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Poisoning is contact with a substance that results in toxicity. Symptoms vary, but certain common syndromes may suggest particular classes of poisons. Diagnosis is primarily clinical, but for some poisonings, blood and urine tests can help. Treatment is supportive for most poisonings; specific antidotes are necessary for a few. Prevention includes labeling drug containers clearly and keeping poisons out of the reach of children.
Most poisonings are dose-related. Dose is determined by concentration over time. Toxicity may result from exposure to excess amounts of normally nontoxic substances. Some poisonings result from exposure to substances that are poisonous at all doses. Poisoning is distinguished from hypersensitivity and idiosyncratic reactions, which are unpredictable and not dose-related, and from intolerance, which is a toxic reaction to a usually nontoxic dose of a substance.
Poisoning is commonly due to ingestion but can result from injection, inhalation, or exposure of body surfaces (eg, skin, eye, mucous membranes). Many commonly ingested nonfood substances are generally nontoxic (see Table 1: Poisoning: Substances Usually Not Dangerous When Ingested* ); however, almost any substance can be toxic if ingested in excessive amounts.
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Table 1
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| Substances Usually Not Dangerous When Ingested* |
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Adhesives
Antibiotics, topical
Antifungals, topical
Barium sulfate
Bathtub toys (floating)
Blackboard chalk (Ca carbonate)
Bleach, hypochlorite (Na hypochlorite concentration < 6% and Na hydroxide concentration < 0.5%)
Candles (insect-repellent type may be toxic)
Carbowax (polyethylene glycol)
Carboxymethylcellulose (dehydrating material packed with drugs, film, and other products)
Castor oil
Cetyl alcohol
Cigarettes (small amounts ingested by a child)
Clay, art and craft
Contraceptives
Corticosteroids, topical
Crayons (children's; marked A.P., C.P., or C.S. 130–46)
Detergent, dishwashing, liquid
Dichloral (herbicide)
Diaper rash cream and ointment
Dry cell battery (alkaline)
Fabric softeners, solid sheets
Glow products (eg, glow sticks, glow necklaces)
Glycerol
Glyceryl monostearate
Graphite
Gums (eg, acacia, agar, ghatti)
Ink (amount in one ballpoint pen)
Iodide salts
Kaolin
Lanolin
Linoleic acid
Linseed oil (not boiled)
Lipstick
Lotion, calamine (excluding products with antihistamines or local anesthetics)
Lozenges, throat (without local anesthetics)
Magnesium silicate (antacid)
Make-up
Matches
Methylcellulose
Mineral oil (if not aspirated)
Newspaper
Paint, water-color or water-based
Paraffin, chlorinated
Pencil lead (graphite)
Perfumes and colognes
Petrolatum jelly
Plant food (household)
Polyethylene glycols
Polyethylene glycol stearate
Polysorbate
Putty
Shaving cream
Silica (silicon dioxide)
Soap (bath or dishwashing)
Spermaceti
Starch and sizing
Stearic acid
Talc (except when inhaled)
Titanium dioxide
Toothpaste (with or without fluoride)
Triacetin (glyceryl triacetate)
Vitamins, children's multiple with or without iron
Vitamins, multiple without iron
Zinc oxide
Zirconium oxide
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*This table is intended only as a guide. Substances may be combined with phenol, petroleum distillate vehicles, or other toxic chemicals. A poison control center should be consulted for up-to-date information. Almost any substance can be toxic if ingested in sufficient amounts.
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Accidental poisoning is common among young children, who are curious and ingest items indiscriminately despite noxious tastes and odors; usually, only a single substance is involved. Poisoning is also common among older children, adolescents, and adults attempting suicide; multiple drugs, including alcohol, acetaminophen, and other OTC drugs, may be involved. Accidental poisoning may occur in the elderly because of confusion, poor eyesight, mental impairment, or multiple prescriptions of the same drug by different physicians.
