Abstract
Background:
Relative to first time (primary) cardiac surgery, revision cardiac surgery is associated with increased transfusion requirements, but studies comparing these cohorts were done before patient blood management (PBM) and blood conservation measures were commonplace. The current study was done as an update to determine if this finding is still evident in the PBM era.
Methods:
Primary and revision cardiac surgery cases were compared in a retrospective database analysis at a single tertiary care referral center. Two groups of patients were assessed: 1) Those having isolated coronary artery bypass (CAB) or valve surgery, and 2) all other cardiac surgeries. Intraoperative and whole hospital transfusion requirements were assessed for the 4 major blood components.
Results:
Compared to the primary cardiac surgery patients, the revision surgery patients required ≈2-fold more transfused units intraoperatively (P<0.0001), and ≈2 to 3-fold more transfused units for the whole hospital stay (P<0.0001). Intraoperative massive transfusion (>10 red blood cell units) was substantially more frequent with revision vs. primary cardiac surgery; 2.6 vs. 0.1%; P<0.0001 for isolated CAB or valve, and 6.1% vs. 1.9%; P<0.0001 for all other cardiac surgeries. Revision surgery was an independent risk factor for both moderate (6–10 red blood cell units) and massive intraoperative transfusion.
Conclusions:
In the era of PBM, with restrictive transfusion strategies and a variety of methods for blood conservation, revision cardiac surgery patients continue to have substantially greater transfusion requirements relative to primary cardiac surgery patients. This difference in transfusion requirement was greater than what has been previously reported in the pre-PBM era.
Introduction:
With increased longevity, more patients are having revision cardiac surgery, which presents additional challenges relative to first-time (primary) cardiac surgeries. Blood loss and transfusion requirements are both increased with revision cardiac surgery, likely due to scar tissue, adhesions, and increased operative time. Bracey and colleagues reported a 75% increase in blood components transfused with revision compared to primary coronary artery bypass (CAB) surgery, however this was more than 20 years ago, before patient blood management (PBM) programs were commonplace.1 Since then, new studies supporting lower hemoglobin (Hb) transfusion triggers and new methods of intraoperative blood conservation have been introduced, both of which may influence overall blood utilization.2,3
The purpose of the current study was to assess transfusion requirements for patients undergoing revision compared to primary cardiac surgery in the era of patient blood management. In this retrospective database review, we included both isolated CAB or valve (aortic or mitral) and all other cardiac surgery patients, and evaluated both intraoperative and whole hospital transfusion requirements for all four major blood components. Our hypothesis was that revision cardiac surgery patients continue to have greater transfusion requirements relative to primary surgery patients, despite newer methods of blood conservation and patient blood management techniques. Our findings should be clinically relevant by allowing appropriate planning and preparation for blood availability, as well as targeted methods of blood conservation in these most challenging cases.
Methods:
After approval by the institutional review board, we acquired electronic medical record data for cardiac surgery cases at a single tertiary care center (Johns Hopkins Hospital) from April 2010 until June 2016. We used three sources: a web-based intelligence portal (IMPACT Online; Haemonetics Corp, USA), our anesthesia information management system (AIMS) (MetaVision; iMDsoft Corp, USA), and the Society of Thoracic Surgeons (STS) National Database. We excluded patients with missing data from any of these datasets. We also excluded pediatric cardiac cases (age <18 years old) and trans-aortic valvular replacement (TAVR) procedures. During the time frame of the study, the methods of blood conservation, many of which have been adopted at our institution, are listed in Table 1. Although these were not universally used in all cardiac surgery patients, these methods have been used with increasing frequency at our institution over the past 7 years.
Table 1.
Methods of blood conservation
| 1. Early diagnosis and treatment of preoperative anemia |
| 2. Discontinuing herbal supplements that interfere with coagulation |
| 3. Judicious decision-making for when to not operate (risk exceeds benefit) |
| 4. Minimizing laboratory testing |
| 5. Low volume, microtainers for phlebotomy |
| 6. In-line blood-return devices for indwelling arterial and central venous catheters |
| 7. Tolerating lower hemoglobin levels |
| 8. Intraoperative autologous blood salvage |
| 9. Intraoperative autologous normovolemic hemodilution |
| 10. Meticulous surgical technique |
| 11. Perioperative antifibrinolytics (tranexamic acid, epsilon aminocaproic acid) |
| 12. New methods of electrocautery |
| 13. Topical sealants and hemostatic agents |
| 14. Avoiding perioperative hypothermia |
| 15. Intentional moderate hypotension |
| 16. Point-of-care coagulation testing |
Classification of Surgery and Transfusion
Utilizing the AIMS data, we searched for the procedure “redo sternotomy”, which is the designation for any revision cardiac surgery at our institution. We then used the STS database to classify surgical procedures into four groups: 1) primary isolated CAB or valve (mitral or aortic), 2) revision isolated CAB or valve (mitral or aortic), 3) primary other cardiac surgery, and 4) revision other cardiac surgery. A CAB combined with any other major cardiac procedure (e.g. valve) was included in the “other cardiac surgery” category.
