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MP 3.01.02 Opioid Antagonists Under Heavy Sedation or General Anesthesia as a Technique of Opioid Detoxification

Medical Policy    
Mental Health
Original Policy Date
Last Review Status/Date
Reviewed with literature search/12:2012
  Return to Medical Policy Index


Our medical policies are designed for informational purposes only and are not an authorization, or an explanation of benefits, or a contract.  Receipt of benefits is subject to satisfaction of all terms and conditions of the coverage.  Medical technology is constantly changing, and we reserve the right to review and update our policies periodically.


The use of relatively high doses of opioid antagonists under deep sedation or general anesthesia is a technique for opioid detoxification and is known as ultra-rapid detoxification. It is a potential alternative to standard detoxification that allows patients to avoid the acute symptoms associated with initial detoxification. Ultra-rapid detoxification is used in conjunction with maintenance treatments e.g., oral opioid antagonists and psychosocial support.

The traditional treatment of opioid addiction involves substituting the opiate (i.e., heroin) with an equivalent dose of a longer-acting opioid antagonist, i.e., methadone, followed by tapering to a maintenance dose. Methadone maintenance therapy does not resolve opioid addiction but has been shown to result in improved general health, retention of patients in treatment, and a decrease in the risk of transmitting human immunodeficiency virus (HIV) or hepatitis. However, critics of methadone maintenance point out that this strategy substitutes one drug of dependence for the indefinite use of another. Detoxification followed by abstinence is another treatment option, which can be used as the initial treatment of opioid addiction or offered as a final treatment strategy for patients on methadone maintenance. Detoxification is associated with acute symptoms followed by a longer period of protracted symptoms (i.e., 6 months) of withdrawal. Although typically not life-threatening, acute detoxification symptoms include irritability, anxiety, apprehension, muscular and abdominal pains, chills, nausea, diarrhea, yawning, lacrimation, sweating, sneezing, rhinorrhea, general weakness, and insomnia. Protracted withdrawal symptoms include a general feeling of reduced well-being and drug craving. Relapse is common during this period.

Detoxification may be initiated with tapering doses of methadone or buprenorphine (an opioid agonist-antagonist), treatment with a combination of buprenorphine and naloxone (an opioid antagonist), or discontinuation of opioids and administration of oral clonidine and other medications to relieve acute symptoms. However, no matter what type of patient support and oral medications are offered, detoxification is associated with patient discomfort, and many patients may be unwilling to attempt detoxification. In addition, detoxification is only the first stage of treatment. Without ongoing medication and psychosocial support after detoxification, the probability is low that any detoxification procedure alone will result in lasting abstinence. Opioid antagonists, such as naltrexone, may also be used as maintenance therapy to reduce drug craving and thus reduce the risk of relapse.

Dissatisfaction with current approaches to detoxification has led to interest in using relatively high doses of opioid antagonists, such as naltrexone, naloxone, or nalmefene under deep sedation with benzodiazepine or general anesthesia. This strategy has been referred to as "ultra-rapid," "anesthesia-assisted," or "one-day" detoxification. The use of opioid antagonists accelerates the acute phase of detoxification, which can be completed within 24–48 hours. Since the patient is under anesthesia, the patient has no discomfort or memory of the symptoms of acute withdrawal. Various other drugs are also administered to control acute withdrawal symptoms, such as clonidine (to attenuate sympathetic and hemodynamic effects of withdrawal), ondansetron (to control nausea and vomiting), and somatostatin (to control diarrhea). Hospital admission is required if general anesthesia is used. If heavy sedation is used, the program can potentially be offered on an outpatient basis. Initial detoxification is then followed by ongoing support for the protracted symptoms of withdrawal. In addition, naltrexone may be continued to discourage relapse.

Ultra-rapid detoxification may be offered by specialized facilities. Neuraad™ Treatment Centers, Nutmeg Intensive Rehabilitation, and Center for Research and Treatment of Addiction (CITA) are examples. These programs typically consist of 3 phases: a comprehensive evaluation, inpatient detoxification under anesthesia, and finally, mandatory post-detoxification care and follow-up. The program may be offered to patients addicted to opioid or narcotic drugs such as opium, heroin, methadone, morphine, meperidine, hydromorphone, fentanyl, oxycodone, hydrocodone, or butorphanol. Once acute detoxification is complete, the opioid antagonist naltrexone is often continued to decrease drug craving, with the hope of reducing the incidence of relapse.

Regulatory Status

In October 2002, Reckitt Benckiser received U.S. Food and Drug Administration (FDA) approval to market a buprenorphine monotherapy product, Subutex®, and a buprenorphine/naloxone combination product, Suboxone®, for use in opioid addiction treatment.


