Oxygen Consumption-based Assessments of Hemodynamics in Neonates Following Congenital Heart Surgery (Oxy-CAHN Study)

Study Results

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-12-31

Study Completion Date

2019-01-29

Brief Summary

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The purpose of the Oxy-CAHN study is to improve the monitoring capabilities of newborn infants recovering from congenital heart surgery. Currently, we utilize important but unsophisticated measures, such as vital signs and lactate measurements, to monitor these patients. Although they are useful in categorizing patients as well or unwell, these signs currently lack the power quantify a patient's risk for cardiac arrest. More to the point, they are mostly indirect measures of what we really are assessing, which is tissue oxygen delivery.

Our group has signiﬁcant expertise with devices which quantify the amount of oxygen that a baby consumes every minute. Historically, these values are more commonly used in combination with other measures to assess nutritional and metabolism status. In critically ill patients, however, the volume of oxygen consumed by a patient may be limited by the amount of oxygen their circulation delivers. This may represent a critical relationship, which has been previously described, but not exploited for the purpose of identifying patients with critically low oxygen delivery.

The aims of this study are therefore (1) to demonstrate that oxygen consumption can be safely and precisely measured continuously in newborns undergoing one of two common congenital heart surgeries, (2) to determine whether postoperative circulatory failure is associated with a precedent change in oxygen consumption, and (3) to determine whether the addition of the oxygen-based measurements (including oxygen consumption and venous oxygen saturations) to standardly measured parameters will add power in predicting which patients will experience postoperative circulatory failure.

If successful, this study may improve our capacity to non-invasively and continuously monitor patients following the highest risk congenital heart surgeries, and in the future,to create an algorithm which quantiﬁes a patients risk for having a cardiac arrest. This may permit providers to intervene on these patients earlier, improving the morbidity and mortality associated with congenital heart disease.

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Detailed Description

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Conditions

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Transposition of the Great Vessels Hypoplastic Left Heart Syndrome Oxygen Consumption Based Assessment of Hemodynamics

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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HLHS

Patients undergoing palliative repair.

Group Type EXPERIMENTAL

General Electric Healthcare E-COVX Gas Monitoring Module for VO2 Measurments

Intervention Type DEVICE

Breath to breath VO2 measurements

Edwards Continuous SVO2 Catheter and Monitoring System - 4.5 fr

Intervention Type DEVICE

Edwards continuous SVO2 measurement system

TGA

Surgical repair of TGA.

Group Type ACTIVE_COMPARATOR

General Electric Healthcare E-COVX Gas Monitoring Module for VO2 Measurments

Intervention Type DEVICE

Breath to breath VO2 measurements

Edwards Continuous SVO2 Catheter and Monitoring System - 4.5 fr

Intervention Type DEVICE

Edwards continuous SVO2 measurement system

Interventions

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General Electric Healthcare E-COVX Gas Monitoring Module for VO2 Measurments

Breath to breath VO2 measurements

Intervention Type DEVICE

Edwards Continuous SVO2 Catheter and Monitoring System - 4.5 fr

Edwards continuous SVO2 measurement system

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients from birth to 6 months of age
2. HLHS AND no prior operations AND planned S1P or HPOR d-TGA/IVS AND planned ASO
3. Written parental informed consent

Exclusion Criteria

1. Weight \< 2 kg
2. Disease speciﬁc A. HLHS patients: Infants whose surgical plan includes a neonatal biventricularrepair will be excluded.

B. d-TGA/IVS patients: Newborns with any additional cardiac defect other than an atrial septal defect will be excluded.
3. Patients on ECMO preoperatively
4. Clinically signiﬁcant tracheo-esophageal ﬁstula or known preoperative air leak

Minimum Eligible Age

1 Day

Maximum Eligible Age

6 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No