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68 Interventions in Alzheimer’s Disease <strong>KCE</strong> Reports 111<br />
One should note that among <strong>the</strong> 168 patients who started ChEIs within 6 months after<br />
institutionalization 101 patients (60%) received <strong>the</strong>ir first prescription in a hospital<br />
setting. The distribution of <strong>the</strong> ROB/RVT-MR/MRS types used for <strong>the</strong> first charge is<br />
given below.<br />
Figure 3: ChEI use by ROB/RVT-MR/MRS type<br />
TYPE Discont'd Continued Started<br />
ROB A N 1 31 33<br />
ROB B N 4 72 52<br />
ROB C N 0 5 6<br />
ROB Cd N 4 32 15<br />
ROB O N 0 19 29<br />
RVT B N 4 37 17<br />
RVT C N 0 2 4<br />
RVT Cd N 4 30 12<br />
Total N 17 228 168<br />
These results illustrate ChEIs are prescribed mainly in patients who are not in <strong>the</strong><br />
highest classes (C) of dependency based on <strong>the</strong> Katz ADL scale. It should also be noted<br />
that <strong>the</strong> net change in ChEI use associated with institutionalization is thus an increase in<br />
<strong>the</strong> number of patients on ChEIs. The appropriateness of starting ChEIs after<br />
institutionalization was questioned by some of <strong>the</strong> external experts of this project.<br />
Among <strong>the</strong> patients with ChEI prescriptions in 2006, 466 patients (31%) resided in<br />
ROB/RVT-MR/MRS. If we assume that among <strong>the</strong> 40000 patients on ChEIs in 2008 31%<br />
or 12400 patients reside in a ROB/RVT-MR/MRS, <strong>the</strong> following can be derived. This<br />
would mean that 12400 (or 36%) of <strong>the</strong> estimated 34000 AD patients in ROB/RVT-<br />
MR/MRS receive a ChEI. This also means that about 27600 (69%) of <strong>the</strong> estimated<br />
41000 AD patients residing at home receive a ChEI.<br />
6.3.3 Routine use of new diagnostic markers<br />
The table below shows <strong>the</strong> patients who are tested, and also shows <strong>the</strong> number of tests<br />
over <strong>the</strong> period 2002-2006 for <strong>the</strong> 2502 patients in our study database. We do not<br />
know <strong>the</strong> reason for doing <strong>the</strong> test nor what analyses were exactly performed.<br />
Table 18: Number of tests and patients tested in 2002-2006 period among<br />
<strong>the</strong> 2502 patients who started ChEI <strong>the</strong>rapy.<br />
Test N tests N patients (% of 2502 patients)<br />
MRI 605 472 (18.9%)<br />
CSF 83 65 (2.6%)<br />
PET 78 72 (2.9%)<br />
DNA 42 33 (1.3%)<br />
MRI = MRI of head; CSF = lumbar puncture; PET = PET scan or functional scintigraphic test code<br />
used in case centre not registered for PET; DNA = genetic test based on DNA hybridization<br />
Test volumes for Belgium in this patient group can be estimated by multiplying <strong>the</strong>se<br />
numbers with a factor of 20. We could not study <strong>the</strong> reason why <strong>the</strong> test or procedure<br />
was performed, but as <strong>the</strong> timing of <strong>the</strong> test/procedure was often close to <strong>the</strong> start of<br />
ChEI <strong>the</strong>rapy in <strong>the</strong> majority of cases, we can assume that most tests/procedures were<br />
performed in <strong>the</strong> context of dementia diagnostic work-up.<br />
We conclude that <strong>the</strong> new proposed markers are not routinely used during <strong>the</strong> study<br />
period. According to <strong>the</strong> external experts consulted for this project <strong>the</strong>se markers, eg<br />
CSF markers, are used in selected patients and mainly in university centres. 130