Sepsis Clinical Trial
— GAPPSSOfficial title:
Genotypes and Phenotypes in Pediatric SIRS and Sepsis (GAPPSS)
Verified date | April 2018 |
Source | Seattle Children's Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this investigation is to longitudinally quantify host gene expression and serum proteins in children with infectious and non-infectious SIRS. The investigators hypothesize that children with non-infectious SIRS, with bacterial infection associated SIRS, or with viral infection associated SIRS will exhibit distinct patterns of host gene expression and serum proteins. The investigators further hypothesize that it should be possible to discover sets of mRNA or protein biomarkers that will permit unambiguous diagnosis of non-infectious SIRS, SIRS associated with bacterial infection, and SIRS associated with viral infection.
Status | Completed |
Enrollment | 104 |
Est. completion date | December 31, 2017 |
Est. primary completion date | December 31, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 38 Weeks to 18 Years |
Eligibility |
A. INSI group: systemic inflammation, in the absence of culture positive infection. Cardiac
surgery patients, n=30. Inclusion Criteria: - Admission to the CICU AND - Age ~1-18 years AND - Weight exceeding 10 kg - Vascular catheter capable of providing the blood draw or anticipated orders for venipuncture for clinical labs AND - Status post open heart surgery requiring cardiopulmonary bypass AND - Parents speak English AND - Not previously enrolled in the GAPPSS investigation Exclusion Criteria: - Pre- or post-operative culture positive infection OR - Not expected to survive the CICU stay OR - Ward of the state OR - Concurrent malignancy or autoimmune disorder B. CSSS (Clinical Severe Sepsis Syndrome) group: systemic inflammation, in the presence of highly suspected or documented bacterial infection. Children with clinical severe sepsis, n = 40. In this group, the investigators will enroll children who are immunocompetent as well as children who are immunocompromised. Inclusion Criteria: - Admitted to the PICU AND - Age newborn (>38 weeks EGA)-18 years AND - Weight equal to or greater than 4 kg AND - Vascular catheter capable of providing the blood draw or anticipated orders for venipuncture for clinical labs AND - At least one organ dysfunction (severe sepsis) AND - Parents speak English AND - SIRS (systemic inflammatory response syndrome) AND - Strongly suspected or documented source of infection - Not previously enrolled in the GAPPSS investigation Exclusion Criteria: - PICU nosocomial primary infection accounting for the sepsis event - Not expected to survive the PICU stay - Ward of the state C. Viral Infection group. Severe respiratory dysfunction in the presence of PCR -documented viral infection. Children with clinical severe viral sepsis, n=6. In this group, the investigators will enroll children who are immunocompetent as well as children who are immunocompromised. Inclusion Criteria: - Admitted to the PICU AND - Age newborn (>38 weeks EGA)-18 years AND - Weight equal to or greater than 4 kg AND - Vascular catheter capable of providing the blood draw or anticipated orders for venipuncture for clinical labs AND - Parents speak English AND - Severe respiratory dysfunction requiring invasive or non-invasive positive pressure mechanical ventilation support AND - Positive PCR verifying a viral infection - Not previously enrolled in the GAPPSS investigation Exclusion Criteria: - PICU nosocomial primary infection accounting for the sepsis event - Not expected to survive the PICU stay - Ward of the state |
Country | Name | City | State |
---|---|---|---|
United States | Seattle Children's Hospital | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
Seattle Children's Hospital | Immunexpress |
United States,
Mathias B, Mira JC, Larson SD. Pediatric sepsis. Curr Opin Pediatr. 2016 Jun;28(3):380-7. doi: 10.1097/MOP.0000000000000337. Review. — View Citation
McHugh L, Seldon TA, Brandon RA, Kirk JT, Rapisarda A, Sutherland AJ, Presneill JJ, Venter DJ, Lipman J, Thomas MR, Klein Klouwenberg PM, van Vught L, Scicluna B, Bonten M, Cremer OL, Schultz MJ, van der Poll T, Yager TD, Brandon RB. A Molecular Host Resp — View Citation
Weiss SL, Fitzgerald JC, Pappachan J, Wheeler D, Jaramillo-Bustamante JC, Salloo A, Singhi SC, Erickson S, Roy JA, Bush JL, Nadkarni VM, Thomas NJ; Sepsis Prevalence, Outcomes, and Therapies (SPROUT) Study Investigators and Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network. Global epidemiology of pediatric severe sepsis: the sepsis prevalence, outcomes, and therapies study. Am J Respir Crit Care Med. 2015 May 15;191(10):1147-57. doi: 10.1164/rccm.201412-2323OC. Erratum in: Am J Respir Crit Care Med. 2016 Jan 15;193(2):223-4. — View Citation
Zimmerman J, Sullivan E, Sampson D, McHugh L, Yager T, Seldon T. 1024: Sensitive and Specific Diagnosis of Sepsis in Critically Ill Children Utilizing Host Gene Expression. Critical Care Medicine 2015; 43 (12), 258. doi: 10.1097/01.ccm.0000474855.13970.46
Zimmerman JJ, Sullivan E, Yager TD, Cheng C, Permut L, Cermelli S, McHugh L, Sampson D, Seldon T, Brandon RB, Brandon RA. Diagnostic Accuracy of a Host Gene Expression Signature That Discriminates Clinical Severe Sepsis Syndrome and Infection-Negative Sys — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Gene Expression Levels | Gene expression levels (quantitative) will be compared between CSSS, INSI and viral infection groups, in a search for signatures that can discriminate these groups | Day 1 of admission to the pediatric intensive care unit (PICU) | |
Secondary | Serum Protein Expression Profiles | Serum protein expression profiles (semi-quantitative) will be compared between CSSS and INSI groups, in a search for signatures that can discriminate the two groups | Day 1 of admission to the pediatric intensive care unit (PICU) |
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