eMedicine Specialties > Emergency Medicine > Toxicology

Toxicity, Cocaine: Differential Diagnoses & Workup

Author: Lynn Barkley Burnett, EdD, MS, LLB(c), Medical Advisor, Fresno County Sheriff's Department; Attending Consultant-in-Chief and Chairman, Medical Ethics, Clinical Faculty, Community Medical Centers; Adjunct Professor of Forensic Pathology, National University Master of Forensic Science Program
Coauthor(s): Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School
Contributor Information and Disclosures

Updated: Nov 10, 2008

Differential Diagnoses

Angina Pectoris
Status Epilepticus
Cardiomyopathy, Dilated
Syncope
Coma
Toxicity, Amphetamine
Delirium Tremens
Toxicity, Anticholinergic
Delirium, Dementia, and Amnesia
Toxicity, Antidepressant
Epistaxis
Toxicity, Antihistamine
Heat Exhaustion and Heatstroke
Toxicity, Hallucinogen
Hypertensive Emergencies
Toxicity, MDMA
Hypoglycemia
Toxicity, Monoamine Oxidase Inhibitor
Myocardial Infarction
Toxicity, Neuroleptic Agents
Neuroleptic Malignant Syndrome
Toxicity, Phencyclidine
Pediatrics, Status Epilepticus
Toxicity, Selective Serotonin Reuptake Inhibitor
Pediatrics, Tachycardia
Toxicity, Sympathomimetic
Personality Disorders
Toxicity, Thyroid Hormone
Pneumothorax, Iatrogenic, Spontaneous and Pneumomediastinum
Ventricular Fibrillation
Pneumothorax, Tension and Traumatic
Withdrawal Syndromes
Rhabdomyolysis
Schizophrenia
Shock, Septic

Other Problems to Be Considered

CNS structural considerations (eg, hematoma, tumor, emboli, abscess, contusion)
Drug withdrawal
Exogenous toxins
Hypoxemia
Intracranial hemorrhage
Mania
Seizures
Serotonin syndrome
Thiamine deficiency
Thyroid storm
Thyrotoxicosis
Xanthine toxicity
Water and electrolyte imbalance

Workup

Laboratory Studies

  • No laboratory studies are indicated if the patient has a clear history and mild symptoms.
  • If history is absent or if the patient has moderate-to-severe toxicity, appropriate laboratory tests may be ordered to assess the following:
    • Complete blood cell count (CBC)
    • Electrolytes level
    • Glucose level
    • Pregnancy test
    • Calcium level
    • BUN level
    • Creatinine level
    • Arterial blood gases (ABGs) analysis
    • Creatine kinase (CK) level: An elevated CK level is nonspecific. In 19 patients with elevated CK levels, 5 had documented MI, and 14 had intramuscular injections or other muscle trauma. A CK level may be used to help rule out rhabdomyolysis.
    • Urinalysis (UA)
      • A UA should include inspection to detect myoglobinuria. In cocaine-induced rhabdomyolysis, a dipstick UA reveals an orthotoluidine reaction positive for heme in 75% of patients, findings positive for protein in 67%, and microscopic hematuria in some. On a urine drug screen, Drano or bleach can mask cocaine; alkaline urine may raise this suspicion.
      • Desipramine and amantadine, prescribed to reduce cravings for cocaine, may cause false-positive results on urine tests for amphetamines.
    • Toxicology
      • Urine, blood, gastric contents, and unknown substances found on patients or, such as on mustaches, may be sent for toxicologic evaluation. (Include the patient's clinical history and differential diagnosis of the toxins in question to guide the laboratory evaluations). However, high plasma cocaine concentrations are rarely observed because cocaine has a short half-life of 30-45 minutes. Furthermore, numerous studies have demonstrated that toxicology screens rarely change the clinical treatment of patients.
      • Although concentrations higher than 1 mg/L are generally associated with toxicity, deaths have been reported with blood levels of 0.1-20.9 mg/L. Because of this wide range of toxicity, quantitative blood levels of cocaine or metabolites are generally not clinically useful.
    • Half-life
      • Cocaine exhibits first-order kinetics over a wide dose range; therefore, after 5 half-lives (approximately 4 h), virtually all of the cocaine should have been converted to its metabolites. Hollander et al concur, indicating that urinary cocaine may be detected for 4-8 hours after a single intranasal dose. However, Lewin, Goldfrank, and Weisman maintain that most cocaine is excreted in the urine within 24 hours of ingestion.22
      • Benzoylecgonine may be present in urine for as long as 60 hours after single use and for as long as 22 days after the cessation of heavy cocaine use. If the ratio of benzoylecgonine to cocaine found in the urine is less than 100:1, either the cocaine was ingested less than 10 hours before collection of the sample or ongoing liberation of cocaine is occurring from a body package.
  • Also consider tests of the following:
    • Cardiac markers in patients with chest pain
    • Lactate dehydrogenase (LDH) level, aspartate aminotransferase (AST, formerly serum glutamic-oxaloacetic transaminase [SGOT]) level, prothrombin time (PT), activated partial thromboplastin time (aPTT), CSF, and cultures of blood and urine in patients with elevated temperatures
    • Serum osmolality and ketones in patients with altered mental status

