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Hemodiafiltration-A Technique for Physiological Correction of Priming Solution in Pediatric Cardiac Surgery: An In
Pankaj Garg1, Arvind Kumar Bishnoi1, Kartik Patel1
1Department of Cardiovascular and Thoracic Surgery, U. N. Mehta Institute of Cardiology and Research Center and B.J. Medical College, New Civil Hospital, Ahmedabad, 380016, Gujarat, India.
Insights
Hemodiafiltration effectively corrects metabolic abnormalities in stored packed red blood cells (PRBCs) used for pediatric cardiopulmonary bypass (CPB) priming. This method rapidly restores physiological balance, improving patient safety during CPB procedures.
Area of Science:
- Biomedical Engineering
- Cardiovascular Surgery
- Transfusion Medicine
Background:
- Pediatric cardiopulmonary bypass (CPB) requires priming with packed red blood cells (PRBCs).
- Stored PRBCs have unphysiological metabolic compositions that worsen with storage duration.
- Correcting these metabolic abnormalities before CPB is recommended.
Purpose of the Study:
- To test if hemodiafiltration of the prime with 0.45% saline can reduce metabolic load and achieve a physiological state.
- To compare hemodiafiltration with direct removal and ultrafiltration for correcting metabolic abnormalities in PRBCs.
Main Methods:
- An in vitro study using 45 neonatal CPB circuits primed with 100 mL of PRBCs (3-20 days storage).
- Circuits were divided into three groups: direct removal, ultrafiltration, and hemodiafiltration.
- Blood gas analyses were performed before and after crystalloid removal.
Main Results:
- Both direct removal and ultrafiltration significantly reduced the metabolic load (P < 0.001) but did not reach physiological levels.
- Hemodiafiltration significantly improved metabolic parameters (lactate, pH, bicarbonates) to near physiological ranges (P < 0.001).
- Sodium and potassium levels also shifted significantly towards physiological ranges with hemodiafiltration (P < 0.001).
Conclusions:
- Hemodiafiltration is a simple, efficient, and rapid method for correcting biochemical parameters in stored PRBCs.
- This technique effectively reduces the metabolic load of PRBCs towards physiological levels before CPB initiation.
- Hemodiafiltration enhances the safety and efficacy of pediatric CPB by optimizing the blood prime composition.
Abstract:
Pediatric cardiopulmonary bypass (CPB) circuit invariably requires priming with packed red blood cells (PRBCs). Metabolic composition of stored PRBCs is unphysiological and becomes worse with increasing duration of storage. It is recommended to correct these abnormalities before initiation of CPB. We tested the hypothesis that hemodiafiltration of the prime with 0.45% saline is sufficient for reducing the metabolic load and reaching a physiologic state. In an in vitro study, 100 mL of blood each from 45 units of PRBCs stored for 3-20 days were used for priming the 45 neonatal CPB circuits. Based upon the method used for removal of excess crystalloid from the prime, circuits were divided into three groups. Group 1: Direct removal through manifold line. Group 2: Ultrafiltration of prime. Group 3: Hemodiafiltration of the prime. Blood gas analyses were obtained from the PRBCs and from the prime before and after removal of crystalloid. Both direct removal of crystalloid and ultrafiltration resulted in significant reduction in biochemical and metabolic load of blood (P < 0.001). However, the final composition of the prime was far from being physiological. Hemodiafiltration resulted in improvement of metabolic parameters to near physiological range (lactate: 33.8 ± 4.44 vs. 14 ± 2.53 mg/dL, pH: 7.05 ± 0.15 vs. 7.34 ± 0.06, bicarbonates: 4.83 ± 0.59 vs. 27.6 ± 2.94 meq/L; P < 0.001). Similarly, sodium (147.76 ± 12.73 vs. 144.6 ± 5.96 meq/L) and potassium (9.6 ± 2.83 vs. 4.23 ± 0.37 meq/L) also changed significantly (P < 0.001) to near physiologic range. Hemodiafiltraion of final prime is a simple, efficients and rapid method of correcting the biochemical parameters and reducing the metabolic load of stored PRBCs towards the physiological range before initiating the CPB.
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