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Cannabis-based medicines and the perioperative physician

Abstract

The increasing availability of cannabis for both recreational and medicinal purposes means that anaesthetists will encounter an increasing number of patients taking cannabis-based medications. The existing evidence base is conflicted and incomplete regarding the indications, interactions and long-term effects of these substances. Globally, most doctors have had little education regarding the pharmacology of cannabis-based medicines, despite the endocannabinoid system being one of the most widespread in the human body. Much is unknown, and much is to be decided, including clarifying definitions and nomenclature, and therapeutic indications and dosing. Anaesthetists, Intensivists, Pain and Perioperative physicians will want to contribute to this evidence base and attempt to harness such therapeutic benefits in terms of pain relief and opiate-avoidance, anti-emesis and seizure control. We present a summary of the pharmacology of cannabis-based medicines including anaesthetic interactions and implications, to assist colleagues encountering these medicines in clinical practice.

Introduction

Cannabis use for medicinal purposes was first documented in 2900 BC in China, when Emperor Shen Nong described benefit for rheumatism and malaria (Pertwee 2015) and later in Ancient Egyptian texts (Pertwee 2015; Zlas et al. 1993). In the United Kingdom (UK), Queen Victoria’s personal physician Sir John Russell Reynolds issued a tincture containing cannabis for her Majesty’s menstrual cramps (David 2017), subsequently publishing his 30 years’ worth of experience with the drug (Reynolds 1890).

Discussion in medical journals, the mainstream and social media around the use of cannabis for medicinal and non-medicinal purposes has increased recently, especially following the legalisation of cannabis for recreational use in Canada (Government of Canada 2018a) and the UK government’s decision to make cannabis-based medicines (CBMs) available for prescription by doctors on the specialist register (Department of Health and Social Care 2018).

The actual, social and economic legitimisation of cannabis and its medicinal derivatives makes it likely increasing numbers of patients will present on this class of medicines. Perioperative physicians will require a sound understanding of their pharmacology and evidence base, and may wish to exploit this group of compounds for therapeutic purposes in the perioperative period.

A search of Pubmed was conducted in February 2019 utilising the search terms cannab* and the AND function for the following search terms individually; anaes*, marijuana, pain, nausea, surgery and pharmaco*. Abstracts were then screened for their applicability, with full texts reviewed. This was supplemented by a review of recent publications from governmental and regulatory organisations relating to CBMs, with backward reference searching. A search of individual governmental websites looking for legislation around cannabis and cannabinoid use was also undertaken in September 2019.

The pharmacology of novel psychoactive compounds (“legal highs”) is outside the scope of this review.

The global position

The availability of CBMs varies geographically and there is no global consensus on how cannabis and CBMs should be regulated. International stakeholders and regulators, including the United Nations (International Drug Policy Consortium 2016; Transnational Institute and Global Drug Policy Observatory 2016) and World Health Organisation (WHO) have been inconsistent in their approach. The WHO’s Expert Committee on Drug Dependences’ recent review (Ghebreyesus 2019) recommended to the United Nations Office on Drugs and Crime (UNODC) that the rescheduling within the International Drug Control Conventions occurs for cannabis and cannabis resin, dronabinol, tetrahydrocannabinol and extracts and tinctures of cannabis. They also repeated their recommendation to remove cannabidiol (CBD) preparations (with not more than 0.2% delta-9-THC) from the International Drug Control Conventions. The UNODC subsequently delayed its vote on these recommendations, but despite this, many countries are proceeding to legalise or reschedule cannabis and/or CBMs, broadening public availability, with the UK the most recent country to reschedule CBMs. Table 1 details the current status of cannabis and CBMs in selected countries for medical use. The recreational use of cannabis is currently legalised in Uruguay, Canada and certain states within the USA (United Nations Office on Drugs and Crime 2019).

Table 1 Current legal status of Cannabis and CBMs in selected countries

Definitions of cannabis and cannabinoids

Cannabis

The Cannabis genus encompasses three major species; Cannabis sativa, Cannabis indica and Cannabis ruderalis. The number of identifiable extractable compounds has increased dramatically from 60 (Ashton 1999) to over 500 in the last 20 years (Beaulieu et al. 2016), of which over 100 are cannabinoids (Bie et al. 2018).

Cannabinoids

Cannabinoids are endogenous in humans, animals and plants, or synthetically produced, acting as ligands at the cannabinoid receptors. Cannabinoids can be psychoactive, for example delta-9-tetrahydrocannabinol (d9THC), delta-8-tetrahydrocannabinol (d8THC), cannabinol (CBN) or non-psychoactive, for example cannabidiol (CBD). Table 2 lists their classification, as well as examples of currently available CBMs (Pertwee 2015; Beaulieu et al. 2016; Zendulka et al. 2016; Yeon Kong et al. 2018; Hauser et al. 2018a; Barnes 2018; National Institute for Health and Care Excellence 2014; Rice and Cameron 2017; Krcevski-Skvarc et al. 2018).

Table 2 Classification of cannabinoids and some commercially available preparation

Pharmacology of cannabinoids

Mode of action

The endocannabinoid system consists of both cannabinoid (CB) receptors and neurotransmitters, the plasma concentrations of which are normally at low levels. They are synthesised in the postsynaptic neurone (Hosking and Zajicek 2008) in response to stimuli including pain, stress, inflammation and are involved in the homeostasis of various body systems (Pertwee 2015). Antinociceptive effects occur via their actions as retrograde transmitters at presynaptic inhibitory CB1 receptors (Hauser et al. 2018a). Both CB1 and CB2 receptors are G protein coupled receptors (Gi,Go) with stimulation reducing cAMP production through the inhibition of adenylyl cyclase, resulting in an action on voltage gated calcium and potassium channels depressing neuronal excitability and reducing neurotransmitter release (Zendulka et al. 2016; Hauser et al. 2018a; Hosking and Zajicek 2008).

CB1 receptors are found in the cortex (thalamus, medulla, periaqueductal gray matter, descending pain pathways), spinal cord (descending pain pathways, dorsal horn) and peripherally on primary afferent sensory neurones where they outnumber the mu receptor, suggesting a potential mechanism for the modulation and treatment of neuropathic pain (Kumar et al. 2001).

CB2 receptors are involved in immunomodulation, with receptors distributed in the spleen, macrophages and Kupffer cells. It is increasingly recognised that the endocannabinoid system plays a crucial role in the maintenance of microglial activity through actions at CB1 and CB2 receptors, reducing neuro-inflammation (Bie et al. 2018; Bilkei-Gorzo et al. 2018). Relatively few CB2 receptors are found in the nervous system (Lucas et al. 2018), but they are inducible in the dorsal horn following inflammation or injury, with increased receptor concentration found in neuropathic pain models and receptor activation limiting the acute inflammatory process contributing to nociceptor sensitisation (Bie et al. 2018; Hosking and Zajicek 2008).

Exogenous and endogenous cannabinoids have differing effects at the CB1 and CB2 receptors. THC is an agonist at both, whilst CBD is a non-competitive antagonist at CB1 receptors at high concentrations, an inverse agonist at CB2 receptors and causes allosteric modulation of both CB receptors (Pertwee 2015; Lucas et al. 2018; Expert Committee on Drug Dependence 2018). The cannabinoid compounds, particularly CBD, have additional actions within the nervous system through signalling at a multitude of other receptors. This includes adenosine, serotonergic, adrenergic, nicotinic acetylcholine, glycine, nuclear peroxisome proliferator activated receptors (PPARs) and transient receptor potential (TPRV) ion channels (Capsaicin target). Anaesthetists should also note their actions at the opioid, NMDA and gamma amino butyric acid (GABA) receptors (Zendulka et al. 2016; Hauser et al. 2018a; Expert Committee on Drug Dependence 2018; Meng et al. 2017; Koppel et al. 2014).

Opioid system interaction

The cannabinoid and opioid systems are closely linked, with the activation of both opioid and cannabinoid receptors mediating common intracellular signalling mechanisms (Manzanares et al. 1999; Abrams et al. 2011; Scavone et al. 2013; Cohen et al. 2019; Pertwee et al. 2010). Opioid and cannabinoid receptors are found within the same cells and neurones in the central nervous system, with cannabinoids acting at kappa and delta receptors to increase endogenous opioid synthesis and release. Notably, the administration of opioid antagonists has been shown to block some of the effects of delta 9THC (Manzanares et al. 1999). The presence of opioid and cannabinoid receptors in noradrenergic pathways may have a role in the treatment of opiate withdrawal (Scavone et al. 2013).