Imaging Studies

  • General chest radiography
    • Obtain a chest radiograph in patients with chest pain, hypoxia, or moderate-to-severe toxicity. The chest image of drug users may reveal diffuse granulomatous changes resulting from chronic parenteral abuse due to the injection of inert insoluble ingredients of oral preparations or insolubles used to cut cocaine (eg, talc). Septic pulmonary emboli appear round or wedge shaped; they may clear rapidly or cavitate. Aspiration pneumonitis and noncardiogenic pulmonary edema also may be demonstrated. Pulmonary abscesses may become evident after aspiration pneumonitis or after an intravenous injection of bacteria or toxic organic or inorganic materials.
    • Chest images may occasionally reveal a needle, catheter, or fragment thereof, which was lost during drug injection. An aneurysm or pseudoaneurysm may be noted if the person was mainlining, or directly injecting, into a central artery or vein; this finding is an indication for further imaging studies. Up to 50% of posteroanterior (PA) chest images may demonstrate normal findings, with pneumomediastinum demonstrable only on lateral views.
    • To evaluate an inflamed area (abscess or cellulitis) or nonhealing wound in an intravenous drug user, include a radiograph, and look for foreign bodies, such as needles or parts thereof, metal, glass, or painted materials, that may have become imbedded after trauma. A radiograph of the infected area also may reveal subcutaneous emphysema produced by gas-forming organisms in an anaerobic infection.
    • Skeletal images may reveal osteomyelitis or fractures. However, osteomyelitis may not be demonstrable on plain images for 1-2 weeks, and other imaging studies should be performed if such a diagnosis is considered. Fractures are a concern because people under the influence of a drug may have injury that they do not recognize because of their intoxication.
  • Chest radiography to investigate body packing
    • Swallowed packets of cocaine may rupture, resulting in acute cocaine poisoning. They may also critically obstruct the esophagus or small bowel, typically at the ileocecal valve. The drug packets typically weigh 1-12 g.
    • Begin with plain images of the abdomen to search for packages. However, the rate of false-negative results is 1.2-33%, which may be because drug packages may not produce a radiographically visible outline or because shadows caused by constipation may obscure the silhouette.
    • Results from ultrasonography are commonly disappointing.
    • Contrast-enhanced study of the bowel or abdominal CT may be the only way of identifying the packages.
    • Regular radiologic examination is imperative to confirm successful transit of packages through the GI tract.
    • McCarron and Wood reported a series of 75 patients with suspected body packing of cocaine who were evaluated with kidneys, ureters, and bladder (KUB) radiography. Cocaine packages (15-175 per individual) were retrieved from 48 patients. In 73%, the KUB images showed foreign bodies. KUB findings were negative in 3% of patients with cocaine packages in the rectum and in another 16% who subsequently passed 15-135 packages.23
    • McCarron and Wood identified 3 types of packages, with the following physical and radiographic characteristics and risk for rupture23 :
      • Type 1: Condoms, toy balloons, or fingers of latex gloves contained cocaine in loose white powder form. Typically, the package material was stuffed with cocaine, tied, folded back on itself, and tied again at the opposite end. A variation involved wrapping a package with masking tape to make a small bundle, then covering it with 2 more condoms tied with fishing line. Type 1 packages radiographically appeared as well-defined circular or cigar-shaped white opacities. Ties, if radiographically apparent, had a rosette appearance. If gas halos were observed, they were irregular. This type of cocaine package posed the highest risk for breakage or leaching.
      • Type 2: About 5-7 layers of tubular latex, with a smooth tie on each end, covered white or light yellow matted cocaine powder. On direct inspection of the bundles, they appeared light yellow and were relatively large and uniform in size. These radiopaque bundles were oblong. When viewed radiographically, gas halos were present and regular, but no ties were apparent. Type 2 packages were less susceptible to breaking than type 1 packages.
      • Type 3: Yellow, hardened cocaine paste wrapped in aluminum foil, then wrapped again with 3-5 layers of tubular latex and securely tied at both ends. These packages were hard, smaller than type 1 and type 2 packages, and irregularly sized. They did not appear as foreign bodies on abdominal images. No breakage or leaching of cocaine was reported with this type of package.
    • The risk of bag rupture or leaching increases if the bag remains in the GI tract for a long period. In one series, 2 patients had sloughed pieces of wrapping, and 1 had evidence of leaching. After the container believed to be the last has passed, Perrone and Hoffman recommend imaging (eg, Gastrografin upper-GI series with small-bowel follow through) to ensure that the GI system has been fully purged of all packets.24
  • The ACEP recommends brain CT in patients presenting with first-time seizures. Perrone and Hoffman recommend CT scans of the head in all patients with cocaine-associated seizures because intracranial pathology often causes the seizures.24

