Phenylephrine: Difference between revisions
ClaireLewis (talk | contribs) |
ClaireLewis (talk | contribs) No edit summary |
||
(9 intermediate revisions by 6 users not shown) | |||
Line 2: | Line 2: | ||
*Type: [[Vasopressors]] | *Type: [[Vasopressors]] | ||
*Dosage Forms: | *Dosage Forms: | ||
*Common Trade Names: | *Common Trade Names: Neosynephrine | ||
==Adult Dosing== | ==Adult Dosing== | ||
=== | ===Hypotension=== | ||
*Start 100- | *Start 100-200 mcg/min then taper down | ||
**40- | **40-60 mcg/min works for most | ||
*"[[Push dose pressors|Push dose]]" | |||
**Inject 1ml (10mg) into 100ml NS Bag = 100mcg/ml | |||
**Draw this into a syringe, each ml is 100mcg | |||
**Give in 0.5-2ml (50-200mcg) alloquots q2-5min | |||
===Low Flow [[Priapism]]=== | |||
*Dilute phenylephrine 1mg in 9mL NS for final concentration of 100mcg/mL | |||
**For 500 mcg/ml, take 0.5 ml of 10mg/ml phenylephrine, and dilute in 9.5 cc NS | |||
*Inject base of penis with 29-Ga needle (after blood aspiration to confirm position) | |||
**100-500 mcg every 3-5min (max 1000 mcg) until resolution or 1 hour | |||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
*Hypotension/Shock | |||
**IV Bolus: 5-20mcg/kg q10-15min prn, 1st dose should not exceed 500mcg with a max dose of 1000mcg | |||
**IV Infusion: 0.1-0.5mcg/kg/min, titrate to desired BP | |||
*Nasal Congestion (OTC) | |||
**4-<6yrs: 2.5mg q4hr prn for <7 days | |||
**6-<12yrs: 5mg q4hr prn for <7 days | |||
==Special Populations== | ==Special Populations== | ||
Line 23: | Line 40: | ||
==Contraindications== | ==Contraindications== | ||
*Allergy to class/drug | *Allergy to class/drug | ||
*Severe hypertension | |||
*Ventricular tachycardia | |||
*Closed angle glaucoma | |||
*Caution if: | |||
**Heart failure or cardiogenic shock (cardiac output may decrease with increased SVR) | |||
**Spinal cord injury or other autonomic dysfunction (may experience exaggerated increase in blood pressure) | |||
**Hyperthyroidism | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
*Baroreceptor-mediated reflex bradycardia | *Baroreceptor-mediated reflex bradycardia, particularly in patients with preexisting cardiac dysfunction or severe CAD | ||
*If extravasates use phentolamine | *If extravasates use phentolamine | ||
===Serious=== | ===Serious=== | ||
*Bradycardia | |||
*pulmonary edema | |||
*Metabolic acidosis | |||
*Decreased renal perfusion | |||
*Extravasation | |||
===Common=== | ===Common=== | ||
*Hypertension | |||
*Anxiety | |||
*Headache | |||
*Rebound congestion, sneezing | |||
*Nausea, gastric irritation | |||
==Pharmacology== | ==Pharmacology== | ||
*Half-life: | *Half-life: 2-3h | ||
*Metabolism: | *Metabolism: extensively in intestinal wall, moderately in liver | ||
*Excretion: | *Excretion: Urinary | ||
*Mechanism of Action: | *Mechanism of Action: selective α<sub>1</sub> agonist causes vasoconstriction | ||
===Primary Receptor=== | ===Primary Receptor=== | ||
* | *α<sub>1</sub> | ||
===Relative Effects=== | ===Relative Effects=== | ||
*↑SVR | *↑SVR | ||
Line 45: | Line 78: | ||
==Notes== | ==Notes== | ||
*Use with caution in patients with spinal cord injury-related bradycardia | *Use with caution in patients with spinal cord injury-related bradycardia | ||
*Useful for treatment of vasodilatory shock when norepinephrine or dopamine have precipitated tachyarrhythmias | *Useful for treatment of vasodilatory shock when norepinephrine or [[dopamine]] have precipitated tachyarrhythmias | ||
