Severe acute poisoning with encephalopathy:
This is amedical emergency and the following measures must
be undertaken immediately –
BAL
4 mg/kg immediately (in children).
Cranial
CT scan: to rule out cerebral oedema.
––
If there is cerebral oedema, it can be managed by the following measures:
--
Controlled hyperventilation, maintaining an arterial CO2
tension of 25 to 30 mmHg, can reduce intracranial pressure in patients with
rapidly worsening mental status, lateralising neurologic findings or evidence
of impending herniation. Prolonged hyperventilation is not desirable in
general. Monitor intracranial pres-sure continuously. Monitor cardiovascular
function, renal function, and serum electrolytes carefully.
-- Diuretics
»» Mannitol 20%:Adult:1 to 1.5 gm/kg by infusion over 10
to 20 minutes. Child: 0.5 to 1 gm/kg
by IV infusion over 10 to 20 minutes.
»» Glycerol: 0.3 to 1 gm/kg orally.
»» Loop Diuretics: Furosemide and/or
ethacrynic acid may be useful as an adjunct in the treatment of cerebral
oedema.
»» Corticosteroids:
⌂⌂
Dexamethasone—low dose - 16 mg/day in
divided doses.
⌂⌂
Dexamethasone—high dose— 1 to 2
mg/kg/day in divided doses.
·
KUB: to rule out lead chips in GI
tract.
·
For seizures: Treat seizures with
intravenous diazepam (Adult: up to 10
mg slowly, repeat if necessary;
Children: 0.1
to 0.3 mg/kg slowly). Seizures from leadencephalopathy may be resistant to
anticonvulsant therapy; barbiturate coma and aggressive control of ICP may be
needed.
·
Foley catheterisation: to monitor
urinary specificic gravity, sediment, lead level.
·
CaNa2
EDTA 75 mg/kg/day IV infusion.
·
After the initial dose of BAL,
repeat the same dose at 4 hourly intervals until blood lead level falls below
40 mcg/100 ml. Then reduce BAL to 12 mg/kg/day in 3 divided doses.
·
Reduce CaNa2
EDTA to 50 mg/kg/day as condition improves.
––
Continue the above regimen until patient is asymptomatic and can tolerate oral
chelation with D-penicillamine or DMSA.
Severe acute poisoning without
encephalopathy: (BL morethan 70 mcg/100 ml) –
·
BAL 12 mg/kg/day.
·
EDTA 50 mg/kg/day.
·
Discontinue BAL when the BL falls
below 40 mcg/100 ml, but continue EDTA for 5 more days.
·
Change to oral chelation
subsequently which may have to be continued until the BL falls below 15 mcg/100
ml, or 3 months have been completed.
Moderate poisoning: (BL
between 45 and 70 mcg/100 ml) –
·
EDTA 50 mg/kg/day.
·
When blood lead falls below 40
mcg/100 ml, begin oral chelation.
Mild poisoning: (BL
between 20 and 35 mcg/100 ml) –
·
D-Penicillamine 30 mg/kg/day in 3
divided doses. Start with ¼th of the calculated dose. Double this after 1 week.
Double again (to full dose) after 1 week. Continue this until the BL falls to
less than 15 mcg/100 ml, or 3 months have been completed.
·
In addition to the above protocol,
the following supportive measures must be instituted as applicable –
·
Thiamine 10 to 50 mg/kg is said to
improve neurological
·
In acute poisoning, or in the event
of radiopacities in the GI tract on x-ray, stomach wash can be done.
·
Lead colic usually responds to IV
calcium gluconate.
·
Correct iron deficiency if present.*
·
IV fluids, (maintain specific
gravity of urine under 1020).
·
If intracranial pressure is high due
to cerebral oedema, administer mannitol or steroids as required (vide supra). Organic lead poisoning is
mainly managed symptomatically. Chelation is done only if there is production
of inorganic lead in the body from organic lead.
·
After one round of chelation
therapy, allow an interval of 2 weeks and then esimate the BL. Repeat chelation
if neces- sary. Rebounds are common. And finally the sine qua non of treament of heavy metal poisoning: remove the
patient from the source of exposure. In recent times, a new chelating agent
called Succimer has been introduced
in the management of lead poisoning in Western countries. It is said to be more
efficacious and less toxic.
·
BL less than 10 mcg/100 ml—Re-evaluate and rescreen patients
in 1 year. No additional action required.
·
BL 10–19 mcg/100 ml—Lead education and referrals should be
provided. If the result of screening test is 10–14 mcg/100 ml, perform
diagnostic test for lead on venous blood within 3 months, and at least one
follow-up test within 3 months. If the result of screening test is 15–19
mcg/100 ml, perform diagnostic test for lead on venous blood within 2 months,
and at least one follow-up test within 2 months. Follow according to guidelines
in 20–44 mcg/100 ml range if BL persists in 15–19 mcg/100 ml range.
·
BL 20–44 mcg/100 ml—Lead education and referrals should be
provided. Provide clinical evaluation and management. If the result of
screening test is 20–29 mcg/100 ml, perform diagnostic test for lead on venous
blood within 1 month. If the result of screening test is 30–44 mcg/100 ml,
perform diagnostic test for lead on venous blood within 1 week. Follow-up
testing should be performed every 1 to 2 months.
·
BL 45–69 mcg/100 ml—Lead education and refer-rals should be
provided. Provide coordination of care (case management) within 48 hours.
Perform clinical evaluation and management within 48 hours. Provide diagnostic
testing within 24–48 hours and follow-up testing (in accordance with chelation
therapy, at least once a month).
·
BL equal to or greather than 70
mcg/100 ml - A medical emergency. Hospitalise the patient and begin immediate
chelation therapy.
·
Employees whose blood lead level is
equal to or greater than 50 mcg/100 ml should be temporarily removed from
exposure until their blood lead level is at or below 40 mcg/100 ml.
·
Employees may also be removed from
exposure for medical reasons even if their blood lead levels are within 40
mcg/100 ml.
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