Other Tests

  • Obtain a 12-lead ECG in patients with chest pain; hypoxia; dyspnea; an irregular, rapid, or slow pulse; altered mental status; or moderate-to-severe toxicity.
    • Of 48 patients admitted to an ICU with cocaine-induced chest pain, 86% had abnormal ECG findings, but only 6% were found to have sustained a MI.
    • The Brugada sign has been noted in cocaine users. This finding should prompt consideration of its implications for sudden cardiac death.
  • Coma has several possible etiologies in the cocaine-toxic patient, including the second (nonconvulsive) stage of status epilepticus. Therefore, immediate STAT EEG is indicated in patients presenting with unexplained coma in whom this is thought to be a possibility.

Procedures

  • Renzi recommends lumbar puncture (LP) to rule out intracranial hemorrhage in patients with persistent headache after the patient's BP is normalized and contraindications are ruled out on head CT.25
    • When LP is considered for this possible indication, remember that headaches are common in cocaine users secondary to decreased uptake of serotonin.
    • Consider LP in all patients with hyperthermia or altered mental status.

More on Toxicity, Cocaine

Overview: Toxicity, Cocaine
Differential Diagnoses & Workup: Toxicity, Cocaine
Treatment & Medication: Toxicity, Cocaine
Follow-up: Toxicity, Cocaine
References

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Further Reading

Keywords

cocaine toxicity, cocaine ingestion, cocaine poisoning, benzoylmethylecgonine, blow, coke, crack, snow, toot, nose candy, freebase, club drug, rock, Erythroxylon coca, ecgonine, norcocaine, ethylbenzoylecgonine, cocaethylene, cocaine-induced myocardial infarction, cocaine-induced MI, speedball, ischemic stroke, hemorrhagic stroke, subarachnoid hemorrhage, hyperthermia, agitated delirium, excited delirium, acute coronary syndromes, cocaine-associated rhabdomyolysis, hyperthermia, ventricular dysrhythmias, myocarditis, microfocal fibrosis, contraction band necrosis, tachydysrhythmias, cardiac arrest, coronary atherosclerosis, dilated cardiomyopathy, cocaine-induced seizures, cocaine-associated seizures, neuroleptic malignant syndrome, NMS, dystonic reactions, bradykinesia, akinesia, akathisia, pseudoparkinsonism, catalepsy, neuroleptic-induced dystonias, sudden death, psychostimulant-induced hyperthermia, myoglobinuria, acute tubular necrosis, acidemia, aortic dissection, pneumothorax, pneumopericardium, pneumomediastinum, pulmonary hemorrhage, pulmonary infarction, diffuse alveolar hemorrhage, neurogenic pulmonary edema, exacerbation of asthma, eosinophilic lung disease, chronic diffuse interstitial pneumonia, sudden infant death syndrome, SIDS, pulmonary hypertension, transient pulmonary infiltrates, crack lung, nasal septum perforation, bronchiolitis obliterans organizing pneumonia, granulomatosis, sinusitis, epiglottitis, bronchitis, cellulose granulomas in lung, panlobular emphysema, alveolar accumulation of carbonaceous material, airway burns, tracheal stenosis, hypersensitivity pneumonitis, toxic encephalopathy, neurogenic syncope, movement disorders, cocaine-induced hypertension, crack dancing, mesenteric ischemia, renal infarction, cocaine-associated cerebral vasculitis, central retinal artery occlusion, blurring of vision, endophthalmitis, optic neuropathy, corneal ulcerations, hallucinations, anxiety, depression, delirium, paranoia, toxic psychosis, cocaine bingeing, pocket shot, necrotizing angiitis, acquired immunodeficiency syndrome, AIDS, thrombophlebitis, cellulitis, talc-induced hepatitis, subacute bacterial endocarditis, SBE, foreign-particle pulmonary emboli, tetanus, cotton fever, malaria

