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ULY CLINIC

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ULY CLINIC

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19 Februari 2026, 01:06:27

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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:

  1. Binding sulfhydryl (-SH) groups

  2. Inhibiting enzymes

  3. Increasing oxidative stress

  4. Damaging neuronal microtubules

  5. 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

  1. Tanzania Ministry of Health. Standard Treatment Guidelines and Essential Medicines List. Latest edition.

  2. World Health Organization. Mercury and health. Geneva: WHO; 2017.

  3. Clarkson TW, Magos L, Myers GJ. The toxicology of mercury. N Engl J Med. 2003;349:1731-1737.

  4. ATSDR. Toxicological profile for mercury. Agency for Toxic Substances and Disease Registry; 2022.

  5. Goldfrank LR, et al. Goldfrank’s Toxicologic Emergencies. 11th ed. McGraw-Hill; 2019.

  6. Nelson LS, Howland MA. Heavy metal poisoning. In: Tintinalli’s Emergency Medicine. 9th ed. McGraw-Hill; 2020.

  7. Bernhoft RA. Mercury toxicity and treatment. J Environ Public Health. 2012;2012:460508.


Imeandikwa:

14 Novemba 2020, 14:58:51

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