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Acute poisoning guidelines for initial management
1. ACUTE POISONING
GUIDELINES FOR INITIAL
MANAGEMENT
Prof. Dr. Saad S Al Ani
Senior Pediatric Consultant
Head of Pediatric Department
Khorfakkan Hospital
Sharjah ,UAE
saadsalani@yahoo.com
2. INTRODUCTION
• The majority of poisonings are
accidental, especially in the under-5
age group
• Intentional overdoses and substance
abuse are seen in older children
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
3. CONT.
• Deaths in children from poisoning are
becoming increasingly rare
• Factors responsible for this decline
include:
1. Introduction of child-resistant
containers
2. Reducing the pack sizes of aspirin and
acetaminophen
3. More effective management
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
4. HOW CHILDREN DIFFER FROM ADULTS
• Pediatric patients may be particularly
vulnerable to certain toxins at specific
stages of childhood.
• Breast fed infants may be exposed to
drugs or toxins excreted in breast milk;
neonates have immature metabolic
capabilities
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
5. CONT.
• Toddlers, as they develop exploratory
hand-to-mouth activity, may be
exposed to a wide range of potential
hazards
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
6. GENERAL PRINCIPLES
Assess:
Type of ingestion (drug, preparation)
Time of incident
Amount of ingestion (include all medication
that was potentially in the bottle or packet
when calculating)
Weight of child
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
7. GENERAL PRINCIPLES
Cont.
Is the ingestion potentially harmful?
Beware of the possibility of mixed overdose
Beware of the possibility of inaccurate dose
reporting on history taking
If mixed or undetermined ingestion
Paracetamol level should be done
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
8. GENERAL PRINCIPLES
Management
Airway
Breathing
Circulation
Removal of poison (if necessary)
Emesis
No role in the hospital setting
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
9. GENERAL PRINCIPLES
Cont.
Activated Charcoal
The treatment of choice for most ingestions.
Most effective when given within first hour.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
11. GENERAL PRINCIPLES
Cont.
Whole Bowel Irrigation has a limited role
in treatment of some slow release
preparations
Gastric Lavage has a very limited role in
treatment and should not be used without
consultation.
Specific antidotes may be available and
serum drug levels may help in treatment
decisions
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
12. GENERAL PRINCIPLES
Cont.
All acts of deliberate self harm must be
taken extremely seriously.
All intentional self poisonings in
adolescents require admission
If unexplained symptoms exist a urinary
drug screen may be indicated
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
13. INITIAL ASSESSMENT AND MANAGEMENT
The initial priority in treating poisoned
children is the standard ABC
(airway, breathing, and circulation)
resuscitation approach
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
14. A: ASSESS AIRWAY PATENCY
By looking, listening, and feeling for
air movement.
If there is no air movement, try to open
the airway with simple maneuvers such
as the jaw thrust or the use of airway
adjuncts.
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
15. CONT.
Certain ingested agents may predispose
to airway edema and
obstruction, including caustic
agents, angiotensin-converting enzyme
inhibitors, and plants containing
calcium oxalate crystals
(e.g. Dieffenbachia and
Philodendron house plants)
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
16. B: ASSESS THE ADEQUACY OF BREATHING
It is important to remember that
succinylcholine may cause prolonged
block in children who have a reduced
cholinesterase concentration due to
exposure to cocaine or
organophosphate compounds:
prolonged apneas of up to 7 h have
been described.
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
17. CONT.
Observing ventilatory frequency, use of
accessory muscles, breath sounds, and
oxygen saturations.
Reduced respiratory effort may require
bag-valve-mask ventilation until a
definitive airway can be secured
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
18. C: ASSESS THE CIRCULATION
In terms of cardiovascular status (heart
rate, arterial pressure, and capillary
refill) and the effect of circulatory
inadequacy on other organs (mental
state, urine output, skin
temperature, and colour).
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
19. CONT.
Hypotension should initially be treated
with a 20 ml/ kg crystalloid
bolus, remembering that if it is caused
by specific toxins such as β-
blockers, the specific antidote should
also be given, for example, glucagon
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
20. CONT.
Arrhythmias associated with poisoning
are best treated by:
i. Correcting precipitating factors (e.g.
hyperkalaemia and acidosis)
ii. Administering the appropriate
antidote;
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
21. CONT.
Children in cardiac arrest should be
treated according to standard guidelines
(e.g. The Advanced Cardiac Life
Support protocol), although it is
important to address the need for a
specific antidote, for example, sodium
bicarbonate for tricyclic antidepressant
(TCA) poisoning
http://emedicine.medscape.com/pediatrics_general/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
24. SALICYLATES POISONING
Cont.
