Module 6: Opioid agonist treatment (OAT) initiation and stabilization phase Flashcards

1
Q

What is the name of the Canadian guideline for OUD management?

A

CRISM (Canadian Research Initiative in Substance Use)
(unclear what year)

CAMH also has a guideline: Opioid Agonist Therapy: A Synthesis of Canadian Guidelines for Treating Opioid Use Disorder – Canadian Opioid Use Disorder Clinical Guidelines (2021)

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2
Q

Prescribing practices for narcotics

A
  • written or faxed prescriptions only
  • no refills permitted
  • dose in mg (write dose in words)
  • new start vs dose increase or decrease
  • start and end dates (“inclusive”)
  • specific days for observed doses
  • specific days for carries
  • for methadone: “doses should be dispensed in orange juice
  • for bup/nlx: “sublingual administration”
  • for bup/nlx don’t specific # of tablets, just dose, frequency, duration and allow pharmacist to figure out required number of tablets
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3
Q

Physician requirements for prescribing methadone

A

> “effective May 19, 2018, exemption is no longer required to prescribe methadone for opioid use disorder”

> CPSO: “As with all areas of practice, physicians must only prescribe methadone if they have the knowledge, skill, and judgment necessary to do so safely and effectively. Physicians and other health-care professionals can obtain the necessary training and education by completing the Centre for Addiction and Mental Health’s Opioid Use Disorder Treatment course and Opioid Dependence Treatment Certificate Program.2”

  • In other words: you should do the CAMH training course
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4
Q

Physician requirements for prescribing bup/nlx

A

nothing mentioned on CPSO
Probably should have training.

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5
Q

Prescription practices when starting / changing dose

A

“Cancel previous prescriptions”
“Dose change”

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6
Q

What should happen to OAT prescription upon admission to hospital?

A

Should be cancelled at community pharmacy so that
- admission is communicated
- avoids errors in dose changes / prescriptions

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7
Q

What should be communicated to client at initiation

A
  • effects / side-effects / toxicity / interaction with other opioids
  • bup/nlx starts at 2-4mg, requires few weeks to optimum dose
  • methadone starts 15-30mg, risk of toxicity
  • withdrawal symptoms until dose optimized
  • risk reduction: naloxone kit, small doses, do not use alone
  • missed doses and apparent intoxication at pharmacy
  • written agreement
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8
Q

Buprenorphine time of onset (peak plasma concentration)

A

1 hour

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9
Q

Buprenorphine half-life

A

32 hours on average

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10
Q

Initiating bup/nlx: what describes moderate withdrawal?

A

COWS 13+

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11
Q

Initiating bup/nlx: estimated wait times to moderate withdrawal?

A

short-acting opioids: 12h+
long-acting opioids: 12-24h+
methadone: 36h to 3-5 days
fentanyl: tricky because it accumulates in fat tissue, risk of precipitated withdrawal

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12
Q

What makes a high risk for precipitated withdrawal when starting bup/nlx in fentanyl users?

A

accumulates in fat tissue, so effective half-life is prolonged
risk of precipitated withdrawal even when moderate withdrawal sx or 12h+ since last use

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13
Q

initiating bup/nlx: microdosing – the big idea

A

avoid any moderate-severe withdrawal symptoms by gently introducing partial-agonism of bup/nlx:
1. using full agonist therapy (e.g. methadone)
2. while slowly increasing bup/nlx dose over a week

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14
Q

initiating bup/nlx: microdosing – the protocol

A
  1. Start with a low dose of bup/nlx (e.g. 0.5mg) overlapping with other opioid use.
  2. Implement small (e.g., 0.5–1 mg) daily dose increases of bup/nlx, over five to seven days.
  3. Cease opioid use abruptly after reaching a total daily dosage of 12 mg of bup/nlx.
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15
Q

initiating bup/nlx: microdosing – target populations

A
  • use illicit fentanyl and fentanyl analogues (b/c unpredictable withdrawal)
  • may not reliably attend appointments due to work commitments or social instability
  • cannot tolerate moderate to severe withdrawal.
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16
Q

initiating bup/nlx: conventional approach – induction day

A

if COWS > 13,
0. prescriptions for supportive meds (clonidine, loperamide, dimenhydrinate)
1. client -> pharmacy for first dose
2. returns (not driving self)
3. re-assessed over 3 hours to confirm no precipitated withdrawal

17
Q

initiating bup/nlx: conventional approach – initial dose

A

2-4mg

consider also one to two 2mg tabs PRN for withdrawal symptoms
max 12mg total in one day

18
Q

initiating bup/nlx: conventional approach – titration

A

day 1: 2-4mg once + 2mg x 1-2 tabs PRN withdrawal
day 2: doubled (4-8mg once), max 24mg po daily
day 3: doubled again (8-16mg once), max 24mg po daily
etc.
stop when no withdrawal x 1 day

19
Q

initiating bup/nlx: conventional approach – titration – elderly

A

slower titration:
increase by 2-6mg every one to two days max 24mg daily

same stopping criteria: stop when no withdrawal x 1 day

20
Q

long-acting bup: formulations

A

implants (q6month, abstinence prior, up to 8mg SL daily)
subq (qmonthly, no abstinence required, 8-24mg SL x 7 days prior)

21
Q

methadone – time to steady state

A

5-10 days (half life 36 hours on average)

22
Q

methadone – initiation – key determinate to chose starting dose

A

risk of methadone toxicity
high risk = low opioid tolerance (i.e. low potency use, low frequency use)

23
Q

methadone – initiation / titration – high risk of toxicity

A

high risk: low potency use, low frequency of use

max 10mg, then increase by 5mg every 5 days

24
Q

methadone – initiation / titration – moderate risk of toxicity

A

moderate risk: established tolerance (by UDT/hx), high risk factors for resp depression (COPD, depressant use, elderly)

5-20mg, then increase by 5-10mg every 3-5 days

25
Q

methadone – initiation / titration – low risk of toxicity

A

low risk: established tolerance + no risk factors for resp depression

5-30mg, then increase 5-15mg every 3-5 days

26
Q

SROM – target population

A

very high tolerance (e.g. fentanyl use) + failed bup/nlx or methadone

27
Q

SROM – initiation / titration

A

1 week induction phase

not using methadone (e.g. using heroin):
1. start 30-60mg, increase by 30-60mg q2days, max 200-800mg daily

using methadone (i.e. switching from methadone to SROM):
1. start at 1:4 methadone:SROM dose
2. target 1:6 or 1:8

28
Q

iOAT – indications

A

severe opioid IVDU despite methadone or bup/nlx
high risk of medical complications with continued IVDU
capacity to attend 3 times daily for observed (self-)administration

29
Q

iOAT – formulations

A

Hydromorphone or diacetylmorphine

30
Q

iOAT – dosing

A
  • Hydromorphone: 10mg TID, increase by max total 30mg / day, max 200mg/dose
  • Diacetylmorphine: 20mg TID, increase by max total 60mg / day, max 400mg/dose
31
Q

iOAT – co-prescriptions

A

methadone or SROM to avoid cravings in between injections (ie. overnight)