Abstract
Objective:
Rates of mental illness among young people remain elevated, and the utilization of youth mental health services is expected to increase. Yet, there is limited knowledge on real-world medication usage and prescribing at these services. Hence, the aim of this study was to explore the medication prescribing patterns at a headspace center, an Australian youth mental health service.
Methods:
A retrospective cross-sectional study of medical records was conducted. Demographic data, clinical information, prescribed medications, and reasons for use of young people who attended an intake assessment at headspace Camperdown over a 13-month period, February 2021–February 2022, were analyzed. Data collection focused on medication molecule, strength, dose, prescriber designation, and indication. Data were analyzed descriptively.
Results:
Records for 608 participants were included. The median age at intake was 19.9 years old (interquartile range: 16.1–22.4), and most participants identified as female (n = 372, 61.2%). Anxiety (n = 246, 40.5%) and low mood (n = 95, 15.6%) were the most common presenting concerns. Almost half of participants (n = 291, 47.9%) reported using medication/s at intake, and almost one in five participants (n = 119, 19.6%) were prescribed a medication at the service. The most prescribed medications at headspace were melatonin (24.0%) and quetiapine (12.3%), as well as the antidepressants escitalopram (15.1%), sertraline (11.2%), and fluoxetine (7.3%).
Conclusions:
This study provides insights into the prescribing practices at a single headspace center. Further investigations are needed to explore the impacts of off-label prescribing for young people, particularly in relation to melatonin and quetiapine, where safety and efficacy in young people have not been well established.
Introduction
Globally, one in seven people aged 10–17 years old experience a mental disorder, most commonly depression, anxiety, and behavioral concerns (World Health Organization, 2021). In Australia, young people report higher rates of mental illness than any other age-group, with almost two in five people (38.8%) aged 16–24 years experiencing a mental illness in any 12-month period, representing close to half (45.5%) of females and one third (32.4%) of males in this age-group (Australian Bureau of Statistics, 2020–22). Young people are more likely to seek help for mental health concerns compared with other age-groups, yet rates of mental illness in young people remain high, and the utilization of mental health services is expected to increase (Australian Bureau of Statistics, 2020–22).
Psychosocial interventions, such as psychoeducation or psychological therapies, are considered first-line treatment for young people with depression and anxiety disorders before pharmacological interventions are trialed (National Institute for Health and Care Excellence [NICE], 2019; Andrews et al., 2018). Despite this, and in line with global trends (Zito et al., 2008; Barczyk et al., 2020; Tsai et al., 2017), the dispensing of psychotropic medications for Australian children and adolescents doubled from 2013 to 2021 (Wood et al., 2023), as did the prevalence of psychotropic polypharmacy in this age-group (Wood et al., 2023). Psychotropic medication use in young people remains a subject of debate due to the limited safety and efficacy data in this age-group (Hetrick et al., 2021; Vitiello et al., 2009). The impacts of adverse effects in young people may be less well known compared with adults, partially attributable to concerns regarding inclusion of young people in clinical research (Wolraich, 2003). Despite limited data, untreated mental illness during childhood can have a lasting impact in later life, leading to lower life satisfaction, poorer health outcomes, and suicidal ideation (Schlack et al., 2021). Hence, psychotropic medications may be used despite the lack of licensed indications for this age-group (Parens and Johnston, 2008).
While there is research exploring the prevalence of psychotropic medication use in young people in Australia with population-level data (Wood et al., 2023; Rasmussen et al., 2019; Karanges et al., 2014), little is known about the use of medications within youth mental health services (Rickwood et al., 2023; Rickwood et al., 2015). One previous study focusing on psychotropic medication use in young people with moderate to severe mental health problems found over half of young people aged 12–17 were prescribed psychotropic medications, with one fifth receiving psychotropic polypharmacy (Dharni and Coates, 2018). The use of psychotropic medications within early intervention youth mental health services focusing on mild to moderate mental illness, such as headspace, is unknown (Rickwood et al., 2023).