NMDA system interaction

The NMDA receptor NR1 subunit is closely coupled to CB1 receptors, with the histidine triad nucleotide binding protein 1 (HINT 1) thought to be the pivotal modulator, exerting a negative control on NMDA receptors. HINT-1 gene deletion results in loss of CB1 inhibition of the NMDA receptor (Rodríguez-Muñoz et al. 2016). CB1 receptors have both presynaptic (reduced release of glutamate into synaptic cleft) and post-synaptic (intracellular NMDA signalling) effects (Rodríguez-Muñoz et al. 2016).

NMDA receptor activity stimulates the release of endocannabinoids, resulting in negative feedback reducing NMDA receptor numbers. It has been postulated that exo-cannabinoids are more potent inhibitors of the NMDA receptor than endocannabinoids (Pacheco et al. 2019; Ferreira et al. 2018), with exo-cannabinoids causing neural dysfunction and NMDA receptor hypofunction through alteration in the balance of NMDA-CB receptor regulation (Rodríguez-Muñoz et al. 2016).

The endocannabinoid system also regulates NMDA receptor activity by preventing over activation, neuroprotection from excitotoxicity and downregulating their activity (Rodríguez-Muñoz et al. 2016; Pacheco et al. 2019; Sánchez-Blázquez et al. 2014).

Gamma amino butyric acid

Gamma amino butyric acid (GABA) and CB1 receptors are closely localised in multiple cortical regions, including the hypothalamus, hippocampus and cortex (Cohen et al. 2019; Lotsch et al. 2018). CB1 receptors are expressed on GABAergic neurons, helping to regulate astrocyte and microglial activity, and hence neuroinflammation (Bilkei-Gorzo et al. 2018).

In preclinical studies, cannabinoids inhibit GABA release, through activation of CB1 receptors (Pertwee 2015; Laaris et al. 2011). They inhibit GABA uptake from the CNS extracellular space (Laaris et al. 2011), and cause allosteric modulation of GABA receptors (Bakas et al. 2017). Limited human studies show altered levels of GABAergic functions with chronic cannabis use, which may contribute to psychological effects (Cohen et al. 2019).

Pharmacokinetics

Absorption

The absorption of vaporised cannabinoids is rapid, with peak plasma concentrations observed within 10 min. THC’s bioavailability after inhalation ranges from 10 to 35%, and CBD 31% varying with device used and size of the particles (Kumar et al. 2001; Lucas et al. 2018; Karschner et al. 2011).

Oral bioavailability of CBM is low, at 2–20% for both CBD and THC (Lucas et al. 2018; Karschner et al. 2011; Anderson and Chan 2016) mainly due to extensive first pass metabolism (Lucas et al. 2018). Onset of action is 0.5–2 h due to slow intestinal absorption resulting in a longer duration of action (Kumar et al. 2001; Bridgeman and Abazia 2017).

An oromucosal spray preparation (nabiximols; Sativex ®) has a reported bioavailability similar to oral THC or intermediate between the oral and inhaled routes (Lucas et al. 2018; Expert Committee on Drug Dependence 2018; Karschner et al. 2011; Anderson and Chan 2016).

Transdermal administration is reported, with the permeability of CBD and CBN higher than d9THC and d8THC (Therapeutic Goods Administration 2017), but their hydrophobic nature means transdermal absorption is poor and requires permeation enhancement (Lucas et al. 2018).

Distribution

Volume of distribution varies by cannabinoid studied, with a VD of 32 L/kg for CBD (intravenous administration), and 3.4 L/kg for THC (inhalation administration) (Lucas et al. 2018), which is said to follow a three-compartment model (Heuberger et al. 2015). Cannabinoids are highly lipid soluble (Kumar et al. 2001) with rapid penetration through the blood–brain barrier (Ashton 1999), the placenta and into breast milk (Lucas et al. 2018). This also leads to accumulation in fatty tissue, with continued activity following cessation.

Metabolism

The cannabinoids are mainly hydroxylated and glucuronidated in the liver by the cytochrome P450 family of isoenzymes (Kumar et al. 2001; Lucas et al. 2018; Karschner et al. 2011; Ujváry and Hanuš 2016). Some metabolites are equipotent to the parental compounds (Yeon Kong et al. 2018; Rong et al. 2017). THC is metabolised to over 80 metabolites by various isoenzymes, including CYP1A1, CYP1A2, CYP1B1, CYP2B6, CYP2A6, CYP2C9 and CYP3A4. Inhibition of CYP3A4 may result in clinically apparent interactions with oxycodone (Pertwee 2015; Zendulka et al. 2016; Hauser et al. 2018a; Lucas et al. 2018).

CBD is metabolised to over 100 metabolites by isoenzymes CYP1A1, CYP1A2, CYP3A4, CYP2C9 and CYP2D6, the most abundant metabolite being the hydroxylated 7-COOH CBD derivative (Lucas et al. 2018; Ujváry and Hanuš 2016). Inhibition of CYP2D6 and CYP3A4 results in interactions with oxycodone, benzodiazepines and haloperidol (Hauser et al. 2018a; Karschner et al. 2011; Ujváry and Hanuš 2016). Oral CBD increases clobazam (and active metabolite) plasma levels (CYP2C19 interaction) (Ujváry and Hanuš 2016), resulting in dose reductions of clobazam in recent randomised controlled trial (RCTs) (Thiele et al. 2018). Prolonged use of CBD results in CYP1A1 induction (Ujváry and Hanuš 2016).

Cannabinol is metabolised via CYP2C9 and CYP3A4, with no evidence cytochrome P450 interactions (Zendulka et al. 2016).

The significance of these interactions is uncertain as they have occurred either in vitro or in excess of clinically relevant concentrations.

Elimination/excretion

Clearance of cannabinoids is estimated to be 38.8 L/h to 53 L/h (Heuberger et al. 2015), with long terminal half-lives due to their lipophilicity. In regular users, this is extended, with measurable plasma concentrations of THC over 24 h after last administration. Fifteen percent of cannabinoid metabolites undergo enterohepatic recycling, prolonging their action (Ashton 1999).

THC and metabolites are mainly excreted in faeces (65–80%) and urine (20–35%) (Ashton 1999; WHO Expert Committee on Drug Dependence 2018). THC’s elimination half-life is 56 h in occasional and 28 h in chronic users (Ashton 1999) with urinary metabolites measurable 14 days post exposure (Vandrey et al. 2017). Nabilone’s (Cesamet ®; synthetic THC) elimination half-life is shorter than THC, at 2–4 h, yet 16% of a single dose is reportedly measurable at 7 days post administration (Ashton 1999).

CBD metabolites and unchanged drug are mainly excreted in the urine with an elimination half-life of 2–5 days (Lucas et al. 2018; Anderson and Chan 2016; Ujváry and Hanuš 2016).

Pharmacodynamics (of relevance to the perioperative physician)

Cardiovascular system

Tachycardia due to CB1 agonism in cardiac myocytes has been reported (Kumar et al. 2001; Lucas et al. 2018), but was not noted following intravenous administration of d9THC (Vandrey et al. 2017). Bradycardia, hypotension, an increased cardiac output and myocardial oxygen demand have been described (Dickerson 1980; Bryson and Frost 2011). These effects are potentially exacerbated by sympathomimetic agents although the mechanism of action is unclear (Lucas et al. 2018). Effects may be cannabinoid specific, with CBD (Expert Committee on Drug Dependence 2018) not reported to effect heart rate or blood pressure, and THC possibly having anticholinergic effects through depletion of acetylcholine stores (Dickerson 1980).

Central nervous system

Effects are well described largely in relation to their abuse as a recreational drug, including psychomotor impairment, sedation, dizziness, euphoria, disorientation and confusion. Effects may be enhanced if administered with other CNS depressant drugs, for example opioids or benzodiazepines, and have been observed in a clinical setting (Kumar et al. 2001; Lucas et al. 2018).

The behavioural and long-term psychological effects (including dependence) of cannabis are widely reported (Pertwee 2015; Kumar et al. 2001; Nugent et al. 2017), and not reiterated here. Some evidence suggests the abuse potential of CBMs, likelihood of withdrawal phenomena and mental health morbidity is low (Pertwee 2015; Aragona et al. 2009), but trials are of short duration and do not examine long term effects. Evidence suggests chronic cannabis use impairs learning, memory and attention, and causes complex mental health disorders (Pertwee 2015; Nugent et al. 2017; National Academies of Sciences Engineering and Medicine 2017; Campbell et al. 2018). Further research is needed to determine relevance to CBM use.

Respiratory system

There is no clear evidence of respiratory system effects when administered by routes other than smoking. This may be due to the absence of cannabinoid receptors in the brainstem (Kumar et al. 2001).

Perioperative practitioners should be alert to the recent warning from the FDA around the use of vaping THC oil (US Food and Drug Administration 2019). This followed on from a multitude of reports of severe pulmonary disease development associated with vaping of THC products (Layden et al. 2019). Any patient presenting in the perioperative period with new onset respiratory disease and a history of vaping THC should therefore be thoroughly evaluated with this kept in mind.