Occasionally, people are poisoned by someone who intends to kill or disable them (eg, to rape or rob them). Drugs used to disable (eg, scopolamine, benzodiazepines, γ-hydroxybutyrate) tend to have sedative or amnestic properties or both. Rarely, parents, who may have some medical knowledge, poison their children because of unclear psychiatric reasons or a desire to cause illness and thus gain medical attention (a disorder called Munchausen syndrome by proxy—see Somatoform and Factitious Disorders: Munchausen Syndrome by Proxy).
After exposure or ingestion and absorption, most poisons are metabolized, pass through the GI tract, or are excreted. Occasionally, tablets (eg, aspirin, iron, enteric-coated drugs) form large concretions (bezoars) in the GI tract, where they tend to remain, continuing to be absorbed and causing toxicity.
Symptoms and Signs
Symptoms and signs vary depending on the substance (see Table 8: Poisoning: Symptoms and Treatment of Specific Poisons ). Also, different patients poisoned with the same substance may present with very different symptoms. However, 6 clusters of symptoms (toxic syndromes, or toxidromes) occur commonly and may suggest particular classes of substances (see Table 2: Poisoning: Common Toxic Syndromes (Toxidromes)). Patients who ingest multiple substances are less likely to have symptoms characteristic of a single substance.
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Table 2
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| Common Toxic Syndromes (Toxidromes) |
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Syndrome
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Symptoms
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Common Causes
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Anticholinergic
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Tachycardia, hyperthermia, mydriasis, warm and dry skin, urinary retention, ileus, delirium (“mad as a hatter, blind as a bat, red as a beet, hot as a hare, and dry as a bone”*)
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Antihistamines
Atropine
Belladonna alkaloids
Jimson weed
Mushrooms (some)
Psychoactive drugs (many)
Scopolamine
Tricyclic antidepressants
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Cholinergic, muscarinic
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Salivation, lacrimation, urination, defecation, GI cramps, emesis (mnemonic device: SLUDGE)
or
Diarrhea; urination; miosis; bronchorrhea, bradycardia, and bronchoconstriction; emesis; lacrimation; and salivation (mnemonic device: DUMBELS)
Wheezing
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Carbamates
Mushrooms (some)
Organophosphates
Physostigmine
Pilocarpine
Pyridostigmine
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Cholinergic, nicotinic
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Mydriasis, tachycardia, weakness, hypertension and hyperglycemia, fasciculations, sweating (mnemonic device: MTWT[h]FS)
Abdominal pain, paresis
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Black widow spider bites
Carbamates
Nicotine
Organophosphates (some)
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Opioid
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Hypoventilation, hypotension, miosis, sedation, possibly hypothermia
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Opioids (eg, diphenoxylate, fentanyl, heroin, methadone, morphine, pentazocine, propoxyphene)
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Sympathomimetic
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Tachycardia, hypertension, mydriasis, agitation, seizures, diaphoresis, hyperthermia, psychosis (after chronic use)
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Amphetamines
Caffeine
Cocaine
Ephedrine
Herbal and synthetic marijuana and common substitutes
MDMA (Ecstasy)
Phenylpropanolamine
Theophylline
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Withdrawal
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Tachycardia, hypertension, mydriasis, diaphoresis, agitation, restlessness, seizures, hyperreflexia, piloerection, yawning, abdominal cramps, lacrimation, hallucinations
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Withdrawal from any of the following:
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*From Carroll L: Alice's Adventures in Wonderland. London, MacMillan & Co., 1865.
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MDMA = methylenedioxymethamphetamine.
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Symptoms typically begin soon after contact but, with certain poisons, are delayed. The delay may occur because only a metabolite is toxic rather than the parent substance (eg, methanol, ethylene glycol, hepatotoxins). Ingestion of hepatotoxins (eg, acetaminophen, iron, Amanita phalloides mushrooms) may cause acute liver failure that occurs one to a few days later. With metals or hydrocarbon solvents, symptoms typically occur only after chronic exposure to the toxin.
