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CBRNE - Incapacitating Agents, Opioids/Benzodiazepines - Diagnosis and Differentials

Author Information and Disclosures

Contents

Clinical

History: An event involving an opioid or benzodiazepine aerosolized incapacitating agent would probably create confusion and panic; cause multiple serious injuries or fatalities; and necessitate a major emergency medical service, police, and/or military response.
  • Large numbers of casualties could overwhelm any community's emergency response services.
  • Chaos may occur following such an event.
  • In the early phases of an emergency response, the agent would probably be unknown, and the history may be misleading and inaccurate.
  • Physical examination is the key to identifying the causative agent.

Physical: Following exposure to either an aerosolized opioid or benzodiazepine incapacitating agent, the presentation would be a syndrome consistent with opioid or benzodiazepine toxicity, respectively. These syndromes can vary, depending on the opioid or benzodiazepine agent used. In addition, findings may vary, depending on the patient's preexisting medical problems, the treatment provided by first responders, and the potential complications of the intoxication. For example, if hypoxic brain injury occurs, the characteristic miosis seen in an opioid syndrome may be replaced by fixed dilated pupils.

  • Opioid intoxication
    • Respiratory depression manifesting as hypoventilation, apnea, and airway occlusion may be present.
    • Central nervous system depression manifesting as fatigue, somnolence, ataxia, and/or coma may be present.
    • Miosis may be present. Intoxication with the opioids meperidine and propoxyphene does not typically cause miosis, and normal papillary size is regularly maintained; however, neither of these agents has been associated with aerosolization. Mydriasis may occur in patients with severe toxicity because of anoxic brain injury. Miosis may be limited by preexisting medical conditions, such as a history of previous cataract surgery.
    • Cardiovascular manifestations of opioid toxicity may include hypotension secondary to arteriolar and venous dilation. Both tachycardia secondary to hypotension or hypoxia and bradycardia secondary to a reduction of direct central nervous system stimulation may be observed. If hypoventilation becomes prominent, hypoxia-induced cardiac arrhythmias may occur.
  • Benzodiazepine intoxication
    • Respiratory depression manifesting as hypoventilation, apnea, and airway occlusion may be present.
    • Central nervous system depression manifesting as drowsiness, somnolence, ataxia, nystagmus, and/or coma may be present.
    • Cardiovascular manifestations of benzodiazepines may include hypotension, tachycardia, and bradycardia. Hypoxia-induced cardiac arrhythmias may occur.

Differentials

CBRNE - Chemical Warfare Agents
CBRNE - Cyanides, Hydrogen
CBRNE - Incapacitating Agents, 3-Quinuclidinyl Benzilate
CBRNE - Incapacitating Agents, Agent 15
CBRNE - Incapacitating Agents, Cannabinoids
CBRNE - Incapacitating Agents, LSD
CBRNE - Nerve Agents, Binary: GB2, VX2
CBRNE - Nerve Agents, G-series: Tabun, Sarin, Soman
CBRNE - Nerve Agents, V-series: Ve, Vg, Vm, Vx
Toxicity, Barbiturate
Toxicity, Benzodiazepine
Toxicity, Clonidine
Toxicity, Cyanide
Toxicity, Gamma-Hydroxybutyrate
Toxicity, Hallucinogen
Toxicity, Narcotics
Toxicity, Organophosphate and Carbamate

Workup

Lab Studies:
  • The use of laboratory studies in the treatment of patients potentially exposed to opioid or benzodiazepine incapacitating agents should initially focus on the potential complications associated with those sedatives. Additional laboratory tests can also be conducted in an attempt to identify the diagnosis of the incapacitating agent if the specific agent is unknown to the clinicians.
  • Rapid urine drug screenings (immunoassays) are available and may assist health care professionals in making a diagnosis. However, these immunoassays do have a number of limitations. Opioid immunoassays are directed toward morphine. Many synthetic opioids, such as fentanyl, show no cross-reactivity with these assays. Testing for benzodiazepines is complicated because numerous benzodiazepines have substantially different structures. Results may be positive for diazepam, but negative for other benzodiazepines (eg, clonazepam).
  • Performing a complete blood count, electrolyte tests, clotting studies, and renal and liver function tests is reasonable in any person who has potentially been exposed to an incapacitating agent.
  • If the patient is comatose, performing a urine myoglobin and/or creatine phosphokinase test is warranted to exclude rhabdomyolysis. Hyperkalemia, hyperphosphatemia, and hypocalcemia may occur in association with rhabdomyolysis. The lactate level may also be elevated in these patients.
  • If the incapacitating agent is unknown, obtain extra blood and urine samples. Subsequent testing can be performed to confirm the causative agent.
Imaging Studies:
  • A patient who has potentially been exposed to an opioid or a benzodiazepine incapacitating agent and who is comatose may be at risk for aspiration pneumonia. Obtain a chest radiograph.
  • If the etiology of a patient's altered mental status is uncertain, performing a head CT scan to exclude other intracranial processes is reasonable.

Other Tests:

  • Both opioids and benzodiazepines may be associated with bradycardia. However, stress occurring in response to a situation associated with an exposure to aerosolized opioids or benzodiazepines may lead to tachycardia. Patients who are exposed to these agents and have preexisting cardiac disease may be at risk for cardiac ischemia. Perform an ECG to exclude these potential problems.
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Bibliography

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Synonyms And Related Keywords

incapacitating agent; opioid; fentanyl; carfentanil; alfentanil; sufentanil; benzodiazepine; diazepam; chemical warfare agents; chemical, biological, radiological, nuclear, and explosive threat agents; chemical weapons; benzodiazepine toxicity; opioid toxicity

Author Information and Disclosures

Author: Christopher P Holstege, MD, FACEP, FACMT, Associate Professor of Emergency Medicine and Pediatrics, University of Virginia; Director, Division of Medical Toxicology, Center of Clinical Toxicology; Medical Director, Blue Ridge Poison Ctr, Associate Medical Toxicology Fellowship Director, VA Dept of Health

Coauthor(s): Alexander Baer, MD, Staff Physician, Department of Emergency Medicine, University of Virginia School of Medicine

Christopher P Holstege, MD, FACEP, FACMT, is a member of the following medical societies: American Academy of Clinical Toxicology, American Academy of Emergency Medicine, American Association for the Advancement of Science, American College of Emergency Physicians, American College of Medical Toxicology, American Medical Association, Christian Medical and Dental Society, Medical Society of Virginia, Society for Academic Emergency Medicine, and Wilderness Medical Society

Editor Information

Editor(s): Suzanne White, MD, Medical Director, Regional Poison Control Center at Children's Hospital, Program Director of Medical Toxicology, Associate Professor, Departments of Emergency Medicine and Pediatrics, Wayne State University School of Medicine; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Rick Kulkarni, MD, Medical Director, Assistant Professor of Surgery, Section of Emergency Medicine, Yale-New Haven Hospital; John Halamka, MD, Chief Information Officer, CareGroup Healthcare System, Assistant Professor of Medicine, Department of Emergency Medicine, Beth Israel Deaconess Medical Center; Assistant Professor of Medicine, Harvard Medical School; and Robert G Darling, MD, FACEP, Assistant Professor of Military and Emergency Medicine, Uniformed Services University of the Health Sciences, F Edward Hebert School of Medicine; Director, Center for Disaster and Humanitarian Assistance Medicine

 
 
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