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New Zealand Autism Spectrum Disorder Guideline - Ministry of Health

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Part 4: Treatment and management <strong>of</strong> ASD<br />

Part 4<br />

therefore, many recommendations are based<br />

on short-term studies or expert opinion.<br />

Many medications utilised for children and<br />

adolescents with ASD have been developed<br />

for and tested in adults. Because <strong>of</strong> important<br />

potential differences in pharmacokinetics<br />

(metabolism etc) and pharmacodynamics<br />

(effects on the body and mind), findings from<br />

the adult literature should be applied to children<br />

and adolescents with significant caution.<br />

Studies involving children and adolescents<br />

are slow to take place and numbers included<br />

in studies small. Prescription <strong>of</strong> many agents<br />

will, by necessity, therefore be ‘<strong>of</strong>f-label’ when<br />

applied to children with autism (that is, outside<br />

manufacturers’ recommendations) 292 . Parents,<br />

carers and pr<strong>of</strong>essionals need to be aware <strong>of</strong> the<br />

implications <strong>of</strong> this practice.<br />

In addition, the response to medications used to<br />

treat co-morbidities may be different for children<br />

with ASD so that special care is needed when<br />

prescribing in this group. For example, many<br />

children with ASD have coexisting significant<br />

ADHD symptomatology. While this may<br />

<strong>of</strong>ten improve significantly with stimulants,<br />

stimulants may increase anxiety and stereotyped<br />

behaviour. Stimulants may therefore be less<br />

useful in some children with autism. There is<br />

evidence that suggests that some children with<br />

ASD become over-focused when on stimulant<br />

medication, and repetitive and obsessional<br />

behaviour may be exacerbated 293 .<br />

Clearly, for reasons <strong>of</strong> brevity, this review<br />

cannot address the vast literature on the use <strong>of</strong><br />

psychoactive medications in disorders other<br />

than ASD. This means that any prescriber<br />

working with children with ASD must have<br />

a good working knowledge <strong>of</strong> psychiatric<br />

disorders, their diagnosis and treatment, and<br />

indeed <strong>of</strong> all psychoactive drugs, including their<br />

safety and efficacy. If the prescriber does not<br />

have this knowledge, then access to a child and<br />

adolescent psychiatrist or other appropriately<br />

knowledgeable prescriber is necessary. Where<br />

there is clear and properly diagnosed evidence<br />

<strong>of</strong> another mental health disorder (eg, ADHD),<br />

the child or person with ASD has should be<br />

treated according to evidence-based treatment<br />

guidelines for that disorder. However,<br />

prescribers must make it clear that the treatment<br />

may not improve ASD symptoms, and must<br />

ensure that there is monitoring for side effects<br />

(including worsening <strong>of</strong> ASD core symptoms<br />

like obsessional anxiety).<br />

Some medications currently in use in children<br />

with ASD in <strong>New</strong> <strong>Zealand</strong> are relatively new<br />

medications. It is essential that both clinicians<br />

and parents appreciate that there is therefore<br />

very limited information on long-term safety.<br />

As children with challenging behaviour<br />

may remain on these medications for many<br />

years, both prescribers and parents need to<br />

understand that there is an element <strong>of</strong> risk in<br />

the use <strong>of</strong> such drugs.<br />

The therapeutic use <strong>of</strong> a large number <strong>of</strong><br />

different medications and other approaches such<br />

as biological agents and dietary approaches (see<br />

section 4.5 Other interventions) has been studied<br />

in ASD and related disorders, but not many<br />

are supported by rigorous evidence. Some<br />

<strong>of</strong> the studies have only assessed classes <strong>of</strong><br />

medications, rather than individual agents. The<br />

most commonly studied agents are risperidone,<br />

fenfluramine, secretin and naltrexone. Some<br />

<strong>of</strong> the evidence for medications may be biased<br />

because the studies have been funded by the<br />

manufacturers. Medications for which little or<br />

no evidence base exists are not necessarily less<br />

effective, but it is recommended that clinicians<br />

avoid using medications for which evidence <strong>of</strong><br />

efficacy is not available.<br />

A useful summary <strong>of</strong> issues in paediatric<br />

psychopharmacological prescribing may be<br />

found in a number <strong>of</strong> reviews by experts,<br />

although only the first <strong>of</strong> these is autism<br />

specific 294-296 .<br />

146<br />

<strong>New</strong> <strong>Zealand</strong> <strong>Autism</strong> <strong>Spectrum</strong> <strong>Disorder</strong> <strong>Guideline</strong>

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