Presentation is loading. Please wait.

Presentation is loading. Please wait.

PESTICIDE POISONING Shiromini Nissanka Research Officer National Poisons and Drug Information Centre.

Similar presentations


Presentation on theme: "PESTICIDE POISONING Shiromini Nissanka Research Officer National Poisons and Drug Information Centre."— Presentation transcript:

1 PESTICIDE POISONING Shiromini Nissanka Research Officer National Poisons and Drug Information Centre

2 WHAT IS A TOXIC SUBSTANCE ? Any substance which is harmful to the environment and humans. There are naturally occurring toxins and synthetic toxins. Toxic Substance Natural Toxins Synthetic Toxins Poisonous plants Pesticides SnakesIndustrial chemicals Other poisonous animalsHousehold products

3 WHAT IS A PESTICIDE ? A Pesticide is a chemical use to prevent, destroy or repel pests. Pests can be Insects, Mice, Weeds, Fungi or Microorganisms such as Bacteria and Viruses. Pesticides - Insecticides Weedicides Rodenticides Fungicides

4 INSECTICIDES Organophosphates - Baytex EC 50, Harcros Demro Carbamates - Baygon Fly Bait Organochlorine - Aldrin Pyrethroids - Baygon mosquito coil

5 WEEDICIDES Paraquat - Gramoxone Propanil DPA Glyphosate - Roundup Chlorophenoxy - MCPA

6 RODENTICIDES & FUNGICIDES Zinc phosphide- Run rat Coumarins- Racumin Brodifacoum- Klerat Pellets Sulphur - Morisal WP, Dithiocarbamate - Metaxil

7 TYPE & ROUTE OF POISONING AccidentalOral SuicidalInhalation HomicidalDermal OccupationalEye contact

8 ORGANOPHOSPHATES AND CARBAMATES Group of chemicals share a common mechanism of cholinesterase inhibition and hence can cause similar symptoms. –Phosphorylation of the acetylcholinesterase (AChE) at nerve endings. –Loss of available AChE results accumulation of acetylcholine at receptor sites and effector organ to become over stimulated by the excess acetylcholine.

9 ORGANOPHOSPHATES AND CARBAMATES Contd. Clinical Features are based on excessive cholinergic stimulation. Unlike organophosphate poisoning, carbamate poisoning tend to be of shorter duration because the inhibition of nerve tissue AChE is reversible.

10 CLINICAL FEATURES Eye contact: Irritation or pain, lacrymation, swelling, blurring of vision. Inhalation: Cough, difficulty in breathing, bronchitis, pneumonia. Ingestion: Nausea, vomiting, diarrhoea, sweating, salivation, small or pin point pupils, muscle twitching, fasciculation.

11 ORGANOCHLORINES Very few organochlorines are used now as pesticides. Organochlorines are very toxic if ingested or inhaled. Some are readily absorbed through the intact skin. Skin contact: Dermatitis Inhalation: Inhalation can give rise to irritation of eyes, nose, throat and cough. Ingestion: Nausea, vomiting, diarrhoea, abdominal pain, headache, dizziness, convulsions and coma.

12 PYRETHRINS & PYRETHROIDS Pyrethrum is an insecticide extracted from chrysanthemum flower. Active ingredients of pyrethrum are known as pyrethrins. Synthetic compounds structurally related to pyrethrins are known as pyrethroids. Inhalation: Allergic manifestations such as wheezing.

13 PYRETHRINS & PYRETHROIDS Contd… Ingestion: After ingestion pyrethrums have low toxicity, vomiting, epigastric pain and diarrhoea are the common features. Eye contact: Lacrymation, oedema of the eyelids. Skin contact: Allergic dermatitis.

14 PARAQUAT Paraquat is a widely used herbicide in Sri Lanka. It is a safe herbicide because it is inactivated by contact with soil. Paraquat is commonly used as suicidal poison in this country. Paraquat has life threatening effects on the gastrointestinal tract, kidney, liver and other organs. The lung is the primary target organ of paraquat poisoning.

15 PARAQUAT Contd… Recently a new paraquat formulation with INTEON technology (containing an alginate that converts to a gel under stomach acid conditions, increased levels of emetic and purgative) was developed in order to reduce oral toxicity. However ingestion of INTEON is still very likely to be lethal. Skin contact: prolonged contact will produce blistering, abrasion and ulceration. Although absorption across intact skin is slow, abraded or eroded skin allows efficient absorption.

16 PROPANIL & CHLOROPHENOXY COMPOUNDS Propanil is a selective herbicide of low toxicity. However, in self poisoning with large doses methaemogloninaemia is cause, which can be fatal. Chlorophenoxy compounds are well absorbed from the gastrointestinal tract. They are less well absorbed from the lung. Cutaneous absorption appears to be minimal.

17 GLYPHOSATE Glyphosate is a non-selective herbicide, typically marketed as an aqueous solution of 41% isopropylamine glyphosate, 15% polyoxyethyleneamine surfactant and various minor components including anti- foaming and colour agents, biocides and inorganic ions to produce pH adjustment. Ingestion of concentrated formulations may cause epigastric pain, dysphagia, nausea, vomiting, oral ulceration, diarrhoea and haemetemesis in severe cases leading to hypovolaemic shock.

18 RODENTICIDES Coumarins, indandiones and brodifacoum are used as rodenticides. They are fairly safe for human beings due to the low concentration of the active ingredient. Their toxicity is due to depression of the synthesis of factors essential for coagulation of blood.

