History

The Ontario Cohort Study builds on the successes of two previous database and infrastructure projects called the:
  • HIV Ontario Observational Database (HOOD)
  • HIV Ontario Information Infrastructure Project (HIIP)

The HIV Ontario Observational Database was:

  • Created in 1994
  • Funded by the Positive Action Fund with contributions from Burroughs-Wellcome
  • Housed at Sunnybrook Health Sciences Centre
  • Led by Anita Rachlis, Peggy Millson and Greg Robinson
  • Governed by a committee that included a majority representation of community members and people with HIV
  • Designed as a retrospective (to the last HIV negative test result or date of HIV diagnosis) and prospective (data collection every six months) study with socio-demographic and behavioural data collected at enrolment
  • A voluntary, anonymous cohort study enrolled 3,431 participants by 1999

The HIV Information Infrastructure Project was:

  • Created in 1998 with the formation of the OHTN
  • Mandated to extend HOOD to include clinical management systems to facilitate the delivery of care
  • Enhanced HOOD to improve the efficiency of data gathering through electronic data extraction
  • Transitioned HOOD to the OHTN in 2000
  • Led by Anita Rachlis and Peggy Millson until 2001 when Ahmed Bayoumi because the lead investigator
  • Governed by a committee chaired by Don Kilby with a majority representation of people with HIV
  • Expanded to include clinical management systems and an updated electronic version of HOOD (e-HOOD) in 2005.  This expansion allowed for on-site electronic data collection in clinics and offices of health care providers using paper medical charts

Each year, over 1,000 Ontarians are diagnosed with HIV - and more are infected but not yet diagnosed.