Rosen & Barkin's 5-Minute Emergency Medicine Consult (60 page)

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Authors: Jeffrey J. Schaider,Adam Z. Barkin,Roger M. Barkin,Philip Shayne,Richard E. Wolfe,Stephen R. Hayden,Peter Rosen

Tags: #Medical, #Emergency Medicine

BOOK: Rosen & Barkin's 5-Minute Emergency Medicine Consult
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ETIOLOGY
  • Many drugs contain anticholinergic properties:
    • Mild at therapeutic doses
    • Life threatening in overdose
  • Anticholinergic substances:
    • Antihistamines
    • Belladonna alkaloids and synthetic congeners
    • Antiparkinsonian drugs
    • Cyclic antidepressants
    • Antipsychotics (neuroleptics)
    • Mydriatics
    • Skeletal muscle relaxants (orphenadrine, cyclobenzaprine)
    • Antispasmodics
    • Mushrooms—
      Amanita muscaria, Amanita pantherina
    • Plants—deadly nightshade, mandrake, henbane
    • Jimson weed—smoked or ingested
DIAGNOSIS
SIGNS AND SYMPTOMS
History
  • Onset and duration of symptoms
  • Type and extent of ingestion/exposure
Physical-Exam
  • Classic toxidrome:

    • Mad as a hatter”

      altered mental status

    • Hot as a hare”
      —hyperthermia

    • Red as a beet”
      —flushed skin

    • Dry as a bone”
      —dry skin and mucous membranes

    • Blind as a bat”
      —blurred vision secondary to mydriasis
  • General:
    • Hyperthermia
    • Altered mental status
  • Ocular:
    • Unreactive mydriasis
    • Inability to accommodate
  • Cardiovascular:
    • Sinus tachycardia
    • Dysrhythmias (rare except in massive ingestions)
    • Hypotension/HTN
    • Cardiogenic pulmonary edema
  • Pulmonary:
    • Tachypnea
    • Respiratory failure
  • GI:
    • Decreased/absent bowel sounds
    • Dysphagia
    • Decreased GI motility
    • Decreased salivation
  • Genitourinary (GU):
    • Urinary retention
  • Integument:
    • Decreased sweating
    • Flushed skin
    • Dry skin and mucous membranes
  • CNS:
    • Altered mental status
    • Auditory or visual hallucinations
    • Coma
    • Seizures
ESSENTIAL WORKUP

Diagnosis based on clinical presentation and an accurate history

DIAGNOSIS TESTS & NTERPRETATION
Lab
  • Urine toxicologic screen if clinically indicated
  • Electrolytes, BUN, creatinine, and glucose
  • CBC
  • Creatine phosphokinase (CPK) if suspected rhabdomyolysis
  • Urinalysis
  • Acetaminophen and salicylate levels:
    • Detects occult ingestion (e.g., Tylenol PM)
Imaging

ECG:

  • Sinus tachycardia most common
  • QRS prolongation
  • AV blockade
  • Bundle branch block pattern
  • Dysrhythmias
DIFFERENTIAL DIAGNOSIS
  • Sympathomimetic intoxication
  • Withdrawal syndrome
  • Acute psychiatric disorders
  • Sepsis
  • Thyroid disorder
TREATMENT
PRE HOSPITAL

Transport all pills/pill bottles involved in overdose for identification in ED.

