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CARBONYL FLUORIDE

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Classification   |    Detailed evidence-based information

Substances Included Synonyms

Therapeutic Toxic Class

    A) Carbonyl fluoride is a fluorophosgene compound.

Specific Substances

    A) No Synonyms were found in group or single elements
    1.2.1) MOLECULAR FORMULA
    1) C-F2-O

Available Forms Sources

    A) USES
    1) Carbonyl fluoride is a chemical intermediate used in organic synthesis. It is a significant source of exposure in the thermal decomposition of fluoropolymers(ACGIH, 2001).

Overview

Life Support

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

Clinical Effects

    0.2.1) SUMMARY OF EXPOSURE
    A) Human toxicity data are minimal, but exposures to high concentrations would be expected to cause strong irritation or burns to eyes, lungs, skin, and mucous membranes.
    B) This gas readily hydrolyzes to form hydrogen fluoride and carbon dioxide. Refer to the medical management on HYDROGEN FLUORIDE exposure for more information.
    0.2.4) HEENT
    A) This substance is corrosive. Carbonyl fluoride gas and vapors are extremely irritating to the mucous membranes of the eyes, nose, throat, and mouth.
    0.2.5) CARDIOVASCULAR
    A) Chest pain may occur.
    0.2.6) RESPIRATORY
    A) Shortness of breath, respiratory irritation, bronchitis, and pulmonary edema may occur.
    0.2.7) NEUROLOGIC
    A) Extreme malaise and weakness may precede death.
    0.2.9) HEPATIC
    A) Enlarged nuclei and fatty infiltration have been seen in experimental animals.
    0.2.10) GENITOURINARY
    A) Glucose, protein, ketones, occult blood, and increased urinary fluoride levels may occur.
    0.2.14) DERMATOLOGIC
    A) Skin irritation may be present.
    0.2.20) REPRODUCTIVE
    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.
    B) At the time of this review, no data were available to assess the teratogenic potential of this agent.
    0.2.21) CARCINOGENICITY
    A) At the time of this review, no data were available to assess the carcinogenic potential of this agent.
    0.2.22) OTHER
    A) Carbonyl fluoride is highly corrosive to skin and mucous membranes. Hydrogen fluoride is corrosive in high concentrations. Exposure can result in pneumonitis, eye damage, gastrointestinal erosion, and severe burns.
    1) Refer to the medical management on HYDROGEN FLUORIDE for more information.

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) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Rule out corrosive GI tract injury with GI consult and endoscopy. Evaluate for and correct hypocalcemia, hypomagnesemia.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) Systemic toxicity with severe hypocalcemia, hypomagnesemia, acidosis and ventricular dysrhythmia can develop after ingestion or rectal instillation of small amounts, after inhalation, or after dermal exposure to large surface areas or high concentration products. Begin appropriate respiratory and hemodynamic support for critically ill patients. The mainstays of therapy are aggressive correction of hypocalcemia, treatment of hypomagnesemia and avoidance of acidosis. Give empiric calcium. Maintain serum calcium levels in high-normal range. Give appropriate analgesia. If sudden death is avoided in the first 24 hours, prognosis is good; although recovery may be prolonged. Treat patients with dysrhythmias or hypotension with calcium chloride (via central line or large bore catheter) and sodium bicarbonate 1 to 2 mEq/kg IV to serum pH of 7.5. In cases of cardiac arrest, give calcium chloride 3 to 5 g IV bolus and sodium bicarbonate 1 to 2 mEq/kg IV to serum pH of 7.5, vasopressors and defibrillation in addition to advanced cardiac life support measures.
    2) INGESTION: Large amounts of oral calcium and/or IV calcium chloride immediately. Administer sufficient intravenous calcium to maintain serum calcium levels at high-normal. Patients also may require magnesium supplementation. Animal models suggest that acidemia may worsen prognosis.
    C) DECONTAMINATION
    1) PREHOSPITAL: For ingestions, immediately give a substance containing calcium (milk, calcium carbonate antacids) or magnesium (magnesium containing antacids or laxatives). No activated charcoal. Do NOT induce emesis.
    2) HOSPITAL: No activated charcoal. If very recent ingestion of large volume, aspirate with soft nasogastric tube and then instill calcium or magnesium solutions (ie, antacids, laxatives).
    D) AIRWAY MANAGEMENT
    1) Perform early in patients with severe intoxication after ingestion or inhalation.
    E) ANTIDOTE
    1) Calcium in high doses (calcium gluconate or chloride) binds the fluoride atoms to avert tissue injury and systemic fluorosis.
    F) HYPOCALCEMIA
    1) Administer calcium empirically to any patient with a potentially severe exposure while awaiting laboratory results. Monitor serum calcium. Repeat calcium replenishment as needed to maintain calcium concentrations in the high-normal range. CALCIUM CHLORIDE: ADULT DOSE: 1 g (10 mL of 10% solution) IV infused over 5 minutes; may repeat after 10 minutes. PEDIATRIC DOSE: 10 to 25 mg/kg (0.1 to 0.25 mL/kg) per dose up to a maximum single dose of 5 mL (500 mg) IV infused over 5 minutes; may repeat after 10 minutes. Treat patients with dysrhythmias or hypotension with calcium chloride and sodium bicarbonate 1 to 2 mEq/kg IV to a serum pH of 7.5.
    G) HYPOMAGNESEMIA
    1) Correct known and suspected hypomagnesemia with intravenous magnesium sulfate. DOSE: ADULT: 1 to 2 g diluted in 250 mL D5W or NS infused IV, may be repeated as necessary. PEDIATRIC: 25 to 50 mg/kg IV infusion over 30 to 60 minutes; repeat dose as necessary; max 2 g/dose. Monitor serum magnesium. Repeat as needed.
    H) CARDIAC ARREST
    1) Advanced cardiac life support measures. Give calcium chloride 3 to 5 g IV bolus and sodium bicarbonate 1 to 2 mEq/kg IV to a serum pH of 7.5, vasopressors and defibrillation.
    I) ENHANCED ELIMINATION
    1) Fluoride is removed by dialysis, but patients with severe toxicity will likely be hemodynamically unstable.
    0.4.3) INHALATION EXPOSURE
    A) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Supportive care, nebulized bronchodilators, and give calcium gluconate nebulizer treatments.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) Calcium gluconate 2.5 to 5% nebulizer treatments. Nebulized beta agonists for bronchospasm, humidified oxygen. Intravenous calcium if systemic toxicity or hypocalcemia develop.
    C) DECONTAMINATION
    1) PREHOSPITAL: Remove from inhalation source and administer oxygen.
    2) HOSPITAL: Administer 100% 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) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Normal saline eye irrigation (NOT calcium solution). Give analgesia.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) Irrigate eyes with copious amounts of normal saline; NOT a calcium solution. Slit lamp exam and ophthalmology consult.
    C) DECONTAMINATION
    1) PREHOSPITAL: Irrigate eyes with copious saline or water.
    2) HOSPITAL: Irrigate exposed eyes with normal saline. 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) MANAGEMENT OF MILD TO MODERATE TOXICITY
    a) Thoroughly irrigate skin immediately after exposure. Patients with early decontamination do well. Patients with pain should be treated with topical calcium therapy. TOPICAL: Treat with calcium gluconate or carbonate gel (1 g calcium gluconate in 40 g (about 40 mL) water-soluble lubricant = 2.5% gel; alternative is 10 10-g tablets crushed to fine powder + 20 mL water-soluble lubricant mixed into a slurry; apply thin coat to burn, then place hand in glove containing 10 mL slurry for 4 hours). SUBCUTANEOUS: Inject 0.5 mL/cm(2) with 10% calcium gluconate for topical treatment failures (not commonly used).
    b) Do not use calcium chloride for bier block procedures. Calcium chloride is irritating to the tissues and may cause injury.
    2) MANAGEMENT OF SEVERE TOXICITY
    a) Patients with pain not responding to topical calcium can be treated with regional venous or arterial perfusion. These methods are particularly effective for HF exposures involving the digits. BIER BLOCK: Inject IV 10 to 40 mL calcium gluconate in 50 mL normal saline for 20 minutes. ARTERIAL: 10 to 20 mL of 10% calcium gluconate in 50 mL D5W. Infuse over 4 hours via radial or brachial artery. The arterial catheter may be placed in normal position (not inverted).
    b) Do not use calcium chloride for bier block procedures. Calcium chloride is irritating to the tissues and may cause injury.
    3) DECONTAMINATION
    a) PREHOSPITAL: For dermal exposure, remove clothing and irrigate skin thoroughly with water.
    b) HOSPITAL: Irrigate exposed skin. 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.

