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Article

Can Artificial Intelligence Improve the Appropriate Use and Decrease the Misuse of REBOA?

by
Mary Bokenkamp
1,†,
Yu Ma
2,*,†,
Ander Dorken-Gallastegi
1,
Jefferson A. Proaño-Zamudio
1,
Anthony Gebran
1,
George C. Velmahos
1,
Dimitris Bertsimas
2,‡ and
Haytham M. A. Kaafarani
1,‡
1
Trauma, Emergency Surgery, and Surgical Critical Care, Massachusetts General Hospital, Boston, MA 02114, USA
2
Operations Research Center, Massachusetts Institute of Technology, Cambridge, MA 02142, USA
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work as first authors.
These authors also contributed equally to this work as senior authors.
Bioengineering 2025, 12(10), 1025; https://doi.org/10.3390/bioengineering12101025
Submission received: 22 May 2025 / Revised: 30 August 2025 / Accepted: 17 September 2025 / Published: 25 September 2025
(This article belongs to the Section Biosignal Processing)

Abstract

Background: The use of resuscitative endovascular balloon occlusion of the aorta (REBOA) for control of noncompressible torso hemorrhage remains controversial. We aimed to utilize a novel and transparent/interpretable artificial intelligence (AI) method called Optimal Policy Trees (OPTs) to improve the appropriate use and decrease the misuse of REBOA in hemodynamically unstable blunt trauma patients. Methods: We trained and then validated OPTs that “prescribe” REBOA in a 50:50 split on all hemorrhagic shock blunt trauma patients in the 2010–2019 ACS-TQIP database based on rates of survival. Hemorrhagic shock was defined as a systolic blood pressure ≤90 on arrival or a transfusion requirement of ≥4 units of blood in the first 4 h of presentation. The expected 24 h mortality rate following OPT prescription was compared to the observed 24 h mortality rate in patients who were or were not treated with REBOA. Results: Out of 4.5 million patients, 100,615 were included, and 803 underwent REBOA. REBOA patients had a higher rate of pelvic fracture, femur fracture, hemothorax, pneumothorax, and thoracic aorta injury (p < 0.001). The 24 h mortality rate for the REBOA vs. non-REBOA group was 47% vs. 21%, respectively (p < 0.001). OPTs resulted in an 18% reduction in 24 h mortality for REBOA and a 0.8% reduction in non-REBOA patients. We specifically divert the misuse of REBOA by recommending against REBOA in cases where it leads to worse outcomes. Conclusions: This proof-of-concept study shows that interpretable AI models can improve mortality in unstable blunt trauma patients by optimizing the use and decreasing the misuse of REBOA. To date, these models have been used to predict outcomes, but their groundbreaking use will be in prescribing interventions and changing outcomes.

1. Introduction

The use of resuscitative endovascular balloon occlusion of the aorta (REBOA) in trauma continues to be highly controversial due to conflicting mortality data and procedure-associated complications such as limb ischemia, vascular injury, and reperfusion effects. Of the retrospective and prospective studies available, some have shown increased mortality [1,2] while others have claimed decreased mortality [3,4,5]. Similarly, the studies vary in the reporting of the procedure-associated complications [1,2,3,4,5,6,7,8]. Its use was born during the Korean War as a temporary solution to control noncompressible torso hemorrhage in military personnel [9]. While the use of REBOA in civilian trauma could be similarly beneficial, studies have not shown consistent results [1,2,3,4,5,6,7,8], and randomized control trials for its use have been difficult to design, as the real emergent nature of the situation warrants its use [10,11,12]. As such, the indication and contraindications of its use continue to be a hotly debated subject at almost every trauma surgery conference and journal.
In recent years, our surgical-engineering collaborative group has successfully applied the power of Artificial Intelligence (AI) methodologies to surgical patients, first focusing on risk prediction problems using OCT and now, in this current study, on treatment prescription problems using OPT. The key difference between OCT and OPT is that although they both present similar single-tree structures, OCT is a prediction-driven problem, where the goal is to make an estimate of how likely an outcome would occur. In contrast, OPT is a prescription-driven problem, where the goal is to make a concrete decision about treatment to optimize an outcome (in our case, reduce mortality rate). The transition from OCT to OPT signals the progression from outcome-estimation-based methods to decision-based methods. We have previously leveraged a novel and interpretable AI technique called Optimal Classification Trees (OCT) to predict risk and outcomes in emergency general surgery [13] and trauma patients [14]. This resulted in two accurate and transparent algorithms that were translated into interpretable and user-friendly smartphone applications. These applications have since been downloaded and are in use by thousands of surgeons worldwide. For the present study, we aspired to utilize a different AI methodology developed at the Massachusetts Institute of Technology (MIT) called Optimal Policy Trees (OPT) [15,16]. Unlike OCTs, which are “predictive”, OPTs are “prescriptive”. These trees work to “prescribe” the best treatment for different patient subgroups to achieve the best possible outcome of interest. The aim of this study was to utilize OPTs to improve the appropriate use and decrease the misuse of REBOA in hemodynamically unstable blunt trauma patients.

