Anxiety and depression
Anxiety is one of the most common comorbidities with autism. There are links to difficulties with social communication and therefore the internal discomfort that can be experienced when in groups, going to new environments and when experiencing change. Talking-based therapies, in particular cognitive behaviour therapy, have good supporting evidence.18 These techniques are harder to use in children and adults with a severe autism spectrum disorder who find working in a therapeutic relationship and speaking to a therapist about distressing feelings to be intolerable. Drugs have a role when anxiety is interfering in the functional life of a child, such as avoiding school, losing friendships or ceasing activities that were previously enjoyable.
The first-line drugs are selective serotonin reuptake inhibitors (SSRIs) such as sertraline, fluoxetine and fluvoxamine.19 The onset adverse effects of fluvoxamine,20 which include agitation and anxiety, limit its use as a first-line drug. It is often used after a failed trial of sertraline or fluoxetine.
To provide the low doses required for some SSRIs, a compounding chemist may be needed to prepare a low-concentration liquid form.
Sertraline, fluoxetine and fluvoxamine can be used for depressive disorders, however there are less research data from children with autism spectrum disorder and a mood disorder. Treatment is considered on a case- by-case basis after specialist assessment.3 There is the risk for increased suicidal thinking occurring when using SSRIs. The harm–benefit ratio for each patient needs to be considered as well as monitoring for an increase in suicidal thinking in the first two weeks of treatment.11
Mood lability
Children with autism spectrum disorder who present with externalising behaviours, which are behaviours that are targeted toward the external environment when distressed such as physical aggression, threats and destroying property, often have a labile mood. They also often have learning disorders, poor self-regulation and behavioural problems at school.
Sodium valproate can be helpful with aggression and is also used to treat irritability and mood lability.21 There are insufficient data to indicate the use of other mood stabilisers. Sodium valproate has many adverse effects including nausea, poor attention, skin reactions including Stevens-Johnson syndrome, and liver toxicity. It is best avoided in females because of its teratogenicity and has also been associated with polycystic ovary syndrome.
Tics and Tourette syndrome
Clonidine is the first-line treatment for tics and Tourette syndrome. There is evidence that atypical antipsychotics such as aripiprazole can also be used for treatment. Aripiprazole reduces the symptoms of Tourette syndrome, and can be used when there is little response to psychological interventions or when there is a contraindication or no response to clonidine.22 Aripiprazole may be better tolerated than clonidine.23
Irritability and aggression
Aggression is one of the most common sources of concern for parents of children with autism spectrum disorder. It can cause large interruptions in their schooling, relationships, their ability to leave the home and it can greatly disrupt a family.
Often antipsychotics such as aripiprazole and risperidone have been used to help treat irritability and problem behaviours in children and adolescents with autism spectrum disorder.24,25 In Australia, risperidone is approved by the Therapeutic Goods Administration for irritability and aggression in autism in patients under 18 years of age. However, the risks with risperidone include weight gain, elevated lipids, blood glucose and prolactin, and interruption of puberty. Aripiprazole has been used in other countries, in particular the USA, as it causes less weight gain and has less effect on prolactin. It is not as sedating as risperidone and this can cause difficulties for families if they have been using risperidone to settle night-time aggression and to improve sleep.
Before prescribing, record height, weight, menarche and regularity of menstruation, blood glucose, fasting lipids and prolactin. Monitor these again after one month and then six-monthly. An increase in prolactin or the development of abnormal muscle movements requires the drug dose to be lowered and a review of the antipsychotic therapy.
At present, due to small sample sizes and open- label studies, there is insufficient evidence to show that antipsychotics such as olanzapine, quetiapine, ziprasidone or clozapine are effective in autism spectrum disorder.10,11 There is also little evidence that older antipsychotics, antiepileptic drugs and glutaminergic modulators (such as ketamine and memantine) are helpful in managing aggression.25 Sodium valproate can be tried if antipsychotics are not effective or the patient cannot tolerate them.21
For some patients with a poor response to risperidone and aripiprazole, off-label use of an alternate antipsychotic can be considered.26
Attention deficit hyperactivity disorder
ADHD is a common comorbidity with autism spectrum disorder.7,27 The drugs used in treatment are the same as those used for ADHD alone, namely methylphenidate, dexamfetamine, guanfacine and atomoxetine.27 Stimulant treatment improves the symptoms of ADHD in patients with autism spectrum disorder. Atomoxetine can assist with inattentive ADHD and patients with comorbid anxiety symptoms. The adverse effects include nausea and fatigue.28
Insomnia
Insomnia and sleep disorders affect close to 80% of people with autism spectrum disorder, and often present as a sleep onset disorder. Behavioural management is the mainstay of treatment.
There are few drugs that are useful for sleep disorders in children. Benzodiazepines are not recommended. Antipsychotics should also be avoided because of their high risk of adverse effects. Melatonin is often used to manage sleep disorders in children, partly because it is available over-the-counter in overseas countries. It has a low risk of adverse effects and dependency.29 Clonidine in low dose (50–200 microgram at night) has also been used, in particular when the insomnia is secondary to stimulant treatment.11