For this study, we selected all participants who entered the SHCS between 1 January 1996 and 31 December 2008. The seven SHCS centres, 13 affiliated hospitals and 33 private collaborating physicians from all regions of the country were addressed in formal correspondence to provide aggregated (i.e. unidentifiable) numbers of HIV-positive persons not participating in the SHCS during their first clinical visit in 2008. Collected information

included geographical region of origin, gender, injecting drug use (IDU) and whether the patient was on ART. After two rounds of reminders via email and/or telephone, the response rate was 40 of 53 (75%) clinics or private physicians, and those that responded included all seven SHCS centres and all large institutions providing HIV care. Among participants not known to have died, we defined LTFU as no further cohort visit during at least 1 year after the last visit. selleck chemicals llc We distinguished seven geographical regions of patients’ origin SB203580 clinical trial according to an adopted UNAIDS classification of nationalities [15]. Because of the small numbers of persons in care and their similar

demographic characteristics, we merged the Caribbean and Latin America into one region and combined the USA, Canada, Australia and New Zealand with northwestern Europe. Thus, the regions were: (1) Northwestern countries (Switzerland, Andorra, Austria, Belgium, Denmark, Finland, France, Germany, the UK, Iceland, Ireland, Liechtenstein, Luxemburg, Monaco, the Netherlands, Norway, Sweden, USA, Canada, Australia and New Zealand); (2) sub-Saharan Africa; (3) Southern Europe (Spain, Portugal, Italy, Greece, Malta and San Marino); (4) Latin America/Caribbean; (5) Southeastern Asia; (6) Eastern Europe/Central Asia; and (7) Northern Africa/Middle East. The SHCS collects information on ethnicity, categorized as White, Black, Asian and Hispano-American. Because there was a congruent picture between nationality and ethnicity in five out

of the seven regions described above (>96% of participants), we did not analyse the data for ethnicity separately. Demographic and clinical characteristics at inclusion were analysed for three calendar periods (1996–1999, 2000–2003 and 2004–2008) to determine trends over time. Methane monooxygenase Cox proportional hazards models were fitted to examine the effects of region of origin, gender, age, education, IDU, clinical HIV disease stage and treatment status on the probability of ceasing to participate in the SHCS. CD4 cell count was also fitted as a time-updated covariable. Because of evidence of an interaction [likelihood ratio test (LRT) P<0.001] between region of origin and gender, we analysed the risk for LTFU separately for women and men. Data from the survey on SHCS participation were analysed using logistic regression. Because the group of former participants was very small (3.