2. Materials and Methods

2.1. Patient Population

The American College of Surgeons Trauma Quality Improvement Program (ACS-TQIP) Participant Use Data Files (PUFs) for the years 2010–2019 were used as the data source. As demonstrated in Figure 1, patients age > 16 who suffered a blunt traumatic injury and arrived at the hospital in hemorrhagic shock were included. Hemorrhagic shock was defined as a systolic blood pressure (SBP) ≤ 90 or a transfusion requirement of ≥ 4 units of red blood cells (RBCs) within the first 4 h of hospital arrival. Patients were excluded if they were transferred in the first 24 h or were missing data for age or length of stay (LOS). Patients who underwent REBOA placement within 4 h of hospital arrival were identified using ICD-10 procedure codes (04L03DZ, 04L03DJ, 04L04DZ, 02LW3DJ, 04L04ZZ).
Figure 1. Flowchart for the study population. The overall cohort size is 100,615 after applying the exclusion criteria.

2.2. Data Points

Multiple data points were collected. To ensure the OPTs would prescribe REBOA in a clinically meaningful way, the only data points that were utilized in the creation of the trees were those that would be obtainable in the trauma bay. For example, at the point of deciding whether to use REBOA or not, the surgeon would know the patient’s approximate age and initial vitals, but would not know the volume of blood products the patient would receive, nor their ISS. These independent variables utilized were age, sex, admission physiology (SBP, pulse, temperature, Glasgow Coma Scale (GCS), respiratory rate, pulse oximetry), use of supplemental oxygen, intubation in the emergency department (ED), height, weight, body mass index (BMI), signs of life upon ED arrival, hospital teaching status, and ACS verification level. Major injuries that could be suspected or diagnosed during the primary and secondary survey or initial radiological workup in the trauma bay were also included. These were pelvic fracture, femur fracture, hemothorax, pneumothorax, and thoracic aorta injury. Along a similar line of thinking, we included procedures that the patient may undergo in the trauma bay. These were chest tube placement, transfusion of RBC, and transfusion of whole blood. A time constraint of one hour was placed on these to capture procedures that were performed immediately upon arrival. The ED diagnoses and procedures were identified using ICD-10 codes (Tables S1 and S2).
Additional patient- and injury-related data points were analyzed separately to provide a more comprehensive picture of the overall cohort. The patients were stratified into two groups for comparison: those who underwent REBOA within 4 h of hospital arrival (REBOA) and those who did not (No REBOA). The data points analyzed included blood products transfused within 4 h of hospital arrival (red blood cells (RBC), fresh frozen plasma (FFP), platelets (PLT), and cryoprecipitate (Cryo), AIS, ISS, hemorrhage control procedures required within 4 h of hospital arrival (laparotomy, thoracotomy/sternotomy, extremity vascular, preperitoneal pelvic packing (PPP), external fixation (EF) of pelvis, angioembolization (AE) of pelvis), and comorbidities. Laparotomy, thoracotomy/sternotomy, angioembolization, and extremity vascular are procedures tracked by ACS-TQIP. PPP and EF were identified using ICD-10 procedure codes (Table S2).