We examined allogeneic blood requirements in both intraoperative and whole hospital time periods for red blood cell (RBC), fresh frozen plasma (FFP), platelets (PLTS), and cryoprecipitate (CRYO). One unit of PLTS was considered to be an apheresis single donor bag, and one unit of CRYO was considered to be one dose (5 pooled units). CRYO data were not available for the intraoperative period, but intraoperative CRYO units were included in the whole hospital data. Based on total number of intraoperative RBC units transfused, we further stratified transfusion requirements into moderate transfusion (6–10 RBC units) and massive transfusion (>10 RBC units) patients based on prior literature.4
Statistical analysis
Results are reported as proportions, mean ± SD, and median (interquartile range). Proportions were compared by Chi-squared tests and/or Fisher’s Exact tests where appropriate. Normally distributed continuous data were compared by unpaired student’s t-tests, and non-normally distributed continuous data by Mann-Whitney U tests. In particular, mean ± SD are reported for transfusion requirements to allow comparison with prior literature on this topic, which reported transfusion requirements in mean ± SD. A multinomial logistic regression model was used to examine whether revision cardiac surgery (relative to primary surgery) was independently associated with increased whole hospital transfusion requirements. Variables to include in the model were considered a priori based on parameters known to influence transfusion rates (preoperative hemoglobin, body mass, gender, duration of surgery, P2Y12 inhibitors, patient age, Charlson Comorbidity Index). Data were analyzed using JMP version 12.0.2 (SAS Institute, Cary North Carolina) and Stata 12.0 (StataCorp; College Station, TX). P < 0.05 defined significance.
Results:
Patients Characteristics
Data were available on 5800 patients. Patient characteristics for the four cohorts (primary vs. revision; isolated CAB or valve vs. other cardiac surgery) are shown in Table 2. The procedures in the “other cardiac surgery” category are listed in Table 3. Of note, 284/5800 (4.9%) patients underwent procedures through a minimally invasive thoracotomy approach. As expected, there were differences in patient characteristics between the primary and the revision groups. Mean age was increased in the primary surgery patients in the other cardiac surgery group. Coagulopathy was more prevalent in the revision group, for both the isolated CAB or valve, and the other cardiac surgery patients. P2Y12 inhibitors were taken in equal proportions in the primary and the revision groups. As expected, duration of surgery, duration of bypass, and duration of cross-clamp were increased with revision surgery in both the isolated CAB or valve and the other cardiac surgery groups. There were small but significant differences as the preoperative hemoglobin was lower, the INR higher, and the platelet count lower in the revision groups.
Table 2.
Characteristics of Cardiac Surgery Patientsa
| Isolated CAB/Valve Surgery | Other Cardiac Surgery | |||||
|---|---|---|---|---|---|---|
| Primary (n = 3,122) | Revision (n = 154) | P-Value | Primary (n = 2,214) | Revision (n = 310) | P-Value | |
| Age in years, mean ± SD | 64 ± 12 | 63 ± 15 | 0.396 | 60 ± 16 | 54 ± 18 | < 0.0001 |
| Male, n (%) | 2,226 (71.30%) | 107 (69.48%) | 0.628 | 1,376 (62.15%) | 191 (61.61%) | 0.8553 |
| Comorbiditiesb | ||||||
| Hypertension, n (%) | 2,065 (78.10%) | 87 (65.91%) | 0.0018 | 1,204 (63.17%) | 163 (59.49%) | 0.241 |
| Pulmonary, n (%) | 397 (15.02%) | 19 (14.39%) | 0.845 | 342 (17.94%) | 32 (11.68%) | 0.0073 |
