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Review

The cannabis withdrawal syndrome: current insights

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Pages 9-37 | Published online: 27 Apr 2017

Abstract

The cannabis withdrawal syndrome (CWS) is a criterion of cannabis use disorders (CUDs) (Diagnostic and Statistical Manual of Mental Disorders – Fifth Edition) and cannabis dependence (International Classification of Diseases [ICD]-10). Several lines of evidence from animal and human studies indicate that cessation from long-term and regular cannabis use precipitates a specific withdrawal syndrome with mainly mood and behavioral symptoms of light to moderate intensity, which can usually be treated in an outpatient setting. Regular cannabis intake is related to a desensitization and downregulation of human brain cannabinoid 1 (CB1) receptors. This starts to reverse within the first 2 days of abstinence and the receptors return to normal functioning within 4 weeks of abstinence, which could constitute a neurobiological time frame for the duration of CWS, not taking into account cellular and synaptic long-term neuroplasticity elicited by long-term cannabis use before cessation, for example, being possibly responsible for cannabis craving. The CWS severity is dependent on the amount of cannabis used pre-cessation, gender, and heritable and several environmental factors. Therefore, naturalistic severity of CWS highly varies. Women reported a stronger CWS than men including physical symptoms, such as nausea and stomach pain. Comorbidity with mental or somatic disorders, severe CUD, and low social functioning may require an inpatient treatment (preferably qualified detox) and post-acute rehabilitation. There are promising results with gabapentin and delta-9-tetrahydrocannabinol analogs in the treatment of CWS. Mirtazapine can be beneficial to treat CWS insomnia. According to small studies, venlafaxine can worsen the CWS, whereas other antidepressants, atomoxetine, lithium, buspirone, and divalproex had no relevant effect. Certainly, further research is required with respect to the impact of the CWS treatment setting on long-term CUD prognosis and with respect to psychopharmacological or behavioral approaches, such as aerobic exercise therapy or psychoeducation, in the treatment of CWS. The up-to-date ICD-11 Beta Draft is recommended to be expanded by physical CWS symptoms, the specification of CWS intensity and duration as well as gender effects.

Introduction

Cannabis is a psychotropic substance with widespread recreational use worldwide, surpassed only by nicotine and alcohol.Citation1 Its use continues to be high in West and Central Africa, Western and Central Europe, Australasia, and North America, where recently an increase in the prevalence of past year cannabis use was recorded in the USA (12.6%).Citation1 In Europe, prevalence rates of annual cannabis use rise in Nordic countries (7%–18%) and France (22%). They decline in Spain, UK, and Germany (currently 12%), and there is an increase in the number of treatment demands for cannabis-related problems across EuropeCitation2 and the USA.Citation3 Although such prevalence rates are useful to indicate consumption trends, it is doubted whether these rates are relevant to reflect a health risk. Approximately 1% of European adolescents and young adults use cannabis daily or almost daily (defined as use on ≥20 days in the last month),Citation2 a consumption pattern which is more likely to produce cannabis-related disabling disorders.Citation4,Citation5 The prevalence of cannabis dependence (Diagnostic and Statistical Manual of Mental Disorders – Fourth Edition – Text Revision [DSM-IV-TR]) is highest in Australasia (0.68%), followed by North America (0.60%), Western Europe (0.34%), Asia Central (0.28%), and southern Latin America (0.26%).Citation4 In Germany, ~0.5% of the adult population have a cannabis dependence diagnosis.Citation6 Most of the other regions of the world providing data report a prevalence of cannabis dependence of <0.2%.Citation4 There is a significant positive correlation between the region’s economic situation and the prevalence of cannabis dependence.Citation4 A hallmark of cannabis dependence (Diagnostic and Statistical Manual of Mental Disorders – Fourth Edition [DSM-IV] or International Classification of Diseases [ICD]- 10) as well as cannabis use disorder (CUD) (Diagnostic and Statistical Manual of Mental Disorders – Fifth Edition [DSM-5]) is the cannabis withdrawal syndrome (CWS) that characteristically occurs after quitting a regular cannabis use abruptly.

Although there was early evidence from animal experimentsCitation7 and despite observations in humans in every decade,Citation8,Citation9 CWS entity was doubted before the 1990s, when a new cannabis wave started to roll in worldwide, particularly in affluent regions.Citation4 This was related with a mounting number of patients seeking treatment due to various cannabis-related disorders, including cognitive deficits, psychosis, and dependence.Citation4,Citation5 Considering these populations and also nontreatment-seeking cannabis-dependent individuals, larger retrospective clinical trialsCitation10,Citation11 demonstrated that discontinuation of regular cannabis use is frequently followed by waxing and waning behavioral, mood and physical symptoms such weakness, sweating, restlessness, dysphoria, sleeping problems, anxiety, and craving, which are subsequently positively associated with relapse to cannabis use.Citation11Citation19 However, other studies did not find this association.Citation20 CWS was further validated by epidemiological,Citation21,Citation22 retrospective,Citation11,Citation19,Citation23 and prospective outpatientCitation12,Citation13,Citation20,Citation24Citation26 and inpatient laboratory studiesCitation27Citation30 (). Based on this research, diagnostic criteria of CWS were newly included in DSM-5 ().Citation31 In ICD-10, CWS is still vaguely definedCitation32 and awaits due definition in ICD-11.Citation33 More recent clinical inpatient detoxification studies arranging controlled abstinence conditions confirmed the entity of CWS.Citation34Citation36 The CWS was also verified in youths and adolescents (aged 13–19 years), who sought treatment for their disabilitating cannabis dependence.Citation18,Citation37Citation40

