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Registered medical practitioners undertaking health monitoring are required to be experienced in health monitoring and have an understanding of the potential adverse health effects of inorganic arsenic, and to use their clinical knowledge to advise on health monitoring of workers.
Arsenic is widely distributed in rocks and soil. In its inorganic form, arsenic is highly toxic. Occupational exposure to arsenic occurs in mining and refining processes. This includes roasting arsenopyrite ore and the smelting of minerals such as gold, lead, zinc and copper. Arsenic is also present in mining waste, the waste disposal industry, some manufacturing and laboratories. It is used, and has historically been used, in metal alloys, pigments, ceramic enamels, anti-fouling paints, pesticides, rat poison, and leather hide and wood preservation. In the marine environment, inorganic arsenic is taken up by fish, shellfish and algae (including seaweed) and is stored as organic arsenical compounds. These compounds are considered non-toxic. Arsenobetaine is the major species of organic arsenic in fish. In contrast, arsenosugars are the major species of organic arsenic in seaweed. Inorganic arsenic enters the body via inhalation or ingestion. In occupational exposure, the respiratory tract is the major portal of entry. Arsenic compounds, such as arsenic trioxide, are soluble in bodily fluids and cleared rapidly from the lungs. Relevantly, 80-90 per cent of arsenic trioxide is absorbed by the gastrointestinal tract. Less soluble arsenic compounds (calcium arsenate, lead arsenate, arsenic sulphide) are retained in the lungs. Dermal absorption of these compounds is likely to be low. Inorganic arsenic binds to red blood cells and is deposited in the liver, kidneys, muscle, bone, hair, skin and nails. Arsenic also readily crosses the placental barrier and can potentially result in adverse effects on the foetus. Arsenic is metabolised by the reduction of pentavalent arsenic (As(V)) to trivalent arsenic (As(III)), and methylation to less toxic metabolites (monomethylarsonic acid (MMAv) and dimethylarsinic acid (DMAv)). Methylation is triggered after about eight hours. Trivalent arsenic is more toxic than pentavalent arsenic. Inorganic arsenic is rapidly excreted via the kidneys, of which 10-20 per cent is excreted unchanged, 10-20 per cent as MMAv and 60-80 per cent as DMAv. Excretion commences within the first few hours after exposure. Most of the arsenic is excreted in the urine within three days (with a half-life of one to two days). However, it may take weeks to completely eliminate a single dose. Symptoms from exposure vary depending on the dose, chemical form, mode and duration of exposure, as well as individual characteristics and health status. Arsenic is a local irritant to mucous membranes and causes eye irritation, nose irritation, epistaxis and nasal septum perforation. Acute poisoning results in acute abdominal pain, nausea, vomiting, diarrhoea, cramps in the extremities, restlessness and spasms. There may be cardiac arrhythmias, liver toxicity, kidney failure and peripheral neuropathy, convulsions, dehydration, shock and death at very high doses. Skin folds (nose, mouth, axillae, scrotum) with moist surfaces are susceptible to local irritation, vesiculitis, folliculitis and ulcers. Arsenic also causes skin hyperpigmentation, hyperkeratosis and sensitisation. The skin changes are the most obvious signs of chronic inorganic arsenic toxicity. Chronic poisoning may cause peripheral neuropathy, cardiomyopathy and arrythmias, as well as non-malignant pulmonary changes. Inorganic arsenic is classified as a carcinogen (Group 1, IARC). The metabolites, MMAv and DMAv, are classified as possible carcinogens (Group 2B, IARC). Chronic arsenic exposure is associated with skin, lung and bladder cancers. Skin cancers include basal cell carcinoma and squamous cell carcinoma. Smoking has also been shown to increase the risk of lung cancer in workers exposed to arsenic. Health monitoring consists of: The registered medical practitioner has an important role in educating and reinforcing good personal hygiene and safe work practices. This includes: Arsenic levels in urine are indicative of exposure over the previous two to three days. Measurement of inorganic As(III), As(V) and the metabolites (DMAv and MMAv) is the preferred method for biological monitoring (inorganic arsenic). Urinary total arsenic analysis includes contributions from dietary (organic) sources of arsenic. If total urinary arsenic (non-speciated) analysis is used and the levels exceed 35 µg/L, the registered medical practitioner should instruct the pathology laboratory to automatically perform speciation. Consumption of seafood contributes to the level of urinary arsenic. Arsenobetaine in fish and shellfish is excreted unchanged in urine. Some molluscs also contain DMAv. Arsenosugars in seaweed are metabolised to DMAv. This can affect the results of urinary inorganic arsenic analysis. Tobacco smokers may have slightly higher levels of urinary arsenic. This is due to the presence of arsenic in cigarettes, which in turn creates a potentially reduced capacity for the elimination of arsenic. The registered medical practitioner determines whether the worker may or may not continue working with arsenic. The registered medical practitioner also: When urinary arsenic (inorganic) is 35 µg/L or more, the registered medical practitioner: The registered medical practitioner must complete the WorkSafe Health monitoring form notification: Other The registered medical practitioner must then notify WorkSafe by forwarding reports and test results to safety@demirs.wa.gov.auSource
Toxicokinetics
Health effects
Health monitoring
Health counselling
Biological monitoring
Biological exposure standard for inorganic arsenic
Sample collection
Timing
Frequency
Contractors
Health monitoring outcomes
Removal of workers
Notification requirements
Further information
Safe Work Australia
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