ANH in Complex Cardiac Surgery: A Prospective Randomized Study

Bleeding in cardiac surgery is a frequent complication. Despite transfusion algorithms and point of care coagulation testing, transfusion of erythrocytes, platelets, and plasma is very common even in low risk cardiac surgery¹. Previous studies demonstrate that allogeneic blood transfusions occur in 40-90% of cardiac surgery².

Packed red blood cells (PRBCs) are associated with worse short-term and long-term outcomes including mortality, renal failure and neurologic complications. Patients who receive a blood transfusion during a cardiac surgical hospitalization have a 70% increase in mortality compared to patients who did not receive a transfusion³.

Acute normovolemic hemodilution (ANH) is a blood conservation technique that may decrease allogeneic blood transfusion in cardiac surgery. Most of the literature for ANH has been studied in low-risk cardiac surgery, such as coronary artery bypass grafting and isolated valve surgery⁴. There is a paucity of evidence for ANH in high-risk cardiac surgery, such as aortic surgery and adult congenital heart disease surgery. Rates of transfusion in high-risk cardiac surgery are more common than low risk cardiac surgery, therefore, ANH may offer significant potential benefits. However, it is unknown whether ANH is safe and effective in high-risk cardiac surgery. The goal of this study is to assess the effect of ANH on outcomes in patients undergoing high-risk cardiac surgery. We tested the primary hypothesis that ANH reduces perioperative transfusion of erythrocytes within 72 hours following cardiopulmonary bypass. Secondarily, we tested the hypothesis that ANH reduces intraoperative erythrocyte transfusion and erythrocyte transfusion within 24 and 48 hours following cardiopulmonary bypass.

Patient characteristics, intraoperative variables, laboratory results, and clinical outcomes were summarized overall in Table 1, Table 2, Table 3 and by study group (ANH vs control) using means and standard deviations for continuous variables and frequencies with percentages for categorical variables. Comparisons between groups were conducted using independent-sample t-tests for continuous variables and chi-square tests for categorical variables. For transfusion-related outcomes (e.g., perioperative and intraoperative pRBCs, platelets, FFP, cryoprecipitate), which exhibited skewed distributions, log transformation was applied prior to conducting group comparisons with t-tests. Additional comparisons for secondary outcomes, such as ICU and hospital length of stay, were also assessed using t-tests. All analyses were conducted using SPSS version 28 (IBM Corp., Armonk, NY) and R version 4.1.0 (R Foundation for Statistical Computing, Vienna, Austria). All tests were two-tailed, and p-values < 0.05 were considered statistically significant.

Sixty-one patients that met both inclusion and exclusion criteria were enrolled in the study between February 2022 and May 2023. After randomization, 32 patients (52%) were assigned to the ANH arm while the remaining 29 patients were assigned to the control group. Participant demographics and perioperative features are shown in Table 1

Baseline characteristics between the ANH and control groups were comparable except that participants in the ANH group were found to be younger (50.9 ± 18.6 vs 60.3 ± 14.8; p = 0.034). The preoperative hematologic and coagulation profiles between both groups were similar. Furthermore, no differences between groups were noted in the estimated/calculated and actual post-dilutional hematocrit.

Intraoperative characteristics are presented in Table 2. As demonstrated in Table 2, no statistical differences in CPB time, aortic cross-clamp time, circulatory arrest time, or number of pump runs were observed between groups. The lowest recorded temperature on CPB was statistically higher in the ANH group compared to controls (32.1 ± 4.3 °C vs 29.6 ± 5.4 °C; p=0.050). Intraoperative administration of crystalloid and colloid as well as heparin and protamine were similar between both groups. There was comparable utilization of antifibrinolytics (aminocaproic acid or tranexamic acid), desmopressin, prothrombin complex concentrate and recombinant factor VIIa in both groups. Utilization of inotropic support was the same between both groups. No intragroup difference was observed in the incidence and medical management of vasoplegia.

