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This is a prospective, observational study of patients undergoing open GI surgery. At the time of operation, samples will be collected from the incision site and GI tract. The study will follow patients up to 30 days postoperatively, monitoring for signs of SSI. Samples will be taken from all patients who develop SSI. Sequencing will be performed on a subset of samples based on our specific aims.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients undergoing open GI surgery | Patients with SSI |
| |
| Control group | age-, sex-, diagnosis-, and wound class-matched control patients without SSI |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| No intervention | Other | samples from the incision site and GI tract collected |
|
| Measure | Description | Time Frame |
|---|---|---|
| alpha diversity composition | Alpha diversity composition at the surgical incision site at multiple time points | Baseline, Day 30 post-op |
| microbial community composition | microbial community composition at the surgical incision site at multiple time points | Baseline, Day 30 post-op |
| pathogenic strain of bacteria | Pathogenic strain of bacteria at SSI compared with pathogens isolated from skin and/or GI tract microbiome | Baseline, Day 30 post-op |
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Inclusion Criteria:
Exclusion Criteria:
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adults over the age of 18 years, who are undergoing open abdominal surgery with a midline incision.
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| Name | Affiliation | Role |
|---|---|---|
| Jennifer Rickard | University of Minnesota | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Minnesota | Minneapolis | Minnesota | 55414 | United States |
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samples from the incision site and GI tract