19 BANNED PESTICIDES 1970 – Endrin 1976 – DDT 1980 – Chlordimeform 1980 – Dieldrin 1980 – Phosphamidon 1980 – Thallium sulpht – 2,4,5-T 1984 – Ethyl parathion 1984 – Methyl parathion Aldrin 1986 – Lindane 1987 – HCH (mixed Isomers) 1987 – Mercury cpds – Arsenic (arsenites and arsenates) 1988 – Hepatachlor 1989 – Leptophos Captafol 1990 –Dichloropropane

20 BANNED PESTICIDES Contd – Aldicarb 1990 – Quintozene (PCNB) 1994 – Pentachlorophenol 1995 – Methamidophos 1995 – Monocrotophos (restricted to coconut) 1996 – Chlordane Endosulfan

21 FIRST AID Skin contact:  Remove contaminated clothes carefully.  Wash the skin with running water for at least 15 minutes.  Do not use any local application without seeking medical advice.

22 FIRST AID Contd…  Wash eyes with running water for at least 15 minutes.  Do not use any eye drops without seeking medical advice.  If there is visual impairment seek medical advice from an Ophthalmologist.

23 FIRST AID Contd… Inhalation: Remove the patient away from the source and encourage deep breathing of fresh air. Ingestion: Do not induce emesis because some pesticides have corrosive effects and some may contain hydrocarbons as solvents. If patient is semiconscious or unconscious keep the patient in Neck extended position.

24 Management of Organophosphate and Carbamate poiosning Contd… Atropine: The following features of cholinergic syndrome is an indication for atropine therapy. Poor air entry in to the lungs due to bronchorrhoea and bronchospasm. Excessive sweating Bradycardia Hypotension Miosis

25 Management of Organophosphate and Carbamate poiosning Contd… Initial dose: 1.8 – 3 mg, 3-5 of 0.6 mg vials rapidly IV into a fast flowing IV drip depending on the condition. After 5 min. check the five parameters and if there is no improvement double the dose.

26 Management of Organophosphate and Carbamate poiosning Contd… Once atropinised clinical features: –Clear lungs –Adequate heart rate ( > than 80 beats/m.) –Blood pressure (> 80 mmHg systolic) –Dry skin –Pupils no longer pinpoint –Set up an infusion with 10-20% of total amount of atropine.

27 Management of Organophosphate and Carbamate poiosning Contd… Target end points for atropine therapy. Clear chest on ausculatation with no wheeze. Heart rate between beats/min. Pupils no longer pinpoint. Systolic blood pressure > 80 mmHg. Dry axillae.

28 Management of Organophosphate and Carbamate poiosning Contd… Excess atropine causes confusion, urinary retention, hyperthermia, bowel ileus and tachycardia. In this condition atropine should be ceased and the patient reviewed after 30 min. to see whether the features of toxicity have settled. When atropine toxicity settles 70-80% of the previous rate.

29 Management of Organophosphate and Carbamate poiosning Pralidoxime: Give 30 mg/kg loading dose of pralidoxime over min. followed by a continuous infusion of 8-10 mg/kg per hour until clinical recovery (for example hours after atropine is no longer required or the patient is extubated) or 7 days which is later. Less severely poisoned patients can be given intermittent doses (1 gram 6 hourly by slow IV bolus over 10 – 20 mins). Oximes are not required for carbamate poisoning.

30 Management of Organochlorine poisoning For convulsions give diazepam 5-10 mg IV slowly (Paediatric dose 0.2 mg/kg). Repeat if necessary. Up to 40 mg/day can be given orally as maintenance dose. Continue diazepam for 3-4 days after convulsions have been controlled. 10 ml of 10% calcium gluconate IV can also be used to control convulsions.

31 Management of Paraquat poisoning An absorbent (Fuller’s earth or Activated charcoal) should be given orally or via a nasogastric tube as early as possible. The dose of Fuller’s earth is 1 litre of 15% aqueous suspension (Paediatric dose 15 ml/kg body weight). If Fuller’s earth is not available give activated charcoal g dissolved in 200 ml of water (Paediatric dose 15 ml/kg body weight).

32 Management of Propanil poisoning If symptoms of methaemoglobinaemia are present (tachycardia, tachopnoea or confusion) or if the levels are over 30%, give 1% methylene blue 0.1 ml/kg IV over 5 minutes. The same dose may be repeated within 1 hour if there is no improvement. If IV preparation is not available give methylene bluee 300 mg daily orally. If methylene blue is not available give ascorbic acid 1 g IV twice daily.

33 Management of Rodenticide poisoning If there has been no bleeding, but the PT is prolonged, give vitamin K mg orally two to four times a day (paediatric dose 0.4 mg/kg/dose). For prolonged PT with less severe bleeding, give vitamin K1 10 to 15 mg SC or IM (for a child 1 to 5 mg). In severe haemorrhage with prolonged prothrombin time (PT) give vitamin K1 (phytomenadione) 20 mg by slow IV injection (0.6 mg/kg for children under 12 years). In severe bleeding, it may be necessary to give fresh frozen plasma or fresh blood.

34 THANK YOU


Download ppt "PESTICIDE POISONING Shiromini Nissanka Research Officer National Poisons and Drug Information Centre."

Similar presentations


Ads by Google