Table 1 Clinical and laboratory studies on human CWS in the past 20 years

Table 2 Marijuana Withdrawal Checklist (MWC)

There is a consistent evidence that CWS occurs in ~90% of the patients being diagnosed with cannabis dependence according to ICD-10 or DSM-IVCitation12,Citation13,Citation38,Citation41,Citation42 (). Among them, most often, male adolescents and young adults demonstrated a significant loss of quality of life during their cannabis dependence as measured by disability-adjusted life years in the Global Burden of Disease 2010 Study (cf and in http://journals.plos.org/plosone/article?id=info:doi/10.1371/journal.pone.0076635, accessed November 25, 2016).Citation4

Recent studies revealed that 35%–75% patients seeking outpatient cannabis detoxification developed a CWS post-cessation, which usually seemed to be mild to moderate in severity.Citation11Citation13,Citation15,Citation16,Citation19 However, most of the cannabis dependents developed a CWS of greater severity.Citation36 Adult cannabis dependents were shown to develop a severe CWS likelier than adolescent frequent users.Citation24,Citation37 A prolonged and heavier cannabis use predicts a stronger CWS.Citation12,Citation13,Citation19 It was confirmed again more recently that the occurrence of CWS is a highly specific indicator of a cannabis dependence, particularly in adolescents and young adults.Citation42

This review intends to provide a synthesis of current evidence on the biology and clinical characteristics of the human CWS and its treatment. In addition, it includes information on the role of CWS in the course of CUDCitation31 or cannabis dependence.Citation22,Citation43

Materials and methods

This study is a review of the current literature on human CWS. The search for articles was performed on the PubMedCitation44 (Med-line) and Scopus,Citation45 using the a combination of the search terms “cannabis withdrawal,” “humans,” “epidemiology,” “disability,” “clinical studies,” “clinical trials,” “case reports,” “cannabis use disorder,” “cannabis dependence,” “treatment,” “psychotherapy,” “psychosocial,” “exercise,” “occupational therapy,” “pharmacotherapy,” and “potency”. In addition, an active search for related literature was carried out in the reference lists of the selected publications. In total, 2,440 documents were screened, and mainly those studies providing information on human CWS and those published in English or German (N=101) were considered. Articles published up to November 25, 2016, were included.

Human biological background

The cannabis plant contains >420 chemical compounds of which 61 being cannabinoids themselves being defined to bind to cannabinoid 1 and 2 (CB1, CB2) receptors.Citation46 Regular cannabis use is associated with neuroanatomic abnormalities within brain regions with a high density of CB1 receptors, particularly the hippocampus and prefrontal cortex.Citation47,Citation48 It is assumed that, the main psychoactive ingredient of cannabis, the partial CB1 receptor agonist delta-9-tetrahydrocannabinol (THC) is involved in the etiology of this damage,Citation47 which certainly awaits further study. For instance, a contribution of receptor-independent mechanisms of cannabinoidsCitation49,Citation50 as well as distress due to psychiatric CUD or CWS cannot as yet be excluded. A crucial role of THC in the genesis of CWS in humans is demonstrated by 1) pharmacokinetic studies showing a hysteresis effect between the decrease in plasma THC and onset of CWS,Citation51,Citation52 2) an abstinence syndrome following oral THCCitation12,Citation13 and THC analogs,Citation53 3) alleviation of CWS by oral THC and THC analogs,Citation29,Citation54,Citation55 and 4) the occurrence of CWS-like symptoms after quitting recreational intake of synthetic cannabinoid (SC) receptor agonists, often being full CB1 receptor agonists, differing from THC being a partial agonist.Citation56,Citation57 The withdrawal syndrome of SCs binding closer to CB1 receptors than THC seemed to be stronger than CWS and obviously showed characteristics unknown to CWS, such as seizures.Citation58 Otherwise, single cases of patients with diagnosed epilepsy who quit regular cannabis use are reported to exacerbate,Citation59 which is attributed to an anticonvulsive effect of cannabis.Citation46 The psychoactive potency of bred cannabis products sold for recreational use has been increasing in many markets over the past decade,Citation1,Citation2 which could lead to a stronger withdrawal syndrome than usually known for cannabis. Intriguingly, there is one case report regarding improvement of CWS following the administration of cannabidiol,Citation60 another constituent of cannabis, shown to reverse some adverse effects of THC in the laboratory.Citation61 The cardiovascular functioning seemed to be scarcely altered during CWS.Citation62 Although the endocannabinoid system is involved in the regulation of most of the other peripheral organ systems, the immune system and the gut, too, we are unaware of any such study on the contribution of these organs to human CWS. Notably, applying a CB1 receptor antagonist (rimonabant) to cannabis-dependent patients substituted with THC analogs did not precipitate a relevant CWS.Citation63 This may be due to the low doses of rimonabant applied (20 and 40 mg) or the CWS-generating mechanisms that are at least partly independent upon CB1 receptors.Citation49,Citation50 Cannabis users with opioid dependence are less likely to experience CWS,Citation64 which may indicate the contribution of the endogenous opioid system. In a laboratory study, the µ-opioid receptor antagonist naltrexone was recently shown to reduce self-administration of active cannabis and its related subjective positive effects on heavy cannabis users.Citation65 The authors are unaware of any study having directly examined the effect of naltrexone on the CWS under naturalistic conditions.