Ingested and absorbed toxins generally cause systemic symptoms. Caustics and corrosive liquids damage mainly the mucous membranes of the GI tract, causing stomatitis, enteritis, or perforation. Some toxins (eg, alcohol, hydrocarbons) cause characteristic breath odors. Skin contact with toxins can cause various acute cutaneous symptoms (eg, rashes, pain, blistering); chronic exposure may cause dermatitis. Inhaled toxins are likely to cause symptoms of upper airway injury if they are water-soluble (eg, chlorine, ammonia) and symptoms of lower airway injury and noncardiogenic pulmonary edema if they are less water-soluble (eg, phosgene). Inhalation of carbon monoxide, cyanide, or hydrogen sulfide gas can cause organ ischemia or cardiac or respiratory arrest. Eye contact with toxins (solid, liquid, or vapor) may damage the cornea, sclera, and lens, causing eye pain, redness, and loss of vision.
Some substances (eg, cocaine, phencyclidine, amphetamine) can cause severe agitation, which can result in hyperthermia, acidosis, and rhabdomyolysis.
Diagnosis
The first step of diagnosis is to assess the overall status of the patient. Severe poisoning may require rapid intervention to treat airway compromise or cardiopulmonary collapse.
Poisoning may be known at presentation. It should be suspected if patients have unexplained symptoms, especially altered consciousness (which can range from agitation to somnolence to coma). If purposeful self-poisoning occurs in adults, multiple substances should be suspected.
History is often the most valuable tool. Because many patients (eg, preverbal children, suicidal or psychotic adults, patients with altered consciousness) cannot provide reliable information, friends, relatives, and rescue personnel should be questioned. Even seemingly reliable patients may incorrectly report the amount or time of ingestion. When possible, the patient's living quarters should be inspected for clues (eg, partially empty pill containers, a suicide note, evidence of recreational drug use). Pharmacy and medical records may provide useful information. In potential workplace poisonings, coworkers and supervisors should be questioned. All industrial chemicals must have a material safety data sheet (MSDS) readily available at the workplace; the MSDS provides detailed information about toxicity and any specific treatment.
In many parts of the world, information about household and industrial chemicals can be obtained from poison control centers. Consultation with the centers is encouraged because ingredients, first-aid measures, and antidotes printed on product containers are occasionally inaccurate or outdated. Also, the container may have been replaced, or the package may have been tampered with. Poison control centers may be able to help identify unknown pills based on their appearance. The centers have ready access to toxicologists. The telephone number of the nearest center is often listed with other emergency numbers in the front of the local telephone book; the number is also available from the telephone operator or, in the US, by dialing 1-800-222-1222. More information is available at the American Association of Poison Control Centers web site (www.aapcc.org).
Physical examination sometimes detects signs suggesting particular types of substances (eg, toxidromes, breath odor, needle tracks suggesting IV drug use, stigmata of chronic alcohol use).
Even if a patient is known to be poisoned, altered consciousness may be due to other causes (eg, CNS infection, head trauma, hypoglycemia, stroke, hepatic encephalopathy, Wernicke encephalopathy), which should also be considered. Attempted suicide must always be considered in older children, adolescents, and adults who have ingested a drug. After such patients are stabilized, psychiatric intervention should be considered.
Testing:
In most cases, laboratory testing provides limited help. Standard, readily available tests to identify common drugs of abuse (often called toxic screens) are qualitative, not quantitative. These tests may provide false-positive or false-negative results and they check for only a limited number of substances. Also, the presence of a drug of abuse does not necessarily indicate that the drug caused the patient's symptoms or signs. Urine drug screening is used most often but has limited value and usually detects classes of drugs or metabolites rather than specific drugs. For example, an opioid urine immunoassay test does not detect fentanyl or methadone but does react with very small amounts of morphine or codeine analogues. The test used to identify cocaine detects a metabolite rather than cocaine itself.