| Renal, n (%) | 398 (15.05%) | 18 (13.64%) | 0.6524 | 294 (15.42%) | 50 (18.25%) | 0.2386 |
| Coagulopathy, n (%) | 150 (5.67%) | 18 (13.64%) | 0.0011 | 144 (7.56%) | 34 (12.41%) | 0.0095 |
| Obesity, n (%) | 484 (18.31%) | 22 (16.67%) | 0.6304 | 253 (13.27%) | 22 (8.03%) | 0.01 |
| Diabetes, n (%) | 771 (29.16%) | 29 (21.97%) | 0.0678 | 364 (19.10%) | 41 (14.96%) | 0.0921 |
| Charlson Comorbidity Index, med (IQR) | 2 (1 – 3) | 2 (1 – 3) | 0.65 | 2 (1 – 3) | 2 (1 – 3) | 0.4038 |
| Weight (kg), mean ± SD | 87 ± 20 | 86 ± 20 | 0.6048 | 85 ± 21 | 83 ± 21 | 0.1037 |
| P2Y12 Inhibitorc, n (%) | 412 (13.20%) | 21 (13.64%) | 0.9518 | 127 (5.74%) | 15 (4.84%) | 0.3193 |
| Surgical Characteristics | ||||||
| Duration of Surgery, min ± SD | 257 ± 97 | 310 ± 106 | < 0.0001 | 281 ± 117 | 358 ± 142 | < 0.0001 |
| Bypass Time, min ± SD | 99 ± 40 | 134 ± 48 | < 0.0001 | 134 ± 59 | 182 ± 82 | < 0.0001 |
| Cross Clamp Time, min ± SD | 65 ± 26 | 72 30 | 0.0014 | 86 ± 38 | 105 ± 49 | < 0.0001 |
| First Hb, mean ± SD | 13.1 ± 2.0 | 12.6 ± 2.1 | 0.0021 | 13.0 ± 2.0 | 12.5 ± 2.4 | 0.0004 |
| First Hct, mean ± SD | 39.1 ± 5.3 | 38.0 ± 5.9 | 0.025 | 38.9 ± 5.6 | 37.8 ± 6.2 | 0.0021 |
| First INR, mean ±SD | 1.1 ± 0.4 | 1.3 ± 1.0 | 0.0034 | 1.3 ± 0.7 | 1.5 ± 1.0 | < 0.0001 |
| First PLT, mean ± SD | 223 ± 80 | 211 ± 80 | 0.092 | 223 ± 83 | 208 ± 74 | 0.0031 |
| % Massively Transfused | ||||||
| > 5 Units RBC in OR, n (%) | 52 (1.67%) | 20 (12.99%) | < 0.0001 | 169 (7.63%) | 64 (20.65%) | < 0.0001 |
| > 10 Units RBC in OR, n (%) | 4 (0.13%) | 4 (2.60%) | 0.0003 | 41 (1.85%) | 19 (6.13%) | < 0.0001 |
Kg= kilograms; Hb = hemoglobin; Hct= hematocrit; INR= international normalized ratio; PLT= platelet
All values are expressed using the number of patients with non-missing data as the denominator
ICD-9 and ICD-10 discharge codes available through the Impact Online database were used to identify comorbidities
Defined as having received P2Y12 inhibitors within 5 days of surgery
Table 3.
Percentage of Types of Cases within Other Cardiac Surgery Category
| Category | Frequency | Percentage |
|---|---|---|
| VAD | 109 | 4.32 |
| Transplanta | 148 | 5.86 |
| Aortic Arch | 127 | 5.03 |
| Ascending/Descending Aorta | 544 | 21.55 |
| Myectomy | 123 | 4.87 |
| Cardiac Masses | 56 | 2.22 |
| Congenital | 86 | 3.41 |
| Other valveb | 249 | 9.87 |
| CAB/Valve combined | 540 | 21.39 |
| Otherc | 542 | 21.47 |
VAD= ventricular assist device
Heart or lung transplant
Tricupsid valve repair/replacement, pulmonic repair/replacement, and multiple valvular procedures
Combined procedures not easily definable or very low frequency. i.e., Ross procedure AND subaortic membrane resection
Patients that were brought back to the operating room after their initial cardiac surgery were included in the analysis. The vast majority of the time, these patients are brought back due to excessive bleeding in the cardiac surgical ICU. There were 307 patients brought back for excessive bleeding out of 5800 total patients, or 5.3%. There were 4.85% in the primary sternotomy group (259/5336) versus 10.3% (48/464) of the revision sternotomy patients (P<0.001).
Incidence of Transfusion
As shown in Figure 1, for all patients (both the isolated CAB/valve group and the other cardiac surgery group), the percentage of patients requiring transfusion over the whole hospital stay and intraoperatively was greater in the revision than the primary surgery group for RBCs, FFP, PLTS, and CRYO (P<0.01 for all blood components). The greater incidence of transfusion in the revision patients ranged from a ≈30–50% increase (for RBCs) to ≈60–100% increase (for FFP, PLTS, and CRYO).
Figure 1.