Abstinence-induced craving is associated with reduced amygdala volumes in frequent adolescent cannabis users, which was also found in adult alcohol and cocaine users.Citation66 Thus, the specificity of this finding for CWS is doubted and may represent a more general precursor of substance abuse itself;Citation66 that is, early stress in life.Citation67,Citation68 With respect to the three “a”s of CWS (anger, aggression, and anxiety) (), the threat-related amygdala reactivity was shown to be inversely related to the level of cannabis use in adolescents with comorbid cannabis dependence and major depression.Citation69 This finding may reflect the neurobiological basis of these transient, mostly short-lasting CWS symptoms, thus possibly being even rebound “amygdala-related” symptoms after quitting regular cannabis use. Nevertheless, the CWS symptoms could persist even longer in genetically or epigenetically more susceptible individuals upon withdrawal.

Regular cannabis intake is related to a desensitization and downregulation of human cortical and subcortical CB1 receptors. This starts to reverse within the first 2 days of abstinence and the receptors return to normal functioning after ~4 weeks of abstinence,Citation70 which could constitute a neurobiological time frame for the duration of CWS, not taking into account cellular and synaptic long-term neuroplasticity elicited by long-term cannabis use before cessation, for example, being possibly responsible for craving. In support, cannabis dependents were recently shown to have a robust negative correlation between CB1 receptor availability in almost all brain regions and their withdrawal symptoms after 2 days of cannabis abstinence which in turn resolved in the next 28 days of abstinence.Citation71

If compared with nonusers, long-term cannabis users were demonstrated to have greater brain activity during cannabis cues relative to natural reward cues (ie, fruit itself being superior to neutral cues) in the orbitofrontal cortex, striatum, anterior cingulate gyrus, and ventral tegmental area.Citation72 The users had positive correlations between neural response to cannabis cues in the fronto-striatal-temporal regions and subjective craving, cannabis-related problems, serum levels of THC metabolites, and the intensity of CWS. All of which were not found in non-cannabis users,Citation72 suggesting a sensitization and specificity of the brain response to cannabis cues in long-term cannabis users.Citation72

In the San Francisco Family Study, some symptoms of CWS, craving and cannabis-related paranoia were found to be heritable,Citation73 which could have been confounded by the heritability of age at first-ever use, for instance. It was suggested that genetic factors determine whether an individual may try or use cannabis; however, environmental factors are more crucial in determining whether a person develops dependence or not.Citation73 Recent findings provide evidence that the use of nicotine, alcohol, or cannabis shares genetic and environmental pathways on the way to develop a substance use disorder.Citation74 Regular intake of alcohol, nicotine, cannabis, or other drugs of abuse alters the stress response sustainablyCitation75 and, thereby, may precipitate a substance use disorder.

Characteristics of CWS

Considering the cannabis research of the last 20 years,Citation12,Citation13,Citation16,Citation18Citation20,Citation31 there was no doubt that cessation of heavy or prolonged cannabis use is most likely followed by typical symptoms, such as

  1. irritability

  2. nervousness/anxiety

  3. sleep difficulty

  4. decreased appetite or weight loss

  5. depressed mood

  6. one of the following physical symptoms such as abdominal pain, shakiness/tremors, sweating, fever, chills, or headache.

According to DSM-5,Citation31 CWS (292.0) is diagnosed if three or more of these symptoms (1–6) develop within ~1 week after quitting cannabis use abruptly.Citation31 Withdrawal severity and duration can vary widely between individuals and fluctuate depending on the amount of prior cannabis use, context of cessation (eg, outpatient vs inpatient, voluntary vs involuntary), personality traits, psychiatric and somatic comorbidity, current life stressors, previous experiences, expectations, support, and severity of dependence.Citation12,Citation13 Women seeking treatment for CUD were shown to generate more frequent and more severe withdrawal symptoms than men after quitting their frequent cannabis use.Citation36,Citation76,Citation77 However, older studies did not reveal this gender effect ().

Additional heavy tobacco use was reported to be associated with stronger irritability during the CWS of adolescents.Citation40 Black adolescents were shown to have lower withdrawal complaints and experience less severe depressed mood, sleep difficulty, and nervousness/anxiety than non-Black adolescents.Citation40 In youths with conduct disorder, this disorder antedated cannabis use.Citation38

Currently, psychometrically validated cannabis withdrawal scales are unavailable. Several versions to measure CWSCitation11Citation13,Citation16,Citation18,Citation24,Citation78 were developed, some of which compared with each user by Gorelick et al.Citation19 All these versions were based on the Marijuana Withdrawal Checklist (MWC) of Budney et al.Citation24 The MWC was originally designed with 22 items that assessed mood, behavioral, and physical symptoms and was revised to a 15-item version comprising these items that had been most frequently endorsed during cannabis withdrawalCitation12,Citation13,Citation26,Citation37 (). Later, this version builds the construct of the DSM-5 definition of CWSCitation31 (), which, however, does not consider cannabis craving and nausea.Citation31

Regarding the course of the overall CWS, there were two different types described in the available literature ( and ). One peaked between the second and sixth abstinence day (type A)Citation11,Citation15,Citation16,Citation19,Citation20,Citation23,Citation26,Citation27,Citation35,Citation36,Citation56,Citation79 and the other decreased continuously following cannabis cessation (type B).Citation28,Citation34,Citation39 It is assumed that type-A CWS includes more intoxication symptoms which vanished during the first few days post-cessation, thereby unmasking the “pure” CWS.Citation36 A negative correlation with serum levels of THC at admission, which would support this assumption, was found in type A.Citation35,Citation36 Type-B CWS was not investigated to this subject. Alternative explanations are that the contribution of single items (cf and ) differed between types A and B or more patients without a measurable CWS were included in the group of patients producing a type-B course.

