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Pre Bypass Ultrafiltration (PBUF) in Children Requiring Cardiopulmonary Bypass (PBUF)

Primary Purpose

Congenital Heart Disease

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Use of prebypass ultrafiltration (PBUF)
Sponsored by
Boston Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congenital Heart Disease

Eligibility Criteria

1 Day - 1 Year (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients < 8 kilograms and < 1 year (to ensure that all patients receive steroids at initiation of CPB) undergoing an index cardiac operation for that hospitalization (using a single PBUF protocol)

Exclusion Criteria:

  • Patients undergoing repeat cardiac surgery within the same admission
  • Patients undergoing transplants as their index surgery
  • Patients undergoing Ventricular assist device implantation as their index surgery

Sites / Locations

  • Boston Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control

Study

Arm Description

Standard of care

PBUF used prior to Cardiopulmonary bypass

Outcomes

Primary Outcome Measures

Glucose in milligrams per deciliter (mg/dL). Normal range 61 to 199 mg/dL
Differences in glucose (mg/dl) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Sodium in milliequivalents per liter (mEq/L). Normal range 135 to 148 mEq/L
Differences in sodium (mEq/L) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Potassium in milliequivalents per liter (mEq/L). Normal range 3.2 to 4.5 mEg/L
Differences in potassium (mEq/L) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Lactate in milliequivalents per liter (mEq/L). Normal range 0.5 to 2.2 mEq/L
Differences in lactate (mEq/L) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU

Secondary Outcome Measures

Osmolality in milli osmoles per kilogram (mOsm/Kg). Normal Range 276- 295 mOsm/kg
Differences in osmolality in mOsm/Kg in final prime, first blood draw after CPB and on arrival to cardiac intensive care unit (CICU) for PBUF versus standard care.
Plasma free hemoglobin in milligrams per deciliter (mg/dL). Normal < 5 mg/dL.
Differences in plasma free hemoglobin in mg/dL in final prime, first blood draw after CPB and on arrival to cardiac intensive care unit (CICU) for PBUF versus standard care.
Inotrope use
Differences in vasoactive inotrope score between the PBUF and standard care groups at the following time points: i. Between cessation of CPB and admission to CICU as measured by vasoactive inotrope score (VIS) ii. In CICU as measure by VIS/ 24 hours for first 72 hours
Body wall edema as measured daily weights in kilograms (Kg)
Differences in body wall edema as measure by daily weights in Kg between the PBUF and standard care groups.
Body wall edema as measured daily weights in kilograms (Kg)
Differences in body wall edema as measure by daily weights in Kg between the PBUF and standard care groups.
Initial ventilation duration in days and hours
Differences in ventilation duration, Initial (days, hours) until first extubation between the PBUF and standard care groups.
Reintubation as a proportion subjects needing reintubation in each group Reintubation
Difference in proportion of subjects requiring unplanned reintubation for respiratory failure between the PBUF and standard care groups.
Total ventilation duration (days, hours)
Difference in total ventilation duration (includes all periods on the ventilator including period following unplanned reintubation for respiratory failure between the PBUF and standard care groups.
Postoperative Cardiac intensive care unit (CICU) length of stay (LOS) in days,
Difference in postoperative CICU LOS in days between the PBUF and standard care groups.
Postoperative hospital LOS
Difference in postoperative hospital LOS in days between the PBUF and standard care groups.
Composite of major adverse events (Postoperative extra corporeal membrane oxygenation (ECMO), reoperation for bleeding, reoperation for low cardiac output state, circuit clotting events) and mortality. Yes or No
Difference in proportion subjects who have a composite event between the PBUF and standard care groups.

