- Joined
- Sep 7, 2008
- Messages
- 60
- Reaction score
- 7
Is anyone prescribing Suboxone in their practice? I'm primarily interventional pain, but just wondered if anyone had experience with this side of Pain Medicine? Pros and Cons? Thanks.
That's opiate rotation and not getting off opiates. My pen has the feature of writing a taper of any opiate that they are currently on, often without need to pen a new Rx.I find it useful to take the patients treatment course to completion. I don't take on heroin addicts or the like, just help get the people I treat off the opioids.
That's opiate rotation and not getting off opiates. My pen has the feature of writing a taper of any opiate that they are currently on, often without need to pen a new Rx.
I think suboxone should come from addiction psych only.
Not necessary. If used in the "occasional" appropriate patient (selected by you the pain doctor), it can do wonders. While most of the things written about on this board talk about our worst of the worst drug abusing patients, there are many patients are truly sick of taking pills and are having trouble with tapering. With the economy being how it was the past few years, giving patients a fast taper is sometimes a recipe for disaster in terms of work performance. The patients have to motivated to do this, and understand that suboxone doesn't work well for pain, but rather will at least bring their pill taking under control. Most of these selected patients quickly become more willing to try other modalities of treatment, and most do eventually become better. Anecdotally, I've seen quite a few patients who we select for suboxone treatment at the clinic start tapering lower over the course of 12-18 months. Interestingly, even patients who have been on high doses of opioids, usually settle on taking between 8-12mg of suboxone daily.
Self selecting patients for suboxone. Hmm. Thats not pain. Thats addiction. Proactive addiction.
But to a federal agrncy it can appear as if you are mainaining addicts yo allow ongoing injections.
JAMA Intern Med. 2014 Oct 20. doi: 10.1001/jamainternmed.2014.5302. [Epub ahead of print]
Primary Care-Based Buprenorphine Taper vs Maintenance Therapy for Prescription Opioid Dependence: A Randomized Clinical Trial.
Fiellin DA1, Schottenfeld RS2, Cutter CJ1, Moore BA2, Barry DT2, O'Connor PG1.
Author information
Abstract
IMPORTANCE:
Prescription opioid dependence is increasing and creates a significant public health burden, but primary care physicians lack evidence-based guidelines to decide between tapering doses followed by discontinuation of buprenorphine hydrochloride and naloxone hydrochloridetherapy (hereinafter referred to as buprenorphine therapy) or ongoing maintenance therapy.
OBJECTIVE:
To determine the efficacy of buprenorphine taper vs ongoing maintenance therapy in primary care-based treatment for prescriptionopioid dependence.
DESIGN, SETTING, AND PARTICIPANTS:
We conducted a 14-week randomized clinical trial that enrolled 113 patients with prescription opioiddependence from February 17, 2009, through February 1, 2013, in a single primary care site.
INTERVENTIONS:
Patients were randomized to buprenorphine taper (taper condition) or ongoing buprenorphine maintenance therapy (maintenancecondition). The buprenorphine taper was initiated after 6 weeks of stabilization, lasted for 3 weeks, and included medications for opioid withdrawal, after which patients were offered naltrexone treatment. The maintenance group received ongoing buprenorphine therapy. All patients received physician and nurse support and drug counseling.
MAIN OUTCOMES AND MEASURES:
Illicit opioid use via results of urinanalysis and patient report, treatment retention, and reinitiation ofbuprenorphine therapy (taper group only).
RESULTS:
During the trial, the mean percentage of urine samples negative for opioids was lower for patients in the taper group (35.2% [95% CI, 26.2%-44.2%]) compared with those in the maintenance group (53.2% [95% CI, 44.3%-62.0%]). Patients in the taper group reported more days per week of illicit opioid use than those in the maintenance group once they were no longer receiving buprenorphine (mean use, 1.27 [95% CI, 0.60-1.94]vs 0.47 [95% CI, 0.19-0.74] days). Patients in the taper group had fewer maximum consecutive weeks of opioid abstinence compared with those in the maintenance group (mean abstinence, 2.70 [95% CI, 1.72-3.75] vs 5.20 [95% CI, 4.16-6.20] weeks). Patients in the taper group were less likely to complete the trial (6 of 57 [11%] vs 37 of 56 [66%]; P < .001). Sixteen patients in the taper group reinitiated buprenorphine treatment after thetaper owing to relapse.
CONCLUSIONS AND RELEVANCE:
Tapering is less efficacious than ongoing maintenance treatment in patients with prescription opioiddependence who receive buprenorphine therapy in primary care.