Figure 1 Courses of overall CWS post-cessation. The CWS usually lasts up to 3 weeks and its average peak severity (burden) is comparable to that of a moderate depression or alcohol withdrawal syndrome or in outpatient settings, similar to that of a tobacco withdrawal syndrome. Data from previous studies.Citation14,Citation36,Citation79

Abbreviation: CWS, cannabis withdrawal syndrome.
Figure 1 Courses of overall CWS post-cessation. The CWS usually lasts up to 3 weeks and its average peak severity (burden) is comparable to that of a moderate depression or alcohol withdrawal syndrome or in outpatient settings, similar to that of a tobacco withdrawal syndrome. Data from previous studies.Citation14,Citation36,Citation79

Figure 2 Mean and standard deviation of the (A) CWS checklist (MWC score according to previous studiesCitation24,Citation26,Citation37) and (B) the Clinical Global Impression Scale (CGI-S ScoreCitation80) during the course of the study. Reduced sample sizes on day 12 (n=35) and day 16 (n=28) due to regular dismissals and missed assessments are indicated by dashed lines. The effect size according to Cohen (Cohen’s d) was 1.1 for the CWS (day 1 to day 16), Cohen’s d ≥0.8 is defined to reflect a strong effect.Citation130 Vertical imaginary Y-axis: severity scores. Horizontal imaginary X-axis: time course.

Note: Reproduced from Drug Alcohol Depend, 143, Bonnet U, Specka M, Stratmann U, Ochwadt R, Scherbaum N, Abstinence phenomena of chronic cannabis-addicts prospectively monitored during controlled inpatient detoxification: cannabis withdrawal syndrome and its correlation with delta-9-tetrahydrocannabinol and -metabolites in serum, 189–197. Copyright (2014), with permission from Elsevier.Citation36
Abbreviations: CWS, cannabis withdrawal syndrome; MWC, Marijuana Withdrawal Checklist.
Figure 2 Mean and standard deviation of the (A) CWS checklist (MWC score according to previous studiesCitation24,Citation26,Citation37) and (B) the Clinical Global Impression Scale (CGI-S ScoreCitation80) during the course of the study. Reduced sample sizes on day 12 (n=35) and day 16 (n=28) due to regular dismissals and missed assessments are indicated by dashed lines. The effect size according to Cohen (Cohen’s d) was 1.1 for the CWS (day 1 to day 16), Cohen’s d ≥0.8 is defined to reflect a strong effect.Citation130 Vertical imaginary Y-axis: severity scores. Horizontal imaginary X-axis: time course.

Figure 3 Mean rating of single symptoms of the MWC (MWC score according to previous studiesCitation24,Citation26,Citation37); 4-point scale (0 = none, 1 = mild, 2 = moderate, 3 = heavy). Note the delayed occurrence of strange dreams.Citation25 Vertical imaginary Y-axis: severity scores. Horizontal imaginary X-axis: time course.

Note: Reproduced from Drug Alcohol Depend, 143, Bonnet U, Specka M, Stratmann U, Ochwadt R, Scherbaum N, Abstinence phenomena of chronic cannabis-addicts prospectively monitored during controlled inpatient detoxification: cannabis withdrawal syndrome and its correlation with delta-9-tetrahydrocannabinol and -metabolites in serum, 189–197. Copyright (2014), with permission from Elsevier.Citation36
Figure 3 Mean rating of single symptoms of the MWC (MWC score according to previous studiesCitation24,Citation26,Citation37); 4-point scale (0 = none, 1 = mild, 2 = moderate, 3 = heavy). Note the delayed occurrence of strange dreams.Citation25 Vertical imaginary Y-axis: severity scores. Horizontal imaginary X-axis: time course.

In the following, the course of a CWS ( and ) is presented, which was recorded during a controlled inpatient detoxification treatment of a sample consisting of long-term cannabis users (N=39, 38 Caucasians, 8 females, median age: 27 years, median daily cannabis use: 2.5 g, median duration of daily cannabis use: 36 months).Citation36 Their cannabis consumption was in the upper range if compared with other clinical studies on CWS.Citation11,Citation12,Citation16,Citation20,Citation34 All patients of this sample developed a considerable CWS.Citation36 Although this study was conducted in a large detoxification ward of a university hospital residing in a metropolitan area (Ruhr Area, Germany), it lasted 5 years (2006–2011) to find 39 appropriate patients seeking treatment due to a current sole cannabis dependence without a competing additional substance use (except for tobacco) or active comorbidity to measure a CWS as pure as possible.Citation36 This study aimed to apply both MWCCitation24 and the Clinical Global Impression Scale (CGI-S)Citation80 to this sample to make the severity of CWS comparable to the severity of other psychiatric disorders.Citation36 The course of the single items is shown in . Cronbach’s α coefficients were 0.67, 0.78, and 0.73 on days 4, 8, and 12, respectively.Citation36 The MWC applied to this sample achieved α coefficients comparable to that of the CWS criteria proposed for DSM-5 (0.75)Citation19 and to that of the original MWC of Budney et al (0.77).Citation12,Citation24

