Table 2

Factors relating to DMT eligibility in memory clinics in North and East London and the specialist cognitive service at the National Hospital for Neurology and Neurosurgery

Entire memory clinic cohort (n=517)Site 1 (n=100)Site 2 (n=100)Site 3 (n=100)Site 4 (n=126)Site 5 (n=89)Specialist cognitive service (n=500; 177 AD included in analysis)
Dementia/AD diagnosis potentially eligible for DMT367 (71%)73 (73%)68 (68%)76 (76%)88 (70%)62 (70%)177
Formal cognitive assessment documented within 18 months482 (93%)*156 (88%)
MMSE ≥20*397 (77%)71 (71%)82 (82%)75 (75%)101 (80%)68 (76%)74 (47%)
Rockwood frailty score ≤5†320 (75%†)69 (69%)70 (70%)76 (76%)105 (83%)NA107 (60%)
Potentially eligible for DMT¶276 (53%)41 (41%)42 (42%)61 (61%)76 (60%)56 (63%)68 (38%)
Neuroimaging performed, n (%)‡388 (75%)95 (95%)50 (50%)70 (70%)85 (68%)88 (99%)177 (100%)
MRI results available, n (%)239 (46%)73 (73%)23 (23%)55 (55%)29 (23%)59 (66%)174 (98%)
Amyloid biomarkers assessed (plasma/CSF/amyloid-PET), n (%)2‡ (0.4%)0 (0%)NANANA2‡ (2%)109§ (62%)
FDG-PETNANANANANANA4 (2%)
  • *Or equivalent ACE/RUDAS.

  • †Data not available for site 5 so excluded from all proportions.

  • ‡Does not capture where imaging performed from primary care prior to referral.

  • ‡In a small proportion of memory clinics, plasma p-tau was assessed.

  • §In the specialist cognitive clinic, CSF or amyloid-PET was assessed.

  • ¶Calculated as those with potentially eligible diagnosis, MMSE ≥20 and Rockwood ≤5. Where Rockwood missing for site 5, patients were included if they had a potentially eligible diagnosis and MMSE ≥20. Those patients with only MMSE available (i.e. those without Rockwood) were excluded from the cohort described in figure 2.

  • ACE, Addenbrooke’s Cognitive Examination; AD, Alzheimer’s disease; CSF, cerebrospinal fluid; DMT, disease-modifying therapy; FDG-PET, fluorodeoxyglucose positron emission tomography; MMSE, Mini-Mental State Examination; PET, positron emission tomography; RUDAS, Rowland Universal Dementia Assessment Scale.