The percentage of patients requiring any transfusion of the four major blood components were compared between revision and primary cardiac surgery patients. Isolated coronary artery bypass (CAB) / valve and all other cardiac surgeries were analyzed as separate subgroups, and whole hospital and intraoperative transfusion requirements are shown. There was a clear increase in the percentage of patients requiring all the blood components when revision surgeries were compared to primary surgeries. (All P-values <0.001)
Magnitude of Transfusion Requirements
As shown in Figure 2, all types of revision surgeries had an approximate 2-fold increase in the mean number of units transfused intraoperatively for all blood components (P<0.0001 for all comparisons). For the whole hospital course, all types of revision surgeries had an approximate 2 to 3-fold increase in mean number of units transfused for all blood components (P<0.0001 for all comparisons).
Figure 2.
Mean red blood cell (RBC), plasma (FFP), platelets (PLTS), and cryoprecipitate (CRYO) units transfused were compared between revision and primary cardiac surgery patients. Isolated coronary artery bypass (CAB)/valve and all other cardiac surgeries were analyzed as separate subgroups, and whole hospital and intraoperative transfusion requirements are shown. Revision surgery was associated with a 2 to 3-fold increase in blood utilization for isolated CAB/valve, and a 2-fold increase in other cardiac surgeries.
The relative incidence of moderate (6–10 RBC units) and massive (>10 RBC units) intraoperative transfusions was also examined, as shown in Figure 3. Moderate transfusion during surgery was substantially more frequent with revision vs. primary cardiac surgery, for both isolated CAB/valves (10.4 vs. 1.5%; P<0.0001), and for all other cardiac surgeries (14.5% vs. 5.8%; P<0.0001). Similarly, massive transfusion during surgery was substantially more frequent with revision vs. primary cardiac surgery for isolated CAB/valves (2.6 vs. 0.1%; P<0.0001) and for all other cardiac surgeries (6.1% vs. 1.9%; P<0.0001).
Figure 3.
The incidence of intraoperative moderate (6–10 RBC units) and massive (>10 RBC units) transfusion was substantially higher in the revision compared to the primary cardiac surgery patients. (All P-values < 0.001)
The independent contribution of revision surgery to moderate and massive intraoperative transfusion was examined using multivariable multinomial logistic regression, with risk adjustment for age, weight, gender, operative time, first hemoglobin, Charlson score, and anti-platelet medications (Table 4). Revision surgery independently increased the risk of both moderate and massive transfusions. The magnitude of increased risk was greater among CAB/valve patients, compared with other surgeries.
Table 4:
Relative Risk Ratio of Intraoperative Red Cell Unit Transfusion for Revision Cardiac Surgery Compared to Primary Surgery
| Unadjusted | Adjusted* | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Relative Risk Ratio | Confidence Interval | P-value | Relative Risk Ratio | Confidence Interval | P-value | |||||
| CAB/ Valve | ||||||||||
| 0 Units (reference) | ||||||||||
| 1–5 units | 1.9 | 1.4–2.7 | <0.001 | 1.8 | 1.14–2.9 | 0.01 | ||||
| 6–10 units (moderate transfusion) | 10.2 | 5.5–18.9 | <0.001 | 8.1 | 3.7–17.9 | <0.001 | ||||
| > 10 units (massive transfusion) | 30.6 | 7.5–125.1 | <0.001 | 22.9 | 3.0–174.8 | 0.003 | ||||
| Other | ||||||||||
| 0 Units (reference) | ||||||||||
| 1–5 units | 2.1 | 1.6–2.7 | <0.001 | 2.1 | 1.5–3.0 | <0.001 | ||||
| 6–10 units (moderate transfusion) | 4.2 | 2.9–6.3 | <0.001 | 2.5 | 1.5–4.4 | 0.001 | ||||
| > 10 units (massive transfusion) | 5.6 | 3.1–10.0 | <0.001 | 2.4 | 1.1–5.4 | 0.03 | ||||
Adjusted for age, weight, gender, surgery time, first hemoglobin, Charlson score, and anti-platelet medications
Discussion:
The primary findings in our study are that revision cardiac surgery patients have a substantially greater transfusion requirement relative to first time (primary) cardiac surgery patients. In fact, the difference between revision and primary surgery in the current study with regard to transfusion requirements was greater than was reported over 20 years ago by Bracey et al. before current PBM practices were commonplace, and prior to the randomized trials supporting restrictive transfusion strategies.1–3,5 In general, our findings demonstrate a 2–3 fold greater transfusion requirement for patients having revision surgery, compared to a 75% increase previously reported.1
This increased transfusion requirement for revision surgeries suggests that the newer methods of blood management may not be very effective in reducing transfusion requirements in revision surgeries. Revision cardiac surgery may require more blood than we are able to save by using blood management methods, such as cell salvage, hemoconcentrators, acute normovolemic hemodilution (ANH), lower hemoglobin triggers and targets, smaller phlebotomy tubes, complete rewarming, and viscoelastic point of care testing. However, we are hopeful that continuing these blood conservation methods along with modifying our surgical strategies, may help us eventually to achieve less blood utilization for these challenging patients.