*In patients with ↓LV function, unopposed | *In patients with ↓LV function, unopposed α<sub>1</sub> may lead to decreased CO or myocardial ischemia | ||
**However clinical trials do not support these effects when used in clinically appropriate dose range | **However clinical trials do not support these effects when used in clinically appropriate dose range | ||
===Indication=== | ===Indication=== | ||
*Neurogenic Shock | *Neurogenic Shock | ||
*Second line agent for septic shock | |||
==See Also== | ==See Also== | ||
http://www.atsjournals.org/doi/abs/10.1164/rccm.201006-0972CI?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dpubmed#readcube-epdf | |||
==References== | ==References== | ||
<references/> | |||
[[Category:Pharmacology]] [[Category:Critical Care]] | |||
[[Category:Pharmacology]] |
Revision as of 21:39, 23 September 2019
General
- Type: Vasopressors
- Dosage Forms:
- Common Trade Names: Neosynephrine
Adult Dosing
Hypotension
- Start 100-200 mcg/min then taper down
- 40-60 mcg/min works for most
- "Push dose"
- Inject 1ml (10mg) into 100ml NS Bag = 100mcg/ml
- Draw this into a syringe, each ml is 100mcg
- Give in 0.5-2ml (50-200mcg) alloquots q2-5min
Low Flow Priapism
- Dilute phenylephrine 1mg in 9mL NS for final concentration of 100mcg/mL
- For 500 mcg/ml, take 0.5 ml of 10mg/ml phenylephrine, and dilute in 9.5 cc NS
- Inject base of penis with 29-Ga needle (after blood aspiration to confirm position)
- 100-500 mcg every 3-5min (max 1000 mcg) until resolution or 1 hour
Pediatric Dosing
- Hypotension/Shock
- IV Bolus: 5-20mcg/kg q10-15min prn, 1st dose should not exceed 500mcg with a max dose of 1000mcg
- IV Infusion: 0.1-0.5mcg/kg/min, titrate to desired BP
- Nasal Congestion (OTC)
- 4-<6yrs: 2.5mg q4hr prn for <7 days
- 6-<12yrs: 5mg q4hr prn for <7 days
Special Populations
- Pregnancy Rating: C
- Lactation: infant risk cannot be ruled out
- Renal Dosing
- Adult
- Pediatric
- Hepatic Dosing
- Adult
- Pediatric
Contraindications
- Allergy to class/drug
- Severe hypertension
- Ventricular tachycardia
- Closed angle glaucoma
- Caution if:
- Heart failure or cardiogenic shock (cardiac output may decrease with increased SVR)
- Spinal cord injury or other autonomic dysfunction (may experience exaggerated increase in blood pressure)
- Hyperthyroidism
Adverse Reactions
- Baroreceptor-mediated reflex bradycardia, particularly in patients with preexisting cardiac dysfunction or severe CAD
- If extravasates use phentolamine
Serious
- Bradycardia
- pulmonary edema
- Metabolic acidosis
- Decreased renal perfusion
- Extravasation
Common
- Hypertension
- Anxiety
- Headache
- Rebound congestion, sneezing
- Nausea, gastric irritation
Pharmacology
- Half-life: 2-3h
- Metabolism: extensively in intestinal wall, moderately in liver
- Excretion: Urinary
- Mechanism of Action: selective α1 agonist causes vasoconstriction
Primary Receptor
- α1
Relative Effects
- ↑SVR
- ↓HR (reflex bradycardia)
Notes
- Use with caution in patients with spinal cord injury-related bradycardia
- Useful for treatment of vasodilatory shock when norepinephrine or dopamine have precipitated tachyarrhythmias
- In patients with ↓LV function, unopposed α1 may lead to decreased CO or myocardial ischemia
- However clinical trials do not support these effects when used in clinically appropriate dose range
Indication
- Neurogenic Shock
- Second line agent for septic shock