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CYANURIC FLUORIDE

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Classification   |    Detailed evidence-based information

Substances Included Synonyms

Therapeutic Toxic Class

    A) Cyanuric fluoride is a fluorinated triazine.

Specific Substances

    A) No Synonyms were found in group or single elements
    1.2.1) MOLECULAR FORMULA
    1) C3-F3-N3

Available Forms Sources

    A) FORMS
    1) Cyanuric fluoride is a colorless liquid (HSDB, 2003).
    B) SOURCES
    1) Cyanuric fluoride can be prepared from cyanuric chloride using a fluorinating agent, such as pentavalent antimony chlorofluoride, silver monofluoride, potassium fluoride, sodium fluoride, potassium fluorosulfinate, or sulfur tetrafluoride (HSDB, 2003).
    C) USES
    1) Cyanuric fluoride is commercially available for biochemical applications. In particular, it is used as a specific reagent for tyrosine. Fiber-reactive dyes based on cyanuric fluorides is also an emerging major application (HSDB, 2003).

Overview

Life Support

    A) This overview assumes that basic life support measures have been instituted.

Clinical Effects

    0.2.1) SUMMARY OF EXPOSURE
    A) Very little information is available about cyanuric fluoride and its potential toxicity. The material readily penetrates through the skin, and is quite irritating. At the time of this review, NO DATA INDICATING THAT CYANIDE POISONING CAN OCCUR FOLLOWING EXPOSURE were found.
    1) Should an exposed patient exhibit signs or symptoms of CYANIDE POISONING, REFER to the POTASSIUM CYANIDE management for evaluation and treatment recommendations.
    B) Most of the clinical effects and treatment recommendations below are derived from information regarding the similar chlorinated derivative, CYANURIC CHLORIDE, classified as a moderately toxic substance.
    1) Respiratory tract, skin, and severe eye irritation has been demonstrated in experimental animals exposed to cyanuric chloride. Respiratory tract irritation occurred in exposed humans.
    2) In humans, repeated dermal exposure to low concentrations of cyanuric chloride did not cause irritation, although serious irritation and dermal necrosis have occurred in experimental animals exposed directly to the material.
    3) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals. Subacute feedings of 37 mg/kg per day for 5 weeks caused no ill effects in rabbits.
    4) One older rat study without controls and using only a small number of animals found that cyanuric chloride is a relatively weak carcinogen, causing an increased incidence of fibroadenomas at injection sites, and tumors of the mammary glands, uterus, and prostate. This study has been criticized for several reasons, and does not provide adequate evidence that cyanuric chloride is carcinogenic.
    C) When cyanuric fluoride is heated to decomposition, highly irritating and toxic fumes of fluorides and oxides of nitrogen are released. Exposure to these products of combustion would be predicted to cause eye and respiratory tract irritation, and could lead to the development of chemical pneumonitis or noncardiogenic pulmonary edema.
    D) It is unknown whether or not systemic fluoride poisoning could occur following cyanuric fluoride absorption. However, it would be prudent to observe for such effects as hypocalcemia, hypomagnesemia, hyperkalemia, cardiac dysrhythmias, respiratory depression, hyperactive reflexes with tetany, and hypocoagulability.
    0.2.4) HEENT
    A) Eye irritation, corneal ulceration, and excessive lacrimation were noted in experimental animals following direct contact with the similar compound, cyanuric chloride. Exposure to the products of combustion of cyanuric fluoride, fluoride and oxides of nitrogen, would be predicted to cause irritation of the nose and throat.
    0.2.5) CARDIOVASCULAR
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, death might occur from cardiac failure or respiratory paralysis. Hypocalcemia with QT prolongation is possible. Dysrhythmias consistent with hyperkalemia have been reported in systemic fluoride poisoning.
    0.2.6) RESPIRATORY
    A) Respiratory tract irritation was seen in both human volunteers and experimental animals exposed to fumes of the similar compound, cyanuric chloride. Inhalation of cyanuric chloride dust by rats at a concentration of 1.88 mg/m(3) 4 hours daily for 2 and 1/2 months caused respiratory tract irritation with a fatality rate of 30 percent.
    B) Exposure to the fluoride and oxides of nitrogen cyanuric fluoride thermal decomposition products would be predicted to cause respiratory tract irritation with chemical pneumonitis or noncardiogenic pulmonary edema.
    C) In systemic fluoride poisoning, respirations are first stimulated, then depressed. Death usually is from respiratory paralysis.
    0.2.7) NEUROLOGIC
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, blood calcium could decrease causing an increase in skeletal muscle excitability, hyperactive reflexes, painful spasms (particularly in the extremities), weakness and tetanic contractures 3 to 5 hours later.
    0.2.8) GASTROINTESTINAL
    A) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals.
    0.2.12) FLUID-ELECTROLYTE
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, serious hypocalcemia or fatal hyperkalemia might occur; hypomagnesemia could also develop.
    0.2.13) HEMATOLOGIC
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, reduction of serum calcium could decrease the clotting ability of blood.
    0.2.14) DERMATOLOGIC
    A) Cyanuric fluoride readily penetrates all layers of the skin in rabbits. The similar compound, cyanuric chloride, causes skin irritation on direct contact.
    0.2.19) IMMUNOLOGIC
    A) The similar compound, cyanuric chloride, caused immunosuppression which decreased antibody affinity in immunized rabbits. This effect has not been reported in exposed humans.
    0.2.20) REPRODUCTIVE
    A) CYANURIC FLUORIDE -
    1) At the time of this review, no data were available to assess the possible reproductive hazards of cyanuric fluoride in humans.
    B) CYANURIC CHLORIDE -
    1) The similar compound, cyanuric chloride, was not teratogenic in chick embryos.
    C) No information about possible male reproductive effects was found in available references at the time of this review.
    0.2.21) CARCINOGENICITY
    A) CYANURIC FLUORIDE -
    1) At the time of this review, no data was available to assess the potential carcinogenicity of cyanuric fluoride.

Laboratory Monitoring

    A) Obtain at least hourly serum electrolytes including serial total or ionized calcium, magnesium, and potassium levels. Total calcium may not reflect true hypocalcemia, but usually has a more rapid turnaround. Therapy should be directed toward signs and symptoms of toxicity. Serum fluoride level may be used to confirm HF exposure. Obtain ABGs and chest X-ray in symptomatic patients.
    B) Obtain serial ECGs looking for signs of hypocalcemia (prolonged QTc interval) and hyperkalemia (peaked T waves). Institute continuous cardiac monitoring.

Treatment Overview

    0.4.2) ORAL/PARENTERAL EXPOSURE
    A) Attempt immediate administration of a fluoride binding substance: milk (one-half to one glassful), chewable calcium carbonate tablets, milk of magnesia or a liquid antacid. Avoid large amounts of liquid, as this may induce vomiting.
    B) Do not induce vomiting.
    C) HYPOCALCEMIA may occur. Correct with IV CALCIUM CHLORIDE (10 percent solution). ADULT: 2 to 4 mg/kg (0.02 to 0.04 mL/kg) infused slowly and repeated as necessary. PEDIATRIC: 10 to 30 mg/kg (0.1 to 0.3 mL/kg) infused slowly and repeat as necessary. Ideally, further doses should be based on measured deficits of ionized calcium. It may be necessary to exceed manufacturer's recommended rate and dose of administration to correct hypocalcemia.
    D) HYPOMAGNESEMIA may occur. Correct with IV MAGNESIUM SULFATE: ADULT 2 grams is diluted in 50 to 100 mL of D5W and administered over 5 minutes. PEDIATRIC: 25 to 50 mg/kg diluted to less than 10 mg/mL and infused over 5 to 10 minutes. Repeat doses may be necessary.
    E) HYPERKALEMIA - Patients with ECG changes (particularly QRS widening) or serum potassium greater than 7.5 require aggressive therapy. Administer 10 percent calcium chloride or calcium gluconate intravenously. ADULT DOSE: 5 to 10 mL/dose over 1 to 5 minutes; may repeat after 10 minutes. PEDIATRIC DOSE: 0.2 to 0.3 mL/kg/dose up to a maximum of 5 mL/dose.
    1) Intravenous administration of sodium bicarbonate enhances intracellular shift of potassium. Use 8.4 percent solution (1 mEq/mL). ADULT DOSE: 50 mL/dose over 5 minutes, repeated every 20 to 30 minutes as required. PEDIATRIC DOSE: 1 to 2 mL/kg/dose every 2 to 4 hours or as required.
    2) Administration of glucose and insulin facilitates intracellular potassium shift. ADULT DOSE: 50 mL of 50 percent solution together with 5 to 10 units of regular insulin intravenously over 5 minutes. PEDIATRIC DOSE: 0.25 to 0.5 mL/kg/dose IV followed by 1 unit regular insulin IV for every 4 grams glucose infused; may repeat every 10 to 30 minutes.
    F) Observe and evaluate patient for oral and GI burns. Consider NG suction if less than 90 minutes since ingestion.
    G) Endoscopy is recommended after ingestion of high concentration (greater than 20%) products, intentional ingestions of large amounts, or in patients with drooling, stridor, abdominal pain, or repeated vomiting.
    0.4.3) INHALATION EXPOSURE
    A) INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm.
    B) ACUTE LUNG INJURY: Maintain ventilation and oxygenation and evaluate with frequent arterial blood gases and/or pulse oximetry monitoring. Early use of PEEP and mechanical ventilation may be needed.
    C) OBSERVATION - Carefully observe patients with inhalation exposure for the development of abnormal systemic signs or symptoms and administer symptomatic treatment as necessary. Signs and symptoms of pulmonary edema may be delayed for 24 to 72 hours in some cases.
    D) INITIAL TREATMENT - Administer 100 percent humidified supplemental oxygen with assisted ventilation as required. Exposed skin and eyes should be copiously washed with water. Mild inhalational symptoms may be treated with 2.5% calcium gluconate nebulization.
    0.4.4) EYE EXPOSURE
    A) Irrigate promptly with crystalloid solution. Carefully evaluate for eye damage; exposure to dilute solutions may result in delayed signs and symptoms of ocular damage. The patient should be evaluated by an ophthalmologist following appropriate decontamination.
    0.4.5) DERMAL EXPOSURE
    A) OVERVIEW
    1) DECONTAMINATION - Remove all exposed clothing and jewelry taking necessary precautions to prevent secondary exposure to health care providers. Irrigate exposed areas promptly with copious amounts of water for at least 30 minutes. Carefully evaluate for eye damage and systemic toxicity.
    2) CALCIUM GLUCONATE OR CARBONATE GEL - Use of 2.5 percent to 33 percent calcium gluconate or carbonate gel or slurry, either placed into a surgical glove into which the affected hand is then placed, or applied onto the exposed dermis, has been recommended. This therapy is more easily administered and less painful than infiltration. In cases where concentrated HF exposure involving the nail and/or nailbed, splitting or removing the nail(s) to treat the nailbed injury has been advocated.
    3) CALCIUM INFUSION - Regional intravenous infusion of calcium gluconate is a therapeutic option in HF burns of the forearm, hand, or digits as adjunct to topical therapy or if topical therapy is unsatisfactory. Intra-arterial calcium infusion for digital HF burn is also a therapeutic option and may be considered if regional intravenous calcium gluconate is ineffective.
    4) CALCIUM GLUCONATE INFILTRATION - Continued tissue destruction and pain may be minimized by subcutaneous administration of calcium gluconate. Local infiltration with CALCIUM GLUCONATE may be considered if (1) exposure results in immediate tissue damage or (2) erythema and pain persist following adequate irrigation. Infiltrate each cm(2) of affected dermis and subcutaneous tissue with about 0.5 mL of 10 percent CALCIUM GLUCONATE using a 30 gauge needle. Repeat as needed to control pain. CAUTION: Avoid administering large volumes as this will result in decreased tissue perfusion and potential necrosis.
    5) DO NOT USE CALCIUM CHLORIDE - Calcium chloride is irritating to the tissues and may cause injury.