Opioid antagonists under heavy sedation or anesthesia is considered investigational as a technique for opioid detoxification (i.e., ultra-rapid detoxification).

Policy Guidelines

No applicable information

Benefit Application
BlueCard/National Account Issues 

Opioid dependence is considered a mental disorder, thus claims for ultra-rapid detoxification may be adjudicated under the mental health benefits.


Assessment of ultra-rapid opioid detoxification will focus on data reporting the severity and duration of withdrawal symptoms and the short- and long-term outcomes of maintenance of abstinence in distinct populations of patients, based on type and duration of addiction. Efficacy outcomes will be balanced against the safety considerations of deep sedation or general anesthesia in conjunction with naloxone.

This policy was originally created in 2002 and was updated regularly with searches of the MEDLINE database. The most recent literature search was performed for the period October 2011 through October 2012. Following is a summary of the key literature to date:

In 2010, a Cochrane review by Gowing and colleagues on opioid antagonists under heavy sedation or anesthesia for opioid withdrawal was published. (1) A total of 9 studies including 1,109 participants were eligible for inclusion; there were 8 randomized controlled trials (RCTs) and 1 non-randomized controlled trial. Four studies compared the intervention to conventional approaches of withdrawal, and 5 compared different regimens of antagonist-induced withdrawal. In 5 of the studies, all participants were withdrawing from heroin or other short-acting opioids; in 3 studies, they were using heroin and/or methadone and, in 1 study, all participants were withdrawing from methadone.

Due to differences in study designs (e.g., antagonist and anesthesia or sedation regimens, comparison interventions, outcome variables, etc.), few pooled analyses could be conducted. Findings from 3 trials (total n=240) comparing antagonist-induced and conventional withdrawal were pooled for several outcome variables. The number of participants completing maintenance treatment was significantly higher in the antagonist-induced group than in the conventional treatment group (relative risk [RR]: 4.28; 95% confidence interval [CI]: 2.91-6.30). The number of participants who continued maintenance treatment or were abstinent at 12 months also favored the antagonist-induced group (RR: 2.77; 95% CI: 1.37-5.61). Safety data from these 3 studies were not pooled. One of the studies reported no adverse effects, and 1 only reported adverse effects in patients who received octreotide during the anesthetic procedure; 7 out of these 11 patients (64%) experienced vomiting and/or diarrhea. The third study reported 3 serious adverse events, all of which occurred in the anesthesia group. There were no pooled analyses of the results of studies that evaluated the efficacy of differing opioid antagonist withdrawal regimens. One meta-analysis of safety data from 2 studies (total n=572) found a statistically significantly higher rate of adverse events with heavy sedation compared to light sedation (RR: 3.21; 95% CI: 1.13-9.12). Other adverse events included high rates of vomiting in several studies and, in 1 study, episodes of irregularities in respiratory patterns during withdrawal.

The authors of the Cochrane review commented that, due to variability among the trials, “it is not possible to identify ‘standard’ treatment regimens for antagonist-induced withdrawal in conjunction with heavy sedation or anesthesia.” They concluded that “the increased risk of clinically significant adverse events associated with withdrawal under heavy sedation or anesthesia make the value of anesthesia-assisted antagonist-induced withdrawal questionable.”

Several of the trials are described in more detail below:

Collins and colleagues reported on the results of a trial of 106 heroin addicts who were randomly assigned to undergo detoxification with an anesthesia-assisted rapid opioid detoxification, buprenorphine-assisted rapid opioid detoxification, or clonidine-assisted opioid detoxification. (2) All patients received an additional 12 weeks of outpatient naltrexone maintenance. Mean withdrawal severities were similar among the 3 groups, and treatment retention in the 12-week follow-up period was also similar. However, the anesthesia procedure was associated with 3 potentially significant life-threatening adverse events. The authors concluded that the data did not support the use of general anesthesia for heroin detoxification.

Favrat and colleagues published an RCT from a European center in 2006. The trial reported that the initial improvement in rate of opiate detoxification and abstinence (3 months) with anesthesia was not maintained with longer-term follow-up; both groups (36 patients treated with anesthesia and 34 with classical clonidine detoxification) showed less than 5% abstinence after 12 months. (3)

Among the published RCTs are several that focused on treatment regimens that varied only in the level or type of sedation used and did not include a control group of patients that did receive rapid detoxification. (4-6) In 2011, Nasr and colleagues in Egypt compared ultra-rapid detoxification under general anesthesia with and without dexmedetomidine. (6) Another study, by Seoane and colleagues, compared rapid intravenous detoxification treatment under either monitored light intravenous sedation or unmonitored deep intravenous sedation. (5) No conclusions can be drawn from these studies about the relative efficacy of rapid detoxification and standard methods.

