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Organophosphorus
poisoning
PREPARED BY:
RN Arpana Bhusal
BNS
Contents
 Introduction
 Causes
 Sign and symptoms
 Treatment
 Prevention
 References
Introduction
 Organophosphate
poisoning is poisoning due
to organophosphates (OPs). Organop
hosphates are used as insecticides,
medications, and nerve agents.
 Symptoms include increased saliva and
tear production, diarrhea, vomiting, small
pupils, sweating, muscle tremors, and
confusion.
 Other names: Organophosphate toxicity
 Causes: organophosphates
 Organophosphates are phosphate
esters that irreversiblely inhibit AChE
• These are highly toxic
• These chemicals are nerve poisions
and have been used in warfare, in
bioterrorism, and as agricultural
insecticides
Causes
1. Inhalation of sprays or dusts of
insecticides.
2. Contamination of skin of agricultural
workers.
3. Contamination of crops or food.
4. Accidental or intentional ingestion of
insecticides.
5. War gases in the chemical war.
SYMPTOMS
Symptoms
1. Muscarinic effects:
• Bradycardia and hypotension.
• Bronchoconstriction and increased
bronchial
secretion.
• Excessive sweating, salivation and
lacrimation.
• Miosis. (
• Nausea, vomiting, abdominal cramps
and
diarrhea.
• Urinary incontinence
 2. Nicotinic effect:
• Muscle twitches followed by
weakness.
• Neuromuscular blockade of
diaphragm and the intercostal muscles
3 CNS effects:
• Restlessness, insomnia, tremors and
confusion.
• Convulsions and coma.
• Depression of respiratory and
cardiovascular system.
 Death is usually due to respiratory
failure
Investigation
• Routine bloods,
• ECG and
• chest x-ray
• Markedly depressed serum
cholinesterase activity below normal
range
 Altered arterial blood gases (acidosis),
serum electrolytes, and serum
creatinine in response to respiratory
distress and shock within 1 to 6 hours
Management
1. Ensure adequate airways protection
–If the patient has respiratory distress
intubate early (avoid succinylcholine!)
2. Ensure adequate oxygenation – give
high flow oxygen via a face mask.
3. Ensure adequate circulation – insert
cannula and give iv fluids
 Give atropine until patient is fully
atropinised. Start with 0.05mg/Kg of
atropine iv (2-4mg depending on patient
weight).
-Repeat every 15 mins until full
atropinisation.
-Aim for pulse rate >80 beats per minute
and systolic blood pressure >80mm/Hg.
Increase atropine bolus dose until
response occurs
 5. Start atropine infusion when
atropinisation achieved
– 0.05mg/kg/hour.
-E.g. for a 70kg patient give 3.5 mg of
atropine per hour as an infusion.
 6. Monitor patient ever 15 minutes.
- If the dose of atropine is too low
cholinergic features will re occur.
- If the dose of atropine is too high
agitation, pyrexia, reduced bowel
sounds and urinary retention will occur
– then reduce atropine infusion
 7. If patient presents within 24 hours
of
exposure and has signs of moderate
to severe organophosphate poisoning
give pralidoxime (PAM)250mg iv.
– repeat after 2 hours.
- Note give parlidoxime after initial
atropine bolus.
 Perform a 12 lead ECG – treat
arrhythmias as
necessary, intravenous magnesium
maybe
helpful
 9. Monitor patient for secretions, pulse
rate (use cardiac monitor), pupil size,
blood pressure, oxygen saturation and
pulse.
- The aim of treatment is to excessive
oral and respiratory secretions and
prevent respiratory failure.
- Adequate atropinisation is indicated
by
reduction of secretions.
 10. Control fits with boluses of
diazepam – give10mg ivi. Diazepam is
also useful for delirium and agitation in
these patients.
-Note agitation may be due to excess
atropine
 11. There is no evidence to support
the use of activated charcoal or gastric
lavage.
 12. Remove contaminated clothing
(wear gloves) and dispose of as
hazardous material.
- Wash the Patient thoroughly with
soap and water
 13. As soon as patient is stable start to
reduce atropine infusion slowly over
24 hours.
-Infusion may need to be increased if
symptoms and signs recur
 Patients with minor exposure to
organophosphates can be discharged
if asymptomatic after 12 hours of
observation.
Prevention
 Protective gear should include
covering the head and neck, wearing
a mask or respirator, and using eye
protection.
 Any exposure to organophosphates
should be washed off immediately with
water and a mild alkaline soap.
 Avoid the use of detergents, as they
may increase absorption by removing
the skin's protective oil.
References
 (http://www.who.int/hiv/pub/imai/en/ac
utecarerev2_e.pdf,@2021/7/09 at 3pm.
 https://www.Mayoclinic.org/disease-
conditions/op-poisoning/diagnosis-
treatment/drc-20356236 @2021/7/8 at
6pm.
