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J Thorac Cardiovasc Surg 2005;130:654
© 2005 The American Association for Thoracic Surgery
Cardiopulmonary Support and Physiology |
McGill University, Montreal, Quebec, Canada.
Received for publication November 3, 2004; revisions received February 8, 2005; accepted for publication February 15, 2005. * Address for reprints: Sandra Dial, MD, MSc, Department of Critical Care, SMBD Jewish General Hospital, McGill University, Montreal, and Respiratory Epidemiology and Clinical Research Unit, Montreal Chest Institute, 3650 St Urbain, Room K1.14, Montreal, Quebec, Canada, H2X 2P4. (Email: sandra.dial{at}mcgill.ca).
| Abstract |
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METHODS: We performed a prospective cohort study of 613 adult patients who underwent coronary artery bypass grafting in 3 tertiary, university-affiliated hospitals during the period from October 1, 2000, to March 31, 2001.
RESULTS: Low intraoperative hematocrit levels (<19%) were found in 131 (24%) patients who had operations performed with extracorporeal circulation compared with in 3 (4%) patients with operations performed off pump. In multivariate analysis this was associated with older age, female sex, lower preoperative hemoglobin levels, lower body surface area, longer duration on bypass, and use of higher total volumes with more hydroxyethyl starch in the circuit. Low intraoperative hematocrit levels did not predict excessive postoperative hemorrhage (>1 L of mediastinal drainage in the first 12 hours). This occurred in 26% (n = 140) of patients undergoing on-pump operations and in 25% of patients undergoing off-pump operations and in multivariate analysis was associated with male sex, longer pump times, not receiving aprotinin, and operations performed by certain surgeons but not with total circuit or hydroxyethyl starch volume.
CONCLUSIONS: We observed that the risk factors for the development of a low intraoperative hematocrit level and excessive postoperative bleeding differed. Our results suggest that decreasing these outcomes in patients undergoing cardiac surgery requires a comprehensive approach, including limiting hemodilution, particularly in female subjects with lower preoperative hemoglobin levels, and careful attention to surgical hemostasis.
| Introduction |
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After observing differences in practices in cardiac surgery in the 3 affiliated hospitals at our university, we prospectively evaluated the occurrence and risk factors for excessive postoperative hemorrhage and low intraoperative hematocrit values.
| Methods |
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None of the hospitals had written transfusion protocols. As antifibrinolytic agents, aprotinin was routinely used in hospital A, whereas tranexamic acid was routinely used in the other 2 hospitals. During the time of the study, aprotinin was temporarily unavailable from the manufacturer, and as a result, 46 patients in hospital A underwent cardiac surgery without any antifibrinolytic agent. All patients were admitted to the intensive care unit (ICU) postoperatively, and retransfusion of shed mediastinal blood was practiced at all sites.
Data were collected prospectively on 613 consecutive patients who had undergone coronary artery bypass graft (CABG) procedures only without any valvular operations from October 1, 2000, to March 31, 2001, in hospitals B and C and from December 1, 2000 to March 31, 2001, in hospital A. A total of 545 procedures were performed on pump, and 68 were performed off pump across the 3 sites. The study was approved by the research ethics committees of the participating institutions.
Data Collection
The following data were collected from standardized data collection sheets.
Preoperative characteristics included age, sex, body surface area, Parsonnet score,
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history of prior cardiac surgery, premorbid diagnoses (eg, diabetes mellitus, hypertension, renal failure, coagulation disorders, and left ventricular dysfunction), and whether surgical intervention was required within 6 hours (ie, an emergency procedure). We also recorded preoperative use of drugs that impair hemostasis, such as aspirin, clopidogrel, heparin, or warfarin, as well as preoperative hemoglobin level, international normalized ratio, partial thromboplastin time, and platelet count.
Intraoperative factors included identity of the primary surgeon, antifibrinolytic agent used, time on extracorporeal circulation, lowest intraoperative hematocrit level recorded, type and number of blood products transfused intraoperatively, highest recorded activated clotting time, and total number of grafts, including whether arterial or vein grafts were used.
