Skip to main content

The impact of bleeding on outcomes following lung transplantation: a retrospective analysis using the universal definition of perioperative bleeding

Abstract

Background

Lung transplantation (LT) represents a high-risk procedure for end-stage lung diseases. This study describes the outcomes of patients undergoing LT that require massive transfusions as defined by the universal definition of perioperative bleeding (UDPB).

Methods

Adult patients who underwent bilateral LT at a single academic center were surveyed retrospectively. Patients were grouped by insignificant, mild, or moderate perioperative bleeding (insignificant-to-moderate bleeders) and severe or massive perioperative bleeding (severe-to-massive bleeders) based on the UDPB classification. Outcomes included 1-year survival and primary graft dysfunction (PGD) of grade 3 at 72 h postoperatively. Multivariable models were adjusted for recipient age, sex, body mass index (BMI), Lung allocation score (LAS), preoperative hemoglobin (Hb), preoperative extracorporeal membrane oxygenation (ECMO) status, transplant number, and donor status. An additional multivariable model was created to find preoperative and intraoperative predictors of severe-to-massive bleeding. A p-value less than 0.05 was selected for significance.

Results

A total of 528 patients were included, with 357 insignificant-to-moderate bleeders and 171 severe-to-massive bleeders. Postoperatively, severe-to-massive bleeders had higher rates of PGD grade 3 at 72 h, longer hospital stays, higher mortality rates at 30 days and one year, and were less likely to achieve textbook outcomes for LT. They also required postoperative ECMO, reintubation for over 48 h, tracheostomy, reintervention, and dialysis at higher rates. In the multivariate analysis, severe-to-massive bleeding was significantly associated with adverse outcomes after adjusting for recipient and donor factors, with an odds ratio of 7.73 (95% CI: 4.27–14.4, p < 0.001) for PGD3 at 72 h, 4.30 (95% CI: 2.30–8.12, p < 0.001) for 1-year mortality, and 1.75 (95% CI: 1.52–2.01, p < 0.001) for longer hospital stays. Additionally, severe-to-massive bleeders were less likely to achieve textbook outcomes, with an odds ratio of 0.07 (95% CI: 0.02–0.16, p < 0.001). Preoperative and intraoperative predictors of severe/massive bleeding were identified, with White patients having lower odds compared to Black patients (OR: 041, 95% CI: 0.22–0.80, p = 0.008). Each 1-unit increase in BMI decreased the odds of bleeding (OR: 0.89, 95% CI: 0.83–0.95, p < 0.001), while each 1-unit increase in MPAP increased the odds of bleeding (OR: 1.04, 95% CI: 1.02–1.06, p < 0.001). First-time transplant recipients had lower risk (OR: 0.16, 95% CI: 0.06–0.36, p < 0.001), whereas those with DCD donors had a higher risk of severe-to-massive bleeding (OR: 3.09, 95% CI: 1.63–5.87, p = 0.001).

Conclusion

These results suggest that patients at high risk of massive bleeding require higher utilization of hospital resources. Understanding their outcomes is important, as it may inform future decisions to transplant comparable patients.

Peer Review reports

Background

Lung transplantation (LT) is a complex procedure for patients with end-stage lung disease that offers hope and a survival benefit [1]. LT survival, however, has lagged compared to other solid organ transplantations [2, 3].

The decision to transplant a patient entails consideration of many factors, including the severity of lung disease, efficacy of alternative treatments, the patient’s general health status, and likelihood of success [4]. As demand for LT increases, selecting recipients who will maximally benefit is necessary, [5] and selection criteria should consider patient demographics, comorbidities, and potential complications [6].

Perioperative bleeding during LT and the need for transfusion poses significant risks to transplanted organs [7]. For example, a growing body of evidence suggests that large-volume transfusion negatively impacts graft function (i.e. primary graft dysfunction (PGD)) which may translate into chronic allograft dysfunction (CLAD), and shorten overall survival. Consequently, understanding the preoperative risks for bleeding before LT can help inform decisions about whether or not to transplant an individual.

Increased bleeding, as defined by the universal definition of perioperative bleeding (UDPB), requires additional blood products and is associated with increased morbidity and mortality in various cardiac surgical settings [8]. In this study, we applied this definition of massive bleeding retrospectively to our LT cohort in order to describe the impact of increased bleeding on outcomes for those recipients based on the UDPB. In some instances, bleeding is unanticipated but often it can be predicted based on the patient’s history or current clinical situation. It is our hope that the insights from this retrospective analysis will inform clinical decision-making around the appropriateness of LT in patients at high risk of increased bleeding and transfusion.