• Initial respiratory alkalosis (may be
transient), followed by paradoxical
aciduria (pH <6), then metabolic
acidosis & Hypokalemia (± ongoing
respiratory alkalosis).
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
25. SALICYLATES POISONING
Patients Requiring Treatment
Acute ingestion ≥ 150mg/kg
All symptomatic patients
Ingestion of unknown quantity
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
26. SALICYLATES POISONING
Investigations
Serum salicylate level at presentation (on
patients requiring treatment), and 2 hrly if
symptomatic or enteric coated preparation.
(Need to call the RCH lab to get test run
urgently as it is sent to RMH for analysis)
Urea & electrolytes, creatinine, acid-
base, glucose
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
27. SALICYLATES POISONING
Management
Asymptomatic
Charcoal 1g/kg (if <1 hour since ingestion unless
enteric coated preparation)
Observe 6 hours & discharge if still asymptomatic
If enteric coated preparations, serial salicylate levels
(2 hourly)
Admit if levels have not plateaued at 6 hours post
ingestion
I.V. bicarbonate infusion 1mmol/kg/hr to correct any
acidosis (pH <7.3)
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
28. SALICYLATES POISONING
Cont.
Symptomatic
All symptomatic patients require urgent medical
assessment and investigations as above.
Charcoal 1g/kg unless altered conscious state
(protect airway first)
I.V. fluid resuscitation to correct dehydration (use
N. Saline)
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
29. SALICYLATES POISONING
Symptomatic (Cont.)
I.V. bicarbonate infusion 1mmol/kg/hr, after
initial slow bolus of 2mmol/kg, (keep urine pH
>7.5)
Potassium replacement as required
Worsening symptoms, convulsion, coma, contact
I.C.U. for respiratory support hemodialysis
Salicylate level >7mmol/l following an acute
poisoning contact I.C.U. for consideration of
hemodialysis.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
31. PARACETAMOL POISONING
Patients Requiring Management
1. Acute ingestion of > 200 mg/kg
2. Ingestion of unknown quantity
3. Repeated supratherapeutic ingestion of
> 100mg/kg/day
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
32. PARACETAMOL POISONING
Assessment
Consider the possibility of co
ingestions, either accidental or deliberate
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
33. PARACETAMOL POISONING
Management
Activated charcoal is not useful in liquid
ingestions due to rapid absorption
Activated charcoal 1 g/kg may be considered
in a cooperative patient seen within 1 hour of
tablet or capsule ingestion.
Serum paracetamol level at (or as soon as
possible after) 4 hours post ingestion
determines the need for N-acetyl cysteine
(NAC) administration. (see nomogram)
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
34. PARACETAMOL POISONING
There is no benefit in measuring
paracetamol level earlier than 4 hours
It is safe to wait for the paracetamol level to
decide on the need for NAC in all cases that
present within 8 hours of ingestion.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
35. PARACETAMOL POISONING
Cont.
Patients who present > 8 hours after a toxic
ingestion / symptoms of toxicity (RUQ pain or
tenderness, nausea, vomiting) should be
commenced on NAC immediately.
The decision to continue or cease NAC is then
based on the paracetamol level.
Delaying NAC administration beyond 8 hours is
associated with a progressive increased risk of
liver injury.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
36. PARACETAMOL POISONING
There is little evidence to guide management
in repeated supratherapeutic doses. Potential
toxicity should be assessed when:
> 200 mg/kg (or 10g) ingested over a 24
hour period
> 150 mg/kg/day (or 6 g) ingested over a 48
hour period
> 100 mg/kg/day ingested over a 72 hour
period
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
40. PARACETAMOL POISONING
N- Acetyl cysteine (NAC) Infusion
Instructions
The standard administration of NAC is a 3
stage infusion giving a total dose of 300
mg/kg:
1. 150 mg/kg over the first hour
2. 50 mg/kg over the next 4 hours
3. 100mg/kg over the next 16 hours
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
41. PARACETAMOL POISONING
Cont.
For patients > 110 kg, calculate the dose based
on 110 kg body weight.
NAC may be diluted in 5% dextrose or 0.9%
saline (normal saline).
