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A systematic review and economic model of the effectiveness and ...

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MPH, DEX <strong>and</strong> ATX improve hyperactivity<br />

<strong>and</strong> QoL (as assessed using CGI as a<br />

proxy) compared with placebo. The validity<br />

<strong>of</strong> <strong>the</strong> results is not known for studies <strong>of</strong> MPH<br />

<strong>and</strong> DEX, given <strong>the</strong> poor reporting <strong>of</strong> study<br />

methodology in <strong>the</strong> majority <strong>of</strong> <strong>the</strong>se trials.<br />

The recent trials on ATX are likely to be more<br />

reliable.<br />

There were very few head-to-head studies<br />

comparing MPH, DEX <strong>and</strong> ATX. No significant<br />

differences between <strong>the</strong> various drugs in terms <strong>of</strong><br />

efficacy or side-effects were found, mainly owing<br />

to a lack <strong>of</strong> evidence.<br />

The main conclusions from this report are:<br />

● Drug <strong>the</strong>rapy seems to be superior to no drug<br />

<strong>the</strong>rapy.<br />

● No significant differences between <strong>the</strong> various<br />

drugs in terms <strong>of</strong> efficacy or side-effects were<br />

found, mainly owing to a lack <strong>of</strong> evidence.<br />

● The additional benefits from BT (in<br />

combination with drug <strong>the</strong>rapy) are uncertain.<br />

Chapter 8<br />

Conclusion<br />

© Queen’s Printer <strong>and</strong> Controller <strong>of</strong> HMSO 2006. All rights reserved.<br />

Health Technology Assessment 2006; Vol. 10: No. 23<br />

The main additional feature <strong>of</strong> <strong>the</strong> <strong>economic</strong><br />

<strong>model</strong> is <strong>the</strong> consideration <strong>of</strong> costs. Given <strong>the</strong> lack<br />

<strong>of</strong> evidence for any differences in <strong>effectiveness</strong><br />

between <strong>the</strong> drugs, <strong>the</strong> <strong>model</strong> tends to be driven<br />

by drug costs, which differ considerably.<br />

Research recommendations<br />

● Future trials examining MPH, DEX <strong>and</strong> ATX<br />

should include <strong>the</strong> assessment <strong>of</strong> tolerability<br />

<strong>and</strong> safety as a priority. Reporting should be<br />

st<strong>and</strong>ardised <strong>and</strong> transparent. Researchers<br />

should refer to <strong>the</strong> CONSORT approach to<br />

study design. 159<br />

● Longer term follow-up <strong>of</strong> individuals<br />

participating in trials could fur<strong>the</strong>r inform<br />

policy makers <strong>and</strong> health pr<strong>of</strong>essionals. Such<br />

data could potentially distinguish between <strong>the</strong>se<br />

drugs in a clinically useful way.<br />

● In addition, research examining whe<strong>the</strong>r<br />

somatic complaints are actually related to drug<br />

treatment or to <strong>the</strong> disorder itself would be<br />

informative.<br />

129

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