For most substances, blood levels cannot be easily determined or do not help guide treatment. For a few substances (eg, acetaminophen, aspirin, carbon monoxide, digoxin, ethylene glycol, iron, lithium, methanol, phenobarbital, phenytoin, theophylline), blood levels may help guide treatment. Many authorities recommend measuring acetaminophen levels in all patients with mixed ingestions because acetaminophen ingestion is common, is often asymptomatic during the early stages, and can cause serious delayed toxicity that can be prevented by an antidote. For some substances, other blood tests (eg, PT for warfarin overdose, methemoglobin levels for certain substances) help guide treatment. For patients who have altered consciousness or abnormal vital signs or who have ingested certain substances, tests should include serum electrolytes, BUN, creatinine, serum osmolality, glucose, coagulation studies, and ABGs. Other tests (eg, methemoglobin level, carbon monoxide level, brain CT) may be indicated for certain suspected poisons or in certain clinical situations.
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Table 3
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| Common Specific Antidotes |
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Toxin
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Antidote
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Acetaminophen
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N-Acetylcysteine
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Anticholinergics
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Physostigmine*
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Benzodiazepines
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Flumazenil*
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Black widow spider bite
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Lactrodectus antivenom
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Botulism
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Botulinum antitoxin
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β-Blockers
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Glucagon
IV fat emulsion
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Ca channel blockers
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Ca
IV insulin in high doses with IV glucose
IV fat emulsion
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Carbamates
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Atropine
Pralidoxime chloride
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Crotaline snake bites (US)
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Crotalinae polyvalent immune Fab (ovine)
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Cyanide
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Hydroxocobalamin
Cyanide antidote kit (includes amyl nitrate, Na nitrite, and Na thiosulfate)
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Digitalis glycosides (eg, digoxin, digitoxin, oleander, foxglove)
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Digoxin-specific Fab fragments
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Ethylene glycol
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Fomepizole
Ethanol
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Heavy metals
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Chelating drugs (see Table 4: Poisoning: Guidelines for Chelation Therapy)
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Iron
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Deferoxamine
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Isoniazid
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Pyridoxine (vitamin B6)
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Methanol
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Fomepizole
Ethanol
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Methemoglobin-forming agents (eg, aniline dyes, some local anesthetics, nitrates, nitrites, phenacetin, sulfonamides)
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Methylene blue
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Methotrexate
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Leucovorin (folinic acid)
Glucarpidase (carboxypeptidase-G2)
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Opioids
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Naloxone
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Organophosphates
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Atropine
Pralidoxime
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Scorpion envenomation (Centruroides sp)
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Centruroides immune F(ab')2
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Sulfonylurea
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Octreotide
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Thallium
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Prussian blue
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Tricyclic antidepressants
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NaHCO3
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Unfractionated heparin
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Protamine
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Warfarin
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Vitamin K
Fresh frozen plasma
Prothrombin complex concentrate (PCC)
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*Use is controversial.
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Fab = fractionated antibodies.
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For certain poisonings (eg, due to iron, lead, arsenic, other metals, or to packets of cocaine or other illicit drugs ingested by so-called body packers), plain abdominal x-rays may show the presence and location of ingested substances.
For poisonings with drugs that have cardiovascular effects or with an unknown substance, ECG and cardiac monitoring are indicated.
If blood levels of a substance or symptoms of toxicity increase after initially decreasing or persist for an unusually long time, a bezoar, a sustained-release preparation, or reexposure (ie, repeated covert exposure to a recreationally used drug) should be suspected.