Full Information

First Posted
May 29, 2018
Last Updated
February 14, 2022
Sponsor
Boston Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03576534
Brief Title
Pre Bypass Ultrafiltration (PBUF) in Children Requiring Cardiopulmonary Bypass
Acronym
PBUF
Official Title
Pre Bypass Ultrafiltration (PBUF) Improves Intraoperative Glucose, Sodium, Potassium and Lactate Levels in Children Requiring Cardiopulmonary Bypass
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Terminated
Why Stopped
Given SARS CoV2 pandemic, we had difficulty enrolling patients in the proposed time frame
Study Start Date
October 3, 2019 (Actual)
Primary Completion Date
September 13, 2021 (Actual)
Study Completion Date
September 13, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Children's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Newborn babies and children with congenital heart defects who need heart surgery need to be placed on the heart-lung machine for heart surgery. In order to use the heart-lung machine, the investigators have to use blood and other fluids to fill the tubing. During the operation, ultrafiltration is carried out as standard of care to remove extra fluid. Modified ultrafiltration is also performed after surgery. In this study, the investigators are looking to use the filter additionally before surgery. Using the pre bypass filtration before the subject is placed on the heart-lung machine will allow the investigators to better normalize electrolytes in the blood/fluid mixture used in the heart lung machine. This technique is called pre-bypass ultrafiltration, or PBUF (pronounced "P" Buff). The investigators are conducting a study to see if using PBUF to better normalize electrolytes in the blood will make a difference. The investigators have been adding fluids to prime the heart-lung machine in two different ways. The investigators believe both methods are safe and acceptable but hypothesize that there may be subtle differences in electrolytes and fluid status when one technique is used as opposed to the other. The investigators believe that neither technique introduces risk since both are currently used in practice. The standard method adds blood to the heart-lung machine. The alternate method adds blood to the heart-lung machine and then additional fluid is added and removed to more normalize the electrolytes. The investigators plan to randomized subjects undergoing heart surgery to receive the standard priming method versus PBUF to determine if there is any difference in outcomes. Laboratory and clinical data collected as part of clinical care will be used to determine difference sin outcomes. There will be no additional blood taken for this study. There are no known risks to PBUF. The benefits include helping investigators determine if PBUF does or does not make a difference to how subjects recover after surgery. The investigators believe that providing more normal blood values will either improve the subjects' outcome or have no benefit. The investigators do not anticipate increased risks. Given COVID -19 restrictions, the study is on hold.
Detailed Description
Research question: Can PBUF provide more physiologic values for glucose, sodium, potassium and lactate throughout the cardiopulmonary bypass period without an increased incidence of adverse events? Background: The values for glucose, sodium, potassium and lactate in blood primes for subjects weighing less than 8 kg are known to be non-physiologic. The process of priming the cardiopulmonary bypass circuit is not standardized across institutions and there are several methods used to correct for known prime value issues. The investigators documented the prime values for 20 subjects weighing less than 8 kg and then performed pre-bypass ultrafiltration (PBUF) on the prime for those same circuits to achieve more physiologic prime values. The investigators were cautious not to implement too significant of a change as the investigators assessed the technique and documented that plasma-free hemoglobin importantly did not rise and that measured osmolality was still slightly above the normal range. Study type: Prospective randomized controlled study. Hypothesis: The investigators hypothesize that pre cardiopulmonary bypass ultrafiltration (PBUF) can provide more physiologic prime values for glucose, sodium, potassium and lactate. Plasma-free hemoglobin will not increase with the technique. Osmolality will be maintained slightly above the normal range. PBUF will not negatively impact clinical outcome measures and may improve them. Specific Aim 1 To determine if use of PBUF will result in more physiologic values for glucose, sodium, potassium and lactate during and immediately after cardiopulmonary bypass. Specific Aim 2 To determine if PBUF can be achieved with no increase in plasma free hemoglobin while maintaining plasma osmolality within acceptable range during and immediately after cardiopulmonary bypass. Specific Aim 3 To determine if use of PBUF will result in improved clinical outcomes after surgery on cardiopulmonary bypass. Randomization: Prior to surgery, subjects will be randomized to one of the two study groups using a randomly permuted blocks design. Statistical analysis: Analyses will be performed on an intention to treat basis. Comparisons of subject characteristics and outcomes will be made using the two-sample t test or Wilcoxon rank sum test for continuous variables, and Fisher's exact test for categorical variables. If imbalances in patient factors exist between the two groups, linear and logistic regression will be used to compare outcomes for the groups adjusting for these potential confounders. Sample size calculation: Sample size is calculated for comparisons of subjects in the normal range of values for the PBUF and standard care groups. This will be done separately for glucose, sodium, potassium, and lactate; each comparison will be performed at the 0.0125 level of significance. If 70% of standard care subjects are in the normal range versus 90% of PBUF subjects, a total of 176 subjects (88 per group) would be required to achieve 80% power. With 350 eligible subjects that meet inclusion criteria based on 2017 numbers and 75% consent rate the investigators will be able to enroll 260 subjects in 1 year. Given COVID-19 restrictions, the study is on hold.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized Control Trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard of care