Immune system

Animal studies suggest that high-dose cannabinoids impair cell-mediated and humoral immunity (Kumar et al. 2001), and low-dose CBD causes immune stimulation (Expert Committee on Drug Dependence 2018). The clinical relevance in humans is unclear.

Interactions of note for the perioperative physician

Induction agents/volatiles

Effects of cannabinoids on dosing of volatile and intravenous anaesthetic agents is equivocal, with evidence limited to animal studies, case reports and two limited human studies.

Ether anaesthesia is prolonged in mice and rats by cannabidiol, d8THC and d9THC (Chesher et al. 1974). Halothane anaesthesia is prolonged and dose requirements reduced in dogs after THC administration (Stoelting et al. 1973), with similar effects noted in mice with isoflurane administration (Schuster et al. 2002). Little is known about the interaction between cannabinoids and modern inhalational anaesthetics.

Animal studies have shown cannabidiol, d8THC and d9THC prolong barbiturate anaesthesia in mice and rats (Chesher et al. 1974) and THC administration increases the doses of thiopentone and propofol required for sedation (Brand et al. 2008). A cannabis extract premedication in dogs resulted in quicker onset and longer lasting anaesthesia with propofol (Kumar et al. 2010). One postulated mechanism is the increased Andamide (endocannabinoid) levels in the brain with propofol, with the inhibition of the enzyme fatty acid amide hydrolyses (FAAH), which normally terminates Anandamides activity, thought to be key (Schelling et al. 2006).

There is limited evidence of the effect of cannabinoid exposure on anaesthesia in humans. Case reports suggest increased anaesthetic requirements with non-medicinal cannabis use (Richtig et al. 2015; Symons 2002). A prospective trial found significantly increased propofol dosing for induction and LMA insertion in cannabis users versus controls (Flisberg et al. 2009). Studies utilising bispectral index monitoring (BIS) found no differences between cannabis users and non-users with the bolus dose of propofol required to achieve a BIS of < 60 (Flisberg et al. 2009). Higher BIS values have been noted for patients under steady state volatile anaesthesia who were administered nabiximols (Sativex®) as a premedication versus controls (Ibera et al. 2018).

These results should be interpreted cautiously given the limited number of participants, the applicability of extrapolating animal studies to human practice, use of unknown quantities of non-prescribable CBMs (except one study) and uncertainties about prior cannabis consumption (Flisberg et al. 2009). Additionally in the electroencephalogram (EEG)/depth of anaesthesia studies, it is unclear if the effects are a result of cannabinoids on the EEG or the effect of cannabinoid-anaesthetic interaction.

In summary, there is minimal evidence base as to the effects of the current agents, with animal studies relating to older agents only (ether, halothane, isoflurane). The evidence for intravenous agents is conflicting and of poor quality, but propofol requirements may be higher. There is a current research opportunity for investigation into the interaction with newer agents in humans.

Opioids

Cannabinoid agonists facilitate endogenous opioid signalling and increase concentrations of endogenous opioids (Scavone et al. 2013; Abrams 2016).

In animal studies (Abrams 2016; Maguire and France 2018), cannabinoids and opioids are synergistic, with the analgesic efficacy of cannabinoids not reduced when opioid antagonists are administered. Human findings are variable; statistically significant reductions in pain scores, and similar opioid pharmacokinetics (with the exception of a reduced Cmax in the morphine group) pre and post vaporised cannabis use was found in chronic opioid users (morphine/oxycodone) (Abrams et al. 2011). In contrast, a small study found higher pain scores and greater rescue analgesia requirements post operatively in cannabis users, versus non-cannabis users (Jefferson et al. 2013). Chronic cannabinoid and cannabis users undergoing orthopaedic procedures showed higher post-operative pain scores without a significant increase in post-operative opioid consumption (Liu et al. 2018). All these studies have limited numbers of participants, and methodological issues that may confound the results.

In summary, cannabinoids and opioids are synergistic for both wanted and unwanted effects. Chronic cannabis users may have higher pain scores; it is unclear whether this is pathophysiological or a behavioral component of drug use.

Ketamine

Ketamine induces endogenous cannabinoid release (Pacheco et al. 2019; Ferreira et al. 2018), which may partially explain its role in anti-nociception. The psychomotor side effects of ketamine are enhanced with CBD administration, but no adverse behavioural or cardiovascular effects have been noted (Hallak et al. 2011).

Gabapentinoids

Gabapentin’s mechanism of action is via α2δ subunits on voltage-dependent calcium channels, with reduction in neural transmission. Similarly, activation of the CB receptor results in inhibition of the voltage dependent calcium channel (Pertwee 2015; Lile et al. 2016). Animal studies have shown the synergistic action of gabapentin and THC when used for the treatment of neuropathic pain, at the expense of increased side effects of THC (Atwal et al. 2017).

Human studies are limited; in multiple sclerosis, the combination of THC and gabapentin improved pain scores in neuropathic pain (Turcotte et al. 2015). High-dose gabapentin for management of cannabis tolerance produces THC like effects, and when gabapentin was used in combination with THC, these effects were seen to be increased, suggesting overlap of pharmacological actions (Lile et al. 2016).

In summary, the gabapentinoids and cannabinoids have overlapping pharmacological actions, with increased therapeutic and side effects when combination dosing is used.

Dexmedetomidine

There is limited evidence regarding potential interactions between cannabinoids and Dexmedetomidine. Animal studies have shown that a synthetic THC derivative (CP55,940) has additive or synergistic analgesic effects when administered with Dexmedetomidine, depending on the nociceptive stimulus utilised (Tham et al. 2005). The study failed to explain the mechanism of this apparent synergy; however, given the similar intracellular signalling mechanisms (calcium, potassium and cyclic AMP) activated by these medications and the close locality of the target receptors in the periaqueductal grey and substantia gelatinosa, receptor interaction is postulated (Tham et al. 2005).

Given the lack of current evidence around interactions in humans, further research should focus on this area.

Medical conditions where cannabinoids are recommended

A variety of National and Governmental organisations have provided reviews on the use of CBMs, producing recommendations with a varying hierarchy of evidence (Department of Health and Social Care 2018; Ghebreyesus 2019; Therapeutic Goods Administration 2017; Health Products Regualtory Authority 2017; National Academies of Sciences Engineering and Medicine 2017). Here, we review the commoner indications for CBMs.

Chronic pain

Information on the use of cannabinoids for chronic pain comes from trials, systematic reviews (SR), meta-analyses (MA) and organisational reports. The outcomes vary, and are limited by factors including study design, moderate to high risk of bias (Hauser et al. 2018a), limited participants (most recent SR/MA (Stockings et al. 2018a) identified 104 studies, 21 with > 100 participants), short duration of exposure to the cannabinoid (median eight weeks (Stockings et al. 2018a)) and varying definitions of “chronic pain”. Many studies within these systematic reviews are notable for high withdrawal rates in the treatment arms (Stockings et al. 2018a; Mucke et al. 2018).

The most recent SR concluded that the number needed to harm (NNTH) for cannabinoid use in chronic pain was 6 (opioids NNTH = 5) (Stockings et al. 2018a) with a number needed to treat (NNT) of 24 (30% reduction in pain). This compares unfavourably with opioids (NNT 4.3), pregabalin (7.7) and tricyclics (NNT 3.6) (Stockings et al. 2018a). When the pain intensity reduction (versus placebo) was pooled, it was equivalent to a 3 mm reduction on a 100 mm visual analogue scale. Taken with a higher risk of an adverse event and trial withdrawal (Stockings et al. 2018a), the authors suggested that whilst there was moderate evidence for pain reduction with cannabinoids compared with placebo (higher quality evidence for MS and neuropathic related pain), it seemed unlikely that cannabinoids are highly effective for chronic non-cancer pain.

Other SR/MAs make varying comments on the strength of the evidence, including weak recommendations (Meng et al. 2017), low strength (Rodríguez-Muñoz et al. 2016), moderate (Therapeutic Goods Administration 2017; Mucke et al. 2018; Whiting et al. 2015) (30% reduction pain relief), moderate to high (Aviram and Samuelly-Leichtag 2017), strong or “conclusive” (Abrams 2018) evidence for the use of cannabinoids in chronic pain. Others suggest a moderate to high risk of bias, concluding the evidence base is insufficient to make well found conclusions about the use of CBMs for cancer and non-cancer pain (Hauser et al. 2018b). Additionally, a large observational cohort study in Australia disputed cannabis use as an adjunct to reduce opiate consumption (Sánchez-Blázquez et al. 2014).