Range Of Toxicity

    A) In animals, the toxicity has been shown to be about that of hydrogen fluoride.
    B) The TLV is 2 ppm.

Clinical Effects

Summary Of Exposure

    A) Human toxicity data are minimal, but exposures to high concentrations would be expected to cause strong irritation or burns to eyes, lungs, skin, and mucous membranes.
    B) This gas readily hydrolyzes to form hydrogen fluoride and carbon dioxide. Refer to the medical management on HYDROGEN FLUORIDE exposure for more information.

Heent

    3.4.1) SUMMARY
    A) This substance is corrosive. Carbonyl fluoride gas and vapors are extremely irritating to the mucous membranes of the eyes, nose, throat, and mouth.
    3.4.3) EYES
    A) IRRITATION - Carbonyl fluoride is a strong eye irritant (HSDB, 2004).
    3.4.5) NOSE
    A) IRRITATION - Carbonyl fluoride is a strong mucous membrane irritant (HSDB, 2004).
    3.4.6) THROAT
    A) IRRITATION - Carbonyl fluoride is a strong mucous membrane irritant (HSDB, 2004).
    B) DRYNESS - Dryness or a burning sensation of the throat may occur following slight gassing (CHRIS, 2004).

Cardiovascular

    3.5.1) SUMMARY
    A) Chest pain may occur.
    3.5.2) CLINICAL EFFECTS
    A) CHEST PAIN
    1) Chest pain may be present following exposure (CHRIS, 2004).

Respiratory

    3.6.1) SUMMARY
    A) Shortness of breath, respiratory irritation, bronchitis, and pulmonary edema may occur.
    3.6.2) CLINICAL EFFECTS
    A) RESPIRATORY SYMPTOM
    1) Seven patients were exposed to various chlorofluorocarbons (freons) and their thermal decomposition prodoucts. Decomposition products were thought to include carbonyl fluoride although air sampling was not conducted. Acute respiratory symptoms were present in all patients. Symptoms were mild and self-limited in 3 of the 7 patients. Cough, dyspnea, signs of reactive airway dysfunction syndrome, and pulmonary function changes lasted for several months to years in the other 4 patients(Piirila et al, 2003).
    B) ACUTE LUNG INJURY
    1) Rats were exposed to 310 ppm for 1 hour. At autopsy, the lungs showed focal hemorrhage and pulmonary edema(ACGIH, 2001).
    C) BRONCHITIS
    1) Bronchitis may occur following exposure (CHRIS, 2004).
    D) IRRITATION SYMPTOM
    1) Carbonyl fluoride is a strong irritant of the mucous membranes (Budavari, 1996; HSDB , 1993).
    E) DYSPNEA
    1) Shortness of breath may be present following exposure (CHRIS, 2004).

Neurologic

    3.7.1) SUMMARY
    A) Extreme malaise and weakness may precede death.
    3.7.2) CLINICAL EFFECTS
    A) MUSCLE WEAKNESS
    1) In experimental animals, death was preceded by extreme malaise and weakness (Anon, 1981).

Hepatic

    3.9.1) SUMMARY
    A) Enlarged nuclei and fatty infiltration have been seen in experimental animals.
    3.9.2) CLINICAL EFFECTS
    A) STEATOSIS OF LIVER
    1) FATTY INFILTRATION - Livers of rats exposed to sublethal doses of polytetrafluoroethylene and carbonyl fluoride had enlarged nuclei and fatty infiltration of the cells(ACGIH, 2001).

Genitourinary

    3.10.1) SUMMARY
    A) Glucose, protein, ketones, occult blood, and increased urinary fluoride levels may occur.
    3.10.2) CLINICAL EFFECTS
    A) ABNORMAL URINE
    1) In experimental animals exposed to sublethal doses of polytetrafluoroethylene and carbonyl fluoride, glucose, protein, ketones, and occult blood were detected in the urine(ACGIH, 2001).
    2) URINARY FLUORIDE - In rats given 32 ppm of carbonyl difluoride in 5 daily 1-hour exposures, urinary fluoride increased to 42 mg/L (HSDB, 2004).

Dermatologic

    3.14.1) SUMMARY
    A) Skin irritation may be present.
    3.14.2) CLINICAL EFFECTS
    A) SKIN IRRITATION
    1) Carbonyl fluoride is a strong skin irritant (Budavari, 1996; HSDB, 2004).

Reproductive

    3.20.1) SUMMARY
    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.
    B) At the time of this review, no data were available to assess the teratogenic potential of this agent.
    3.20.2) TERATOGENICITY
    A) LACK OF INFORMATION
    1) At the time of this review, no data were available to assess the teratogenic potential of this agent.
    3.20.3) EFFECTS IN PREGNANCY
    A) LACK OF INFORMATION
    1) 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 CAS353-50-4 (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) At the time of this review, no data were available to assess the carcinogenic potential of this agent.
    3.21.3) HUMAN STUDIES
    A) LACK OF INFORMATION
    1) At the time of this review, no data were available to assess the carcinogenic potential of this agent.

