Overall, the findings suggest medical publications in Australia construct medicinal cannabis as a legitimate medicine whose regulation is being driven by the community. Cannabis is complex to prescribe and access, does not have a strong evidence base to support its use, and also carries safety concerns. At the same time, the outlook on cannabis research data is largely positive. Findings for primary sources indicate a prioritisation of peer-reviewed journals or government reports, voices from medical associations or foundations, as well as government and university researchers. In the following section we discuss the most prominent frames and sources, those that were less prominent, and intonation.
Article intonation
Cannabis is frequently framed in positive terms in medical publications in Australia (Fig. 3). These articles framed cannabis as a legitimate medicine that should be legalised and that carried promising research findings. Positive articles also framed the community push for medicinal cannabis as well as the complexities of doctor prescribing and patient access. It is worth noting that negative articles did not appear until 2015, the year before medicinal cannabis was legalised in Australia. The heightened period of negatively toned articles occurred across the period when access was being streamlined across most of the country, with the introduction of the special access scheme and authorised prescriber access. Intonation is further considered in the following sections exploring the framing results.
Cannabis as legitimate (n = 28)
The articles positively characterise cannabis as a legitimate therapeutic option in the Australian healthcare landscape. In contrast, only two articles during the whole period framed cannabis as an illegitimate substance or approach to therapeutic care. Reports with legitimacy framings start in 2000 with a Medical Journal of Australia ‘Viewpoint’ article about cannabinoids and the endocannabinoid system, which had been discovered 8 years earlier. Legitimacy framings occur in at least three articles a year between 2013 and 2018 and are most predominant in 2014 and 2019 with a total of five articles in those years. These framings occurred most consistently in Australian Doctor (n = 17), Medical Journal of Australia (n = 5), Medical Observer (n = 3), and Australian Medicine (n = 3). The items were predominantly news stories (n = 20), followed by editorials (n = 3), original research or reviews (n = 2), one book review in the MJA, and one 2018 case study in Australian Doctor by the country’s first registered cannabis prescribing physician, Dr Vicki Kotsirilos. Reports framing cannabis as a legitimate therapeutic option were predominantly positive in tone (n = 21), with fewer (n = 6) carrying a mixed tone, and one neutral article.
Professionally speaking, legitimation has been a historically significant process for doctors in Australia and is integral to their social capital reinforcing their elite professional status (Willis 1989). Indeed, this is not just relevant to their professional dominance, but necessarily relates also to the medical objects that doctors integrate into their medical repertoire. As discussed earlier, professional medical publications assist to reinforce the legitimacy of the doctor at the helm of primary healthcare practice in Australia. If doctors are permitted via the legal system to prescribe medicinal cannabis to those patients with specified conditions, then it makes sense that doctors’ publications contribute to legitimising discourse about cannabis through news reports, where it can become integrated into the doctors’ repertoire of medicines and medical objects. The frequency of legitimisation framings in these doctors’ publications is consistent with the findings from the Karanges et al. (2018) study, which found that many GPs regarded cannabis as a legitimate medicine and supported its availability as a prescribed medicine for certain conditions—a medicine that carried potential therapeutic benefit for patients.
The following excerpts offer a glimpse into the legitimisation framings, drawing on notions of scientific evidence and safety, carrying a strong rhetoric of pathos:
A civilised and compassionate country that supports evidence-based medicine and policy should acknowledge that medicinal cannabis is acceptably effective and safe, and probably also cost-effective, especially when the costs of resource use and improvement to the lives and functionality of patients and carers are considered. (MJA, 16 December 2013)
Victorian Health Minister Jill Hennessy said children with severe epilepsy would be the first group to have access to the drug, beginning next year. “We’re starting with these children with severe epilepsy, whose lives have been shown to improve so significantly, because we know these children often don’t make it [into] adulthood,” Ms Hennessy told the ABC. “We want to improve their quality of life.” (AM, 19 April 2016)
This next quotation, from Australian Doctor (2019), invokes the history of penicillin as a ‘natural medicine’ that was accepted by the medical profession as a legitimate medicine some 70 years earlier:
“About 70 years ago another natural medicine came into the medical arena,” writes Professor Nutt, of the Imperial College in London. “This was welcomed enthusiastically by UK doctors, even though there had been no placebo-controlled trials of its efficacy because it was seen to fulfil a major clinical need. “That drug was penicillin. If today’s medical profession could embrace cannabis in the same way as it did penicillin, then the true value of this plant medicine should rapidly be realised.” (Australian Doctor Pharmacy News 7 May 2019).