Routine use of anti-fibrinolytics is one of many strategies to decrease blood product utilization in cardiac surgery. Epsilon-aminocaproic (EACA) and its pharmacologic mechanism was first discovered in the early 1960’s but did not become clinically recognized and used until the late 1980’s.6 Due to cardiopulmonary bypass causing accelerated thrombin generation, dysfunctional platelets and fibrinolysis, aprotinin and lysine-analogs (EACA and tranexamic acid) became popular to attenuate bleeding.7 In a Cochrane review by Henry et al., the relative risk of needing an allogeneic RBC transfusion with tranexamic acid and EACA compared to controls were 0.61 (95% confidence interval [CI] 0.53 to 0.70) and 0.81, respectively (95% CI 0.67 to 0.99). Our institution started routinely using EACA in the late 1990’s, and it remains the routine practice today.8
Additionally, in this new era of patient blood management, many anesthesiologists use viscoelastometry to help guide transfusion of plasma, platelets, and cryoprecipitate. There have been algorithms developed specifically targeting cardiac surgical patients.9 A recent meta-analyses by Wikkelso et al. of trials utilizing viscoelastometry (TEG and ROTEM) algorithms found a significant reduction in bleeding and transfusion.10 Such algorithms were published in 1999, and used sporadically in our institution until the past decade, when a formal algorithm was adopted as routine practice.
Strategies to reduce transfusion have been driven by the results of both randomized and observational studies. The two most recent trials supporting restrictive transfusion strategies in cardiac surgery add to the evidence from an earlier study (also by Bracey and colleagues), that giving more blood than is necessary to cardiac surgery patients does not improve outcomes5. The TRACS and TITRe2 trials, in 2010 and 2015 respectively, demonstrated noninferiority in the primary outcomes between a restrictive vs. liberal postoperative transfusion strategy.2,3 In revision cardiac surgery, specifically, George et al. found that revision sternotomy heart transplant recipients had increased blood product usage, and that increased transfusion of products was independently associated with short and long-term mortality.11 Many other observational studies have reported the increased morbidity and mortality associated with incremental amounts of blood transfusion.4,12,13 Although the results of observational studies must be interpreted with caution, the 2011 Update to the Society of Thoracic Surgeons and Society of Cardiovascular Anesthesiologists Blood Conservation Guidelines noted that transfusing beyond the recommended guidelines only increases risk and cost for cardiac surgery patients.14
Surgeons also approach revision sternotomy cases differently from primary cases. First, a decision is made whether to commence cardiopulmonary bypass (CPB) prior to sternotomy. The disadvantage to this conservative approach is a longer time on CPB. Secondly, surgeons may use different equipment, including an oscillating saw to try and prevent entering into a large vessel or anterior cardiac chamber. Thirdly, hemostatic agents, such as Floseal™ (Baxter International, Deerfield IL) may be used for both primary and revision sternotomy cases. Although the surgical technique may be different for revision cases, we have not been able to identify techniques that we feel could improve outcomes; indeed many of the differences in techniques were developed specifically to improve safety in this population. Thus, newer strategies in transfusion and surgical practice warranted a new look at whether revision cardiac surgery patients continue to require more transfused blood components relative to primary cardiac surgery patients, as was shown two decades ago.
Not surprisingly, there was a significantly increased duration of surgery and duration of cardiopulmonary bypass for revision cardiac surgery relative to primary surgery. Increased time on CPB may result in more inflammation, leading to impaired hemostasis and increased blood loss, and consequently increased transfusion requirements. As mentioned previously, CPB can increase fibrinolysis, cause a consumptive coagulopathy, and lead to dysfunctional platelets. Increasing duration of CPB and its’ associated risk of more allogeneic blood units transfused is a common finding.12,15,16 Parr et al. found that increased CPB time had an adjusted odds ratio (OR) of 1.33 (95% CI 1.14–1.54) in their primary outcome of transfusion of >2 units of RBCs and an adjusted OR of 1.36 (95% CI 1.16–1.60) of needing mediastinal re-exploration or receipt of cryoprecipitate, FFP, or platelets during hospitalization.15 Although viscoelastic point-of-care testing, antifibrinolytic drugs, acute normovolemic hemodilution, cell salvage and use of hemoconcentrators have been effective in reducing transfusions overall in cardiac surgery, the increased duration of CPB in revision cases is likely an contributing cause of increased transfusion requirements.
