Valeurs seuils pour le rapport coût-efficacité en soins de santé - KCE
Valeurs seuils pour le rapport coût-efficacité en soins de santé - KCE
Valeurs seuils pour le rapport coût-efficacité en soins de santé - KCE
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
50 ICER Thresholds <strong>KCE</strong> Reports 100<br />
Key points<br />
• In the UK, a discussion is ongoing on the use of ICER threshold values.<br />
Curr<strong>en</strong>tly the UK uses an explicit threshold range of £20 000 to £30 000<br />
per QALY gained.<br />
• Implicit threshold values based on past allocation <strong>de</strong>cisions were<br />
published in Australia (AU$69 900 / QALY gained), New Zealand<br />
(NZ$20 000 / QALY gained) and Canada (range of acceptance: dominant<br />
to $80 000 per QALY gained, range of rejection: $31 000 to $137 000 per<br />
QALY gained).<br />
• Thresholds values or ranges proposed by individuals or institutions were<br />
found in the USA (50 000$/QALY), in the Netherlands (€80 000 per<br />
QALY gained) and in Canada (20 000 - 100 000$/QALY).<br />
• The lower and upper limit for the social WTP for a QALY in the US was<br />
estimated to be 109 000$/QALY and 297 000$/QALY respectively.<br />
• With the exception of the UK, no explicit ICER threshold value (or<br />
range) is used in the countries examined.<br />
• In all countries <strong>de</strong>cision making is not so<strong>le</strong>ly based on cost-effectiv<strong>en</strong>ess<br />
consi<strong>de</strong>rations. The technology is assessed based on the threshold range<br />
together with other criteria. In the pres<strong>en</strong>ce of high ICERs, those other<br />
criteria become more important.<br />
• In most countries it appears that interv<strong>en</strong>tions with a low ICER are more<br />
likely to become accepted than interv<strong>en</strong>tions with a high ICER.<br />
3.6 THE USE OF ICER THRESHOLD VALUES IN BELGIUM<br />
Additional to the international comparison a limited field study explored the use of<br />
cost-effectiv<strong>en</strong>ess evaluations in health care reimbursem<strong>en</strong>t <strong>de</strong>cisions in Belgium. We<br />
focused on two committees: the Drug Reimbursem<strong>en</strong>t Committee (DRC or<br />
CTG/CRM) and the Technical Committee for Implants (TCI or TRI/CTI), both having an<br />
important ro<strong>le</strong> in reimbursem<strong>en</strong>t <strong>de</strong>cisions.<br />
3.6.1 Background on DRC and TCI<br />
The <strong>de</strong>cision to reimburse pharmaceutical products and <strong>de</strong>vices in Belgium is tak<strong>en</strong> by<br />
the Minister of Social Affairs after consultation with the Minister of Budget, but the<br />
Minister is advised on these matters by the DRC and the TCI respectively. Both<br />
committees are organised within the NIHDI but their structure, working procedures<br />
and place in the <strong>de</strong>cision making process are differ<strong>en</strong>t.<br />
The DRC advises the Minister of Social Affairs directly. Although the advice is not<br />
strictly binding, the Minister can only <strong>de</strong>viate from the advice formulated by the DRC<br />
for social or budgetary reasons. The composition of the DRC and the procedures for<br />
formulating a reimbursem<strong>en</strong>t proposal for a pharmaceutical product are stipulated in<br />
two Royal Decrees, approved on 21/12/2001. 165, 166 The DRC is composed of<br />
repres<strong>en</strong>tatives of sickness funds (the mutualities), universities, medical doctors and<br />
pharmacists. Repres<strong>en</strong>tatives of the pharmaceutical industry, the Ministry of Economic<br />
Affairs, the Ministry of Budget, the Ministry of Social Affairs, the Ministry of Public<br />
Health and the NIHDI can att<strong>en</strong>d the meetings and participate in the discussions but<br />
have no voting rights. The DRC has to formulate an advice within strict time limits: the<br />
<strong>de</strong>cision to reimburse a pharmaceutical product has to be tak<strong>en</strong> within 180 days after<br />
the submission of a reimbursem<strong>en</strong>t request fi<strong>le</strong> by a pharmaceutical company. The<br />
advice of the DRC with respect to reimbursem<strong>en</strong>t has to reach the Minister of Social<br />
Affairs at day 150 at the latest.