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Effects of transfusion load and suction pressure on renal function in intraoperative salvage autotransfusion

Abstract

Although some investigations have been performed to determine the effects of transfusion load and suction pressure on renal function during intraoperative salvage autotransfusion, the precise threshold is still undetermined. A total of 625 patients undergoing surgery with the Continuous AutoTransfusion System (CATSplus) were enrolled and divided into groups according to the utilized suction pressure and transfusion volume. Plasma free hemoglobin (FHB) and creatinine clearance (CCr) were assayed to indicate the renal function. Both 0.03 MPa suction (≥4-unit load) and >5 units transfusion changed the levels of FHB and CCr significantly when measured 24 h post-operation compared to pre-operation. Under 0.02 MPa suction (≥4-unit load), the alteration of FHB and CCr returned to normal after 24 h. Under 3 units transfusion, the levels of FHB and CCr at 6 and 12 h post-operation changed significantly compared to pre-operation (P<0.05 or P<0.01, respectively), and this alteration could be restored to normal at 72 h post-operation. After an exhaustive investigation, less than 4 units transfusion and less than 0.03 MPa suction pressure are recommended for intraoperative salvage autotransfusion.

Intraoperative salvage autotransfusion; Plasma-free hemoglobin; Creatinine clearance


Introduction

Besides financial burden, allogenic transfusion remains a challenge considering the risk of developing transfusion-transmitted virus and bacterial infections, acute lung injury and circulatory overload, hemolytic and allergic reactions, variant Creutzfeldt-Jakob disease, and even death (11. East JM, Viau-Lapointe J, Mccredie VA. Transfusion practices in traumatic brain injury. Curr Opin Anesthesiol 2018; 31: 219–226, doi: 10.1097/ACO.0000000000000566.
https://doi.org/10.1097/ACO.000000000000...
2. Roberts GH. Transfusion-related acute lung injury (TRALI). Clin Lab Sci 2004; 17: 133–135. 3. Seifried E, Mueller MM. Blood transfusion: one unit too much or one unit too few-which strategy poses the smallest risk to the patient? ISBT Sci Series 2017; 13.44. Polanco-García M, Capielo AM, Miret X, Chamero A, Sainz J, Revilla E, et al. Effectiveness of a patient blood management protocol on reduction of allogenic red blood cell transfusions in orthopedic surgery. Med Clin 2019; 152: 90–97, doi: 10.1016/j.medcli.2018.04.021.
https://doi.org/10.1016/j.medcli.2018.04...
). Thus, intraoperative blood salvage should be considered. With carefully selected surgical patients, intraoperative salvage autotransfusion can provide erythrocytes of a higher quality with less blood storage and immunological challenge (55. Catling S, Wrench I. Cell salvage at caesarean section: the need for an evidence-based approach. BJOG 2010; 117: 122–123, doi: 10.1111/j.1471-0528.2009.02394.x.
https://doi.org/10.1111/j.1471-0528.2009...
,66. Craig EK, Yazer MH, Waters JH. Red blood cell salvage analysis from clotted blood. Blood Transfus 2019; 17: 146–150, doi: 10.2450/2018.0008-18.
https://doi.org/10.2450/2018.0008-18...
). Considering the risks, intraoperative salvage autotransfusion may be more cost-effective than allogeneic transfusion. The global medical community has increasingly moved from allogeneic towards autologous blood transfusions.