It can also be diluted in combination dextrose-
saline solutions not exceeding these
concentrations including 0.45% saline in 5%
dextrose, and 0.9% saline in 5% dextrose.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
42. PARACETAMOL POISONING
For adolescent / adult:
1. 150 mg/kg in 250 or 500 ml over 1
hour
2. 50 mg/kg in 500 ml over 4 hours
3. 100 mg/kg in 1000 ml over 16 hours
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
44. IRON POISONING
Background
Iron is found in several different forms in
different medicines.
The important ingestion is the amount of
elemental iron not the iron salt.
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
47. ASSESSMENT
Patients Requiring Assessment
1. Ingestion of > 40 mg/kg elemental iron.
(approximately > ½ tablet/kg or 6.5 ml
syrup/kg)
2. Ingestion of an unknown quantity.
3. Any symptomatic patients
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
48. HISTORY AND EXAMINATION
Initial symptoms:
Usually occur within 20 minutes
Nausea, vomiting, diarrhea, abdominal
pain, hypotension, Hematemesis, fever
Gastrointestinal symptoms related to the corrosive
nature of iron may occur without systemic
toxicity, however any symptoms require iron levels.
Lack of symptoms within the first 6 hours makes
significant toxicity unlikely.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
49. HISTORY AND EXAMINATION
Latent period:
There is often 6-24 hour latent period when
initial symptoms resolve, before overt
systemic toxicity
Thus improvement over this time may be a
result of improvement or deterioration
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
50. HISTORY AND EXAMINATION
Other symptoms:
Usually appear at 6-24 hours and last 12-24
Tachycardia, vasoconstriction, hypotension
and shock
Metabolic acidosis can occur.
These are related to fluid shifts from
intravascular to extravascular compartments
and cellular hypoxia
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
51. HISTORY AND EXAMINATION
Multiple organ failure:
Occurs 12-48 hours after ingestion
Particularly hepatic failure
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
52. Management
ABC
Supportive therapy to maintain adequate
blood pressure and electrolyte balance is
essential
I.V. fluid resuscitation 20 ml/kg
Potassium and glucose administration as
necessary.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
53. Investigations
Asymptomatic patients:
If tablet ingestion do AXR and if negative -
does not need further investigation or
observation
If unknown amount or >60mg/kg ingested
need serum iron levels 4 hourly until falling
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
54. All symptomatic patients should have the
following investigations:
AXR if tablet ingestion
ABG/CBG (acidosis)
Glucose (hyperglycaemia)
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
55. Cont.
Serum iron
Peak levels are usually seen at 4 hours.
Levels taken after four hours may underestimate
toxicity because the subject iron may have either been
distributed into tissues or be bound to ferritin.
In the case of slow release or enteric coated
tablets, levels should be repeated at six to eight hours as
absorption may be erratic.
Once desferroxamine is commenced, iron levels are not
accurate at most labs using automated methods
(including RCH)
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
56. Cont.
FBE (leukocytosis)
U&E & Cr
X-match
Clotting (reversible early coagulopathy and late
coagulopathy secondary to hepatic injury)
LFTs
AXR may be helpful in evaluating gastrointestinal
decontamination after treatment if tablets have been
ingested.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
57. Cont.
Decontamination
Charcoal is of no benefit.
Decontamination of choice is whole bowel irrigation
(WBI) with naso-gastric colonic lavage solution
30ml/kg/hr until rectal effluent clear (contraindicated if
there are signs of bowel obstruction or haemorrhage).
WBI is indicated:
If AXR reveals tablets, or capsules ingested
In symptomatic patients
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
58. Antidote:
Desferroxamine is a chelating agent which
forms a water soluble desferroxamine-iron
complex.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
59. Consider desferroxamine in:
Serum iron levels > 90 micromol/l
Level 60 - 90 micromol/l and tablets visible on
XRay or symptomatic
(nausea, vomiting, diarrhea, abdominal
pain, haematemesis, fever)
Any patient with significant symptoms of altered
conscious
state, hypotension, tachycardia, tachypnea, or
worsening symptoms irrespective of ingested dose
or serum iron level.
Do not wait for iron level if altered conscious
state, shock, severe acidosis (pH <7.1), or
worsening symptoms but commence
Desferroxamine without delay.
