Critical Illness, Trauma
Conditions
Keywords
trauma, critical illness, injury
Brief summary
The purpose of this research study is to gather clinical and biologic information from severely injured patients to better understand and characterize the host response to injury and inflammation across several domains. This information may improve outcome prediction, improve clinical treatment of injured patients, and permit the construction of non-biologic computerized models of illness that can be utilized to represent the host response in future research efforts. This study is designed as the calibration of a mathematical model of this response with predictive capabilities. The central hypothesis governing this study is that adaptive immune elements are crucial to determining the outcome of complex inflammatory scenarios. We propose to test these hypotheses in the following interrelated Specific Aims: Specific Aim 1: To develop a robust mathematical model describing trauma/hemorrhage-induced inflammation in humans, its pathologic consequences, and possible therapies. Specific Aim 2: To translate the mathematical model to humans and create software aimed at individualized clinical decision-making. Specific Aim 3: To determine the prevalence of an IL-1 receptor-associated kinase (IRAK-1) variant haplotype located on the X-chromosome in an injured population, and to characterize differences in the pro-inflammatory response across gender, relative to the IRAK-1 haplotype. Specific Aim 4: To determine if increased arginase activity previously observed in isolated peripheral blood mononuclear cells of trauma patients is a consequence of the presence of contaminating activated granulocytes or a particular subset of an arginase positive monocyte subset.
Interventions
None listed
Sponsors
National Institute of General Medical Sciences (NIGMS)
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Trauma patient cohort inclusion criteria: * Present for treatment of their acute, blunt or penetrating injuries to the University of Pittsburgh Medical Center within 6 hours of injury * Age greater than or equal to 18 years * Intact cervical spinal cord * Are admitted to the Intensive Care Unit Trauma patient cohort
Exclusion criteria
* Anticipated survival \< 24 hrs * Anticipated survival \< 28 days due to pre-existing condition * Traumatic Brain injury (GCS ≤8 after ICU admission) AND brain CT abnormality within 12 hr of injury * Inability to obtain consent from the subject or their legally authorized representative. * Pre-existing immunosuppression * Transplant recipient * Chronic high doses of steroids (\>20 mg prednisone equivalents/day) * Significant likelihood of high dose steroids (e.g. spinal cord injury) * Oncolytic drug(s) therapy within the past 14 days * Known HIV positive status and CD4 count \< 200 cells/mm3 * Admission to the ICU primary for substance withdrawal. * Inability to obtain 1st blood sample within 24 hours of injury. Healthy volunteer cohort inclusion: * Age greater than or equal to 18 years * Weight \> 110 pounds * no recent illness or infection in the last two weeks * no recent hospitalization or trauma in the last month Healthy volunteer cohort exclusion: * wt \< 110 lbs * infection or illness in the last two weeks * Hospitalization or trauma in the last month
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Multiple Organ Failure | 48 hours |
Countries
United States
Contacts
Primary ContactStacy D Stull, MS
Outcome results
None listed