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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TABLE 96 Results <strong>of</strong> <strong>the</strong> sensitivity analysis employing alternative estimates <strong>of</strong> resource use<br />
no treatment. Again, strategy 9 is not ruled out by<br />
dominance or extended dominance, but <strong>the</strong> cost<br />
per QALY gained compared with strategy 7 is<br />
outside <strong>the</strong> range normally considered costeffective<br />
(£5,808,184).<br />
Sensitivity to structural assumption<br />
regarding MPH<br />
A major structural assumption in <strong>the</strong> <strong>model</strong> is that<br />
a patient who has failed treatment with one<br />
formulation <strong>of</strong> MPH would not <strong>the</strong>n receive a<br />
different formulation <strong>of</strong> <strong>the</strong> same drug. However,<br />
if failure on IR-MPH was due to non-compliance,<br />
or because a midday dose was simply unworkable<br />
for <strong>the</strong> patient, ER-MPH may be a relevant<br />
treatment option. The effect <strong>of</strong> compliance on<br />
response rates to IR-MPH <strong>and</strong> ER-MPH is<br />
reflected in <strong>the</strong> <strong>model</strong>. However, <strong>the</strong> <strong>model</strong>, <strong>and</strong><br />
<strong>the</strong> trial data, do not identify <strong>the</strong> proportion <strong>of</strong><br />
Health Technology Assessment 2006; Vol. 10: No. 23<br />
Strategy Order <strong>of</strong> treatments received Cost (£) QALYs Cost per QALY (£)<br />
(compared with)<br />
1 IR-MPH – ATX – DEX – no treatment 1006 0.8279 D<br />
2 ER-MPH8 – ATX – DEX – no treatment 1233 0.8273 D<br />
3 ER-MPH12 – ATX – DEX – no treatment 1250 0.8278 D<br />
4 ATX – IR-MPH – DEX – no treatment 1250 0.8278 D<br />
5 ATX – ER-MPH8 – DEX – no treatment 1320 0.8277 D<br />
6 ATX – ER-MPH12 – DEX – no treatment 1327 0.8274 D<br />
7 IR-MPH – DEX – ATX – no treatment 920 0.8283 D<br />
8 ER-MPH8 – DEX – ATX – no treatment 1105 0.8277 D<br />
9 ER-MPH12 – DEX – ATX – no treatment 1190 0.8284 D<br />
10 ATX – DEX – IR-MPH – no treatment 1242 0.8281 D<br />
11 ATX – DEX – ER-MPH8 – no treatment 1261 0.8281 D<br />
12 ATX – DEX – ER-MPH12 – no treatment 1259 0.8278 D<br />
13 DEX – IR-MPH – ATX – no treatment 887 0.8288 14,939<br />
14 DEX – ER-MPH8 – ATX – no treatment 944 0.8287 D<br />
15 DEX – ER-MPH12 – ATX – no treatment 945 0.8286 D<br />
16 DEX – ATX – IR-MPH – no treatment 946 0.8288 D<br />
17 DEX– ATX – ER-MPH8 – no treatment 965 0.8288 D<br />
18 DEX– ATX – ER-MPH12 – no treatment 963 0.8285 D<br />
19 No treatment 48 0.7727 –<br />
D, dominated.<br />
TABLE 97 Cost-<strong>effectiveness</strong> <strong>of</strong> ER-MPH8, ER-MPH12, ATX <strong>and</strong> no treatment in patients for whom a midday dose <strong>of</strong> medication is<br />
unsuitable<br />
Strategy Order <strong>of</strong> treatments received Cost (£) QALYs Cost per QALY (£)<br />
(compared with)<br />
19 No treatment 1223 0.7731 –<br />
20 ATX only 1517 0.8093 D<br />
22 ER-MPH8 only 1360 0.8053 4251 (vs 19)<br />
23 ER-MPH12 only 1427 0.8140 7670 (vs 22)<br />
D, dominated.<br />
© Queen’s Printer <strong>and</strong> Controller <strong>of</strong> HMSO 2006. All rights reserved.<br />
non-responders that fail owing to lack <strong>of</strong><br />
compliance. As such, this sensitivity analysis<br />
considers a hypo<strong>the</strong>tical cohort <strong>of</strong> patients for<br />
whom a midday dose <strong>of</strong> medication is considered<br />
unsuitable. This includes patients who have failed<br />
on IR-MPH or DEX where <strong>the</strong> clinician can<br />
identify that <strong>the</strong> reason for failure is non-response.<br />
Also included are patients for whom <strong>the</strong> clinician<br />
judges a midday dose <strong>of</strong> medication to be<br />
unworkable.<br />
The <strong>model</strong> is a simple comparison <strong>of</strong> ER-MPH8,<br />
ER-MPH12 <strong>and</strong> ATX <strong>and</strong> no treatment. The<br />
results <strong>of</strong> <strong>the</strong> analysis are shown in Table 97. They<br />
show that in this selected patient population, ATX<br />
is dominated by ER-MPH12. Hence in those<br />
patients for whom a midday dose <strong>of</strong> medication is<br />
unsuitable, through non-compliance or for o<strong>the</strong>r<br />
reasons, ER-MPH12 would precede ATX in any<br />
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