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
60. Dose: Desferroxamine 15 mg/kg/hr I.V. The rate
is reduced after four to six hours so that the total
intravenous dose in general does not exceed 80
mg/kg/24 hours.
Desferroxamine -iron complex is renally excreted.
If oliguria or anuria develop, peritoneal dialysis
or hemodialysis may become necessary to remove
ferrioxamine.
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
61. It is difficult to determine the endpoint for
chelation therapy.
Significant poisoning usually requires 12 -
16 hours,
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
62. Cont.
It is recommended to continue desferroxamine
until:
Patient is asymptomatic.
decontamination complete
anion-gap acidosis resolved
Iron level (if measurable) is <54 micromol/L
Desferroxamine has been associated with
pulmonary toxicity and should be used with
caution if indications persist >24 hours.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
IRON POISONING
64. Hydrocarbons Include:
Petrol
Kerosene
Lighter Fluid
Mineral Turpentine
Paraffin Oil
Lubricating Oil
Furniture Polishes
2 Stroke Fuel
Diesel Fuel
White Spirit
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
HYDROCARBON POISONING
65. Assessment
Main complication is Aspiration Pneumonitis
C.N.S. toxicity can be evident (either depression or
excitement)
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
HYDROCARBON POISONING
66. Symptoms:
Coughing, choking, respiratory distress
ataxia, drowsiness, coma, convulsions
persistent burping (particularly seen after
petrol ingestion
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
HYDROCARBON POISONING
67. Keep nil orally charcoal is contraindicated.
Asymptomatic
Observe 6hours
Discharge if remains asymptomatic
Arrange review by LMO the following day
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
68. Symptomatic
If develops respiratory symptoms
(aspiration), do CXR & O2 saturation
Give O2 to maintain saturation > 94%
If stable, admit to general medical ward
If increasing O2 requirements or increased
respiratory distress contact I.C.U.
If altered conscious state at any time contact
I.C.U.
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Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT (CONT.)
70. Alkalis include:
Drain cleaners, Oven cleaners
Automatic dish washing liquids & powders
Laundry detergents, Ammonia
Portland cement
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ALKALIS POISONING
71. pH of >11.5 is likely to cause significant GI
ulceration
Attempt to obtain container to check
contents and strength of substance.
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ALKALIS POISONING
72. Corrosive potential varies with concentration of
specific ingredients and preparations, ie liquid
preparations are more likely to cause esophageal
burns than powders.
Check preparations with Poisons Information Centre
to determine whether ingested substance is
weak, strong, irritant or corrosive in nature.
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ALKALIS POISONING(CONT.)
73. Toxicity
Exposure may lead to severe burns of
GIT, especially esophagus
Absence of mouth or pharyngeal ulcers does
not preclude gastro- oesophageal lesions
Symptoms: May be minimal
Pain
Nausea & vomiting, drooling or refusing to eat
and drink
Stridor, respiratory distress
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6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ASSESSMENT
74. Activated charcoal is contraindicated
If asymptomatic treat with fluid dilution:
10ml/kg of water (max 250ml)
If asymptomatic after 4 hours and able to
eat and drink the patient can be safely
discharged
If any symptoms, contact surgical
registrar, & admit for oesophagoscopy
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
76. CARBAMAZEPINE, PHENYTOIN, SODIUM
VALPROATE, PHENOBARBITONE
Assessment
CNS
Ataxia, drowsiness, coma, convulsions
GIT
Nausea & Vomiting
CVS
Hypotension, Arrhythmias
Drug levels are available for some anticonvulsants e.g.
carbamazepine, phenytoin, phenobarbitone
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ANTICONVULSANT POISONING
77. All symptomatic patients
Acute ingestion of unknown quantity
Carbamazepine ingestion of >20mg/kg (for
patients not on maintenance treatment) or
the greater of more than twice the daily
dose or 20mg/kg for patients on
maintenance treatment
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
PATIENTS REQUIRING TREATMENT
78. Charcoal 1g/kg unless altered conscious state (protect
airway first)
Mild symptoms (e.g. ataxia, blurred vision)
observe 4 hours, discharge if symptom free
Moderate or persistent symptoms (after 4 hours of
observation)
Admit for observation
Severe symptoms
Depressed conscious state or cardiac arrhythmias
contact I.C.U. .
