (dose)
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5-10mg
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Dexamethasone (duration)
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variable
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Dexamethasone (onset)
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1 hour
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Naloxone (dose)
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40-100 mcg
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Naloxone (duration)
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20-60 minutes
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Naloxone (onset)
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2 minutes
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Ketoralac (dose)
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30 or 60mg
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Ketoralac (duration)
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4-6 hours
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Ketoralac (onset)
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30 minutes
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Indigo Carmine
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(40mg/5ml vial) 5mg
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Furosemide (dose)
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20-40mg IV (up to 200mg/dose for acute pulmonary edema) 20-80mg PO (qday or q6-8 hrs for edema, HTN; not to exceed 600mg/day)
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Lasix (duration)
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2 hours IV 6-8 hours PO
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Lasix (onset)
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5 min IV 30 min IM 30-60 min PO/SL
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Lasix (peak)
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<15min IV 1-2 hours PO/SL
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Oxytocin (dose)
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0.5-8 mU/min
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Hemabate/ Carboprost tromethamine (dose)
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250mcg IM initial repeat PRN q 1.5-3.5 hours
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Methergine/ Methylergonovine (dose)
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0.2 mg IM q2-4 (not to exceed 5 doses) (Then 0.2-0.4 mg PO q6-8 hours for 2-7 days)
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Sublimaze/Fentanyl (IV dose)
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25-100mcg
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Sublimaze/Fentanyl (IV duration)
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0.5-1 hour
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Fentanyl (peak)
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20-30 minutes
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Sublimaze/Fentanyl (IV onset)
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2-5 minutes
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Hydromorphone (IV onset)
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15-30 minutes
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Hydromorphone (IV duration)
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4-5 hours
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Hydromorphone (IV dose)
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0.25 mg -1mg
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Hydromorphone (peak)
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30-90 minutes
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Morphine (IV dose)
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2-10mg
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Morphine (IV duration)
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4-5 hours
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Morphine (IV onset)
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20 minutes
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Morphine (IV peak)
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30-60 minutes
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Sufentanil (IV dose)
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0.5 mcg/kg
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Sufentanil (IV onset)
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1-3 minutes
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Sufentanil (IV duration)
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dose dependent
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Remifentanil (IV induction and infusion dose)
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0.5-1 mcg/kg (induction) 0.05-2 mcg/kg/min (infusion)
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Remifentanil (IV onset)
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1 minute
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Remifentanil (IV duration)
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5-10 minute
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Remifentanil (peak)
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1 minute
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Midazolam (onset)
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IV 1-2 minutes IM 15 minutes PO 30 minutes
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Midazolam (duration)
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IV 20-50 minutes IM up to 6 hours
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Midazolam (IM, IV, Induction dose)
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IM 0.07 mg/kg IV 0.02-0.03 mg/kg Induction 0.1-0.2 mg/kg
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Edrophonium (dose)
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0.05-0.1 mg/kg
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Edrophonium (duration)
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30-60 minutes
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Edrophonium (onset)
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5-10 minutes
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Atropine (dose)
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0.4-1mg IV (bradycardia) (NMB Reversal 10 mcg/kg with edrophonium 0.02 mg/kg peds)
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Atropine (duration)
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2-6 hours
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Atropine (onset)
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30-60 seconds
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Neostigmine (dose)
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0.05 mg/kg max dose 5mg (w/ robinul 0.2mg for every 1 mg of neostig)
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Neostigmine (duration)
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45-90 minutes
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Neostigmine (onset)
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5-15 minutes
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Glycopyrrolate (dose)
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IV 0.1-0.2 mg for bradycardia 0.2 mg for every 1mg of neostig or 10 mcg/kg
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Glycopyrrolate (onset)
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1-3 minutes
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Glycopyrrolate (duration)
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Vagal effects about 2 hours, decreased salivation for 7 hours
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Vasopressin (dose)
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Bolus 10-20 units 0.04-0.1 unit/min
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Vasopressin (duration)
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10-30 minutes
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Vasopressin (onset)
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1-5 minutes
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Vasopressin (peak)
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5 minutes
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Ephedrine (dose)
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5-10mg
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Ephedrine (onset)
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less than 1 minute
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Ephedrine (duration)
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10- 60 minutes
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Atracurium
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0.5 mg/kg
