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ULY CLINIC
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ULY CLINIC
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19 Februari 2026, 01:06:27
Mercury toxicity
Mercury toxicity is a systemic toxicological emergency caused by exposure to elemental, inorganic, or organic mercury compounds. Mercury is a heavy metal that has no physiological role in the human body and is toxic at very low concentrations.
Exposure may occur through:
Inhalation of mercury vapour
Ingestion of contaminated food or chemicals
Percutaneous absorption through skin
Injection (rare but reported)
Occupational exposure
Mercury distributes widely and accumulates particularly in:
Brain (central nervous system)
Kidneys
Liver
Peripheral nerves
Fetus (crosses placenta)
Breast milk
The toxicity depends on the chemical form, because each form targets different organs.
2. Types and Toxicokinetics
Form | Common Source | Main Target Organ | Key Toxic Effect |
Elemental mercury (Hg⁰) | Thermometers, gold mining | Brain | Neurotoxicity |
Inorganic mercury (Hg⁺, Hg²⁺ salts) | Batteries, disinfectants | GI tract & kidneys | Corrosive injury |
Organic mercury (methylmercury) | Contaminated fish | CNS | Neurodegeneration |
Absorption
Route | Absorption rate |
Inhalation | Very high (≈80%) |
Ingestion (elemental) | Minimal |
Ingestion (organic) | Almost complete |
Skin | Slow but significant |
Distribution
Mercury binds sulfhydryl groups → enzyme inhibition → mitochondrial failure → neuronal death.
Organic mercury crosses:
Blood-brain barrier
Placenta
Elimination
Urine
Feces
Breast milk
Hair and nails (chronic exposure marker)
Half-life:
Elemental: 40–60 days
Organic: up to 3 months
3. Risk Factors
Occupational
Gold mining
Dentistry
Battery manufacturing
Fluorescent bulb handling
Laboratory workers
Environmental
Fish from contaminated waters
Industrial pollution
Improper waste disposal
Broken thermometers in enclosed rooms
Patient-related
Children (hand-to-mouth exposure)
Pregnant women
Chronic kidney disease
Malnutrition
Poor ventilation housing
4. Pathophysiology
Mercury causes toxicity by:
Binding sulfhydryl (-SH) groups
Inhibiting enzymes
Increasing oxidative stress
Damaging neuronal microtubules
Causing mitochondrial dysfunction
5. Clinical Manifestations
Symptoms vary according to mercury type.
A. Inorganic Mercury Poisoning
Gastrointestinal (corrosive phase)
Ash-gray mucous membranes
Severe abdominal pain
Haematochesia
Vomiting
Metallic taste
Foul breath
Oral cavity
Stomatitis
Gingivitis
Loosening of teeth
Excess salivation
Systemic
Hypovolaemic shock
Acute kidney injury
Renal tubular necrosis
B. Organic Mercury Poisoning (Neurotoxic phase)
Early neurological signs
Paresthesias
Peripheral neuropathy
Fatigue
Irritability
Progressive neurological syndrome
Scotomata
Visual field constriction (tunnel vision)
Ataxia
Hearing loss
Dysarthria
Tremor
Movement disorders
Advanced toxicity
Mental deterioration
Paralysis
Coma
Death
6. Diagnostic Criteria
Suspect mercury poisoning if:
Neurological deterioration + fish exposure
Gingivitis + kidney injury
Occupational exposure history
Unexplained neuropathy
Concentric visual field loss
7. Investigations
Laboratory tests
Blood mercury level (recent exposure)
Urine mercury level (chronic exposure)
FBC
Renal function tests
Electrolytes
Specialized tests
Hair mercury level (chronic methylmercury)
Toenail mercury level
CSF mercury level (severe neurotoxicity)
Imaging
Abdominal X-ray (ingested mercury visible)
Brain MRI (chronic poisoning → cortical atrophy)
8. Management
Treat immediately once suspected — do NOT wait for laboratory confirmation.
8.1 Initial Stabilization (ABC)
Secure airway
Give oxygen
IV access
Treat shock
8.2 Non-Pharmacological Treatment
Decontamination
Remove patient from exposure
Remove contaminated clothing
Copious skin irrigation
Gastrointestinal management
Gastric lavage (only if visible mercury on X-ray)
Activated charcoal
Whole bowel irrigation (selected cases)
Supportive care
IV fluids
Electrolyte correction
Dialysis if renal failure
Surgical intervention
Remove mercury lodged in intestine/colon if persistent source.
8.3 Chelation Therapy
Chelation binds mercury → increases urinary excretion.
First line: Succimer (DMSA)
Dose:
10 mg/kg PO every 8 hrs for 5 days
Then 10 mg/kg every 12 hrs for 14 days(Max 500 mg per dose)
Preferred because:
Oral
Safer
Effective for children
Acute Inorganic Mercury: Dimercaprol (BAL)
Dose:
Day 1: 5 mg/kg IM once
Day 2–11: 2.5 mg/kg IM every 12 hrs
Additional options (specialist use)
DMPS
Penicillamine (rare)
8.4 Dialysis
Indicated when:
Renal failure
Very high mercury levels
Severe electrolyte imbalance
9. Complications
Chronic kidney disease
Peripheral neuropathy
Blindness
Cerebellar degeneration
Developmental delay (children)
Fetal malformations
Death
10. Special Populations
Pregnancy
Mercury crosses placenta → fetal brain injury
Children
More severe neurological damage
Chronic exposure
May present as psychiatric illness:
Memory loss
Personality change
Depression
Tremor (erethism)
11. Prognosis
Exposure | Outcome |
Acute treated early | Good recovery |
Chronic organic exposure | Permanent neurologic damage |
Renal failure | May become permanent |
Fetal exposure | Irreversible |
12. Prevention
Do’s
Keep medicines and poisons secured
Child-resistant containers
Keep original containers
Read labels carefully
Don’ts
Leave containers open
Transfer chemicals
Remove labels
Store tablets in purse/envelope
Refer to medicine as sweets
Take medicine in front of children
13. Public Health Prevention
Avoid contaminated fish
Occupational protective equipment
Proper disposal of industrial waste
Ventilate indoor spills
Avoid mercury-containing cosmetics
References
Tanzania Ministry of Health. Standard Treatment Guidelines and Essential Medicines List. Latest edition.
World Health Organization. Mercury and health. Geneva: WHO; 2017.
Clarkson TW, Magos L, Myers GJ. The toxicology of mercury. N Engl J Med. 2003;349:1731-1737.
ATSDR. Toxicological profile for mercury. Agency for Toxic Substances and Disease Registry; 2022.
Goldfrank LR, et al. Goldfrank’s Toxicologic Emergencies. 11th ed. McGraw-Hill; 2019.
Nelson LS, Howland MA. Heavy metal poisoning. In: Tintinalli’s Emergency Medicine. 9th ed. McGraw-Hill; 2020.
Bernhoft RA. Mercury toxicity and treatment. J Environ Public Health. 2012;2012:460508.