Range Of Toxicity

    A) Median lethal doses for the similar compound, cyanuric chloride, were 350 mg/kg in mice and 485 mg/kg in rats.
    B) The irritant threshold for fumes of the similar compound, cyanuric chloride, in humans was 0.3 mg/m(3) for a one-minute exposure.
    C) Application of 200 mg of the similar compound, cyanuric chloride, caused skin irritation in rabbits, followed by ulceration with repeated exposures. A dose of 3000 mg of cyanuric chloride applied to rabbit skin caused no deaths, although severe irritation developed.
    D) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals. Subacute feedings of 37 mg/kg per day of cyanuric chloride for 5 weeks caused no ill effects in rabbits. No effects were seen in rats fed 20 mg/kg of cyanuric chloride for 30 days; a reduced weight gain was seen at doses of 100 and 500 mg/kg daily.

Clinical Effects

Summary Of Exposure

    A) Very little information is available about cyanuric fluoride and its potential toxicity. The material readily penetrates through the skin, and is quite irritating. At the time of this review, NO DATA INDICATING THAT CYANIDE POISONING CAN OCCUR FOLLOWING EXPOSURE were found.
    1) Should an exposed patient exhibit signs or symptoms of CYANIDE POISONING, REFER to the POTASSIUM CYANIDE management for evaluation and treatment recommendations.
    B) Most of the clinical effects and treatment recommendations below are derived from information regarding the similar chlorinated derivative, CYANURIC CHLORIDE, classified as a moderately toxic substance.
    1) Respiratory tract, skin, and severe eye irritation has been demonstrated in experimental animals exposed to cyanuric chloride. Respiratory tract irritation occurred in exposed humans.
    2) In humans, repeated dermal exposure to low concentrations of cyanuric chloride did not cause irritation, although serious irritation and dermal necrosis have occurred in experimental animals exposed directly to the material.
    3) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals. Subacute feedings of 37 mg/kg per day for 5 weeks caused no ill effects in rabbits.
    4) One older rat study without controls and using only a small number of animals found that cyanuric chloride is a relatively weak carcinogen, causing an increased incidence of fibroadenomas at injection sites, and tumors of the mammary glands, uterus, and prostate. This study has been criticized for several reasons, and does not provide adequate evidence that cyanuric chloride is carcinogenic.
    C) When cyanuric fluoride is heated to decomposition, highly irritating and toxic fumes of fluorides and oxides of nitrogen are released. Exposure to these products of combustion would be predicted to cause eye and respiratory tract irritation, and could lead to the development of chemical pneumonitis or noncardiogenic pulmonary edema.
    D) It is unknown whether or not systemic fluoride poisoning could occur following cyanuric fluoride absorption. However, it would be prudent to observe for such effects as hypocalcemia, hypomagnesemia, hyperkalemia, cardiac dysrhythmias, respiratory depression, hyperactive reflexes with tetany, and hypocoagulability.

Heent

    3.4.1) SUMMARY
    A) Eye irritation, corneal ulceration, and excessive lacrimation were noted in experimental animals following direct contact with the similar compound, cyanuric chloride. Exposure to the products of combustion of cyanuric fluoride, fluoride and oxides of nitrogen, would be predicted to cause irritation of the nose and throat.
    3.4.3) EYES
    A) IRRITATION
    1) Eye irritation was noted in experimental animals following direct contact with the similar compound, cyanuric chloride (Blagodatin, 1968; HSDB, 2004).
    B) ULCERATION - Corneal ulceration was noted in experimental animals following direct contact with the similar compound, cyanuric chloride (Blagodatin, 1968).
    C) LACRIMATION - Excessive lacrimation was noted in experimental animals following direct contact with the similar compound, cyanuric chloride (Blagodatin, 1968).
    3.4.5) NOSE
    A) IRRITATION - Exposure to the products of combustion of cyanuric fluoride, fluoride and oxides of nitrogen (Lewis, 1996), would be predicted to cause irritation of the nose and throat.
    3.4.6) THROAT
    A) IRRITATION - Exposure to the products of combustion of cyanuric fluoride, fluoride and oxides of nitrogen (Lewis, 1996), would be predicted to cause irritation of the nose and throat.

Cardiovascular

    3.5.1) SUMMARY
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, death might occur from cardiac failure or respiratory paralysis. Hypocalcemia with QT prolongation is possible. Dysrhythmias consistent with hyperkalemia have been reported in systemic fluoride poisoning.
    3.5.2) CLINICAL EFFECTS
    A) CONDUCTION DISORDER OF THE HEART
    1) SUMMARY: Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, cardiac dysrhythmias secondary to hypocalcemia or hyperkalemia can occur(Heifetz & Horowitz, 1986a; Clancy, 2002).
    2) Prolongation of the QT interval (hypocalcemia) may be an ECG finding (Clancy, 2002).
    3) Hyperkalemia resulting in peaked T-waves on the ECG may also be present (Clancy, 2002). Dysrhythmias consistent with hyperkalemia have been reported in systemic fluoride poisoning(Baltazar et al, 1980a; McIvor et al, 1987).
    4) CASE REPORT: Dysrhyrthmias consistent with hyperkalemia (ie, marked peaking of T-waves) were reported in a fatal overdose. The patient developed refractory ventricular fibrillation(Baltazar et al, 1980a).

Respiratory

    3.6.1) SUMMARY
    A) Respiratory tract irritation was seen in both human volunteers and experimental animals exposed to fumes of the similar compound, cyanuric chloride. Inhalation of cyanuric chloride dust by rats at a concentration of 1.88 mg/m(3) 4 hours daily for 2 and 1/2 months caused respiratory tract irritation with a fatality rate of 30 percent.
    B) Exposure to the fluoride and oxides of nitrogen cyanuric fluoride thermal decomposition products would be predicted to cause respiratory tract irritation with chemical pneumonitis or noncardiogenic pulmonary edema.
    C) In systemic fluoride poisoning, respirations are first stimulated, then depressed. Death usually is from respiratory paralysis.
    3.6.2) CLINICAL EFFECTS
    A) IRRITATION SYMPTOM
    1) Respiratory tract irritation was seen in both human volunteers and experimental animals exposed to fumes of the similar compound, cyanuric chloride (Blagodatin, 1968; HSDB, 2004).
    2) Inhalation of dust from the similar compound, cyanuric chloride, by rats at a concentration of 1.88 mg/m(3) 4 hours daily for 2 and 1/2 months caused respiratory tract irritation with a fatality rate of 30 percent (CHEMINFO , 1990).
    3) Exposure to the products of combustion of cyanuric fluoride, fluoride and oxides of nitrogen (Lewis, 1996), would be predicted to cause respiratory tract irritation.
    B) PNEUMONITIS
    1) Exposure to the products of combustion of cyanuric fluoride, fluoride and oxides of nitrogen (Lewis, 1996), would be predicted to cause eye and respiratory tract irritation, and could lead to the development of chemical pneumonitis or noncardiogenic pulmonary edema.
    C) PARALYSIS
    1) In systemic fluoride poisoning, respirations are first stimulated, then depressed. Death usually is from respiratory paralysis (Heifetz & Horowitz, 1986).

Neurologic

    3.7.1) SUMMARY
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, blood calcium could decrease causing an increase in skeletal muscle excitability, hyperactive reflexes, painful spasms (particularly in the extremities), weakness and tetanic contractures 3 to 5 hours later.
    3.7.2) CLINICAL EFFECTS
    A) HYPERREFLEXIA
    1) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, blood calcium could decrease causing an increase in skeletal muscle excitability, hyperactive reflexes, painful spasms (particularly in the extremities), weakness and tetanic contractures 3 to 5 hours later (Arena, 1985).