Methods

Patients and study design

This was a retrospective cohort study of patients undergoing bilateral orthotopic lung transplantations (BOLT) at a single-center, large-volume LT program. Approval from the Institutional Review Board (IRB) was obtained prior to the initiation of this study (Pro00093325). Patients were included in the cohort if they were identified as undergoing LT between January 1, 2017, and July 31, 2022. Multi-visceral transplantation patients and patients who underwent a single orthotopic LT were excluded. The final cohort (n = 528) contained patients over 18 years old who underwent BOLT. The UDPB was used to separate patients into two groups: patients with insignificant, mild, or moderate bleeding (insignificant-to-moderate bleeders) (n = 357) and patients with severe or massive bleeds (severe-to-massive bleeders) (n = 171) [9]. The UDPB stratifies patients into five classes based on nine clinical events that occur during surgery or within the first postoperative day, including blood loss, delayed sternal closure, and need for blood products. Patients were dichotomized by groups; classes 0 to 2 were insignificant-to-moderate bleeders, and classes 3 and 4 were categorized as severe-to-massive bleeders. Patients were divided into two groups to emphasize severity and acuity of presentation, enabling clearer comparisons of outcomes. Furthermore, this dichotomization reduced the comparison groups to allow for enhanced statistical analysis.

Variables

Characteristics for lung recipients were collected, including age, gender, body mass index (BMI), preoperative diagnosis, pulmonary hypertension, mean pulmonary artery pressure (MPAP), lung allocation score (LAS), previous lung surgery, including prior LT, or pleural procedure, left ventricular ejection fraction, preoperative extracorporeal membrane oxygenation (ECMO), preoperative ventilation status, and preoperative labs including the International Normalized Ratio (INR), creatine (Cr), hemoglobin (Hb), and platelet counts. Donor variables such as age, gender, BMI, smoking status, donation after circulatory death (DCD), donation after brain death (DBD), and a medical history of hypertension or cancer were also collected. Additionally, operative characteristics, including the use and type of extracorporeal life support (ECLS) such as venovenous (VV) ECMO and venoarterial (VA) ECMO, duration of ECLS, duration of total ischemia, the intraoperative administration of tranexamic acid (TXA), and the presence of intraoperative complications were recorded.

At our institution, the algorithm for mechanical support during LT primarily involves routine use of VA ECMO, while CPB is reserved for emergencies or cases involving concomitant heart surgery [10]. Anticoagulation is managed using activated clotting time targets of 180–220 s for VA ECMO and > 400 s for CPB, with additional monitoring of platelet counts, fibrinogen levels, and rotational thromboelastometry (ROTEM) at the first lung reperfusion.

Outcomes

The primary outcome of interest was the occurrence of PGD grade 3 at 72 h after LT. PGD was defined according to the International Society for Heart and Lung Transplantation [8]. Several secondary outcomes were analyzed in relation to UDPB classification, including one-year mortality, hospital length of stay (LOS), and textbook outcome which is a composite outcome measure that aggregates intraoperative complications, need for postoperative interventions, readmission to the ICU or hospital within 30 days, length of stay exceeding the 75th percentile for LT patients, mortality within 90 days, acute rejection within 30 days, grade 3 primary graft dysfunction at 48–72 h, use of postoperative extracorporeal membrane oxygenation, tracheostomy within 7 days, inpatient dialysis, reintubation, and extubation more than 48 h after the transplant [11, 12]. The measurement of textbook outcome has been associated with improved post-transplant survival and reliability in center-level LT performance [13].

UDPB classification of bleeding assesses hemostasis, need for blood products, need for surgical reexploration, and salvage treatment [9]. Clinical bleeding evidence, laboratory evidence of coagulopathy, and established transfusion algorithms guided the decision to transfuse blood products or perform further intervention [14].

Statistical analyses

Descriptive statistics were calculated to provide a summary of the cohort’s outcomes, with frequencies and percentages used to summarize categorical variables. Continuous variables were compared using the Mann-Whitney U test and independent samples t-test. The Mann-Whitney U test compared medians of two independent groups when data deviated from normality or sample sizes were small, while the independent samples t-test compared means under normality and homogeneity of variance assumptions. The chi-squared test and Fisher exact test examined associations between categorical variables, with the Fisher exact test applied to small sample sizes or violated chi-square test assumptions. Univariate and multivariable regression models for the bleeding groups were performed on outcomes including textbook outcomes, PGD grade 3 at 72 h, one-year mortality, and hospital LOS. Multivariable logistic regression models were adjusted for recipient age, sex, BMI, LAS, group diagnosis, preoperative ECMO status, number of transplants, preoperative Hb, and donor status (DCD vs. DBD). Variables were selected by fellowship trained cardiothoracic surgeons and anesthesiologist based on clinical relevance and pertinence to outcomes of interest.

Additionally, univariate analysis evaluated the significance of these variables. Multicollinearity between variables in the multiple regression models was assessed using the variance inflation factor (VIF). All VIFs were below 3, indicating low multicollinearity, which was not considered an issue. Variables were used in their recorded format whenever possible. If a typically continuous variable was summarized as categorical, it was due to differing recording methods between data sources, ensuring the most complete dataset with the lowest rate of missingness.

Missing data rates were monitored, with the highest rate at 9% (LV Eject) in the Recipient table, while all other rates were below 5%, making imputation unnecessary. Preoperative ECMO data were intentionally missing due to non-use. PGD, textbook outcomes, and mortality outcomes had no missing data, and only 4 cases (< 1%) lacked hospital discharge dates, which excluded them from hospital length of stay regression models.