Intraoperative salvage autotransfusion is reported to affect post-operative renal function (77. Song Y, Li R, Gu XH, Gong XJ, Zhang G, Wu SM, et al. Effects of blood washing and autotransfusion during cardiopulmonary bypass on erythrocyte immune and kidney function [in Chinese]. Zhonghua Yi Xue Za Zhi 2006; 86: 2293–2296.,88. Murphy GJ, Rogers CS. Safety, efficacy, and cost of intraoperative cell salvage and autotransfusion after off-pump coronary artery bypass surgery: a randomized trial. J Thoracic Cardiovasc Surg 2005; 130: 20–28, doi: 10.1016/j.jtcvs.2004.12.006.
https://doi.org/10.1016/j.jtcvs.2004.12....
). In the process of retrieving and transfusion of hematochezia, erythrocytes are sucked, filtered, and separated by vacuum aspiration, which will cause some degree of hemolysis-related deterioration of renal function. In order to achieve maximum clinical benefit and minimum adverse effect, the negative suction pressure, the size of the suction tip, and the air contact during suction were investigated in a previous report, and it is estimated that air contact is a major concern (99. An SB, Choi ES, Ahn W. Suction conditions for minimizing the production of free hemoglobin during blood salvage using an autotransfusion apparatus. Korean J Anesthesiol 2011; 60: 266–271, doi: 10.4097/kjae.2011.60.4.266.
https://doi.org/10.4097/kjae.2011.60.4.2...
). The Fresenius Kabi Continuous AutoTransfusion System is standardly utilized to aspirate in the middle of the pool of blood to minimize air contact (1010. Reents W, Babin-Ebell J, Misoph MR, Schwarzkopf A, Elert O. Influence of different autotransfusion devices on the quality of salvaged blood. Ann Thorac Surg 1999; 68: 58–62, doi: 10.1016/S0003-4975(99)00472-5.
https://doi.org/10.1016/S0003-4975(99)00...
), and the balance between the volume of transfusion and vacuum suction pressure was assessed in that investigation. In order to minimize the mechanical breakage of recycled erythrocytes, the vacuum suction pressure is recommended to not exceed 0.02 MPa (150 mmHg) by previous research (1111. Waters JH, Brandon W, Yazer MH, Kameneva MV. Modification of suction-induced hemolysis during cell salvage. Anesth Analg 2007; 104: 684–687, doi: 10.1213/01.ane.0000255208.96685.2e.
https://doi.org/10.1213/01.ane.000025520...
), while others found that erythrocytes are not affected even at 0.04 Mpa (1212. Huidan L, Fengjiang Z, Zhihao P, Xiaofei C, Lina Y, Min Y. Effects of washed autologous blood transfusion on erythrocytic fragility in salvaged blood from diabetics [in Chinese]. Zhonghua Yi Xue Za Zhi 2014; 94: 491–494.). It is believed that the concentration of free hemoglobin (FHB) in the recovered blood is positively correlated with the occurrence of hepato-renal function insufficiency, and up to 1 g/L FHB can cause renal function damage. More than five units of autologous blood transfusion could increase the incidence of renal failure after surgery.

This investigation was designed to comprehensively evaluate the effect of transfusion volume and suction pressure on renal function, which will help to set up a unified standard of intraoperative salvage autotransfusion.

Material and Methods

Study subjects

This investigation was performed in Quanzhou First Hospital of Fujian Province, and the protocols were approved by the Ethical Committee of Quanzhou First Hospital. Study design and procedures are shown in Figure S1. A total of 936 typical cases that underwent surgery using the Continuous AutoTransfusion System (CATS®plus, Fresenius Kabi, Germany) were screened from January 2016 to December 2018. Inclusion criteria were: over 18 years of age; willing to participate and sign an informed consent; and underwent orthopedic surgery, cardiovascular surgery, organ transplant surgery, brain surgery, emergency surgery, and other surgeries. Exclusion criteria were: surgical patients with comorbidities such as hypertension, diabetes mellitus, chronic obstructive pulmonary disease, and chronic renal disease; surgical field blood contaminated with digestive, bile, urine, and amniotic fluid; surgical field blood at risk of contamination in open trauma; blood conservation beyond 6 h; patients with infectious diseases; patients with malignant tumors and those who died during or within 72 h after surgery; patients with kidney injury before operation. After evaluation, a total of 625 eligible patients were enrolled in the final investigation.