CWS severity in comparison with other psychiatric conditions

As outlined earlier, the severity of CWS is positively related to the cumulative amount and potency of cannabis used before cessation,Citation12,Citation13,Citation19 gender,Citation36,Citation76,Citation77 and several environmentalCitation12,Citation13,Citation73 as well as heritableCitation73 factors. Therefore, its naturalistic severity varies a lot. There are some evidences that the discomfort due to CWS is similar to that found during tobacco withdrawalCitation14,Citation79 or a moderate alcohol withdrawal syndrome.Citation36 Inpatients detoxifying from heavy cannabis use were rated to be “moderately ill” at the peak of CWS according to CGI-S.Citation36 For a first orientation, inpatients suffering from acute schizophrenic episodes and patients with acute depressive episodes in outpatient settings have been rated in the majority to be “severely ill” and “moderately ill,” respectively.Citation36 Strong CWS can mimic eating disorders associated with gastrointestinal symptoms, food avoidance, and weight loss of adolescents.Citation81

The role of nausea in CWS

There is one case report of severe nausea being associated with CWS.Citation82 In the last years, increasing cases with a cannabis-hyperemesis syndrome were noticed, which characteristically occurred in frequent and long-term cannabis users and vanished in their next 5–20 abstinent days.Citation83Citation85 In order to differentiate this condition from CWS, we studied the course of the item “nausea” in the “cannabis burdened” sample mentioned earlier and found no correlation (r=−0.14 to 0.19) with the other items of MWC, whose internal consistency did not change, if “nausea” was excluded from the scale.Citation36 Thus, we found no evidence of nausea being a characteristic element in the orchestra of the CWS, which confirms the previous results of others.Citation11,Citation12,Citation19

Nevertheless, nausea seems to be a less common cannabis withdrawal symptom than chills, shaking, sweating, depressed mood, and stomach pain.Citation13 This is supported by the observation that nausea can occur more pronounced in the female CWS than in the male CWS.Citation76,Citation77

A retrospective chart review found preliminary evidence that “nausea and vomiting” might emerge more frequently in the withdrawal syndrome of SC agonists ()Citation56 often being full agonists at the CB1 receptor, other than the partial agonist THC.Citation57 Is this a clue that nausea breaks through when very potent agonists are removed from CB1 receptors? On the other hand, “severe nausea and vomiting” were key symptoms of the intoxication syndrome following the intravenous application of crude marijuana extractsCitation86 and are typical signs for the overdosing of smoking or swallowing cannabis preparations,Citation46,Citation86 including the first-ever intake experience. However, low to moderate amounts of cannabis preparations or THC analogs have well-known antiemetic properties.Citation46

Treatment of CWS

Cannabis detoxification treatment is usually performed in outpatient settings. However, in the case of a moderate or severe dependence syndrome, low psychosocial functioning or moderate or severe psychiatric comorbidity, an inpatient treatment is required. In Germany, inpatient cannabis detoxification is ideally performed in specialized wards following a “qualified detoxification” protocol. This includes supportive psychosocial interventions, psychoeducation, non-pharmacological symptom management, occupational and exercise therapy, professional care, as well as medical and psychiatric diagnostics and therapy of comorbid conditions. The treatment duration is related to the severity of the comorbidity or the CUD. An inpatient detoxification treatment on grounds of the diagnosis of “cannabis dependence” alone is mostly not accepted by the German health care providers, and they prima vista doubted the existence of a treatment-relevant CWS. This point of view may have a historical background, because many physicians consider cannabis to be a “soft drug,” as probably 20 years ago it contained lower THC contents.Citation87Citation90 This view may change with a clear definition of CWS in current diagnostic classification systems, such as DSM-5.Citation31 As a rule of thumb, an “acute” inpatient detoxification treatment lasts between a few days and up to 3 weeks. In case of a too high psychiatric comorbidity and too low psychosocial functioning for an outpatient treatment, the patients could be transferred into specialized inpatient rehabilitation wards. Because this post-acute treatment approach is paid by the German Person Fund (DRV), a substantial formal request is required. The rehabilitation treatment normally lasts for several weeks and is a special feature of the German health care system. In Germany, most of the cannabis patients entering outpatient (28,000 individuals in 2014) and inpatient (3,367 individuals in 2014) rehab programs show additional problems with the co-use of alcohol (7%–14%), opioids (30%–55%), cocaine (45%–60%), stimulants (45%–70%), and pathological gambling (6%–18%).Citation91 This pattern of comorbidity is common in other high-income countries.Citation1

The effects of behavioral approaches on the mitigation of CWS were not intentionally studied, even though a beneficial action of aerobic exercise therapy can be assumed.Citation92

Currently, there are no approved medications for the treatment of CUD. Nevertheless, various pharmaceuticals have been studied in small (N<80) controlled, mostly outpatient or laboratory pilot trials: lithium, antidepressants (bupropion, nefazodone, venlafaxine, fluoxetine, escitalopram, and mirtazapine), anticonvulsants (divalproex and gabapentin), norepinephrine reuptake inhibitor (atomoxetine), glutamate modulator and mucolytic agent (N-acetylcysteine), muscle relaxants (baclofen), anxiolytic (buspirone), antipsychotics (quetiapine), and CB receptor agonists (dronabinol and nabiximols).Citation55,Citation93 The antidepres sants, atomoxetine, lithium, buspirone, and divalproex had no relevant effect on the CWS or had worsened it.Citation55,Citation93 For instance, venlafaxine was shown to aggravate CWS and, thus, was accused to uphold cannabis smoking.Citation94 Quetiapine (200 mg/day) improved appetite and sleep quality during the CWS but worsened marijuana craving and drove self-administration of marijuana.Citation95 A more recent open pilot study reported a decrease of cannabis use within 8 weeks of quetiapine treatment (25–600 mg).Citation96