We performed an additional multivariable logistic regression analysis to find predictors of severe-to-massive bleeding. A stepwise selection was performed to identify the most significant predictors for severe-to-massive bleeding. Initially, a model with no predictors was considered and a full model including all variables from the recipient table (Table 1), as well as Donor Status (DBD vs. DCD) and total ischemic time. Intraoperative variables were excluded to avoid conceptual overlap with UDPB status. Stepwise selection iteratively added and removed variables to determine the best prediction model based on the Akaike Information Criterion (AIC) [15]. The final model included recipient race (White vs. Black), BMI, MPAP, preoperative ECMO, first transplant status, and Donor Status (DCD vs. DBD) as significant predictors. Statistical significance was determined by a p-value less than 0.05, with analysis conducted by a certified statistician in R version 4.2.2 [16,17,18,19,20].

Table 1 Demographic and clinical characteristics of recipients

Results

Patient cohort

There were 642 patients who underwent LT, with 61 patients excluded for undergoing multi-visceral transplantation and 53 excluded for receiving a single orthotopic LT. In total, 528 patients fulfilled inclusion criteria, with 357 insignificant-to-moderate bleeders and 171 severe-to-massive bleeders (Fig. 1). Within the study cohort, there were 432 who had a clamshell incision and 7 patients who underwent a sternotomy. Postoperatively, there were 71 patients who had an open chest requiring delayed closure and 429 patients without delayed closure. Among all transplant recipients, 301 (57.0%) were male, with an average age of 56.6 [50,67] years old and an average BMI of 24.3 ± 3.8 (Table 1).

Fig. 1
figure 1

Patient Cohort Selection

Recipient and donor demographics

Severe-to-massive bleeders were younger, (55.00 [37.50, 64.00] vs. 63.00 [54.00, 68.00]; p < 0.001), had lower BMIs (23.26 ± 3.83 vs. 24.85 ± 3.74); p < 0.001), and were more often female (49.7% v. 39.8%; p = 0.039). There were severe-to-massive bleeders distributed across all the different disease subtypes noted with the most common being restrictive lung disease (64.9%). severe-to-massive bleeders did not significantly differ from insignificant-to-moderate bleeders in terms of race (p = 0.078).

Donors for the severe-to-massive bleeders had higher rates of DCD compared to the donors for the insignificant-to-moderate bleeders (22.2% vs. 10.7%; p = 0.001) (Table 2). Other demographic data, including donor sex (p = 0.769), age (p = 0.474), BMI (p = 0.689), history of hypertension (p = 0.394), and history of cancer (p = 0.735) were similar between bleeding groups.

Table 2 Donor demographic and clinical characteristics

Preoperative status

Severe-to-massive bleeders had higher rates of pulmonary vascular disease (7.0% v. 1.4%; p = 0.007) defined as mean pulmonary arterial pressures over 25 mmHg, higher mean pulmonary artery pressures (26.00 [22.00, 32.00] mmHg vs. 25.00 [20.00, 30.00] mmHg; p = 0.010), and higher rates of moderate (10.3% vs. 8.2%) and severe (6.1% vs. 1.4%) right ventricular dysfunction (p = 0.029). Conversely, there was no difference in the left ventricular ejection fraction between the two groups (p = 0.933). Severe-to-massive bleeder patients had higher lung allocation scores 54.14 ± 20.21 vs. 46.72 ± 12.55; p < 0.001) and were more frequently receiving their second (12.5% vs. 2.2%) or third (1.8% v. 0.6%) transplant (p < 0.001). Severe-to-massive bleeders were more likely to require preoperative ventilation (16.4% vs. 1.4%; p < 0.001) and less likely to present as an outpatient (68.4% vs. 83.2%; p < 0.001). ECMO bridging was more often required for severe-to-massive bleeders (16.4% vs. 1.4%; p < 0.001). The severe-to-massive bleeding group was more frequently anemic with lower preoperative Hb (11.80 [9.85, 13.10] vs. 12.60 [11.47, 13.70]; p < 0.001) but INR (p = 0.132) and creatinine (p = 0.757) labs. The severe-to-massive bleeding group had slightly higher median platelet counts compared to the insignificant-to moderate bleeders (12.20 [11.30, 13.38] vs. 11.90 [11.30, 12.80]; p = 0.038).

Intraoperative support

Severe-to-massive bleeders experienced a higher median total ischemic time (484.50 [424.00, 563.25] minutes vs. 432.50 [380.75, 505.25] minutes; p < 0.001) (Table 3). They were also more likely to require VV ECMO (7.8% vs. 3.4%) and CPB (14.0% vs. 4.5%) during their operation compared to insignificant-to-moderate bleeders (p < 0.001). Intraoperative VA ECMO need was similar between groups. However, severe-to-massive bleeders required intraoperative tranexamic acid (28.1% v. 5.3%; p < 0.001) at higher rates and had higher incidences of intraoperative complications (13.5% vs. 1.7%; p < 0.001).