2.3. Outcome Definitions

The primary outcome targeted by the OPT model for improvement was 24 h mortality. Secondary outcomes, analyzed separately, included hospital complications (catheter-associated urinary tract infection (CAUTI), central line-associated blood stream infection (CLABSI), superficial surgical site infection (SSI), deep SSI, organ space SSI, sepsis, pressure ulcer, deep vein thrombosis (DVT), pulmonary embolism (PE), compartment syndrome, cardiac arrest, myocardial infarction (MI), acute respiratory distress syndrome (ARDS), ventilator-associated pneumonia (VAP), acute kidney injury (AKI), and unplanned intubation, return to OR, or ICU admission), ventilator days, ICU LOS, and in-hospital mortality. For the purpose of this study, we focus our analysis only on the primary outcome due to its immediate importance in the clinical setting we consider.

2.4. Optimal Policy Trees

To create our AI-based prescriptive models, we used an innovative and interpretable machine learning methodology called OPT [15,16]. OPT leverages the power of mixed-integer programming by formulating the policy prescription problem as an optimization problem. The OPT method has been shown to achieve superior solutions to traditional machine-learning single-tree methods such as Classification and Regression Trees (CART) on various real-world datasets [15,16]. In comparison to other interpretable methods such as decision rules and CART, the OPT method achieves such performance by automatically exploring the best decision path combinations that optimize the reward, in our case, reduced mortality rate. Unlike many other “black box” machine-learning algorithms, such as Regress and Compare [17] or Causal Forest [18], OPT can make informed and accurate decisions without sacrificing intuitive understanding of how each decision is made. Specifically, such ensemble methods rely on the assembly of multiple weak decisions in order to arrive at the final decisions, thus often making it difficult for physicians to decipher the exact decision paths. On the other hand, OPT offers direct interpretability as a one-tree model, providing direct visibility of the decision path. The ability to follow a transparent, concise decision path allows clinicians to understand exactly how each factor is incorporated into the decision-making process.
Another important class of comparison methods is graph-based analytics, which has been successfully applied across a range of domains, including healthcare [19,20,21]. These approaches have the potential to complement our OPT method due to their abilities to capture richer relational structures that go beyond independent variable modeling. This advantage is especially important due to trauma patients’ often interdependent injuries (i.e., pelvic and femoral fractures). For example, the MEGA framework [19] uses structural features such as triangle motifs to model tightly connected substructures and distance centrality to quantify network influence. Knowledge graphs [20] offer another paradigm for representing hierarchical relationships, where nodes correspond to medical entities (e.g., symptoms, diagnoses, treatments) and edges encode their semantic or causal links. These graph representations can be further enriched with Graph Neural Networks (GNNs) [21], which learn low-dimensional embeddings that preserve both feature information and relational structure, enabling downstream tasks such as patient stratification, treatment effect estimation, and outcome prediction. Future work could explore hybrid approaches that integrate the interpretability of OPT with the representational richness of graph analytics by using graph-derived embeddings as inputs into prescriptive tree models or combining graph-based patient similarity networks with rule-based decision paths.
Through OPT, we produced a prescriptive model to improve 24 h mortality in blunt hemodynamically unstable trauma patients who did or did not undergo REBOA placement. There were essentially five steps to accomplish this. First, the study population and data points as described above were isolated. Second, missing values for independent variables were imputed using a machine-learning method called Optimal Impute [22]. Third, reward estimation was performed. This step estimates the probability that a given observation (patient) is assigned a given treatment (REBOA vs. No REBOA) and the probability of outcome (24 h mortality) for each observation under each treatment option. Random forest classifiers are used to make these estimations. Doubly robust estimation is then used to construct reward matrices. These rewards are used to train an OPT to prescribe new treatments in such a way that the risk of 24 h mortality is reduced in comparison with the current risk of 24 h mortality.
The fourth step involved model training and evaluation. Models are trained on a training and testing split of 50:50 to ensure sufficient data is saved to achieve high-quality reward estimation on the test set. Grid search is applied to select the best combination of hyperparameters (i.e., minimum number of samples in leaf, maximum depth of tree, complexity parameter) such that the best reward minimization is achieved in the training set. Specifically, the decision nodes are selected and pruned automatically, given these selected hyperparameters, which can also be interpreted as additional constraints that limit how complex the resulting tree will become. To avoid any information from the training set leaking through to the out-of-sample evaluation, instead of directly using the rewards from our existing reward estimator trained on the training set, we estimate a new set of reward estimators using only the test set and evaluate the policy against these rewards. Finally, the best-performing tree was evaluated for clinical integrity and logic. If any inconsistencies were noted (for example, accidental inclusion of independent variables that would not be known at the time of REBOA placement), the dataset was adjusted, and these steps were repeated until the final tree was obtained.
OPT could also be interpreted as a general framework that could be aimed at achieving several important clinical sub-tasks, such as patient stratification and treatment assignment. For example, the resulting tree would naturally separate the original patient population into subgroups, or leaves, where each subgroup represents a patient cohort whose characteristics are aligned or considered homogenous within themselves. For each subgroup, a treatment is assigned to optimally maximize the reward of this group. In this regard, OPT should be considered as a tool beyond the clinical setting we have considered here, and can be applied even more generally to other relevant cases.