Contributor Information and Disclosures

Author

Lynn Barkley Burnett, EdD, MS, LLB(c), Medical Advisor, Fresno County Sheriff's Department; Attending Consultant-in-Chief and Chairman, Medical Ethics, Clinical Faculty, Community Medical Centers; Adjunct Professor of Forensic Pathology, National University Master of Forensic Science Program
Lynn Barkley Burnett, EdD, MS, LLB(c) is a member of the following medical societies: American Academy of Hospice and Palliative Medicine, American Association for the Advancement of Science, American Association of Suicidology, American Cancer Society, American College of Sports Medicine, American Heart Association, American Professional Society on the Abuse of Children, American Public Health Association, American Society for Bioethics and Humanities, American Society of Law Medicine and Ethics, American Stroke Association, Association of Military Surgeons of the US, Christian Medical & Dental Society, European Society for Trauma and Emergency Surgery, European Society of Cardiology, European Society of Intensive Care Medicine, European Society of Paediatric and Neonatal Intensive Care, Faculty of Forensic and Legal Medicine of the Royal College of Physicians of London, International Homicide Investigators Association, New York Academy of Sciences, Royal College of Surgeons of Edinburgh, Royal Society of Medicine, Society for Academic Emergency Medicine, Society of Critical Care Medicine, and World Association for Disaster and Emergency Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School
Jonathan Adler, MD is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: eMedicine.com, Inc. Consulting fee Consulting

Medical Editor

Miguel C Fernandez, MD, FAAEM, FACEP, FACMT, Associate Clinical Professor; Medical and Managing Director, South Texas Poison Center, Department of Surgery/Emergency Medicine and Toxicology, University of Texas Health Science Center at San Antonio
Miguel C Fernandez, MD, FAAEM, FACEP, FACMT is a member of the following medical societies: American Academy of Clinical Toxicology, American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Medical Toxicology, Society for Academic Emergency Medicine, and Texas Medical Association
Disclosure: Nothing to disclose.

Pharmacy Editor

John T VanDeVoort, PharmD, ABAT, Director of Pharmacy, Sacred Heart Hospital
John T VanDeVoort, PharmD, ABAT is a member of the following medical societies: American Academy of Clinical Toxicology and American Society of Health-System Pharmacists
Disclosure: Nothing to disclose.

Managing Editor

John G Benitez, MD, MPH, FACMT, FACPM, FAAEM, Associate Professor, Department of Medicine, Clinical Pharmacology Division, Vanderbilt University; Managing Director, Tennessee Poison Center
John G Benitez, MD, MPH, FACMT, FACPM, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine, American College of Medical Toxicology, American College of Preventive Medicine, Society for Academic Emergency Medicine, Undersea and Hyperbaric Medical Society, and Wilderness Medical Society
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Asim Tarabar, MD, Assistant Professor, Department of Surgery, Section of Emergency Medicine, Yale University School of Medicine; Consulting Staff, Department of Emergency Medicine, Yale-New Haven Hospital
Disclosure: Nothing to disclose.

 
 
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