For the primary outcome, there was no statistical difference in total postoperative pRBC transfusions between the ANH and control group (0.2 ± 0.5 units vs 0.3 ± 0.6 units; p = 0.402) as shown in Table 3. Receipt of ANH was associated with a lower incidence of total perioperative pRBC transfusion (0.6 ± 1.2 units vs 2.7 ± 6.8 units; p = 0.030/0.049). Total perioperative transfusion of all other fractionated blood products, including platelets (0.8 ± units vs 1.9 ± 2.4 units; p=0.010), cryoprecipitate (0.5 ± 0.7 vs 1.3 ± 2.0; p=0.016) and FFP (0.5 ± 1.0 vs 2.3 ± 6.2 units; p=0.013), was significantly lower in the ANH group compared to controls. Participants in the ANH group received significantly fewer intraoperative transfusions of pRBC (0.4 ± 1.2 vs 2.6 ± 7.0 units; p=0.037), platelets (0.8 ± 1.2 units vs 1.9 ± 2.4 units; p=0.0.13, logtrans), FFP (0.4 ± 0.9 vs 2.5 ± 6.4 units; p=0.003) and cryoprecipitate (0.5 ± 0.7 vs 1.3 ± 2.1 units; p=0.012, logtrans). Postoperative transfusions of pRBCs, platelets, FFP and cryoprecipitate at 24, 48 and 72 hours did not differ between ANH and control groups.

With respect to secondary clinical outcomes, ANH participants had statistically shorter ICU (3.7 ± 1.9 vs 5.4 ± 3.6 days; p=0.020) and hospital (6.7 ± 2.1 vs 9.5 ± 7.7 days; p = 0.048) length of stays (Table 5). There were no statistically significant differences in postoperative intubation time, left ventricular systolic function, and re-exploration for bleeding. The incidence of neurologic complications including stroke and renal failure requiring dialysis were the same between groups. Perioperative myocardial injury/infarction and death occurred a similar frequency in the ANH and control groups.

Our study ANH in Complex Cardiac Surgery is a prospective, randomized, controlled study conducted at a large academic university hospital. We embarked on this study with the idea that ANH has been shown to be a safe and efficacious blood conservation strategy in low-risk cardiac surgery and has been shown to diminish red blood cell transfusion⁸. There have been no known prospective, randomized trials looking at ANH in complex cardiac surgery. The patients included in the study had complex valve, aortic, valve-CABG, redo sternotomy and adult congenital heart open-heart procedures requiring cardiopulmonary bypass. Our study excluded any single valve procedures, CABG surgery, heart transplants and patients with acute heart failure, left ventricular ejection fraction lower than 35%, anemia, recent transfusion, infection, malignancy, and dialysis dependent renal failure. All patients had ROTEM and laboratory driven standardized transfusion guidelines in the perioperative period, and there were no complications experienced in the study. There was a single neurological death in the control group.

The primary outcome of decreased PRBC transfusion in the perioperative period was statistically significant over the cumulative 72-hour perioperative interval. The intraoperative period had similar PRBC transfusion rates in both the study and control groups. We attributed this finding to the case selection. Both the control and ANH groups incurred heavy bleeding and required red blood cell transfusion which remained necessary and similar in both groups during that immediate, operative period. However, when we evaluated the total PRBC transfusion over the 72-hour perioperative interval, we found the difference in total red cell transfusion between the ANH and control groups to be different with the ANH group requiring significantly diminished red cell transfusion requirements. These findings have important clinical and economic implications. Transfusions of all blood products are known to be resource and cost- intensive and have been shown to increase perioperative complications, morbidity and mortality. In cardiac surgery, pulmonary and cardiac dysfunction, neurologic impairment, infection and renal failure are major concerns and have been increased in patients receiving transfusions⁹. Therefore, incorporating a blood conservation strategy like ANH which may reduce transfusion requirements and diminish exposure to blood products may reduce morbidity, mortality and costs.

Important statistically significant secondary outcomes including diminished transfusion of platelets, cryoprecipitate, FFP, total blood product transfusion, decreased length of intensive care unit stay and decreased length of hospital stay were seen in the ANH group. The clinical impact of reduced transfusion on complex cardiac surgical patients is most likely multifactorial. Kotake et. al. found a difference in autologous blood transfusion-induced inflammatory responses between ANH and preoperatively donated autologous blood. The Kotake group reported that ANH blood transfusions were associated with a smaller concentration of inflammatory mediators such as interleukin 10 and neutrophil elastase than autologous blood bank blood¹⁰. Liker et al. previously described the cardioprotective effects of ANH in patients undergoing coronary artery bypass surgery due to the hemodilution-induced blood viscosity. Cardio-protection may be associated with improved oxygen supply and consumption balance¹¹. A reduction in postoperative pulmonary infections has previously been described, although no difference in ventilator days was seen in the study by Zhou et al¹². as well as our group. Our study had a limit of 700 cc of ANH blood removal. There was a greater benefit with a larger volume of ANH blood removed. The most common amount removed was 600 cc due to the collection bag size and ratio of preservation fluid (citrate phosphate dextrose adenine). The average volume removed was 652 cc. 8-10 cc/kg was the recommended removal volume. However, there were ten patients who received 700- 1000 cc of ANH. In these patients, whole blood removed and reinfused was well tolerated. A single ACHD patient weighing 133 kg had 1000 cc removed due to high hematocrit (48%) and good hemodynamics per the care team. This practice was consistent with the report of Goldberg et al13. and the meta-analysis by Barile et al⁸.

