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CBRNE - Nerve Agents, Binary: GB2, VX2: Follow-up
Updated: Dec 19, 2007
Follow-up
Further Inpatient Care
- Admit all patients with liquid exposures for observation, even if initially asymptomatic. Onset of symptoms with these exposures may be delayed as long as 18 hours.
- After a vapor exposure with only minimal symptoms, the patient can usually be discharged home.
- Admit patients who have more than simple miosis for observation and further inpatient care.
Further Outpatient Care
- Patients who are discharged from the hospital do not usually require further instructions or care. Nerve agents have not been associated with organophosphate-induced delayed neuropathy. Advise patients with miosis not to drive at night until their visual deficit resolves, which may take several weeks.
- Posttraumatic stress disorder is common after terrorist events; patients may need a psychiatric evaluation or referral.
Inpatient & Outpatient Medications
- The cornerstone of management is the early use of antidotes (atropine and pralidoxime). No evidence supports the use of long-term therapy after the acute phase is over.
Transfer
- Prompt delivery of antidotes is of foremost importance in these patients. Transfer to a higher level of care facility may be arranged after decontamination, antidote administration, and stabilization of the patient.
Complications
- Patients with status epilepticus or hypoxemia may experience anoxic brain injury.
Prognosis
- If patients recover from the acute effects of the exposure, chronic effects are generally not expected. Subtle behavioral and cognitive changes have been noted to persist for days to weeks after the initial exposure. Patients may have permanent sequelae if they experienced anoxia during the acute phase of the poisoning.
Patient Education
- For excellent patient education resources, visit eMedicine's Bioterrorism and Warfare Center. Also, see eMedicine's patient education articles Chemical Warfare and Personal Protective Equipment.
Miscellaneous
Medicolegal Pitfalls
- Careful documentation of physical findings, response to treatment, and laboratory parameters are important.
- In the case of a terrorist attack, any collected data can be used to prosecute the perpetrators.
- In the case of occupational (eg, military, research laboratories) accidents, data are needed to make recommendations for follow-up care and to determine dates of possible return to work. Documentation of an occupational exposure to a nerve agent such as VX also helps with improving safety in the workplace.
Special Concerns
- Information regarding nerve agents has been gathered mainly from accidental exposures or volunteer studies in military personnel. No experience is available on the difference in effects or outcome for special populations such as pregnant, pediatric, or geriatric populations.
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| Treatment & Medication: CBRNE - Nerve Agents, Binary: GB2, VX2 |
Follow-up: CBRNE - Nerve Agents, Binary: GB2, VX2 |
| Multimedia: CBRNE - Nerve Agents, Binary: GB2, VX2 |
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Further Reading
For a discussion about Novichok agents, see Chemical Weapons Disarmament in Russia: Problems and Prospects.
Keywords
nerve agents, binary agents, GB2, VX2, sarin, chemical warfare, acetylcholinesterase inhibitors, AChE inhibitors, GA, tabun, GD, soman, chemical weapons, GB, VX, GD2, acetylcholine, cholinergic overstimulation, organophosphate, carbamate, pralidoxime chloride, Protopam, 2-PAM, anticholinergics, oximes, AChE reactivator, muscarinic receptor
Follow-up: CBRNE - Nerve Agents, Binary: GB2, VX2