Globally, regulatory bodies have come to different conclusions. The Health Products Regulatory Authority (HPRA) of Ireland does not support CBMs as a treatment in chronic pain (Health Products Regualtory Authority 2017). The European Pain Federations recent position paper recommended CBMs be considered for chronic neuropathic pain, but as a third line agent, and stated there was insufficient evidence for CBMs for non-neuropathic chronic non-cancer pain (Hauser et al. 2018a). This is in direct contrast to the National Academies of Science Engineering and Medicine (NASEM) review on the health effects of cannabis and cannabinoids (National Academies of Sciences Engineering and Medicine 2017) which concluded that there was conclusive or substantial evidence for the use cannabis or cannabinoids for the treatment of pain in adults.

In summary, CBMs have a higher NNT than opioids, pregabalin or TCA, with a clinically insignificant pooled pain reduction of 3 mm on 100 mm VAS, and are thus unlikely to be effective in chronic, non-cancer pain, non-neuropathic pain. Additionally, other problems include study design and high withdrawal rates in intervention arms, with Cannabinoids demonstrating a higher risk of adverse events.

Nausea and vomiting secondary to chemotherapy

Nabilone (UK) and dronabinol (USA) are used to treat intractable post-chemotherapy nausea and vomiting (Abrams 2018), with the HPRA of Ireland recently permitting its use for this indication (Health Products Regualtory Authority 2017).

Reviews of cannabinoids for this indication have found them to be better than placebo (Whiting et al. 2015; Smith et al. 2015; Layeeque et al. 2006) of similar (Smith et al. 2015; Lewis et al. 1994) or better efficacy than antiemetics (dopamine antagonists) (Whiting et al. 2015), but with patients preferring CBMs (Smith et al. 2015). These reviews do not compare CBMs with steroids or serotonin (5HT3) antagonists. One randomised controlled trial utilising ondansetron as a comparator (Meiri et al. 2007) was stopped early due to recruitment difficulties, and had numerous methodological limitations including being underpowered for the authors conclusion that dronabinol was as efficacious as ondansetron.

The quality of evidence for the use of CBMs in preventing chemotherapy induced nausea and vomiting has been described as low (Whiting et al. 2015; Smith et al. 2015), “sometimes effective” (Therapeutic Goods Administration 2017) or conclusive/substantial evidence of benefit (Abrams 2018).

In summary, no completed studies have utilised modern antiemetics as a comparator, but cannabinoids are better than placebo, and display equivalent efficacy with dopamine antagonists. Further research will help determine the appropriate usage of CBM for nausea and vomiting.

Multiple sclerosis

Nabiximols (Sativex®) is licensed for multiple sclerosis (MS)-induced spasticity (Department of Health and Social Care 2018), which affects 17% of MS sufferers, with a similar proportion using cannabis for symptom control (Rice and Cameron 2017).

Previous MA/SR have produced various conclusions on the strength of the evidence of CBMs in MS-induced spasticity, ranging from low quality to conclusive evidence (Therapeutic Goods Administration 2017; Health Products Regualtory Authority 2017; Rice and Cameron 2017; Koppel et al. 2014; Whiting et al. 2015; Abrams 2018). A recent systematic review of reviews (Nielsen et al. 2018) for the use of cannabinoids in MS concluded that whilst the quality of the evidence from included studies was very low to low, five of the eleven reviews concluded that there was sufficient evidence for reduction in spasticity and/or pain in MS. However, the authors stated that despite the positive findings, the effect was small (Nielsen et al. 2018).

In summary, CBMs have a small positive effect on muscle spasticity, but the evidence quality is low.

Epilepsy

The United States Food and Drug Administration (FDA) (US Food and Drug Administration 2018) has recently approved cannabidiol oral solution (Epidiolex®) for the treatment of two forms of rare epilepsy in children aged over 2 years of age; Lennox-Gastaut syndrome and Dravet syndrome (Thiele et al. 2018; Devinsky et al. 2018; Devinsky et al. 2017). Most evidence is on the use of CBD, with the overall quality of the evidence in adults being limited (Koppel et al. 2014; Abrams 2018; Gloss and Vickrey 2014; Stockings et al. 2018b). Meta-analysis results pool effects in adults and children, with conclusions being influenced by the aforementioned paediatric studies (Sánchez-Blázquez et al. 2014; Devinsky et al. 2018; Devinsky et al. 2017; Gloss and Vickrey 2014; Stockings et al. 2018b). Outside of the USA, CBM use for epilepsy is not recommended in the UK (Department of Health and Social Care 2018), Ireland (Health Products Regualtory Authority 2017) and only once conventional treatments have failed in Australia (Therapeutic Goods Administration 2017).

In summary, the evidence base supports the use of CBD in children with certain neurological conditions, but not in adults.

Other

The NASEM review has considered CBMs for the treatment of other conditions, as detailed in Table 3 (Abrams 2018).

Table 3 Potential indications for CBM and evidence base

Potential future uses in perioperative medicine

Nausea and vomiting prophylaxis and treatment

There is a paucity of evidence on the effects on post-operative nausea and vomiting (PONV). Nabilone (Cesamet®) (Lewis et al. 1994; Levin et al. 2017) and intravenous THC (Kleine-Brueggeney et al. 2015) have been shown to be ineffective for PONV. Nabilone premedication compared with placebo (Levin et al. 2017) or metoclopramide (Lewis et al. 1994) had no effect on PONV. Intravenous THC similarly showed a lack of effect, with early trial cessation due to an intolerable side effect profile (Kleine-Brueggeney et al. 2015).

Combination therapy (dronabinol and prochlorperazine) compared with routine care showed a reduction in the incidence of PONV, yet the retrospective nature and multiple confounders means the evidence has to be carefully interpreted (Layeeque et al. 2006).

Perioperative pain management

A systematic review looking at the efficacy of cannabinoids for acute pain management suggested no role for cannabinoids (Stevens and Higgins 2017).

For perioperative pain management, a small number of RCTs have been conducted with two studies suggesting benefit (Jain et al. 1981; Holdcroft et al. 2006). The first (Jain et al. 1981) showed significantly improved post-operative pain scores compared with placebo, but at the expense of increased side effects including drowsiness and dysphoria. The second (Holdcroft et al. 2006), a dose escalation study, with an oral capsule mixture of THC/cannabidiol (and other plant-based cannabinoid extracts) reported a similar NNT as other rescue analgesics, but with significantly increased side effects including sedation and nausea. The applicability of these results is limited by methodological issues and the small number of participants.

Six other studies (Ostenfeld et al. 2011; Beaulieu 2006; Buggy et al. 2003; Seeling et al. 2006; Kalliomäki et al. 2013; Guillaud et al. 1983) investigating the perioperative use of CBMs for analgesia showed no improvement in pain scores; one (Beaulieu 2006) showing significantly higher pain scores.

If CBMs are to be introduced into the clinical pharmacopoeia for perioperative analgesia, the potential for synergy with concurrently administered opioids (especially slow release formulations) in the perioperative period should be considered. One of the main concerns, and as recently highlighted by both the Anaesthesia Patient Safety Foundation (APSF) and ANZCAs faculty of pain medicine (Anaesthesia Patient Safety Foundation 2018; Australia and New Zealand College of Anaesthetists Faculty of Pain Medicine 2018) is the potential for opioid induced ventilatory impairment (OIVI) (Australia and New Zealand College of Anaesthetists Faculty of Pain Medicine 2018). We would recommend sedation soring be undertaken in these patients, as well as standardised order sets as recently recommended by the APSF (Anaesthesia Patient Safety Foundation 2018) and ANZCA (Australia and New Zealand College of Anaesthetists Faculty of Pain Medicine 2018).

In summary, cannabinoids may improve pain relief as part of multi-modal approach. There is an increased risk of adverse side effects including increased sedation and subsequent ventilatory impairment.

The future of CBMS

Further clarification on the role of non-CBD CBMs is expected later this year with the forthcoming UNODC vote on rescheduling as recommended by the WHO, increasing the focus on this group of medicines. With time, this may help to improve the evidence base, define clinical indications including potential therapeutic applications in perioperative medicine and provide outcome data from longer term use, which is currently lacking (Health Products Regualtory Authority 2017; Fitzcharles and Eisenberg 2018).

This latter point is arguably the most important, and whilst cannabis use per se has been associated with some cancers (prostate, glioma, cervical) and psychiatric morbidity, the quality of the evidence is limited, and it is uncertain if long-term effects of CBMs can be extrapolated from long term cannabis use (Nugent et al. 2017; National Academies of Sciences Engineering and Medicine 2017; Campbell et al. 2018).

