Antegrade Autologous Blood Reinfusion After CPB
Condition(s) studied
Investigational drug(s) / intervention(s)
Antegrade Pump Blood Reinfusion: Adult patients undergoing cardiac surgery with cardiopulmonary bypass in whom antegrade pump blood reinfusion is performed at the end of bypass using the crystalloid chase technique, as part of routine clinical practice.
No Anterograde Pump Blood Reinfusion: Adult patients undergoing cardiac surgery with cardiopulmonary bypass in whom anterograde pump blood reinfusion is not performed at the end of bypass. Standard institutional clinical management is applied.
Study summary
This prospective observational study aims to evaluate the effect of antegrade pump blood reinfusion using the crystalloid "chase" technique on postoperative transfusion requirements in adult patients undergoing cardiac surgery with cardiopulmonary bypass. At the end of cardiopulmonary bypass, blood remaining within the cardiopulmonary bypass circuit is reinfused antegradely through the arterial line using a crystalloid chase, without collection or storage. Blood remaining within the bypass circuit after surgery represents a valuable source of autologous blood, and its reinfusion may contribute to perioperative blood conservation strategies. Patients receiving antegrade pump blood reinfusion via the chase technique will be compared with those managed without reinfusion, without any intervention by the investigators. The primary outcome is postoperative blood transfusion requirement.
Eligibility
Primary outcome measure(s)
- Postoperative Blood Transfusion Requirement — From the end of surgery to 24 hours postoperatively
Incidence of allogeneic blood transfusion within the first 24 hours after surgery.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Kocaeli City Hospital | Kocaeli | Izmit | Recruiting |
More Kocaeli City Hospital trials in Turkey
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07420582 on ClinicalTrials.gov ↗ ← All trials in Turkey