Treatment
Seriously poisoned patients may require assisted ventilation or treatment of cardiovascular collapse. Patients with impaired consciousness may require continuous monitoring or restraints. The discussion of treatment for specific poisonings, below and in Table 3: Poisoning: Common Specific Antidotes, Table 4: Poisoning: Guidelines for Chelation Therapy, and Table 8: Poisoning: Symptoms and Treatment of Specific Poisons , is general and does not include specific complexities and details. Consultation with a poison control center is recommended for any poisonings except the mildest and most routine.
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Table 4
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| Guidelines for Chelation Therapy |
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Chelating Drug*
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Metal
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Dosage†
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Deferoxamine
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Iron
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See Poisoning: Treatment
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Dimercaprol, 10% in oil
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Antimony
Arsenic
Bismuth
Copper salts
Gold
Lead
Mercury
Thallium*
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3–4 mg/kg via deep IM injection q 4 h on day 1, 2 mg/kg IM q 4 h on day 2, 3 mg/kg IM q 6 h on day 3, then 3 mg/kg IM q 12 h for 7–10 days until recovery
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Edetate Ca disodium (Ca disodium edathamil) diluted to ≤ 3%
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Cobalt
Lead
Zinc
Zinc salts
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25–35 mg/kg via deep IM injection or IV slowly (over 1 h) q 12 h for 5–7 days, followed by 7 days without the drug; then repeated
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Penicillamine
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Arsenic
Copper salts
Gold
Lead
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5–7.5 mg/kg po qid (usual starting dose is 250 mg qid) to a maximum adult dose of 2 g/day
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Succimer
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Arsenic (occupational exposure in adults)
Cadmium salts
Lead if children have blood lead levels > 45 μg/dL (> 2.15 μmol/L)
Lead (occupational exposure in adults)
Mercury (occupational exposure in adults)
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10 mg/kg po q 8 h for 5 days, then 10 mg/kg po q 12 h for 14 days
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*Thallium salts are chelated with varying success by this drug (see thallium salts in Table 8: Poisoning: Symptoms and Treatment of Specific Poisons ).
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†Dosages depend on type and severity of poisoning.
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Initial stabilization:
Treatment of any systemic poisoning begins with airway, breathing, and circulatory stabilization (see Cardiac Arrest: Cardiopulmonary Resuscitation (CPR) in Adults).
If patients have apnea or compromised airways (eg, foreign material in the oropharynx, decreased gag reflex), an endotracheal tube should be inserted. If patients have respiratory depression or hypoxia, supplemental O2 or mechanical ventilation should be provided as needed.
In patients with apnea, IV naloxone (2 mg in adults; 0.1 mg/kg in children) should be tried while airway support is maintained. In opioid addicts, naloxone may precipitate withdrawal, but withdrawal is preferable to apnea. If respiratory depression persists despite use of naloxone, endotracheal intubation and continuous mechanical ventilation are required. If naloxone relieves respiratory depression, patients are monitored; if respiratory depression recurs, patients should be treated with another bolus of IV naloxone or endotracheal intubation and mechanical ventilation. Using a low-dose continuous naloxone infusion to maintain respiratory drive without precipitating withdrawal has been suggested but in reality is very difficult to accomplish.
If patients have altered consciousness, blood glucose should be measured immediately at bedside, or IV dextrose (50 mL of a 50% solution for adults; 2 to 4 mL/kg of a 25% solution for children) should be given empirically. For adults with suspected thiamine deficiency (eg, alcoholics, undernourished patients), thiamine 100 mg IV is given with or before glucose.
Hypotension is treated with IV fluids. If fluids are ineffective, invasive hemodynamic monitoring may be necessary to guide fluid and vasopressor therapy. The first-choice vasopressor for most poison-induced hypotension is norepinephrine 0.5 to 1 mg/min IV infusion, but treatment should not be delayed if another vasopressor is more immediately available.
Topical decontamination:
Any body surface (including the eyes) exposed to a toxin is flushed with large amounts of water or saline. Contaminated clothing, including shoes and socks, and jewelry should be removed.