Putatively beneficial agents

There is evidence for an improvement of CWS with gabapentin (1200 mg/day).Citation97 The efficacy of the THC analogs dronabinol and nabiximols (plus cannabidiol) in reducing CWS is demonstrated in three small but well-controlled outpatient studies.Citation98Citation101 An improvement of the dependence syndrome or craving was not found.Citation98Citation101 Although innovative compounds, high costs of dronabinol or nabiximols may limit not only the use but also the abuse of these drugs. A significant effect of the THC substitution on the severity of cannabis dependence, craving, or cannabis-related problems was not found yet.Citation98Citation101 Nabiximols is a drug containing two of the main active cannabinoids, namely, THC and cannabidiol, and has been approved in some countries for the treatment of spasticity of multiple sclerosis (MS).Citation99Citation101 It is an oral spray formulation, and each puff of 100 µL contains 2.7 mg of THC and 2.5 mg of cannabidiol. A treatment with six puffs over the day revealed >10 times smaller blood THC concentrations than the blood concentrations known to produce psychotropic effects.Citation102 For the nabiximols regimes in the treatment of CWS, cannabis users had been instructed to take eight sprays qidCitation99,Citation100 or a maximum of four sprays every hour (up to 40 sprays/day).Citation101 Oral dronabinol had been administered in 20 mg doses three times a day.Citation98 The effectiveness of N-acetylcysteine (1200 mg/day) on CWS was not assessed directly, but this agent was shown to reduce relapse markers in the urine alongside a large (N=116) well-controlled study.Citation103 A recent laboratory study demonstrated the efficacy of the THC analog nabilon.Citation104

Because sleep difficulty is the withdrawal symptom that is assumed to be most associated with relapse to cannabis use,Citation105 a few sleeping medications were tested in the CWS treatment with first promising results for mirtazapineCitation30 and zolpidemCitation106,Citation107 during the first days of abstinence, necessarily taking care for zolpidem’s potential misuse. Nevertheless, both the drugs had no effects on CWS in general or relapse prevention.Citation30,Citation107

The withdrawal syndrome of SC receptor agonistsCitation56 awaits further characterization and may respond to benzodiazepines and quetiapine.Citation108

Impact on CUD or dependence

The CWS is part of a CUD (DSM-5)Citation31 and dependence-syndrome (ID-10, DSM-IV-R)Citation32,Citation43 being characterized by frequent, heavy, or prolonged cannabis use. The importance of the treatment of CWS on the maintenance of cannabis use or substance use trajectories over time is unclear and awaits further study. From previous literature, there is small evidence for both 1) CWS treatment initiated abstinence or dose reductionCitation12,Citation13 and 2) CWS treatment does not influence cannabis use in the following.Citation18,Citation20,Citation42,Citation109 Frequent cannabis users had reported that withdrawal symptoms negatively influence their desire and ability to quit.Citation12,Citation13,Citation18,Citation105 Two actual studies on adolescents and young adults found no association of CWS with abstinence rates being monitored up to 3 monthsCitation20 and 1 year posttreatment,Citation109 which confirmed the previous finding of Arendt et al.Citation20 Furthermore, patients with CWS relapsed sooner than those without CWS.Citation20 Patients recognizing a problem with CWS were associated with better abstinence rates than patients not recognizing a problem with CWSCitation42 pointing to a potential value of psychoeducation, an approach to be further studied in the management of CUD.

Abstaining from cannabis was reported to be followed by an increase of alcohol and tobacco use, which decreased again after continuation of cannabis use.Citation110 CWS in people with schizophrenia is associated with behavioral change, including relapse with cannabis and increased tobacco use.Citation111 “Religious support” and “prayer” were self-identified by cannabis users to be the most helpful quitting strategies and both were associated with higher 1-month and 1-year abstinence rates in these population.Citation111 Furthermore, the symptom severity of patients with posttraumatic stress disorder was positively associated with the use of cannabis (probably taken as a “self-medication”), cannabis use problems, and severity of CWS.Citation112

Studies that compared the effectiveness of outpatient versus inpatient treatments with respect to the severity and prognosis of CUD, especially their differential efficacy on long-term relapse prevention, dose reduction, or psychosocial functioning, are missing. At the end of a 16-day lasting inpatient detoxification treatment (qualified detox) of heavy cannabis users, the following effect sizes were found (Cohen’s d): 1.1 (CWS), 1.4 (cognition), psychiatric symptoms (0.8–0.9).Citation113 The bothersome global distress of this sample had improved significantly during the qualified detox ().

