Sandbox vidit: Difference between revisions
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{{familytree | | | | | | C01 | | | | | | C02 | | | | | | | |C01=Short acting opioids|C02=Long acting opioids}} | {{familytree | | | | | | C01 | | | | | | C02 | | | | | | | |C01=Short acting opioids|C02=Long acting opioids}} | ||
{{familytree | | | | | | |!| | | | | | | |!| | | | | | | | |}} | {{familytree | | | | | | |!| | | | | | | |!| | | | | | | | |}} | ||
{{familytree | | | | | | D01 | | | | | | D03 | | | | | | | | |D01=<div style="float: left; text-align: left"> ❑ Discontinue short acting opioids <br> ❑ Look for withdrawal symptoms (12-24 hours after last dose)</div>|D03=<div style="float: left; text-align: left">❑ Taper down long acting opioids<br> | {{familytree | | | | | | D01 | | | | | | D03 | | | | | | | | |D01=<div style="float: left; text-align: left"> ❑ Discontinue short acting opioids <br> ❑ Look for withdrawal symptoms (12-24 hours after last dose)</div>|D03=<div style="float: left; text-align: left"> ❑ Taper down long acting opioids<br> | ||
:❑ Methadone to ≤ 30 mg/day | :❑ Methadone to ≤ 30 mg/day | ||
:❑ LAAM to ≤ 40 mg/48 hours<br> | :❑ LAAM to ≤ 40 mg/48 hours<br> | ||
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:❑ For LAAM: 48+ hours after last dose</div>}} | :❑ For LAAM: 48+ hours after last dose</div>}} | ||
{{familytree | | | | | | |)|-|-|-|v|-|-|-|(| | | | | | |}} | {{familytree | | | | | | |)|-|-|-|v|-|-|-|(| | | | | | |}} | ||
{{familytree | | | | | | E01 | | E02 | | E03 | | | | | |E01=<div style="float: left; text-align: left">'''Withdrawal symptoms present:'''<br> ❑ Administer buprenorphine/naloxone 4/1 mg <br> ❑ Observe for 2+ hours</div> |E02=<div style="float: left; text-align: left"> '''Withdrawal symptoms absent:''' <br> ❑ Reevaluate the suitability for induction </div> |E03==<div style="float: left; text-align: left">'''Withdrawal symptoms present:'''<br>❑ Administer buprenorphine 2 mg<BR>❑ Observe 2+ hours</div>}} | {{familytree | | | | | | E01 | | E02 | | E03 | | | | | |E01=<div style="float: left; text-align: left">'''Withdrawal symptoms present:'''<br> ❑ Administer buprenorphine/naloxone 4/1 mg <br> ❑ Observe for 2+ hours </div> |E02=<div style="float: left; text-align: left"> '''Withdrawal symptoms absent:''' <br> ❑ Reevaluate the suitability for induction </div> |E03==<div style="float: left; text-align: left">'''Withdrawal symptoms present:'''<br> ❑ Administer buprenorphine 2 mg <BR> ❑ Observe 2+ hours</div>}} | ||
{{familytree | | | | | | |)|-|-|-|v|-|-|-|(| | | | | | |}} | {{familytree | | | | | | |)|-|-|-|v|-|-|-|(| | | | | | |}} | ||
{{familytree | | | | | | F01 | | F02 | | F03 | | | | | |F01=<div style="float: left; text-align: left">'''Withdrawal symptoms not relieved:'''<br>❑ Repeat | {{familytree | | | | | | F01 | | F02 | | F03 | | | | | |F01=<div style="float: left; text-align: left">'''Withdrawal symptoms not relieved:''' <br> ❑ Repeat buprenorphine 4mg (up to maximum of 8mg/24 hours <br> ❑ Naloxone 1 mg (up to maximum of 2 mg/24 hours)</div>|F02=<div style="float: left; text-align: left">'''Withdrawal symptoms relieved:'''<br> ❑ Day 1 dose established <BR> ❑ Send home patient <BR> ❑ Patient should return on day 2 for forward induction</div> |F03==<div style="float: left; text-align: left">'''Withdrawal symptoms not relieved:''' <br> ❑ Repeat<br> | ||
:❑ Buprenorphine 2mg (up to maximum of 8mg/24 hours)</div> }} | :❑ Buprenorphine 2mg (up to maximum of 8mg/24 hours)</div> }} | ||
{{familytree | | | | | | |`|-|-|-|v|-|-|-|'| | | | | | | | | |}} | {{familytree | | | | | | |`|-|-|-|v|-|-|-|'| | | | | | | | | |}} |
Revision as of 16:33, 7 February 2014
Induction: (day 1) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Identify the opioid's the patient has been using | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Short acting opioids | Long acting opioids | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
❑ Discontinue short acting opioids ❑ Look for withdrawal symptoms (12-24 hours after last dose) | ❑ Taper down long acting opioids
❑ Look for withdrawal symptoms:
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Withdrawal symptoms present: ❑ Administer buprenorphine/naloxone 4/1 mg ❑ Observe for 2+ hours | Withdrawal symptoms absent: ❑ Reevaluate the suitability for induction | = Withdrawal symptoms present: ❑ Administer buprenorphine 2 mg ❑ Observe 2+ hours | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Withdrawal symptoms not relieved: ❑ Repeat buprenorphine 4mg (up to maximum of 8mg/24 hours ❑ Naloxone 1 mg (up to maximum of 2 mg/24 hours) | Withdrawal symptoms relieved: ❑ Day 1 dose established ❑ Send home patient ❑ Patient should return on day 2 for forward induction | = Withdrawal symptoms not relieved: ❑ Repeat
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Withdrawal symptoms relieved: ❑ Day 1 dose established ❑ Send home patient ❑ Patient should return on day 2 for forward induction | Withdrawal symptoms not relieved: Manage withdrawal symptoms symptomatically
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Induction-day 2 forward | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
On return withdrawal symptoms absent: ❑ Administer a daily dose established equal to total buprenorphine & naloxone administered on previous day | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
On return withdrawal symptoms present: ❑ Administer dose equal to Total amount of buprenorphine & naloxone administered on previous day + 4mg of buprenorphine (up to maximum of 12mg on day 2) & 1mg of naloxone (up to maximum of 3mg on day 2) ❑ Observe 2+ hours | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Withdrawal symptoms relieved: ❑ Daily buprenorphine & naloxone dose established | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Withdrawal symptoms not relieved: ❑ Administer buprenorphine 4 mg (up to maximum of 16mg on day 2) & naloxone 1 mg (up to maximum of 4 mg on day 2) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Withdrawal symptoms relieved: ❑ Daily buprenorphine & naloxone dose established | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Withdrawal symptoms not relieved: Manage withdrawal symptoms symptomatically
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Stabilization phase (1-2 months): ❑ Transition when patient has:
❑ As patient stabilizes, transition to alternate day or every third day regimen by doubling and tripling daily doses respectively | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Maintenance phase: ❑ Maintain at same dose as daily stabilization dose
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- ↑ 1.0 1.1 O'Connor, PG.; Waugh, ME.; Carroll, KM.; Rounsaville, BJ.; Diagkogiannis, IA.; Schottenfeld, RS. (1995). "Primary care-based ambulatory opioid detoxification: the results of a clinical trial". J Gen Intern Med. 10 (5): 255–60. PMID 7616334. Unknown parameter
|month=
ignored (help) - ↑ 2.0 2.1 Strang, J.; Bearn, J.; Gossop, M. (1999). "Lofexidine for opiate detoxification: review of recent randomised and open controlled trials". Am J Addict. 8 (4): 337–48. PMID 10598217.