Therefore, further research is required, and whilst one of the longest follow up studies of cannabis use in a medical setting (Ware et al. 2015) suggested no difference in serious adverse events between controls and cannabis users, the short duration of this and other studies involving CBMs limits conclusions on long-term safety (Hauser et al. 2018c). Long-term data on CBMs is now being collected through patient registries (national and pharmaceutical led) and observational studies providing reporting of adverse effects (Krcevski-Skvarc et al. 2018). Achieving greater clarity on the benefits and harms of CBMs may be affected by the legalisation of cannabis for recreational use in some territories (United Nations Office on Drugs and Crime 2018).

Conclusions

There are marked discrepancies in the literature regarding grading of the evidence base and the strength and quality of the resultant recommendations.

It is clear that with the increasing trend for legalisation of this class of medicines, and the large number of patients we as a specialty are involved with, the perioperative team need to have a broader understanding of the pharmacology interactions, and potential uses this group of drugs has.

As the evidence base increases, CBMs could become part of the perioperative teams’ armamentarium to help provide an opiate sparing multimodal analgesia regime as well as having a role in the management of common post-operative complications such as nausea and vomiting.

Availability of data and materials

Not applicable.

Abbreviations

BIS:

Bispectral Index

CB:

Cannabinoid

CBD:

Cannabidiol

CBN:

Cannabinol

CBM:

Cannabis-based medicines

CYP:

Cytochrome P450

D8THC:

Delta-8-tetrahydrocannabinol

D9THC:

Elta-9-tetrahydrocannabinol

EEG:

Electroencephalogram

GABA:

Gamma amino butyric acid

HPRA:

Health Products Regulatory Authority

MA:

Meta-analysis

MS:

Multiple sclerosis

NASEM:

National Academies of Science Engineering and Medicine

NNT:

Number needed to treat

NNTH:

Number needed to harm

PONV:

Post-operative nausea and vomiting

RCT:

Randomised controlled trial

SR:

Systematic review

THC:

Tetrahydrocannabinol

UK:

United Kingdom

USA:

United States of America

WHO:

World Health Organisation

References

  1. Abrams DI. Integrating cannabis into clinical cancer care. Curr Oncol. 2016;23:S8–14.

  2. Abrams DI. The therapeutic effects of Cannabis and cannabinoids: an update from the National Academies of Sciences, Engineering and Medicine report. Eur J Intern Med. 2018;49:7–11.

  3. Abrams DI, Couey P, Shade SB, Kelly ME, Benowitz NL. Cannabinoid–opioid interaction in chronic pain. Clin. Pharmacol Ther. 2011;90:844–51.

  4. Aguilar BS, Gutiérrez V, Sánchez L, Nougier M. Medicinal cannabis policies and practices around the world. International Drug Policy Consortium. 2018. http://fileserver.idpc.net/library/Medicinal%20cannabis%20briefing_ENG_FINAL.PDF. .

  5. Anaesthesia Patient Safety Foundation. Using the 2018 guidelines from the Joint Commission to kickstart your hospitals program to reduce opioid induced ventilatory impairment. 2018. https://www.apsf.org/article/using-the-2018-guidelines-from-the-joint-commission-to-kickstart-your-hospitals-program-to-reduce-opioid-induced-ventilatory-impairment/ Accessed 8 Sept 2019.

  6. Anderson GD, Chan L. Pharmacokinetic drug interactions with tobacco, cannabinoids and smoking cessation products. Clin Pharmacokinet. 2016;55:1353–68.

  7. Aragona M, Onesti E, Tomassini V, et al. Psychopathological and cognitive effects of therapeutic cannabinoids in multiple clerosis: A double-blind, placebo controlled, crossover study. Clin Neuropharmacol. 2009;32:41–7.

  8. Argentinian government. Enrollment in the National Register of Patients in Cannabis Treatment. Government of Argentina. 2018. https://www.argentina.gob.ar/inscribirse-en-el-registro-nacional-de-pacientes-en-tratamiento-con-cannabis-recann. Accessed 24 Nov 2018.

  9. Ashton CH. Adverse effects of cannabis and cannabinoids. Br J Anaesth. 1999;83:637–49.

  10. Atwal N, Casey SL, Mitchell VA, Vaughan CW. Neuropharmacology THC and gabapentin interactions in a mouse neuropathic pain model. Neuropharmacology. 2017;144:115–21.

  11. Australia and New Zealand College of Anaesthetists Faculty of Pain Medicine. Position statement on the use of slow release opioid preparations in the treatment of acute pain. 2018. http://www.anzca.edu.au/resources/endorsed-guidelines/position-statement-on-the-use-of-slow-release-opio Accessed 10 Sept 2019

  12. Australia and New Zealand College of Anaesthetists Faculty of Pain Medicine. Statement on principles for identifying and preventing opioid induced ventilatory impairment (OIVI). http://www.anzca.edu.au/resources/endorsed-guidelines/oivi-statement Accessed 12 Sept 2019.

  13. Australian Government Department of Health. Therapeutic Goods Administration. Access to medicinal cannabis products. Austalian Government. 2018. http://www.tga.gov.au/access-medicinal-cannabis-products-1. Accessed 4 Sept 2019

  14. Aviram J, Samuelly-Leichtag G. Efficacy of Cannabis-based medicines for pain management: a systematic review and meta-analysis of randomized controlled trials. Pain Physician. 2017;20:E755–96.

  15. Bakas T, Van Nieuwenhuijzen PS, Devenish SO, Mcgregor IS, Arnold JC, Chebib M. The direct actions of cannabidiol and 2-arachidonoyl glycerol at GABA A receptors. Pharmacol. Res. 2017;119:358–70.

  16. Barnes MP. The case for medical cannabis—an essay. BMJ. 2018;362:k3230.

  17. Beaulieu P. Effects of nabilone, a synthetic cannabinoid, on postoperative pain. Can J Anesth. 2006;53(8):769–75.

  18. Beaulieu P, Boulanger A, Desroches J, Clark AJ. Medical cannabis: considerations for the anesthesiologist and pain physician. Can J Anaesth. 2016;63:608–24.

  19. Bie B, Wu J, Foss JF, Naguib M. An overview of the cannabinoid type 2 receptor system and its therapeutic potential. Curr Opin Anesthesiol. 2018;31:407–14.

  20. Bilkei-Gorzo A, Albayram O, Ativie F, Chasan S, Zimmer T. Cannabinoid 1 receptor signaling on GABAergic neurons influences astrocytes in the ageing brain. PLoS One. 2018;13(8):1–21.

  21. Brand PA, Paris A, Bein B, et al. Propofol sedation is reduced by δ9-tetrahydrocannabinol in mice. Anesth Analg. 2008;107:102–6.

  22. Brazilian Government. Anvisa sets rules for sale of cannabidiol based medicine. Government of Brazil. 2016. http://www.brasil.gov.br/noticias/saude/2016/11/anvisa-define-regras-para-venda-de-medicamentos-a-base-de-canabidiol. .

  23. Bridgeman MB, Abazia DT. Medicinal cannabis: history, pharmacology, and implications for the acute care setting. Pharm. Ther. 2017;42:180–8.

  24. Broich K. Annual Report 2017/18. Federal Institute for Drugs and Medical Devices. 2018. https://www.bfarm.de/SharedDocs/Downloads/EN/BfArM/Publikationen/AnnualReport2017-18.pdf?__blob=publicationFile&v=4.

  25. Bryson EO, Frost EAM. The perioperative implications of tobacco, marijuana, and other inhaled toxins. Int Anesthesiol Clin. 2011;49:103–18.

  26. Buggy DJ, Toogood L, Maric S, Sharpe P, Lambert DG, Rowbotham DJ. Lack of analgesic efficacy of oral δ-9-tetrahydrocannabinol in postoperative pain. Pain. 2003;106:169–72.

  27. Campbell G, Hall WD, Peacock A, et al. Effect of cannabis use in people with chronic non-cancer pain prescribed opioids: findings from a 4-year prospective cohort study. Lancet Public Health. 2018;3:e341–50.

  28. Chesher GB, JAckson DM, Starmer GA. Interaction of cannabis and general anaesthetic agents in mice. Br J Pharmacol. 1974;50:593–9.

  29. Cohen K, Abraham W, Aviv W. Modulatory effects of cannabinoids on brain neurotransmission. Eur J Neurosci. 2019. https://doi.org/10.1111/ejn.14407.

  30. Constitutional Court of South Africa. Minister of Justice and Constitutional Development and others v Prince CCT108/17. Constitutional Court of South Africa. 2017. https://www.concourt.org.za/index.php/judgement/260-minister-of-justice-and-constitutional-development-and-others-v-prince-cct108-17. Accessed 4 Sept 2019

  31. Dame Sally Davies. The therapeutic and medicinal benefits of Cannabis based products-a review of recent evidence. London: Cannabis Scheduling Review Part 1; 2018.

