This document summarizes guidelines for treating exposure to various chemical and radiological agents. It provides details on the mechanisms and dosing of antidotes for nerve agents (atropine, benzodiazepines, 2-PAM), cyanide (nitrites, sodium thiosulfate), botulinum toxin (antitoxin), thallium (Prussian blue), and radiation (potassium iodide, Prussian blue). It emphasizes the importance of rapid administration of the correct antidote to prevent lasting effects of exposure and maximize survival.
Disorders of the neuromuscular junction include Myasthenia gravis, Lambert-Eaton myasthenic syndrome, Botulism, Tetanus, Strychnine intoxication, Organophosphates poisoning and neuromyotonia. Pharmacology of the NMJ is also reviewed in brief.
this is all medicine are used in anesthesia so as student are in field of anesthesia you can find this attachment, may it will help you to know more about this general anesthetics drugs if you got a questions you contact me inbox
this presentation is based on anticonvulsants which are used to cure or to control the disturbance created in brain by abnormal discharging of neurons which is termed as epilepsy.
Disorders of the neuromuscular junction include Myasthenia gravis, Lambert-Eaton myasthenic syndrome, Botulism, Tetanus, Strychnine intoxication, Organophosphates poisoning and neuromyotonia. Pharmacology of the NMJ is also reviewed in brief.
this is all medicine are used in anesthesia so as student are in field of anesthesia you can find this attachment, may it will help you to know more about this general anesthetics drugs if you got a questions you contact me inbox
this presentation is based on anticonvulsants which are used to cure or to control the disturbance created in brain by abnormal discharging of neurons which is termed as epilepsy.
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Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
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Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
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Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
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Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
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Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
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Chemical terrorism attacks - update on antidotes - handout
1. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Chemical Terrorism Attacks: Update on Antidotes
Nerve agents
Vapour exposures immediate symptoms (seconds to minutes)
Dermal exposures delayed (minutes to 18 hours)
Farooq Khan MDCM
PGY3 FRCP-EM
McGill University
November 14
th
2011
2. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Mark-1 Kit
Atropine
Mechanism Atropine acts at muscarinic cholinergic receptors as a competitive antagonist. It is used to counter
muscarinic effects, and administration will result in drying of secretions, alleviating bronchospasm, and reversing central
apnea. Given within the first 5 minutes, it can prevent organophosphate-induced seizures
Delivery autoinjector is more effective than IM injections using a conventional syringe, can go through clothing or
protective garments. Additional atropine doses should be administered IV once access is obtained
Dosing
Field treatment for severe poisoning is three autoinjectors or 6 mg initially with retreatment q 5-10 min
The initial intravenous dose should be 2 mg for adults or 0.02 mg/kg for children
Atropine doses should be repeated q 5 min until the therapeutic endpoint is reached (ie, until pulmonary
secretions are dried [reflected by improved oxygenation] and ease of breathing [or ease of ventilation])
Typical total dose required after nerve agent poisoning has ranged from 5 to 20 mg (up to 200mg in cases)
Precautions. Excessive doses of atropine can result in deleterious effects including delirium, agitation, and tachycardia
and hypertension. Atropine will likely not improve miosis or skeletal muscle paralysis; therefore, reversal of these effects
is not a therapeutic endpoint.
Benzodiazepines
Indications
Any patient who has significant symptoms from nerve agent exposure to prevent seizure and neuronal damage
Infused rapidly to unresponsive patients who may have nonconvulsive seizures due to the onset of paralysis
Alleviate extreme anxiety
3. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Dose/delivery
Diazepam 10 mg IM auto-injector in the field, Midazolam IM/IV in hospital
2-PAM
Neither atropine nor benzodiazepines will alleviate symptoms affecting the nicotinic system.
Over time, nerve agents will form an irreversible covalent bond with AChE in a process termed aging.
Once aging occurs, the patient will not regain vital functions, such as muscle strength or respiratory drive, until
new enzyme is synthesized (may take weeks to months)
Oxime reactivates AChE if administered before aging
Indications. 2-PAM should be given to any patient exposed to an organophosphate nerve agent who is showing any
systemic toxicity. This is particularly true if there are fasciculations or weakness.