Figure 4 Significant improvement (p<0.001) of the subjective global distress of adult heavy cannabis users during inpatient qualified detoxification as measured by the Symptom Checklist 90, revised version (SCL-90-R).Citation129 Y-axis: percent of the sample (N=35); X-axis: global distress according to T-values: T<60: normal global distress; T>70: severe global distress;Citation129 T1 = admission day and T16 = last day (day 16) of the controlled inpatient qualified detoxification treatment.Citation113

Note: Reproduced from Dtsch Med Wochenschr, 141(2), Bonnet U, Specka M, Scherbaum N, Häufiger Konsum von nichtmedizinischem Cannabis, 126–131. Copyright (2016), with permission from Georg Thieme Verlag.Citation113
Figure 4 Significant improvement (p<0.001) of the subjective global distress of adult heavy cannabis users during inpatient qualified detoxification as measured by the Symptom Checklist 90, revised version (SCL-90-R).Citation129 Y-axis: percent of the sample (N=35); X-axis: global distress according to T-values: T<60: normal global distress; T>70: severe global distress;Citation129 T1 = admission day and T16 = last day (day 16) of the controlled inpatient qualified detoxification treatment.Citation113

At present, the effectiveness of different cannabis detoxification treatments on the course of the CUD has not been studied in depth. Outpatient treatment programs improved the psychosocial functioning and dropped the cannabis use for a while.Citation12,Citation13 Currently, only a few long-term follow-ups are available, so far showing no sustaining improvement of CUD subsequent to outpatient detoxification attempts.Citation18,Citation20,Citation42,Citation109

Discussion

With the definition of the DSM-5 criteria,Citation31 the CWS comes of age. Genetic influences on cannabis withdrawal were described to be the same as those affecting cannabis abuse and dependence.Citation114 Beyond that, the existence of the CWS has solid neurobiological underpinnings since it was found that the availability of brain CB1 receptor in cannabis dependents was inversely associated with the occurrence of CWS.Citation70,Citation71 After 4 weeks of abstinence, the anomalies of CB1 receptors binding had been normalized in cannabis dependents, thus giving a rough time frame of the duration of CWS,Citation70,Citation71 which apt to the clinical observations that have been obtained in the past 20 years (). Two different courses of CWS might result from the different contribution of cannabis residual symptoms assumed to be initially more prominent in the type A than in type B CWS.Citation36 Looking at a key symptom of cannabis use, such as “increase in appetite,”Citation5,Citation7 this was indeed reported more often in the first days of the type A CWS ().Citation19,Citation20,Citation35

Mood and behavioral symptoms, namely, insomnia, dysphoria, and anxiety, are the key symptoms of the CWS ( and ). Similar symptoms occurred in the obesity treatment with the CB-1 receptor antagonist rimonabant (also known as SR14171) and were the reason why rimonabant was withdrawn from the market in 2008.Citation115 Possibly, a “sustained CWS” had been precipitated when the effects of the physiological tone of endogenous endocannabinoids on brain and peripheral CB1 receptors were impeded by receptor antagonists, even in non-addicted but susceptible individuals. In support, the neurocircuitries involved in the regulation of stress, anxiety, and mood (such as the serotonergic, noradrenergic, and dopaminergic systems) were demonstrated to be sensitive to CB-1 receptor antagonists.Citation115

Influence of alcohol and tobacco

Regular alcohol drinking might influence the clinical expression of the CWS, and this is not through the overlapping alcohol withdrawal symptoms. Continuous exposure to ethanol, in either cell culture or rodent models, led to an increase in endocannabinoid levels that resulted in downregulation of the CB1 receptor and uncoupling of this receptor from downstream G protein signaling pathways.Citation116 A similar downregulation of CB1 receptors was found in multiple brain regions of chronic drinkers.Citation116 Alcoholic drinks were reported to be co-used by 33%–46% of regular cannabis users. The rates of co-use for cocaine, stimulants, and hallucinogens were 37%–43%, 30%–52%, and 36%–42%, respectivelyCitation1,Citation2,Citation116 – all putatively being able to influence the course and intensity of the CWS. Approximately 90% of cannabis users are also tobacco smokers, possibly reflecting the common route of administration, and even synergistic and compensatory actions of cannabis and tobacco as well as genetic and epigenetic factors assumed to mediate addiction vulnerability.Citation117,Citation118 More specifically, smoking tobacco use was shown to increase the number of cannabis dependence symptomsCitation119 and precipitated cannabis relapse.Citation120 Vice versa, cannabis use decreased the likelihood of abstaining from tobacco.Citation117,Citation118 There is a preliminary evidence that simultaneous tobacco and cannabis abstinence predicts better psychosocial treatment outcomes.Citation117,Citation118 There is still a paucity of clinical studies on this important subject, although alcohol, tobacco, and cannabis were consistently identified to be the substances with earliest onset of use, the highest prevalence of lifetime use, and the highest prevalence of lifetime disorder.Citation1Citation6,Citation74

Choice of treatment setting

In comparison with outpatient programs, inpatient detoxifications can provide strict abstinence conditions and, thus, can be used to better differentiate CWS from comorbidity, but are much more expensive and usually not the first choice of patients seeking treatment due to CUD. However, 1) the inability to initiate cannabis abstinence due to bothersome CWS, 2) the continuous co-use of other harmful drugs of dependence, or 3) the coexistence of other disabling psychiatric or somatic complaints give reasons for the medical necessity of an inpatient detoxification program, the duration of which depends on the intensity of the withdrawal symptoms and concomitant complaints.Citation5,Citation113 At this juncture, the duration of an inpatient detoxification program of heavy cannabis users is recommended to be not less than 14 days, ideally 21 days, taken into account that their pure CWS itself usually lasted up to 14–21 days (),Citation12,Citation13,Citation36,Citation113 and the diagnosing of potentially underlying comorbidity is more sensitive from then on. It remains a challenge of future in-depth studies to compare the impact of outpatient and inpatient treatment programs on the long-term course and disability of substance use disorders, which applies to CUD, too.