Table 3 Intraoperative factors

Postoperative outcomes

PGD grade 3 at 72 h was more common in severe-to-massive bleeders (32.7% v. 5.9%; p < 0.001) (Table 4). Severe-to-massive bleeders had longer hospital stays (40.00 [25.00, 78.00] vs. 20.00 [16.00, 30.00]; p < 0.001) and elevated mortality rates at 30 days (7.0% vs. 0.6%; p < 0.001) and one year (22.2% vs. 7.3%; p < 0.001). This cohort was less likely to achieve textbook outcomes for LT (2.9% vs. 35.6%; p < 0.001). Indeed, they were more dependent on postoperative ECMO within 72 h (48.0% vs. 9.2%; p < 0.001), reintubation for over 48 h (24.6% vs. 13.4%; p < 0.001), or tracheostomy placement (30.4% v. 9.5%; p < 0.001). Severe-to-massive bleeders had higher rates of patients among the top quartile for hospital LOS (46.2% vs. 14.0%; p < 0.001). This subgroup also required reintervention (62.6% vs. 35.6%; p < 0.001) and dialysis (26.9% vs. 4.5%; p < 0.001) more frequently. Correspondingly, 90-day mortality were greater (12.9% vs. 1.1%; p < 0.001). However, biopsy proven rejection at 30 days (p = 0.097) was similar between groups.

Table 4 Outcomes by Bleeding Group in lung transplant recipients

Regression analysis

Univariate analysis against PGD3 at 72 h showed that relative to insignificant-to-moderate bleeding, severe-to-massive bleeding increased rates of PGD3 at 72 h (OR = 7.79, 95% CI: 4.59–13.69, p < 0.001) (Fig. 2). Severe-to-massive bleeding significantly extinguished odds of achieving textbook outcomes, (OR = 0.05, 95% CI = 0.02–0.12, p < 0.001), while over tripling risks one-year mortality rate (OR = 3.64, 95% CI = 2.13–6.29, p < 0.001) (Table 5). Hospital LOS also showed a significant association, with an odds ratio of 1.89 (95% CI: 1.66–2.14, p < 0.001), indicating a longer hospital stays for patients with severe-to-massive bleeding.

Fig. 2
figure 2

Univariable and Multivariable Analysis for the Odds Ratio of severe-to-massive Bleeders. The multivariable models adjusted for recipient’s age, sex, body mass index, group diagnosis, lung allocation score, preoperative hemoglobin, preoperative ECMO status (Y/N), transplant number (first transplant Y/N), and donor status

Table 5 Regression analysis by Bleeding Group in lung transplant recipients

In the multivariate analysis, severe-to-massive bleeding remained significantly associated with adverse outcomes after controlling for confounding characteristics. Severe-to-massive bleeding was independently associated with an increased rate of PGD3 at 72 h (OR = 7.73, 95% CI = 4.27–14.4, p < 0.001) and significantly reduced the likelihood of achieving textbook outcomes (OR = 0.07, 95% CI = 0.02–0.16, p < 0.001). Being categorized in this bleeding group also raised odds of one-year mortality (OR = 4.30, (95% CI = 2.30–8.12, p < 0.001) and was associated with prolonged hospital LOS (OR = 1.75, 95% CI = 1.52–2.01).

There were several preoperative and intraoperative predictors associated with bleeding for the multivariable analysis using bleeding as an outcome. White patients had lower odds of experiencing severe/massive bleeding compared to Black patients (Table 6). Each 1-unit increase in BMI was associated with an 11% reduction in the odds of severe-to-massive bleeding. Additionally, each 1-unit increase in MPAP resulted in a 4% increase in the odds of severe-to-massive. First-time transplant recipients had an 84% lower risk of severe/massive bleeding compared to those undergoing subsequent transplants. Additionally, recipients with DCD donors had a 209% increase in the odds of severe/massive bleeding.

Table 6 Multivariable logistic regression analysis with bleeding as an outcome

Discussion

Among the 32.4% (n = 171/528) of patients in the severe-to-massive group, we discovered higher rates of worse outcomes. Most notably, were more likely to have PGD grade 3, had higher one-year mortality rates, and were less likely to achieve textbook outcomes while still requiring longer hospital stays. This relationship held true for both the univariate and multivariate regression.

Multiple studies have examined the impact of transfusion of different blood products on LT outcomes [21,22,23,24,25,26]. The current study adds to the current literature by demonstrating the association between increased transfusion requirements and adverse outcomes. The findings of this study highlight the significant impact of massive bleeds on the outcomes of LT recipients. Patients who experienced massive bleeds demonstrated higher rates of PGD, reinforcing the notion that severe bleeding during the perioperative period may be associated with an increased risk of graft dysfunction [27]. Diamond et al., in a multicenter study comprised of 1,255 lung LT recipients across 10 different centers found that the use of over one liter of PRBCs was associated with severe PGD at 48 to 72 h postoperatively [28]. Similarly, requiring over four units of PRBCs has been known to increase rates of grade 3 PGD at 72 h [29]. Preventing and managing massive bleeding in patients who are at higher risk of bleeding is essential as PGD has previously been associated with increase morality extending up to 10 years after LT [30, 31]. The exact mechanisms underlying the development of PGD are not fully understood, but several factors have been implicated in its pathogenesis. One mechanism is ischemia-reperfusion injury [32, 33], which triggers a cascade of inflammatory responses, oxidative stress, and ultimately cell damage and dysfunction [34].