2.5. Measurement of Model Performance

All propensity and outcome estimations are evaluated using the area under the receiver operating characteristic curve (ROC AUC). The AUC measures the ability of a model to discriminate between the outcomes of interest (24 h mortality) and has been used extensively for binary classification problems due to its superior ability to account for problems such as class imbalance.

2.5.1. Policy Evaluation

The expected 24 h mortality rate following OPT prescription was compared to the observed 24 h mortality rate in patients who were or were not treated with REBOA. This was achieved by calculating the average predicted probability of mortality under the treatments prescribed by the tree for the test set compared to the average probability of mortality under the treatment assignments that were observed. These results are reported as the absolute risk reduction (ARR). This was also calculated for each terminal leaflet of the tree to identify where the largest benefits were achieved by the prescriptive model.

2.5.2. Other Statistical Analysis

The REBOA and No REBOA patient groups were compared using descriptive statistics. Categorical variables were compared using Pearson’s chi-squared test, and continuous variables with the Kruskal–Wallis test. Categorical variables were reported as the number of patients (percentage), and continuous variables were reported as median (interquartile range [IQR]). The level of significance was set at a p-value of <0.05. All analyses were performed using STATA v.17 (StataCorp 2021, College Station, TX, USA).

3. Results

Out of a total of 4.5 million patients, 121,465 suffered blunt trauma and arrived at the hospital in hemorrhagic shock. After applying the aforementioned exclusion criteria, 100,615 patients comprised the study population. Within this group, 803 (0.8%) underwent REBOA within 4 h of hospital arrival, and 99,812 (99.2%) did not.

3.1. Baseline Characteristics

The characteristics of REBOA vs. No REBOA patients utilized in the creation of OPTs are displayed in Table 1. These are all data points that would have been theoretically known or obtainable during the primary and secondary surveys. In summary, the REBOA patients were younger with a median age of 48 (IQR = 29, 61, p < 0.001) and mostly male (69.1%). They had a slightly higher SBP and pulse on arrival. The median GCS of REBOA patients was 3 (IQR = 3, 14) compared to 14 (IQR = 3, 15) for No REBOA patients. The majority of REBOA placements occurred at ACS Level 1 facilities (86.7%). Regarding ED procedures, 64.6% of REBOA patients underwent transfusion of RBCs vs. 19.9% of No REBOA patients. Of the ED diagnoses evaluated, REBOA patients had more injuries of all types, with pneumothorax being the most common (46.8%).
The other injury-related characteristics of REBOA vs. No REBOA patients that were not included in the creation of OPTs are displayed in Table 2. REBOA patients received more units of all blood products (RBC, FFP, PLT, Cryo). The median ISS for REBOA vs. No REBOA patients was 34 (IQR = 26, 45) and 21 (IQR = 10, 33), respectively. The highest AIS body region score for REBOA patients was the thorax, abdomen, and extremity. The most common hemorrhage control procedure performed on REBOA patients within 4 h of hospital arrival was laparotomy (46.5%), followed by pelvic angioembolization (15.2%).