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Succinylcholine induction dose
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0.5-1 mg/kg RSI: 1-1.5 mg/kg
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Succinylcholine onset
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30 sec
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Succinylcholine duration
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4-6 min
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Succinylcholine MOA
Succinylcholine MOA
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binds to nicotinic ACh receptors at the NMJ causing depolarization
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Rocuronium induction dose
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o.6-1.2 mg/kg
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Rocuronium onset
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45-90 sec
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Rocuronium duration
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15-150 min
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Non-depolarizing NMBA MOA
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competitive binding of nicotinic ACh receptors at the NMJ, preventing depolarization
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Cisatracurium induction dose
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0.2 mg/kg
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Cisatracurium onset
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90-120
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Cisatracurium duration
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20-40 min
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Fentanyl dose
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50-150 mcg
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Fentanyl onset
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within 30 sec
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Fentanyl peak
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3-5 min (6.8 min)
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Fentanyl duration
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30-60 min
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Fentanyl MOA
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Mu 1&2 agonist
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Fentanyl issues
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muscle rigidity, bradycardia w/large dose, potency 100x morphine
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Remifentanil dose
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0.05-2 mcg/kg/min
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Remifentanil onset
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within 30 sec
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Remifentanil peak
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3-5 min
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Remifentanil duration
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5-10 min
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Remifentanil metabolism
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plasma cholinesterases
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Dilaudid dose
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0.5-2 mg
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Dilaudid onset
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almost immediate
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Dilaudid peak
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5-20 min
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Dilaudid duration
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2-4 hrs
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Dilaudid issues
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muscle rigidity
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Morphine dose
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1-15 mg
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Morphine onset
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<1 min
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Morphine peak
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5-20 min
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Morphine duration
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2-7 hrs
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Morphine issues
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avoid in asthma and hypotension because of histamine release
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Propofol dose
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1-2 mg/kg
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Propofol maintenance dose
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50-150 mcg/kg/min
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Propofol onset
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30 sec
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Propofol peak
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1 min
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Propofol duration
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5-10 min
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Propofol MOA
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increasing the duration of the GABA-activated opening of the chloride channel with resulting hyperpolarization of cell membranes
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Propofol properties & issues
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anti-emetic hypotension, irritation on injection
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Ketamine dose
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0.5-1 mg/kg
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Ketamine onset
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<30 sec
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Ketamine peak
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1 min
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Ketamine duration
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5-15 min
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Ketamine MOA
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inhibits glutamate @ the NMDA receptor
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Ketamine metabolism
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cytochrome P450 system
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Ketamine S/E
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++ MAP, ++ HR, + CO, no respiratory depression, bronchodilation, analgesic properties, decrease CBF but increase CPP CMRO2 ICP & IOP
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Midazolam dose
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0.1-0.2 mg/kg
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Midazolam onset
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30-60 sec
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Midazolam peak
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3-5 min
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Midzaolam duration
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15-80 min
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Midazolam MOA
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GABA agonist- opening of Cl channels leading to hyper polarization
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Dexmedetomidine dose
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1 mcg/kg over 10 min
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Dexmedetomidine maintenance dose
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0.2-0.7 mcg/kg/min
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Dexmedetomidine peak
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2-6 min
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Dexmedetomidine duration
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0.5-2 hrs
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Dexmedetomidine MOA
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presynaptic Alpha-2 agonist inhibiting Ca channels and activating K channels causing hyperpolarization and decreased release of catecholamine vesicles
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Dexmedetomidine issues
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hypotension & bradycardia
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Neosynephrine dose
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50-100 mcg
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Neosynephrine onset
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<1 min