Legitimacy stories were most commonly associated with framings about the complexity of prescribing, concern about safety issues, the need for legalisation, alternative access issues, positive research findings, and the framing that cannabis is relatively safe. The validity of cannabis as a medicine is also reinforced by the high rate of references to specific conditions: in particular, chronic pain, epilepsy, cancer, and nausea and chemotherapy.
It is rather novel to see a medicine like cannabis be embraced into the mainstream healthcare system in publications that are typically more circumspect towards botanical medicines. This finding contrasts with an earlier study by Lewis (2011a, 2011b) on risk factors in herbal medicine, where a high proportion of doctors found there to be a substantially high rate of reference to risks of plant medicines. Articles typically refer to medicinal cannabis in the context of cannabinoids (notably CBD and THC) as the active constituents, rather than the entourage effect of cannabis sativa as a whole plant (Caldicott et al. 2018). In other words, cannabis is being constructed as a pharmaceutical medicine, rather than a plant medicine. This framing of cannabis as a pharmaceutical is distinct from ‘natural’ or ‘plant’ medicine.
Regulation being driven by community (n = 28)
Unlike many other medicines, cannabis has bypassed more orthodox methods of medicalisation, in terms of how its legalisation has evolved through an unusually bottom-up trend of patients and advocates seeking legitimisation of access to therapeutic use as opposed to a top-down trend where medical experts legitimise the practice (Bone et al. 2018; Fitzcharles and Eisenberg 2018; Bostwick 2012; Martin and Bonomo 2016). Community-driven regulation was a frequent frame across the study period, acknowledging the role of grassroots activism in the legislation process and recognising medicinal cannabis advocacy as part of a social movement. This has been a significant feature of cannabis advocacy around the world, which has seen legalisation of cannabis as an outcome of the work of community-based activists ranging from patients and carers to community dispensaries, occasionally supported by local governments (Penn 2014; Blickman 2014; Frankhauser 2008). This frame did not appear until 2013, a couple of years before new legislation about medical access, reaching its peak in reports in 2017 and 2018, and demonstrating a decline in reports in 2019, once legislation was well established. The tone of these stories is typically positive or mixed:
A group of Queensland mums are seeking to put medical cannabis on the state election agenda, claiming it could “save” their children.
-Hoffman, Tessa ‘Mums lobby for legal cannabis for kids’ Australian Doctor 2015
In the aftermath of this flurry of activity there has been widespread confusion and scepticism among doctors. Many question whether the cart has been put before the horse; whether legislative change has been driven by the passionate campaigns of patients and advocacy groups rather than evidence-based medicine.
-Dunn, Emily ‘Your guide to the clamour for cannabis’ Australian Doctor 2017
Medicinal cannabis certainly has had a very political and community driven introduction in this country.
-AMA Vice President Dr Toney Bartone, ‘Medicinal cannabis – still a lot of misinformation’ Australian Medicine 2017
Like complementary medicine advocates, medicinal cannabis activists have worked to challenge existing policies on cannabis and advocate and even conduct their own research to understand its efficacy, benefits, viability, and social value. This is a strong feature of health social movements (Brown and Zavestoski 2004) and regular reference to the ‘driven by the community’ framing in these articles conveys an awareness—which may not necessarily be manifestly articulated—that medicinal cannabis is a medicine being strongly advocated by citizens such as ‘Queensland mums’ (Hoffman 2015), or ‘patients and advocacy groups’ (Dunn 2017).