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) BLOOD/SERUM CHEMISTRY
    1) Significant exposures may result in liver or kidney damage, based on animal studies. Monitoring electrolytes, liver and kidney function may be beneficial in such exposures.
    4.1.4) OTHER
    A) OTHER
    1) MONITORING
    a) If respiratory tract irritation is present, monitor arterial blood gases and chest x-ray.
    2) ECG
    a) Obtain serial ECGs, looking for signs of hypocalcemia (prolonged QTc interval) and hyperkalemia (peaked T waves). Institute continuous cardiac monitoring.

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) PREHOSPITAL: For DERMAL exposure, remove clothing and irrigate skin thoroughly with water. Remove from INHALATION source and administer oxygen. Irrigate EYES with copious saline or water. For INGESTION, immediately give a substance containing calcium (milk, calcium carbonate antacids) or magnesium (magnesium containing antacids or laxatives). No activated charcoal. Do NOT induce emesis.
    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) 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) CALCIUM CHLORIDE
    a) ADULT DOSE: 1 g (10 mL of 10% solution) IV infused over 5 minutes; may repeat after 10 minutes (Jones & Flanagan, 2004; Saxena, 1989; Anon, 2000).
    b) PEDIATRIC DOSE: 10 to 25 mg/kg (0.1 to 0.25 mL/kg) per dose up to a maximum single dose of 5 mL (500 mg) IV infused over 5 minutes; may repeat after 10 minutes (Jones & Flanagan, 2004; Barkin, 1986; Anon, 2000).
    c) CALCIUM FOR INJECTION is available as three salts; calcium chloride, calcium gluconate, and calcium gluceptate.
    d) 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). However, other studies have suggested that hepatic metabolism may not be required for calcium gluconate (Martin et al, 1990).
    e) Calcium chloride is very irritating, and is ideally given via a central venous catheter. It may cause hypotension and bradycardia. Calcium salts are incompatible with bicarbonate (Chameides, 1988; Saxena, 1989; Anon, 2000).
    3) Monitor ECG continuously and at least hourly serial total or ionized calcium, magnesium, potassium levels during therapy. Suspect hypocalcemia and/or hypomagnesemia when QTc interval is prolonged.
    4) Treat aggressively with intravenous calcium in the presence of any ECG or clinical signs of hypocalcemia while serum calcium levels are pending.
    C) 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 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.
    D) 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 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 et al, 1987).
    2) CALCIUM CHLORIDE
    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) ADULT DOSE: 1 g (10 mL of 10% solution) IV infused over 5 minutes; may repeat after 10 minutes (Jones & Flanagan, 2004; Saxena, 1989; Anon, 2000).
    c) PEDIATRIC DOSE: 10 to 25 mg/kg (0.1 to 0.25 mL/kg) per dose up to a maximum single dose of 5 mL (500 mg) IV infused over 5 minutes; may repeat after 10 minutes (Jones & Flanagan, 2004; Barkin, 1986; Anon, 2000).
    d) CALCIUM FOR INJECTION is available as three salts; calcium chloride, calcium gluconate, and calcium gluceptate.
    e) 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). However, other studies have suggested that hepatic metabolism may not be required for calcium gluconate (Martin et al, 1990).
    f) Calcium chloride is very irritating, and is ideally given via a central venous catheter. It may cause hypotension and bradycardia. Calcium salts are incompatible with bicarbonate (Chameides, 1988; Saxena, 1989; Anon, 2000).
    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.
    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) 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.
    G) 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.
    H) 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% has been recommended (Trevino et al, 2001; Trevino et al, 1983; Tsonis et al, 2008).
    2) CASE SERIES - The use of calcium gluconate nebulization was reported in 13 workers exposed to 150 to 200 ppm 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 (Lee et al, 1993).
    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 - Five workers presented to the emergency department 4 hours after inhalation exposure to HF fumes. 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).
    5) CASE REPORT - A 52-year-old man with severe dyspnea from HF exposure was given 5% calcium gluconate solution via a nebulizer, and completely recovered by day 21 (Kono et al, 2000).
    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, 1983a).
    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 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, 1987).
    C) HYPOCALCEMIA
    1) Hypocalcemia in the absence of clinical tetany may occur following dermal exposure (Tepperman, 1980). Check patient for a positive Trousseau's or Chvostek's sign.
    2) MANAGEMENT OF MILD TO MODERATE TOXICITY
    a) Thoroughly irrigate skin immediately after exposure. Patients with early decontamination do well. Patients with pain should be treated with topical calcium therapy. TOPICAL: Treat with calcium gluconate or carbonate gel (1 g calcium gluconate in 40 g (about 40 mL) water-soluble lubricant = 2.5% gel; alternative is 10 10-g tablets crushed to fine powder + 20 mL water-soluble lubricant mixed into a slurry; apply thin coat to burn, then place hand in glove containing 10 mL slurry for 4 hours). SUBCUTANEOUS: Inject 0.5 mL/cm(2) with 10% calcium gluconate for topical treatment failures (not commonly used).
    b) Do not use calcium chloride for bier block procedures. Calcium chloride is irritating to the tissues and may cause injury.
    3) MANAGEMENT OF SEVERE TOXICITY
    a) Patients with pain not responding to topical calcium can be treated with regional venous or arterial perfusion. These methods are particularly effective for HF exposures involving the digits. BIER BLOCK: Inject IV 10 to 40 mL calcium gluconate in 50 mL normal saline for 20 minutes. ARTERIAL: 10 to 20 mL of 10% calcium gluconate in 50 mL D5W. Infuse over 4 hours via radial or brachial artery. The arterial catheter may be placed in normal position (not inverted).
    b) Do not use calcium chloride for bier block procedures. Calcium chloride is irritating to the tissues and may cause injury.
    4) Monitor ECG continuously and at least hourly serial total or ionized calcium, magnesium, potassium levels during therapy. Suspect hypocalcemia and/or hypomagnesemia when 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.
    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 magnesiu 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 nailplate 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) In animals, the toxicity has been shown to be about that of hydrogen fluoride.
    B) The TLV is 2 ppm.

Minimum Lethal Exposure

    A) GENERAL/SUMMARY
    1) The minimum lethal human dose to this agent has not been delineated.

Maximum Tolerated Exposure

    A) GENERAL/SUMMARY
    1) The maximum tolerated human exposure to this agent has not been delineated.
    B) ANIMAL DATA
    1) In animals, the toxicity has been shown to be about as much as hydrogen fluoride (ACGIH, 2001).
    2) There is a cumulative toxic effect on rats exposed to daily HF, a hydrolysis product of carbonyl fluoride (ACGIH, 1986).

