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5%) were excluded as they were not released from prison during the follow-up period due to parole rejection check details or being remanded in custody on new charges. A further 257 (19.4%) and 214 (16.2%) participants were excluded from analysis due to a complete lack of follow-up data and/or study ��exposure�� data (ie, 1-month PCP contact), respectively. The remaining participants (N=847, 63.9%) were included in the analyses. Compared with those excluded from analysis (N=478), this study sample was less likely to identify participants as Indigenous, significantly older, and was more likely to report social visits in prison, to have no history of juvenile incarceration, to screen negative for ID, to report having a postrelease supervisory order, to report current non-CNS medication use, to report a lifetime chronic condition, and to report no hepatitis C exposure (table 1). Table?1 Passports cohort characteristics overall and by current study inclusion status Follow-up interview occurrence The mean (��SD) time to each follow-up was 39 (��15), 109 (��25) and 219 (��44) days postrelease for the 1, 3 and 6-month follow-up interviews, respectively. One-month follow-up PCP contact Overall, 394 participants (46.5%) reported PCP contact prior to the 1-month follow-up interview. Participant characteristics are presented overall and according to 1-month PCP contact in table 2. The majority of the cohort was male (77.7%; n=658) and the mean (��SD) age of participants GSK J4 solubility dmso was 34.2��11.6?years. Females (57.7%) were 78.3% (p older (37.4��12.9?years) than the no-PCP-contact group (31.5��9.6?years, pS6 Kinase overall and by 1-month PCP contact status One-month follow-up PCP contact and health service utilisation Unadjusted Kaplan-Meier survival curves comparing type-specific service utilisation rates between the PCP-contact and no-PCP-contact groups are displayed in figure 1. Compared to the no-PCP-contact group, the PCP-contact group exhibited higher rates of utilisation of mental health, AOD, hospital and subsequent PCP services well beyond 180?days of follow-up, where the number of participants ��at-risk�� was still substantial. Subsequent PCP service utilisation shows a delay in incidence of approximately 90?days, as assessment began at the 3-month follow-up for this outcome (figure 1).