Complexity of prescribing and patient access (n = 25)
These articles make salient the point that the process by which medicinal cannabis is prescribed is exceedingly complex for doctors and their patients. For example:
…there are several hurdles to be jumped before the script can be actioned. First, doctors will first need to be approved by the government as registered prescribers of cannabis-based medicine. Then, for each patient’s prescription, they will need to apply for approval to the TGA and NSW Health, providing clinical evidence to support their application. Doctors are also expected to have tried other medical and nonmedical interventions before resorting to a cannabis-based product.…AMA NSW spokesman Clinical Associate Professor Saxon Smith…says that while the rules come into effect on Monday, the implementation process will be lengthy and it could be months before the first script is approved…
-Hoffman, Tessa ‘Green light for unapproved cannabis scripts’ Australian Doctor 2016
For doctors trying to support patients, navigating medicinal cannabis prescribing pathways can be torturous. It is still up to individual practitioners to reconcile the clinical evidence, come to a view about its therapeutic appropriateness and complete the appropriate processes for accessing medicinal cannabis products.
-Gill, Kate and Brell, Ruanne ‘How to navigate the logistical labyrinth that is medicinal cannabis’ Medical Observer 2018
The high rate of references to ‘access’ (n = 190) and derivatives of the word ‘prescribe’ (n = 303) generated by word mapping correlate with the frequency of framings about the complexity of prescribing and patient access. Practitioners can register with the TGA for special prescriber access in order to be able to prescribe for large numbers of patients without seeking TGA approval for each individual patient. Alternatively, for the Special Access Schemes (SAS) A and B,Footnote 3 they make a case to the regulator for each individual patient for whom they wish to prescribe medicinal cannabis. This submission process has two effects. The first is that doctors are resistant to becoming prescribers because of the complexity and difficulty of the process and the labour required in order to either become registered or to make submissions for individual cases. Doctors are forced into a position of making a crude, self-cost-benefit analysis as to the worth of undertaking this process. The second element is that owing to the difficulties of following legitimate prescription routes, a natural consequence of this will be for patients to seek remedies through self-prescription and self-medication. This creates a double regulatory bind. On the one hand, we have the resistance by practitioners because of the complexity; on the other, we have the illegal route taken by self-prescribing patients because of the challenges of trying to obtain prescriptions from a doctor. Even in countries where legalisation of cannabis is total, its therapeutic uses are held back by recognisable obstacles, such as lack of education (St Pierre et al. 2020), stigmatisation (St Pierre et al. 2020; Balneaves et al. 2018), and regulatory hurdles (Abuhasira et al. 2018)
Safety concerns (n = 23)
Concern about safety issues for medicinal cannabis use was a frame in the study with word mapping showing the words ‘risk’ or ‘risks’ occurring 152 times across articles, ‘safety’ or ‘safe’ were used 134 times, and ‘harm’ or ‘harms’ 46 times. It is important to note that the most concentrated periods for stories framing safety concerns about cannabis were in 2019 (n = 7) and 2018 (n = 4), with three items carrying such framings in 2016 and 2017. This indicates that the focus on cannabis risk is a more recent phenomenon articulated across these medical publications, and understandably coincides with the period following legislation, after which increasingly aware patients were requesting legal access to cannabis and doctors were starting to register and prescribe it.
In an article from 2016, ANU physician and researcher, Dr David Caldicott, addresses the anxieties of doctors in this field (Woodhead 2016):
“The message for clinicians is that they shouldn’t be afraid. There are already very well-developed [medical cannabis] markets out there, so we don’t have to reinvent the wheel. It’s very hard to argue that you are going to harm anybody with a regimen that will be very tightly regulated. And clinicians should not be expected to prescribe something with which they are not comfortable or prescribe something prior to them having the opportunity to learn everything they want to know about it.”
This can be contrasted with another 2016 article from Medical Observer quoting an addiction specialist based at the Royal Adelaide Hospital, who articulated a strong level of safety concern for potential harm on brain development in children and young people:
Medicinal cannabis trials in children and teens should not go ahead unless there is evidence they won’t cause long-term harm to the developing brain, an addiction medicine specialist says.