Continuous autotransfusion procedure

The CATSplus circuit was primed and purged with 3000 mL saline (0.9%) mixed with 30,000 IU of sodium heparin. A double-lumen suction catheter specific for blood collection was utilized to salvage the bloodshed from the surgical field. Salvaged blood was suctioned with different vacuum pressures according to the study design (0.01, 0.015, 0.02, and 0.03 MPa), and further collected into the reservoir of the CATSplus. High-quality wash performed with the CATSplus was processed to minimize the residual FHB (<100 mg/dL), and the separated erythrocytes were further collected and transfused into the patients. Residual heparin levels were guaranteed to be less than or equal to 0.1 IU/mL in all post-treatments to minimize the clinical risk for intra- or post-operative hemorrhage.

Demographical and hematological variables

Age, gender, body mass index (BMI), and smoking habit were obtained and recorded. Hematological variables, such as blood urea nitrogen (BUN), blood creatinine, aspartate aminotransferase (AST), alanine aminotransferase (ALT), plasma FHB, and creatinine clearance (CCr), were measured.

Statistical analysis

GraphPad Prism v7.0 software (GraphPad Software, Inc., USA) was used to analyze the data. Numerical variables are reported as means±SD. Categorical data are reported as percentage (%) and were compared between groups by Pearson chi-squared and Fisher's Exact tests. Because the data of FHB and CCr were not in a normal distribution (Kolmogorov Smirnov, P<0.05), the Mann Whitney test was used to test the statistical significance of FHB and CCr. A significance level of P<0.05 was used in all tests.

Results

Clinical characteristics

Preoperative data (BMI, serum BUN, blood creatinine, AST, and ALT) of participants involved in this investigation are reported in Table 1. Age, gender, smoking habit, as well as types of surgery are also indicated in Table 1. The participants were further randomly assigned to different groups according to the volume of blood transfusion (2, 3, 4, 5, and >5 units) and suction pressure (0.01, 0.015, 0.02, and 0.03 MPa) (Table 2).

Table 1
Characteristics of study subjects.
Table 2
Subjects were assigned to different number of transfusion units and pressures of intraoperative salvage autotransfusion.

Transfusion load and suction pressure related to risk of renal function damage

Postoperative renal function change was indicated by the alteration of plasma FHB and CCr. A significant difference in FHB and CCr 24 h post-operation compared with pre-operation in the case of 0.03 MPa suction and ≥4 units transfusion and 0.02 MPa and >5 units transfusion (P<0.05 or P<0.01) (Table 3 and Table 4) was found, which indicated that both >5 units transfusion and 0.03 MPa suction plus ≥4 units transfusion would increase the risk of renal function damage.

Table 3
Plasma free hemoglobin (mg/dL) content in pre- and post-operative patients at 24 h.
Table 4
Creatinine clearance (mL·min-1·(1.73 m2)-1) in pre-operative and 24 h post-operative patients.

Less than 4 units of transfusion volume caused no harm to renal function

To decipher the relative long-term effect of transfusion volume and suction pressure on the risk of developing renal function damage, a time-course detection and analysis were performed. Under the situation of 0.02 MPa suction (>5 units transfusion), the levels of FHB and CCr altered significantly compared with the pre-operation condition at 6, 12, 24, and 72 h, as expected (P<0.05 or P<0.01, Table 5). Three units transfusion caused no change in FHB and CCr, while the change of FHB and CCr returned to normal after 24 h post-operation with 4 units transfusion, and all of these indicated that a transfusion volume less than four units should be safe.

Table 5
Plasma free hemoglobin (FHB) and creatinine clearance (CCr) in pre-operative and 6, 12, 24, and 72 h post-operative patients under 0.02 Mpa pressure.