Gastrointestinal

    3.8.1) SUMMARY
    A) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals.
    3.8.2) CLINICAL EFFECTS
    A) BURN OF GASTROINTESTINAL TRACT
    1) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals(HSDB, 2004).
    3.8.3) ANIMAL EFFECTS
    A) ANIMAL STUDIES
    1) GASTRIC ULCER
    a) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals (HSDB, 2004).

Hematologic

    3.13.1) SUMMARY
    A) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, reduction of serum calcium could decrease the clotting ability of blood.
    3.13.2) CLINICAL EFFECTS
    A) BLOOD COAGULATION PATHWAY FINDING
    1) Should systemic fluoride poisoning occur following absorption of cyanuric fluoride, reduction of serum calcium could decrease the clotting ability of blood (Arena, 1985).

Dermatologic

    3.14.1) SUMMARY
    A) Cyanuric fluoride readily penetrates all layers of the skin in rabbits. The similar compound, cyanuric chloride, causes skin irritation on direct contact.
    3.14.2) CLINICAL EFFECTS
    A) SKIN ABSORPTION
    1) Cyanuric fluoride readily penetrates all layers of the skin in rabbits (Griffiths, 1972).
    B) SKIN IRRITATION
    1) The similar compound, cyanuric chloride, causes skin irritation on direct contact (Blagodatin, 1968; HSDB, 2004).

Immunologic

    3.19.1) SUMMARY
    A) The similar compound, cyanuric chloride, caused immunosuppression which decreased antibody affinity in immunized rabbits. This effect has not been reported in exposed humans.

Reproductive

    3.20.1) SUMMARY
    A) CYANURIC FLUORIDE -
    1) At the time of this review, no data were available to assess the possible reproductive hazards of cyanuric fluoride in humans.
    B) CYANURIC CHLORIDE -
    1) The similar compound, cyanuric chloride, was not teratogenic in chick embryos.
    C) No information about possible male reproductive effects was found in available references at the time of this review.
    3.20.2) TERATOGENICITY
    A) HUMANS
    1) CYANIDE has been linked with congenital cretinism (deformities, dwarfism, and mental insufficiency) due to thyroid deficiency in regions of the world where cassava is a major part of the diet (Anon, 1972). The critical period is the first trimester, and damage can be prevented with iodine supplements (Anon, 1972).
    2) FLUORIDE can produce mottling of the deciduous (baby) teeth. It is believed that osteosclerosis is not a risk from prenatal exposure to fluoride (Hodge & MacGregor, 1982).
    B) ANIMAL STUDIES
    1) Cyanide has also been teratogenic and has affected the fertility of laboratory animals.
    2) Chemicals which liberate cyanide are also known to be teratogenic in animals. This is especially true of the aliphatic nitriles (Willhite, 1981; Smith, 1981; Willhite, 1980), including acrylonitrile (Buchter & Peter, 1984) and acetonitrile (Willhite, 1983).
    3) Cyanuric chloride, a related substance, was not teratogenic when injected into chick embryos(HSDB, 2004). This result would suggest, but certainly would not prove, that the cyanuric compounds do not behave like cyanide for reproductive effects.
    3.20.3) EFFECTS IN PREGNANCY
    A) LACK OF INFORMATION
    1) LACK OF INFORMATION
    a) At the time of this review, no data were available to assess the potential effects of exposure to this agent during pregnancy or lactation.

Carcinogenicity

    3.21.1) IARC CATEGORY
    A) IARC Carcinogenicity Ratings for CAS675-14-9 (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004):
    1) Not Listed
    3.21.2) SUMMARY/HUMAN
    A) CYANURIC FLUORIDE -
    1) At the time of this review, no data was available to assess the potential carcinogenicity of cyanuric fluoride.
    3.21.3) HUMAN STUDIES
    A) CYANURIC FLUORIDE -
    1) At the time of this review, no data was available to assess the potential carcinogenicity of cyanuric fluoride.
    3.21.4) ANIMAL STUDIES
    A) CYANURIC CHLORIDE -
    1) The similar compound, cyanuric chloride, was tested in rats: 10 of 34 survivors had sarcomas at the injection sites and fibroadenomata of the mammary glands, uterus, and prostate occurred in 8 of 45 rats in a feeding study (Pliss, 1966).
    2) These studies have been criticized for several reasons, and do not provide adequate evidence that cyanuric chloride is carcinogenic (CHEMINFO , 1990).

Genotoxicity

    A) CYANURIC FLUORIDE -
    1) At the time of this review, no data were available to assess the possible genotoxicity of cyanuric fluoride.
    B) CYANURIC CHLORIDE -
    1) The similar compound, cyanuric chloride, was not mutagenic in 4 Salmonella typhimurium strains with or without rat liver extracts.

Laboratory Monitoring

Monitoring Parameters Levels

    4.1.1) SUMMARY
    A) Obtain at least hourly serum electrolytes including serial total or ionized calcium, magnesium, and potassium levels. Total calcium may not reflect true hypocalcemia, but usually has a more rapid turnaround. Therapy should be directed toward signs and symptoms of toxicity. Serum fluoride level may be used to confirm HF exposure. Obtain ABGs and chest X-ray in symptomatic patients.
    B) Obtain serial ECGs looking for signs of hypocalcemia (prolonged QTc interval) and hyperkalemia (peaked T waves). Institute continuous cardiac monitoring.
    4.1.2) SERUM/BLOOD
    A) ACID/BASE
    1) BLOOD GASES
    a) Monitor arterial blood gases and/or pulse oximetry in patients with significant exposure.
    2) Monitoring pulse oximetry is an alternative to arterial blood gases.
    B) BLOOD/SERUM CHEMISTRY
    1) This agent may cause hepatotoxicity. Monitor liver function tests in patients with significant exposure.
    2) This agent may cause nephrotoxicity. Monitor renal function tests and urinalysis in patients with significant exposure.
    3) If systemic fluoride poisoning is suspected, monitor serum potassium, calcium, and magnesium levels.
    C) COAGULATION STUDIES
    1) Baseline coagulation studies should be obtained and monitored if systemic fluoride poisoning is suspected.
    4.1.4) OTHER
    A) OTHER
    1) PULMONARY FUNCTION TESTS
    a) If respiratory tract irritation is present, it may be useful to monitor pulmonary function tests.
    2) ECG
    a) Obtain serial ECGs looking for signs of hypocalcemia (prolonged QTc interval) and hyperkalemia (peaked T waves). Institute continuous cardiac monitoring.

Radiographic Studies

    A) CHEST RADIOGRAPH
    1) If respiratory tract irritation is present, monitor chest x-ray.

Treatment

Life Support

    A) Support respiratory and cardiovascular function.

Patient Disposition

    6.3.1) DISPOSITION/ORAL EXPOSURE
    6.3.1.1) ADMISSION CRITERIA/ORAL
    A) Patients with a history of significant exposures or with significant symptomatology should be admitted to an intensive care unit and observed with continuous ECG monitoring for a minimum of 24 to 48 hours (Caravati, 1988).

Monitoring

    A) Obtain at least hourly serum electrolytes including serial total or ionized calcium, magnesium, and potassium levels. Total calcium may not reflect true hypocalcemia, but usually has a more rapid turnaround. Therapy should be directed toward signs and symptoms of toxicity. Serum fluoride level may be used to confirm HF exposure. Obtain ABGs and chest X-ray in symptomatic patients.
    B) Obtain serial ECGs looking for signs of hypocalcemia (prolonged QTc interval) and hyperkalemia (peaked T waves). Institute continuous cardiac monitoring.

Oral Exposure

    6.5.1) PREVENTION OF ABSORPTION/PREHOSPITAL
    A) DILUTION
    1) FLUORIDE BINDING - Attempt immediate administration of a fluoride binding substance. Options include milk (one-half to one glassful), chewable calcium carbonate tablets, or milk of magnesia. Avoid large amounts of liquid, since this may induce vomiting.
    B) EMESIS/NOT RECOMMENDED
    1) Do NOT induce vomiting.
    6.5.2) PREVENTION OF ABSORPTION
    A) SUMMARY
    1) FLUORIDE BINDING - Attempt immediate administration of a fluoride binding substance which includes milk (one-half to one glassful), chewable calcium carbonate tablets, or milk of magnesia. Avoid large amounts of liquid, since this may induce vomiting.
    2) The precise amount of oral calcium required is unknown. One protocol for oral decontamination used 2400 mg of elemental calcium every two hours until hospital admission (Browne, 1982). This is equivalent to 12 TUMS(R) tablets (contain 200 milligrams each), 11 ROLAIDS CALCIUM RICH(R) tablets (contain 220 milligrams each), or 8 TUMS EXTRA STRENGTH(R) tablets (contain 300 milligrams each) per dose. Milk contains approximately 300 milligrams elemental calcium per 8 ounces.
    B) EMESIS/NOT RECOMMENDED
    1) Do not induce vomiting.
    C) NASOGASTRIC SUCTION
    1) Consider careful nasogastric suction or lavage with a small (18 Fr) soft tube for patients with significant ingestions who present within 90 minutes of exposure and have not spontaneously vomited. CALCIUM GLUCONATE 10 percent may be added to the lavage fluid.
    2) Brushite (calcium phosphate, dibasic, dihydrate) suspension is superior in inactivating hydrofluoric acid when compared to apatite (calcium orthophosphate, basic) suspension, calcium gluconate solution, or skim milk in an in vitro model of acute fluoride poisoning (Larsen & Jensen, 1991).
    a) Hydrofluoric acid containing test solutions were prepared by dissolving sodium fluoride in hydrochloric acid to produce three solutions, each with a pH of 4.5 (solution I), 4.0 (solution II), or 2.1 (solution III).
    b) The solutions provide a source of calcium that reacts with hydrofluoric acid producing calcium fluoride.
    c) The table below illustrates the percentage of fluoride removed by calcium fluoride formation in vitro.
    SOLUTION
    CALCIUMSOURCE I II III
    pH%FpH%FpH%F
    Brushite 0.16 g/mL7.2887.0992.490
    Brushite 0.16 g/mL7.2756.5642.156
    Apatite 0.58 g/mL7.4347.0383.4100
    Apatite 0.058 g/mL7.4306.6252.184
    Calcium gluconate0.24 g/mL4.8873.6602.29
    Skim Milk 0.1 g/mL7.1466.9334.58.3