Among the adverse events reported in the Cochrane review, vomiting under sedation is particularly worrisome due to the threat of aspiration. Techniques reported to minimize this risk include intubation, use of prophylactic antibiotics, and the use of medication to diminish the volume of gastric secretions. Several deaths occurring either during anesthesia or immediately thereafter have been reported. (7-10) Also, deaths subsequent to ultra-rapid detoxification have been reported. (11) Of particular concern is the fact that the use of opioid antagonists results in loss of tolerance to opioids, rendering patients susceptible to overdose if they return to pre-detoxification dosage of illicit drugs. (12)


Ultra-rapid detoxification is an opioid detoxification technique that uses relatively high doses of opioid antagonists under deep sedation or general anesthesia. The paucity of controlled trials and lack of a standardized approach to ultra-rapid detoxification does not permit scientific conclusions regarding the safety or efficacy of ultra-rapid detoxification compared to other approaches that do not involve deep sedation or general anesthesia. Moreover, there are concerns about adverse effects, including life-threatening or potentially life-threatening events. Thus, this technology is considered investigational.

Practice Guidelines and Position Statements

In 2007, the National Institute for Health and Clinical Excellence issued clinical practice guidelines on “drug misuse, opioid detoxification.” (13) The guidelines include the following statement regarding ultra-rapid detoxification, “Ultra-rapid detoxification under general anesthesia or heavy sedation (where the airway needs to be supported) must not be offered. This is because of the risk of serious adverse events, including death.”

In 2007, the American Psychiatric Association Work Group on Substance Use Disorders released a practice guideline for the treatment of patients with substance use disorders. (14) The practice guideline included the following recommendation: “Anesthesia-assisted rapid opioid detoxification (AROD) is not recommended because of lack of proven efficacy and adverse risk-benefit ratios.”

In 2005, the American Society of Addiction Medicine published a public policy statement regarding opiate detoxification under sedation or anesthesia (update of their 2000 statement). (15) It included the following position statements:

“Opioid detoxification alone is not a treatment of opioid addiction. ASAM does not support the initiation of acute opioid detoxification interventions unless they are part of an integrated continuum of services that promote ongoing recovery from addiction.

Ultra-Rapid Opioid Detoxification (UROD) is a procedure with uncertain risks and benefits, and its use in clinical settings is not supportable until a clearly positive risk-benefit relationship can be demonstrated. Further research on UROD should be conducted.

Although there is medical literature describing various techniques of Rapid Opioid Detoxification (ROD), further research into the physiology and consequences of ROD should be supported so that patients may be directed to the most effective treatment methods and practices.”

Medicare National Coverage

Medicare Policy (16)

Medicare Coverage Issues Manual—Medical Procedures

Section 35-42, Withdrawal Treatment for Narcotic Addictions, states: “Withdrawal is an accepted treatment for narcotic addiction, and Part B payment can be made for these services if they are provided by the physician directly or under his personal supervision and if they are reasonable and necessary. In reviewing claims, reasonableness and necessity are determined with the aid of the contractor’s medical staff.

Drugs that the physician provides in connection with this treatment are also covered if they cannot be self-administered and meet all other statutory requirements.”

Section 35-22.2, Treatment of Drug Abuse (Chemical Dependency), states:

“We recognize that there are similarities in approach to treatment of drug abuse and alcohol detoxification. However, the intensity and duration of treatment for drug abuse may vary (depending on the particular substance(s), duration of use, and the patient’s medical and emotional condition) from the duration of treatment or intensity needed to treat alcoholism. Accordingly, when it is medically necessary for a patient to receive detoxification and/or rehabilitation for drug substance abuse as a hospital inpatient, coverage for that care is available. Coverage is also available for treatment services that are provided in the outpatient department of a hospital to patients who, for example, have been discharged from an inpatient hospital stay for the treatment of drug substance abuse or who require treatment but do not require the availability and intensity of services found only in the inpatient hospital setting. The coverage available for these services is subject to the same rules generally applicable to the coverage of an outpatient hospital. The services must be reasonable and necessary for the treatment of the individual’s condition. Decisions regarding reasonableness and necessity of treatment, the need for inpatient hospital level of care, and lengths of treatment should be made by intermediaries based on accepted medical practice with the advice of their medical consultant.”



