hta_ knee intro.qxp - Ministero della Salute
hta_ knee intro.qxp - Ministero della Salute
hta_ knee intro.qxp - Ministero della Salute
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The data loss due to a narrow study question, inclusion criteria, 5 year survival cut-off, and<br />
focused outcomes is another potential limit of our study (see figure 9.1 that depicts the various<br />
levels and causes of data loss through the study). For example the 50 year limit entailed the exclusion<br />
of some large studies which reported ages in aggregate or as ranges (i.e. 18-75). Some of<br />
these studies probably reported data which were relevant to our study, but had to be excluded to<br />
avoid confounding and preserving our focus on OA.<br />
In addition, our analyses are based on costs and effectiveness estimates which may not be<br />
generalisable across nations or even regions of the same system. This is shown by the difference<br />
in some effectiveness profiles for the same model of prostheses between the two registers. The<br />
availability of more individual data from registers would have allowed more sophisticated comparisons<br />
to be made, adjusted for example by risk factors such as level of physical activity, age and<br />
co-morbidities. Finally, one of the manufacturers also told us that our weighted costs estimates<br />
grossly overestimated the costs of their products, probably unfavourably impacting on their ICERs.<br />
While this may be so, we had to rely on what respondents told us. Their cost data in turn reflected<br />
local purchase prices, i.e. reality.<br />
Figure 9.1: Flow of data loss through the study.<br />
Objecttive<br />
Reeport’s<br />
Survey Systematic<br />
review<br />
DATA INPUT<br />
Arthroplasty<br />
register<br />
Economic<br />
evaluation<br />
Data collection<br />
Questionnaire not evaluable<br />
(outcome, ( ppopulation, p follow-up) p)<br />
(incorrectly compiled)<br />
Reporting<br />
Inclusion Criteria<br />
(format and content)<br />
(prostheses not in use in<br />
Italy Italy, follow - up < 5 years years,<br />
Objecti<br />
population, clinical<br />
Data sharing<br />
indication)<br />
ive<br />
Partial information<br />
(effectiveness or price)<br />
CONCLUSIONS AND RECOMENDATIONS<br />
Report’s<br />
O<br />
61