Suction pressure less than 0.03 MPa caused no harm to renal function

The effect of suction pressure on renal function was further investigated under the 3 units transfusion. The changes of FHB and CCr at 6 and 12 h post-operation was significant compared with pre-operation (P<0.05 or P<0.01), while such changes were restored to normal at 72 h post-operation at 0.03 MPa suction (Table 6). Only at the 6-h time-point was a FHB change observed at 0.02 MPa suction, which was restored at 12 h post-operation. All of these indicated that the recommended pressure for vacuum suction should be less than 0.03 MPa.

Table 6
Plasma free hemoglobin (FHB) and creatinine clearance (CCr) in pre-operative and 6, 12, 24, and 72 h post-operative patients under 3 transfusion units.

Discussion

In this investigation, both FHB and CCr were utilized to indicate renal function. Intraoperative salvage hemolysis can release FHB, which can precipitate in the renal tubules with resultant tubular dysfunction (1313. You D, Garcia AP, Ferridebarros F, Parsons D. Hemolysis following intraoperative cell salvage replacement in a scoliosis patient with sickle cell trait: a case report. Spine 2017; 42: E1331–E1333, doi: 10.1097/BRS.0000000000002211.
https://doi.org/10.1097/BRS.000000000000...
14. Gregoretti S. Suction‐induced hemolysis at various vacuum pressures: implications for intraoperative blood salvage. Transfusion 1996; 36: 57–60, doi: 10.1046/j.1537-2995.1996.36196190516.x.
https://doi.org/10.1046/j.1537-2995.1996...
1515. Sikorski RA, Rizkalla NA, Yang WW, Frank SM. Autologous blood salvage in the era of patient blood management. Vox Sang 2017; 112: 499–510, doi: 10.1111/vox.12527.
https://doi.org/10.1111/vox.12527...
). In intraoperative salvage autotransfusion, the washing process can remove FHB before re-infusion, and less than 100 mg/dL FHB is recommended to minimize the effect on renal function. Such concentration of FHB is well below the standard of banked blood, which will show no deleterious effects on renal function after transfusion. CCr is a parameter that can be utilized to assess the excretory function of the kidneys (1616. Wyss M, Kaddurahdaouk R. Creatine and creatinine metabolism. Physiol Rev 2000; 80: 1107–1213, doi: 10.1152/physrev.2000.80.3.1107.
https://doi.org/10.1152/physrev.2000.80....
17. Wada H, Kanda J, Akahoshi Y, Nakano H, Ugai T, Yamasaki R, et al. Impact of estimated glomerular filtration rate based on plasma cystatin C and serum creatinine levels before allogeneic hematopoietic cell transplantation. Hematology 2018; 23: 271–276, doi: 10.1080/10245332.2017.1396026.
https://doi.org/10.1080/10245332.2017.13...
1818. Mangan C, Stott MC, Dhanda R. Renal physiology: blood flow, glomerular filtration and plasma clearance. Anaesth Intens Care Med 2018: S1472029918300584.), and renal dysfunction can be defined as a decrease of CCr (<60 mL/min) (1919. Klodell CT, Richardson JD, Bergamini TM, Spain DA. Does cell-saver blood administration and free hemoglobin load cause renal dysfunction? Am Surg 2001; 67: 44–47.).