-Worsley, Rachel ‘Addiction expert slams medicinal cannabis for kids’ Medical Observer 2016
Doctors are understandably highly attuned to matters of risk and their awareness of it constantly underpins much of their practice. Accompanied by efficacy and quality, safety is a primary category used to assess the viability of new medicinal substances at the regulatory level as being integral to evidence-based medicine, not to mention a fundamental principle of primary health care. As a new medicine—and a plant-based one at that—it is perhaps surprising that framings about safety concerns were not more prominent across these publications. This finding can be contrasted with a study of MJA articles about herbal medicine across a 42-year period (Lewis 2011a, 2011b), which found that the majority of MJA items in the study referred to herbal medicine risk. It is unclear whether doctors are feeling completely reassured by laboratory and clinical trial research into medicinal cannabis. The dearth of articles addressing traditional usage or acknowledging validity of traditional usage suggests that this may not be a highly valued attribute in doctors’ publications.
Overall, the safety concern framings did not negate the use of medicinal cannabis, and arguably functioned to demonstrate the legitimacy of cannabis as a pharmacological and pharmaceuticalised substance, as reflected here:
“We need to have proper trials and regulate it as a medication just like any other medication…It’s not about trying to deny access to the drug, but we also want to make sure that we don’t do any harm. We want to make sure that people are actually getting the drug for the right reasons, and that it’s actually going to benefit them in the future.”
-Rollins, Adrian ‘Cannabis meds? Follow the evidence, says AMA’ Australian Medicine 2015
This point about pharmaceuticalisation is reinforced by the word mapping, which revealed very substantial distinctions between the comparatively low frequency of the word “plant” (n = 28) and more pharmaceutically-oriented terms, such as “cannabidiol” (n = 154) or “CBD” (n = 142), and “THC” (n = 106) which as discussed earlier refer to particular isolated active constituents (cannabinoids) contained in the whole plant. A purely pharmaceuticalised orientation towards medicinal cannabis discourse is, however, not so straightforward. Across the period, images of the whole plant and raw plant materials were far more common than photographs of the manufactured and bottled product or of clinical research or laboratory images. This could relate to the availability, access, and cost of using particular images for publishers, and undoubtedly the aesthetic appeal of the bright, green cannabis foliage. At the same time, it highlights a tension between cannabis as a pharmaceutical substance or a ‘drug’ and cannabis as a plant.
With the exception of articles in the MJA, cannabis safety concerns were often discussed generally, rather than specifically, expressing the safety concerns about cannabis as an unfamiliar and unknown entity, rather than something proven to be dangerous. When specifics were mentioned it related to long-term usage, dosage, and side-effects. The concern about safety based on lack of familiarity, rather than confirmed risks of cannabis as a medicine, is echoed in research of doctors’ attitudes towards unconventional therapies by Newell and Sanson-Fisher (2000) and Lin et al. (2005) and a more recent study that highlighted concerns from gastroenterologists in Australia (Benson et al. 2020).
A previous study of representations of herbal medicines in the MJA across a 42-year period by Lewis (2011a, 2011b) indicated that the most frequent references to risks about herbal medicines were associated with adverse events and toxicity in particular, as well as a lower frequency of mentions of drug interactions, and dosage. Word text searches within NVivo for this study indicated a higher reference to dosage (n = 23), followed by adverse events (n = 15) and toxicity (n = 9), and drug interactions (n = 4).
Importantly, the framing of concerns about safety did not function to delegitimise the value of cannabis as a medicine. Whilst concerns are articulated about safety in 20% of reports, cannabis appears to be a trusted medical object in these doctors’ publications.
