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. 2010 Nov 17;36(1):19–28. doi: 10.1159/000321712

Table 4.

Details of included studies

Source/condition Design Population/denominator Timescale Case ascertainment method Diagnostic method Outcome Potential bias/methodological limitations
Nath et al. (2001) [9] PSP Population-based study of prevalence 3 substudies;
  • National study: population of 59,236,500

  • North East study: population of 2,589,240

  • Community study (35 GP catchments in Newcastle-upon-Tyne): population of 259,998; populations all based on 1998 census figures for the UK

Prevalence on January 1, 1999
  • National study: case ascertainment not complete

  • Regional study: direct referral of cases from all neurologists in the region, correspondence reviews, database screening, inpatient hospital sources

  • Community study: screening of GP records for potential patients followed by review of records and structured interview and clinical examination

Possible or probable cases based on NINDS- SPSP criteria
  • National study: prevalence of 1.0/100,000

  • Regional study: prevalence of 3.1/100,000

  • Community study: prevalence of 6.5/100,000

Smaller population denominator at each level of study led to more extensive capture methods, hence the greater prevalence in smaller denomination studies; national study did not use active case ascertainment methods and thought up to 81% of cases unidentified

PSP = Progressive supranuclear palsy; GP = general practitioner; NINDS-SPSP = National Institute of Neurological Disorders and Society for Progressive Supranuclear Palsy.