Patients with severe-to-massive bleeds required a higher frequency of reinterventions and dialysis, suggesting severe bleeding may exert systemic complications and impact the overall health of transplant recipients. For example, acute kidney injuries have been associated with LT [35], likely exacerbated by pulmonary insults, ultimately requiring higher rates of dialysis [36,37,38].

Another important finding was the prolonged LOS observed in patients with massive bleeds, which has been associated with increased mortality up to five years post-transplant [39]. Prolonged stays may be attributed to the complex management of bleeding complications, additional interventions, and the overall compromised clinical condition sustained from massive bleeding episodes. Outside of patient outcomes, prolonged hospitalization drains healthcare resources and contributes to healthcare costs [40, 41].

The optimization of patients prior to transplantation is essential. In lower acuity settings, characteristics such as anemia enjoy higher incidence among severe-to-massive bleeders are worth optimizing. Intraoperatively, bleeding may be managed prophylactically and while it happens. TXA, prothrombin complex concentrate (PCC), factor VIIa, and low-dose heparin infusions represent methods that decrease the risk of bleeding. Some hemostatic interventions may encounter limitations when ECMO is employed, calling for careful risk-benefit analysis. Patients with right ventricular dysfunction and pulmonary hypertension require longer mechanical circulatory support runs, which demands conservative use of medical interventions to prevent coagulation. Balancing bleeding risks and thrombotic complications associated with prolonged mechanical circulatory support is imperative for optimizing outcomes in this challenging patient population. It is important to note that these interventions may have unavoidable interactions that impact outcomes following LT.

Perhaps more important than optimization and intraoperative initiatives to limit bleeding is the careful selection and management of potential LT recipients. The current study may have included patients deemed to have a lower risk of bleeding complications based on preoperative assessments, such as evaluation of anemia, coagulation profiles, and identification of potential bleeding risk factors. These efforts in patient selection and risk stratification may have resulted in a cohort with a lower overall incidence of massive bleeding. To that end, the worse outcome in severe-to-massive bleeders raises pivotal questions: firstly, the appropriateness of the transplantation for these patients, and secondly, the selection between BOLT and single orthotopic lung transplantations (SOLT) procedures. Previous research has demonstrated that although BOLT generally has improved long-term outcomes, short-term outcomes may be better in SOLT, and patients with increased risk of peri-operative mortality (such as high risk of massive bleeds) may benefit from SOLT [42]. The differences in indications between BOLT and SOLT may also contribute to the outcomes demonstrated in the two procedures and future studies should focus on elucidating these interactions. Preoperative assessment and optimization are equally essential and should be considered in conjunction to limit bleeding complications.

A previous study found the rate of massive bleeding ranged between 19% and 33% [22]. Our combined rate of severe and massive bleeding aligns with prior literature, although our incidence of massive bleeding was even lower at 12.9%. The current study’s lower rate of massive transfusion can be explained by several factors. Over time, advancements in surgical techniques and perioperative management of bleeding may have contributed to reduced intraoperative bleeding and subsequent lower transfusion requirements.

This is one of the first studies applying the UDPB to LT [8]. Applying this definition offers several benefits. First, having a standardized definition facilitates consistency and comparability across studies, enhancing the accuracy and reliability of research findings. Downstream, this facilitates the pooling of data from different centers, enabling a more comprehensive analysis of outcomes and the development of evidence-based practices. The UDPB also allows clinicians to classify patients postoperatively and identify patients at higher risk for worse outcomes. By accurately defining and categorizing massive bleeding, the UDPB aids in risk stratification, facilitating the identification of high-risk patients who may require additional monitoring and interventions.

There are several limitations to this current study. This study is retrospective, limiting the conclusions that can be drawn. Second, typically sicker patients (e.g., bridged patients) require higher rates of transfusions, and thus will have worse outcomes postoperatively. Although this could potentially confound the results, the multivariable regression in the study accounted for various factors (e.g., LAS, group diagnosis, etc.) to mitigate the impact of baseline illness severity on outcomes and isolate the impact of bleeding. The study, however, offers the benefit of utilizing our center’s large volume to find a large cohort of patients requiring massive transfusions. Using the UDPB provides the benefit of easily allowing for comparison across different studies and centers.

This study emphasizes the importance of carefully considering the risk of massive bleeding and transfusion in the selection and management of LT recipients. The results underscore the substantial utilization of hospital resources associated with patients at high risk of massive bleeding, including prolonged LOS and increased morbidity and mortality rates. Understanding the outcomes of this high-risk subgroup is critical, as it can inform future decisions regarding the transplantation of comparable patients. Implementing strategies to prevent and effectively manage massive bleeds during LT is vital to optimize patient outcomes and allocate healthcare resources efficiently. Ultimately, this study helps to provide a comprehensive understanding of the associated clinical outcomes, resource utilization, and potential risks, which can inform clinical decision-making and improve patient care in this high-risk population.

