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Red blood cell damage during experimental prolonged perfusion with membrane oxygenation using fresh human blood

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

G. Friberg

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

B. Liu

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

N. Al-Khaja

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

A. Belboul

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

G. Mellgren

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

D. Roberts

Department of Thoracic and Cardiovascular Surgery, Sahlgrenska Sjukhuset and Department of Pediatric Surgery, Ostra Sjukhuset, University of Gothenburg

The effects of prolonged perfusion of oxygenated blood have previously been studied with respect to haemolysis and cell morphology. The aim of this study was to examine the effect of mechanical trauma on the microrheology of red blood cells during experimental prolonged perfusion with membrane oxygenation (PPMO). Red blood cell damage was assessed by blood rheological parameters using a St George's filtrometer. Red blood cell filtration rate (RFR, µl/s), clogging rate (RBC-CR, 10²%/ml), clogging particle (RBC-CP, 106/ml), mean corpuscular volume (MCV) and haematocrit (Hct) were analysed at the start of PPMO and after 24, 48 and 72 hours. RFR values were 81.3 ± 3.7 at the start, 79.2 ± 7.6 (24 h, p < 0.01), 42.3 ± 8.4 (48 h, p < 0.001) and 25.1 ± 7.0 (72 h, p < 0.001). The mean RBC-CR was 2.45 ± 0.53 at the start; this increased to 3.58 ± 0.9, 6.62 ± 0.92 and then reduced to 4.77 ± 1.39 at 24 (p < 0.0001), 48 (p < 0.0001) and 72 (p < 0.02) hours respectively. Mean RBC-CP at the start was 3.29 ± 0.55; this increased to 3.42 ± 0.72, 5.29 ± 0.68 and 6.09 ± 1.07 at 24, 48 and 72 hours respectively (NS at 24 h and 48 h, p < 0.04 at 72 h). The mean MCV (fl) at the start was 86 ± 4; this increased to 101 ± 2, 111 ± 4 and 119 ± 4 at 24, 48 and 72 hours respectively (p < 0.001). Mean Hct (%) at the start was 33 ± 2; this increased to 38 ± 2, 38 ± 2 and 48 ± 2 at 24, 48 and 72 hours respectively (p < 0.05 at 24 and 48 hours, p < 0.001 at 72 hours). The mean pH and CO ₂ (kPa.s) levels were 7.38 ± 0.04 and 4.1 ± 0.7 respectively. This study suggested that there was a continuous loss of red cell rheology during PPMO, which could lead to disturbed microcirculation, thereby increasing the risk of organ ischaemia, hypoxia, dysfunction and failure.

Perfusion, Vol. 8, No. 3, 225-232 (1993)
DOI: 10.1177/026765919300800305


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