Framings of research evidence (poor evidence n = 24 and positive findings n = 19)
Framings of research evidence in these articles demonstrate a pattern of acceptance of cannabis that is correlated with the level of evidence available for the particular condition it is treating. This is consistent with the findings from Karanges et al. (2018). The framings on positive or promising evidence, as well as the distinct concern about the lack of evidence, are an acknowledgement that evidence to support medicinal cannabis usage is a necessary and desirable outcome. Rare are the framings of negative research findings that suggest cannabis is not safe, efficacious or effective, or an invalid therapeutic option. Given that cannabis is a plant-based product, which in the regulatory context may consist of a standardised extract of CBD or THC, a synthetic version of either of the two, or a whole plant extract, the apparent openness in these publications to the potentialities of cannabis might be contrasted with the response to a product like Hypericum performatum (St John’s Wort), which has a solid evidence base for use in people with mild to moderate depression (Linde et al. 2008). Despite this evidence, St John’s Wort is not supported in primary care medicine in Australia, nor is it a registered medicine. An important question here might be: why is medicinal cannabis regarded as more valid and viable than another plant that has sound evidence of efficacy to support its usage, like St John’s Wort? What makes cannabis so distinct from another plant medicine like St John’s Wort? This is a question for further research but it is not merely a matter of evidence, but also sociocultural and political matters, not to mention economics. The matter of standardisation is also relevant, given the pharmacological complexity of whole plant medicines in comparison to the process of isolating active constituents and creating a standardised extract that has eliminated the wide variabilities of the whole plant. Arguably, the representation of medicinal cannabis as a controllable, ‘pharmaceuticalisable’ product is an important part of the discourse on safety and evidence. Framings that directly addressed standardisation, however, were surprisingly few (n = 5). We shall now look at some of the less common frames.
Less common frames
The scale of the opioid crisis and accompanying news coverage that depicts the risks and harms caused by the over-prescription of opioids and the influence of pharmaceutical companies in promulgating this culture of over-prescription has been huge (Stoicea et al. 2019). When we searched using the term ‘opioid crisis’ across Australian Doctor issues, for example, we found 57 articles. Thus, we had anticipated more articles addressing cannabis as an alternative option for pain relief in these publications. While there were seven such reports, all of which referred positively to the potentialities of cannabis as an alternative to opioids for pain relief, it is unclear why this framing was less common. It may be due to caution given the lack of robust safety and efficacy data about cannabis in treating pain (Stockings et al. 2018; Moore et al. 2021), although the references to cannabis and chronic pain in this study are substantial.Footnote 4 Moore et al. (2021:S76), however, argue that pain specialists should be included more in such research, for example:
It is telling that a U.S. National Academies of Sciences, Engineering and Medicine report on therapeutic effects of cannabis and cannabinoids, and a later update,Footnote 5 concluded that there is “substantial” evidence that cannabis is an effective treatment for chronic pain in adults. The committee included experts in substance abuse, cardiovascular health, epidemiology, immunology, pharmacology, pulmonary health, neurodevelopment, oncology, pediatrics, public health, and systematic review methodology, but not pain.
Framings that convey commercialisation concerns were surprisingly rare in this study. This is noteworthy, given the scrutiny that has arisen from doctors’ groups in Australia targeting complementary medicines and botanical and nutritional supplements, in particular (Lewis 2019, 2020). The narrative of cannabis as a legitimate and new medicine, laden with not just therapeutic, but commercial possibilities, seems to have evaded such scrutiny and critique, with the exception of one Australian Doctor article, which commented:
But National Cannabinoid Clinics’ financial links with Tilray create unique ethical issues for GPs to navigate,Footnote 6 says Associate Professor Vicki Kotsirilos, a former chair of the RACGP integrative medicine group. (Ausdoc, 10 April 2019, by Geir O’Rourke)
It is possible that doctors are still grappling with the efficacy and benefits of cannabis, along with its risks and all its access and prescribing complexities, before turning their attention to matters of commercialisation, conflicting interests, and ethics. It also may be that for a profession highly familiar with a pharmaceuticalised approach to healthcare, the medicinal cannabis model offers an easy logic, whereby it can be embraced as a medicalised, commercialised, pharmaceutical substance rather than anything resembling herbal medicine.