    d) Additional in vitro studies are needed to confirm the safety and efficacy of these agents for gastric lavage in human fluoride poisoning.
    6.5.3) TREATMENT
    A) SELECTIVE DECONTAMINATION OF THE DIGESTIVE TRACT
    1) FLUORIDE BINDING - Attempt immediate administration of a fluoride binding substance which includes milk (one-half to one glassful), chewable calcium carbonate tablets, or milk of magnesia. Avoid large amounts of liquid, since this may induce vomiting.
    2) The precise amount of oral calcium required is unknown. One protocol for oral decontamination used 2400 mg of elemental calcium every two hours until hospital admission (Browne, 1982). This is equivalent to 12 TUMS(R) tablets (contain 200 milligrams each), 11 ROLAIDS CALCIUM RICH(R) tablets (contain 220 milligrams each), or 8 TUMS EXTRA STRENGTH(R) tablets (contain 300 milligrams each) per dose. Milk contains approximately 300 milligrams elemental calcium per 8 ounces.
    3) ANIMAL STUDY - In one animal study, it was determined that oral decontamination with calcium chloride or magnesium sulfate does not improve survival following hydrofluoric acid ingestion (Delgado & Heard, 2002).
    B) CALCIUM
    1) Patients with significant oral ingestion or dermal exposures are at a high risk to develop hypocalcemia. It has been suggested that 20 milliliters of 10 percent CALCIUM GLUCONATE be added to the first liter of intravenous fluids prophylactically. Further therapy is guided by serial serum calcium levels (Trevino et al, 1983).
    C) HYPOCALCEMIA
    1) Hypocalcemia in the absence of clinical tetany may occur following oral ingestion or dermal exposure (Tepperman, 1980). Check patient for a positive Trousseau's or Chvostek's sign.
    2) Correct known or suspected hypocalcemia with intravenous CALCIUM CHLORIDE (10 percent SOLUTION): ADULT 2 to 4 mg/kg (0.02 to 0.04 mL/kg) with repeat doses as necessary. PEDIATRIC: 10 to 30 mg/kg (0.1 to 0.3 mL/kg) infused slowly with repeat doses as necessary. Ideally, repeat doses should be based on measured deficits of ionized calcium. CALCIUM GLUCONATE (10 percent solution) may also be used, but the dose is 3 times the amount of the dose for calcium chloride.
    a) It may be necessary to exceed the manufacturer's recommended rate of administration to correct hypocalcemia (Manoguerra & Neuman, 1986).
    b) Doses of up to 113 mEq of calcium have been used to successfully treat hydrofluoric acid burns. A dose of 266.7 mEq used in one case resulted in hypercalcemia (Greco et al, 1988).
    c) Treat aggressively with intravenous calcium in the presence of any ECG or clinical signs of hypocalcemia while serum calcium levels are pending.
    D) HYPOMAGNESEMIA
    1) Hypomagnesemia may develop following oral ingestion or dermal exposure and has been associated with QTc prolongation and ventricular dysrhythmias.
    2) Correct known and suspected hypomagnesemia with intravenous
    3) MAGNESIUM SULFATE DOSE
    a) ADULT: 1 to 2 g diluted in 250 mL D5W or NS and infused IV, may be repeated as necessary.
    b) PEDIATRIC: 25 to 50 mg/kg IV infusion over 30 to 60 minutes; repeat dose as necessary; max 2 g/dose (Kleinman et al, 2010; Manrique et al, 2010; Haque & Saleem, 2009)
    4) The maximal therapeutic dose of magnesium use in clinical practice has not been definitively determined. Magnesium sulfate 6 grams loading over 15 minutes followed by 4 grams per hour has been used in the treatment of preeclampsia.
    5) Serial evaluation of the patient's knee jerk reflex is the most important and reliable guide to magnesium treatment. Serum magnesium levels are not a reliable indicator for what is a "therapeutic level". Patient should be monitored with ECG continuously.
    E) HYPERKALEMIA
    1) Patients should be monitored for laboratory and/or ECG evidence of hyperkalemia after ingestion of HF.
    a) ECG changes include peaked T waves in the precordial leads, prolongation of the PR interval and QRS duration, progressive flattening of the P wave, merging of the QRS complex with the T wave to produce a continuous sine wave appearance, and ventricular fibrillation or asystole (Martin et al, 1986; Smith et al, 1985) Williams, 1986).
    b) ECG manifestations of hyperkalemia and/or a serum potassium concentration of 7.5 milliequivalents/liter or greater indicates a medical emergency and requires aggressive therapy and continuous cardiac monitoring.
    c) Fluoride-induced hyperkalemia, once developed, may be irreversible. Therapeutic intervention to prevent development of elevated serum potassium is essential. Note: the beta-adrenergic receptor and the calcium channel do NOT appear to have major roles in fluoride-induced hyperkalemia. Early aggressive therapy with glucose, insulin and/or sodium bicarbonate prior to the development of hyperkalemia was ineffective in dog studies; however, quinidine was shown effective in preventing the K+ efflux from cells and preventing cardiotoxicity in fluoride-toxic dogs. Therapeutic doses of other antidysrhythmics, such as lidocaine, were not effective. Propranolol worsened fluoride-induced cardiotoxicity (Cummings & McIvor, 1988; McIvor & Cummings, 1987).
    d) In an in-vitro model of human erythrocytes, the potassium channel blockers, amiodarone and quinidine, attenuated fluoride-induced hyperkalemia. The authors recommended further in-vivo studies to determine whether amiodarone can enhance survival in fluoride poisoning (Su et al, 2003).
    e) Death is usually the result of delayed sudden cardiovascular collapse with ventricular fibrillation triggered by electrolyte imbalances (hypocalcemia, hypomagnesemia, hyperkalemia). If sudden death is avoided in the first 24 hours, prognosis is good, although recovery may be prolonged. In dog studies, increase in serum potassium levels began at approximately 2 hours postexposure and began to rise exponentially at 6 hours postexposure. Maintain normal or alkalotic pH. Cation exchange resins or dialysis may be the only effective means in which to reverse fluoride-induced hyperkalemia (Cummings & McIvor, 1988; McIvor & Cummings, 1987; McIvor et al, 1987).
    2) CALCIUM
    a) Intravenous calcium has no effect on circulating potassium levels, but it antagonizes cardiac toxicity in patients demonstrating cardiac signs and/or symptoms of hyperkalemia.
    b) Use 10 percent calcium chloride.
    c) ADULT DOSE - 5 to 10 milliliters (500 to 1000 milligrams) intravenously over 1 to 5 minutes; may repeat after 10 minutes.
    d) PEDIATRIC DOSE - 0.2 to 0.3 milliliter/kilogram (20 to 30 milligrams/kilogram) per dose up to a maximum single dose of 5 milliliters (500 milligrams) intravenously over 5 to 10 minutes, repeated up to four times or until serum calcium increases (Barkin, 1986).
    e) CALCIUM FOR INJECTION is available as three salts; calcium chloride, calcium gluconate, and calcium gluceptate.
    f) While the other salts may be used, calcium chloride is the preferred salt for resuscitation since it directly delivers ionized calcium, whereas the other salts must be hepatically metabolized to release ionized calcium (Chameides, 1988).
    g) Calcium chloride is very irritating, and should only be given via a central venous catheter. It may cause hypotension and bradycardia. Calcium salts are incompatible with bicarbonate.
    3) SODIUM BICARBONATE
    a) Administer intravenous sodium bicarbonate to shift potassium intracellularly. Expect 0.5 to 1 milliequivalent/liter reduction in serum potassium for each 0.1 unit rise in blood pH.
    b) A standard syringe contains 50 milliliters of 8.4% solution, 1 milliequivalent/milliliter, 50 milliequivalents/syringe.
    c) ADULT DOSE - 50 milliliters (50 milliequivalents) intravenously over 5 minutes, repeated at 20 to 30 minute intervals.
    d) PEDIATRIC DOSE - 1 to 2 milliliters/kilogram/dose (1 to 2 milliequivalents/kilogram/dose) intravenously every 2 to 4 hours or as required by pH (Barkin, 1986). The onset is 15 minutes, the duration of action 1 to 2 hours (Ellenhorn & Barceloux, 1997).
    4) INSULIN/DEXTROSE
    a) Enhances intracellular potassium shift.
    b) ADULT DOSE - Administer 25 grams of dextrose (250 milliliters of a 10% solution) intravenously over 30 minutes, and then continue the infusion at a slower rate.
    c) Ten units of regular insulin are given subcutaneously or added to the infusion.
    d) ALTERNATIVELY, 50 milliliters of a 50% dextrose solution with 5 to 10 units of regular insulin may be administered intravenously over 5 minutes.
    e) Typically, this regimen will lower serum potassium by 1 to 2 milliequivalents/liter within 30 to 60 minutes with the decrease lasting for several hours.
    f) PEDIATRIC DOSE - 0.5 to 1 gram/kilogram/dose followed by 1 unit of regular insulin intravenously for every 4 grams of glucose infused; may repeat every 10 to 30 minutes (Barkin, 1986).
    g) HYPEROSMOLARITY - It must be remembered that 50 percent dextrose, and even 25% dextrose, are very hyperosmolar and may be sclerosing to peripheral veins (Chameides, 1988); administration of hypertonic solutions via central lines is preferred, if possible.
    F) VENTRICULAR ARRHYTHMIA
    1) Evaluate for and treat hypocalcemia, hypomagnesemia and hyperkalemia. Because amiodarone has potassium channel blocking effects, it may be the preferred antidysrhythmic in the setting of hydrofluoric acid poisoning.
    2) AMIODARONE
    a) AMIODARONE/INDICATIONS
    1) Effective for the control of hemodynamically stable monomorphic ventricular tachycardia. Also recommended for pulseless ventricular tachycardia or ventricular fibrillation in cardiac arrest unresponsive to CPR, defibrillation and vasopressor therapy (Link et al, 2015; Neumar et al, 2010). It should be used with caution when the ingestion involves agents known to cause QTc prolongation, such as fluoroquinolones, macrolide antibiotics or azoles, and when ECG reveals QT prolongation suspected to be secondary to overdose (Prod Info Cordarone(R) oral tablets, 2015).
    b) AMIODARONE/ADULT DOSE
    1) For ventricular fibrillation or pulseless VT unresponsive to CPR, defibrillation, and a vasopressor therapy give an initial dose of 300 mg IV followed by 1 dose of 150 mg IV. For stable ventricular tachycardias: Infuse 150 milligrams over 10 minutes, and repeat if necessary. Follow by a 1 milligram/minute infusion for 6 hours, then a 0.5 milligram/minute. Maximum total dose over 24 hours is 2.2 grams (Neumar et al, 2010).
    c) AMIODARONE/PEDIATRIC DOSE
    1) Infuse 5 milligrams/kilogram as a bolus for pulseless ventricular tachycardia or ventricular fibrillation; may repeat twice up to 15 mg/kg. Infuse 5 milligrams/kilogram over 20 to 60 minutes for perfusing tachycardias. Maximum single dose is 300 mg. Routine use with other drugs that prolong the QT interval is NOT recommended (Kleinman et al, 2010).
    d) ADVERSE EFFECTS
    1) Hypotension and bradycardia are the most common adverse effects (Neumar et al, 2010).
    G) BURN
    1) Patient should be observed and evaluated for evidence of oral and gastrointestinal burns after deliberate ingestions or ingestion of high concentration products. While gastrointestinal burns may occur after ingestion they are generally NOT an immediate life threat.
    H) ENDOSCOPIC PROCEDURE
    1) Endoscopy is recommended after ingestion of high concentration (greater than 20%) products, deliberate ingestion of large amounts of low or high concentration products, or in patients manifesting drooling, stridor, abdominal pain, or repeated vomiting. There is little published information regarding the use of endoscopy and the therapy of mucosal burns after ingestion of hydrofluoric acid.
    I) ACIDOSIS
    1) METABOLIC ACIDOSIS: Treat severe metabolic acidosis (pH less than 7.1) with sodium bicarbonate, 1 to 2 mEq/kg is a reasonable starting dose(Kraut & Madias, 2010). Monitor serum electrolytes and arterial or venous blood gases to guide further therapy.

