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Safety and Efficacy of Acute Normovolemic Hemodilution in Pediatric Cardiac Surgery Patients

The Efficacy and Safety of Acute Normovolemic Hemodilution in Pediatric Cardiac Surgery Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02751645
Enrollment
24
Registered
2016-04-26
Start date
2016-06-30
Completion date
2020-05-31
Last updated
2019-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Defect

Keywords

Pediatric, Cardiac, Surgery

Brief summary

The investigators primary objective is to determine if acute normovolemic hemodilution (ANH) for pediatric cardiac surgical patients decreases the volume of blood products transfused during surgery and the immediate post-operative period as compared to usual care. This study will enroll 24 pediatric heart surgery patients, aged 6 months to 3 years old undergoing either ANH prior to initiating cardiopulmonary bypass or the standard of care procedures for the use of cardiopulmonary bypass.

Detailed description

Blood transfusion has been associated with worse outcomes in pediatric cardiac surgical patients. The major complications associated with it include increased blood loss during and after surgery, kidney disease requiring dialysis, abnormal coagulation profile, increased vasopressor use, and increased time spent on the ventilator and in the intensive care unit. One strategy to minimize blood product administration is acute normovolemic hemodilution (ANH). The investigators primary aim is to determine if ANH for pediatric cardiac surgical patients decreases the volume of blood products transfused during surgery and the immediate post-operative period, compared to usual care. The investigators designed a randomized, controlled, open label study that equally assigns 24 pediatric cardiac surgery patients aged 6 months to 3 years into two groups to receive either ANH prior to initiating cardiopulmonary bypass or usual standard of care. Participants in the ANH arm of the study will have 10 ml/kg of blood removed following anesthetic induction. In order to maintain normal circulating volume, the collected blood will be replaced with an equal volume of 5% albumin. All participants will be treated with a standardized protocol aimed at blood conservation including the use of retrograde arterial and antegrade venous perfusion, small circuit size, intraoperative red blood cell salvage, and low hemoglobin targets to trigger transfusion.

Interventions

ANH is a technique in which a portion of the patients' own blood is removed before any surgical bleeding occurs. It is stored until the end of the operation, at which point it is returned to the patient.

Sponsors

The Gerber Foundation
CollaboratorOTHER
Oregon Health and Science University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 3 Years
Healthy volunteers
No

Inclusion criteria

* Informed signed consent must be obtained by a legally authorized representative. * Must be undergoing an elective surgical repair or palliation of a cardiac defect with the use of the cardiopulmonary bypass machine. * Must be clinically stable at the time of evaluation for eligibility and on the day of randomization.

Exclusion criteria

* Patients who carry a diagnosis of a bleeding disorder. * Patients who have an abnormal coagulation profile as evidenced by a preoperative coagulation screen. * Patients who have received a blood transfusion in the preceding 120 days. * Patients who have a diagnosis of a chromosomal abnormality. * Patients whose participation in the study is deemed unsafe by their primary care team.

Design outcomes

Primary

MeasureTime frameDescription
Effectiveness of ANH to decrease volume of blood products during surgery and the immediate post-operative period.2 DaysThis will be measured by comparing the volume (mL/Kg body weight) of any blood products administered peri-operatively between the two groups.

Secondary

MeasureTime frameDescription
Kidney function2 daysThis will be measured by the change in creatinine on postoperative day 2 from the pre-operative baseline value
Normalization of thromboelastogrpahy (TEG) MA value (maximum amplitude)2 daysThis will be measured by thromboelastography (TEG) test following end of cardiopulmonary bypass
Normalization of thromboelastography (TEG) R value (reaction time)2 daysThis will be measured by thromboelastography (TEG) test following end of cardiopulmonary bypass
Duration of mechanical ventilation and ICU stay8 daysThis value will be recorded and compared for each group.
Final hematocrit, platelet count, PT/PTT on ICU admission1 dayThese lab values will be recorded and compared for each group.
Hematocrit and platelet count on post-operative day 11 daysThese lab values will be recorded and compared for each group.
Time to end of vasoactive support in the first 24 hours post-operation.1 daysThis value will be recorded and compared for each group.
Normalization of thromboelastography (TEG) Alpha Angle value2 daysThis will be measured by thromboelastography (TEG) test following end of cardiopulmonary bypass

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026