The following information provides general guidance and is not meant to substitute for industrial or medical policies, procedures or protocols. Please note that if a terrorist attack results in multiple or mass casualties, triage protocols are likely to be implemented along with mass casualty treatment protocols.
If cyanide poisoning is suspected, the victim should immediately be moved to an area with fresh air. Contaminated clothing should be removed, the skin immediately washed with soap and water and professional medical care should be sought as quickly as possible.
While extremely lethal at high concentrations, if treated quickly, cyanide can be completely eliminated from the victim.
Currently, cyanide poisoning can be treated with prompt administration
of an approved antidote, but cyanide poisoning should be confirmed
by a blood test or other environment sources before administering the antidote.
In the event of multiple victims, the emergency responder and emergency physician will be guided by triage and mass casualty protocols. Sources of additional supplies, including antidotes, are likely to be needed. Community based emergency planning must consider response times and potential cyanide risk when developing community response plans and medical caches stocking levels and locations.
Medical professionals in the United States currently have access to an antidote called the Cyanide Antidote Kit, (also called the Taylor, Lilly or Pasadena Kit). This kit contains three different medicines - amyl nitrite, sodium nitrite and sodium thiosulfate - to be used in a specific sequence: the amyl nitrite is administered as an inhalant, followed by the sodium nitrite and sodium thiosulfate, which are given intravenously.
The nitrites are given to convert hemoglobin in the red blood cell to methemoglobin, which attracts the cyanide away from the cytochrome oxidase and allows the cell to continue the process of aerobic metabolism. Thiosulfate is given to facilitate detoxification of cyanide by the body's own cyanide clearance system.
Learn more about aerobic metabolism
In countries throughout the world, other antidotes have been developed and are currently used by emergency medical personnel in various situations.
Hydroxocobalamin, a precursor of vitamin B12, has been used safely and effectively in France (with the trade name Cyanokit, made by Merck Sant S.A.S.) since 1996 to treat smoke inhalation victims for cyanide exposure, including as an empiric therapy and in cases of suspected cyanide poisoning. While not currently available in the United States, it is being investigated for possible use in the U.S. The mechanism of action of hydroxocobalamin is fairly straightforward. The hydroxocobalamin attaches to the cyanide directly, creating cyanocobalamin, a natural form of vitamin B12, which is excreted in the urine. The advantage of this approach is that methemoglobin is not produced and the oxygen-carrying capacity of the victim's blood is not lowered. Therefore, it is suitable for use in smoke inhalation victims as well as other causes of cyanide poisoning. The most common side effect of hydroxocobalamin is temporary pink discoloration of the skin, urine and mucous membranes.
Dicobalt Ededate is used in the UK to treat cyanide poisoning. Cobalt compounds fixate to the cyanide ion. One 300mg ampule is administered intravenously at a regular rate over one minute followed by 50ml glucose intravenous infusion. The most common side effects include vomiting, hypotension or hypertension, and tachycardia. Dicobalt edetate can be extremely toxic in the absence of cyanide ions and can only be given when the presence of severe cyanide poisoning is detected.
4-dimethylaminophenol (DMAP) is used in Germany as an antidote for severe cyanide poisoning in patients who are in a deep coma and who have dilated non-reactive pupils and deteriorating cardio-respiratory function. DMAP converts part of the hemoglobin of the blood from ferrous hemoglobin to ferric; this creates a pool of binding potential that can divert cyanide from the cytochromes it posions. Patients are given an intravenous dose of 3.25 mg/kg body weight. There are differences in individual susceptibility, which may result in an unacceptably high level of methemoglobin after normal therapeutic doses. Adverse side effects include: hemolyisis, mild headache, dizziness, hyperventilation, cyanosis, and discoloration of the urine.