In addition to examining average transfusion, we also examined the incidence of moderate (6–10 RBC units) and massive (>10 RBC units) transfusion intraoperatively. It is paramount to know how best to prepare for revision cardiac surgery cases, specifically quantities of blood components to prepare, and how quickly these units can be obtained. In our data, 13.0% of the revision isolated CAB or valves and 20.6% of the revision other cardiac surgeries required moderate or massive transfusion. Commonly, slow bleeding occurs at the microvascular level in revision cardiac cases. Uncommonly, these are cases with rapid blood loss upon entering the patient’s chest. Even when using extreme caution, a large vessel, such as the aorta or pulmonary artery or even an anterior heart chamber, such as the right ventricle, can be accidentally punctured. In those moments of rapid bleeding, having a container of RBCs and/or FFP in the operating room helps to facilitate giving blood during sudden hemorrhage. Our data also suggest that plasma and platelets should be rapidly obtainable for revision cardiac surgery cases.
In our analysis, we were unable to quantify the incidence of cardiac rupture on dissection, however we did examine the amount of cell salvage returned to patients intraoperatively. For primary sternotomy patients, a median of 500 mL (IQR 500–750 mL) was returned, while for revision sternotomy patients a median of 600 mL (IQR 500–800 mL) was returned (P<0.01). These estimates underscore our observation that more blood loss occurs in revision sternotomy patients, and may also be a reason for increased utilization of plasma and platelets.
Even after accounting for confounding variables, revision surgery was an independent risk factor for both moderate and massive intraoperative transfusion. Of note, the risk of moderate and massive transfusion was greater in CAB/valve patients compared with other cardiac surgery patients. This may be due to the inherent risk of bleeding associated with those cases that were classified as ‘other cardiac surgeries’, such as aortic root replacements, ascending aorta replacements, aortic arch reconstructions and emergent aortic dissections. These complex aortic surgeries will likely have increased blood utilization in the primary surgery for a variety of reasons and have been shown in other studies to have the highest degree of blood utilization compared to other cardiac surgeries.17 We did not include previous exposure to chest radiation in our analysis but studies have demonstrated increased risk of massive bleeding as well as increased long-term mortality.18,19
The limitations of this study include the single centered nature of the study, and the possibility that results may differ in other centers due to differences in surgical technique or the use of patient blood management practices. Since our institution is a tertiary/quaternary referral center, it may limit the generalizability of our results. Nevertheless, it is important to point out that our results are similar in both the isolated CAB/valve patients as well as the other cardiac surgery group. In our experience, the “other” patients are often the patients who are specifically referred for tertiary/quaternary care. Additionally, the incidence of revision at our institution is similar to other sites in the literature20.
Another possible limitation is the heterogeneity of the surgical cases that were in the other cardiac surgery group. For example, it has been previously noted that lowest temperature on bypass correlates with increased transfusion due to hypothermia causing dysfunctional platelets as well as the increased time for cooling and rewarming on CPB.21 Thus complex cardiac surgeries requiring hypothermic circulatory arrest or involving multiple combined procedures may have increased transfusion requirements. Interestingly, our findings in the isolated CAB or valve group were generally similar to the other cardiac surgery group, suggesting that revision surgery is a strong predictor of increased transfusion, regardless of the type of cardiac surgical procedure.
A final limitation is in how patient blood management (PBM) strategies are phased in over time and how that may affect a retrospective study. In 2014, our institution started to use PBM measures such as acute normovolemic hemodilution and viscoelastic testing algorithms routinely. In 2015, we started using hemoconcentrators on cardiopulmonary bypass routinely. Even though these strategies were phased in over the course of the study time period, we had an equal number of revision cases in the 2010–2013 time period when there was less PBM enacted as we did during the 2014–2016 period when more were being utilized routinely.
In summary, revision cardiac surgery, even in the era of patient blood management, remains a strong predictor of increased transfusion requirements, and the increased transfusion with revision surgery was greater in our study than was reported two decades ago. Perhaps with more aggressive blood conservation techniques, we can reduce transfusion requirements in this high-risk population. Preoperative optimization by diagnosing and treating anemia may be of benefit, as well as correction of coagulopathies prior to surgery. Intraoperative use of autologous normovolemic hemodilution and viscoelastic testing algorithms may also be beneficial. Autologous cell salvage and hemoconcentration (modified ultrafiltration), as well as complete rewarming to prevent residual hypothermia may all be useful to decrease transfusion in these complex revision surgeries.22,23 Our findings may allow anesthesiologists, surgeons, and transfusion medicine specialists to better plan and prepare for these challenging revision cardiac surgery cases.