Inhalation Exposure

    6.7.1) DECONTAMINATION
    A) Move patient from the toxic environment to fresh air. Monitor for respiratory distress. If cough or difficulty in breathing develops, evaluate for hypoxia, respiratory tract irritation, bronchitis, or pneumonitis.
    B) OBSERVATION: Carefully observe patients with inhalation exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary.
    C) INITIAL TREATMENT: Administer 100% humidified supplemental oxygen, perform endotracheal intubation and provide assisted ventilation as required. Administer inhaled beta-2 adrenergic agonists, if bronchospasm develops. Consider systemic corticosteroids in patients with significant bronchospasm (National Heart,Lung,and Blood Institute, 2007). Exposed skin and eyes should be flushed with copious amounts of water.
    6.7.2) TREATMENT
    A) OXYGEN
    1) Administer 100 percent humidified oxygen to patients with abnormal respiratory signs or symptoms.
    B) ACUTE LUNG INJURY
    1) ONSET: Onset of acute lung injury after toxic exposure may be delayed up to 24 to 72 hours after exposure in some cases.
    2) NON-PHARMACOLOGIC TREATMENT: The treatment of acute lung injury is primarily supportive (Cataletto, 2012). Maintain adequate ventilation and oxygenation with frequent monitoring of arterial blood gases and/or pulse oximetry. If a high FIO2 is required to maintain adequate oxygenation, mechanical ventilation and positive-end-expiratory pressure (PEEP) may be required; ventilation with small tidal volumes (6 mL/kg) is preferred if ARDS develops (Haas, 2011; Stolbach & Hoffman, 2011).
    a) To minimize barotrauma and other complications, use the lowest amount of PEEP possible while maintaining adequate oxygenation. Use of smaller tidal volumes (6 mL/kg) and lower plateau pressures (30 cm water or less) has been associated with decreased mortality and more rapid weaning from mechanical ventilation in patients with ARDS (Brower et al, 2000). More treatment information may be obtained from ARDS Clinical Network website, NIH NHLBI ARDS Clinical Network Mechanical Ventilation Protocol Summary, http://www.ardsnet.org/node/77791 (NHLBI ARDS Network, 2008)
    3) FLUIDS: Crystalloid solutions must be administered judiciously. Pulmonary artery monitoring may help. In general the pulmonary artery wedge pressure should be kept relatively low while still maintaining adequate cardiac output, blood pressure and urine output (Stolbach & Hoffman, 2011).
    4) ANTIBIOTICS: Indicated only when there is evidence of infection (Artigas et al, 1998).
    5) EXPERIMENTAL THERAPY: Partial liquid ventilation has shown promise in preliminary studies (Kollef & Schuster, 1995).
    6) CALFACTANT: In a multicenter, randomized, blinded trial, endotracheal instillation of 2 doses of 80 mL/m(2) calfactant (35 mg/mL of phospholipid suspension in saline) in infants, children, and adolescents with acute lung injury resulted in acute improvement in oxygenation and lower mortality; however, no significant decrease in the course of respiratory failure measured by duration of ventilator therapy, intensive care unit, or hospital stay was noted. Adverse effects (transient hypoxia and hypotension) were more frequent in calfactant patients, but these effects were mild and did not require withdrawal from the study (Wilson et al, 2005).
    7) However, in a multicenter, randomized, controlled, and masked trial, endotracheal instillation of up to 3 doses of calfactant (30 mg) in adults only with acute lung injury/ARDS due to direct lung injury was not associated with improved oxygenation and longer term benefits compared to the placebo group. It was also associated with significant increases in hypoxia and hypotension (Willson et al, 2015).
    C) CALCIUM
    1) Administration of nebulized CALCIUM GLUCONATE 2.5 percent has been recommended (Trevino et al, 2001; Trevino et al, 1983).
    2) CASE SERIES - Lee et al (1992) report the use of calcium gluconate nebulization in 13 workers exposed to 150 to 200 parts per million HF gas for 2 minutes. Patients were treated quickly after exposure, and only minor upper respiratory tract irritation was noted. All patients tolerated the treatment without adverse effects. None developed delayed pulmonary edema or any permanent sequelae.
    3) CASE REPORT - Following a one minute exposure to fumes from an anhydrous HF spill in an enclosed area, a male worker experienced immediate upper airway irritation and dyspnea. Three nebulized calcium gluconate treatments were immediately administered with resolution of respiratory complaints. The authors suggested this treatment may have prevented pulmonary injury (Boyer et al, 2000).
    4) CASE SERIES - After 5 workers were exposed to inhalational HF fumes, they presented to the ED 4 hours later. Burning of the mouth and tongue were reported in 3 of the patients and one complained of nausea and abdominal cramps. All patients were administered a 2.5% calcium gluconate nebulized treatment. All symptoms resolved by the end of the treatment. The authors recommend calcium gluconate nebulization therapy for mild symptoms of HF inhalation (Trevino et al, 2001).
    D) Treatment should include recommendations listed in the ORAL EXPOSURE section when appropriate.

