A systematic review and economic model of the effectiveness and ...
A systematic review and economic model of the effectiveness and ...
A systematic review and economic model of the effectiveness and ...
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6<br />
Background<br />
Concerta XL<br />
Concerta XL is administered orally once daily in<br />
<strong>the</strong> morning <strong>and</strong> must be swallowed whole with<br />
<strong>the</strong> aid <strong>of</strong> liquids, <strong>and</strong> must not be chewed,<br />
divided or crushed. Concerta XL may be<br />
administered with or without food. Dosage should<br />
be individualised according to <strong>the</strong> needs <strong>and</strong><br />
responses <strong>of</strong> <strong>the</strong> patient. Dosage may be adjusted<br />
in 18-mg increments to a maximum <strong>of</strong> 54 mg per<br />
day taken once in <strong>the</strong> morning. In general, dosage<br />
adjustment may proceed at approximately weekly<br />
intervals. The manufacturers <strong>of</strong> this drug claim<br />
that its effects last through 12 hours. 26<br />
Dexamfetamine sulphate<br />
(dexamphetamine sulphate)<br />
DEX is a symphathomimetic amine with central<br />
stimulant <strong>and</strong> anorectic activity. It is indicated in<br />
narcolepsy. It is also indicated for children with<br />
refractory hyperkinetic states under <strong>the</strong><br />
supervision <strong>of</strong> a physician specialising in child<br />
psychiatry.<br />
Dexedrine ® (Celltech Pharmaceuticals Ltd) is<br />
available in 5-mg tablets.<br />
The usual starting dosage for children aged<br />
3–5 years is 2.5 mg per day, increased if necessary<br />
by 2.5 mg per day at weekly intervals. For children<br />
aged ≥ 6 years, <strong>the</strong> usual starting dose is 5–10 mg<br />
per day, increasing if necessary by 5 mg at weekly<br />
intervals. The usual upper limit is 20 mg a day<br />
although some older children have needed 40 mg<br />
or more for optimal response.<br />
Atomoxetine hydrochloride 27<br />
ATX is reported to be a selective noradrenaline<br />
reuptake inhibitor. The precise mechanism by<br />
which ATX works on ADHD is not known. It is<br />
currently licensed in <strong>the</strong> USA <strong>and</strong> <strong>the</strong> UK under<br />
<strong>the</strong> br<strong>and</strong> name Strattera ® (Eli Lilly & Co. Ltd).<br />
The manufacturers claim that it is <strong>the</strong> first nonstimulant<br />
medication approved for <strong>the</strong> treatment<br />
<strong>of</strong> ADHD in children ≥ 6 years <strong>of</strong> age. In<br />
adolescents who have shown a clear benefit from<br />
treatment, <strong>and</strong> whose symptoms persist into<br />
adulthood, treatment may be continued into<br />
adulthood. However, starting treatment with<br />
Strattera in adults is not appropriate. It is<br />
indicated as an integral part <strong>of</strong> a total treatment<br />
programme for patients with ADHD.<br />
Strattera is available in 10-, 18-, 25-, 40- <strong>and</strong><br />
60-mg capsules (for oral administration with or<br />
without food).<br />
In children <strong>and</strong> adolescents up to 70 kg body<br />
weight, Strattera should be initiated at a total daily<br />
dose <strong>of</strong> approximately 0.5 mg/kg <strong>and</strong> increased<br />
after a minimum <strong>of</strong> 3 days to a target daily dose <strong>of</strong><br />
approximately 1.2 mg/kg administered ei<strong>the</strong>r as a<br />
single daily dose in <strong>the</strong> morning or as evenly<br />
divided doses in <strong>the</strong> morning <strong>and</strong> late<br />
afternoon/early evening. The total daily dose in<br />
children <strong>and</strong> adolescents should not exceed<br />
1.4 mg/kg or 100 mg, whichever is less.<br />
In children <strong>and</strong> adolescents >70 kg body weight,<br />
Strattera should be initiated at a total daily dose <strong>of</strong><br />
40 mg <strong>and</strong> increased after a minimum <strong>of</strong> 3 days to<br />
a target total daily dose <strong>of</strong> approximately 80 mg<br />
administered as stated above. After 2–4 additional<br />
weeks, <strong>the</strong> dose may be increased to a maximum<br />
<strong>of</strong> 100 mg in patients who have not achieved an<br />
optimal response.