The youth-specific model of care plays a critical role in encouraging readiness to seek help in young people and has been successful in achieving improved outcomes such as increased service uptake and quality of care, in comparison to other non-age-specific models of care (Brimblecombe et al., 2017; Hawke et al., 2019). headspace is Australia’s National Youth Mental Health Foundation, founded in 2006 in response to the increasing prevalence of mental illness among young people and structural problems with existing models of care (McGorry et al., 2007). headspace centers provide youth-friendly, integrated primary care health services to address mental health, physical and sexual health, alcohol and drug use, as well as work and study issues (Rickwood et al., 2023). It has since expanded with over 150 centers across the country and has attracted substantial government funding ($44 million AUD in 2022) (Department of Health and Aged Care, 2022). Despite significant financial investment, there are limited data available about the prescribing of psychotropic medications within youth mental health services and hence a need to better understand the real-world applications of psychotropic medication use in young people within settings such as headspace. Hence, the aim of this study was to explore medication prescribing patterns at a single headspace center.
Materials and Methods
A retrospective cross-sectional study was conducted through an audit of medical records for a cohort of young people who attended an intake assessment at headspace Camperdown in Sydney, Australia, over a 13-month period, between February 1, 2021, and February 28, 2022.
Setting
This study was conducted at headspace Camperdown, Sydney. headspace provides a unique early intervention model of care along with a multidisciplinary team of health care professionals who work together to provide mental health support for people aged 12–25 years old (McGorry et al., 2007). Health care teams at headspace centers may include general practitioners (GPs), psychiatrists, social workers, and psychologists, although the composition of staff varies between centers. During the auditing period, three GPs and three psychiatry registrars provided medical care and were the only prescribers, although not all were employed at the same time. Young people could have medications prescribed at headspace or by an external GP.
Young people can self-refer or be referred by others (e.g., by a GP) as part of their mental health treatment plan (a plan created by a person and their treating doctor that may include treatment options, agreed goals, and access to subsidized mental health care) (Services Australia, 2023). After establishing contact with the center, young people are invited to an initial intake assessment to determine their suitability for the services provided by headspace, which could include medical or mental health consultations. As most young people are undiagnosed at presentation, headspace does not routinely award formal diagnoses as per international classification systems, such as the Diagnostic and Statistical Manual of Mental Disorders (American Psychiatric Association, 2013). Rather, headspace utilizes a clinical staging model where young people are assigned discrete categories (Stages 1–4, where Stage 1a is “help-seeking” such as non-specific symptoms of anxiety or depression; Stage 1b is “attenuated syndrome,” such as specific symptoms of moderate depression; Stage 2 is “discrete disorder,” such as clear episodes of severe depressive disorders; Stage 3 is “persistent or recurrent illness”; and Stage 4 is “chronic debilitating illness”) based on severity of dysfunction and distress (Hickie et al., 2013). For complex presentations (Stages 2 and above) that are unsuitable for the services provided by headspace, the person is referred to external “step-up” care services.
Participants and study processes
All headspace clients are asked to sign a waiver at intake, which includes an item regarding consent for research and quality assurance activities related to the provision of services. This study was a secondary analysis of an existing database that contained de-identified records, demographic data, and clinical information of all young people who attended an intake assessment at headspace Camperdown. For this current study, young people were assigned a unique record number that corresponded to their file in MedicalDirector. Record numbers were used to retrieve phone numbers via MedicalDirector for either the young person or their parent/guardian. Young people were provided an additional electronic consent form using REDCap (Harris et al., 2009). The consent form was sent via text message using MedicalDirector Bluechip Version 4.11 to young people over 16 years of age at the time that this study was conducted (Telstra Health, 2023a). Participants indicated their consent by electronically signing and returning the consent form. Consent to participate was sought from parents or guardians of young people aged 14–15 years old. A second attempt to obtain consent was made one week after the first text message was sent. If no response was obtained after two attempts, reasonable efforts were assumed to have been made to contact the young person, and they were included in the study given they had previously provided consent at intake. If consent was denied, these young people were removed from the data extraction process.
