Sunday, August 5, 2012

Preoperative alcohol cessation prior to elective surgery



Full text source http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD008343.pub2/abstract

Source

It is hard to convince the folks at the Cochrane Database, but a meta-analysis of two randomized studies showed that "intensive alcohol cessation interventions including pharmacological strategies for alcohol withdrawal and relapse prophylaxis" significantly reduced post operative complications with an impressive odds ratio of 0.22 (95% confidence interval (CI) 0.08 to 0.61; p = 0.004)

There was no significant reduction of in-hospital and 30-day mortality. Although the odds ratio was 0.39; the 95% CI was 0.06 to 2.83 (p = 0.35).

The take home message for our work is that admitting people for alcohol withdrawal treatment prior to surgery is a good thing.

Levetiracetam not effective for alcohol dependence in randomized trial


A Double-Blind, Placebo-Controlled Trial Assessing the Efficacy of Levetiracetam Extended-Release in Very Heavy Drinking Alcohol-Dependent Patients.
 2012 Feb 10
PMID: 22324516

Despite promising open label trials this double-blind, randomized, placebo-controlled clinical trial of 130 alcohol-dependent patients who reported very heavy drinking did not show any efficacy in percent abstinence, drinks per drinking day or number of heavy drinking days. There was not even a trend in the medications favor vs placebo.

Levetiracetam XR was titrated during the first 4 weeks to 2,000 mg/d. This target dose was maintained during weeks 5 through 14 and was tapered during weeks 15 and 16.

My take home lessons: 
(1) take open label trials with a grain of salt and
(2) anti-convulsants are different from each other.   

Conversion of Chronic Pain Patients from Full Opioid Agonists to Sublingual Buprenorphine


 2012 Jul;15(3 Suppl):ES59-66.

Conversion of chronic pain patients from full-opioid agonists to sublingual buprenorphine.

Source

Advanced Pain Management and Spine Specialists, Fort Myers, FL.
PMID: 22786462
Complete text as PDF
Retrospective data from 104 patients poorly controlled chronic pain electing to switch from other opiate medications to high dose sublingual buprenorphine.   The mean daily preinduction morphine equivalent dose of opioid was 180 mg.

They appear to have been transitioned easily in an out patient setting
Buprenorphine SL was administered to patients after they had discontinued all opioid medications at least 24 hours prior (48-72 hours for methadone). Initially, 8 mg of buprenorphine SL was given sublingually. Patients were instructed to dissolve an additional dose of 8 mg one hour later if pain or withdrawal symptoms continued. Patients were instructed not to exceed 32 mg of buprenorphine SL daily.
On a 0-10 scale, pain scores decreased by 2.3 on average. The decrease was less for those who had been on higher morphine equivalents, but patients taking > 400mg morphine equivalent still reported the on average a 1.1 point decrease. 



Once patients were converted to buprenorphine and established an effective dose, no escalation in medication use was noted. Patients did not overuse medication and rarely ran out 
early.



Patients were disqualified for the study if they were not on buprenorphine SL for at least 
60 days, were taking buprenorphine SL before the first clinic visit, were noncompliant in the treatment plan, or continued to use opioid medications.  This may have eliminated some patients who did not do well from the final reported success.






Twelve Reasons for Considering Buprenorphine as a Frontline Analgesic in the Management of Pain


 2012 Jul 16. [Epub ahead of print]

Twelve Reasons for Considering Buprenorphine as a Frontline Analgesic in the Management of Pain.

PMID: 22809652

When I am trying to convince patients to switch from their current opiate for chronic pain (which they have usually lost control of, considering that I have these conversations at the Addiction Recovery Service) to buprenorphine and review the advantages, they often ask why didn't their doctor start them buprenorphine instead of morphine, hydrocodone, oxycodone etc. 

This article encourages physicians to consider buprenorphine, specifically the transdermal patch, as a first line agent in the approach to chronic pain.  I have some misgivings about opiate management of chronic pain in any case and find the data that exists fairly unconvincing given the potential for opiate induced hyperalgesia.  However I do concur with this author on the advantages of buprenorphine compared to the full mu agonists that are usually prescribed.

