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Organophosphate Pesticide Poisoning

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31 diapositives · 2.5K Views · Jan 19, 2012

Organophosphate Pesticide Poisoning. Bishan Rajapakse MBChB Otago Emergency Medicine Advanced Trainee, MPhil Student (ANU), South Asian Clinical Toxicology Research Collaboration Sri Lanka. The Case…. Picture yourself in Anuradhapura hospital Sri Lanka – ED/ Medical SHO

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  1. OrganophosphatePesticidePoisoning Bishan Rajapakse MBChB Otago Emergency Medicine Advanced Trainee, MPhil Student (ANU), South Asian Clinical Toxicology Research Collaboration Sri Lanka

  2. The Case…. • Picture yourself in Anuradhapura hospital Sri Lanka – ED/ Medical SHO • Ward 6 , teaming with patients…. • Charge Sister tells you there is a sick patient • 36yo F • Taken 100mls of Dimethoate after a domestic argument • There’s nowhere to run, or hide…. So you see the patient – what do you do?

  3. Organophosphate Pesticide Poisoning

  4. Organophosphate Poisoning in Sri Lanka • Organophosphate pesticide (OP) poisoning kills 300,000 worldwide • In Sri Lanka these are mostly impulsive deliberate self-poisoning in young people

  5. Organophosphate Poisoning in Sri Lanka • Case Fatality rates (CFR) • 10-20% for most • 50-70% for some OP’s • In west CFR • 0.3% from all poisons • Multifactorial • Toxicity of OP’s • Patient transport • Lack of resources • Training • Although less common OP Poisoning is still a problem in West • Occupational exposure • Threat of Chemical warfare

  6. Poisoning at Anuradhapura Hospital in 2005

  7. Mechanism of OP’s

  8. Simplified Acute OP Toxicity • Inactivation of acetylcholinesterase enzyme Organophosphate

  9. Pharmacology of Cholinomimetics according to Katzung • Structure • Simple Alcohols eg edrophonium • Carbamates Eg Neostigmine and Physostigmine (tertiary) • Organophosphates eg Parathion

  10. } Respiratory failure + Death Clinical Syndrome • Clinical Syndrome • Acute Cholinergic: • Central • Peripheral Muscarinic • Peripheral Nicotinic • Intermediate Syndrome • OPIDN: Delayed peripheral neuropathy • Neurocognitive dysfunction

  11. Cholinergic Effects • D iarrhoea • U rination • M iosis • B radycardia, Bronchorrhoea, Bronchospasm • E mesis • L acrimation • S alivation

  12. Nicotinic Effects • Respiratory difficulty • respiratory arrest • diaphragmatic weakness • Muscle Weakness • fasiculations • clonus • tremor • Stimulation of sympathetic nervous system • Mydriasis, hypertension, tachycardia • re-entrant dysrhythmias • cardiorespiratory arrest

  13. CNS effects • Malaise • Memory loss • Confusion • Disorientation • Delirium • Seizures • Respiratory centre depression or dysfunction • Coma

  14. Intermediate Syndrome • Delayed Respiratory Failure • Proximal muscle weakness and cranial nerve lesions • Typically 1-4 days after cholinergic crisis has resolved • Prolonged Effects on Nicotinic receptors • Primary motor end plate degeneration • Clinical importance • Delayed respiratory failure leads to death if not aware of it or prepared for it • Wadia et. al 1974 :Type II Paralysis, Senanayake and Karalliedde 1987

  15. Chronic Effects • Organophosphate induced delayed neuropathy (OPIDN) • 1-3weeks • Peripheral neuropathy • Axonopathy due to Neuropathy Target Esterases (NTE) • Chronic organophosphate induced neuropsychiatric disorder (COPIND)

  16. Management The priorities in management are to: Resuscitation Atropinisation of symptomatic patients Decontamination Other Treatments - Oximes

  17. ? Dose • ? Duration • ? Effectiveness Antidotes • Atropine • Oximes • Expensive • Does treatment affect outcome • Intermediate Syndrome? • OPIDN?

