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Ocupational Poisoning. By : Dr ASLANI OCCUPATIONAL MEDICINE SPECIALIST. Content. Definition Etiology Types of Toxicity Lead Mercury. Introduction. Introduction. HEAVY METALS. CHEMICAL PESTICIDES. ORGANIC SOLVENTS. Gases and vapors. Types of Toxicity. Acute toxicity
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Ocupational Poisoning By : Dr ASLANI OCCUPATIONAL MEDICINE SPECIALIST
Content • Definition • Etiology • Types of Toxicity • Lead • Mercury
Types of Toxicity • Acute toxicity • Chronic toxicity • Irritation and corrosivity • Sensitization • Carcinogenicity • Reproductive toxicity
Types of toxicity continues • Mechanisms of toxicity: • Direct local toxicity to tissues first in contact with the substance • Systemic effects due to the absorption of the substance
Occupational toxicity deals with the chemicals found in the place of work. • Persons working in various industries may be exposed to various agents during • the synthesis, • or through their use during the occupation.
Lead metal • Soft • Malleable • Corrosion resistance • Low melting point 13
Battery manufacturing Chemical industry Gasoline additives production Foundry workers Welders Jewelers Lead miners Pigment manufacturing Plastics industry Pottery workers Radiator repair Soldering of lead Rubber industry products Occupational exposure
Lead in the Environment • Varies from place to place • Soil near roadways • Elevated in soil, water, or air near lead mining or smelting facilities • Near smaller businesses and industries that involve lead
Routes of Entry • Lead gets into the body by the following routes of entry: • Inhalation (breathing) • Ingestion (swallowing) • Skin absorption
Inhalation • Inhalation is the primary route of entry for lead. • Occurs when lead dust or fume is released into the air and inhaled. • welding on steel coated with lead-based paint • Approximately 40 to 50 percent of the lead that is inhaled is absorbed into the body
Ingestion • Lead-based paint was banned from residential because of lead poisoning in children.
Skin absorption • Certain lead compounds can be absorbed through the skin (TEL).
Toxicology Absorption • Respiratory (30 to 40 % ): • Gastrointestinal systems: (10 to 15% ) adults < children • Cutaneous
Toxicology IncreasedAbsorption: Deficient in calcium Iron Phosphorus zinc
Neurological Effects Gastrointestinal Effects Health effects of lead Heme Synthesis Other Renal Effects ReproductiveEffects
Acute Inorganic Lead Toxicity Acute Inorganic Lead Toxicity: Excessive exposure in brief period Acute lead poisoning syndrome. Classic clinical findings : Abdominal colic Constipation Fatigue hemolytic anemia CNS dysfunction. in profound case: Acute encephalopathy with Coma Convulsions papill edema In milder exposures : headaches personality changes
Acute Inorganic Lead Toxicity Acute Inorganic Lead Toxicity: Abdominal colic (lead colic) • it has sometimes been misdiagnosed as • appendicitis, • peptic ulcer, • biliary colic, • pancreatitis, • pelvic inflammatory disease
Chronic Inorganic Lead Toxicity Late effects : Chronic renal failure Hypertension Gout Chronic encephalopathy Classic abdominal colic of acute lead poisoning is absent. Symptoms: Arthralgias Headache Weakness Depression Loss of libido Impotence Sperm count dec.
Physical Exam Lead line
Heath Effects vs Symptomology • Some workers may experience symptoms at lower blood lead levels while others may tolerate very high levels without showing symptoms
Hematologic toxicity Anemia induced by lead:
Effects on the Nervous System • Damage to the brain may also result in behavioral problems, i.e., • Poor memory • Reduced intelligence • Instability of mood(40-70µg/dl) • Visual disturbances • Confusion • Encephalopathy (a degenerative brain disease) may occur.