Eye Exposure

    6.8.1) DECONTAMINATION
    A) Irrigate promptly with crystalloid solution (lactated ringer's or normal saline). Carefully evaluate for eye damage; exposure to dilute solutions may result in delayed signs and symptoms of ocular damage (Caravati, 1988). The patient should be evaluated by an ophthalmologist following appropriate decontamination.
    6.8.2) TREATMENT
    A) IRRIGATION
    1) SUMMARY - Similar to treatment of skin exposure, calcium gluconate solution and benzethonium chloride (benzethonium hydrochloride) have been suggested for treatment of eye exposure. In addition, single irrigation with isotonic sodium chloride or magnesium chloride has been suggested (with repeated irrigation an increase in the frequency of corneal ulceration was reported in rabbit eyes) (Grant & Schuman, 1993).
    2) Based on animal studies, immediate SINGLE 30 minutes irrigation with one liter of water, isotonic sodium chloride or magnesium chloride may provide the most beneficial therapy for ocular exposure to 0.25 M/L or greater of HF. However, multiple irrigations increased the corneal ulceration rate from 6 to 40 percent (McCulley et al, 1983) 1990). Other animal studies suggest that irrigation with 1 percent calcium gluconate solution did not have any significant advantage over saline irrigation and topical treatment only following ocular exposure to 2 percent HF (Beiran et al, 1986).
    3) Monitor eye fluid pH with litmus paper and continue irrigation until ocular pH is in the normal range. The patient should be evaluated by an ophthalmologist following appropriate decontamination (Grant, 1986).
    4) Equivocal results have been reported after immediate copious washing of the eyes, followed by application of ice packs until arrival at a health care facility, then irrigation with 1 percent calcium gluconate for 5 to 10 minutes, and instillation of 1 percent calcium gluconate drops every 2 to 3 hours for 2 to 3 days (Trevino et al, 1983).
    5) Bentur et al (1993) report the case of 33-year-old man who splashed 49 percent HF into his eye. Treatment consisted of immediate flushing with water by the patient followed by further flushing with water for 10 minutes at the worksite and with 1 liter of normal saline 50 minutes later in the emergency department.
    a) Examination at that time revealed chemotic and hyperemic conjunctiva and sloughing of nearly all of the corneal epithelium. The patient was treated with 1 percent calcium gluconate drops (3 drops every 3 hours for 2 days), topical cycloplegia and antibiotics and a mild pressure patch. The epithelial defect healed over the next 4 days and eye exam was normal at 3 months.
    B) EXPERIMENTAL THERAPY
    1) ANIMAL STUDIES - Various eye treatments were tried on animals to determine the most effective method to bind the fluoride ion.
    a) Subconjunctival injection of calcium gluconate is too toxic to the eye.
    b) Injections of isotonic CaCl2, or mixtures of the most common divalent cations of the cornea cause further injury.
    c) Topical ointments of magnesium or magnesium sulfate, irrigation with 0.2 percent hyamine (0.2 percent benzenethonium chloride) or 0.05 percent Zephiran and isotonic CaCl2 were all toxic to the eye.
    C) Treatment should include recommendations listed in the ORAL EXPOSURE section when appropriate.