Conclusion

This retrospective cohort study highlights the impact of severe perioperative bleeding, as defined by the UDPB, on outcomes in LT recipients. Severe-to-massive bleeding was associated with higher rates of PGD grade 3 at 72 h, increased 1-year mortality, lower likelihood of achieving textbook outcomes, and longer hospital stays. These findings underscore the importance of careful patient selection and perioperative management to minimize the risk of severe bleeding and its associated complications. Strategies to prevent and manage bleeding in high-risk patients, including optimizing preoperative status and judicious use of transfusions and hemostatic agents, are crucial for improving outcomes in LT. Further research is needed to explore specific interventions and protocols that can reduce the risk of severe bleeding and improve outcomes in this patient population.

Data availability

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

UDPB:

Universal Definition of Perioperative Bleeding

LT:

Lung Transplantation

PGD:

Primary Graft Dysfunction

BMI:

Body Mass Index

MPAP:

Mean Pulmonary Artery Pressure

LAS:

Lung Allocation Score

ECMO:

Extracorporeal Membrane Oxygenation

INR:

International Normalized Ratio

Cr:

Creatine

Hb:

Hemoglobin

ECLS:

Extracorporeal Life Support

VV ECMO:

Venovenous Extracorporeal Membrane Oxygenation

VA ECMO:

Venoarterial Extracorporeal Membrane Oxygenation

TXA:

Tranexamic Acid

LOS:

Length of Stay

PRBCs:

Packed Red Blood Cells

AKI:

Acute Kidney Injury

ROTEM:

Rotational Thromboelastometry

References

  1. Vock DM, Durheim MT, Tsuang WM, Finlen Copeland CA, Tsiatis AA, Davidian M, Neely ML, Lederer DJ, Palmer SM. Survival Benefit of Lung Transplantation in the modern era of lung allocation. Ann Am Thorac Soc. 2017;14:172–81.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Yusen RD, Edwards LB, Dipchand AI, Goldfarb SB, Kucheryavaya AY, Levvey BJ, Lund LH, Meiser B, Rossano JW, Stehlik J. The Registry of the International Society for Heart and Lung Transplantation: thirty-third adult lung and heart-lung transplant Report-2016; focus theme: primary diagnostic indications for transplant. J Heart Lung Transpl. 2016;35:1170–84.

    Article  Google Scholar 

  3. Bos S, Vos R, Van Raemdonck DE, Verleden GM. Survival in adult lung transplantation: where are we in 2020? Curr Opin Organ Transpl. 2020;25:268–73.

    Article  Google Scholar 

  4. Leard LE, Holm AM, Valapour M, Glanville AR, Attawar S, Aversa M, Campos SV, Christon LM, Cypel M, Dellgren G, et al. Consensus document for the selection of lung transplant candidates: an update from the International Society for Heart and Lung Transplantation. J Heart Lung Transpl. 2021;40:1349–79.

    Article  Google Scholar 

  5. Beeckmans H, Bos S, Vos R. Selection criteria for lung transplantation: controversies and New Developments. Semin Respir Crit Care Med. 2021;42:329–45.

    Article  PubMed  Google Scholar 

  6. Vandervest KM, Zamora MR. Recipient risk factors and lung transplant outcomes. Curr Opin Organ Transpl. 2013;18:531–6.

    Article  CAS  Google Scholar 

  7. Madisetty J, Wang C. Transfusion Medicine and Coagulation Management in Organ Transplantation. Anesthesiol Clin. 2017;35:407–20.

    Article  PubMed  Google Scholar 

  8. Snell GI, Yusen RD, Weill D, Strueber M, Garrity E, Reed A, Pelaez A, Whelan TP, Perch M, Bag R, et al. Report of the ISHLT Working Group on Primary Lung Graft Dysfunction, part I: definition and grading-A 2016 Consensus Group statement of the International Society for Heart and Lung Transplantation. J Heart Lung Transpl. 2017;36:1097–103.

    Article  Google Scholar 

  9. Dyke C, Aronson S, Dietrich W, Hofmann A, Karkouti K, Levi M, Murphy GJ, Sellke FW, Shore-Lesserson L, von Heymann C, Ranucci M. Universal definition of perioperative bleeding in adult cardiac surgery. J Thorac Cardiovasc Surg. 2014;147:1458–e14631451.

    Article  PubMed  Google Scholar 

  10. Pollak AL, Poisson J, Cooter M, Barac Y, Bryner B, Haney J, Hartwig MG, Klapper J, Zaffiri L, Welsby I, et al. Effects of a goal Directed Transfusion protocol on severe primary graft dysfunction after lung transplantation. J Heart Lung Transplantation. 2020;39:S330.