Workplace Standards

    A) ACGIH TLV Values for CAS353-50-4 (American Conference of Governmental Industrial Hygienists, 2010):
    1) Editor's Note: The listed values are recommendations or guidelines developed by ACGIH(R) to assist in the control of health hazards. They should only be used, interpreted and applied by individuals trained in industrial hygiene. Before applying these values, it is imperative to read the introduction to each section in the current TLVs(R) and BEI(R) Book and become familiar with the constraints and limitations to their use. Always consult the Documentation of the TLVs(R) and BEIs(R) before applying these recommendations and guidelines.
    a) Adopted Value
    1) Carbonyl fluoride
    a) TLV:
    1) TLV-TWA: 2 ppm
    2) TLV-STEL: 5 ppm
    3) TLV-Ceiling:
    b) Notations and Endnotes:
    1) Carcinogenicity Category: Not Listed
    2) Codes: Not Listed
    3) Definitions: Not Listed
    c) TLV Basis - Critical Effect(s): LRT irr; bone dam
    d) Molecular Weight: 66.01
    1) For gases and vapors, to convert the TLV from ppm to mg/m(3):
    a) [(TLV in ppm)(gram molecular weight of substance)]/24.45
    2) For gases and vapors, to convert the TLV from mg/m(3) to ppm:
    a) [(TLV in mg/m(3))(24.45)]/gram molecular weight of substance
    e) Additional information:

    B) NIOSH REL and IDLH Values for CAS353-50-4 (National Institute for Occupational Safety and Health, 2007):
    1) Listed as: Carbonyl fluoride
    2) REL:
    a) TWA: 2 ppm (5 mg/m(3))
    b) STEL: 5 ppm (15 mg/m(3))
    c) Ceiling:
    d) Carcinogen Listing: (Not Listed) Not Listed
    e) Skin Designation: Not Listed
    f) Note(s):
    3) IDLH: Not Listed

    C) Carcinogenicity Ratings for CAS353-50-4 :
    1) ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Carbonyl fluoride
    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 ; Listed as: Carbonyl fluoride
    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 CAS353-50-4 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
    1) Not Listed

Toxicity Information

    7.7.1) TOXICITY VALUES

Pharmacology Toxicology

Toxicologic Mechanism

    A) Hydrogen fluoride is released by the hydrolysis of carbonyl fluoride and will inhibit succinic dehydrogenase in the kidney(ACGIH, 2001).

Physicochemical

Physical Characteristics

    A) Carbonyl fluoride is a colorless, hygroscopic gas or a light yellow compressed liquid with a sharp, pungent odor (AAR, 1987; Lewis, 2000; ITI, 1985; HSDB, 2004).
    1) Carbonyl fluoride is unstable in the presence of moisture or water, and hydrolyzes instantly to release hydrogen fluoride (ITI, 1985; Lewis, 2000; Budavari, 1996).
    2) Carbonyl fluoride is available in a technical grade of 97 mole percent minimum purity and a commercial grade of 100 percent purity (Sax & Lewis, 1987; CHRIS, 2004).