  32. David JM. Medical Marijuana the evidence, clinical practice and its consequences. AAFP national conference. 2017. https://www.aafp.org/dam/AAFP/documents/events/nc/handouts/nc17-med-marijuana.pdf. Accessed 24 Sep 2018.

  33. Department of Agriculture, Forestry and Fisheries. Agriculture, Forestry and Fisheries on Constitutional Court ruling on decriminalisation of cultivation and use of cannabis in SA. . South African Government. 2018. https://www.gov.za/speeches/agriculture-forestry-and-fisheries-constitutional-court-ruling-decriminalisation. Accessed 4 Sept 2019

  34. Department of Health and Social Care. Medical cannabis: information and resources. UK government. 2018. https://www.gov.uk/government/collections/medicinal-cannabis-information-and-resources Accessed 28 August 2019.

  35. Department of Health Ireland. Clinical Guidance on Cannabis for Medical Use. Department of Health Ireland. 2018. https://health.gov.ie/wp-content/uploads/2018/07/Clinical-guidance-on-cannabis-for-medical-use.pdf. Accessed 24 Nov 2018

  36. Devinsky O, Croos H, Laux L, et al. Trial of cannabidiol for drug-resistant seizures in the Dravet syndrome. N Engl J Med. 2017;376:2011–20.

  37. Devinsky O, Patel AD, Cross JH, et al. Effect of cannabidiol on drop seizures in the Lennox–Gastaut syndrome. N Engl J Med. 2018;378:1888–97.

  38. Dickerson SJ. Cannabis and its effect on anesthesia. J Am Assoc Nurse Anesth. 1980;48:526–8.

  39. Expert Committee on Drug Dependence. Cannabidiol (CBD) critical review report. Geneva: World Health Organization; 2018.

  40. Ferreira RCM, Castor MGM, Piscitelli F, Di Marzo V, IDuarte IDG, Romero TRL. The involvement of the endocannabinoid system in the peripheral antinociceptive action of ketamine. J. Pain. 2018;19:487–95.

  41. Fitzcharles MA, Eisenberg E. Medical cannabis: a forward vision for the clinician. Eur J Pain. 2018;22:485–91.

  42. Flisberg P, Paech MJ, Shah T, Ledowski T, Kurowski I, Parsons R. Induction dose of propofol in patients using cannabis. Eur J Anaesthesiol. 2009;26:192–5.

  43. Ghebreyesus TA. Forty first meeting of the expert committee on drug dependence; Director General Letter. Switzerland: World Health Organisation; 2019. https://www.who.int/medicines/access/controlled-substances/UNSG_letter_ECDD41_recommendations_cannabis_24Jan19.pdf?ua=1. Accessed 27 Feb 2019

  44. Gloss D, Vickrey B. Cannabinoids for epilepsy (Review). Cochrane Database Syst Rev 2014; 3: Art. No.: CD009270.

  45. Government of Argentina. What will cannabis regulation be like in Argentina? 2019. https://www.argentina.gob.ar/noticias/como-sera-la-regulacion-de-cannabis-en-argentina Accessed 5th September 2019.

  46. Government of Canada. Mandate letter tracker: delivering results for Canadians. Government of Canada. 2018a. https://www.canada.ca/en/privy-council/campaigns/mandate-tracker-results-canadians.html?utm_campaign=not-applicable&utm_medium=vanity-url&utm_source=canada-ca_results. Accessed 21 Nov 2018.

  47. Government of Canada. About Cannabis. Government of Canada. 2018b. https://www.canada.ca/en/health-canada/services/drugs-medication/cannabis/about.html Accessed 4 Sept 2019.

  48. Government of Mexico. COFEPRIS attends within the framework of its legal attributions, the applications for medicinal, personal and playful use of cannabis. Government of Mexico. 2018a. https://www.gob.mx/cofepris/articulos/cofepris-atiende-en-el-marco-de-sus-atribuciones-legales-las-solicitudes-para-uso-medicinal-personal-y-ludico-de-la-cannabis-173520?idiom=es. Accessed 4 Sept 2019

  49. Government of Mexico. They release 38 products with cannabis and its derivatives. Government of Mexico. 2018b. https://www.gob.mx/cofepris/articulos/liberan-38-productos-con-cannabis-y-sus-derivados-182739?idiom=es. Accessed 4 Sept 2019.

  50. Government of Mexico. COFEPRIS attends within the framework of its legal attributions, the request for medicinal, personal and recreational use of cannabis. 2018c. https://www.gob.mx/cofepris/es/articulos/cofepris-atiende-en-el-marco-de-sus-atribuciones-legales-las-solicitudes-para-uso-medicinal-personal-y-ludico-de-la-cannabis-173520?idiom=es. Accessed 5 Sept 2019

  51. Government of the Netherlands. Controlled cannabis supply chain experiment. 2019. https://www.government.nl/topics/drugs/controlled-cannabis-supply-chain-experiment Accessed 7th September2019

  52. Guillaud J, Legagneux F, Paulet C, Leoni J, Lassner J. Mortality in Anaesthesia. European Acaemy of Aaesthesiology vol 3 Springer Berlin, Heidelberg. Comparison of Levonantradol 1 or 2mg IM with Pethdiine and Placebo for postoperative analgesia. 1983 .

  53. Hallak JEC, Dursun SM, Bosi DC, et al. The interplay of cannabinoid and NMDA glutamate receptor systems in humans : preliminary evidence of interactive effects of cannabidiol and ketamine in healthy human subjects. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2011;35(1):198–202.

  54. Hauser W, Finn DP, Kalso E, et al. European Pain Federation (EFIC) position paper on appropriate use of cannabis-based medicines and medical cannabis for chronic pain management. Eur J Pain. 2018a;22:1547–64.

  55. Hauser W, Finnerup NB, Moore RA. Systematic reviews with meta-analysis on cannabis-based medicines for chronic pain: a methodological and political minefield. Pain. 2018c;159:1906–7.

  56. Hauser W, Petzke F, Fitzcharles MA. Efficacy, tolerability and safety of cannabis-based medicines for chronic pain management—an overview of systematic reviews. Eur J Pain. 2018b;22:455–70.

  57. Health Canada. Health products containing cannabis or for use with cannabis: guidance for the Cannabis Act, the Food and Drugs Act, and related regulations. Government of Canada 2018. https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/guidance-cannabis-act-food-and-drugs-act-related-regulations/document.html.

  58. Health Products Regualtory Authority. Cannabis for Medical Use-A Scientific Review. Health Products Regulatory Authority. 2017. https://www.hpra.ie/docs/default-source/publications-forms/newsletters/cannabis-for-medical-use%2D%2D-a-scientific-review.pdf?sfvrsn=7. .

  59. Heuberger J, Guan Z, Oyetayo OO, et al. Population pharmacokinetic model of THC integrates oral, intravenous, and pulmonary dosing and characterizes short- and long-term pharmacokinetics. Clin Pharmacokinet. 2015;54:209–19.

  60. Holdcroft A, Maze M, Dore C, Tebbs S, Thompson S. A multicenter dose-escalation study of the analgesic and adverse effects of an oral cannabis extract (Cannador) for postoperative pain management. Anesthesiology. 2006;104(5):1040–6.

  61. Hosking RD, Zajicek JP. Therapeutic potential of cannabis in pain medicine. Br J Anaesth. 2008;101:59–68.

  62. Ibera C, Shalom B, Saifi F, Shruder J, Davidson E. Effects of cannabis extract premedication on anesthetic depth. Harefuah. 2018;157:162–6.

  63. Indian Council of Medical Research, Department of Health Research-Ministry Health and Family Welfare Government of India. Media report November 2018. 2018. https://www.icmr.nic.in/sites/default/files/ICMR_News.pdf Accessed 12th September 2019

  64. International Drug Policy Consortium. The United Nations General Assembly Special Session (UNGASS) on the World Drug Problem. London: Report of Proceedings; 2016.

  65. Jain A, Ryan J, McMahon G, Smith G. Evaluation of intramuscular levonantradol and placebo in acutepostoperative. J Clin Pharmacol. 1981;21:320–6.

  66. Jefferson D, Harding H, Cawich S, Jackson-Gibson A. Postoperative analgesia in the Jamaican cannabis user. J Psychoactive Drugs. 2013;45:227–32.

  67. Kalliomäki J, Segerdahl M, Webster L, et al. Evaluation of the analgesic efficacy of AZD1940, a novel cannabinoid agonist, on post-operative pain after lower third molar surgical removal. Scand. J. Pain. 2013;4:17–22.

  68. Karschner EL, David Darwin W, Goodwin RS, Wright S, Huestis MA. Plasma cannabinoid pharmacokinetics following controlled oral Δ 9-tetrahydrocannabinol and oromucosal cannabis extract administration. Clin Chem. 2011;57:66–75.

