None listed
Conditions
Brief summary
The Critical Illness, Inflammation, and Immunology (CI3) Biobank has been developed to improve insights into the immune mechanisms that contribute to critical illness. Our aims are to develop a world-class biospecimen repository that will support future translational research in this area. Using careful safeguards to protect patient privacy we will link a range of biological specimens to detailed demographic, diagnostic, management, and patient-reported outcome data. Working in partnership with leading researchers we hope to provide new insights into the immunobiology and inflammation in critical illnesses with a focus on identifying novel treatment strategies, improving patient care and outcomes.
Interventions
CI3 Biobank is an open biospecimen repository (biobank) created to facilitate future translational research into conditions such as sepsis, including but not limited to cellular, molecular, transcriptomic, proteomic, metabolomic and genomic projects. Potential participants will be those presenting to the participating institution/s with an infection, inflammation, or immune dysfunction-related diagnosis. Participants will be patients admitted to Intensive Care Unit. They will be separated into 3 groups based on the reason of admission to ICU. Patients with diagnosis or clinical suspicion of sepsis will be categorised to Group A and participants with any non-infective inflammation will be categorized to Group B participants. Both groups will need to have Sequential Organ Failure Assessment (SOFA) > or = 2 (SOFA score greater than or equal to 2) to be eligible for biobank inclusion. Group C is the third category of participants who will have neither any infection nor any inflammation, with SOFA score of 2 or less than 2. Potential participants will be invited directly (or through their Person Responsible) to take part in the Biobank. Consented participants will be enrolled in the Biobank by contributing their biospecimens including blood, urine, cerebrospinal fluid, bronchoalveolar lavage, stool, and tissue samples to biobank. Blood samples will be collected at 5 timepoints: Baseline, day 3, 1 month, 6 months and 12 months from ICU admission. WHODAS questionnaire will be completed by participants at 6 and 12 months. Biospecimens will be de-identified and stored securely for future studies relating to the risk factors, diagnosis, response to treatment and outcomes of inflammation driven critical illnesses. Participation into CI3 Biobank entails blood collection and completing a Health and Disability outcome using World Health Organization Disability Assessment Schedule (WHODAS) 2.0 questionnaire. Blood collection will occur at Baseline, day 3, 1 month, 6 months and 12 months from recruitment. WHODAS questionnaire will be due at 6- and 12-months post enrolment. Participants will have the option to opt out of any these milestones at any point. Participants will be categorised into 3 groups. Group A and B participants will be Admitted to Intensive Care Unit with diagnosis of infection (Group A) and non-infective inflammation (Group B) both with Sequential Organ Failure Assessment (SOFA) = 2 (greater than or equal to 2) . Group C participants are healthy (no infection and inflammation) participants with SOFA score </= 2 (less than or equal to 2) who may be in ICU or healthy volunteers.
Sponsors
Eligibility
Inclusion criteria
Inclusion Criteria • Adults (18 years of age and older) • Admitted to Intensive Care Unit with diagnosis of infection (Group A participants) or non-infective inflammation (Group B participants) with Sequential Organ Failure Assessment (SOFA) =/> 2 (Greater than or equal to 2) OR Any healthy person/volunteers with No infection or organ dysfunction (Group C) with Sequential Organ Failure Assessment (SOFA) =/< 2 (Group C participants, (less than or equal to 2) • Participant or Person Responsible able to provide consent • Biospecimens collection within 72 hours of admission
Exclusion criteria
Exclusion criteria - Age less than 18 years - Participant or Person Responsible unable to provide verbal or written consent - >72 hours of ICU admission