Molecular Weight

    A) 66.01

References

General Bibliography

    1) 40 CFR 372.28: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Lower thresholds for chemicals of special concern. National Archives and Records Administration (NARA) and the Government Printing Office (GPO). Washington, DC. Final rules current as of Apr 3, 2006.
    2) 40 CFR 372.65: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Chemicals and Chemical Categories to which this part applies. National Archives and Records Association (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Apr 3, 2006.
    3) 49 CFR 172.101 - App. B: Department of Transportation - Table of Hazardous Materials, Appendix B: List of Marine Pollutants. National Archives and Records Administration (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Aug 29, 2005.
    4) 49 CFR 172.101: Department of Transportation - Table of Hazardous Materials. National Archives and Records Administration (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Aug 11, 2005.
    5) 62 FR 58840: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 1997.
    6) 65 FR 14186: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
    7) 65 FR 39264: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
    8) 65 FR 77866: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
    9) 66 FR 21940: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2001.
    10) 67 FR 7164: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2002.
    11) 68 FR 42710: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2003.
    12) 69 FR 54144: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2004.
    13) AAR: Emergency Handling of Hazardous Material in Surface Transportation, Hazardous Materials Systems (BOE), Association of American Railroads, Washington, DC, 1987, pp 140.
    14) ACGIH: Documentation of the Threshold Limit Values and Biological Exposure Indices, 5th ed, Am Conference of Govt Ind Hyg, Inc, Cincinnati, OH, 1986.
    15) ACGIH: Documentation of the Threshold Limit Values and Biological Exposure Indices, 7th ed, Am Conference of Govt Ind Hyg, Inc, Cincinnati, OH, 2001.
    16) AIHA: 2006 Emergency Response Planning Guidelines and Workplace Environmental Exposure Level Guides Handbook, American Industrial Hygiene Association, Fairfax, VA, 2006.
    17) American Conference of Governmental Industrial Hygienists : ACGIH 2010 Threshold Limit Values (TLVs(R)) for Chemical Substances and Physical Agents and Biological Exposure Indices (BEIs(R)), American Conference of Governmental Industrial Hygienists, Cincinnati, OH, 2010.
    18) Anon: American Heart Association/International Liaison Committee on Resuscitation: Guidelines 2000 for Cardiopulmonary Resuscitation and emergency Cardiovascular Care: an international consensus on science. Circulation 2000; 102:I1-I384.
    19) Anon: Information Profiles on Potential Occupational Hazards: Carbonyl Fluoride, Center for Chemical Hazard Assessment, Syracuse Research Corporation, Arlington, VA, 1981.
    20) Artigas A, Bernard GR, Carlet J, et al: The American-European consensus conference on ARDS, part 2: ventilatory, pharmacologic, supportive therapy, study design strategies, and issues related to recovery and remodeling.. Am J Respir Crit Care Med 1998; 157:1332-1347.
    21) Barkin RM: Emergency Pediatrics, 2nd ed, CV Mosby Co, St. Louis, MO, 1986.
    22) Boyer EW, Walker N, & Woolf A: Inhalational exposure to hydrogen fluoride treated with nebulized calcium gluconate (abstract). Clin Toxicol 2000; 38:545.
    23) Brower RG, Matthay AM, & Morris A: Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Eng J Med 2000; 342:1301-1308.
    24) Budavari S: The Merck Index, 12th edition, Merck & Co, Inc, Whitehouse Station, NJ, 1996.
    25) CHRIS : CHRIS Hazardous Chemical Data. US Department of Transportation, US Coast Guard. Washington, DC (Internet Version). Edition expires 1989; provided by Truven Health Analytics Inc., Greenwood Village, CO.
    26) CHRIS: CHRIS Hazardous Chemical Data. US Department of Transportation, US Coast Guard. Washington, DC (Internet Version). Edition expires 2004; provided by Truven Health Analytics Inc., Greenwood Village, CO.
    27) Caravati EM: Acute hydrofluoric acid exposure. Am J Emerg Med 1988; 6:143-150.
    28) Cataletto M: Respiratory Distress Syndrome, Acute(ARDS). In: Domino FJ, ed. The 5-Minute Clinical Consult 2012, 20th ed. Lippincott Williams & Wilkins, Philadelphia, PA, 2012.
    29) Chameides L: Textbook of Pediatric Advanced Life Support, American Heart Association, Dallas, TX, 1988.
    30) Cummings CC & McIvor ME: Fluoride-induced hyperkalemia: the role of Ca2+-dependent K+ channels. Am J Emerg Med 1988; 6:1-3.
    31) DFG: List of MAK and BAT Values 2002, Report No. 38, Deutsche Forschungsgemeinschaft, Commission for the Investigation of Health Hazards of Chemical Compounds in the Work Area, Wiley-VCH, Weinheim, Federal Republic of Germany, 2002.
    32) Delgado JH & Heard K: Oral decontamination with calcium or magnesium salts does not improve survival following hydrofluoric acid ingestion. J Toxicol Clin Toxicol 2002; 40(5):697.
    33) EPA: Search results for Toxic Substances Control Act (TSCA) Inventory Chemicals. US Environmental Protection Agency, Substance Registry System, U.S. EPA's Office of Pollution Prevention and Toxics. Washington, DC. 2005. Available from URL: http://www.epa.gov/srs/.
    34) ERG: Emergency Response Guidebook. A Guidebook for First Responders During the Initial Phase of a Dangerous Goods/Hazardous Materials Incident, U.S. Department of Transportation, Research and Special Programs Administration, Washington, DC, 2004.
    35) Grant WM & Schuman JS: Toxicology of the Eye, 4th ed, Charles C Thomas, Springfield, IL, 1993.
    36) Grant WM: Toxicology of the Eye, 3rd ed, Charles C Thomas, Springfield, IL, 1986, pp 490-492.
    37) HSDB : Hazardous Substances Data Bank. National Library of Medicine. Bethesda, MD (Internet Version). Edition expires 1993; provided by Truven Health Analytics Inc., Greenwood Village, CO.
    38) HSDB : Hazardous Substances Data Bank. National Library of Medicine. Bethesda, MD (Internet Version). Edition expires 2004; provided by Truven Health Analytics Inc., Greenwood Village, CO.
    39) Haas CF: Mechanical ventilation with lung protective strategies: what works?. Crit Care Clin 2011; 27(3):469-486.
    40) Haque A & Saleem AF: On admission hypomagnesemia in critically ill children: Risk factors and outcome. Indian J Pediatr 2009; 76(12):1227-1230.
    41) Hojer J, Personne M, Hulten P, et al: Topical treatments for hydrofluoric acid burns: a blind controlled experimental study. J Toxicol Clin Toxicol 2002; 40(7):861-866.
    42) IARC Working Group on the Evaluation of Carcinogenic Risks to Humans : IARC Monographs on the Evaluation of Carcinogenic Risks to Humans: 1,3-Butadiene, Ethylene Oxide and Vinyl Halides (Vinyl Fluoride, Vinyl Chloride and Vinyl Bromide), 97, International Agency for Research on Cancer, Lyon, France, 2008.
    43) IARC Working Group on the Evaluation of Carcinogenic Risks to Humans : IARC Monographs on the Evaluation of Carcinogenic Risks to Humans: Formaldehyde, 2-Butoxyethanol and 1-tert-Butoxypropan-2-ol, 88, International Agency for Research on Cancer, Lyon, France, 2006.
    44) IARC Working Group on the Evaluation of Carcinogenic Risks to Humans : IARC Monographs on the Evaluation of Carcinogenic Risks to Humans: Household Use of Solid Fuels and High-temperature Frying, 95, International Agency for Research on Cancer, Lyon, France, 2010a.
    45) IARC Working Group on the Evaluation of Carcinogenic Risks to Humans : IARC Monographs on the Evaluation of Carcinogenic Risks to Humans: Smokeless Tobacco and Some Tobacco-specific N-Nitrosamines, 89, International Agency for Research on Cancer, Lyon, France, 2007.
    46) IARC Working Group on the Evaluation of Carcinogenic Risks to Humans : IARC Monographs on the Evaluation of Carcinogenic Risks to Humans: Some Non-heterocyclic Polycyclic Aromatic Hydrocarbons and Some Related Exposures, 92, International Agency for Research on Cancer, Lyon, France, 2010.
    47) IARC: List of all agents, mixtures and exposures evaluated to date - IARC Monographs: Overall Evaluations of Carcinogenicity to Humans, Volumes 1-88, 1972-PRESENT. World Health Organization, International Agency for Research on Cancer. Lyon, FranceAvailable from URL: http://monographs.iarc.fr/monoeval/crthall.html. As accessed Oct 07, 2004.
    48) ICAO: Technical Instructions for the Safe Transport of Dangerous Goods by Air, 2003-2004. International Civil Aviation Organization, Montreal, Quebec, Canada, 2002.
    49) ITI: Toxic and Hazardous Industrial Chemicals Safety Manual, The International Technical Information Institute, Tokyo, Japan, 1985, pp 110-111.
    50) International Agency for Research on Cancer (IARC): IARC monographs on the evaluation of carcinogenic risks to humans: list of classifications, volumes 1-116. International Agency for Research on Cancer (IARC). Lyon, France. 2016. Available from URL: http://monographs.iarc.fr/ENG/Classification/latest_classif.php. As accessed 2016-08-24.
    51) International Agency for Research on Cancer: IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. World Health Organization. Geneva, Switzerland. 2015. Available from URL: http://monographs.iarc.fr/ENG/Classification/. As accessed 2015-08-06.
    52) Jones AL & Flanagan RJ: Calcium Salts. In: Dart RC, Caravato EM, McGuigan MA, et al, eds. Medical Toxicology, 3rd ed. Lippincott Williams & Wilkins, Philadelphia, PA, 2004.
    53) Kleinman ME, Chameides L, Schexnayder SM, et al: 2010 American Heart Association guidelines for cardiopulmonary resuscitation and emergency cardiovascular care. Part 14: pediatric advanced life support. Circulation 2010; 122(18 Suppl.3):S876-S908.
    54) Kollef MH & Schuster DP: The acute respiratory distress syndrome. N Engl J Med 1995; 332:27-37.
    55) Kono K, Watanabe T, Dote T, et al: Successful treatments of lung injury and skin burn due to hydrofluoric acid exposure. Int Arch Occup Environ Health 2000; 73 Suppl:93-97.
    56) Kraut JA & Madias NE: Metabolic acidosis: pathophysiology, diagnosis and management. Nat Rev Nephrol 2010; 6(5):274-285.