Dermal Exposure

    6.9.1) DECONTAMINATION
    A) DERMAL DECONTAMINATION
    1) Remove all exposed clothing and jewelry taking necessary precautions to prevent secondary exposure to health care providers (i.e., wear protective clothing, gloves, etc). Irrigate all exposed areas promptly with copious amounts of water or crystalloid solution (lactated ringer's or normal saline) for at least 30 minutes. Carefully evaluate for eye damage; exposure to dilute solutions may result in delayed signs and symptoms of ocular damage. The patient should be evaluated by an ophthalmologist following appropriate decontamination.
    6.9.2) TREATMENT
    A) SKIN FINDING
    1) DERMAL DECONTAMINATION
    a) Exposure to dilute solutions (6 percent to 11 percent) hydrofluoric acid is best treated by immediately washing all exposed areas with copious amounts of water or crystalloid solution (lactated ringer's or normal saline) for at least 30 minutes while removing all potentially contaminated clothing and jewelry. Take necessary precautions to prevent secondary exposure to health care providers. Carefully evaluate for ocular damage when dermal exposure involves the face.
    b) Exposure to dilute HF solutions may result in delayed signs and symptoms of ocular damage. If ocular exposure has occurred, the patient should be evaluated by an ophthalmologist after appropriate decontamination. Calcium gluconate or calcium carbonate gel applied topically to the affected area has been associated with relief of pain at the site of exposure. Systemic toxicity or severe tissue damage is unlikely to occur with small surface area exposures to dilute solutions. Aggressive therapy with calcium gluconate infiltration or calcium gluconate arterial perfusion are not likely to be necessary and may increase tissue damage.
    2) DERMAL ABSORPTION
    a) Dermal exposure to HF can produce hypocalcemia, hypomagnesemia, hyperkalemia, cardiac dysrhythmias, and death (Tepperman, 1980; Proctor et al, 1988; Yamaura et al, 1997).
    B) HYPERKALEMIA
    1) Fluoride-induced hyperkalemia, once developed, may be irreversible. Therapeutic intervention to prevent development of elevated serum potassium is essential. Note: the beta-adrenergic receptor and the calcium channel do NOT appear to have major roles in fluoride-induced hyperkalemia. Early aggressive therapy with glucose, insulin and/or sodium bicarbonate prior to the development of hyperkalemia was ineffective in dog studies; however, quinidine was shown effective in preventing the K+ efflux from cells and preventing cardiotoxicity in fluoride-toxic dogs. Therapeutic doses of other antidysrhythmics, such as lidocaine, were not effective. Propranolol worsened fluoride-induced cardiotoxicity (Cummings & McIvor, 1988; McIvor & Cummings, 1987).
    2) Death is usually the result of delayed sudden cardiovascular collapse with ventricular fibrillation triggered by electrolyte abnormalities (hypocalcemia, hypomagnesemia, hyperkalemia). If sudden death is avoided in the first 24 hours, prognosis is good, although recovery may be prolonged. In dog studies, increase in serum potassium levels began at approximately 2 hours post-exposure and began to rise exponentially at 6 hours post-exposure. Maintain normal or alkalotic pH. Cation exchange resins or dialysis may be the only effective means in which to reverse fluoride-induced hyperkalemia (Cummings & McIvor, 1988; McIvor & Cummings, 1987; McIvor, 1988).
    C) HYPOCALCEMIA
    1) Correct known or suspected hypocalcemia with intravenous CALCIUM CHLORIDE (10 percent SOLUTION): ADULT: 2 to 4 mg/kg (0.02 to 0.04 mL/kg) with repeat doses as necessary. PEDIATRIC: 10 to 30 mg/kg (0.1 to 0.3 mL/kg) infused slowly with repeat doses as necessary. Ideally, repeat doses should be based on measured deficits of ionized calcium. CALCIUM GLUCONATE (10 percent solution) may also be used but the dose is 3 times the amount of the dose for calcium chloride.
    2) It may be necessary to exceed the manufacturer's recommended rate of administration to correct hypocalcemia (Manoguerra & Neuman, 1986).
    3) Doses of up to 113 milliequivalents of calcium have been used to successfully treat hydrofluoric acid burns. A dose of 266.7 milliequivalents used in one case resulted in hypercalcemia (Greco et al, 1988).
    4) Monitor ECG continuously and serial calcium, magnesium, and potassium levels at least hourly during therapy. Suspect hypocalcemia and/or hypomagnesemia if QTc interval is prolonged.
    5) Treat aggressively with intravenous calcium in the presence of any ECG or clinical signs of hypocalcemia while serum calcium levels are pending. Serum levels should be obtained as soon as possible to monitor calcium therapy.
    D) HYPOMAGNESEMIA
    1) Hypomagnesemia may develop after dermal exposure or ingestion and has been associated with QTc prolongation, ventricular dysrhythmias and death.
    2) Correct known and suspected hypomagnesemia with intravenous magnesium sulfate
    3) MAGNESIUM SULFATE DOSE
    a) ADULT: 1 to 2 g diluted in 250 mL D5W or NS and infused IV, may be repeated as necessary.
    b) PEDIATRIC: 25 to 50 mg/kg IV infusion over 30 to 60 minutes; repeat dose as necessary; max 2 g/dose (Kleinman et al, 2010; Manrique et al, 2010; Haque & Saleem, 2009)
    4) Serial evaluation of the patient's knee jerk reflex is the most important and reliable guide to magnesium treatment. Serum magnesium levels are not a reliable indicator for what is a "therapeutic level". Patient should be monitored with ECG continuously.
    E) VENTRICULAR ARRHYTHMIA
    1) Evaluate for and treat hypocalcemia, hypomagnesemia and hyperkalemia. Because amiodarone has potassium channel blocking effects, it may be the preferred antidysrhythmic in the setting of hydrofluoric acid poisoning.
    2) AMIODARONE
    a) AMIODARONE/INDICATIONS
    1) Effective for the control of hemodynamically stable monomorphic ventricular tachycardia. Also recommended for pulseless ventricular tachycardia or ventricular fibrillation in cardiac arrest unresponsive to CPR, defibrillation and vasopressor therapy (Link et al, 2015; Neumar et al, 2010). It should be used with caution when the ingestion involves agents known to cause QTc prolongation, such as fluoroquinolones, macrolide antibiotics or azoles, and when ECG reveals QT prolongation suspected to be secondary to overdose (Prod Info Cordarone(R) oral tablets, 2015).
    b) AMIODARONE/ADULT DOSE
    1) For ventricular fibrillation or pulseless VT unresponsive to CPR, defibrillation, and a vasopressor therapy give an initial dose of 300 mg IV followed by 1 dose of 150 mg IV. For stable ventricular tachycardias: Infuse 150 milligrams over 10 minutes, and repeat if necessary. Follow by a 1 milligram/minute infusion for 6 hours, then a 0.5 milligram/minute. Maximum total dose over 24 hours is 2.2 grams (Neumar et al, 2010).
    c) AMIODARONE/PEDIATRIC DOSE
    1) Infuse 5 milligrams/kilogram as a bolus for pulseless ventricular tachycardia or ventricular fibrillation; may repeat twice up to 15 mg/kg. Infuse 5 milligrams/kilogram over 20 to 60 minutes for perfusing tachycardias. Maximum single dose is 300 mg. Routine use with other drugs that prolong the QT interval is NOT recommended (Kleinman et al, 2010).
    d) ADVERSE EFFECTS
    1) Hypotension and bradycardia are the most common adverse effects (Neumar et al, 2010).
    F) DRUG THERAPY
    1) CALCIUM GEL
    a) SUMMARY
    1) Various topical calcium preparations have been used anecdotally for treatment of exposure to HF solutions of less than 20 percent. Concentrations of calcium gluconate or calcium carbonate range from 2.5 to 33 percent. There are no studies comparing relative efficacy among different concentrations of gel.
    2) The less viscous gel form may be more practical for application to large surface areas, while the concentrated slurry may be more appropriate for smaller areas such as hands or fingers. Topical application of a 2.5% calcium gluconate gel is easier to perform and less painful than infiltration (Brown, 1974; Trevino et al, 1983; El Saadi et al, 1989; Asvesti et al, 1997). Murao (1989) demonstrated in rats dermally exposed to 20% hydrofluoric acid, that irrigation of the affected skin with running water for 10 minutes followed by application of 2.5% calcium gluconate jelly was an effective therapy for reducing fluoride concentrations in urine and tissues surrounding the injured region.
    3) TECHNIQUE
    a) After copious irrigation with water, the gel is typically massaged into the affected area until the pain has subsided for 15 minutes. It must have access to the burn, so cloth or thick necrotic coagulum should be removed. The earlier the initiation of this therapy after exposure, the more rapid the resolution of symptoms may occur (El Saadi et al, 1989).
    b) For hand and/or finger burns, a thin layer of 32.5 percent calcium carbonate slurry was applied directly to the burned area, and 10 milliliters were placed in a surgical glove into which the affected hand was placed. Patients moved or massaged the hand periodically and the glove was changed at 4 hours and again at 8 hours if pain persisted (Chick & Borah, 1990).
    4) COMMERCIAL PRODUCTS AVAILABLE
    a) A commercial gel, "H-F Antidote Gel" is available from Moore & Company, Ltd. Rippleside Commercial Estate, Renwick Rd, Barking, Essex, IG11 05D, England. Also, a 2.5 percent by weight calcium gluconate gel and jelly are available OTC in 25 gram tubes from Pharmascience Inc., Montreal, Quebec (514-340-1114), sold under the name "H-F Antidote Gel".
    b) EXTEMPORANEOUS PREPARATION
    1) CALCIUM GLUCONATE POWDER (METHOD 1) - Add 3.5 grams of calcium gluconate USP to a 5 ounce tube of water-soluble surgical lubricant, such as K-Y Jelly(R). Other soluble calcium salts (such as calcium lactate) may theoretically be substituted for the gluconate salt, but no data exist on use of these salts. Calcium chloride is NOT recommended due to its potential for irritation. IF CALCIUM GLUCONATE POWDER IS NOT AVAILABLE, PREPARE GEL FROM CALCIUM CARBONATE TABLETS AS DIRECTED UNDER METHOD 3.
    2) CALCIUM GLUCONATE POWDER (METHOD 2) - Dissolve 2.5 grams calcium gluconate in 91.25 milliliters of water, heating the water if necessary. Let cool to room temperature. Add 0.25 gram chlorhexidine gluconate and stir. Make a slurry in a separate container of hydroxyethyl cellulose 2 grams and isopropyl alcohol 4 milliliters, and stir. Add slurry to calcium solution, stirring vigorously until a thick gel has formed. Leave overnight before packing (EAPCC, 1987).
    3) CALCIUM CARBONATE TABLETS (METHOD 3) - A 32.5 percent slurry used for treatment of hand or finger burns can be prepared by triturating ten (10 grain) tablets into a fine powder and adding to 20 milliliters of a water-soluble lubricant gel, such as K-Y Jelly(R) (Chick & Borah, 1990). Another method is to gradually add the calcium carbonate powder to K-Y Jelly(R) until a spreadable gel is produced.
    4) CALCIUM GLUCONATE SOLUTION (METHOD 4) - A gel consisting of equal parts of dimethyl sulfoxide and a 10 percent calcium gluconate solution for injection was shown to enhance percutaneous calcium ion absorption in rat skin (Zachary et al, 1986). Cornstarch, methyl cellulose, or other inert thickeners, may be added in order to produce a spreadable gel.
    5) Higher concentrations of calcium gluconate solutions (up to 33 percent) may be used for more serious burns.
    6) HEXAFLUORINE
    a) A newer compound, Hexafluorine, was developed in France for decontamination of HF eye and skin exposures. In a rat study, a 50% HF solution was applied to the shaved backs of rats via a soaked filter paper. After 30 sec, the animals were either rinsed with 500 mL Hexafluorine over a 3 min period, or rinsed with water followed by calcium gluconate 2.5% gel, or rinsed with water only, or given no treatment. A consistent trend toward poorer results with Hexafluorine was observed (Hojer et al, 2002).
    b) EFFICACY
    1) CASE SERIES - A calcium carbonate 32.5 percent slurry was effective in relieving pain within 4 to 6 hours in 8 of 9 patients with hydrofluoric acid hand or finger burns. It was unsuccessful in one patient who did not present until 24 hours after exposure (Chick & Borah, 1990).
    2) ANIMAL STUDY - In a rat model, animals treated with calcium gluconate gel developed a less serious burn than animals treated with benzalkonium chloride, A & D ointment, aloe gel, or magnesium ointment (Bracken et al, 1985).
    3) ANIMAL STUDY - In a rabbit model, calcium gluconate gel was the most effective in preventing severe skin damage. Aluminum and magnesium hydroxide tablets, crushed and mixed with a water-soluble lubricant gel, was also somewhat effective. Magnesium gluconate was no better than control vehicle (Burkhart et al, 1992; Burkhart et al, 1994).
    4) CALCIUM CHLORIDE IS NOT RECOMMENDED BASED ON ITS POTENTIAL FOR IRRITATION.
    5) INTRAVENOUS CALCIUM/MAGNESIUM PERFUSION
    a) Regional intravenous infusion of calcium gluconate, using a technique similar to the Bier block, is a therapeutic option if HF burns of forearm, hand, or digits as adjunct to topical therapy or if topical therapy is unsatisfactory (Graundins et al, 1997; Ryan et al, 1997; Henry & Hla, 1992; Isbister, 2000).
    b) An intravenous cannula is inserted into a vein in the dorsum of the affected hand. The superficial veins of the extremity are exsanguinated by raising the arm for about 5 minutes. This can also be accomplished by application of an Esmarch bandage. When exsanguination is complete the sphygmomanometer cuff is inflated to just above the systolic blood pressure to prevent the arm refilling with blood. The arm is then lowered or the Esmarch bandage removed. Ten to 20 milliliters of 10 percent calcium gluconate solution diluted to 30 to 40 mL with 0.9 percent saline solution is infused. Ischemia is maintained for 25 to 30 minutes; the blood pressure cuff is then sequentially released over 5 minutes.
    c) Intravenous therapy is considered successful if there is absence of pain and tenderness during the hour following treatment. Intraarterial calcium infusion should be considered in cases in which pain or tenderness persists at exposure sites.
    d) ANIMAL STUDY: Williams et al (1994) compared intravenous magnesium sulfate treatment with intradermal calcium gluconate treatment in HF-burned rats.
    e) Rats treated with magnesium sulfate (80 milligrams/kilogram) experienced fewer severe burns (1 of 11 surviving rats; 1 died) than controls (4 of 8 surviving rats; 5 died) or those treated with intradermal calcium (7 of 9 surviving rats; 1 died).
    f) Intravenous magnesium sulfate (0.2 milliequivalent bolus over 2 minutes, followed by 0.2 milliequivalents per kilogram per hour for 4 hours) diminished burn scars and lessening healing time in rabbits with HF burns (Cox & Osgood, 1994). Calcium gluconate infiltration (0.5 ml of 10 percent solution) was as effective in diminishing burn scars and healing time in this model.
    g) ARTERIAL CALCIUM PERFUSION
    1) Intraarterial calcium infusion for digital HF burn is also a therapeutic option and should be considered if regional intravenous calcium gluconate is ineffective. This method should be used on severe distal extremity burns by those physicians who are comfortable with the technique and have experience in the treatment of HF burns (Isbister, 2000).
    2) Several studies have evaluated arterial perfusion of 10 to 20 percent calcium salt (CALCIUM GLUCONATE or CALCIUM CHLORIDE) solutions to treat distal upper extremity HF burns (Kohnlein & Achinger, 1982; Velvart, 1983; Vance et al, 1986; Siegel & Heard, 1992). Intra-arterial infusion should be continued until pain does not recur (Tournoud et al, 1999). In general, pain relief was obtained and wound healing required 2 to 4 weeks.
    3) A long catheter is inserted percutaneously into the radial artery using standard aseptic technique. Intraarterial catheter placement is confirmed by pressure transducer and oscilloscope. If the burn involves only the thumb, index, or long fingers, the catheter is advanced only a few centimeters proximally in preparation for digital subtraction arteriography. If the burn involves the ring or small fingers, the catheter is advanced proximally into the brachial artery because access to the ulnar circulation is necessary.
    4) Following satisfactory placement of the arterial line, digital subtraction arteriography is performed to identify the origin of vascular supply to digits involved. Once the tip of the catheter is in the desired location, a dilute preparation of calcium salts (10 mL of a 10% solution mixed in 40 to 50 mL 5% dextrose) is infused with a pump apparatus into the catheter over 4 hours. Generally, calcium gluconate is used, although calcium chloride may be used in a similar manner. The patient should be observed closely during the infusion period for progression of symptoms and potential complications of the procedure, such as alterations of distal vascular supply.
    5) Following the 4 hour infusion, the arterial line is maintained in place in the usual manner while the patient undergoes an observation period. If typical HF pain returns within 4 hours, a second calcium infusion is repeated. This cycle is repeated until the patient is pain free 4 hours following completion of the calcium infusion.
    6) EFFICACY - The efficacy of this method is difficult to determine since adequate controls were absent in all reports. This technique avoids the painful injections and nail removal required with infiltration therapy. It is able to deliver more calcium ions to the injured tissue. It has not been proven to give superior results to the infiltration technique, however, and requires an invasive vascular procedure, an infusion pump, and hospital admission.
    7) COMPLICATIONS associated with intraarterial calcium infusion, include transient ulnar nerve palsy (believed due to the armboard used for infusion), and median nerve palsy from to hematomas from multiple arterial punctures (Siegal & Heard, 1992).
    8) Continued tissue destruction and associated pain (due to penetration of free fluoride ion into affected tissue) may be minimized by subcutaneous administration of CALCIUM GLUCONATE to form an insoluble (inactive) fluoride salt (Blunt, 1964). This procedure is NOT recommended for digital areas (fingers or toes) unless the physician is experienced with the technique, due to potential for tissue injury from increased pressure.
    9) CALCIUM CHLORIDE should NOT be used because it is irritating and may cause tissue injury.
    10) INDICATIONS - Local infiltration with CALCIUM GLUCONATE may be considered if (1) HF exposure results in immediate tissue damage or (2) erythema and pain persist following adequate irrigation (NOTE: Pain and erythema may be delayed up to 24 hours post exposure depending on the concentration of HF).
    11) Infiltrate each square centimeter of the affected (painful) dermis and subcutaneous tissue with about 0.5 milliliter of 10% CALCIUM GLUCONATE using a 30 gauge needle. Repeat as needed to control pain (Matsuno, 1996).
    12) CAUTION - Avoid administering large volumes of subcutaneous CALCIUM GLUCONATE, as this will result in decreased tissue perfusion and potential necrosis. Exposure of subungual tissue to concentrated hydrofluoric acid often necessitates removal of the nail in order to adequately decontaminate the nailbed and relieve pain (Mayer & Guenlich,1963; Wetherhold & Shepherd, 1965; Dibbell et al, 1970).
    13) IONTOPHORETIC CALCIUM
    a) ANIMAL STUDY - Following experimental 50% HF burns to the nude backs of rats, one group of rats was treated with iontophoresis of calcium chloride with constant voltage at 1.5V and electric current at 20-30 microamps at first, then increased to 100-120 microamps within 5 minutes; total treatment, 30 minutes. Burn areas of this group were reduced significantly when compared to untreated rats, rats treated with calcium gluconate jelly and rats treated with intradermal and subcutaneous calcium gluconate injections. Transdermal transport of calcium appeared to be enhanced in stripped skins by iontophoresis. No adverse effects were observed in normal skins. Limitations of iontophoretic treatment include number of lesions that can be treated simultaneously and size of the lesion (patches are small and unable to cover large areas). Use of iontophoretic delivery of calcium in humans is currently not recommended (Yamashita et al, 2001).
    b) MAGNESIUM
    1) Harris et al (1981) evaluated the efficacy of subcutaneous and intradermal injections of magnesium salts (10% acetate and sulfate) in rats dermally exposed to HF. In this study, the magnesium salts effectively minimized the depth and progression of the HF burn but further studies are needed before these salts can be routinely recommended.
    2) Burkhart et al (1992) found that magnesium gluconate in water soluble lubricant gel (K-Y Jelly(R)) was less effective than calcium gluconate in preventing deep layer skin damage in HF-exposed rabbit skin.
    3) QUATERNARY AMMONIUM SALTS
    a) Soaking the burn in a quaternary ammonium compound solution has been recommended (Wetherhold & Shepherd, 1965; Reinhart et al, 1966), and although successful it is uncomfortable to the patient and difficult to use in awkward or large areas.
    b) In a porcine model of hydrofluoric acid burns topical application of iced benzalkonium chloride (17%) was more effective than topical calcium gluconate gel (2.5%), calcium gluconate injections (5% or 10%), topical calcium acetate (10%) soaks, or benzethonium chloride soaks in reducing the gross size and severity of skin lesions produced after a 9 minute exposure to 38% hydrofluoric acid (Dunn et al, 1992). Calcium acetate soaks (10%) were most effective in reducing the gross size and severity of lesions produced after 15 minutes exposure to 38 percent hydrofluoric acid.
    c) In the same study benzalkonium chloride (17%) soaks, calcium acetate (10%) soaks, calcium gluconate gel (2.5%), and calcium gluconate injection (5%) were all effective in reducing the histologic severity of injury, while benzethonium chloride soaks were less effective and 10% calcium gluconate injection increased the severity of injury (Dunn et al, 1992).
    d) IODINE PREPARATIONS
    1) ANIMAL STUDY - In an animal study, it was determined that postexposure treatment with an iodine ointment was efficacious upon hydrofluoric acid-induced skin burns. Statistically significant reductions of 76% and 68% in ulceration areas were noted at intervals of 5 and 10 minutes between exposure and treatment; however, a weaker effect was observed at a longer time interval of 15 minutes (a 56% reduction in the ulceration area). It was speculated that the protective effect of iodine may be derived from its ability to inhibit apoptosis or proteinase activity crucial for the evoluation of skin damage. The authors suggested the therapeutic usage of these iodine preparations for hydrofluoric acid-induced skin burns (Wormser et al, 2002).
    G) EXCISION
    1) SURGICAL THERAPY
    a) In patients with extensive skin damage over a small surface area and refractory hypocalcemia, immediate excision of the affected skin may be indicated. Packing the wound with benzalkonium chloride solution until calcium status is stable, followed by split-thickness skin grafting, has been recommended (Buckingham, 1988).
    b) In patients without refractory hypocalcemia, immediate excision is not recommended unless necrotic tissue necessitates debridement. A conservative initial approach with local calcium injections has been suggested (Craig, 1964).
    H) NAIL DAMAGE
    1) FINGERNAIL REMOVAL
    a) Exposure of the subungual (nailbed) tissue to HF is particularly painful and difficult to decontaminate. Nail removal is probably not necessary for exposures to concentrations of less than 10%; more concentrated solutions may produce tissue necrosis. The nail plate can be split, lifted, or totally removed in cases of severe exposure to facilitate decontamination and calcium therapy (Roberts et al, 1989). This disfiguring procedure may not be necessary when regional intravenous or intraarterial calcium salt treatment is initiated in a timely manner.
    I) Treatment should include recommendations listed in the ORAL EXPOSURE section when appropriate.