Young people under 14 years of age were not eligible to be included. If record notes on MedicalDirector Bluechip (Telstra Health, 2023a) indicated that a person under 16 years of age did not want their parents or guardians to know they had contacted the service, consent could not be sought; hence, they were not eligible to participate. Similarly, young people who opted out of receiving text messages were not able to be contacted; hence, consent was not able to be obtained, and they were excluded.
Ethics approval
This study was approved by the Human Research Ethics Committee at The University of Sydney (2022/628).
Data collection
An existing database was used containing demographic data and clinical information collected by one researcher (C.M.S.J.) from record files on MedicalDirector Clinical Version 4.22 (Telstra Health, 2023b). Demographic data of interest (age, gender) and clinical information (presenting concerns, clinical stage, occasions of service, number of clinicians seen) were extracted from this database and presented in this current study.
Study data that related to medication use were collected by another researcher (A.D.) and recorded in REDCap (Harris et al., 2009). Where available, medication-related information was collected from mental health treatment plans written by referring physicians and intake assessments conducted by headspace staff, obtained from MedicalDirector Clinical (Telstra Health, 2023b). Medication-related information collected focused on medications the participant reported to be taking prior to the intake assessment and during their time at headspace, up to two years post-intake assessment. Where available, medication name, formulation, strength, dose, directions, instructions relating to titration, indication, and type of prescriber were recorded. Information related to psychotherapy interventions accessed by the participant while at headspace was also collected from patient records. Where indications for medication use were not explicitly stated, the medical notes from the time of prescribing were reviewed, and the reason for use for the medication was inferred.
Data analysis
Data were imported from REDCap (Harris et al., 2009) into Microsoft Excel 2016 for Mac (Microsoft Corporation, 2016) and checked for consistency and completeness. Medications reported at intake and medications prescribed at headspace were categorized according to their anatomical group (1st level), chemical subgroup (4th level), and chemical substance (5th level) in accordance with the Anatomical Therapeutic Chemical (ATC) classification system (WHO Collaborating Centre for Drug Statistics Methodology, 2023). If a medication name was reported to be unknown by the participant at intake, it was excluded from ATC classification. Data were imported into IBM SPSS Statistics Version 24.0 (IBM Corp, 2016) and descriptively analyzed. Frequency counts and percentages were performed for all demographic variables and clinical information of interest. Tests for normality were performed. Means and standard deviations were calculated for continuous variables that were normally distributed, while medians and interquartile ranges (IQR) were calculated for continuous variables that were not normally distributed.
Medication doses were calculated, where the strength of the medication was multiplied by the dosage and frequency to give the total daily dose. Defined daily doses (DDD) were also reported according to the DDD index 2023 (WHO Collaborating Centre for Drug Statistics Methodology, 2023). Analysis was undertaken to determine the types of practitioners who prescribed medications at headspace. Further analysis was conducted to determine the age breakdown of participants who were prescribed antidepressant medications at headspace, as practice guidelines often recommend certain antidepressants for use in younger age-groups (Cleare et al., 2015; National Institute for Health and Care Excellence [NICE], 2019).
Results
In total, 617 people were booked for an intake assessment during the 13-month audit period. Of the young people who were able to be contacted for consent (n = 616), 8 people declined, 15 provided consent, and 585 did not respond to the two text messages and were therefore included. Overall, a total of 608 participants were included in the audit.
Demographics and clinical information
At the intake assessment, study participants had a median age of 19.9 years (IQR: 16.1–22.4), and most identified as female (n = 372, 61.2%) (Table 1). Participants most frequently presented with anxiety concerns (n = 246, 40.5%), low mood (n = 95, 15.6%), and psychological trauma (n = 66, 10.9%). Most participants were assigned a clinical stage of 1a (n = 287, 47.2%) or 1b (n = 245, 40.3%), indicating a mild to moderate level of dysfunction or distress. During their treatment at headspace, participants had a median of 4.0 occasions of service (IQR: 1.0–10.0) and saw a median of 2 clinicians (IQR: 1.0–3.0) for treatment. The median length of treatment was 220.0 days (IQR: 118.5–298.0).