Postoperative factors included hemoglobin and coagulation parameters, need for exploratory reoperation, mortality, length of stay in the ICU and length of hospitalization, mediastinal drainage in the first 12 hours, and number and type of blood products transfused in the postoperative period.
Data Analysis
Two outcomes were selected for analysis: (1) severe intraoperative anemia, which was defined as the development of an intraoperative hematocrit level of less than 19%, and (2) excessive postoperative bleeding, which was defined as mediastinal drainage of greater than 1000 mL in the first 12 hours postoperatively. Blood product transfusions and re-exploration have been suggested as surrogates for bleeding,
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but there is no consensus regarding the criteria for transfusion
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or reoperation.
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These outcomes were also chosen as potential outcomes that would be important triggers for transfusion that would decrease, although not completely control, the effect of variability in practice.
The postoperative period was defined as the time in the ICU up to a maximum of 3 days for patients who stayed longer in the ICU. The perioperative period was defined as the intraoperative and postoperative periods combined. Patients having their procedure performed off pump were analyzed separately.
Differences between patients who did or did not have the 2 major outcomes were tested for statistical significance by using the Student t test for normally distributed data and the Wilcoxon rank test for nonnormal continuous data, whereas
2 tests were used for categorical variables. Multivariate logistic regression was performed to obtain adjusted estimates of the odds with 95% confidence intervals of patient, procedure, and provider factors associated with the development of intraoperative anemia and excessive postoperative bleeding. Variables were included in the multivariate models if they were significantly associated or if there was evidence of a substantial effect on univariate analysis, as well as clinical factors associated with transfusions in previous studies. A nested model was used (PROC GENMOD-SAS) in which the surgeons using the same intraoperative initial circuit volume and similar type of antifibrinolytic agent were compared with each other to assess the independent effect of surgeon. Statistical testing was performed with SAS 8.2 (SAS Institute, Cary, NC).
| Results |
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Excessive postoperative hemorrhage occurred in 26% of the patients whose procedures were performed on pump. The only preoperative patient characteristic associated with excessive postoperative bleeding in univariate analysis was male sex (Table 3). Excessive postoperative bleeding was more likely with longer bypass time, higher number of grafts performed, and certain surgeons (Figure E3) and less likely if aprotinin or tranexamic acid was used. Bleeding was not associated with preoperative aspirin or heparin or with coagulation parameters measured immediately postoperatively. Patients with excessive postoperative bleeding were more likely to be transfused packed cells (Figure E4), had longer ICU lengths of stay, were more likely to undergo re-exploratory surgery, and were more likely to die.
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In multivariate analysis (Table 4) of patients whose procedures were performed on pump, factors associated with intraoperative anemia were those that might reflect greater hemodilution, such as female sex, smaller body surface area, lower preoperative hemoglobin level, and larger initial total and colloid volume in the bypass circuit.
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Severe intraoperative anemia was a stronger predictor of packed cell transfusions, whereas excessive postoperative hemorrhage was a stronger predictor of receiving coagulation factors. Of the patients who had severe intraoperative anemia, 88% were transfused packed cells perioperatively compared with 72% who had excessive postoperative hemorrhage, whereas of the patients who met the criteria for excessive postoperative hemorrhage, 50% received fresh frozen plasma and 33% received platelets compared with only 27% receiving fresh frozen plasma and 17% receiving platelets among the patients with intraoperative anemia (Table 5).
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| Discussion |
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One important inference from these results is that perioperative blood product requirements in cardiac surgery might not all be due to excessive bleeding. Patients who had intraoperative anemia had the same mean volume of mediastinal drainage postoperatively as patients who did not have intraoperative anemia, and less than one third had excessive postoperative bleeding. Many patients who had intraoperative anemia in this study received a transfusion both in the operating room and postoperatively.
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The differences in the use of coagulation factors associated with mediastinal drainage compared with severe intraoperative anemia also support the hypothesis that clinicians are responding differently to the 2 transfusion triggers.