The twelve reasons given are
(1) Buprenorphine is effective in cancer pain(2) buprenorphine is effective in treating neuropathic pain(3) buprenorphine treats a broader array of pain phenotypes than do certain potent mu agonists, is associated with less analgesic tolerance, and can be combined with other mu agonists(4) buprenorphine produces less constipation than do certain other potent mu agonists, and does not adversely affect the sphincter of Oddi(5) buprenorphine has a ceiling effect on respiratory depression but not analgesia(6) buprenorphine causes less cognitive impairment than do certain other opioids(7) buprenorphine is not immunosuppressive like morphine and fentanyl(8) buprenorphine does not adversely affect the hypothalamic-pituitary-adrenal axis or cause hypogonadism(9) buprenorphine does not significantly prolong the QTc interval, and is associated with less sudden death than is methadone(10) buprenorphine is a safe and effective analgesic for the elderly(11) buprenorphine is one of the safest opioids to use in patients in renal failure and those on dialysis(12) withdrawal symptoms are milder and drug dependence is less with buprenorphine
I strongly recommend to read the entire article 

Another recent publication compared 0.4 mg SL buprenorphine favorable to 5 mg IV morphine for ER management of acute fracture.


 2012 Apr;59(4):276-80. Epub 2011 Nov 23.

Sublingual buprenorphine in acute pain management: a double-blind randomized clinical trial.

Jalili M, Fathi M, Moradi-Lakeh M, Zehtabchi S.

Buprenorphine management of both acute and chronic pain will certainly have risks, but it is encouraging to see it's advantages to full opiate agonists being published. 

Buprenorphine Abuse in Finland

 2012 Jul 24. [Epub ahead of print]

Twelve-year trend in treatment seeking for buprenorphine abuse in Finland.

PMID: 22835477

This is a descriptive study of people seeking treatment in Helsinki from 1997 to 2008. There were 4817 total clients including 780 patients who reported that buprenorphine was their primary drug of abuse. They were compared to the 598 who's primary drug of abuse was heroin and the 1249 who's primary drug was amphetamine. (That add's up to 2627 it is unstated what the primary drug for the remaining 2190 patients was). 

Buprenorphine abuse appears to gradually supplant heroin.  The annual proportion of buprenorphine clients increased from 3% in 1998 to 38% in 2008.  Since 2002,  buprenorphine clients were half of all opioid users. Treatment seeking for heroin abuse almost ceased after 2000–2002.  This may be explained by the authors comment "The availability of heroin in the Finnish drug markets has been exiguous [very small] since 2001".

It is unclear how these buprenorphine users began their careers.  Were they heroin users who switched due to market forces, or has buprenorphine become a "gateway drug"? The authors cite another study stating "some buprenorphine users started their IV drug abuse with buprenorphine" but I could not find the original citation. 

Concurrent alcohol abuse in these buprenorphine abuses doubled from 25.5% in 1997–2000
to 54.9% in 2007–2008. 

The authors describe the fascinating recent history of opiates in Finland.  

The availability and abuse of illicit drugs increased in Finland from the early 1990s. As a countermeasure, official opioid substitution treatment programs commenced with buprenorphine (Subutex) and methadone in 1997. Low-dose buprenorphine for pain was marketed prior to this time.

The estimated number of problem drug users in Finland increased from 11,500–16,400 in 1998 to 14,500–19,000 in 2005. Seventy to 80% of problem drug users abused illicitly manufactured amphetamine and the remainder abused opioids. 

Reports of high-dose buprenorphine abuse in Finland date back to the late 1990s and coincide with the initiation of opioid substitution treatment. Among 500 clients of needle exchange services in Finland’s three largest cities between 2000 and 2002, 59% of clients had used buprenorphine intravenously in the previous month. One third used buprenorphine on a daily basis. Buprenorphine was the most frequently used IV drug among IV drug users attending a needle exchange program in Helsink. Buprenorphine abuse was the main reason for treatment seeking in 33%of all clients with substance use disorders in Finland in 2009. Buprenorphine findings in forensic post-mortem investigations have increased from less than 10 cases in 2000 to 104 cases in 2008. 

The buprenorphine/naloxone combination product (Suboxone) was first marketed in Finland in 2006. Since December 2007 it has been the only high-dose formulation of buprenorphine with marketing approval. Single ingredient buprenorphine (Subutex) was withdrawn in 2007 due to concerns about misuse.


The authors note: "buprenorphine clients in Finland differed from prescription opioid users in other countries since they resembled “street users.”  In other countries, prescription opioid users were more likely to receive a legal or higher income, use non-injection routes of administration, have physical health problems (e.g., pain) as a reason for initial opioid use" and this certainly reflects our own experience here in Seattle.