 January 17, 2013.op poisoning.
https://www.slideshare.net@2021/07/07 at
2pm.
 www.medicostuff.com
Op poisoning
Op poisoning

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Op poisoning

  • 1.
  • 3. Contents  Introduction  Causes  Sign and symptoms  Treatment  Prevention  References
  • 4. Introduction  Organophosphate poisoning is poisoning due to organophosphates (OPs). Organop hosphates are used as insecticides, medications, and nerve agents.  Symptoms include increased saliva and tear production, diarrhea, vomiting, small pupils, sweating, muscle tremors, and confusion.  Other names: Organophosphate toxicity  Causes: organophosphates
  • 5.  Organophosphates are phosphate esters that irreversiblely inhibit AChE • These are highly toxic • These chemicals are nerve poisions and have been used in warfare, in bioterrorism, and as agricultural insecticides
  • 6. Causes 1. Inhalation of sprays or dusts of insecticides. 2. Contamination of skin of agricultural workers. 3. Contamination of crops or food. 4. Accidental or intentional ingestion of insecticides. 5. War gases in the chemical war.
  • 8. Symptoms 1. Muscarinic effects: • Bradycardia and hypotension. • Bronchoconstriction and increased bronchial secretion. • Excessive sweating, salivation and lacrimation. • Miosis. ( • Nausea, vomiting, abdominal cramps and diarrhea. • Urinary incontinence
  • 9.  2. Nicotinic effect: • Muscle twitches followed by weakness. • Neuromuscular blockade of diaphragm and the intercostal muscles
  • 10. 3 CNS effects: • Restlessness, insomnia, tremors and confusion. • Convulsions and coma. • Depression of respiratory and cardiovascular system.  Death is usually due to respiratory failure
  • 11. Investigation • Routine bloods, • ECG and • chest x-ray • Markedly depressed serum cholinesterase activity below normal range
  • 12.  Altered arterial blood gases (acidosis), serum electrolytes, and serum creatinine in response to respiratory distress and shock within 1 to 6 hours
  • 13.
  • 14. Management 1. Ensure adequate airways protection –If the patient has respiratory distress intubate early (avoid succinylcholine!) 2. Ensure adequate oxygenation – give high flow oxygen via a face mask. 3. Ensure adequate circulation – insert cannula and give iv fluids
  • 15.  Give atropine until patient is fully atropinised. Start with 0.05mg/Kg of atropine iv (2-4mg depending on patient weight). -Repeat every 15 mins until full atropinisation. -Aim for pulse rate >80 beats per minute and systolic blood pressure >80mm/Hg. Increase atropine bolus dose until response occurs
  • 16.  5. Start atropine infusion when atropinisation achieved – 0.05mg/kg/hour. -E.g. for a 70kg patient give 3.5 mg of atropine per hour as an infusion.
  • 17.  6. Monitor patient ever 15 minutes. - If the dose of atropine is too low cholinergic features will re occur. - If the dose of atropine is too high agitation, pyrexia, reduced bowel sounds and urinary retention will occur – then reduce atropine infusion
  • 18.  7. If patient presents within 24 hours of exposure and has signs of moderate to severe organophosphate poisoning give pralidoxime (PAM)250mg iv. – repeat after 2 hours. - Note give parlidoxime after initial atropine bolus.
  • 19.  Perform a 12 lead ECG – treat arrhythmias as necessary, intravenous magnesium maybe helpful
  • 20.  9. Monitor patient for secretions, pulse rate (use cardiac monitor), pupil size, blood pressure, oxygen saturation and pulse. - The aim of treatment is to excessive oral and respiratory secretions and prevent respiratory failure. - Adequate atropinisation is indicated by reduction of secretions.
  • 21.  10. Control fits with boluses of diazepam – give10mg ivi. Diazepam is also useful for delirium and agitation in these patients. -Note agitation may be due to excess atropine
  • 22.  11. There is no evidence to support the use of activated charcoal or gastric lavage.  12. Remove contaminated clothing (wear gloves) and dispose of as hazardous material. - Wash the Patient thoroughly with soap and water
  • 23.  13. As soon as patient is stable start to reduce atropine infusion slowly over 24 hours. -Infusion may need to be increased if symptoms and signs recur
  • 24.  Patients with minor exposure to organophosphates can be discharged if asymptomatic after 12 hours of observation.
  • 25. Prevention  Protective gear should include covering the head and neck, wearing a mask or respirator, and using eye protection.  Any exposure to organophosphates should be washed off immediately with water and a mild alkaline soap.  Avoid the use of detergents, as they may increase absorption by removing the skin's protective oil.
  • 26. References  (http://www.who.int/hiv/pub/imai/en/ac utecarerev2_e.pdf,@2021/7/09 at 3pm.  https://www.Mayoclinic.org/disease- conditions/op-poisoning/diagnosis- treatment/drc-20356236 @2021/7/8 at 6pm.  January 17, 2013.op poisoning. https://www.slideshare.net@2021/07/07 at 2pm.  www.medicostuff.com