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80 - Attention-deficit hyperactivity disorder: prescribing

from VII - Treatment

Published online by Cambridge University Press:  02 January 2018

Matthew Impey
Affiliation:
Sheffield Health and Social Care Trust
Clare Oakley
Affiliation:
Institute of Psychiatry, King's College London
Floriana Coccia
Affiliation:
University of Birmingham
Neil Masson
Affiliation:
NHS Greater Glasgow and Clyde
Iain McKinnon
Affiliation:
National Institute for Health Research, Newcastle University
Meinou Simmons
Affiliation:
Cambridge and Peterborough Foundation Trust
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Summary

Setting

This audit is intended for a child and adolescent mental health service (CAMHS) involved in the initiation and monitoring of medications prescribed for attentiondeficit hyperactivity disorder (ADHD).

Background

The diagnosis of ADHD is frequently made but still controversial. In children, it involves difficulties with concentration, excessive motor activity and impulsivity in a variety of environments (National Institute for Health and Clinical Excellence, 2008). Alongside behavioural interventions, medications are an important form of treatment and can be taken as short- or long-acting preparations. First-line treatments are stimulants (methylphenidate or dexamfetamine) or atomoxetine.

Standards

Audit criteria were based upon the National Institute for Health and Clinical Excellence's Technology Appraisal 98, Methylphenidate, Atomoxetine and Dexamfetamine for ADHD in Children and Adolescents (2006). This document looks specifically at ADHD medications. The target for meeting all standards was 100%.

ᐅ Drug treatments in ADHD are initiated by an appropriately qualified healthcare professional with expertise in ADHD. (In our locality, this could be either a CAMHS consultant or a paediatrician with specialist experience. In other regions, specialist nurses or pharmacists may also be able to initiate these medications.)

ᐅ Drug treatment is based on a comprehensive assessment and diagnosis. This was taken to require at least three assessments and use of a common rating questionnaire, for example the Conner's rating scale.

ᐅ Where drug treatment is appropriate, methylphenidate, atomoxetine or dexamfetamine is offered.

ᐅ The decision regarding choice of product considers:

  • ▹ the presence of comorbid conditions

  • ▹ adverse effects

  • ▹ specific compliance issues

  • ▹ the potential for drug diversion or misuse (stimulant medications are controlled substances and could be used illicitly by the patient or others)

  • ▹ preferences of the child and parents or guardians.

  • Method

    Data collection

    Prescribing information was taken from multidisciplinary case notes from two sites. The sample included all the available notes (a total of 48 patients).

    Data analysis

    Outcomes were defined by how closely the standard met the target for completion. Comparisons were descriptive rather than statistical.

    Resources required

    People

    The data could be collected by one person. If multiple sites are used, local collection can be performed by different individuals and later analysed as a whole.

    Time

    Data collection can take place over any period of time.

    Type
    Chapter
    Information
    Publisher: Royal College of Psychiatrists
    Print publication year: 2011

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