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Neosynephrine peak
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<1 min
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Neosynephrine duration
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15-20 min
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Neosynephrine indication & MOA
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hypotention w/o bradycardia selective alpha-1 agonist causing vasoconstriction of arterioles and venuoles
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Neosynephrine issues
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bradycardia
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Ephedrine indication & MOA
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hypotension w/ bradycardia & bronchospasm Beta & Alpha agonist mix direct & indirect
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Ephedrine dose
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5-20 mg
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Ephedrine onset
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immediate
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Ephedrine peak
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2-5 min
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Ephedrine duration
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10-60 min
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Ephedrine issues
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increased risk of arrhythmia
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Epinephrine indication & MOA
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other vasopressors fail, total spinal, bronchospasm Alpha & Beta agonist, increased HR, bronchodilator
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Epinephrine dose
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2-10 mcg
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Epinephrine onset
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<1 min
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Epinephrine peak
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<1 min
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Epinephrine duration
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5-10 min
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Esmolol indication & MOA
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Tachycardia, HTN Selective Beta-1 antagonist
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Esmolol dose
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0.5-1 mg/kg
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Esmolol onset
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1-2 min
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Esmolol peak
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5 min
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Esmolol duration
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10 min
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Esmolol metabolism
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RBC esterases
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Metoprolol indication & MOA
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HTN, SVT, Acute MI Selective Beta-1 antagonist
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Metoprolol dose
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2-15 mg
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Metoprolol onset
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<15 min
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Metoprolol peak
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20 min
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Metoprolol duration
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5-8 hrs
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Metoprolol contraindications
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bradycardia & heart block
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Labetalol indications & MOA
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HTN Alpha & Beta antagonist (1:7 - Alpha/Beta)
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Labetalol dose
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2.5-20 mg
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Labetalol onset
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2-5 min
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Labetalol peak
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5-15 min
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Labetalol duration
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2-4 hrs
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Labetalol contraindications
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asthma, HF, bradycardia
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Hydralazine indications & MOA
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HTN, SVR reduction in CHF patients activation of K channels causing hyperpolarization of smooth cells preventing vasoconstriction (requires Nitric Oxide for vasodilation)
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Hydralazine dose
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0.1-0.2 mg/kg
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Hydralazine onset
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5-20 min
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Hydralazine peak
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10-80 min
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Hydralazine duration
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2-4 hrs
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Hydralazine S/E
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reflexive bradycardia (minimal with co-administration w/Beta Blocker)
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A 23 yo F presents to your office for an evaluation of her third molars. Teeth #1 and #16 are erupted/malposed, and #17 and #32 are slightly mesioangular PBIs. On history you discover that she has asthma and smokes cigarettes, 1 PPD for the past 10 years. Her medications include Advair Inhaler BID, Proventil prn, and orthotrycycline BCP (although she occasionally misses a dose and she has not had her period for a couple months). On further questioning, you also find out that she takes a MVI, additional vit E, and an herbal "mood pack" containing St John's Wort, ecchinacea, ginko biloba, and garlic. She wants to be "asleep" during her surgery. What questions would you ask this patient, pertaining to the findings in the medical history?
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Aside from CC, HPI, PMedHx, PSurHx, FamHx, ALL, ROS... How frequent and severe are the asthma attacks, what precipitates them, has she ever been to the ER or hospitalized for them. Is she sexually active, and is there a possibility she could be pregnant?
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What are your concerns and perioperative recommendations for any of the medications or supplements that this patient is taking?
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I am concerned that she is not very compliant with her BCPs. I am also concerned about the additional vitamin E and herbals, which can cause excessive bleeding. I would instruct her to stop those supplements 2 weeks prior to any surgical procedure. In addition, I would counsel her to use alternate forms of birth control for the remainder of her current menstrual cycle if antibiotics are prescribed during treatment, because they can render BCPs ineffective.
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What is Advair?
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A combination B2 agonist/corticosteroid inhaled asthma medication used for prevention, not acute attacks. It contains salmeterol (slow acting B2 agonist) and fluticasone (corticosteroid), and comes in a diskus inhaler, that is activated by the patient's inhalation.
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Describe your physical examination:
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I perform a head & neck exam, visualization/palpation/auscultation, cervical LAD, TMJ exam, intraoral exam looking for soft tissues lesions, infections, ulcerations, and evaluate the airway using the mallampati classification (I - entire pharynx visualized, II - most of uvula visualized, III - only soft palate visualized, IV - soft palate not visible) & physical factors like mandibular position/size and ability to extend neck. I look at pupils for size and reactivity, and assess CN V & VII function as pertinent to any potential surgical procedures. I auscultate the heart and lungs.