    Article  Google Scholar 

  11. Halpern SE, Moris D, Gloria JN, Shaw BI, Haney JC, Klapper JA, Barbas AS, Hartwig MG. Textbook Outcome: definition and analysis of a Novel Quality measure in lung transplantation. Ann Surg. 2021;277:350–7.

    Article  Google Scholar 

  12. Halpern SE, Wright MC, Madsen G, Chow B, Harris CS, Haney JC, Klapper JA, Bottiger BA, Hartwig MG. Textbook outcome in lung transplantation: planned venoarterial extracorporeal membrane oxygenation versus off-pump support for patients without pulmonary hypertension. J Heart Lung Transpl. 2022;41:1628–37.

    Article  Google Scholar 

  13. Krischak MK, Au S, Halpern SE, Olaso DG, Moris D, Snyder LD, Barbas AS, Haney JC, Klapper JA, Hartwig MG. Textbook surgical outcome in lung transplantation: analysis of a US national registry. Clin Transpl. 2022;36:e14588.

    Article  CAS  Google Scholar 

  14. Pollak AL, Poisson J, Cooter M, Barac YD, Bryner B, Haney J, Hartwig MG, Klapper J, Zaffiri L, Welsby I, et al. Effects of a goal Directed Transfusion protocol on severe primary graft dysfunction after lung transplantation. J Heart Lung Transplantation. 2020;39:S330.

    Article  Google Scholar 

  15. Klee EW. Data Mining for Biomarker Development: a review of tissue specificity analysis. Clin Lab Med. 2008;28:127–43.

    Article  PubMed  Google Scholar 

  16. Akoglu H. User’s guide to correlation coefficients. Turk J Emerg Med. 2018;18:91–3.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Kassambara A. rstatix: Pipe-Friendly Framework for Basic Statistical Tests. 2021.

  18. Massicotte P, Eddelbuettel D. gtrendsR: Perform and Display Google Trends Queries. 2022.

  19. R Core Team. R: a Language and Environment for Statistical Computing. 4.2.0 edition. R Foundation for Statistical Computing; 2022.

  20. Wickham H. ggplot2. Springer-Verlag New York; 2009.

  21. Klapper JA, Hicks AC, Ledbetter L, Poisson J, Hartwig MG, Hashmi N, Welsby I, Bottiger BA. Blood product transfusion and lung transplant outcomes: a systematic review. Clin Transpl. 2021;35:e14404.

    Article  Google Scholar 

  22. Cernak V, Oude Lansink-Hartgring A, van den Heuvel ER, Verschuuren EAM, van der Bij W, Scheeren TWL, Engels GE, de Geus AF, Erasmus ME, de Vries AJ. Incidence of massive transfusion and overall transfusion requirements during lung transplantation over a 25-Year period. J Cardiothorac Vasc Anesth. 2019;33:2478–86.

    Article  PubMed  Google Scholar 

  23. Borders CF, Suzuki Y, Lasky J, Schaufler C, Mallem D, Lee J, Carney K, Bellamy SL, Bermudez CA, Localio AR, et al. Massive donor transfusion potentially increases recipient mortality after lung transplantation. J Thorac Cardiovasc Surg. 2017;153:1197–e12031192.

    Article  PubMed  Google Scholar 

  24. Benson AB, Burton JR Jr., Austin GL, Biggins SW, Zimmerman MA, Kam I, Mandell S, Silliman CC, Rosen H, Moss M. Differential effects of plasma and red blood cell transfusions on acute lung injury and infection risk following liver transplantation. Liver Transpl. 2011;17:149–58.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Bhaskar B, Zeigenfuss M, Choudhary J, Fraser JF. Use of recombinant activated factor VII for refractory after lung transplant bleeding as an effective strategy to restrict blood transfusion and associated complications. Transfusion. 2013;53:798–804.

    Article  CAS  PubMed  Google Scholar 

  26. Ong LP, Sachdeva A, Ramesh BC, Muse H, Wallace K, Parry G, Clark SC. Lung transplant with cardiopulmonary bypass: impact of blood transfusion on rejection, function, and late mortality. Ann Thorac Surg. 2016;101:512–9.

    Article  PubMed  Google Scholar 

  27. Crespo MM, Clancy CJ, Pilewski JM, Bermudez C, Jarido V, Johnson B, Haider SS, Bhama J, Toyoda Y, Morrell M, et al. Primary graft dysfunction (PGD) vs transfusion-related lung injury (TRLI) in lung transplantation (LT): can these entities be differentiated based on the current ISHLT PGD definition? J Heart and. 2012;31:S248.

    Google Scholar 

  28. Diamond JM, Lee JC, Kawut SM, Shah RJ, Localio AR, Bellamy SL, Lederer DJ, Cantu E, Kohl BA, Lama VN, et al. Clinical risk factors for primary graft dysfunction after lung transplantation. Am J Respir Crit Care Med. 2013;187:527–34.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Subramaniam K, Loor G, Chan EG, Bottiger BA, Ius F, Hartwig MG, Daoud D, Zhang Q, Wei Q, Villavicencio-Theoduloz MA, et al. Intraoperative red blood cell transfusion and primary graft dysfunction after lung transplantation. Transplantation. 2023;107:1573–9.