    57) Larsen MJ & Jensen SJ: Inactivation of hydrofluoric acid by solutions intended for gastric lavage. Pharmacol Toxicol 1991; 68:447-448.
    58) Lee DC, Wiley JF II, & Snyder JW II: Treatment of inhalational exposure to hydrofluoric acid with nebulized calcium gluconate (Letter). J Occup Med 1993; 35:470.
    59) Lewis RJ: Sax's Dangerous Properties of Industrial Materials, 10th ed, John Wiley & Sons, New York, NY, 2000.
    60) Link MS, Berkow LC, Kudenchuk PJ, et al: Part 7: Adult Advanced Cardiovascular Life Support: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 2015; 132(18 Suppl 2):S444-S464.
    61) Manrique AM, Arroyo M, Lin Y, et al: Magnesium supplementation during cardiopulmonary bypass to prevent junctional ectopic tachycardia after pediatric cardiac surgery: a randomized controlled study. J Thorac Cardiovasc Surg 2010; 139(1):162-169.
    62) Martin ML, Hamilton R, & West MF: Potassium. Emerg Med Clin North Am 1986; 4:131-144.
    63) Martin TJ, Kang Y, Robertson KM, et al: Ionization and hemodynamic effects of calcium chloride and calcium gluconate in the absence of hepatic function. Anesthesiology 1990; 73(1):62-65.
    64) McCulley JP, Whiting DW, & Petitt MG: Hydrofluoric acid burns of the eye. J Occup Med 1983; 25:447-450.
    65) McIvor ME & Cummings CC: Sodium fluoride produces a K+ efflux by increasing intracellular Ca2+ through Na+-Ca2+ exchange. Toxicol Lett 1987; 38:169-176.
    66) McIvor ME, Cummings CE, & Mower MM: Sudden cardiac death from acute fluoride intoxication: the role of potassium. Ann Emerg Med 1987; 16:777-781.
    67) McIvor ME: Delayed fatal hyperkalemia in a patient with acute fluoride intoxication.. Ann Emerg Med 1987; 16:1165-1167.
    68) NFPA: Fire Protection Guide to Hazardous Materials, 13th ed., National Fire Protection Association, Quincy, MA, 2002.
    69) NHLBI ARDS Network: Mechanical ventilation protocol summary. Massachusetts General Hospital. Boston, MA. 2008. Available from URL: http://www.ardsnet.org/system/files/6mlcardsmall_2008update_final_JULY2008.pdf. As accessed 2013-08-07.
    70) NRC: Acute Exposure Guideline Levels for Selected Airborne Chemicals - Volume 1, Subcommittee on Acute Exposure Guideline Levels, Committee on Toxicology, Board on Environmental Studies and Toxicology, Commission of Life Sciences, National Research Council. National Academy Press, Washington, DC, 2001.
    71) NRC: Acute Exposure Guideline Levels for Selected Airborne Chemicals - Volume 2, Subcommittee on Acute Exposure Guideline Levels, Committee on Toxicology, Board on Environmental Studies and Toxicology, Commission of Life Sciences, National Research Council. National Academy Press, Washington, DC, 2002.
    72) NRC: Acute Exposure Guideline Levels for Selected Airborne Chemicals - Volume 3, Subcommittee on Acute Exposure Guideline Levels, Committee on Toxicology, Board on Environmental Studies and Toxicology, Commission of Life Sciences, National Research Council. National Academy Press, Washington, DC, 2003.
    73) NRC: Acute Exposure Guideline Levels for Selected Airborne Chemicals - Volume 4, Subcommittee on Acute Exposure Guideline Levels, Committee on Toxicology, Board on Environmental Studies and Toxicology, Commission of Life Sciences, National Research Council. National Academy Press, Washington, DC, 2004.
    74) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for 1,2,3-Trimethylbenzene (Proposed). United States Environmental Protection Agency. Washington, DC. 2006k. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d68a&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    75) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for 1,2,4-Trimethylbenzene (Proposed). United States Environmental Protection Agency. Washington, DC. 2006m. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d68a&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    76) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for 1,2-Butylene Oxide (Proposed). United States Environmental Protection Agency. Washington, DC. 2008d. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648083cdbb&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    77) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for 1,2-Dibromoethane (Proposed). United States Environmental Protection Agency. Washington, DC. 2007g. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064802796db&disposition=attachment&contentType=pdf. As accessed 2010-08-18.
    78) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for 1,3,5-Trimethylbenzene (Proposed). United States Environmental Protection Agency. Washington, DC. 2006l. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d68a&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    79) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for 2-Ethylhexyl Chloroformate (Proposed). United States Environmental Protection Agency. Washington, DC. 2007b. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648037904e&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    80) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Acrylonitrile (Proposed). United States Environmental Protection Agency. Washington, DC. 2007c. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648028e6a3&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    81) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Adamsite (Proposed). United States Environmental Protection Agency. Washington, DC. 2007h. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020fd29&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    82) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Agent BZ (3-quinuclidinyl benzilate) (Proposed). United States Environmental Protection Agency. Washington, DC. 2007f. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064803ad507&disposition=attachment&contentType=pdf. As accessed 2010-08-18.
    83) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Allyl Chloride (Proposed). United States Environmental Protection Agency. Washington, DC. 2008. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648039d9ee&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    84) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Aluminum Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005b. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    85) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Arsenic Trioxide (Proposed). United States Environmental Protection Agency. Washington, DC. 2007m. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480220305&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    86) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Automotive Gasoline Unleaded (Proposed). United States Environmental Protection Agency. Washington, DC. 2009a. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7cc17&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    87) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Biphenyl (Proposed). United States Environmental Protection Agency. Washington, DC. 2005j. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064801ea1b7&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    88) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Bis-Chloromethyl Ether (BCME) (Proposed). United States Environmental Protection Agency. Washington, DC. 2006n. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648022db11&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    89) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Boron Tribromide (Proposed). United States Environmental Protection Agency. Washington, DC. 2008a. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064803ae1d3&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    90) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Bromine Chloride (Proposed). United States Environmental Protection Agency. Washington, DC. 2007d. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648039732a&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    91) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Bromoacetone (Proposed). United States Environmental Protection Agency. Washington, DC. 2008e. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064809187bf&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    92) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Calcium Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005d. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    93) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Carbonyl Fluoride (Proposed). United States Environmental Protection Agency. Washington, DC. 2008b. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064803ae328&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    94) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Carbonyl Sulfide (Proposed). United States Environmental Protection Agency. Washington, DC. 2007e. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648037ff26&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    95) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Chlorobenzene (Proposed). United States Environmental Protection Agency. Washington, DC. 2008c. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064803a52bb&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    96) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Cyanogen (Proposed). United States Environmental Protection Agency. Washington, DC. 2008f. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064809187fe&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    97) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Dimethyl Phosphite (Proposed). United States Environmental Protection Agency. Washington, DC. 2009. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7cbf3&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    98) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Diphenylchloroarsine (Proposed). United States Environmental Protection Agency. Washington, DC. 2007l. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020fd29&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    99) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Ethyl Isocyanate (Proposed). United States Environmental Protection Agency. Washington, DC. 2008h. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648091884e&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    100) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Ethyl Phosphorodichloridate (Proposed). United States Environmental Protection Agency. Washington, DC. 2008i. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480920347&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    101) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Ethylbenzene (Proposed). United States Environmental Protection Agency. Washington, DC. 2008g. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064809203e7&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    102) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Ethyldichloroarsine (Proposed). United States Environmental Protection Agency. Washington, DC. 2007j. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020fd29&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    103) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Germane (Proposed). United States Environmental Protection Agency. Washington, DC. 2008j. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480963906&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    104) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Hexafluoropropylene (Proposed). United States Environmental Protection Agency. Washington, DC. 2006. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064801ea1f5&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    105) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Ketene (Proposed). United States Environmental Protection Agency. Washington, DC. 2007. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020ee7c&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    106) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Magnesium Aluminum Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005h. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    107) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Magnesium Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005g. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    108) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Malathion (Proposed). United States Environmental Protection Agency. Washington, DC. 2009k. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064809639df&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    109) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Mercury Vapor (Proposed). United States Environmental Protection Agency. Washington, DC. 2009b. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a8a087&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    110) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Methyl Isothiocyanate (Proposed). United States Environmental Protection Agency. Washington, DC. 2008k. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480963a03&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    111) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Methyl Parathion (Proposed). United States Environmental Protection Agency. Washington, DC. 2008l. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480963a57&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    112) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Methyl tertiary-butyl ether (Proposed). United States Environmental Protection Agency. Washington, DC. 2007a. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064802a4985&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    113) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Methylchlorosilane (Proposed). United States Environmental Protection Agency. Washington, DC. 2005. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5f4&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    114) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Methyldichloroarsine (Proposed). United States Environmental Protection Agency. Washington, DC. 2007i. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020fd29&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    115) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Methyldichlorosilane (Proposed). United States Environmental Protection Agency. Washington, DC. 2005a. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c646&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    116) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Nitrogen Mustard (HN1 CAS Reg. No. 538-07-8) (Proposed). United States Environmental Protection Agency. Washington, DC. 2006a. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d6cb&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    117) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Nitrogen Mustard (HN2 CAS Reg. No. 51-75-2) (Proposed). United States Environmental Protection Agency. Washington, DC. 2006b. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d6cb&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    118) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Nitrogen Mustard (HN3 CAS Reg. No. 555-77-1) (Proposed). United States Environmental Protection Agency. Washington, DC. 2006c. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d6cb&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    119) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Nitrogen Tetroxide (Proposed). United States Environmental Protection Agency. Washington, DC. 2008n. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648091855b&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    120) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Nitrogen Trifluoride (Proposed). United States Environmental Protection Agency. Washington, DC. 2009l. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480963e0c&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    121) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Parathion (Proposed). United States Environmental Protection Agency. Washington, DC. 2008o. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480963e32&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    122) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Perchloryl Fluoride (Proposed). United States Environmental Protection Agency. Washington, DC. 2009c. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7e268&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    123) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Perfluoroisobutylene (Proposed). United States Environmental Protection Agency. Washington, DC. 2009d. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7e26a&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    124) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Phenyl Isocyanate (Proposed). United States Environmental Protection Agency. Washington, DC. 2008p. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648096dd58&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    125) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Phenyl Mercaptan (Proposed). United States Environmental Protection Agency. Washington, DC. 2006d. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020cc0c&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    126) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Phenyldichloroarsine (Proposed). United States Environmental Protection Agency. Washington, DC. 2007k. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020fd29&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    127) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Phorate (Proposed). United States Environmental Protection Agency. Washington, DC. 2008q. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648096dcc8&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    128) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Phosgene (Draft-Revised). United States Environmental Protection Agency. Washington, DC. 2009e. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a8a08a&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    129) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Phosgene Oxime (Proposed). United States Environmental Protection Agency. Washington, DC. 2009f. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7e26d&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    130) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Potassium Cyanide (Proposed). United States Environmental Protection Agency. Washington, DC. 2009g. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7cbb9&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    131) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Potassium Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005c. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    132) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Propargyl Alcohol (Proposed). United States Environmental Protection Agency. Washington, DC. 2006e. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020ec91&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    133) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Selenium Hexafluoride (Proposed). United States Environmental Protection Agency. Washington, DC. 2006f. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020ec55&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    134) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Silane (Proposed). United States Environmental Protection Agency. Washington, DC. 2006g. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d523&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    135) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Sodium Cyanide (Proposed). United States Environmental Protection Agency. Washington, DC. 2009h. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7cbb9&disposition=attachment&contentType=pdf. As accessed 2010-08-15.