Both studies reported a reduction in PRBC transfusion by using an ANH blood conservation technique and described a dose-dependent response in which patients receiving larger volume ANH had diminished blood bank blood requirements. It is possible that previous studies using small and medium volume ANH failed to show benefit due to the reduced ANH volume13.

The use of cell saver blood scavenging technique, antifibrinolytic medication with tranexamic acid and aminocaproic acid along with ROTEM evaluation likely augmented our ANH blood conservation and may be considered standard practice in cardiac surgery. However, it is unknown to what extent these practices may have impacted our study. We used these techniques on all patients enrolled in the study.

A trend toward the early use of recombinant coagulation factors such as Factor VII concentrate, Prothrombin complex concentrate (PCC, Kcentra) and Factor IX complex (Profiline) is evolving in cardiac surgical practice¹⁴. In our study, PCC was used as a rescue technique after it was determined the coagulopathy was severe and required recombinant factors based on ROTEM and minimal response to transfused blood products. We had four patients who required the use of PCC. Two of the patients were adult congenital heart disease cases with complex repairs with redo sternotomies who required circulatory arrest. One of the ACHD patients was a control and the other received ANH. The other two patients were complex, double valve, hemiarch cases and both were randomized to the control arm. Three of these patients required hypothermia to below 24 degrees or circulatory arrest and the fourth case experienced an aortic cross clamp time of 150 min at 32 degrees. In these cases, it is thought that profound hypothermia and prolonged cardiopulmonary bypass contributed to the significant, refractory coagulopathy.

The human factor of the ANH technique and process should be appreciated. The process adds another level of complexity to an already complicated procedure. The technique requires vigilance in removing a large amount of blood volume from a hemodynamically fragile patient in a sterile fashion with the appropriate amount of anticoagulant. The blood must be oscillated to prevent clot formation and reinfused within an 8-hour period. However, the benefits of the technique are that the autologous whole blood once collected serves as an in operating room “blood bank” for the patients to receive undiluted, fresh whole blood which contains red cells and critical coagulation factors in a proportionally appropriate amount without the risks of foreign blood product exposure. In our study, there were no clot formations reported. No wastage of ANH blood units occurred, and no complications were reported with respect to collection or reinfusion. All patients had a rigorous screening process which calculated the pre- and post-dilutional hematocrits that would have been anticipated after the ANH removal and the dilutional hematocrit anticipated on cardiopulmonary bypass. Patients with a dilutional hematocrit lower than 22% were excluded from the study. There was no difference in lactate levels, incidence of AKI, decreased brain saturation, hemodynamic instability, incidence of cardiac ischemia or other complications in either the ANH or control groups. This screening process was an additional level of safety that helped us select appropriate patients for the study. Patient selection for the ANH technique is vital as well as meticulous technique to avoid hemodynamic compromise. Attention to positioning in Trendelenburg during collection and gentle fluid administration during removal of blood and replacement cannot be overlooked. With appropriate patient selection and meticulous technique, the safety of ANH was confirmed in our prospective, randomized study.

The primary limitations of our study include the unblinded nature of the study due to the technique required, small sample size secondary to the single study site and rigorous patient screening process, and early termination of the study. There was a possible effect of individual physician practice as well as the effect of having the ready, in-place ANH autologous blood units available and ready to give during the immediate post- bypass period, which is frequently characterized by vasoplegia and hypovolemia. All our participating physicians mentioned the convenience of having immediate volume and whole blood ready to infuse as a benefit of the technique when treating complex cardiac surgical patients. This also may have influenced the surgical team from requesting further blood products thus impacting the total products transfused. This may have contributed to a possible performance bias.

This single center, prospective randomized controlled study demonstrated ANH in complex cardiac surgical patients to be safe and effective in reducing the allogenic blood product transfusion of PRBCs, FFP, platelets and cryoprecipitate in the perioperative period. While the efficacy of ANH has been shown in previous studies, there has not been a prospective trial evaluating the technique in complex cardiac surgical cases. While additional studies are needed to identify subgroups which may benefit more from the technique of ANH and the optimal volume; the technique of using ANH as part of a blood conservation strategy is safe and may diminish exposure to blood products as well as show positive outcomes such as decreased ICU and hospital length of stay.

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