21: Restarting Medications after OD Flashcards

1
Q

What are the “7 Principles” to guide restarting meds after an OD?

1) look for opportunities for…..

2) ___ vs_____
3) ___vs _____
4) Is the pt experiencing _____?
5)
6) Is a _______ likely?
–> must ask, what we given anythign to pt to treat their poisioning that now might interact if we restart med?
–> and are we SWITCHIGN antidepressants, whcih may need a washout period?

7) Implementation and minimizing___

A

1) Do they even need the med? look for opportunities for deprescribing.

2) Risk vs Benefit
3) PK vs Toxicokinetics
4) Is the pt experiencing withdrawal/discontinuation syndrome?
5) Is there a blood level that can be done?
–> USUALLY, if pt’s levels are in therapeutic range, they can be restarted on meds.

6) Is a drug interaction likely?
–> must ask, what we given anythign to pt to treat their poisioning that now might interact if we restart med?
–> and are we SWITCHIGN antidepressants, whcih may need a washout period?

7) Implementation and Minimizing risk

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2
Q

If someone OD’s once, are they more likely to OD again vs someone who’s never?

A

yes!

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3
Q

Principle 2: Risk vs. Benefit

  • What is the FIRST question should you ask when asseessing this?
  • what are 3 other questions to ask?
A

What’s the worst possible thing that could hapen if I restart the med right now?

1) does pt look toxic?
2) Pt disposition? and where are they going? home? psych unit? icu? a monitored bed?

2) are they a risk to themslelves or others if they continue to hold antipsychotics for ex?

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4
Q

Principle 2:
- What are 4 characteristics of HIGH RISK situations, where you might considering delaying re-start.

A
  • If still actively CNS depressed.
  • Displaying elements of cardiotoxicity.
  • If they’ve OD’d on a HYPOGLYCEMIC agent (sulfonylurea), have to be able to show they can control blood sugar withotu exogenous glu drip or octreotide antidote. Must show overnight fast = can control sugards on own.
  • If showing any signs of opiate toxidrome.
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5
Q

Principle 3: Kinetics

  • 97% of drugs are eliminated in how many half lives?
  • 99.9%?
A
  • 5 half lives.
  • 99.9% in 10 half lives. [from steady state]
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6
Q

Principle 3: Kinetics

  • How many days does it take for MOST pts to recover from an overdose?
A

1-4 days.

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7
Q

Principle 3: Kinetics

  • What are some important considerations when assessing kinetics of ODs? (4)
A
  • ACTIVE METABOLITES: Are we considering active metabolites from drugs.
  • GENETIC VARIATION IN CYP ENZYMES:
  • SATURATION OF ENZYMES: what other factors can saturate enzymes?
  • CHANGES IN PHYSL MILIEU: Changing blood/urine pH can affect elim of certain drugs
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8
Q

Principle 4: is the pt in withdrawal?

What acronym can you used to assess withdrawal sx? what does it stand for?

A

Flu like symptoms
Insomnia
Nausea
Imbalance
Sensory Disturbances
Hyperarousal (Agitation/Anxiety)

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9
Q

What are the most likely culprits leading to withdrawal?

A
  • SSRIs
  • SNRIs
  • Baclofen
  • Opiates
  • Benzodiazepines
  • Ethanol
  • Beta-blockers
  • Clonidine
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10
Q

Which drug is known for mimicking brain death on overdose?

A

Baclofen

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11
Q

What is an unlikely drug associated with withdrawal?

  • what does it look like clinically?
  • what is the trx? (2)
A

baclofen! GABA-B agent.

It looks like ALCOHOL WITHDRAWAL. {think: ACHAT - ass hat}
Agitation
Confusion
Hallucinations
Autonomic volatility
Tremors

  • Restart at LOWER dose then titrate up slowly.
  • Can use BENZOS.
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12
Q

Principle 7:
- Which drug should you restart first?

A

most clinically imp. drug first; if multiple are imp, restart one with SHORTEST HALF LIFE first.

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13
Q

repeat OD is most likely in _____ months after first OD

A

9-10mths

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14
Q

CEASE stands for

A

Current medications, Estimate RISK, Assess for individual Pt, Sort + plan + implement, Eliminate and follow up

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15
Q

T or F: Toxicokinetics ≠ pharmacokinetics

A

T

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16
Q

____________ withdrawal may see shock like sensations

A

venlafaxine

17
Q

T or F: toxicity can occur below therapeutic levels

A

T

18
Q

T or F: many drugs have TDM order sets

A

F- few

19
Q

T or F: decisions to restart meds should be individualized and guided by multiple pt factors, as it is not well described in literature for post OD pts

A

T