Activated charcoal:
Charcoal is usually given, particularly when multiple or unknown substances have been ingested. Use of charcoal adds little risk (unless patients are at risk of vomiting and aspiration) but has not been proved to reduce overall morbidity or mortality. When used, charcoal is given as soon as possible. Activated charcoal adsorbs most toxins because of its molecular configuration and large surface area. Multiple doses of activated charcoal may be effective for substances that undergo enterohepatic recirculation (eg, phenobarbital, theophylline) and for sustained-release preparations. Charcoal may be given at 4- to 6-h intervals for serious poisoning with such substances unless bowel sounds are hypoactive. Charcoal is ineffective for caustics, alcohols, and simple ions (eg, cyanide, iron, other metals, lithium). The recommended dose is 5 to 10 times that of the suspected toxin ingested. However, because the amount of toxin ingested is usually unknown, the usual dose is 1 to 2 g/kg, which is about 10 to 25 g for children < 5 yr and 50 to 100 g for older children and adults. Charcoal is given as a slurry in water or soft drinks. It may be unpalatable and results in vomiting in 30% of patients. Administration via a gastric tube may be considered, but caution should be used to prevent trauma caused by tube insertion or aspiration of charcoal; potential benefits must outweigh risks. Activated charcoal should probably be used without sorbitol or other cathartics, which have no clear benefit and can cause dehydration and electrolyte abnormalities.
Gastric emptying:
Gastric emptying, which used to be well-accepted and seems intuitively beneficial, should not be routinely done. It does not clearly reduce overall morbidity or mortality and has risks. Gastric emptying is considered if it can be done within 1 h of a life-threatening ingestion. However, many poisonings manifest too late, and whether a poisoning is life threatening is not always clear. Thus, gastric emptying is seldom indicated and, if a caustic substance has been ingested, is contraindicated (see Poisoning: Caustic Ingestion).
If gastric emptying is used, gastric lavage is the preferred method. Gastric lavage may cause complications such as epistaxis, aspiration, or, rarely, oropharyngeal or esophageal injury. Syrup of ipecac has unpredictable effects, often causes prolonged vomiting, and may not remove substantial amounts of poison from the stomach. Syrup of ipecac may be warranted if the ingested agent is highly toxic and transport time to the emergency department is unusually long, but this is uncommon in the US.
For gastric lavage, tap water is instilled and withdrawn from the stomach via a tube. The largest tube possible (usually > 36 French for adults or 24 French for children) is used so that tablet fragments can be retrieved. If patients have altered consciousness or a weak gag reflex, endotracheal intubation should be done before lavage to prevent aspiration. Patients are placed in the left lateral decubitus position to prevent aspiration, and the tube is inserted orally. Because lavage sometimes forces substances farther into the GI tract, stomach contents should be aspirated and a 25-g dose of charcoal should be instilled through the tube immediately after insertion. Then aliquots (about 3 mL/kg) of tap water are instilled, and the gastric contents are withdrawn by gravity or syringe. Lavage continues until the withdrawn fluids appear free of the substance; usually, 500 to 3000 mL of fluid must be instilled. After lavage, a 2nd 25-g dose of charcoal is instilled.
Whole-bowel irrigation:
This procedure flushes the GI tract and theoretically decreases GI transit time for pills and tablets. Irrigation has not been proved to reduce morbidity or mortality. Irrigation is indicated for any of the following:
A commercially prepared solution of polyethylene glycol (which is nonabsorbable) and electrolytes is given at a rate of 1 to 2 L/h for adults or at 25 to 40 mL/kg/h for children until the rectal effluent is clear; this process may require many hours or even days. The solution is usually given via a gastric tube, although some motivated patients can drink these large volumes.
