None listed
Conditions
Brief summary
Up to 80% of people discharged from the ICU experience various physical, cognitive, and/or psychological complications and enduring impairment, termed ‘post intensive care syndrome’ (PICS). The prevalence and burden of PICS remains uncertain, and current interventions are not effective longer-term; further research into prevention, early diagnosis and intervention of this syndrome is considered internationally is a priority. The interlinked aims of this study are 1. To describe the predictors, correlates and prevalence of PICS, and 2. To use this information to develop screening, diagnostic and outcome measures for use in research and clinical practice.
Interventions
Discharged from a participating ICU - Participants contacted via preferred method (telephone, email, post) at 6 weeks and 6 months post ICU discharge. - At both timepoints, participants complete validated self-reported measures for physical & cognitive function, as well as depression, anxiety and PTSD symptoms. - A retrospective electronic medical record audit is conducted for all participants that complete at least 6 week follow-up measures described above. - The medical record audit will collect demographic information, presenting complaint, ICU length of stay, APACHE score, Charlston Comorbidity Index, results of delirium screening measures, as well as hospital codes for icu complications as well as readmissions between the date of discharge, and the date 6 month follow-up was due.
Sponsors
Eligibility
Inclusion criteria
People discharged from participating ICUs will be eligible to participate if they are: • Aged 18 years or over • Residing in Australia • Sufficiently fluent in English to complete recruitment and data collection processes (assessed at time of seeking permission to contact 6 weeks post discharge) • Provide consent to collection of data from their medical records AND at least partial data from questionnaires at 6 weeks post ICU discharge.
Exclusion criteria
• Patients whose life expectancy at discharge is estimated by their clinical team to be less than 12 months • Age <18 years • Unable or unwilling to provide consent to participate for the duration of the study • Provide consent, but do not provide data at 6 weeks post ICU discharge