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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<br>
{{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 4mg (up to maximum of 8mg/24 hours)
:❑ 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
❑ Methadone to ≤ 30 mg/day
❑ LAAM to ≤ 40 mg/48 hours

❑ Look for withdrawal symptoms:

❑ For methadone: 24+ hours after last dose
❑ For LAAM: 48+ hours after last dose
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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
❑ Buprenorphine 2mg (up to maximum of 8mg/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:
Manage withdrawal symptoms symptomatically
Clonidine 0.2 mg every 4 hours, tapered after day 3,[1]
or
Lofexidine 0.2 mg BD daily, titrated to 1.2 mg BD daily [2]
❑ Chlordiazepoxide as needed
❑ Return next day for repeat induction attempt
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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
Clonidine 0.2 mg every 4 hours, tapered after day 3,[1]
or
Lofexidine 0.2 mg BD daily, titrated to 1.2 mg BD daily [2]
❑ Chlordiazepoxide as needed
❑ On subsequent induction days, if the patient returns experiencing withdrawal symptoms, continue increasing dose (up to a maximum of buprenorphine 32 mg/day & naloxone 8 mg/day
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stabilization phase (1-2 months):
❑ Transition when patient has:
❑ No withdrawal symptoms
❑ Minimal or no side effects
❑ No uncontrollable craving for opioid agonists
❑ Begin with buprenorphine/naloxone combination, increasing dose by 2/0.5-4/1 mg per week till stabilization is achieved, most stabilizing at 16/4-24/6 mg
❑ 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
❑ Decide total treatment duration based on:

❑ Stable housing & income
❑ Patients motivation, doctors comfort in tapering
❑ Presence of psychosocial support
❑ Absence of legal support
❑ Other drugs & alcohol abuse
 
 
 
 
 
 
 
 
 
  1. 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. 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.