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The purpose of this study is to better understand if transesophageal echocardiography during cardiac surgery can predict problems with kidney function after cardiac surgery.
Informed consent will be obtained prior to surgery. Preoperative demographic and baseline clinical data will be collected. We will assess the patient's risk of postoperative AKI using the validated Cleveland clinic score based on preoperative risk factors and calculate the European System Operative Score Risk Evaluation score (EuroSCORE II). After standard anesthesia induction and intubation, a TEE probe will be inserted by a cardiac anesthesiologist, who is certified in intraoperative echocardiography. We will use a standard ultrasound machine (EPIQ 7 Philips;Philips, Bothell, WA). Images of the right or left kidney along with Doppler flow and velocities will be obtained prior to cardiopulmonary bypass (CPB), after CPB, and after chest closure. Images of the portal vein with Doppler flow and velocity will be obtained prior to CPB, after CPB, and after chest closure. Vitals signs and hemodynamic data will be collected concurrently during these times. (See Data Sheet) Concurrent ECG will be obtained to identify the phases of the cardiac cycle. Mean arterial pressure (MAP) will be maintained within 20% of baseline MAP with bolus or continuous infusion of vasopressors (phenylephrine, norepinephrine, epinephrine, vasopressin, ephedrine). Cardiopulmonary bypass management will be standard, with target systemic blood flow of 2.4L/min/m2. Postoperative data will include urine output, serum creatinine, calculated GFR (using Modification of Diet in Renal Disease [MDRD] method) hospital and ICU length of stay, and 30-day mortality.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Upcoming cardiac surgery | Subjects in this group will have an upcoming cardiac surgery with the use of cardiopulmonary bypass and no pre-existing renal insufficiency or failure |
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| Measure | Description | Time Frame |
|---|---|---|
| Portal vein pulsatility | Pulsed-wave Doppler measurement of portal vein flow and portal hypertension | intra-operative measurement |
| Measure | Description | Time Frame |
|---|---|---|
| Renal resistance index | A sonographic index to assess for renal arterial disease measured via pulsed-wave Doppler | intra-operative measurement |
| ICU length of stay | Length of ICU stay at any point for 30 days post-operation will be recorded |
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Inclusion Criteria:
Exclusion Criteria:
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Subjects will be included who are scheduled for a standard of care cardiac surgery with the use of cardiopulmonary bypass at the University of Chicago Medical Center who meet the study's inclusion and exclusion criteria.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Chicago | Chicago | Illinois | 60637 | United States |
Individual participant data will not be shared
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| 30 days post-operation |
| Hospital length of stay | Length of Hospital stay up to 30 days post-operation will be recorded | 30 days post-operation |
| 30-day mortality | Standard measure post | 30 day post-operation |