JAMA Psychiatry. 2013 Dec;70(12):1347-54. doi: 10.1001/jamapsychiatry.2013.2216.
A randomized, double-blind evaluation of buprenorphine taper duration in primary prescription opioid abusers.
Sigmon SC1, Dunn KE, Saulsgiver K, Patrick ME, Badger GJ, Heil SH, Brooklyn JR, Higgins ST.
Author information
Abstract
IMPORTANCE:
Although abuse of prescription opioids (POs) is a significant public health problem, few experimental studies have investigated the treatment needs of this growing population.
OBJECTIVE:
To evaluate, following brief stabilization with a combination of buprenorphine hydrochloride and naloxone hydrochloride dihydrate, the relative efficacy of 1-, 2-, and 4-week buprenorphine tapering regimens and subsequent naltrexone hydrochloride therapy in PO-dependent outpatients.
DESIGN, SETTING, AND PARTICIPANTS:
A double-blind, 12-week randomized clinical trial was conducted in an outpatient research clinic. Following a brief period of buprenorphine stabilization, 70 PO-dependent adults were randomized to receive 1-, 2-, or 4-week tapers followed by naltrexone therapy.
INTERVENTION:
During phase 1 (weeks 1-5 after randomization), participants visited the clinic daily; during phase 2 (weeks 6-12), visits were reduced to thrice weekly. Participants received behavioral therapy and urine toxicology testing throughout the trial.
MAIN OUTCOMES AND MEASURES:
The percentage of participants negative for illicit opioid use, retention, naltrexone ingestion, and favorable treatment response (ie, retained in treatment, opioid abstinent, and receiving naltrexone at the end of the study).
RESULTS:
Opioid abstinence at the end of phase 1 was greater in the 4-week compared with the 2- and 1-week taper conditions (P = .02), with 63% (n = 14), 29% (n = 7), and 29% (n = 7) of participants abstinent in the 4-, 2-, and 1-week conditions, respectively. Abstinence at the end of phase 2 was also greater in the 4-week compared with the 2- and 1-week conditions (P = .03), with 50% (n = 11), 16% (n = 4), and 20% (n = 5) of participants abstinent in the 4-, 2-, and 1-week conditions, respectively. There were more treatment responders in the 4-week condition (P = .03), with 50% (n = 11), 17% (n = 4), and 21% (n = 5) of participants in the 4-, 2-, and 1-week groups considered responders at the end of treatment, respectively. Retention and naltrexone ingestion also were superior in the 4-week vs briefer tapers (both P = .04). Experimental condition (ie, taper duration) was the strongest predictor of treatment response, followed by buprenorphine stabilization dose.
CONCLUSIONS AND RELEVANCE:
This study represents a rigorous experimental evaluation of outpatient buprenorphine stabilization, brief taper, and naltrexone maintenance for treatment of PO dependence. Results suggest that a meaningful subset of PO-dependent outpatients may respond positively to a 4-week taper plus naltrexone maintenance intervention.
When I triage opioid addiction and CNP, the addiction dx goes to the head of the line. Opioid addiction is a potentially fatal diagnosis whereas CNP never is. I think part of the heavy lifting is the difficult discussion that, as experts, we are aware that MANY opioid abusers masquerade as CNP patients to obtain drugs. In a similar vein, CNP is not a ticket to life-long Suboxone Tx, addiction may be.
It's a snake that eats itself: Honestly, I don't think that medicine is sophisticated enough to differentiate between the two in most circumstances...it's another distinction without a difference a la Mark Sullivan's Terribly Sad Life Syndrome...
http://www.jpain.org/article/S1526-5900(08)00801-8/abstract
SLS can indeed be differentiated from acute pain on fMRI. The homunculus for pain
has been mapped. And a lot of the smart researchers working on it realize that certain
intake instruments - PCS, SFMPQ, etc - predict the fMRI results with very good accuracy.
http://www.ncbi.nlm.nih.gov/pubmed/23574118
...Oregon Medicaid considers fMRI experimental for diagnosing SLS...
Read Apakarian's fMRI work carefully. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411898/bin/NIHMS383388-supplement-1.pdf
Incidently, one of his post-docs - Pascal Tretreault - is coming to speak at Jim Shames conference in May.
I'm familiar with it: The problem is that it's a non-starter in our current health system and if the implications are really followed forward it is not what payers necessarily want to hear...it could result in a favorable coverage determination for neuromodulation therapy or rTMS for "central pain"/SLS/etc.
The actuarial data suggest that it is cheaper to do nothing and wait for patients with SLS to die.