Effects on the Nervous System • Peripheral neuropathy: • Weakness and/or paralysis of the hands or legs can cause "wrist drop" or "foot drop". • Motor-sensory neuropathy • Asymmetry • NEW • Months to years of high dose lead • exposure (eg, blood lead concentrations >80 μg/dL) may be associated with a • predominantly motor peripheral neuropathy
Effects on the Kidneys • Often damage is not detected until it’s too late • Increase BUN and Cr. until 50-70%of the nephron destroyed. • NEW • Months to years of high dose lead • exposure (eg, blood lead concentrations >80 μg/dL) may be associated with a • predominantly nephropathy • characterized by interstitial fibrosis and • nephrosclerosis.
Lead and hypertension • Increase mortality heart disease and stroke
Effects on the Reproductive System • FemaleReproductive Health andPregnancy: • Reduces fertility • Spontaneous abortion
Organic lead skin absorption Acute or sub acute CNS symptoms and signs (TEL): Early symptoms: insomnia, anorexia, muscle irritability severe poisoning: Agitated encephalopathy, delirium tremens , cerebellar signs( tremor, ataxia), increased DTR. CSF examination usually is normal.
LAB FINDING • Whole blood lead concentration: is the most common and useful laboratory test to confirm exposure • Noninvasive K x-ray fluorescence measurement of lead in bone: a biomarker of long-term cumulative lead exposure, is used predominantly as a research tool. • Measurement of lead in urine following a dose of a chelating agent (chelation challenge testing): correlates satisfactorily in most cases with blood lead test results, and is seldom indicated in clinical practice.
LAB FINDING An elevation in erythrocyte protoporphyrin (often measured as zinc protoporphyrin or ZPP): reflects lead-induced inhibition of heme synthesis. Because there is a time lag of several weeks associated with lead-induced elevation in ZPP, the finding of a blood lead of ≥30 μg/dL with no concurrent increase in ZPP suggests that the lead exposure was of recent onset.
OSHA standard • whole BLL : • 1.every 6 months if BLL <40 µg/dl • 2.every 2 months If BLL>40 µg/dl until 2times BLL <40 µg/dl • 3.monthly during removal • Removal from exposure: • 1. worker BLL>60 µg/dl • 2. worker average BLL >50 µg/dl • 3. worker at risk of health impairment
OSHA standard • NEW • Current OSHA lead standards that require medical removal from elevated workplace lead exposure when blood lead levels exceed 50 or 60 μg/dL were enacted several decades ago and offer insufficient protection
OSHA standard • NEW • An expert panel in 2007 recommended that removal be initiated for a single blood lead level greater than 30 μg/dL, or when two successive blood lead levels measured over a 4-week interval are ≥20 μg/dL. • The longer-term goal should be for workers to maintain blood lead levels <10 μg/ dL
Primary Prevention of Lead Poisoning Engineering controlsSubstitution of less hazardous material Isolation via containment structure Ventilation via local exhaust systemPersonal protective equipmentRespirator utilizationWork practices Personal hygiene practices Periodic inspection/maintenance of control equipment
Exposure • elemental mercury:is a liquid at room temperature with a substantial vapor pressure • Inorganic mercury salts:(mercuric sulphide (HgS), mercuric oxide (HgO) and mercuric chloride (HgCl2)) • organic mercury: • short-chain alkyl: methyl mercury salts • long-chain alkyl • non-alkyl organic compounds: phenyl mercury
General consideration • Toxicity: • Specific form and compounds • Route of exposure • Dose • Age • Bind to sulfhydryl groups and interfere with numerous cellular enzyme systems.
Elemental mercury • Heavy shiny silver-white metal • liquid or vapor at room temperature
Elemental mercury • Occupational exposure: • Extraction of mercury & silver & gold • Burning fossil fuels (high- sulfur coal) • Maintenance work on furnaces, flues • Chloralkali production plants ( use of mercury in the electrolysis of salt) • Dentist & dental technicians
Elemental mercury • Absorption: • Inhalation is major route of exposure (pulmonary retention is more than 80%) • Skin and gastrointestinal absorption are poor (0.1%) • Heating increase absorption • Elimination : - urine