Midterm Pre & postlab (Antidotes) Flashcards

(46 cards)

1
Q

A processed charcoal that is obtained from the burning of carbonaceous substances. It involves extensive treatment w/ steam, CO2, O2, ZnCl, H2SO4, H3PO4, at 500-900°F that increases surface area.

A. Activated Charcoal
B. EDTA
C. N-acetylecysteine
D. Naloxone

A

A. Activated Charcoal

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2
Q

they are significantly bound?

A

Organic molecules

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3
Q

they are generally less well bound?

A

LMW & polar compounds

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4
Q

they are also not appreciably bound?

A

certain inorganic salts

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5
Q

this antidote has an adsorption at a ratio of approximately 10:1 and administered in1g/kg PO or gastric tube as aqueous suspension?

A

Activated charcoal

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6
Q

chelating agent especially for lead intoxication; hypercalcemia

A

Ethylenediaminetetraacetic acid (EDTA)

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7
Q

in chronic chronic Pb exposure, a medical condition characterized by high levels of calcium in the blood?

A

Hypercalcemia

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8
Q

the BLL that can be considered as Pb poisoning?

A

> 150mcg/dL

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9
Q

Dosing of EDTA for adult and children?

A

Adult: 2-4g or 30-50mg/kg
Children: 1000-1500mg/m2

IV q24H as continuous IV dil. 2-4mg/mL in NS or D5%
symptomatic: admin. for 3-5days

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10
Q

a precursor to glutathione, direct sulfhydryl binding agent; an antioxidant that helps neutralize the toxic metabolites of APAP that can damage the liver?

A

N-acetylcysteine (NAC)

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11
Q

Dosing of NAC:

A

140mg/kg LD dil. in juice or soda
MD: 70mg/kg q4H

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12
Q

competitive opioid antagonist; takes effect 1-2 mins. after IV. Used in opioid overdose

A

Naloxone

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13
Q

longer elimination t1/2 and DoA; discontinued in US. Used to treat alcohol dependence.

A

Nalmefene

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14
Q

active Po; prevent recidivism in patients detoxified after opioid abuse, and reduce alcohol craving.

A

Naltrexone

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15
Q

Dosing of Naloxone:

A

Adults: 0.4-2mg IV initially, repeat at 2-3 mins. interval; 0.4-0.8mg/h continuous IV (NS or D5%), titrate for effect.

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16
Q

Specific chelating agent for iron (free)

A

Deferoxamine

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17
Q

it is water soluble & renally excreted as (?)

A

Red ferrioxamine complex…orange-pink/vin rose

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18
Q

Dosing of Deferoxamine:

A

5 mg/kg/h IV increasing over 15 mins as tolerated,
do not exceed 15mg/kg/h

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19
Q

enzyme that converts a small portion of the drug into a toxic metabolite known as N-acetyl-p-benzoquinone imine (NAPQI).

A

P450 (CYP2E1)

20
Q

product of the combination of glutathione to NAPQI to form nontoxic substance?

A

Cysteine & Mercapturic acid conjugates

21
Q

Dosing of Paracetamol poisoning:

A

Children: >200mg/kg
Adults: 6-7g

22
Q

Early manifestations of Paracetamol poisoning

A

anorexia & NV

23
Q

After 24-48 hrs. manifestations of Paracetamol poisoning

A

AST & ALT levels rise; evident hepatic necrosis

24
Q

Paracetamol poisoning is diagnosed by?

A

Nomogram; electrolytes (anion gap), liver enzymes

25
a tool used to assess the risk of liver damage following paracetamol overdose.
Rummack-Matthew nomogram
26
chemical asphyxiant binds to these to block the aerobic utilization of oxygen?
cellular cytochrome oxidase
27
a much less toxic compound that is excreted in the urine?
Thiocyanate
28
level of Hydrogen cyanide to be considered as cyanide poisoning:
150-200ppm
29
level of ingested Na or K salts to be considered as cyanide poisoning:
200mg
30
Antidote for Cyanide poisoning
Hydrocobalamin Nithiodote
31
Universal antidote is composed of:
2 parts AC 1 part TA 1 part MgO
32
forms a protective film relieving inflammation and irritation
Demulcent
33
Examples of demulcent:
Milk egg albumin (egg white)
34
this prevents absorption by binding with heavy metals
Demulcent
35
Cyanide poisoning is diagnosed by:
lactic acidosis elevatad venous O2 saturation "bitter" almond odor
36
Abrupt onset of profound toxic effects present in cyanide poisoning shortly after exposure:
Headache Nausea Dyspnea (SOB) Confusion
37
2 active ingredients of Nithiodote:
Na nitrite inj. IV Na thiosulfate IV
38
Management of Poisoning:
1. Accurate history taking 2. Stabilization of patient’s condition 3. Physical examination 4. Laboratory examination 5. Decontamination 6. Poison-specific treatment – antidote 7. Disposition
39
History Taking: 5 W’s
Who – demographics (name, age, weight, etc.) What – identify the drug/ toxin and dose When – time and date Where – route of administration and the geographic location Why – intentional or accidental
40
Emergency evaluation treatment:
A-irways, B-reathing, C-irculation, D-isability, E-xposure
41
Essential Laboratory Tests:
• Serum osmolality and osmolar gap • Electrolytes • Serum glucose • BUN and creatinine • Liver profile • Urinalysis • ECG • Pregnancy test • Tests to detect specific chemical/drug levels
42
Decontamination:
• Wash skin and irrigate eyes • Emesis or gastric lavage • Charcoal or cathartic • Hemodialysis, Hemoperfusion
43
neutralizes the poison by changing its chemical nature or oxidize the poison into non-toxic or insoluble form. Ex, Na thiosulfate
Chemical antidote
44
one that prevents absorption of the poison. Ex. AC
Mechanical antidote
45
one that counteracts the effects of poison by producing opposing physiologic effect. Ex. Naloxone
Physiologic antidote
46
work by forming a complex with the metal ion, which can then be excreted from the body through urine or feces. Ex. EDTA
Chelating agents