  18. Does the patient need atropine? • How much and for how long

  19. A t r o p i n i z a t i o n A t r o p i n e r e q u i r e m e n t 2 4 1 6 8 C l e a r l u n g s P o o r a i r e n t r y i n t o l u n g s c a u s e d b y b r o n c h o s p a s m a n d b r o n c h o r r h o e a 4 0 D r y a x i l l a e E x c e s s i v e s w e a t i n g 3 0 S y s t o l . B P > ( H y p o t e n s i o n ) 8 0 m m H g 2 0 H e a r t r a t e > ( B r a d y c a r d i a ) 8 0 / m i n N o m i o s i s 1 0 ( M i o s i s ) 0 0 5 1 0 1 5 m i n a f t e r f i r s t a t r o p i n e d o s e Scheme of atropinization (endpoints to be reached) • Eddleston M, Buckley NA, Mohamed F, Senarathna L, Hittarage A, Dissanayake W, Azhar S, Sheriff MHR, Dawson AH. Speed of initial atropinisation in significant organophosphorus pesticide poisoning - a comparison of recommended regimens. Journal of Toxicology – Clinical Toxicology 2004;6:865-875.

  20. Atropine • Loading • Doubling dose regime e.g. 2 4 8 16 mgs every 5 minutes • Maintenance • Continuous infusion < 3mg/hr • 10-20% of loading dose/hour • Endpoints • Clear chest on auscultation with no wheeze • Heart rate >80 beats/min • Withdrawal • Atropine toxicity • Clinical Improvement

  21. What if you give too much Atropine ? • Anticholinergic Syndrome: • Hot as hell • Blind as a bat • Red as a beet • Dry as a bone • Mad as a hatter • A sensitive indicator for ingestion, but poor predictor for toxicity. • Full syndrome is rare

  22. Gastrointestinal Decontamination ?

  23. Our Decision should depend on a risk/benefit analysis • Nothing • Emesis • Gastric Lavage • Activated Charcoal • Whole bowel irrigation

  24. Risk of Intervention • Aspiration • Impaired GCS + Unprotected Airway • Emesis, Lavage, Charcoal (worse with cathartics) • Trauma • Oesphageal Injury • Emesis, Lavage, Charcoal • Electrolyte Abnormalities • Forced Emesis, Cathartics • Cardiac Arrest • Toxin induced bradycardia + Vagal Tone • Induced emesis, Lavage • Cost

  25. Summary of Experimental Evidence • Ideal settings • Little benefit in outcomes after 1 hour • Activated Charcoal is equivalent or better than emesis or lavage • Position statement: single-dose activated charcoal. J Toxicol Clin Toxicol 1997;35:721-41. • Position statement and practice guidelines on the use of multi-dose activated charcoal in the treatment of acute poisoning. J Toxicol Clin Toxicol 1999;37:731-51.

  26. Oximes • Ineffective in some situations • Ageing • Variation between organophosphates • Effective protocols not established • Variation in use • Zero – 24 grams a day • Expensive • USA $30-600 / gram • India $6- 9 / gram • Sri Lanka 55 cents / gram • Unlikely to address Non-ACh effects

  27. Alternate sites for antidotes • Protect AChE • Supply AChE • Reduce ACh • Protect ACh Receptor • Reduce OP Load • Multiple Mechanisms

  28. Other Treatments under investigation • Magnesium • Reduces acetylcholine release • Blockage pre-synaptic calcium channels • Limited human studies • Clonidine • Decrease the presynaptic synthesis and release of acetylcholine. • Central nervous system > peripheral cholinergic synapses • Diazepam • Diazepam reduces respiratory failure (rats) and cognitive deficit (primates) • Postulate “uncoordinated stimulation of the respiratory centres decreases phrenic nerve output”.

  29. The Case…. • Picture yourself in Anuradhapura hospital Sri Lanka – ED/ Medical SHO • Ward 6 , teaming with patients…. • Charge Sister tells you there is a sick patient • 36yo F • Taken 100mls of Dimethoate after a domestic argument • There’s nowhere to run, or hide…. So you see the patient – what do you do?

  30. Summary • OP’s are Indirect Cholinomimetic • Block AChE, prolonged duration of ACh in synapse • Effects • Muscarinic, Nicotinic, CNS • Respiratory failure and Death result from this • Treatment • ABC’s, Atropine, Decontaminate, Oximes • Important also in West