3.2. Outcomes

The primary and secondary outcomes analyzed are reported in Table 3. In summary, REBOA patients had a 46.9% 24 h mortality rate vs. 20.9% in No REBOA patients (p < 0.001, Table 3). This rate was the target of the OPT model, which is discussed in the next section. The in-hospital mortality rates for REBOA vs. No REBOA patients were 61.8% and 30.8%, respectively (p < 0.001). The rates of several complications, such as CAUTI, deep SSI, sepsis, pressure ulcer, DVT, PE, compartment syndrome, cardiac arrest, AKI, and unplanned return to OR, were statistically higher. In addition, REBOA patients had more ventilator and ICU days.

3.3. OPT and 24 h Mortality

Figure 2 shows the OPT model for prescribing REBOA or No REBOA to blunt trauma patients in hemorrhagic shock to improve 24 h mortality. The tree is transparent and interpretable with a relatively small number of decision branches. Each rectangular box represents a “leaf”, and the data point the model used at each as a branch point is listed below it. Within each leaf, either “Prescribe No REBOA” or “Prescribe REBOA” is the treatment the model prescribed. The “N” number of patients at each leaf is also reported. The color of the terminal leaflets represents each treatment and the prescription strength. The blue color corresponds to REBOA and red to No REBOA. If the color is very solid or dark, it means the prescription in that node is very confident. If the color is pale or light, it means that the difference between prescribing REBOA vs. No REBOA is less prominent.
Figure 2. The Optimal Policy Tree (OPT) Model. The final model prescribes REBOA versus No REBOA to improve 24 h mortality in hemodynamically unstable blunt trauma patients.
Starting at the top of the tree at Leaf #1, one can appreciate the “Prescribe No REBOA” and N = 50,308, which represents the 50:50 training to testing split that was performed. The first branch point asks if the patient had a pulse or not. If present, the next Leaf #15 states “Prescribe No REBOA.” The model suggests these patients not receive REBOA yet, but to have a more confident prescription, one needs to continue going through the tree. The next branch point is SBP. If SBP is obtainable, Leaf #19 prescribes No REBOA and is the terminal leaf. If SBP is not obtainable, the tree asks about GCS. If the GCS ≥ 5, the model prescribes No REBOA. If the GCS < 5, the tree prescribes REBOA.
Returning to Leaf #1, we can follow the model to the left for patients with no pulse. The next Leaf #2 uses pneumothorax as a branch point. If there is no pneumothorax, the model next asks about GCS. If GCS ≥ 6, the model prescribes No REBOA. If GCS < 6, the model prescribes REBOA. The next branch point uses SBP of 68. For patients with an obtainable SBP ≥ 68, the model prescribes No REBOA, and for patients with SBP < 68, the model prescribes REBOA. The tree can be similarly followed through each leaf and branch point to the terminal leaflets.
The ARR in 24 h mortality rate for the overall study population, REBOA patients, and No REBOA patients can be visualized in Figure 3. The ARR in the overall study population and No REBOA patients was about the same at 0.9% and 0.8%, respectively. The ARR was largest amongst REBOA patients, with the original cohort having a 47% 24 h mortality rate and a prescribed 29% 24 h mortality rate, resulting in an ARR of 18%. When the terminal leaflets were examined, the largest benefit was seen at leaflet #5 (ARR = 7.98%) and #17 (ARR = 5.44%) (Table 4).
Figure 3. Absolute risk reduction (ARR). The ARR of 24 h mortality for the overall study population, REBOA patients, and No REBOA patients demonstrates a particular advantage for those who were prescribed REBOA.