Clinical Information and Demographic Data (n = 608)
Includes gender fluid, transgender males, transgender females, non-binary, and unknown genders.
Includes generalized anxiety, social anxiety, phobias, panic, social isolation, and stress.
ADHD, attention-deficit/hyperactivity disorder; IQR, interquartile range; OCD, obsessive compulsive disorder; ODD, oppositional defiant disorder.
Medications prescribed prior to intake
At the intake assessment, 291 participants (47.9%) were currently taking at least one medication (Table 2). The most common types of medications were nervous system drugs (n = 250, 47.7%), genitourinary system and sex hormone drugs (n = 96, 18.2%), and respiratory system drugs (n = 46, 8.7%) (Table 3). Of the nervous system drugs, antidepressants (n = 116, 46.4%), hypnotics and sedatives (n = 48, 19.2%), and psychostimulants (n = 36, 15.2%) were most frequently reported, and the most common individual medications were melatonin (n = 43, 17.3%), escitalopram (n = 35, 14.1%), and sertraline (n = 22, 8.8%) (Table 4).
Medication Use Overview (n = 608)
Classification of Medications by ATC 1st Level (Anatomical Group)
ATC, Anatomical Therapeutic Chemical.
Classification of Nervous System Drugs by ATC Therapeutic Subgroup (3rd Level) and Chemical Substance (5th Level)
Bold data corresponds to the number of medications prescribed within the following therapeutic subgroups: antidepressants, hypnotics and sedatives, antipsychotics.
Only licensed for non-psychiatric indications in Australia (Australian Medicines Handbook Pty Ltd, 2023).
Psychostimulant medications are not prescribed at headspace.
Analgesics such as opioids (N02A), other analgesics and antipyretics (N02B), and anti-migraine preparations (N02C).
Medications prescribed at headspace
Of 608 participants, 119 participants (19.6%) were prescribed a medication while at headspace (Table 2). Of the 259 instances of medications prescribed at headspace, the most common types were nervous system drugs (n = 179, 69.1%), particularly, antidepressants (n = 90, 50.3%), hypnotics and sedatives (n = 46, 25.7%), and antipsychotics (n = 30, 16.8%). The most frequently prescribed individual medications were melatonin (n = 43, 24%), escitalopram (n = 27, 15.1%), and quetiapine (n = 22, 12.3%). Escitalopram (n = 27, 15.1%), sertraline (n = 20, 11.2%), and fluoxetine (n = 13, 7.3%) were the most prescribed antidepressants (Table 4). Of the top three most prescribed antidepressants, the majority were prescribed to participants aged 18 years or above (n = 36, 70.6%) and, to a lesser extent, participants aged 18 or under (n = 15, 29.4%). Fluoxetine was most commonly prescribed for those under 18 years of age (n = 7, 46.7%), while escitalopram (n = 16, 44.4%) and sertraline (n = 15, 41.7%) were more commonly prescribed to participants aged 18 and over.
More than half of participants taking a psychotropic medication were also concurrently receiving psychotherapy from headspace (n = 137, 59.8%). GPs prescribed the majority of medications (n = 187, 72.2%), followed by psychiatric registrars (n = 72, 27.8%). Maintenance doses of individual medications, which were prescribed more than once at headspace (n = 15), were also analyzed. Of these, the doses of eight types of medications (n = 8, 53.3%) were found to exceed the DDD (Table 5).
Maintenance Dose Range of Medications Prescribed at headspace (n = 259)
Excluded from the table (n = 1): agomelatine, amitriptyline, lemborexant, lithium, lurasidone, and temazepam.
The assumed average maintenance dose per day for a drug used for its main indication in adults.
XR: extended release.