The authors do not comment as to whether Finland's switch from pure buprenorphine to buprenorphine/naloxone in 2007 has lead to any change.  The combination product is intended to reduce IV use.  It does appear that countries where pure buprenorphine was introduced that misuse and diversion has been a bigger problem.  On the other hand, prescribing practices may play a larger role.  Overall this story from Finland may be a helpful cautionary tale and encourage holding our buprenorphine patients as accountable as we are able.

Norwegian experience with pregnant women on buprenorphine and methadone

 2012 Jul 25. 

Neonatal outcomes following in utero exposure to methadone or buprenorphine: A National Cohort Study of opioid-agonist treatment of Pregnant Women in Norway from 1996 to 2009.

PMID: 22841456

This study is a non randomized look at neonatal outcomes in Norway.  It is non randomized so should be interpreted cautiously but does have some unexpected findings.

The authors recruited women in three waves: 1996 to 2003 (n = 51), 2005 to 2007 (n = 36), and  2004 to 2009 (n = 52). They only looked at women having their first child on opiate maintenance treatment and the authors believe they captured approx 65% of all women meeting this criteria in Norway from 1996-2009. [Estimating that only 210 women had first children on maintenance treatment during this 13 year period, a surprisingly low number].  The authors reviewed records, spoke with women in the third trimester and had follow up calls post partum, on average on year after delivery. 

As an aside, when they compare drug testing to maternal interviews they note "self-report reveals more use of drugs than does urine drug screening"

These women were not randomly assigned. The authors note "The inclusion criteria for both medications are the same and both medications are provided by the same health professionals in any part of the country" but don't give any indication as to how local providers might decide to offer methadone vs buprenorphine.  They authors tracked 90 pregnancies on methadone and 49 on buprenorphine.

Women on methadone were found to have longer histories of opiate dependence.  They also had more use of other opiates in late pregnancy.  Very different from our experience 90% of the women were on opiate maintenance treatment prior to conception, with a median length of 18 months.  Average dose of methadone 90 mg, average buprenorphine 13 mg.  


Buprenorphine babies were heavier, longer and had larger head circumferences than the
methadone-exposed newborns.  Methadone babies were 2944g (6.4lbs) ± 649g (910–4624), buprenorphine babies 3254g (7.2 bls)  ± 569 (973–4200).  When they adjusted for presumed relevant covariants only the head size remained statistically significant.  There were no differences in gestational ages or apgars.  The c-section rate was 28% on methadone, only 15% on buprenorphine, but htis was not statistically significant.

There are surprising results in the NAS treatment for these babies.
There was no difference in the occurrence of NAS between these two groups. 58% of methadone babies were treated and 60% of buprenorphine babies.  Our clinical experience in Seattle is very different were almost all of methadone babies have Finnegan scores requiring treatment of NAS. 

The length of NAS treatment was nearly significantly different between the groups (p = 0.05); with buprenorphine-exposed neonates tending to have shorter treatment for NAS but not by much.  38.6 days of methadone babies and 27.7 days for buprenorphine babies.   When they adjusted for co-variants the difference decreased and was not longer statistically significant.

The authors note the length of treatment is much longer than in the MOTHERS trial and comment "Another possible explanation for the long average treatment of NAS in our study is that most hospitals in Norway have little experience with the treatment of NAS, and
therefore are more cautious when tapering down the NAS medication of the newborn."

They did not report type of medication given for NAS or on the total medication used. In the MOTHERS randomized trial there was a striking 90% decrease in the total morphine needed for buprenorphine exposed babies.  


Subgroup analysis showed that women using any drugs (opiates, benzodiazepines, cannabis and/or amphetamine) early or late in pregnancy had significantly longer NAS treatment, 40 days vs 28 days. 

Finally, two neonates exposed to buprenorphine in pregnancy were born with malformations, one child with spina bifida and one child with gastroschisis.  It is assumed these are not related to buprenorphine.

In conclusion: this study may not inform our practice much.  These women were unusual in that almost all were on maintenance treatment before pregnancy and there was little additional drug use.  They were not randomized to buprenorphine vs methadone and the authors give little clue how the patient or clinician might have assigned them.  The buprenorphine babies were slightly larger.  There as little difference in the NAS treatment reported.

It is interesting how both the MOTHERS trial and this report show much fewer methadone babies requiring NAS treatment than our clinical experience has show.