4. Discussion

Utilizing a novel, transparent, and interpretable AI methodology called OPT, we have thus created a proof-of-concept model for the prescription of REBOA in hemodynamically unstable blunt trauma patients that can potentially decrease the 24 h mortality of this high-risk population. The OPT model resulted in an ARR of 24 h mortality of 0.8% in No REBOA patients and 18% in REBOA patients. In other words, our model showed very minimal improvement in 24 h mortality when prescribing REBOA to those who did not receive it in real life, and a large improvement in 24 h mortality when prescribing No REBOA to patients who did. These results suggest REBOA is potentially being overused in this patient population.
This is the first study to our knowledge that employs AI to elucidate indications for REBOA. Furthermore, this is the first study to utilize OPTs for decision-making in trauma. We perceive this model as a prototype for the use of AI to assist surgeons in decision-making, rather than advocating that this decision tree be the new guide for REBOA use. Further studies with more granular data can lead to a more powerful OPT tree and decision-making tool creation.
Over the past few decades, substantial effort has been made to study the use REBOA for aortic occlusion in hemorrhaging trauma patients [1,2,3,4,5,6,7,8,9,10,11,12,23,24]. Despite these endeavors, there are currently no universally agreed-upon indications for use, and mixed data on outcomes keep the debate alive. Although minimally invasive, REBOA has been suggested to have significant complications, including common femoral artery injury, aortoiliac injury, balloon rupture, and sequelae from prolonged aortic occlusion such as spinal cord injury, AKI, and multisystem organ failure [10,11]. A recent study by Moore et al. prospectively observed patients from six US Level 1 trauma centers and found balloon inflation to increase SBP and achievement of return of spontaneous circulation (ROSC) in more than 50% of patients in cardiac arrest [23]. These centers used a new ER-REBOA catheter, supporting the notion that advances in technology may improve outcomes surrounding REBOA use.
While these new results are encouraging, one of the most concerning aspects of REBOA remains the discrepancy in mortality outcomes reported. Two well-known studies have shown increased rates of mortality [1,2]. Other studies have shown improved survival in various trauma populations [3,4,5]. In the updated joint statement from the American College of Surgeons Committee on Trauma, American College of Emergency Physicians, National Association of Emergency Medical Services Physicians, and National Association of Emergency Medical Technicians, the authors note that none of the current evidence has shown that REBOA improves outcomes or survival compared to the current standard of treatment. While some studies show promising improvements, and the technology and technique of REBOA continue to evolve, our results suggest that REBOA was overused in the last few years and perhaps highlight the lack of indications and variation in use among different trauma centers.
The concern of bias that can be accidentally built into predictive and prescriptive AI models is real [25,26]. In this study, the difficulty was mainly the lack of additional, dynamic, and nuanced data points available in the trauma bay but not in the database for decision-making. While we did our best to simulate the pieces of information that would be known, this was certainly a limitation. Such data limitations require future work to obtain access to and leverage more granular, clinically relevant trauma data. Another source of potential bias in data could also arise from the imputation method, where the exact values of the parameters chosen and the methodology chosen could influence the final values obtained. This is an explanation for why seemingly irrelevant variables were used by the model, such as BMI and pulse oximetry (Figure 2). The AI algorithms are only as adept as the data used to create and train them [26].
Alternatively, it was also intriguing to note which variables the algorithm did and did not use, as this shows how influential they were in altering the outcome of interest. While BMI and pulse oximetry seem inconsequential, there may be an underlying significance we have yet to uncover as surgeon-scientists. It is also possible that these points point to potential artifacts of the database itself or limitations in the imputation process, and the study would benefit from more granular and clinically complete datasets in future works. Interestingly, the model did not select pelvic fracture, an injury that is often associated with REBOA use. It is also worth discussing the fact that the leaflets with the highest ARR were #5 and #17. Leaf #5 prescribes REBOA to patients who have an absent pulse, no pneumothorax, GCS < 6, and SBP < 68. Leaf #17 prescribes REBOA to patients who have a pulse, no obtainable SBP, and a GCS < 5. Our model aligns with the general indications that have been used for REBOA to date: hypotensive blunt trauma patients.
There are several other limitations to this study. First, the AI model was constructed using retrospective data from a large national databank that was not designed with REBOA in mind. There is no data on what model of REBOA was used, introducer sheath size, time to access, insertion, inflation, and associated SBP at those times, level of aortic occlusion, or duration of aortic occlusion. Second, ACS-TQIP also has no data on the FAST exam, which is a critical missing piece of information for REBOA use. Third, there are only a small number of high-volume trauma centers that use REBOA, and this could have a clustering effect in the data. Fourth, the presence of missing data could contribute to the robustness of the overall patient cohort evaluation. Given these issues, we emphasize the need for more granular data applied to future models to refine the existing model. We applied Optimal Imputation in our study, but other imputation methods can also be applied as new information regarding the nature of the data becomes available. Similarly, we also acknowledge that certain variables are collected at the 4 h cutoff after admission, which could be unavailable at the time of REBOA decision. We conducted this study using these features due to the selection of the TQIP dataset, as well as ensuring a reasonable data sample size. We also acknowledge that it would be helpful to conduct a similar validation study on a more recent dataset once one becomes available. In addition to the tree-based method we utilized in the existing manuscript, we also note that other methods, such as graph-based approaches, could also complement our approach by providing insights such as hierarchical structures between features. Future studies of these approaches should also be explored. Finally, we would like to reiterate our intention that this be appreciated as proof of the conceptual idea behind prescriptive AI methodologies and their use in trauma patients. The key to improving these models will continue to be the application of more granular, robust datasets to be applied to more refined models, which could eventually lead to real-world applications.