  69. Kleine-Brueggeney M, Greif R, Brenneisen R, Urwyler N, Stueber F, Theiler LG. Intravenous Delta-9-tetrahydrocannabinol to prevent postoperative nausea and vomiting: A randomized controlled trial. Anesth Analg. 2015;121:1157–64.

  70. Koppel BS, Brust JCM, Fife T, et al. Systematic review: efficacy and safety of medical marijuana in selected neurologic disorders: report of the Guideline Development Subcommittee of the American Academy of Neurology. Neurology 2014;82:1556–1563

  71. Krcevski-Skvarc N, Wells C, Hauser W. Availability and approval of cannabis-based medicines for chronic pain management and palliative / supportive care in Europe : A survey of the status in the chapters of the European Pain Federation. Eur J Pain. 2018;22:440–54.

  72. Kumar RN, Chambers WA, Pertwee RG. Pharmacological actions and therapeutic uses of cannabis and cannabinoids. Anaesthesia. 2001;56:1059–68.

  73. Kumar SSH, Dass LL, Sharma AK. Cannabis Indica (Bhang) extract as preanaesthetic to propofol anaesthesia in dogs. Journal of Applied Animal Research. 2010;37:125–7.

  74. Laaris N, Good CH, Lupica CR. Δ9 -tetrahydrocannabinol is a full agonist at CB1 receptors on GABA neuron axon terminals in the hippocampus. Neuropharmacology. 2011;59(443):121–7.

  75. Layden JE, Ghinai I, Pray I et al. Pulmonary illness related to e-cigarette use in Illinois and Wisconsin—preliminary report. N Engl J Med 2019. https://doi.org/10.1056/NEJMoa1911614. [Epub ahead of print]

  76. Layeeque R, Siegel E, Kass R, et al. Prevention of nausea and vomiting following breast surgery. Am J Surg. 2006;191:767–72.

  77. Levin DN, Dulberg Z, Chan AW, Hare GM, Mazer D, Hong A. A randomized-controlled trial of nabilone for the prevention of acute postoperative nausea and vomiting in elective surgery. Can J Anesth. 2017;64:385–95.

  78. Lewis IH, Campbell DN, Barrowcliffe MP. Effect of nabilone on nausea and vomiting after total abdominal hysterectomy. Br J Anaesth. 1994;73:244–6.

  79. Lile J, Wesley M, Kelly T, Hays R. Separate and combined effects of gabapentin and 9THC in humans discriminating 9THC. Behav Pharmacol. 2016;27:215–24.

  80. Liu C, Bhatia A, Buzon-Tan A, et al. Weeding out the problem: the impact of preoperative cannabinoid use on pain in the perioperative period. Anesth Analg. 2018. https://doi.org/10.1213/ANE.0000000000003963.

  81. Lotsch J, Weyer-Menkhoff I, Tegeder I. Current evidence of cannabinoid-based analgesia obtained in preclinical and human experimental settings. Eur. J. Pain. 2018;22:471–84.

  82. Lucas CJ, Galettis P, Schneider J. The pharmacokinetics and the pharmacodynamics of cannabinoids. Br J Clin Pharm. 2018;84:2477–82.

  83. Maguire DR, France CP. Antinociceptive effects of mixtures of mu opioid receptor agonists and cannabinoid receptor agonists in rats : Impact of drug and fixed-dose ratio. Eur J Pharmacol. 2018;819:217–24.

  84. Manzanares J, Corchero J, Romero J, Fernández-Ruiz JJ, Ramos J, Fuentes JA. Pharmacological and biochemical interactions between opioids and cannabinoids. Trends Pharmacol Sci. 1999;20:287–94.

  85. Mead A. The legal status of cannabis (marijuana) and cannabidiol (CBD) under U.S. law. Epilepsy Behav. 2017;70:288–91.

  86. Medicines Control Council. Medicines Control Council clarifies access to Cannabis for the treatment of medical conditions. Medicines Control Council. 2016. https://www.sahpra.org.za/documents/5933cac110.14_Media_Release_Cannabis_Nov16_v1.pdf Accessed 4 Sept 2019

  87. Meiri E, Jhangiani H, Vredenburgh JJ, et al. Efficacy of dronabinol alone and in combination with ondansetron versus ondansetron alone for delayed chemotherapy-induced nausea and vomiting. Curr Med Res Opin. 2007;23:533–43.

  88. Meng H, Johnston B, Englesakis M, Moulin D, Bhatia A. Selective cannabinoids for chronic neuropathic pain : a systematic review and meta-analysis. Anesth Analg. 2017;125(5):1638–52.

  89. Mucke M, Phillips T, Radbruch L, Petzke F, Hauser W. Cannabis-based medicines for chronic neuropathic pain in adults (review). Cochrane Database Syst. Rev. 2018;3:CD012182.

  90. National Academies of Sciences Engineering and Medicine. The health effects of cannabis and cannabinoids: the current state of evidence nad recommendations for research. Washington, DC: The National Academies Press; 2017.

  91. National Agency for the Safety of Medicines and Health Products. Decree No. 2013-473 of June 5, 2013 modifying as regards pharmaceutical specialties the provisions of Article R. 5132-86 of the Public Health Code relating to the prohibition of transactions relating to cannabis or its derivatives. Government of France. https://www.legifrance.gouv.fr/affichTexte.do?cidTexte=JORFTEXT000027513604&categorieLien=id. Accessed 24 Nov 2018

  92. National Health Service. Cannabis-based products for medicinal use: Frequently Asked Questions. 2018 https://www.england.nhs.uk/medicines/support-for-prescribers/cannabis-based-products-for-medicinal-use/cannabis-based-products-for-medicinal-use-frequently-asked-questions/#what-are-synthetic-cannabinoids-and-are-they-included-in-the-re-scheduling Accessed 10 Sept 2019

  93. National Institute for Health and Care Excellence. New guidance to tackle inequalities in multiple sclerosis care. National Institute for Health and Care Excellence. 2014. https://www.nice.org.uk/news/article/new-guidance-to-tackle-inequalities-in-multiple-sclerosis-care. Accessed 24 Nov 2018.

  94. National Institute for Health and Care Excellence. NICE draft gudiance and NHS England review highlight need for more research on cannabis-based medicinal products. 2019. https://www.nice.org.uk/news/article/nice-draft-guidance-and-nhs-england-review-highlight-need-for-more-research-on-cannabis-based-medicinal-products Accessed 25 Sept 2019.

  95. New Zealand Ministry of Health. Prescribing cannabis-based products. New Zealand Government: 2018. https://www.health.govt.nz/our-work/regulation-health-and-disability-system/medicines-control/medicinal-cannabis/prescribing-cannabis-based-products. Accessed 4 Sept 2019

  96. New Zealand Parliament. Changes to New Zealand’s drug laws proposed by medicinal cannabis bill. New Zealand Government. 2018. https://www.parliament.nz/en/get-involved/topics/all-current-topics/changes-to-new-zealand-s-drug-laws-proposed-by-medicinal-cannabis-bill. Accessed 4 Sept 2019

  97. Nielsen S, Germanos R, Weier M, et al. The use of cannabis and cannabinoids in treating symptoms of multiple sclerosis: a systematic review of reviews. Curr Neurol Neurosci Rep. 2018;18:8.

  98. Nugent SM, Morasco BJ, O’Neil ME, et al. The effects of cannabis among adults with chronic pain and an overview of general harms a systematic review. Ann Intern Med. 2017;167:319–31.

  99. Office of Medicinal Cannabis. Medicinal Cannabis. Netherlands Ministry of Health. 2018. https://english.cannabisbureau.nl/ Accessed 4 Sept 2019

  100. Office of Medicinal Cannabis Government of the Netherlands. Patients guide medicinal cannabis. 2019. https://english.cannabisbureau.nl/documents/circulars/2018/02/20/patientsguide-medicinal-cannabis Accessed 13 Sept 2019

  101. Ostenfeld T, Price J, Albanese M, et al. A randomized, controlled study to investigate the analgesic efficacy of single doses of the molar tooth extraction. J. Clin. Pain. 2011;27(8):668–76.

  102. Pacheco F, Roberto T, Romero L, Dimitri I, Duarte G. Ketamine induces central antinociception mediated by endogenous cannabinoids and activation of CB 1 receptors. Neurosci. Lett. 2019;699:140–4.

  103. Pertwee R. Handbook of Cannabis. Oxford Scholarship online. 2015. http://www.oxfordscholarship.com/view/10.1093/acprof:oso/9780199662685.001.0001/acprof-9780199662685. Subscription required. Accessed 28 Jan 2019

  104. Pertwee RG, Howlett AC, Abood ME, et al. International union of basic and clinical pharmacology . LXXIX . Cannabinoid receptors and their ligands: beyond CB 1 and CB 2. Pharmacol Rev. 2010;62:588–631.