Range Of Toxicity

Summary

    A) Median lethal doses for the similar compound, cyanuric chloride, were 350 mg/kg in mice and 485 mg/kg in rats.
    B) The irritant threshold for fumes of the similar compound, cyanuric chloride, in humans was 0.3 mg/m(3) for a one-minute exposure.
    C) Application of 200 mg of the similar compound, cyanuric chloride, caused skin irritation in rabbits, followed by ulceration with repeated exposures. A dose of 3000 mg of cyanuric chloride applied to rabbit skin caused no deaths, although severe irritation developed.
    D) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals. Subacute feedings of 37 mg/kg per day of cyanuric chloride for 5 weeks caused no ill effects in rabbits. No effects were seen in rats fed 20 mg/kg of cyanuric chloride for 30 days; a reduced weight gain was seen at doses of 100 and 500 mg/kg daily.

Minimum Lethal Exposure

    A) GENERAL/SUMMARY
    1) At the time of this review, no specific information on the minimun lethal exposure to cyanuric fluoride was found in available references.
    B) ANIMAL DATA
    1) Median lethal doses for the similar compound, cyanuric chloride, were 350 milligrams/kilogram in mice and 485 milligrams/kilogram in rats (Blagodatin, 1968).
    2) Inhalation of dust by rats from the similar compound, cyanuric chloride, at a concentration of 1.88 milligrams/cubic meter 4 hours daily for 2 and 1/2 months caused a 30 percent fatality rate, with respiratory tract irritation and liver and kidney injury in the survivors (CHEMINFO , 1990).

Maximum Tolerated Exposure

    A) GENERAL/SUMMARY
    1) At the time of this review, no specific information on the maximum tolerated exposure to cyanuric fluoride was found in available references.
    2) The irritant threshold for fumes of the similar compound, cyanuric chloride, in humans was 0.3 milligrams/cubic meter for a one-minute exposure (Blagodatin, 1968).
    B) ANIMAL DATA
    1) Application of 200 milligrams of the similar compound, cyanuric chloride, caused skin irritation in rabbits, followed by ulceration with repeated exposures (Blagodatin, 1968).
    2) A dose of 3000 milligrams of cyanuric chloride applied to rabbit skin caused no deaths, although severe irritation developed (CHEMINFO , 1990).
    3) The similar compound, cyanuric chloride, caused corrosive damage to the gastrointestinal tract when fed at high doses to experimental animals (HSDB, 1999).
    4) Subacute feedings of 37 milligrams/kilogram per day of cyanuric chloride for 5 weeks caused no ill effects in rabbits (HSDB, 1999; (CHEMINFO , 1990).
    5) No effects were seen in rats fed 20 milligrams/kilogram of cyanuric chloride for 30 days; a reduced weight gain was seen at doses of 100 and 500 milligrams/kilogram daily (CHEMINFO , 1990).

Workplace Standards

    A) ACGIH TLV Values for CAS675-14-9 (American Conference of Governmental Industrial Hygienists, 2010):
    1) Not Listed

    B) NIOSH REL and IDLH Values for CAS675-14-9 (National Institute for Occupational Safety and Health, 2007):
    1) Not Listed

    C) Carcinogenicity Ratings for CAS675-14-9 :
    1) ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed
    2) EPA (U.S. Environmental Protection Agency, 2011): Not Listed
    3) IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed
    4) NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed
    5) MAK (DFG, 2002): Not Listed
    6) NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed

    D) OSHA PEL Values for CAS675-14-9 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
    1) Not Listed

Toxicity Information

    7.7.1) TOXICITY VALUES
    A) References: RTECS, 2004; Lewis, 1996 EPA, 1985

Physicochemical

Physical Characteristics

    A) Liquid (EPA, 2003)

Molecular Weight

    A) 135.06 (Lewis, 1996)

References

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