5. Conclusions

Our study is a proof-of-concept one to utilize AI non-linear logic to improve the use and decrease the misuse of REBOA. Our algorithms suggest that REBOA may have been overused in blunt hemodynamically unstable trauma patients in the last few years, and improvement of the decision-making with the assistance of AI can potentially result in an 18% ARR in 24 h mortality for patients by avoiding the use of REBOA. Our model is not ready for bedside use, and further studies with more granular data can improve its performance further for clinical practice. However, our study shows the premise that interpretable AI models can, in the future, improve mortality in unstable blunt trauma patients by optimizing decision-making and assisting surgeons in improving outcomes.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/bioengineering12101025/s1. Table S1: Injuries and corresponding ICD-10 codes; Table S2: Procedures and corresponding ICD-10 codes.

Author Contributions

Conceptualization, M.B., Y.M., A.D.-G., J.A.P.-Z., A.G., G.C.V., D.B. and H.M.A.K.; methodology, Y.M. and D.B.; software, Y.M.; validation, M.B., Y.M., A.D.-G., J.A.P.-Z., A.G., D.B. and H.M.A.K.; formal analysis, M.B., Y.M., A.D.-G., J.A.P.-Z., A.G., D.B. and H.M.A.K.; resources, D.B. and H.M.A.K.; data curation, M.B., A.D.-G., J.A.P.-Z. and A.G.; writing—original draft preparation, M.B. and Y.M.; writing—review and editing, M.B., Y.M., A.D.-G., J.A.P.-Z., A.G., G.C.V., D.B. and H.M.A.K.; visualization, M.B. and Y.M.; supervision, D.B. and H.M.A.K.; project administration, D.B. and H.M.A.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research did not receive any specific funding from public, commercial, or not-for-profit agencies.

Institutional Review Board Statement

This study was submitted to and deemed exempt from approval by the Mass General Brigham Institutional Review Board.

Informed Consent Statement

Patient consent was waived due to the dataset being publicly available.

Data Availability Statement

All data and example code are available in the public GitHub repository: https://github.com/yuma-sudo/REBOA_share.git accessed on 16 September 2025.

Acknowledgments

We thank the reviewers for giving insightful reviews and MIT Supercloud for providing computational support.

Conflicts of Interest

The authors have no conflicts of interest or disclosures to report.

