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    Faizah Binti Abdul Rauf

    ORGANOPHOSPHATEPOISONING

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    ORGANOPHOSPHATECOMPOUND

    OP compunds are diverse group ofchemical used in both domestic andindustrial settings

    Examples:

    Insecticides : malathion, parathion,diazinon

    Nerve Gases : soman, sarin, tabun

    Ophthalmic agents: echothiophate,isoflurophate

    Antihelmintics : trichlorfon

    Herbicides : tribufos [DEF], merphos

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    OP POISONING

    Usually from suicidal and accidental events.

    Can occur through

    - inhalation

    - ingestion

    - absorbtion (cutaneous)

    v Generally oral or respiratory exposures

    result in signs or symptoms within threehours.

    v while symptoms of toxicity from dermalabsorption may be delayed up to 12 hours.

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    PATHOTPHYSIOLOGY

    Organophosphorous compounds bind toacetylcholinesterase

    Inhibit acetylcholinesterase

    ACh accumulates throughout the nervoussystem

    Resulting in overstimulation of muscarinicand nicotinic receptors.

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    CLINICAL MANIFESTATION

    Can be divided into 3 categories

    1) Muscarinic effects:

    ) SLUDGE: (Salivation, sweating,Lacrimation, Urination, Diarrhea, GI upset,Emesis)

    ) DUMBELS: (diaphoresis and diarrhea,urination, miosis, bradycardia,bronchospasm, bronchorrhea; emesis,

    lacrimation, sweating and salivation)

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    or SLUDGE BBB

    SLUDGE = Salivation,Lacrimation,Urination,

    Defecation,Gastric Emptying.

    BBB = Bradycardia,

    Bronchorrhea,Bronchospasm.

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    2) Nicotinic effects:

    - diaphoresis, hypoventilation, tachycardia

    - Muscle fasciculations, areflexia, cramps

    and weakness leading to flaccid muscleparalysis.

    3) CNS effects:

    - Anxiety, insomnia, confusion- Resp. depression

    - Seizures and coma

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    In children

    Seizures are more common (22%-25%).

    Lethargy and coma (54%-96%).

    Flaccid muscle weakness,miosis,excessive salivationare common presenting signs

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    ACH: acetylcholine; Epi: epinephrine; NE: norepinephrine; NMJ: neuromuscular

    junction.

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    DIAGNOSIS (clinicalfindings)v 88% of parents initially deny any exposure

    history.

    v petroleum or garlic-like odor.

    v If doubt exists a trial of Atropine (0.01to 0.02 mg/kg) may be employed.

    The absence of signs or symptoms ofanticholinergic effects following atropinechallenge strongly supports the diagnosis

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    DIAGNOSIS (Lababnormalities)

    RBC acetylcholinesterase activity:

    Represents that was found on RBC membranesimilar to that found in neuronal tissue.

    Therefore, more accurately reflects NS AChEinhibitor.

    Determine the effectiveness of antidotetherapy.

    Plasma (or pseudo-) cholinesteraseactivity:

    more easily performed.

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    MANAGEMENT

    1) Initial resuscitation

    v)Deliver 100 % oxygen via facemask

    v)Strongly consider intubation:

    patients who appear mildly poisoned may rapidlydevelop respiratory failure.

    v)Consider volume resuscitation with normalsaline or ringer to treat Bradycardia and

    hypotension.v)Monitor ECG, vital signs every 5-15 min, pulse

    oximetry.

    v) In cases of dermal exposure aggressivedecontamination with complete removal of the

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    2) Drug therapy

    Use activated charcoal within one hour ofan ingestion.

    dosage: 1g/kg body wtAtropine : 1st drug to be given

    Competes with acetylcholine at

    muscarinic receptors.Major use: reduce broncorrhea and

    bronchospasm

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    DOSAGE:

    Adult:

    v Initial dose 2 mg IV bolus.

    v Doubled every 10 min until bronchial secretions andwheezing stop .

    Paeds:

    v Initial dose 0.05 mg/kg IV bolus.

    v Doubled every 10 min until bronchial secretions arecontrolled.

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    v Keep a maintenance dose of atropine for 2-3 days after disappearing of manifestation.

    vTachycardia and mydriasisare notappropriate markers for therapeuticimprovement, as they may indicatecontinued hypoxia, hypovolemia, or

    sympathetic stimulation.

    v Fever, musclefibrillation, and delirium arethe main signs ofatropine toxicitythatindicate that atropine administration should

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    Pralidoxime

    Cholinesterase reactivating agent that areeffective in treating both muscarinic andnicotinic symptoms.

    v Use within 48 hours after poisoning.

    v

    Use with concurrent ofatropine.

    v Effects will be apparent within 30 minutes

    v Dosage: Adult:- 1g IV, Children:- 25-50

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    Benzodiazepine (diazepam)

    -To reduce anxiety and restlessness and tocontrol convulsions

    - Dosage: -5-10 mg IV for anxiety orrestlessness

    -up to 10-20 mg IV for control ofconvulsions.