Dose/Delivery
Mark 1 auto-injector 600mg IM per dose for the field (max
3 injections). IV preferred in hospital.
Initial dose is 1- 2 g diluted in 100mL normal saline
and given over 15-30 min
Initial pediatric dose is 20 to 50 mg/kg up to 2 g
WHO recommendation >30mg/kg bolus then
>8mg/kg/hour infusion to maintain therapeutic levels
due to short t½ (90 min)
For severely poisoned patients: 2 g IM or slow IV
infusion over 15-30 minutes then 500mg/h infusion.
Precautions. Rapid delivery can cause laryngospasm,
rigidity, and self-limited hypertension responding to
phentolamine 5 mg IV
Pediatrics
↑minute ventilation/kg → ↑ risk with exposure
Small airways with bronchospasm and ↑secretions→ ↑rates of respiratory distress/failure
↑prone to seizures
The dose for atropine can be up to 0.05 - 0.1 mg/kg either IV/IO/IM.
40 kg can be administered an adult (2 mg) autoinjector
20 kg can receive a 1-mg autoinjector
10 kg can receive a 0.5-mg autoinjector
The dose for 2-PAM is 25 to 50 mg/kg, up to a total of 2 g.
12 kg will be able to tolerate the dose of one 600-mg 2-PAM autoinjector
Diazepam should be dosed at 0.05 to 0.3 mg/kg IV,
> 30 kg can receive an adult autoinjector
Autoinjector needle is 1 inch, so choose site carefully
Stockpile antidotes if stocks run out, glycopyrrolate (no central effects), scopolamine (more potent central
effects), diphenhydramine, and jimsonweed extract can be used as alternatives
4. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Cyanide
Found in smoke inhalation, industrial accidents, suicide attempts, criminal poisonings and can be potent chemical
weapon.
Primary toxic action is inducing cellular hypoxia through inhibition of cytochrome oxidase, blocking oxidative
phosphorylation → shift from aerobic to anaerobic metabolism causes a depletion of cellular ATP and ↑lactic acid
Effects depend on dose/route/timing
o CNS and cardiac toxicity because these are the most O2-sensitive systems
o Concentrated exposure→ death within minutes (i.e. no time for medical intervention)
o Lesser exposure→ nonspecific symptoms including shortness of breath, hyperventilation, headache,
weakness, and dizziness, which can be attributed to anxiety or other exposures
o Progression to confusion, lethargy, seizures, and coma.
o Neurally mediated tachypnea along with an initial ↑BP
o Can progress to cardiac arrest heralded by bradycardia and hypotension
o Cherry red color and ↑O2 Sat
Cyanide antidote kit
Amyl nitrite, sodium nitrite, and sodium thiosulfate
5. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Mechanism
o Nitrites (amyl and sodium) induce methemoglobinemia
o Cyanide has a ↑affinity for methemoglobin and will leave the mitochondria to bind to it and allow the
mitochondria to resume oxidatitive phosphorylation.