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On auscultation, her lungs are clear and you hear a soft, but unmistakeably present systolic ejection murmur at the left sternal border. She has never been told that she has a murmur. How would you grade the heart murmur?
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Levine scale: 1. The murmur is only audible on listening carefully for some time. 2. The murmur is *faint* but immediately audible on placing the stethoscope on the chest. 3. A loud murmur readily audible but with no palpable thrill. 4. A loud murmur with a palpable thrill. 5. A loud murmur with a palpable thrill. The murmur is so loud that it is audible with only the rim of the stethoscope touching the chest. 6. A loud murmur with a palpable thrill. The murmur is audible with the stethoscope not touching the chest but lifted just off it.
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Location refers to where the heart murmur is usually heard best. There are 4 places on the anterior chest wall to listen for heart murmurs; each of the locations roughly corresponds to a specific part of the heart and should be listened to (through the stethoscope) with the patient lying down, face up. The four locations are?
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Aortic region - the 2nd RIGHT intercostal space. Pulmonic region - the 2nd left intercostal spaces. Tricuspid region - the 5th left intercostal space (STERNAL) Mitral region - the 5th left mid-clavicular intercostal space. (near nipple)
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What are possible etiologies for the murmur?
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Innocent or physiologic murmur, pregnancy, anemia, VSD, tricuspid or mitral valve dysfunction.
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What actions would you take?
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Medical consultation to evaluate the murmur and need for bacterial endocarditis prophylaxis prior to dental/surgical procedures. I would order a urine pregnancy test immediately, and in my hospital setting, I would refer the patient to cardiology, who would evaluate her with auscultation using different maneuvers (left lateral decubitus brings out mitral murmurs and sitting forward accentuates aortic murmurs), likely an ECG, and possibly an echocardiogram to rule out valvular dysfunction.
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What does inhalation do to accentuate the murmur?
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Inhalation leads to an increase in intrathoracic negative pressure, which increases the capacity of pulmonary circulation, thereby prolonging ejection time. This will affect the closure of the pulmonary valve. This finding, also called Carvallo's maneuver, has been found by studies to have a sensitivity of 100% and a specificity of 80% to 88% in detecting murmurs originating in the right heart. specifically positive Carvallo's sign describes the increase in intensity of a tricuspid regurgitation murmur with inspiration.
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On referral to her physician, a pregnancy test is ordered and comes back positive. She is near the end of her first trimester. What is the likely etiology of the murmur?
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Physiologic murmur caused by the hyperdynamic state of pregnancy (increased cardiac output). These murmurs do not require SBE prophylaxis.
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What will you advise her about the timing of her surgery?
answer
She should ideally wait until after delivery. Any procedures that must be performed, are most safely performed in the *2nd trimester* using local anesthesia, although severe infections and trauma must be managed at the time they present in most cases.
question
She develops a moderate to severe pericoronitis involving tooth #32 (with occlusal trauma from tooth #1) during her pregnancy. She has tender right submandibular nodes, localized erythema and swelling around tooth #32 with mild suppuration, and a temperature of 99.8 F. How would you manage this situation?
answer
I would extract tooth #1 with local anesthesia (lidocaine or mepivacaine, but not bupivacaine - it can cause CV collapse) and irrigate the #32 site with Chlorhexidine 0.12% oral rinse, and have the patient irrigate at home BID. I would prescribe PCN 500mg PO QID for 7 days, or Clindamycin 300mg PO QID for 7 days if she is PCN allergic. I would see her in 48 hours for a follow-up appointment.
question
What antibiotics are safe to use during pregnancy?
answer
PCN, cephalosporins, clindamycin
question
What local anesthetics are safe to use?
answer
Lidocaine and mepivacaine
question
What would be your anesthesia plan?
answer
Topical and local anesthesia. Fentanyl and Demerol are ok in small amounts during pregnancy, but benzodiazepines can cause birth defects (such as cleft lip & palate) early in the pregnancy.
question
You are taking out tooth #1 to alleviate a p-cor involving tooth #32. During the procedure the patient becomes light headed. Why is this occurring and what actions are you going to take?
answer
Likely compression of the Vena Cava, with decreased blood return to the heart. The treatment is to place the patient on her left side with her hip slightly elevated. I would also administer supplemental O2 by NC.