Influence of high potency cannabis preparations, gender, and so on

Similar to the cannabis addiction syndrome itself,Citation121 one of its hallmark, the CWS, is based upon complex interactions between drug-induced neurobiological changes, environmental factors, genetic and epigenetic factors, comorbidity, personality traits, gender influences, and stress responsivity, all of which contributing to the high inter- and intrapersonal variations in the composition, annoyance, and duration of the CWS ().Citation12,Citation13,Citation114,Citation121

In addition to an increasing awareness of the existence of the CWS, its increasing emergence in the last 20 years might result from the increasing psychotropic potency of the used marijuana originating from the breeding of strains with high THC (10%–18.5%) and low cannabidiol concentrations (<0.15%) being found especially in high-income countries.Citation1,Citation88Citation90,Citation122 In the Netherlands, the recent cannabidiol content of imported resin was ~7%.Citation90 According to animal experiments, cannabidiol can counterbalance some adverse effects of cannabis,Citation61 and in patient populations, there is mounting evidence of anticonvulsive and antipsychotic properties of cannabidiol.Citation123 Since the early 1950s, it is known that the chemical composition of the resin itself varies with cannabidiol activities between 0% and 50% depending on the provenance of the drug.Citation87 Whether the users of more potent cannabis strains adjust their intake according to the potency is still unclear.Citation88 However, there is first evidence that the occurrence of first-episode psychosis as well as the intensity of the CUD increased alongside the use of high potency cannabis preparations.Citation124,Citation125 This throws an extremely critical light on emerging modern cannabis ingestion methods (“dabbing” or “cannavaping” of cannabis concentrates with 20%–80% THC) used by individuals seeking a more rapid and even bigger than being possible with smoking flowers that THC contents are usually in the range of 2% and 6%.Citation126,Citation127 Marijuana users who had turned to “dabbing” reported higher tolerance and withdrawal experiences.Citation126

The CWS could have an measurement bias regarding a recent finding that it was endorsed more likely by the US than by Dutch cannabis users, which applies to other CUD criteria, such as tolerance, and gender effects on CWS, too.Citation77 In this context, recent studies revealed a consistent gender impact on CWS, because women experienced a stronger CWS ()Citation36,Citation76 and were shown to have a greater susceptibility to developing CUD than men.Citation121,Citation128 Women were also found to be more sensitive to the cannabis than men.Citation121,Citation128 Remarkably, women reported physical CWS complaints more likely, such as nausea and stomach pain ().Citation19,Citation76

CWS in the ICD-11 Beta Draft

In 2018, the 11th revision of the ICD-11 is planned to be published. The so-called Beta-Draft of the chapter about “Mental and Behavioral Disorders” is already available online at http://apps.who.int/classifications/icd11/browse/f/en#/http%3a%2f%2fid.who.int%2ficd%2fentity%2f637576511 (accessed November 25, 2016).Citation33 The current version of this ICD-11 Beta DraftCitation33 lists the usual mood and behavioral CWS symptoms according to DSM-5Citation31 but does not consider physical CWS symptoms.Citation33 We recommend to include at least “nausea” and “stomach pain” into the final version because these symptoms were recently found to be more prominent in the female CWS,Citation76,Citation77,Citation121,Citation128 and yet, it seems likely that the increasing use of high potency cannabis preparations are associated with more physical CWS symptoms. It is also recommended to include a note on the high intra- and interpersonal variability of the CWS intensity and the observation that – if a CWS occurs – it is extra distressing between the first and the third week after quitting a frequent, heavy, or prolonged cannabis use ().Citation12,Citation13,Citation36 Heavy users were shown to experience a CWS whose average severity is comparable to the burden of a moderate depression or moderate alcohol withdrawal syndrome.Citation36 In outpatient settings, the average discomfort of CWS was similar to that of tobacco withdrawal.Citation14,Citation79

Certainly, it awaits future study whether the inhalation of very potent cannabis concentratesCitation126,Citation127 is indeed associated with a further decrease of psychosocial functioning, higher comorbidity, and a stronger CUD and CWS – eventually with more physical features (eg, hyperalgesia, nausea, sweating, tremor, flu-like symptoms)Citation31 than occurring after the cessation of a heavy or prolonged use of traditional non-concentrated cannabis preparations.

Conclusion

The CWS is a criterion of CUDs (DSM-5) and cannabis dependence (DSM-IV-R, ICD-10). Several lines of evidence from human studies indicate that cessation from long-term and regular cannabis use precipitates a specific withdrawal syndrome with mainly mood and behavioral symptoms of light to moderate intensity, which can usually be treated in an outpatient setting. However, comorbidity with mental or somatic disorders, severe CUD, and low social functioning may require an inpatient treatment (preferably a qualified detox) and post-acute rehabilitation or long-term outpatient care. There are promising results with gabapentin and THC analogs in the treatment of CWS. Mirtazapine could improve insomnia, and venlafaxine was found to worsen the CWS. Certainly, further research is required with respect to the impact of the CWS treatment setting on long-term CUD prognosis and with respect to psychopharmacological or behavioral approaches, such as aerobic exercise therapy or psychoeducation, in the CWS treatment. The preliminary up-to-date content for the ICD-11Citation33 (intended to be finally published in 2018) is recommended to be expanded by physical CWS-symptoms, the specification of CWS severity and duration as well as gender effects.

Disclosure

The authors report no conflicts of interest in this work.

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