Discussion
To the best of the authors’ knowledge, this is the first study to present data on the use of psychotropic medications within an early intervention Australian youth mental health service. Previous evaluations of headspace have not included data on medication use or outcomes (Jorm, 2015; Rickwood et al., 2023), yet psychotropic medication use is common in this population and an important part of treatment. Understanding psychotropic medication use in young people is critical to assist with identifying gaps in care. For example, exploring if real-world use aligns with relevant policies and guidelines or if medications are being used for appropriate populations and indications. This study builds on the findings from Dharni and Coates, which found psychotropic medication use is common for young people with moderate to severe mental illness, with medications commonly used “off-label” (Dharni and Coates, 2018).
This audit identified medications possibly being used for indications where the effectiveness or safety evidence is lacking, particularly the use of melatonin and quetiapine for the management of sleep difficulties. This is in line with other recent Australian findings which found quetiapine to be commonly prescribed for insomnia (Dharni and Coates, 2018). Medication use is suspected to be outside of approved indications; however, this was difficult to ascertain due to a lack of documented formal diagnoses at headspace. The frequent prescribing of these medications may suggest that sleep difficulties are prevalent among young people, secondary to primary presenting concerns such as anxiety and low mood. Treatment of depression and anxiety disorders may warrant the use of antidepressants, which accounted for more than half of all psychotropic medications prescribed during the auditing period. For people under the age of 18, clinical practice guidelines recommend fluoxetine (National Institute for Health and Care Excellence [NICE], 2019; Malhi et al., 2021) however, some young people were prescribed antidepressants only approved for use over 18 years of age. More than half of participants who were prescribed an antidepressant also concurrently received psychotherapy at headspace, which aligns with recommendations in clinical practice guidelines (Malhi et al., 2021).
Melatonin was the most common medication reported at intake and prescribed by headspace clinicians in this study. In Australia, melatonin is approved for use in people over the age of 55 with primary insomnia and has recently been approved for use in young people aged 2–18 years with autism spectrum disorder (Therapeutic Goods Administration, 2020; Therapeutic Goods Administration, 2009). However, melatonin continues to be used beyond approved age-groups and indications due to its perceived safety compared with traditional hypnotics (Boafo et al., 2020). Unlike benzodiazepines and non-benzodiazepine hypnotics, melatonin does not appear to cause dependence, and its use has become increasingly popular as a sleep aid for children in recent decades (Hartz et al., 2015; Hartz et al., 2012; Ferracioli-Oda et al., 2013; Lee et al., 2023). Despite increasing use (Klau et al., 2022), there is conflicting evidence on the efficacy of melatonin in young people with sleep difficulties, with a lack of evidence on impacts on quality of sleep and daytime functioning (Edemann-Callesen et al., 2023). Furthermore, the short- and long-term safety of melatonin use in children with insomnia is unknown, with higher relative risks of adverse effects in people under the age of 20 being reported (Händel et al., 2023), highlighting a need for larger and more robust trials investigating the safety and efficacy of melatonin use in young people.
Similarly, this audit revealed substantial prescribing of quetiapine for young people with sleep difficulties. Prescribers may perceive quetiapine as a safer alternative to benzodiazepines due to the potential risk of benzodiazepine addiction; however, the evidence for its use in sleep difficulties is lacking (Kelly et al., 2018; Boafo et al., 2020). Approved indications for quetiapine in young people aged 10–17 years are schizophrenia and bipolar mania (Therapeutic Goods Administration, 2010). Although quetiapine has been shown to be an effective sedative, its safety for insomnia has not been established, hence use for sleep difficulties is off-label (Karsten et al., 2017; Anderson and Vande Griend, 2014). Limited studies have explored quetiapine use for insomnia in the absence of comorbidities, with most studies conducted in adults, and evidence is not necessarily generalizable to younger populations (Anderson and Vande Griend, 2014). Quetiapine, even when prescribed at low doses (<200 mg/day), has been found to result in significant adverse effects such as weight gain and daytime sedation (Coe and Hong, 2012; Anderson and Vande Griend, 2014). Furthermore, quetiapine may be subject to diversion and non-medical use (Kim et al., 2017; Sansone and Sansone, 2010). In light of increasing rates of quetiapine use in Australia (Klau et al., 2022; Brett et al., 2017), there is a need for further prescriber education about the risks of off-label medication use and further research into the safety of this medication in young people.
