The use of near infrared spectroscopy (NIRS) is a technique that has recently been incorporated by several other surgical specialties to measure tissue perfusion, such as in plastic surgery to allow for earlier detection of free flap vascular compromise in the postoperative monitoring protocol, with promising outcomes. IntraOx is a handheld oximeter that uses NIRS to measure tissue oxygen saturation and that has been used as an alternative to indocyanine green (ICG) to assess bowel perfusion in colorectal anastomotic cases. IntraOx is a promising technology that is also sterile and easy to use that can be incorporated into congenital heart surgery procedures to evaluate myocardial perfusion in a time sensitive manner. This technology could also be used on the liver to assess systemic perfusion as another indicator of cardiac function, in conjunction with the intraoperative transesophageal echocardiography (TEE). This could provide more concrete data about not only myocardial perfusion, but systemic perfusion as well. This data could be critical to help surgeons make surgical decisions and may help to improve patient outcomes. This will be a prospective review of the use of the Intra.Ox device during cardiac surgery at different timepoints during the procedure to assess perfusion. This device is FDA-approved for use in adults but not approved for use in children and will be investigational in children. The primary objective of this study is to test whether the Intra.Ox (Vioptix Inc.) using near-infrared spectroscopy to measure tissue oxygen saturation can be used to evaluate myocardial and visceral perfusion at different time points during complex congenital heart surgery, and particularly those involving coronary artery manipulation such as patients undergoing arterial switch operations or stage 1 palliation for hypoplastic left heart syndrome. The investigators would also use this device on the liver to assess systemic perfusion. The secondary objective is to evaluate whether the investigators would be able to use the information from the Intra.Ox device to make clinical decisions that can improve patient outcomes.
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Oxygen saturation
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Liver function test: ALP
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Liver Function Test: AST
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Liver function Test: ALT
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Cardiac function
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Kidney function
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Mortality and major complications
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Lactate
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
pH
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Blood gas: PaO2
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Blood Gas: PaCO2
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Bicarbonate
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Echocardiography qualitative descriptions
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation
Lactate
Timeframe: Day 0 ("baseline") up to 2 weeks post-operation