Intraoperative salvage autotransfusion performed by the CATSplus system has some advantages, such as higher oxygen-carrying capacity and lower volume requirement for transfusion. The efficiency of erythrocyte collection during cell salvage can be attributed to suction pressure. Previous investigations suggest that minimal suction pressures and a suction tip with a relatively large diameter should be adopted to aspirate blood from a surgical field to minimize blood-air interfaces and maximize the efficiency of erythrocyte recovery (1111. Waters JH, Brandon W, Yazer MH, Kameneva MV. Modification of suction-induced hemolysis during cell salvage. Anesth Analg 2007; 104: 684–687, doi: 10.1213/01.ane.0000255208.96685.2e.
https://doi.org/10.1213/01.ane.000025520...
,2020. Michinaga Y, Takano T, Terasaki T, Miyazaki S, Kikuchi N, Okada K. Hemolytic characteristics of three suctioning systems for use with a newly developed cardiopulmonary bypass system. Perfusion 2019; 34: 136–142, doi: 10.1177/0267659118793559.
https://doi.org/10.1177/0267659118793559...
). The fast-moving foams produced by air aspiration during blood suction will burst in the negative pressure environment and generate a mechanical shear force on the erythrocyte (99. An SB, Choi ES, Ahn W. Suction conditions for minimizing the production of free hemoglobin during blood salvage using an autotransfusion apparatus. Korean J Anesthesiol 2011; 60: 266–271, doi: 10.4097/kjae.2011.60.4.266.
https://doi.org/10.4097/kjae.2011.60.4.2...
,2121. Li H, Lykotrafitis G. Erythrocyte membrane model with explicit description of the lipid bilayer and the spectrin network. Biophys J 2014; 107: 642–653, doi: 10.1016/j.bpj.2014.06.031.
https://doi.org/10.1016/j.bpj.2014.06.03...
,2222. Kuck L, Grau M, Simmonds MJ. Recovery time course of erythrocyte deformability following exposure to shear is dependent upon conditioning shear stress. Biorheology 2018; 54: 141–152, doi: 10.3233/BIR-17151.
https://doi.org/10.3233/BIR-17151...
). In this investigation, we found that a suction pressure of less than 0.03 MPa should be used for orthopedic surgery, cardiovascular surgery, organ transplant surgery, brain surgery, and emergency surgery, which can help guide the clinical application of intraoperative salvage autotransfusion. Minimum initial blood volume is required by the CATSplus system to process; in this research, less than four units transfusion was determined for minimal renal function damage (2323. Cyrille B, Goran L, Markus W, Cushing MM, Thorsten H. Evaluation of the minimum volume of salvage blood required for the successful use of two different autotransfusion devices. Paediatr Anaesth 2015; 25: 258–264, doi: 10.1111/pan.12535.
https://doi.org/10.1111/pan.12535...
,2424. Zacharias T, Ahlschwede E, Dufour N, Romain F, Theissen-Laval O. Intraoperative cell salvage with autologous transfusion in elective right or repeat hepatectomy: a propensity-score-matched case-control analysis. Can J Surg 2018; 61: 105–113, doi: 10.1503/cjs.010017.
https://doi.org/10.1503/cjs.010017...
).

