Electronic cigarettes: Difference between revisions

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==Treatment==
==Treatment==
{{Anticholinergic Toxicity}}
{{Anticholinergic Toxicity Treatement}}


==Disposition==
==Disposition==

Revision as of 19:04, 11 June 2014

Background

  • Nicotine containing products that are currently not regulated by the FDA
  • On 4/25/14, the FDA proposed legislation to allow them to regulate e-cigarettes like other tobacco products
  • Nicotine usually suspended in a propylene glycol or vegetable glycerin solution (labeled as %PG/%VG)[1]
  • Increasing toxic exposure to e-cigarettes
  • From Sept 2010 - Feb 2014, there were 16,248 toxic exposures to traditional cigarettes and 2,405 toxic exposures to e-cigarettes[2]
  • Exposures to e-cigarettes increased from 1/month to 215/month over that time period

Product Types

    • Some are fixed products with no refill capabilities (Ex. Blu e-cigarettes) while others can be refilled with replacement nicotine fluid
  • Common strengths include 6mg/ml (low), 12mg/ml (medium-low), 18mg/ml (medium), 24mg/ml (high) and 36mg/ml (Ultra-high)
  • Common refill sizes range from 5ml to 30ml
  • Products come in a variety of flavors that can be enticing to children
  • Bubble gum, root beer, extreme soda, Ecto-cooler, Banana cream pie, toasted marshmallow, etc.

Pathophysiology

  • Fatal intoxications are rare and estimates suggest 60mg as a lethal dose. Traditional cigarettes deliver approximately 2mg of icotine [3]

Absorption

    • Absorbed transdermally, orally and via inhalation

Biphasic presentation

    • Initially excitation secondary to excitation of the presynaptic nAChR which facilitates release of neurotransmitters
    • Second phase characterized by desensitization of the receptors and decreased neurotransmitter release

Clinical Features

  • Highly variable presentation
    • Tobacco is a GI irritant and often causes spontaneous vomiting
    • Biphasic presentation
      • Initially present with excitation, N/V/D, salivation, tachycardia, hypertension, diaphoresis
      • Delayed presentation is hypotension, bradycardia, hypoventilation, fasiculations, seizures, coma, death

Diagnosis

  • Exposure to nicotine containing liquid
  • Toxidrome similar to nicotinism

Work-Up

  • CBC
  • Chem 7
  • Utox

DDx

  • Anticholinergic toxicity

Treatment

Treatment

  • Consider GI decon with Activated Charcoal if patient presents <2 hours after ingestion and remains cooperative

Sedation

  • Decreases the risk of hyperthermia, rhabdo, traumatic injuries
  • Benzos are agents of choice especially increase seizure threshold[4]
    • Repeat boluses every 5-15 minutes as needed to halt seizures and provide adequate sedation
    • Goal: QRS duration < 110 msec

Cholinesterase inhibition

  • Indicated for severe agitation or delirium (esp if unresponsive to benzos)
  • Contraindicated in QRS>100 or Na blockade signs (R' in aVR) and in narrow angle glaucoma
  • Relatively contraindicated in asthma or ileus
  • Physostigmine - strongly consider poison control consult before giving
    • Crosses blood brain barrier, can be used to help make dx
    • Dosing: 0.5mg-1mg IV over 5min (repeat dosing up to 2mg in first hour)[5]
    • Onset of action: 5-10min
    • If partial response, repeat x3
    • If 3 or more administrations are needed over a 6-hour period, start IV infusion (bolus 1-2 mg followed by 1 mg/hour)
    • Stop infusion every 12 hours to determine resolution of the toxidrome
    • Side effects: bradycardia, dysrhythmias, cholinergic excess[6]
    • Always have atropine at the bedside for bradycardia or cholinergic excess</ref>[7]
    • Contraindicated in TCA toxicity (associated with cardiac arrest) and in the presence of bradycardia or AV block

Other therapies

  • Sodium bicarbonate for conduction abnormalities (QRS prolongation)
    • 2 mEq/kg bolus (typically 2-3 amps of bicarb)
    • Begin continuous NaCO3 infusion at 250mL/hr if bolus effective
    • Solution preparation = 1L D5W mixed with 3 ampules NaHCO3

Disposition

  • Admit for symptomatic poisonings

See Also

Source

  1. Carmines EL, Gaworski CL. Toxicological evaluation of glycerin as a cigarette ingredient. Food Chem Toxicol. 2005 Oct;43(10):1521-39
  2. CDC reports. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6313a4.htm
  3. Mayer B. How much nicotine kills a human? Tracing back the generally accepted lethal dose to dubious self-experiments in the nineteenth century. Arch Toxicol. 2014; 88: 5–7
  4. Burns MJ, et al. A comparison of physostigmine and benzodiazepines for the treatment of anticholinergic poisoning. Ann Emerg Med. 2000:35(4):374-381.
  5. Rosenbaum C and Bird SB. Timing and frequency for physostigmine redosing for antimuscarininc toxicity. J Med Toxicol. 2010;6:386-92.
  6. Pentel P and Peterson CD. Aystole complicating physostigmine treatment of tricyclic antidepressant overdose. Ann Emerg Med. 1980 Nov;9(11):588-90.
  7. Nguyen TT, et al. Adverse events from physostigmine: an observational study. Am J Emerg Med. 2018;36:141-2.