In this study the strong association of intraoperative anemia with female sex, lower preoperative hemoglobin level, smaller body surface area, and larger total and colloid volume in the initial pump priming solution suggests that hemodilution was an important contributor to this problem. This is also supported by the almost negligible risk (4%) in patients undergoing off-pump procedures. The occurrence of intraoperative anemia has been shown to be an independent predictor of perioperative mortality and morbidity,
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and strategies to decrease its occurrence might improve outcomes in this population. These strategies would include first decreasing preoperative anemia with practices such as limiting preoperative
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blood taking, use of more microlaboratory techniques, and iron supplementation and perhaps erythropoietin in patients awaiting elective operations. Second, because of the strong association with the larger volumes of priming solution with higher volumes of colloid in the extracorporeal circuit, the volume should be adjusted, taking into consideration patient size, sex, and preoperative hemoglobin concentration, rather than using a fixed volume.
This is supported by previous reports
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of decreases in intraoperative packed cell use with the use of lower prime volume. In a recent study,
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use of hetastarch increased the likelihood of patients undergoing coronary artery surgery receiving 3 or more units of any blood product. The hetastarch might have contributed to greater hemodilution and lower intraoperative hematocrit levels, as well as increased bleeding.
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In our study, higher pump volumes and use of more colloid was strongly associated with intraoperative anemia but not with excessive postoperative bleeding. In the study hospitals, the medium-molecular-weight starches (Pentaspan; Bristol Myers Squibb Canada), for which there are less data on increased bleeding risk, are used.
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The doses of hetastarch used during bypass were fixed and in most patients were less than 15 mL/kg.
Although excessive postoperative hemorrhage has been reported to be one of the most common complications of cardiac surgery,
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relatively few studies have examined this outcome
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because most studies examined perioperative transfusions. It has been suggested that outcomes related to excessive drainage should be examined, such as resternotomy
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and blood product transfusions; our results highlight the limitations of this approach. We noted marked differences in reoperation rates and blood product use in the 3 study sites, which were not related to rates of postoperative bleeding (Table 1) but might reflect practice differences. Therefore, analysis of factors associated with the amount of postoperative bleeding was less likely to be biased than analysis of factors associated with these management decisions. In addition, because postoperative bleeding was associated with longer ICU lengths of stay, transfusions, and a higher mortality, we believe this definition is clinically relevant. In addition, measurement of postoperative mediastinal drainage is objective, routinely performed, and reproducible.
In a prospective study of more than 10,000 patients undergoing cardiac surgery, patient characteristics were not associated with reoperation for postoperative bleeding.
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The authors suggested that reoperation for bleeding might be more related to technical surgical factors rather than patient-related factors. Two other studies have demonstrated that postoperative hemorrhage was associated with surgeon,
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and meticulous surgical technique is frequently mentioned
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as an important means to decrease blood product use in cardiac surgery. These findings are consistent with ours, in which male sex was the only patient characteristic and surgeon was strongly associated with this outcome. We speculated that the association with male sex might have occurred because of the assumption that female subjects have higher bleeding risks, which might have resulted in more meticulous surgical practices in female subjects.
We attempted to include in the multivariate analysis the important factors believed to be associated with increased risk of bleeding and transfusion requirements, as well as the factors that differed among the 3 hospitals. There might be other unmeasured factors that we did not account for that could explain some of the results. Certain variables were also very tightly correlated, such as antifibrinolytic use, volume of prime used in the extracorporeal circuit, and particular surgeon, which limit some of the inferences that can be drawn from the results. In this study neither larger total circuit volumes nor larger HES volumes were associated with excessive mediastinal drainage. Although there have been recommendations that HES not be used in patients undergoing cardiac surgery because of concerns of excess bleeding, we did not find that association in this study, even after adjusting for many clinical variables. The almost exclusive use of aprotinin by the center using the larger volumes of HES might account for our not finding an effect.
There were very few patients who had been exposed to clopidogrel, and no patient had been prescribed low-molecular-weight heparin. We also studied only patients who had bypass procedures alone, without any valvular procedures, and therefore the conclusions might not be applicable to these patient populations. Although repeat surgical interventions were not associated with an increased risk of bleeding in this study, the study might have been underpowered to evaluate this association.
| Conclusions |
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| Acknowledgments |
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| Footnotes |
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| References |
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