The introduction and development of minimally invasive surgery will limit the utilization of intraoperative salvage autotransfusion due less blood loss and transfusion requirements (2525. Frank SM, Rothschild JA, Masear CG, Rivers RJ, Merritt WT, Savage WJ, et al. Optimizing preoperative blood ordering with data acquired from an anesthesia information management system. Anesthesiology 2013; 118: 1286–1297, doi: 10.1097/ALN.0b013e3182923da0.
https://doi.org/10.1097/ALN.0b013e318292...
26. Moua PK, Nguyen CL, Piotrowski DA, Resch MJ, Tabassum T, Noonan K, et al. Surgical sponge blood salvage spinning device design and testing. J Med Eng Technol 2018; 42: 426–434, doi: 10.1080/03091902.2018.1543465.
https://doi.org/10.1080/03091902.2018.15...
2727. Dhariwal SK, Khan KS, Allard S, Wilson M, Moore P. Does current evidence support the use of intraoperative cell salvage in reducing the need for blood transfusion in caesarean section? Curr Opin Obstet Gynecol 2014; 26: 425–430, doi: 10.1097/GCO.0000000000000116.
https://doi.org/10.1097/GCO.000000000000...
). Considering cost-to-benefit ratios, such as lower infection rates and shorter hospital stays, intraoperative salvage autotransfusion can still benefit several patients. In addition, allogeneic transfusion, but not autologous transfusion, could shift an immune deviation towards a T helper 2-type response. Such a shift is associated with a gene transcription profile characteristic of immunosuppression, which may suppress natural killer cells and cytotoxic T-cells, and activate regulatory T cells to down-regulate cellular immunity (2525. Frank SM, Rothschild JA, Masear CG, Rivers RJ, Merritt WT, Savage WJ, et al. Optimizing preoperative blood ordering with data acquired from an anesthesia information management system. Anesthesiology 2013; 118: 1286–1297, doi: 10.1097/ALN.0b013e3182923da0.
https://doi.org/10.1097/ALN.0b013e318292...
,2828. Kirkley SA, Cowles J, Pellegrini VD, Harris CM, Boyd AD, Blumberg N,. Blood transfusion and total joint replacement surgery: T helper 2 (TH2) cytokine secretion and clinical outcome. Transfus Med 2008; 8: 195–204, doi: 10.1046/j.1365-3148.1998.00149.x.
https://doi.org/10.1046/j.1365-3148.1998...
,2929. Kirkley SA. Proposed Mechanisms of Transfusion-Induced Immunomodulation. Clin Diagn Lab Immunol 1999; 6: 652–657, doi: 10.1128/CDLI.6.5.652-657.1999.
https://doi.org/10.1128/CDLI.6.5.652-657...
). Although the long-term immune shifting effect still needs further detailed analysis, intraoperative salvage autotransfusion might be a safe option in the immune context. In addition to renal function, the influence of intraoperative salvage autotransfusion on proinflammatory cytokines, platelet activation, coagulation, fibrinolysis, and hemolysis factors should also be considered in clinical practice, as reported (1010. Reents W, Babin-Ebell J, Misoph MR, Schwarzkopf A, Elert O. Influence of different autotransfusion devices on the quality of salvaged blood. Ann Thorac Surg 1999; 68: 58–62, doi: 10.1016/S0003-4975(99)00472-5.
https://doi.org/10.1016/S0003-4975(99)00...
,3030. Dong P, Che J, Li X, Tian M, Smith FG. Quick biochemical markers for assessment of quality control of intraoperative cell salvage: a prospective observational study. J Cardiothorac Surg 2014; 9: 86, doi: 10.1186/1749-8090-9-86.
https://doi.org/10.1186/1749-8090-9-86...
,3131. van der Merwe M, Lightfoot NJ, Munro JT, Boyle MJ. Intraoperative cell salvage use reduces the rate of perioperative allogenic blood transfusion in patients undergoing periacetabular osteotomy. J Hip Preserv Surg 2019; 6: 277–283, doi: 10.1093/jhps/hnz039.
https://doi.org/10.1093/jhps/hnz039...
), which will be analyzed in a future clinical study. All of these indicate that in addition to the more detailed evaluation of renal function by glomerular filtration rate and blood urea nitrogen, immune function change induced by intraoperative salvage autotransfusion should also be studied.

It must be mentioned that prolonged large-volume autotransfusion may cause coagulopathy due to the dilution of clotting factors with transfusions. Thus, together with appropriate transfusion load and suction pressure, regular coagulation function or close patient monitoring is required (3232. Klein AA, Arnold P, Bingham RM, Brohi K, Clark R, Collis R, et al. AAGBI guidelines: the use of blood components and their alternatives 2016. Anaesthesia 2016; 71: 829–842, doi: 10.1111/anae.13489.
https://doi.org/10.1111/anae.13489...
,3333. Wellesley H, Pownall S. AAGBI Consent guidelines 2017-should the advice about 16 and 17-year-olds be amended? Anaesthesia 2017; 72: 656–657, doi: 10.1111/anae.13883.
https://doi.org/10.1111/anae.13883...
). The long-term effect of the tested transfusion load and suction pressure on renal function was not investigated in this study, and such limitation should also be considered.

Our investigation has both scientific and practical implications for the utilization of intraoperative salvage autotransfusion, which will help clinicians prescribe the appropriate amount of autotransfusion volume and suction pressure.