Findings from this study revealed a variety of medications being used to treat young people experiencing low mood. For the management of depression in young people, practice guideline recommendations differ depending on the severity of illness: mild, moderate, or severe depression. Empirically based guidance recommends psychotherapy as first-line treatment for mild depression, while for moderate to severe depression, combined pharmacology and psychotherapy is recommended (National Institute for Health and Care Excellence [NICE], 2019; Malhi et al., 2021). However, as headspace does not always award or document formal diagnoses, this presents a challenge when assessing the appropriateness of antidepressant choices.
During the audit period, fluoxetine was the only antidepressant licensed in Australia for use in the management of depression in people under the age of 18 and is commonly recommended as first-line treatment for moderate to severe depression in Australian guidelines (Malhi et al., 2021; Therapeutic Goods Administration, 2021). However, escitalopram and sertraline (which is only licensed for the treatment of OCD in people under 18 years of age) were the most prescribed antidepressants at headspace, and, at times, prescribed to people under the age of 18. This is in contrast to population-level studies of young people in Australia that report fluoxetine as the most common antidepressant choice (Klau et al., 2022) and further demonstrates that guidelines are not always adhered to in real-world clinical settings. Clinical practice guidelines may be developed and implemented to improve prescribing and clinical management of certain conditions and patient groups. However, the implementation of such guidelines may not always result in improved prescribing practice. A systematic review of the effects of clinical practice guidelines on the prescribing of mental health medications found that changes in practice are infrequent or minimal, and further work is needed to improve the creation and implementation of such guidelines (Nguyen et al., 2020). Furthermore, many factors are thought to influence prescribing practices (Murshid and Mohaidin, 2017), and prescribing in mental health relies on the management of reported symptoms, unlike objective clinical markers, which can be used when prescribing for many physical health conditions. Future research should investigate how to optimize appropriate psychotropic prescribing in young people.
headspace utilizes a clinical staging model to differentiate between the severity of mental illnesses, which presents challenges to the Australian regulatory framework used for medication prescribing (Hickie et al., 2013). Diagnostic clarity is often needed to justify the prescribing of certain medications listed on the Pharmaceutical Benefits Scheme (PBS). 3 For example, medications classified as “restricted benefit” can only be prescribed for specific therapeutic uses or for specific patient groups. As headspace services focus on early intervention, most people are often transdiagnostic at presentation or do not meet criteria for a mental health diagnosis. Without formal diagnoses, it is difficult to ascertain if medications are being used appropriately and for the approved indications. There are a variety of problems associated with using diagnostic labels in young people, such as associated stigmatization, which may have a psychological impact of increased anxiety, perceived severity of the diagnosis and preference for more invasive treatments (Sims et al., 2021). However, there has been previous research exploring the potential benefits of implementing an indication-based prescribing system in primary care settings (Schiff et al., 2016). The implementation of such a system could permit the identification of drug-indication mismatches and could be utilized to assess medication effectiveness, including for off-label medication use (Grissinger, 2019; Schiff et al., 2016). Despite the lack of formal diagnoses documented, it could be inferred that a medication was prescribed for a mental health purpose based on documented presenting concerns and past medication histories, which demonstrates the importance of conducting an accurate and comprehensive medical and medication history so that indications for medication use can be clearly determined and documented.
