Organophosphate poisoning is caused by exposure to organophosphate compounds found in pesticides and nerve agents. These compounds inhibit the enzyme acetylcholinesterase, leading to accumulation of acetylcholine and overstimulation of nicotinic and muscarinic receptors. Symptoms include bronchoconstriction, vomiting, diarrhea, sweating, muscle weakness and paralysis. Diagnosis is made based on clinical signs and measurement of acetylcholinesterase levels. Treatment involves removal of contaminated clothing, atropine administration to block muscarinic receptors, pralidoxime to reactivate acetylcholinesterase, and supportive care. Complications can include intermediate syndrome of respiratory muscle weakness and organophosphate-
Organophosphate poisoning is caused by exposure to organophosphate compounds found in pesticides and nerve agents. These compounds inhibit the enzyme acetylcholinesterase, leading to accumulation of acetylcholine and overstimulation of nicotinic and muscarinic receptors. Symptoms include bronchoconstriction, vomiting, diarrhea, sweating, muscle weakness and paralysis. Diagnosis is made based on clinical signs and measurement of acetylcholinesterase levels. Treatment involves removal of contaminated clothing, atropine administration to block muscarinic receptors, pralidoxime to reactivate acetylcholinesterase, and supportive care. Complications can include intermediate syndrome of respiratory muscle weakness and organophosphate-
Organophosphate poisoning is caused by exposure to organophosphate compounds found in pesticides and nerve agents. These compounds inhibit the enzyme acetylcholinesterase, leading to accumulation of acetylcholine and overstimulation of nicotinic and muscarinic receptors. Symptoms include bronchoconstriction, vomiting, diarrhea, sweating, muscle weakness and paralysis. Diagnosis is made based on clinical signs and measurement of acetylcholinesterase levels. Treatment involves removal of contaminated clothing, atropine administration to block muscarinic receptors, pralidoxime to reactivate acetylcholinesterase, and supportive care. Complications can include intermediate syndrome of respiratory muscle weakness and organophosphate-
Organophosphate poisoning is caused by exposure to organophosphate compounds found in pesticides and nerve agents. These compounds inhibit the enzyme acetylcholinesterase, leading to accumulation of acetylcholine and overstimulation of nicotinic and muscarinic receptors. Symptoms include bronchoconstriction, vomiting, diarrhea, sweating, muscle weakness and paralysis. Diagnosis is made based on clinical signs and measurement of acetylcholinesterase levels. Treatment involves removal of contaminated clothing, atropine administration to block muscarinic receptors, pralidoxime to reactivate acetylcholinesterase, and supportive care. Complications can include intermediate syndrome of respiratory muscle weakness and organophosphate-
H.O (MU 1) INTRODUCTION • OP Compounds Are Widely Used As Pesticides,Insecticides And Chemical Warfare Agents • OP Compounds Have Been Used More Than 50 Years And Are Still Used In Developing Countries • It Is Believed That B/W 750,000 And 300,0000 OP Poisoning Occur Globally Every Year • Many Studies Estimate That OP Pesticides Cause 300,000 Fetalties Annually In Developing Countries TYPES OF OP COMPOUNDS • NERVE AGENTS • G Agents = Soman,Tabun,Sarin • V AGENTS • INSECTICIDES • Aldicarb,Carbofuran • DIMETHYL COMPOUNDS • Malathion • Fenthion • Dichlorvos • DI ETHYL COPMOUNDS • Parathion • Chlorpyrefos • Diazinon PATHOPHYSIOLOGY • OP Compounds Inhibits The Enzyme Especially Choline Esterase Which Leads To Occumulation Of Acetylcholine In The Cholinergic Synpasis Such As,muscarinic And Nicotinic Receptors,which Results In Acute Cholinergic Phase Followed By Ocassionally In Intermediate Syndrome And Organophophate Induced Delayed Poly Neuropathy CLINICAL FEATURES • ACUTE CHOLINERGIC SYNDROME • Usually starts within few minutes of exposure • It may present with muscarinic and nicotinic feature A. MUCARINIC FEATURES IN PSS i. BRONCHOSPASM & BROCHORROHEA ii. LACRIMATION & MIASIS iii. SALIVATION iv. URINATION v. DIARRHEA & VOMMITING vi. HYPOTENSION & BRADYCARDIA B. NICOTINIC FEATURES IN THE SS i. TACHYCARDIA,HYPERTENSION ii. MYDRIASIS iii. SWEATING CONTINUE…. • NICOTINIC FEATURES IN THE NMJ i. MUSCLE WEAKNESS ii. PARALYSIS iii. FASCICULATIONS
• NICTONIC & MUSCARINIC FEATURES IN THE CNS
i. CONFUSION ii. AGITATIONS iii. COMA iv. RESPIRATORY FAILURE GRADING OF CLINICAL SEVERITY OF OPP MILD MODERATE SEVERE FATAL Rhinorrhea Abdominal Pain Convulsions Coma Sweating Vomitting Pulmonary Edema Convulsions Salivation Diarrhea Respiratory Failure Hypersecretions & Apnea within few minutes after exposure Lacrimation Fasciculations Urinary Incontinance Anxiety ALOC Feacal Incontinance DIAGNOSIS OF OPP • Diagnosis Is Made On The…… 1. Characteristic clinical sign 2. Ideally be confirmed to measure the activity of the butaryl choline esterase in plasma and acetyl choline esterase in red blood cell EMERGENCY AND SUPPORTIVE MEASURE
A. If the agent was recently ingested consider
the gut de-contamination by performing I. Gaustric lavage B. If there is external contamination then Remove the clothes and contact lenses Wash the skin with soap and water MANAGEMENT • Check airway breathing and circulation • Place the patient in the left lateral position as it reduce the risk of stomach contents,makes airway potent and delays the spontaneous absorption of the drug SPECIFIC TREATMENT • ATROPINE Start with 2 mg iv bolus,repeated every 10-25 min untill secretions stopped After 5 minutes of administration check the following parameters Sbp more than 90 mmHg Pulse rate > 80 beats/min Lung fields = Clear Pupils = Dilated Sweating = Stops If above parameters are not corrected double the dose of atropine every 5 minutes untill the above parameters to be corrected CONTINUE…. • Once The Patient Is Stable Start An Infusion Of Atropine Giving Every Hour About 10-20% Of The Total Intial Dose Nedeeded To Stable The Patient • Stop The Atropine Infusion If The Features Of The Toxicity Appears Such As.. Urinary Retention Agitation Hyperthermia Tacchycardia Absent Bowel Sounds • PRALIDOXINE (CONTRATHIONE) Give 30 Mg/Kg IV As Loading Dose Over 10-20 Minutes Followed By The Continues 8-10 Mg/Kg/Hr Maximum Dose Of 12gm In 24 Hr COMPLICATIONS & THEIR MANAGEMENT • INTERMEDIATE SYNDROME o Generally develops quite rapidly in a 1 and 4 days after exposure o About 20% of the patients develop the weakness that spreads from ocular muscles to those of head and neck,proximal limbs and respiratory muscle resulting in the respiratory failure o It may last 2-3 weeks o There is no specific treatment but supportive care including maintainance of airway and ventilations CONTINUE…. • OP INDUCED DELAYED POLY NEUROPATHY It is rare complication that usually occurs 2-3 weeks after acute exposure It is mixed sensory and motor poly neuropathy The early clinical features are the Muscle cramps followed by the numbness and parasthesia proceeding to the flaccid paralysis of the lower limb first followed by the upper limbs There is no specific treatment physiotherapy may limit the deformity Recovery is often incomplete and may be limited to hands and feet Thanks..