Conclusion

Although a more precise design and multi-center investigation are needed, this study showed that less than four units transfusion and less than 0.03 MPa suction pressure may be recommended for intraoperative salvage autotransfusion.

Acknowledgments

The study was supported by the Quanzhou Science and Technology Program Project in Medical and Health (2018Z093).

References

  • 1
    East JM, Viau-Lapointe J, Mccredie VA. Transfusion practices in traumatic brain injury. Curr Opin Anesthesiol 2018; 31: 219–226, doi: 10.1097/ACO.0000000000000566.
    » https://doi.org/10.1097/ACO.0000000000000566
  • 2
    Roberts GH. Transfusion-related acute lung injury (TRALI). Clin Lab Sci 2004; 17: 133–135.
  • 3
    Seifried E, Mueller MM. Blood transfusion: one unit too much or one unit too few-which strategy poses the smallest risk to the patient? ISBT Sci Series 2017; 13.
  • 4
    Polanco-García M, Capielo AM, Miret X, Chamero A, Sainz J, Revilla E, et al. Effectiveness of a patient blood management protocol on reduction of allogenic red blood cell transfusions in orthopedic surgery. Med Clin 2019; 152: 90–97, doi: 10.1016/j.medcli.2018.04.021.
    » https://doi.org/10.1016/j.medcli.2018.04.021
  • 5
    Catling S, Wrench I. Cell salvage at caesarean section: the need for an evidence-based approach. BJOG 2010; 117: 122–123, doi: 10.1111/j.1471-0528.2009.02394.x.
    » https://doi.org/10.1111/j.1471-0528.2009.02394.x
  • 6
    Craig EK, Yazer MH, Waters JH. Red blood cell salvage analysis from clotted blood. Blood Transfus 2019; 17: 146–150, doi: 10.2450/2018.0008-18.
    » https://doi.org/10.2450/2018.0008-18
  • 7
    Song Y, Li R, Gu XH, Gong XJ, Zhang G, Wu SM, et al. Effects of blood washing and autotransfusion during cardiopulmonary bypass on erythrocyte immune and kidney function [in Chinese]. Zhonghua Yi Xue Za Zhi 2006; 86: 2293–2296.
  • 8
    Murphy GJ, Rogers CS. Safety, efficacy, and cost of intraoperative cell salvage and autotransfusion after off-pump coronary artery bypass surgery: a randomized trial. J Thoracic Cardiovasc Surg 2005; 130: 20–28, doi: 10.1016/j.jtcvs.2004.12.006.
    » https://doi.org/10.1016/j.jtcvs.2004.12.006
  • 9
    An SB, Choi ES, Ahn W. Suction conditions for minimizing the production of free hemoglobin during blood salvage using an autotransfusion apparatus. Korean J Anesthesiol 2011; 60: 266–271, doi: 10.4097/kjae.2011.60.4.266.
    » https://doi.org/10.4097/kjae.2011.60.4.266
  • 10
    Reents W, Babin-Ebell J, Misoph MR, Schwarzkopf A, Elert O. Influence of different autotransfusion devices on the quality of salvaged blood. Ann Thorac Surg 1999; 68: 58–62, doi: 10.1016/S0003-4975(99)00472-5.
    » https://doi.org/10.1016/S0003-4975(99)00472-5
  • 11
    Waters JH, Brandon W, Yazer MH, Kameneva MV. Modification of suction-induced hemolysis during cell salvage. Anesth Analg 2007; 104: 684–687, doi: 10.1213/01.ane.0000255208.96685.2e.
    » https://doi.org/10.1213/01.ane.0000255208.96685.2e
  • 12
    Huidan L, Fengjiang Z, Zhihao P, Xiaofei C, Lina Y, Min Y. Effects of washed autologous blood transfusion on erythrocytic fragility in salvaged blood from diabetics [in Chinese]. Zhonghua Yi Xue Za Zhi 2014; 94: 491–494.
  • 13