Acknowledgments
Conflicts of Interests and Sources of Funding:
SMF has been a consultant for Haemonetics (Braintree, MA), Zimmer-Biomet (Warsaw, IN), and Medtronic (Minneapolis, MN). CHB has grant support through NIH K23AG051783–01A1 and the International Anesthesia Research Society. He has received funding from Medtronic for consulting and research that is unrelated to the present study. All other authors have no conflicts to declare.
Contributor Information
Nadia B. Hensley, Department of Anesthesiology/Critical Care Medicine, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Megan P. Kostibas, Department of Anesthesiology/Critical Care Medicine, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Todd Crawford, Department of Surgery, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Pranjal B. Gupta, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Kaushik Mandal, Department of Surgery, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
William W. Yang, Department of Anesthesiology/Critical Care Medicine, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Steven M. Frank, Department of Anesthesiology/Critical Care Medicine, Director, Johns Hopkins Health System Blood Management Program, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Charles H. Brown, 4th, Department of Anesthesiology/Critical Care Medicine, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
References
- 1.Bracey AW, Radovancevic R, Radovancevic B, McAllister HA Jr, Vaughn WK, Cooley DA: Blood use in patients undergoing repeat coronary artery bypass graft procedures: multivariate analysis. Transfusion 1995; 35: 850–4 [DOI] [PubMed] [Google Scholar]
- 2.Hajjar LA, Vincent JL, Galas FR, Nakamura RE, Silva CM, Santos MH, Fukushima J, Kalil Filho R, Sierra DB, Lopes NH, Mauad T, Roquim AC, Sundin MR, Leao WC, Almeida JP, Pomerantzeff PM, Dallan LO, Jatene FB, Stolf NA, Auler JO Jr, Transfusion requirements after cardiac surgery: the TRACS randomized controlled trial. JAMA 2010; 304: 1559–67 [DOI] [PubMed] [Google Scholar]
- 3.Murphy GJ, Pike K, Rogers CA, Wordsworth S, Stokes EA, Angelini GD, Reeves BC, Investigators TI: Liberal or restrictive transfusion after cardiac surgery. N Engl J Med 2015; 372: 997–1008 [DOI] [PubMed] [Google Scholar]
- 4.Johnson DJ, Scott AV, Barodka VM, Park S, Wasey JO, Ness PM, Gniadek T, Frank SM: Morbidity and Mortality after High-dose Transfusion. Anesthesiology 2016; 124: 387–95 [DOI] [PubMed] [Google Scholar]
- 5.Bracey AW, Radovancevic R, Riggs SA, Houston S, Cozart H, Vaughn WK, Radovancevic B, McAllister HA, Cooley DA: Lowering the hemoglobin threshold for transfusion in coronary artery bypass procedures: effect on patient outcome. Transfusion 1999; 39: 1070–7 [DOI] [PubMed] [Google Scholar]
- 6.Butterworth J, James RL, Lin Y, Prielipp RC, Hudspeth AS: Pharmacokinetics of epsilon-aminocaproic acid in patients undergoing aortocoronary bypass surgery. Anesthesiology 1999; 90: 1624–35 [DOI] [PubMed] [Google Scholar]
- 7.Koster A, Schirmer U: Re-evaluation of the role of antifibrinolytic therapy with lysine analogs during cardiac surgery in the post aprotinin era. Curr Opin Anaesthesiol 2011; 24: 92–7 [DOI] [PubMed] [Google Scholar]
- 8.Henry DA, Carless PA, Moxey AJ, O’Connell D, Stokes BJ, McClelland B, Laupacis A, Fergusson D: Anti-fibrinolytic use for minimising perioperative allogeneic blood transfusion. Cochrane Database Syst Rev 2007: CD001886. [DOI] [PubMed] [Google Scholar]
- 9.Shore-Lesserson L, Manspeizer HE, DePerio M, Francis S, Vela-Cantos F, Ergin MA: Thromboelastography-guided transfusion algorithm reduces transfusions in complex cardiac surgery. Anesth Analg 1999; 88: 312–9 [DOI] [PubMed] [Google Scholar]