  105. Republic of Phillipines House of Representatives. An act providing compassionate and right of access to medical cannabis and expanding research into its medicinal properties. Government of Phillipines. 2018. Congress.gov.ph/legisdocs/first_17/CR00402.pdf Accessed 15 Sept 2019

  106. Reynolds JR. Therapeutical uses and toxic effects of cannabis indica. Lancet. 1890;135:637–8.

  107. Rice J, Cameron M. Cannabinoids for treatment of MS symptoms: state of the evidence. Curr Neurol Neurosci Rep. 2017;18:1–10.

  108. Richtig G, Bosse G, Arlt F, Heymann CV. Cannabis consumption before surgery may be associated with increased tolerance of anesthetic drugs: A case report. Int J Case Rep. 2015;6:436–8.

  109. Rodríguez-Muñoz M, Sánchez-Blázquez P, Merlos M, Garzon-Nino J. Endocannabinoid control of glutamate NMDA receptors : the therapeutic potential and consequences of dysfunction. Oncotarget. 2016;34:55840–62.

  110. Rong C, Carmona NE, Lee YL, et al. Drug-drug interactions as a result of co-administering ∆ 9-THC and CBD with other psychotropic agents. Expert Opin Drug Saf. 2017;17:51–4.

  111. Sánchez-Blázquez P, Rodríguez-Muñoz M, Garzón J. The cannabinoid receptor 1 associates with NMDA receptors to produce glutamatergic hypofunction : implications in psychosis and schizophrenia. Front. Pharmacol. 2014;4:1–10.

  112. Scavone J, Sterling R, Van Bockstaele E. Cannabinoid and opioid interactions: implications for opiate dependence and withdrawal. Neuroscience. 2013;248:637–54.

  113. Schelling G, Hauer D, Azad SC, et al. Effects of general anesthesia on anandamide blood levels in humans. Anesthesiology. 2006;104(2):273–7.

  114. Schuster J, Ates M, Brune K, Gühring H. The cannabinoids R(−)-7-hydroxy-delta-6-tetra-hydrocannabinol-dimethylheptyl (HU-210), 2-O-arachidonoylglycerylether (HU-310) and arachidonyl-2-chloroethylamide (ACEA) increase isoflurane provoked sleep duration by activation of cannabinoids 1 (CB1)-recep. Neuroscience Letters. 2002;326:196–200.

  115. Seeling W, Kneer L, Buchele B, et al. Delta(9)-tetrahydrocannabinol and the opioid receptor agonist piritramide do not act synergistically in postoperative pain. Der Anästhesist. 2006;55:391–400.

  116. Smith L, Azariah F, Lavender V, Stoner N, Bettiol S. Cannabinoids for nausea and vomiting in adults with cancer receiving chemotherapy (Review). Cochrane Database Syst Rev. 2015; 11: Art. No. CD009464

  117. Stevens AJ, Higgins MD. A systematic review of the analgesic efficacy of cannabinoid medications in the management of acute pain. Acta Anaesth Scand. 2017;61:268–80.

  118. Stockings E, Campbell G, Hall WD, et al. Cannabis and cannabinoids for the treatment of people with chronic non-cancer pain conditions. Pain. 2018a;159:1932–54.

  119. Stockings E, Zagic D, Campbell G, Weier M, Hall WD, Nielsen S, Herkes GK, et al. Evidence for cannabis and cannabinoids for epilepsy: a systematic review of controlled and observational evidence. J Neurol Neurosurg Psychiatr. 2018b;89:741–53.

  120. Stoelting R, Martz R, Gartner J, Creasser C, Brown D, Forney R. Effects of delta-9-tetrahydrocannibinol on Halothane MAC in dogs. Anesthesiology. 1973;35:521–4.

  121. Symons I. Cannabis smoking and anaesthesia. Anaesthesia. 2002;57:1142.

  122. Tham SM, Angus JA, Tudor EM, Wright CE. Synergistic and additive interactions of the cannabinoid agonist CP55,940 with μ opioid receptor and α 2-adrenoceptor agonists in acute pain models in mice. Br. J. Pharmacol. 2005;144(6):875–84.

  123. Therapeutic Goods Administration. Guidance for the use of medicinal cannabis in Australia Overview. Woden ACT: Australian Government Department of Health; 2017. Version 1

  124. Thiele EA, Marsh ED, French JA, et al. Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial. The Lancet. 2018;391:1085–96.

  125. Transnational Institute, Global Drug Policy Observatory. UNGASS 2016: a broken or broad consensus? UN summit cannot hide growing divergence in the global drug policy landscape. Amsterdam: United Nations; 2016.

  126. Turcotte D, Doupe M, Torabi M, et al. Nabilone as an adjunctive to gabapentin for multiple sclerosis-induced neuropathic pain : a randomized controlled trial. Pain Med. 2015;16:149–59.

  127. Ujváry I, Hanuš L. Human metabolites of cannabidiol: a review on their formation, biological activity, and relevance in therapy. Cannabis Cannabinoid Res. 2016;1(1):90–101.

  128. United Nations Office on Drugs and Crime. Global overview of drug demand and supply. Latest trends, cost-cutting issues. United Nations; 2018. https://www.unodc.org/wdr2018/. Accessed 24 Jan 2019.

  129. United Nations Office on Drugs and Crime. World drug report 2019 Cannabis and Hallucinogens. 2019. https://wdr.unodc.org/wdr2019/prelaunch/WDR19_Booklet_5_CANNABIS_HALLUCINOGENS.pdf. Accessed 15 Sept 2019

  130. Uruguay Government. Ministry of Public Health authorized the sale of medicinal cannabis to a company that met the requirements. Government of Uruguay. 2018. https://www.presidencia.gub.uy/comunicacion/comunicacionnoticias/salud-cannabis-medicinal-venta-empresa-requisitos-basso-msp-ircca. Accessed 4 Sept 2019.

  131. US Food and Drug Administration. FDA and marijuana. In: US Food and Drug Administration; 2016. https://www.fda.gov/NewsEvents/PublicHealthFocus/ucm421163.htm. Accessed 15 Nov 2018.

  132. US Food and Drug Administration. Press announcements—FDA approves first drug comprised of an active ingredient derived from marijuana to treat rare, severe forms of epilepsy. US Food and Drug Administration. 2018 https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm611046.htm Accessed 24 Jan 2019.

  133. US Food and Drug Administration. Vaping Illnesses: consumers can help protect themselves by avoiding Tetrahydrocannabinol (THC) containing vaping products. 2019. https://www.fda.gov/consumers/consumer-updates/vaping-illnesses-consumers-can-help-protect-themselves-avoiding-tetrahydrocannabinol-thc-containing Accessed 9 Sept 2019.

  134. Vandrey R, Herrmann ES, Mitchell JM, et al. Pharmacokinetic profile of oral cannabis in humans: blood and oral fluid disposition and relation to pharmacodynamic outcomes. J Anal Toxicol. 2017;41:83–99.

  135. Ware MA, Wang T, Shapiro S, Collet J. Cannabis for the management of pain: assessment of safety study(COMPASS). J. Pain. 2015;16:1233–42.

  136. Whiting PF, Wolff RF, Deshpande S, et al. Cannabinoids for medical use: a systematic review and meta-analysis. JAMA. 2015;313:2456–73.

  137. WHO Expert Committee on Drug Dependence. Critical review: Delta-9-tetrahydrocannabinol. World Health Organisation. 2018. https://www.who.int/medicines/access/controlled-substances/THCv1.pdf?ua=1. Accessed 24 Nov 2018.

  138. Yeon Kong T, Kim JH, Kyun Kim D, Suk LH. Synthetic cannabinoids are substrates and inhibitors of multiple drug-metabolizing enzymes. Arch Pharm Res. 2018;41:691–710.

  139. Zendulka O, Dovrtělová G, Nosková K, et al. Cannabinoids and cytochrome P450 interactions. Curr Drug Metab. 2016;17:206–26.

  140. Zlas J, Stark H, Seligman J. Early medical use of cannabis. Nature. 1993;363:215.

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SK conceived the idea for the manuscript, both authors acquired, analysed and interpreted the data. Both authors wrote and approved the manuscript.

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PT is a Clinical Fellow in Anaesthesia at Sunnybrook Health Sciences Centre. SK is a Consultant Anaesthetist at University Hospital Southampton.

Correspondence to Patrick Tapley.

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Tapley, P., Kellett, S. Cannabis-based medicines and the perioperative physician. Perioper Med 8, 19 (2019). https://doi.org/10.1186/s13741-019-0127-x

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Keywords

  • Pharmacology
  • Cannabis
  • Cannabinoids
  • Medical marijuana