Arm Title
Study
Arm Type
Active Comparator
Arm Description
PBUF used prior to Cardiopulmonary bypass
Intervention Type
Other
Intervention Name(s)
Use of prebypass ultrafiltration (PBUF)
Intervention Description
In addition to standard of care for cardiopulmonary bypass, in the study arm prebypass ultrafiltration will be performed.
Primary Outcome Measure Information:
Title
Glucose in milligrams per deciliter (mg/dL). Normal range 61 to 199 mg/dL
Description
Differences in glucose (mg/dl) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Time Frame
12 hours
Title
Sodium in milliequivalents per liter (mEq/L). Normal range 135 to 148 mEq/L
Description
Differences in sodium (mEq/L) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Time Frame
12 hours
Title
Potassium in milliequivalents per liter (mEq/L). Normal range 3.2 to 4.5 mEg/L
Description
Differences in potassium (mEq/L) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Time Frame
12 hours
Title
Lactate in milliequivalents per liter (mEq/L). Normal range 0.5 to 2.2 mEq/L
Description
Differences in lactate (mEq/L) at the following time points, and also differences in the percentage of values within the normal range for each time point, for PBUF versus standard care. Final prime value (in the PBUF group after completion of PBUF and prior to cardio pulmonary bypass (CPB), in the control group prior to CPB) First measured levels on bypass - typically 10 minutes post initiation of bypass Last value on CPB Last value in OR First arrival to ICU
Time Frame
12 hours
Secondary Outcome Measure Information:
Title
Osmolality in milli osmoles per kilogram (mOsm/Kg). Normal Range 276- 295 mOsm/kg
Description
Differences in osmolality in mOsm/Kg in final prime, first blood draw after CPB and on arrival to cardiac intensive care unit (CICU) for PBUF versus standard care.
Time Frame
12 hours
Title
Plasma free hemoglobin in milligrams per deciliter (mg/dL). Normal < 5 mg/dL.
Description
Differences in plasma free hemoglobin in mg/dL in final prime, first blood draw after CPB and on arrival to cardiac intensive care unit (CICU) for PBUF versus standard care.
Time Frame
12 hours
Title
Inotrope use
Description
Differences in vasoactive inotrope score between the PBUF and standard care groups at the following time points: i. Between cessation of CPB and admission to CICU as measured by vasoactive inotrope score (VIS) ii. In CICU as measure by VIS/ 24 hours for first 72 hours
Time Frame
72 hours
Title
Body wall edema as measured daily weights in kilograms (Kg)
Description
Differences in body wall edema as measure by daily weights in Kg between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.
Title
Body wall edema as measured daily weights in kilograms (Kg)
Description
Differences in body wall edema as measure by daily weights in Kg between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge) , an average of 15 days.
Title
Initial ventilation duration in days and hours
Description
Differences in ventilation duration, Initial (days, hours) until first extubation between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.
Title
Reintubation as a proportion subjects needing reintubation in each group Reintubation
Description
Difference in proportion of subjects requiring unplanned reintubation for respiratory failure between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.
Title
Total ventilation duration (days, hours)
Description
Difference in total ventilation duration (includes all periods on the ventilator including period following unplanned reintubation for respiratory failure between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.
Title
Postoperative Cardiac intensive care unit (CICU) length of stay (LOS) in days,
Description
Difference in postoperative CICU LOS in days between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.
Title
Postoperative hospital LOS
Description
Difference in postoperative hospital LOS in days between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.
Title
Composite of major adverse events (Postoperative extra corporeal membrane oxygenation (ECMO), reoperation for bleeding, reoperation for low cardiac output state, circuit clotting events) and mortality. Yes or No
Description
Difference in proportion subjects who have a composite event between the PBUF and standard care groups.
Time Frame
Through study completion (until hospital discharge), an average of 15 days.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients < 8 kilograms and < 1 year (to ensure that all patients receive steroids at initiation of CPB) undergoing an index cardiac operation for that hospitalization (using a single PBUF protocol) Exclusion Criteria: Patients undergoing repeat cardiac surgery within the same admission Patients undergoing transplants as their index surgery Patients undergoing Ventricular assist device implantation as their index surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Meena Nathan, MD, MPH
Organizational Affiliation
Boston Children's Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Boston Children's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Pre Bypass Ultrafiltration (PBUF) in Children Requiring Cardiopulmonary Bypass

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