o Sodium thiosulfate acts as a sulfhydryl donor for the enzyme for the enzyme rhodanese that converts cyanide to
the less-toxic renally excreted thiocyanate
Indications to initiate therapy
High index of suspicion
o clusters of patients, structural fire victim, high risk activity (e.g. jeweller, lab worker)
Clinical presentations
o sudden LOC, seizures, HD instability without probable cause
Surrogate markers
o lactate, metabolic acidoses, narrow arteriovenous O2 Sat gap
Dose/delivery
Crush amyl nitrite glass pearls and inhale or administer via BMV until IV line (goal to induce 3-5% MetHb)
Then switch to sodium nitrite IV 300mg (10ml of 3% sol’n) over 2-4min,
Peds: 10mg/kg with normal Hb, 6mg/kg in anemic or unknown Hb child
Sodium thiosulfate 12.5g IV (50ml of 25% sol’n) over 10 min, peds 1.65ml/kg of 25% sol’n
Give with high-level O2 , charcoal for oral exposures
Precautions
Vasodilation, tachycardia, hypotension with high doses of nitrite
↓ O2 carrying capacity with MetHb, avoid in anemic, CO poisoned
Thiosulfate can cause hemolysis in G6PD deficiency
Thiocyanate can be toxic in renal failure (abdo pain, rash, vomiting, CNS dysfunction)
Hydroxycobalamin
Combines with CN to cyanocobalamin a.k.a. Vitamin B12 (safe and renally excreted)
Low threshold of administration given safety profile
Dose
o 70mg/kg, max 5g(adult dose) IV over 15 min
o Each vial of 250ml contains 2.5g, which needs to be diluted in 100ml of NS to bind 250mg of CN
o Repeat dosing in severe toxicity
Combine with sodium thiosulfate but either sequentially or in a different line (inactivated if in the same line)
scavenges NO and prevents hypotension
transient red discoloration of skin and mucus membranes, interferes with lab assays of bili, creat, mg, fe
otherwise safe and preferred over nitrites
Mass exposure
Most patients will not have significant exposures
Patients presenting in cardiac arrest will have low survival
Reserve antidotes for those most likely to survive
Can use thiosulfate alone
6. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Botulism
Clostridial toxins A, B, E, and F
Highly potent (LD 50 of 1μg/kg)
Food water (onset 2h-5 days), aerosolized (onset 3 days), injection
Prevents fusion of synaptic vesicles with presynaptic membrane in PNS (cannot cross BBB) prevents
neurotransmission
Descending weakness, EOMs and bulbar cranial nerves (diplopia/dysarthria/dysphagia) then motor function of
UE then LE. Can affect intercostals and diaphragm needing mechanical ventilation. Spared sensory and
mentation.
Anti-muscarinic effects and nausea vomiting precede neurologic symptoms
Paralysis is irreversible until cleaved protein is regenerated which can last months
Antitoxin
halts progression of paralysis
binds and neutralizes free botulinum toxin
indicated on clinical suspicion (clusters of patients with similar geography etc)
dose 1 vial of Ig IV over 30-60 min diluted 1:10 in NS
1% allergic reaction to horse serum based Ig
Baby-BIG is human derived and recommended in infants
Thallium
Less well known toxic heavy metal odourless and colorless dissolved in water (used in myocardial scintigraphy)
Minimum lethal dose of 12mg/kg
Absorbed from GI tract, causes green discoloration of urine in 1h
Unclear if Interferes with Krebs cycle, glycolysis, and oxidative phosphorylation, or forms stable complexes with
the active sulfhydryl sites on enzymes
Nonspecific symptoms (early GI, mostly neuro)
Reliable early clue for thallium toxicity is an ascending, rapidly progressive painful sensory peripheral
neuropathy (feet)
Delayed alopecia (weeks)
Prussian Blue
Enhances elimination by blocking enteroenteric and enterohepatic recirculation of thallium
Indicated for any patient with toxicity or known exposure
150-250 mg/kg/day divided tid until urinary thallium excretion is <0.5mg/day
No side effects except blue tears and constipation (Dissolve in 50ml of 15% mannitol as cathartic)
Can use activated charcoal as alternative if in low supply of Prussian blue
7. Adapted from Lawrence DT and Kirk MA, Chemical Terrorism Attacks: Update on Antidotes. Emerg Med Clin N Am 25 (2007) 567–595
Radiation
Potassium iodide (KI)
Prevents thyroid cancer in patients exposed to radioactive iodine
Subtotal protection
Must be administered within hours
Indications
o Children, pregnant or lactating women with >0.05 Gy exposure
o Adults over 40 with dose >5 Gy
Dose
o Newborn – 1 month: 16 mg po qd
o Infants and children <3 : 32 mg po qd
o Children 3-18: 65 mg po qd
o Adults: 130 mg po qd
Prussian blue
For cesium-137 (used in radiotherapy and medical devices, could be used in dirty bomb), behaves like
potassium. Physiological t½ of 50-150 days, renally excreted in 4:1 ratio with fecal excretion
↓urine/feces excretion ratio to 1:4 and ↓t ½ by 43%
Dose 3-10g/day
FDA recommendation : 3g bid for adults, 1g tid for children 2-12 ×30days
Mostly non toxic and not absorbed, although not studied in ARS GI syndrome where there is severe
inflammation of mucosa.