- 10.Wikkelso A, Wetterslev J, Moller AM, Afshari A: Thromboelastography (TEG) or rotational thromboelastometry (ROTEM) to monitor haemostatic treatment in bleeding patients: a systematic review with meta-analysis and trial sequential analysis. Anaesthesia 2017; 72: 519–531 [DOI] [PubMed] [Google Scholar]
- 11.George TJ, Beaty CA, Ewald GA, Russell SD, Shah AS, Conte JV, Whitman GJ, Silvestry SC: Reoperative sternotomy is associated with increased mortality after heart transplantation. Ann Thorac Surg 2012; 94: 2025–32 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Koch CG, Li L, Duncan AI, Mihaljevic T, Cosgrove DM, Loop FD, Starr NJ, Blackstone EH: Morbidity and mortality risk associated with red blood cell and blood-component transfusion in isolated coronary artery bypass grafting. Crit Care Med 2006; 34: 1608–16 [DOI] [PubMed] [Google Scholar]
- 13.Yang JC, Sun Y, Xu CX, Dang QL, Li L, Xu YG, Song YJ, Yan H: Correlation between red blood cell transfusion volume and mortality in patients with massive blood transfusion: A large multicenter retrospective study. Exp Ther Med 2015; 9: 137–142 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Society of Thoracic Surgeons Blood Conservation Guideline Task F, Ferraris VA, Brown JR, Despotis GJ, Hammon JW, Reece TB, Saha SP, Song HK, Clough ER, Society of Cardiovascular Anesthesiologists Special Task Force on Blood T, Shore-Lesserson LJ, Goodnough LT, Mazer CD, Shander A, Stafford-Smith M, Waters J, International Consortium for Evidence Based P, Baker RA, Dickinson TA, FitzGerald DJ, Likosky DS, Shann KG: 2011 update to the Society of Thoracic Surgeons and the Society of Cardiovascular Anesthesiologists blood conservation clinical practice guidelines. Ann Thorac Surg 2011; 91: 944–82 [DOI] [PubMed] [Google Scholar]
- 15.Parr KG, Patel MA, Dekker R, Levin R, Glynn R, Avorn J, Morse DS: Multivariate predictors of blood product use in cardiac surgery. J Cardiothorac Vasc Anesth 2003; 17: 176–81 [DOI] [PubMed] [Google Scholar]
- 16.Litmathe J, Boeken U, Feindt P, Gams E: Predictors of homologous blood transfusion for patients undergoing open heart surgery. Thorac Cardiovasc Surg 2003; 51: 17–21 [DOI] [PubMed] [Google Scholar]
- 17.Robich MP, Koch CG, Johnston DR, Schiltz N, Chandran Pillai A, Hussain ST, Soltesz EG: Trends in blood utilization in United States cardiac surgical patients. Transfusion 2015; 55: 805–14 [DOI] [PubMed] [Google Scholar]
- 18.Wu W, Masri A, Popovic ZB, Smedira NG, Lytle BW, Marwick TH, Griffin BP, Desai MY: Long-term survival of patients with radiation heart disease undergoing cardiac surgery: a cohort study. Circulation 2013; 127: 1476–85 [DOI] [PubMed] [Google Scholar]
- 19.Chang AS, Smedira NG, Chang CL, Benavides MM, Myhre U, Feng J, Blackstone EH, Lytle BW: Cardiac surgery after mediastinal radiation: extent of exposure influences outcome. J Thorac Cardiovasc Surg 2007; 133: 404–13 [DOI] [PubMed] [Google Scholar]
- 20.Algarni KD, Elhenawy AM, Maganti M, Collins S, Yau TM: Decreasing prevalence but increasing importance of left ventricular dysfunction and reoperative surgery in prediction of mortality in coronary artery bypass surgery: trends over 18 years. J Thorac Cardiovasc Surg 2012; 144: 340–6, 346 e1 [DOI] [PubMed] [Google Scholar]
- 21.Sniecinski RM, Chen EP, Tanaka KA: Reduced levels of fibrin (antithrombin I) and antithrombin III underlie coagulopathy following complex cardiac surgery. Blood Coagul Fibrinolysis 2008; 19: 178–9 [DOI] [PubMed] [Google Scholar]
- 22.Wang G, Bainbridge D, Martin J, Cheng D: The efficacy of an intraoperative cell saver during cardiac surgery: a meta-analysis of randomized trials. Anesth Analg 2009; 109: 320–30 [DOI] [PubMed] [Google Scholar]
- 23.Carless PA, Henry DA, Moxey AJ, O’Connell D, Brown T, Fergusson DA: Cell salvage for minimising perioperative allogeneic blood transfusion. Cochrane Database Syst Rev 2010: CD001888. [DOI] [PubMed] [Google Scholar]



