Vascular dementia (VaD) is the most common form of dementia after Alzheimer
's disease (AD). However, it is now increasingly recognized that not only i
s VaD a heterogeneous syndrome but also that VaD and AD are not mutually ex
clusive. Thus, the currently used criteria may no longer be sufficient for
an accurate diagnosis of VaD. In addition, although it is widely assumed th
at risk factors for vascular disease are also risk factors for VaD, the evi
dence, in most cases, is circumstantial. For the effective prevention of Va
D, therefore, large-scale and long-term clinical trials are required to inv
estigate the validity of these putative risk factors. These trials should a
lso include the VaD subtypes in their outcome measurements and to this end
a simplified classification system should be adopted. Additional large-scal
e trials are required to facilitate the secondary prevention and symptomati
c treatment of VaD, in particular to investigate the potential application
of several nootropic and neuroprotective drugs. In both cases, these clinic
al trials should aim to move the field of VaD from opinion-based medicine t
o evidence-based medicine. (C) 2001 Elsevier Science Ireland Ltd. All right
s reserved.