    You D, Garcia AP, Ferridebarros F, Parsons D. Hemolysis following intraoperative cell salvage replacement in a scoliosis patient with sickle cell trait: a case report. Spine 2017; 42: E1331–E1333, doi: 10.1097/BRS.0000000000002211.
    » https://doi.org/10.1097/BRS.0000000000002211
  • 14
    Gregoretti S. Suction‐induced hemolysis at various vacuum pressures: implications for intraoperative blood salvage. Transfusion 1996; 36: 57–60, doi: 10.1046/j.1537-2995.1996.36196190516.x.
    » https://doi.org/10.1046/j.1537-2995.1996.36196190516.x
  • 15
    Sikorski RA, Rizkalla NA, Yang WW, Frank SM. Autologous blood salvage in the era of patient blood management. Vox Sang 2017; 112: 499–510, doi: 10.1111/vox.12527.
    » https://doi.org/10.1111/vox.12527
  • 16
    Wyss M, Kaddurahdaouk R. Creatine and creatinine metabolism. Physiol Rev 2000; 80: 1107–1213, doi: 10.1152/physrev.2000.80.3.1107.
    » https://doi.org/10.1152/physrev.2000.80.3.1107
  • 17
    Wada H, Kanda J, Akahoshi Y, Nakano H, Ugai T, Yamasaki R, et al. Impact of estimated glomerular filtration rate based on plasma cystatin C and serum creatinine levels before allogeneic hematopoietic cell transplantation. Hematology 2018; 23: 271–276, doi: 10.1080/10245332.2017.1396026.
    » https://doi.org/10.1080/10245332.2017.1396026
  • 18
    Mangan C, Stott MC, Dhanda R. Renal physiology: blood flow, glomerular filtration and plasma clearance. Anaesth Intens Care Med 2018: S1472029918300584.
  • 19
    Klodell CT, Richardson JD, Bergamini TM, Spain DA. Does cell-saver blood administration and free hemoglobin load cause renal dysfunction? Am Surg 2001; 67: 44–47.
  • 20
    Michinaga Y, Takano T, Terasaki T, Miyazaki S, Kikuchi N, Okada K. Hemolytic characteristics of three suctioning systems for use with a newly developed cardiopulmonary bypass system. Perfusion 2019; 34: 136–142, doi: 10.1177/0267659118793559.
    » https://doi.org/10.1177/0267659118793559
  • 21
    Li H, Lykotrafitis G. Erythrocyte membrane model with explicit description of the lipid bilayer and the spectrin network. Biophys J 2014; 107: 642–653, doi: 10.1016/j.bpj.2014.06.031.
    » https://doi.org/10.1016/j.bpj.2014.06.031
  • 22
    Kuck L, Grau M, Simmonds MJ. Recovery time course of erythrocyte deformability following exposure to shear is dependent upon conditioning shear stress. Biorheology 2018; 54: 141–152, doi: 10.3233/BIR-17151.
    » https://doi.org/10.3233/BIR-17151
  • 23
    Cyrille B, Goran L, Markus W, Cushing MM, Thorsten H. Evaluation of the minimum volume of salvage blood required for the successful use of two different autotransfusion devices. Paediatr Anaesth 2015; 25: 258–264, doi: 10.1111/pan.12535.
    » https://doi.org/10.1111/pan.12535
  • 24
    Zacharias T, Ahlschwede E, Dufour N, Romain F, Theissen-Laval O. Intraoperative cell salvage with autologous transfusion in elective right or repeat hepatectomy: a propensity-score-matched case-control analysis. Can J Surg 2018; 61: 105–113, doi: 10.1503/cjs.010017.
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Supplementary Material

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Publication Dates

  • Publication in this collection
    15 Jan 2021
  • Date of issue
    2021

History

  • Received
    19 May 2020
  • Accepted
    28 Sept 2020
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