Alkaline diuresis:
Alkaline diuresis enhances elimination of weak acids (eg, salicylates, phenobarbital). A solution made by combining 1 L of 5% D/W with 3 50-mEq ampules of NaHCO3 and 20 to 40 mEq of K can be given at a rate of 250 mL/h in adults and 2 to 3 mL/kg/h in children. Urine pH is kept at > 8, and K must be repleted. Hypernatremia, alkalemia, and fluid overload may occur but are usually not serious. However, alkaline diuresis is contraindicated in patients with renal insufficiency.
Dialysis:
Common toxins that may require dialysis or hemoperfusion include
These therapies are less useful if the poison is a large or charged (polar) molecule, has a large volume of distribution (ie, if it is stored in fatty tissue), or is extensively bound to tissue protein (as with digoxin, phencyclidine, phenothiazines, or tricyclic antidepressants). The need for dialysis is usually determined by both laboratory values and clinical status. Methods of dialysis include hemodialysis, peritoneal dialysis, and lipid dialysis (which removes lipid-soluble substances from the blood), as well as hemoperfusion (which more rapidly and efficiently clears specific poisons—see Renal Replacement Therapy).
Specific antidotes:
For the most commonly used antidotes, see Table 3: Poisoning: Common Specific Antidotes. Chelating drugs are used for poisoning with heavy metals and occasionally with other drugs (see Table 4: Poisoning: Guidelines for Chelation Therapy). IV fat emulsions in 10% and 20% concentrations and high-dose insulin therapy have been used to successfully treat several different cardiac toxins (eg, bupivacaine, verapamil).
Ongoing supportive measures:
Most symptoms (eg, agitation, sedation, coma, cerebral edema, hypertension, arrhythmias, renal failure, hypoglycemia) are treated with the usual supportive measures (see elsewhere in The Manual).
Drug-induced hypotension and arrhythmias may not respond to the usual drug treatments. For refractory hypotension, dopamine, epinephrine, other vasopressors, an intra-aortic balloon pump, or even extracorporeal circulatory support may be considered.
For refractory arrhythmias, cardiac pacing may be necessary. Often, torsades de pointes can be treated with Mg sulfate 2 to 4 g IV, overdrive pacing, or a titrated isoproterenol infusion.
Seizures are first treated with benzodiazepines. Phenobarbital or phenytoin can also be used. Severe agitation must be controlled; benzodiazepines in large doses, other potent sedatives (eg, propofol), or, in extreme cases, induction of paralysis and mechanical ventilation may be required.
Hyperthermia is treated with aggressive sedation and physical cooling measures rather than with antipyretics. Organ failure may ultimately require kidney or liver transplantation.
Hospital admission:
General indications for hospital admission include altered consciousness, persistently abnormal vital signs, and predicted delayed toxicity. For example, admission is considered if patients have ingested sustained-release preparations, particularly of drugs with potentially serious effects (eg, cardiovascular drugs). If there are no other reasons for admission, if indicated laboratory test results are normal, and if symptoms are gone after patients have been observed for 4 to 6 h, most patients can be discharged. However, if ingestion was intentional, patients require a psychiatric evaluation.
Prevention
In the US, widespread use of child-resistant containers with safety caps has greatly reduced the number of poisoning deaths in children < 5 yr. Limiting the amount of OTC analgesics in a single container and eliminating confusing and redundant formulations reduces the severity of poisonings, particularly with acetaminophen, aspirin, or ibuprofen. Preventive measures also include clearly labeling household products and prescription drugs, storing drugs and toxic substances in cabinets that are locked and inaccessible to children, promptly disposing of expired drugs by mixing them in cat litter or some other nontempting substance and putting them in a trash container that is inaccessible to children, and using carbon monoxide detectors. Public education measures to encourage storage of substances in their original containers (eg, not placing insecticides in drink bottles) are important. Use of imprint identifications on solid drugs helps prevent confusion and errors by patients, pharmacists, and health care practitioners.
Key Points
Last full review/revision February 2013 by Gerald F. O'Malley, DO; Rika O'Malley, MD
Content last modified March 2013
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