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
81. Charcoal 1g/kg unless altered conscious state (protect
airway first)
Require ECG, cardiac monitoring
Asymptomatic: observe for 6 hours post ingestion and
discharge if have a normal ECG just prior to discharge
All symptomatic patients should be admitted
If widened QRS on ECG commence Sodium Bicarbonate
infusion 1mmol/kg/hr, after initial slow bolus of 2mmol/kg
If altered conscious state, widened QRS or arrhythmia
contact I.C.U. & protect airway
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
82. Assessment
Symptoms
CNS depression, drowsiness, coma
Respiratory depression
Hypotension
Beware additive toxicity with other CNS &
Respiratory depressants
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
BENZODIAZEPINE POISONING
83. Ingestion of ≥3 times recommended dose
for age
All symptomatic patients
Ingestion of unknown quantity
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
PATIENTS REQUIRING OBSERVATION
84. Charcoal is not usually of benefit (due to
low order of toxicity)
If depressed state of consciousness, protect
airway and contact ICU
Antidote available - Flumazenil, not
indicated for ingestions and should only be
used after discussion with consultant staff.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
86. Assessment
CNS
Agitation, hyperventilation, headache, convu
lsions
Cardiovascular
Arrhythmias
GIT
nausea & vomiting (may be
intractable), thirst, diarrhea
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
THEOPHYLLINE POISONING
87. Acute ingestion of ≥ 10mg/kg
Any ingestion while on maintenance
theophylline
Ingestion of unknown quantity
All symptomatic patients
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
PATIENTS REQUIRING TREATMENT
88. Theophylline levels should be determined on all patients
requiring charcoal
Serial levels are required at 2 hours then every 2 hours
until peak reached or decline demonstrated.
If slow release preparation has been taken:
admit, continue levels at 4 hourly intervals after decline or
plateau to ensure detection of secondary peak
Seizures are common at levels >330 micromol/L
Haemoperfusion commonly needed at levels > 550
micromol/L.
U&E, Cr and Glucose on all patients.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
INVESTIGATIONS
89. Asymptomatic
Charcoal 1g/kg
Observe 4 hours. If no
symptoms, discharge if not slow release
medication.
If ingestion of slow release
preparation, admit for observation and
serial drug levelshttp://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
90. Symptomatic
Charcoal 1g/kg initially unless altered conscious state
(protect airway first) then 0.5g/kg 4 hourly, and whole
bowel irrigation with colonic lavage solution 30ml/kg/hr.
Cardiac monitoring
I.V. fluid resuscitation & maintenance of adequate hydration
is vital
If depressed conscious state, arrhythmias or intractable
vomiting contact I.C.U. as likely to need intubation
Severe intoxication may require haemoperfusion
If agitated, may need sedation with a benzodiazepine or
phenobarbitone.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT(CONT.)
93. Fatalities generally occur with blood levels > 86.8mmol/L
(breath alcohol >0.4)
Assessment
Symptoms
Nausea, vomiting, abdominal pain
Hypoglycemia
Ataxia, lethargy, coma, convulsions
Respiratory depression
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ETHANOL POISONING
94. Hypothermia
Hypokalemia, metabolic acidosis
Unexplained drowsiness, hypothermia or hypoglycemia in
adolescents may be ethanol induced. In adolescents ethanol
ingestion often accompanies ingestion of other drugs.
Patients Requiring Treatment
symptomatic patients
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
ETHANOL POISONING(CONT.)
95. Charcoal is of no benefit
Check blood glucose in younger children
Asymptomatic or Mild Symptoms (decreased
inhibition, slight incoordination)
Observe for 2 hours
Give frequent carbohydrate containing drinks
Breath alcohol if possible
If remains symptomatic or symptoms worsen
admit
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT
96. Symptomatic (more than just mild symptoms or
continued symptoms after 2 hours)
Blood ethanol measurement, U& E, Glucose
I.V. fluid
Temperature regulation
Admit.
If unconscious or convulsions contact I.C.U.
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
MANAGEMENT(CONT.)
97. American Association of Poison Control Centers:
http://www.aapcc.org/dnn/Home.aspx
American Academy of Clinical Toxicology:
http://www.clintox.org/index.cfm
Centers for Disease Control and Prevention,
Section on Environmental health:
http://www.cdc.gov/Environmental
http://www.rch.org.au/clinicalguide/guideline_index/Acute_Poisoning_Guidelines_For_Initial_
Management/
6/30/2013 Acute poisoning Prof. Dr. Saad S Al Ani Khorfakkan Hospital
REFERENCES