question
The patient recovers from the p-cor and goes on to an uncomplicated delivery. She presents 6 months later for removal of her remaining third molars. She no longer has a murmur on auscultation. She wants to be "completely asleep" for the surgery this time. What additional questions will you ask her?
answer
Is she breastfeeding? If she is, then she should pump and freeze breast milk to have available for several days after the surgery (until the anesthesia medications and any prescribed narcotic analgesics or antibiotics are out of the patient's system).
question
What is this patient's ASA classification?
answer
ASA 2 ASA 1-Normal healthy patient ASA 2-Controlled systemic disease without functional limitation ASA 3-Severe systemic disease with functional limitation ASA 4-Severe systemic disease that is a constant threat to life ASA 5-Moribund patient, not expected to survive without operation ASA 6-Brain-dead, organ donor (E)-Designator for any patient requiring an emergency operation
question
What are your preoperative instructions for this patient?
answer
Stop the vitamin E and herbals 2 weeks prior to surgery. NPO 6 hours prior, with small amounts of water allowed up to 2 hours prior to surgery. She must perform a urine HCG within 72 hrs prior to the surgery and she must have an adult escort with her to drive her home. She needs to bring her albuterol inhaler with her to the appointment, and continue to use her Advair BID throughout the perioperative period. She should ideally stop smoking several weeks prior to her surgery and refrain from smoking for at least a week postoperatively to minimize her risk of alveolar osteitis or impaired healing. I ask patients to remove any nail polish from their fingernails before the appointment and to wear comfortable, non-restrictive clothing.
question
Describe your anesthetic technique for an OPGA:
answer
I perform and supervise intubated general anesthetic cases in my hospital clinic, as a part of a residency training program. One surgeon performs the anesthesia and another performs the surgery. I have a nurse monitoring and recording vital signs during the procedure and recovery. After an immediate preoperative re-assessment, an 18-20ga peripheral IV is started, and a bag of LR is connected. Any indicated preoperative antibiotics are administered IVPB over 20-30 min. I pre-oxgenate for several minutes while placing monitors (pre-cordial stethoscope, pulse-ox, BP, and EKG leads). I give the patient midazolam for anxiolysis if indicated, but don't usually need it, and avoid it if possible to minimize recovery time. After obtaining the first set of vitals, I give 50 to 100 mcg of fentanyl over several minutes. Until recently, I used to give tubocurarine 3mg IVP, as a defasciculating dose at this point, telling the patient that they may have blurred vision and feel a subjective weakness or difficulty breathing. It has not been available recently. I induce general anesthesia with 2.5mg/kg Propofol IVP. I then make an attempt to mask ventilate the patient in order to assess the airway. If the airway is patent, then I administer Succinycholine 1.5mg/kg IVP, and wait approximately 1 min, until after muscle fasciculations subside. Decadron 8mg IVP is administered if indicated for the procedure. I then perform a direct laryngoscopy and administer approximately 50mg of lidocaine in the trachea with an LTA, to prevent stimulation of the airway with movement of the ETT. Without removing the laryngoscope, I pass an endotracheal tube, watching the cuff go past the cords. The stylet is removed, and the cuff inflated. I then hook up the anesthesia circuit to the ETT and verify position by auscultation, condensation in the ETT, ; ETCO2, and note the tube position at the teeth. The tube is secured and a throat pack placed. I place the patient on 60/40 nitrous oxide/O2 at a flow of about 4-5 l/min, and place them on the ventilator with a TV of approximately 8-10 ml/kg and a rate to keep the ETCO2 around 35. I administer a continuous propofol infusion, using a Baxter infusion pump, initially at 100mcg/kg/min. I administer local anesthetic, and perform the surgery. The propofol is gradually weaned down during the case, and the infusion stopped near the end of the procedure. The nitrous oxide is weaned and the patient placed on 100% O2 as the throat pack is removed. I allow the patient to emerge, through stage 2 (following commands and demonstrating good strength and respiratory pattern), prior to extubation. The patient is asked to open, inhale and hold it, and the bag squeezed to fill the lungs with air, just before dropping the cuff and gently pulling the endotracheal tube. The mask is placed and the patient monitored for adequate respirations prior to transport to the recovery room where the patient is constantly monitored until discharge.