    1. Gowing L, Ali R, White J. Opioid antagonists under heavy sedation or anaesthesia for opioid withdrawal. Cochrane Database Syst Rev 2010; (1):CD002022.
    2. Collins ED, Kleber HD, Whittington RA et al. Anesthesia-assisted vs buprenorphine- or clonidine-assisted heroin detoxification and naltrexone induction: a randomized trial. JAMA 2005; 294(8):903-13.
    3. Favrat B, Zimmermann G, Zullino D et al. Opioid antagonist detoxification under anaesthesia versus traditional clonidine detoxification combined with an additional week of psychosocial support: a randomised clinical trial. Drug Alcohol Depend 2006; 81(2):109-16.
    4. Kienbaum P, Scherbaum N, Thurauf N et al. Acute detoxification of opioid-addicted patients with naloxone during propofol or methohexital anesthesia: a comparison of withdrawal symptoms, neuroendocrine, metabolic and cardiovascular patterns. Crit Care Med 2000; 28(4):969-76.
    5. Seoane A, Carrasco G, Cabre L et al. Efficacy and safety of two new methods of rapid intravenous detoxification in heroin addicts previously treated without success. Br J Psychiatry 1997; 171(October):340-5.
    6. Nasr DA, Omran HA, Hakim SM et al. Ultra-rapid opiate detoxification using dexmedetomidine under general anesthesia. J Opioid Manag 2011; 7(5):337-44.
    7. Bearn J, Gossop M, Strang J. Rapid opiate detoxification treatments. Drug Alcohol Rev 1999; 18(1):75-81.
    8. Dyer C. Addict died after rapid opiate detoxification. BMJ 1998; 316(7126):170.
    9. Gold CG, Cullen DJ, Gonzales S et al. Rapid opioid detoxification during general anesthesia: a review of 20 patients. Anesthesiology 1999; 91(6):1639-47.
    10. Solomont JH. Opiate detoxification under anesthesia. JAMA 1997; 278(16):1318-9.
    11. Brewer C, Laban M, Schmulian C et al. Rapid opiate detoxification and naltrexone induction under general anaesthesia and assisted ventilation: experience with 510 patients in four different centres. Acta Psychiatr Belg 1998; 98:181-9.
    12. American Society of Addiction Medicine. Public Policy Statement on Opioid Antagonist Agent Detoxification Under Sedation Or Anesthesia (OADUSA). J Addict Dis 2000; 19(4):109-12.
    13. National Institute for Health and Clinical Evidence. Drug misuse, opioid detoxification. NICE Clinical Guideline 52. Available online at: Last accessed November, 2012.
    14. Kleber HD, Weiss RD, Anton RF et al. Work Group on Substance Use Disorders. Treatment of patients with substance use disorders. American Psychiatric Association. Am J Psychiatry 2006; 163(8 suppl):5-82.
    15. American Society of Addiction Medicine. Public Policy Statement on Rapid and Ultra Rapid Opioid Detoxification. Available online at: Last accessed November, 2012.
    16. Center for Medicaid and Medicare Services. Medicare Policy 35-22.2. Available online at: Last accessed November, 2012.






No specific CPT code 

ICD-9 Diagnosis 


Opioid type dependence 

ICD-10-CM (effective 10/1/14)


Opioid related disorders code range

ICD-10-PCS (effective 10/1/14)


ICD-10-PCS codes are only used for inpatient services. There is no specific ICD-10-PCS code for this procedure.

  HZ2ZZZZ Substance abuse treatment, detoxification

Type of Service 

Mental Health
Prescription Drug 

Place of Service 

Approved Facility 


Opioid Antagonists Under Heavy Sedation of General Anesthesia as a Technique of Opioid
Detoxification, Opiate, Rapid
Opiate Detoxification, Rapid
Rapid Opiate Detoxification  

Policy History

Date Action Reason
10/08/02 Add to Mental Health section New policy
02/25/04 Replace policy Policy updated with literature review; no change in policy statement
03/15/05 Replace policy Policy updated with literature review; no change in policy statement
12/14/05 Replace policy Policy updated with literature review; no change in policy statement; reference number 19 added
12/12/06 Replace policy Policy updated with literature review; reference numbers 20 and 21 added; no change in policy statement
03/13/08 Replace policy  Policy updated with literature review; no change in policy statement
3/12/2009 Replace policy Policy updated with literature review through January 2009; reference numbers 22 and 23 added; no change in policy statement
12/09/10 Replace policy Policy updated with literature review through October 2010. Rationale extensively rewritten; reference numbers 6 and 19 added; other references re-numbered or removed. No change in policy statement
12/08/11 Replace policy Policy updated with literature review through October 2011. Rationale edited; references removed or renumbered. No change in policy statement.
12/13/12 Replace Policy Policy updated with literature review through October 2012. Reference 6 added; other references re-numbered or removed. No change in policy statement.