The ICON Study: Long-Term Outcomes for ICU Survivors
Author Information
Author(s): Griffiths John A, Morgan Kayleigh, Barber Vicki S, Young J Duncan
Primary Institution: ICS Trials Group, Kadoorie Centre, John Radcliffe Hospital
Hypothesis
What are the long-term health-related quality of life and psychological outcomes for survivors of intensive care treatment?
Conclusion
The ICON study aims to provide comprehensive data on the long-term physical and psychological health of ICU survivors in the UK.
Supporting Evidence
- The study will assess health-related quality of life using validated tools like the SF-36 and EQ-5D.
- Anxiety and depression will be measured using the Hospital Anxiety and Depression Scale (HADS).
- PTSD symptoms will be evaluated with the PTSD Civilian Checklist (PCL-C).
- The study aims to recruit at least 1000 survivors per year, making it the largest prospective cohort study of its kind.
Takeaway
This study is like a big check-up for people who have been in intensive care, to see how they feel and live after they leave the hospital.
Methodology
A multi-centre, longitudinal study assessing health-related quality of life, anxiety, depression, and PTSD symptoms at 3, 6, and 12 months post-ICU discharge.
Potential Biases
There are many potential sources for bias due to the non-randomized nature of the study.
Limitations
The study may face challenges in participant recruitment and potential biases due to its non-randomized design.
Participant Demographics
Participants will be recruited from 20–30 ICUs in the UK, including adults who have experienced at least 24 hours of ICU care.
Digital Object Identifier (DOI)
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