    Article  CAS  PubMed  Google Scholar 

  30. Christie JD, Bellamy S, Ware LB, Lederer D, Hadjiliadis D, Lee J, Robinson N, Localio AR, Wille K, Lama V, et al. Construct validity of the definition of primary graft dysfunction after lung transplantation. J Heart Lung Transpl. 2010;29:1231–9.

    Article  Google Scholar 

  31. Jimenez MJ, Cordova FC, Ferrer N, Gaughan J, Li Y, Criner GJ. Does perioperative blood product transfusions increase the risk of primary graft dysfunction after lung transplantation? Am J Respir Crit Care Med. 2010;181:e943652–943651.

    Google Scholar 

  32. Vlaar AP, Hofstra JJ, Determann RM, Veelo DP, Paulus F, Levi M, Zeerleder S, Vroom MB, Schultz MJ, Juffermans NP. Transfusion-related acute lung injury in cardiac surgery patients is characterized by pulmonary inflammation and coagulopathy: a prospective nested case-control study. Crit Care Med. 2012;40:2813–20.

    Article  PubMed  Google Scholar 

  33. Bittner HB, Richter M, Kuntze T, Rahmel A, Dahlberg P, Hertz M, Mohr FW. Aprotinin decreases reperfusion injury and allograft dysfunction in clinical lung transplantation. Eur J Cardiothorac Surg. 2006;29:210–5.

    Article  PubMed  Google Scholar 

  34. Corash L, Lin JS, Sherman CD, Eiden J. Determination of acute lung injury after repeated platelet transfusions. Blood. 2011;117:1014–20.

    Article  CAS  PubMed  Google Scholar 

  35. Gueler F, Hanke N, Wiese B, Simon A, Haller H, Haverich A, Fegbeutel C. Acute kidney injury after heart-and/or lung transplantation: retrospective analysis of incidence, risk factors and outcome of 1400 patients. Nephrol Dialysis Transplantation. 2013;28:i73.

    Article  Google Scholar 

  36. Tan CS, Jie C, Joe J, Irani ZD, Ganguli S, Kalva SP, Wicky S, Wu S. The impact of transvenous cardiac devices on vascular access patency in hemodialysis patients. Semin Dial. 2013;26:728–32.

    Article  PubMed  Google Scholar 

  37. Imai Y, Parodo J, Kajikawa O, de Perrot M, Fischer S, Edwards V, Cutz E, Liu M, Keshavjee S, Martin TR, et al. Injurious mechanical ventilation and end-organ epithelial cell apoptosis and organ dysfunction in an experimental model of acute respiratory distress syndrome. JAMA. 2003;289:2104–12.

    Article  PubMed  Google Scholar 

  38. Koyner JL, Murray PT. Mechanical ventilation and the kidney. Blood Purif. 2010;29:52–68.

    Article  PubMed  Google Scholar 

  39. Banga A, Mohanka M, Mullins J, Bollineni S, Kaza V, Ring S, Bajona P, Peltz M, Wait M, Torres F. Hospital length of stay after lung transplantation: independent predictors and association with early and late survival. J Heart Lung Transpl. 2017;36:289–96.

    Article  Google Scholar 

  40. Zhan C, Miller MR. Excess length of stay, charges, and mortality attributable to medical injuries during hospitalization. JAMA. 2003;290:1868–74.

    Article  CAS  PubMed  Google Scholar 

  41. Vigneswaran WT, Bhorade S, Wolfe M, Pelletiere K, Garrity ER Jr. Clinical pathway after lung transplantation shortens hospital length of stay without affecting outcome. Int Surg. 2007;92:93–8.

    PubMed  Google Scholar 

  42. Gulack BC, Ganapathi AM, Speicher PJ, Meza JM, Hirji SA, Snyder LD, Davis RD, Hartwig MG. What is the optimal transplant for older patients with idiopathic pulmonary fibrosis? Ann Thorac Surg. 2015;100:1826–33.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

None to declare.

Author information

Authors and Affiliations

Authors

Contributions

KAW: Concept/design, Data analysis/interpretation, Drafting article, Critical revision of article, Approval of article. JKK: Data analysis/interpretation, Drafting article, Critical revision of article, Approval of article, Statistics. MR: Data analysis/interpretation, Critical revision of article, Approval of article, Statistics. BC: Data collection and investigation, Critical revision of article, Approval of article. BAB: Concept/design, Drafting article, Critical revision of article, Approval of article. JAK: Concept/design, Drafting article, Critical revision of article, Approval of article.

Corresponding author

Correspondence to Jacob A. Klapper.

Ethics declarations

Ethics approval and consent to participate

Duke University IRB Pro00093325.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wu, K.A., Kim, J.K., Rosser, M. et al. The impact of bleeding on outcomes following lung transplantation: a retrospective analysis using the universal definition of perioperative bleeding. J Cardiothorac Surg 19, 466 (2024). https://doi.org/10.1186/s13019-024-02952-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13019-024-02952-z

Keywords