INITIAL STABILIZATION/THERAPY
  • Airway, breathing, and circulation (ABCs):
    • Airway control essential
    • Administer supplemental oxygen.
    • IV access
    • Cardiac monitor and pulse oximetry
  • Naloxone, thiamine, D
    50
    (or Accu-Chek) if altered mental status
ED TREATMENT/PROCEDURES
  • Supportive care:
    • IV rehydration with 0.9% NS
    • Standard aggressive cooling measures for hyperthermia
    • Use benzodiazepines for treatment of agitation:
      • Avoid phenothiazines owing to anticholinergic effects.
    • Treat seizures with benzodiazepines and barbiturates.
    • Dysrhythmias:
      • Use standard antidysrhythmics.
      • Avoid class Ia antidysrhythmic owing to the quinidine-like effect of many anticholinergic drugs.
      • Sodium bicarbonate boluses may reverse the quinidine-like effects.
  • Decontamination:
    • Administer activated charcoal for oral ingestions if within 1 hr.
    • Ocular lavage for eyedrop exposure
  • Physostigmine (Antilirium):
    • Reversible acetylcholinesterase inhibitor that crosses the blood–brain barrier
    • Short-term reversal of both central and peripheral anticholinergic effects
    • Indicated in the presence of peripheral anticholinergic signs and the following:
      • Seizures unresponsive to conventional therapy
      • Uncontrollable agitation
    • Use with caution if prolonged QRS is present on ECG owing to risk of dysrhythmias (especially asystole), seizures, and cholinergic crises:
      • Place on cardiac monitor.
      • Observe for cholinergic symptoms.
    • Contraindications:
      • Cyclic antidepressant overdose (potentiates toxicity)
      • Cardiovascular disease
      • Asthma/bronchospasm
      • Intestinal obstruction
      • Heart block
      • Peripheral vascular disease
      • Bladder obstruction
MEDICATION
  • Activated charcoal: 1 g/kg PO
  • Dextrose: 50–100 mL D
    50
    (peds: 2 mL/kg of D
    25
    over 1 min) IV; repeat if necessary
  • Diazepam: 5–10 mg (peds: 0.2–0.5 mg/kg) IV every 10–15 min
  • Dopamine: 2–20 μg/kg/min IV with titration to effect
  • Lorazepam: 2–4 mg (peds: 0.03–0.05 mg/kg) IV every 10–15 min
  • Physostigmine: 0.5–2.0 mg (peds: 0.02 mg/kg) IV over 5 min; repeat if necessary in 30–60 min
  • Phenobarbital: 10–20 mg/kg IV (loading dose); monitor for respiratory depression
  • Thiamine (vitamin B
    1
    ): 100 mg (peds: 50 mg) IV or IM
First Line

Lorazepam or Diazepam

Second Line

Physostigmine (use with caution and consult with medical toxicologist)

FOLLOW-UP
DISPOSITION
Admission Criteria
  • ICU admission for moderate to severe anticholinergic symptoms (agitation control, temperature control, and observation for seizures or dysrhythmias)
  • Any patient receiving physostigmine
Discharge Criteria

Mild and improving symptoms of anticholinergic toxicity after 6–8 hr of ED observation

Issues for Referral
  • Substance abuse referral for patients with recreational anticholinergic abuse
  • Patients with unintentional (accidental) poisoning require poison prevention counseling.
  • Patients with intentional (e.g., suicide) poisoning require psychiatric evaluation.
FOLLOW-UP RECOMMENDATIONS

Appropriate psychiatric referral for intentional ingestions

PEARLS AND PITFALLS
  • Aggressively treat hyperthermia.
  • Antipyretic medications are not effective in toxic hyperthermia.
  • Use physostigmine cautiously and consult with medical toxicologist when available.
ADDITIONAL READING
  • Burns MJ, Linden CH, Graudins A, et al. A comparison of physostigmine and benzodiazepines for the treatment of anticholinergic poisoning.
    Ann Emerg Med
    . 2000;35:374–381.
  • Ceha LJ, Presperin C, Young E, et al. Anticholinergic toxicity from nightshade berry poisoning responsive to physostigmine.
    J Emerg Med
    . 1997;15:65–69.
  • Delaney KA. Anticholinergics and antihistamines (H1 antagonists). In: Ford MD, Delaney KA, Ling LJ, et al., eds.
    Clinical Toxicology
    . Philadelphia, PA: WB Saunders; 2001;472–477.
  • Hidalgo HA, Mowers RM. Anticholinergic drug abuse.
    Ann Pharmacother
    . 1990;24:40.
  • Patel RJ, Saylor T, Williams SR, et al. Prevalence of autonomic signs and symptoms in antimuscarinic drug poisonings.
    J Emerg Med
    . 2004;26(1):89–94.
  • Reilly KM, Chan L, Mehta NJ, et al. Systemic toxicity from ocular homatropine.
    Acad Emerg Med
    . 1996;3:868–871.
CODES
ICD9

971.1 Poisoning by parasympatholytics (anticholinergics and antimuscarinics) and spasmolytics

ICD10

T44.3X1A Poisoning by oth parasympath and spasmolytics, acc, init

ANTIDEPRESSANT POISONING
Patrick M. Lank
BASICS

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