question
The patient desires a general anesthetic and you decide to treat her in the Outpatient Surgery Center of your local hospital. The anesthetist induces anesthesia with Propofol, and is using Sevofluorane for maintenance. What are Propofol and Sevofluorane?
answer
Propofol is a substituted isopropylphenol IV sedative-hypnotic agent used for induction and maintenance of anesthesia. It is in a soybean fat emulsion with egg phosphatide, and is highly lipophilic, which increases it's ability to cross the blood-brain barrier. It produces a dose dependent CNS depression, has a fast onset and short duration, and is easily titrated, but can cause marked hypotension when administered in rapid bolus. The usual induction dose is 2-2.5mg/kg. Infusions of 25-200mcg/kg/min are useful for sedation or maintenance of general anesthesia. Sevofluorane is a fluorinated volatile anesthetic agent with a low blood/gas partition coefficient, therefore a rapid onset and recovery from anesthesia. The MAC is 1.71. It is useful in mask inductions for children, because it has less a less pungent odor and airway irritability than other volatile anesthetics. When used in combination, sevo and propofol may cause profound hypotension.
question
What is MAC, pertaining to volatile anesthetics?
answer
The concentration of an inhaled anesthetic, at 1ATM, that prevents skeletal muscle movement in response to a painful stimulus (skin incision) in 50% of patients. A MAC of 1.3 prevents movement in approximately 95% of individuals undergoing surgery. MAC can be used to compare potency of anesthetic gases.
question
During the case, the anesthetist complains of increasing airway pressures. What could be the cause?
answer
Circuit or ETT obstruction (kinking), airway secretions or mucous plugging, bronchospasm.
question
How should potential bronchospasm be treated intraoperatively, in this intubated patient?
answer
Suction ETT and trachea with suction catheter. Albuterol MDI 8-10 puffs into endotracheal tube on inspiration, through chamber, or a 60cc syringe connected to the anesthesia circuit close to the ETT. If this doesn't work, then epinephrine 0.3mg SC.
question
Near the end of the case, the anesthetist is now complaining that the ETCO2 is abnormally high, and non-responsive to increasing the ventilatory rate. The patient has also become mildly tachycardic. The CRNA asks you what you think is going on?
answer
Suspect Malignant Hyperthermia.
question
What is Malignant Hyperthermia?
answer
An inherited disease that manifests most often in children (1:12,000 pediatric anesthetics, 1:40,000 adult anesthetics). The gene for MH is also the genetic coding site for the calcium release channel of skeletal muscle sarcoplasmic reticulum. It is presumed that a defect in the calcium release channel permits sustained higher concentrations of calcium in the myoplasm and persistent muscle contraction when susceptible patients are exposed to triggering agents (depolarizing muscle relaxants and volatile anesthetics). The eventual result is an extreme hypermetabolic state, leading to respiratory and metabolic acidosis and death is not treated.
question
How do you recognize and treat Malignant Hyperthermia?
answer
Identifying individuals at risk, through a thorough history (and family history) of previous anesthetics is necessary. 70% of MH-susceptible patients have increases of resting concentrations of creatine kinase. The definitive diagnosis of susceptibility to MH requires skeletal muscle biopsy and in vitro isometric contracture testing in the presence of caffeine or halothane, or both. The earliest clinical signs of MH include unexplained sustained elevation in ETCO2, and tachycardia. Arterial hypoxemia, metabolic (due to lactic acidosis) and respiratory acidosis are followed by an eventual profound increase in body temperature (late finding). Treatment includes: initiating the emergency plan/activating EMS, stopping the triggering agent and changing the anesthesia circuit, hyperventilating with 100% O2, administering 2.5mg/kg Dantrolene Sodium IVP and repeat every 10-15 minutes as needed (up to 10mg/kg), initiate active cooling (cold IV saline, gastric lavage with cold saline, surface cooling), Sodium bicarbonate 1-2mEq/kg IV as guided by arterial pH, induce diuresis (hydration, mannitol, lasix), and monitor electrolytes (treat hyperkalemia with insulin and glucose). The patient must be transported to and managed in an ICU setting at the appropriate time.
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