    136) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Sodium Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005i. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    137) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Strontium Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005f. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    138) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Sulfuryl Chloride (Proposed). United States Environmental Protection Agency. Washington, DC. 2006h. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020ec7a&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    139) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Tear Gas (Proposed). United States Environmental Protection Agency. Washington, DC. 2008s. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648096e551&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    140) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Tellurium Hexafluoride (Proposed). United States Environmental Protection Agency. Washington, DC. 2009i. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7e2a1&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    141) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Tert-Octyl Mercaptan (Proposed). United States Environmental Protection Agency. Washington, DC. 2008r. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648096e5c7&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    142) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Tetramethoxysilane (Proposed). United States Environmental Protection Agency. Washington, DC. 2006j. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d632&disposition=attachment&contentType=pdf. As accessed 2010-08-17.
    143) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Trimethoxysilane (Proposed). United States Environmental Protection Agency. Washington, DC. 2006i. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d632&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    144) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Trimethyl Phosphite (Proposed). United States Environmental Protection Agency. Washington, DC. 2009j. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=0900006480a7d608&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    145) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Trimethylacetyl Chloride (Proposed). United States Environmental Protection Agency. Washington, DC. 2008t. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648096e5cc&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    146) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for Zinc Phosphide (Proposed). United States Environmental Protection Agency. Washington, DC. 2005e. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020c5ed&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    147) National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances: Acute Exposure Guideline Levels (AEGLs) for n-Butyl Isocyanate (Proposed). United States Environmental Protection Agency. Washington, DC. 2008m. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=09000064808f9591&disposition=attachment&contentType=pdf. As accessed 2010-08-12.
    148) National Heart,Lung,and Blood Institute: Expert panel report 3: guidelines for the diagnosis and management of asthma. National Heart,Lung,and Blood Institute. Bethesda, MD. 2007. Available from URL: http://www.nhlbi.nih.gov/guidelines/asthma/asthgdln.pdf.
    149) National Institute for Occupational Safety and Health: NIOSH Pocket Guide to Chemical Hazards, U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, Cincinnati, OH, 2007.
    150) National Research Council : Acute exposure guideline levels for selected airborne chemicals, 5, National Academies Press, Washington, DC, 2007.
    151) National Research Council: Acute exposure guideline levels for selected airborne chemicals, 6, National Academies Press, Washington, DC, 2008.
    152) National Research Council: Acute exposure guideline levels for selected airborne chemicals, 7, National Academies Press, Washington, DC, 2009.
    153) National Research Council: Acute exposure guideline levels for selected airborne chemicals, 8, National Academies Press, Washington, DC, 2010.
    154) Neumar RW , Otto CW , Link MS , et al: Part 8: adult advanced cardiovascular life support: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 2010; 122(18 Suppl 3):S729-S767.
    155) Piirila P, Espo T, Pfaffli P, et al: Prolonged respiratory symptoms caused by thermal degradation products of freons. Scand J Work Environ Health 2003; 29:71-77.
    156) Product Information: Cordarone(R) oral tablets, amiodarone HCl oral tablets. Wyeth Pharmaceuticals Inc (per FDA), Philadelphia, PA, 2015.
    157) RTECS : Registry of Toxic Effects of Chemical Substances. National Institute for Occupational Safety and Health. Cincinnati, OH (Internet Version). Edition expires 1989; provided by Truven Health Analytics Inc., Greenwood Village, CO.
    158) RTECS: Registry of Toxic Effects of Chemical Substances.. National Institute for Occupational Safety and Health. Cincinnati, OH (Internet Version). Edition expires 2004; provided by Truven Health Analytics Inc., Greenwood Village, CO.
    159) Sax NI & Lewis RJ: Dangerous Properties of Industrial Materials, 7th ed, Van Nostrand Reinhold Co, New York, NY, 1989, pp 717.
    160) Sax NI & Lewis RJ: Hawley's Condensed Chemical Dictionary, 11th ed, Van Nostrand Reinhold Co, New York, NY, 1987, pp 223.
    161) Saxena K: Clinical features and management of poisoning due to potassium chloride. Med Toxicol Adv Drug Exp 1989; 4:429-443.
    162) Sittig M: Handbook of Toxic and Hazardous Chemicals and Carcinogens, 2nd ed, Noyes Publications, Park Ridge, NJ, 1985, pp 196.
    163) Smith JD, Bia MJ, & DeFronza RA: Clinical disorders of potassium metabolism. In: Arieff AI & DeFronzo RA (Eds): Fluid, Electrolyte, and Acid-Base Disorders, Vol 1, Churchill Livingstone, New York, NY, 1985, pp 413-510.
    164) Stolbach A & Hoffman RS: Respiratory Principles. In: Nelson LS, Hoffman RS, Lewin NA, et al, eds. Goldfrank's Toxicologic Emergencies, 9th ed. McGraw Hill Medical, New York, NY, 2011.
    165) Su M, Chu J, Howland MA, et al: Amiodarone attenuates fluoride-induced hyperkalemia in vitro. Acad Emerg Med 2003; 10(2):105-109.
    166) Tepperman PB: Fatality due to acute systemic fluoride poisoning following a hydrofluoric acid skin burn. J Occup Med 1980; 22:691-692.
    167) Trevino C, Smith G, & Ryan M: Nebulized calcium gluconate for the treatment of respiratory exposure to hydrofluoric acid (abstract). Clin Toxicol 2001; 39:509.
    168) Trevino MA, Herrmann GH, & Sprout WL: Treatment of severe hydrofluoric acid exposures. J Occup Med 1983a; 25:861-863.
    169) Trevino MA, Herrmann GH, & Sprout WL: Treatment of severe hydrofluoric acid exposures.. J Occup Med 1983; 25:861-863.
    170) Tsonis L, Hantsch-Bardsley C, & Gamelli RL: Hydrofluoric acid inhalation injury. J Burn Care Res 2008; 29(5):852-855.
    171) U.S. Department of Energy, Office of Emergency Management: Protective Action Criteria (PAC) with AEGLs, ERPGs, & TEELs: Rev. 26 for chemicals of concern. U.S. Department of Energy, Office of Emergency Management. Washington, DC. 2010. Available from URL: http://www.hss.doe.gov/HealthSafety/WSHP/Chem_Safety/teel.html. As accessed 2011-06-27.
    172) U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project : 11th Report on Carcinogens. U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program. Washington, DC. 2005. Available from URL: http://ntp.niehs.nih.gov/INDEXA5E1.HTM?objectid=32BA9724-F1F6-975E-7FCE50709CB4C932. As accessed 2011-06-27.
    173) U.S. Environmental Protection Agency: Discarded commercial chemical products, off-specification species, container residues, and spill residues thereof. Environmental Protection Agency's (EPA) Resource Conservation and Recovery Act (RCRA); List of hazardous substances and reportable quantities 2010b; 40CFR(261.33, e-f):77-.
    174) U.S. Environmental Protection Agency: Integrated Risk Information System (IRIS). U.S. Environmental Protection Agency. Washington, DC. 2011. Available from URL: http://cfpub.epa.gov/ncea/iris/index.cfm?fuseaction=iris.showSubstanceList&list_type=date. As accessed 2011-06-21.
    175) U.S. Environmental Protection Agency: List of Radionuclides. U.S. Environmental Protection Agency. Washington, DC. 2010a. Available from URL: http://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol27/pdf/CFR-2010-title40-vol27-sec302-4.pdf. As accessed 2011-06-17.
    176) U.S. Environmental Protection Agency: List of hazardous substances and reportable quantities. U.S. Environmental Protection Agency. Washington, DC. 2010. Available from URL: http://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol27/pdf/CFR-2010-title40-vol27-sec302-4.pdf. As accessed 2011-06-17.
    177) U.S. Environmental Protection Agency: The list of extremely hazardous substances and their threshold planning quantities (CAS Number Order). U.S. Environmental Protection Agency. Washington, DC. 2010c. Available from URL: http://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol27/pdf/CFR-2010-title40-vol27-part355.pdf. As accessed 2011-06-17.
    178) U.S. Occupational Safety and Health Administration: Part 1910 - Occupational safety and health standards (continued) Occupational Safety, and Health Administration's (OSHA) list of highly hazardous chemicals, toxics and reactives. Subpart Z - toxic and hazardous substances. CFR 2010 2010; Vol6(SEC1910):7-.
    179) U.S. Occupational Safety, and Health Administration (OSHA): Process safety management of highly hazardous chemicals. 29 CFR 2010 2010; 29(1910.119):348-.
    180) United States Environmental Protection Agency Office of Pollution Prevention and Toxics: Acute Exposure Guideline Levels (AEGLs) for Vinyl Acetate (Proposed). United States Environmental Protection Agency. Washington, DC. 2006. Available from URL: http://www.regulations.gov/search/Regs/contentStreamer?objectId=090000648020d6af&disposition=attachment&contentType=pdf. As accessed 2010-08-16.
    181) Willson DF, Truwit JD, Conaway MR, et al: The adult calfactant in acute respiratory distress syndrome (CARDS) trial. Chest 2015; 148(2):356-364.
    182) Wilson DF, Thomas NJ, Markovitz BP, et al: Effect of exogenous surfactant (calfactant) in pediatric acute lung injury. A randomized controlled trial. JAMA 2005; 293:470-476.
    183) Wormser U, Sintov A, Brodsky B, et al: Protective effect of topical iodine preparations upon heat-induced and hydrofluoric acid-induced skin lesions. Toxicol Pathol 2002; 30(5):552-558.