Challenges were encountered when gathering data on medications prescribed prior to intake, as medication information was not stored in one cohesive part of the medical record. The level of detail of medication information collected during intake assessments varied, with many records lacking details such as strength, dose, and frequency. However, it is unknown whether these details were prompted by the clinician conducting the intake assessment or if this level of detail could not be recounted by the young person. Accurate medication histories are crucial in preventing treatment-related harms. They are essential in detecting changes in clinical signs, which may be the result of drug therapy, and exploring factors which may lead to unnecessary avoidance of a drug (Fitzgerald, 2009). There are various ways to improve medication history taking, including additional education and training for staff who conduct intake assessments or the potential role of a pharmacist within youth mental health services (Shah et al., 2021). Future research could explore interventions and processes to improve medication history taking and the appropriate use of psychotropic medications in youth mental health services, such as exploring the role of an embedded pharmacist. Non-dispensing pharmacists in primary care settings, such as general practice, can provide medication reviews and clinical audits and have demonstrated beneficial clinical outcomes in areas such as asthma and smoking cessation (Deeks et al., 2023).
Strengths and limitations
While previous retrospective cohort studies have been conducted using PBS dispensing data to determine medication usage in Australian children, there have been limited insights into medication usage and prescribing in the context of an Australian youth mental health service. This is the first study to explore the types of medications which have been prescribed to young people at headspace. However, the results of this study should be interpreted in light of relevant limitations. As medication information was largely self-reported by young people during intake assessments, it is possible some medications were undocumented. Diagnosis information was lacking, which made it challenging to examine the appropriateness of prescribed psychotropic medications, and inferences about reasons for medication use were based on clinical notes. On a similar note, the interpretation and reporting of presenting concerns were subjective in nature as they were not based on formal diagnoses. Although the DDD index was used in this study, there is no global definition of DDD for young people, and it was unclear which standardized doses should be used as a reference when conducting drug utilization studies (WHO Collaborating Centre for Drug Statistics Methodology, 2023). Other reference doses, such as those specified in the Australian Medicines Handbook or MIMS, were not used as they would require a formal diagnosis, which was unknown (Australian Medicines Handbook Pty Ltd, 2023; MIMS Australia, 2023). Furthermore, the results of this study pertain specifically to headspace Camperdown, and results may not be generalizable to all headspace centers. However, the sample included in this study appears to be consistent with the broader clientele of headspace centers Australia-wide in relation to demographics and presenting concerns (Rickwood et al., 2023; Rickwood et al., 2014; headspace, 2023). Despite these limitations, this study identifies several avenues for future research, including exploring roles for non-dispensing pharmacists in youth mental health services, investigating the safety and efficacy of medications such as melatonin and quetiapine for children with insomnia, and exploring strategies to improve the quality use of medicines for young people living with mental illness.
Conclusions
This study provided insight into the real-world prescribing patterns at a single Australian youth mental health service. The most prescribed medications were melatonin and quetiapine for sleep difficulties and escitalopram, sertraline, and fluoxetine for low mood. Caution is needed when prescribing medications for potential off-label use, especially when safety and efficacy have not yet been established for use in young people. Further research is warranted to explore the use of clinical practice guidelines in youth mental health settings.
Clinical Significance
This single-centre study found psychotropic medications being prescribed that may not have aligned with presenting concerns, with the most commonly prescribed medications being melatonin and quetiapine.
Footnotes
Acknowledgment
The authors thank the headspace Camperdown staff for their ongoing support.
Authors’ Contributions
A.D.: Data curation, formal analysis, investigation, writing—original draft, writing—review and editing, and visualization. S.E.-D.: Conceptualization, methodology, supervision, and writing—review and editing. J.C.C.: Conceptualization, formal analysis, methodology, supervision, and writing—review and editing. B.H.: Conceptualization, project administration, and writing—review and editing. C.M.S.J.: Project administration, methodology, and writing—review and editing. D.F.: Project administration and writing—review and editing. C.L.O.: Conceptualization, formal analysis, methodology, project administration, supervision, and writing—review and editing.
Data Availability Statement
Data are available upon request to the corresponding author, if in line with ethics approval.
Disclosures
The authors declare that they have no conflicts of interest.
1Practice software for management of patient appointments, SMS reminders, and other administrative workflows.
2Clinical management software used for prescribing and recording of progress notes.