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Figure 1. Flowchart of REBOA and the exclusion criteria to obtain our final study population.
Figure 1. Flowchart of REBOA and the exclusion criteria to obtain our final study population.
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Figure 2. The final REBOA tree selected through validation both computationally and through physician feedback.
Figure 2. The final REBOA tree selected through validation both computationally and through physician feedback.
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Figure 3. REBOA mortality risk reduction across the different patient populations shows that prescribed REBOA treatments consistently reduce mortality rate in comparison to that of original prescriptions.
Figure 3. REBOA mortality risk reduction across the different patient populations shows that prescribed REBOA treatments consistently reduce mortality rate in comparison to that of original prescriptions.
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Table 1. Characteristics of REBOA versus No REBOA patients that were utilized in the creation of OPTs. p-values suggest that the two cohorts are very similar across the board.
Table 1. Characteristics of REBOA versus No REBOA patients that were utilized in the creation of OPTs. p-values suggest that the two cohorts are very similar across the board.
No REBOAREBOAp-Value
N (%)99,812 (99.2%)803 (0.8%)
Age, median (IQR)52 (33, 66)48 (29, 61)<0.001
Sex, n (%) 0.008
    Male64,471 (64.6%)555 (69.1%)
    Female35,317 (35.4%)248 (30.9%)
Admission physiology, median (IQR)
    SBP82 (70, 90)86 (69, 118)<0.001
    Pulse90 (70, 112)108 (80, 130)<0.001
    Temperature36.4 (36, 36.7)36.1 (35.6, 36.5)<0.001
    GCS14 (3, 15)3 (3, 14)<0.001
    Respiratory rate18 (16, 22)20 (16, 25)<0.001
    Pulse oximetry97 (93, 100)97 (91, 100)0.016
Supplemental oxygen, n (%)49,406 (55.4%)547 (79.3%)<0.001
Intubated in ED, n (%)25,577 (25.6%)322 (40.1%)<0.001
Height, median (IQR)172.72 (165, 180)175 (165.1, 180.3)0.034
Weight, median (IQR)80.29 (68, 97)85 (72, 100)<0.001
BMI, median (IQR)26.9 (23.5, 31.7)28.7 (24.7, 33.4)<0.001
Signs of life in ED, n (%) 0.57
    No signs of life8628 (8.6%)74 (9.2%)
    Signs of life91,184 (91.4%)729 (90.8%)
Teaching status, n (%) <0.001
    Community34,933 (35.1%)187 (23.4%)
    Nonteaching11,753 (11.8%)52 (6.5%)
    University52,735 (53.0%)559 (70.1%)
ACS verification level, n (%) <0.001
    149,277 (58.8%)589 (86.7%)
    221,719 (25.9%)80 (11.8%)
    312,848 (15.3%)10 (1.5%)
ED Procedures, n (%)
    Chest tube placement942 (0.9%)24 (3.0%)<0.001
    Transfusion of RBCs19,865 (19.9%)519 (64.6%)<0.001
    Transfusion of whole blood1643 (1.6%)77 (9.6%)<0.001
ED Diagnoses, n (%)
    Pelvic fx9105 (9.1%)287 (35.7%)<0.001
    Femur fx2077 (2.1%)33 (4.1%)<0.001
    Hemothorax6851 (6.9%)160 (19.9%)<0.001
    Pneumothorax20,938 (21.0%)376 (46.8%)<0.001
    Thoracic aorta injury2419 (2.4%)51 (6.4%)<0.001
Abbreviations: SBP: systolic blood pressure, GCS: Glasgow Coma Scale, ED: emergency department, BMI: body mass index, ACS: American College of Surgeons, fx: fracture.
Table 2. Other injury-related characteristics of REBOA versus No REBOA patients that were not included in the creation of OPTs. p-values of the majority of the features suggest the two cohorts are very similar to each other.
Table 2. Other injury-related characteristics of REBOA versus No REBOA patients that were not included in the creation of OPTs. p-values of the majority of the features suggest the two cohorts are very similar to each other.
No REBOAREBOAp-Value
N (%)99,812 (99.2%)803 (0.8%)
Transfusion volume (units) in 4 h, median (IQR)
    RBC5 (4, 9)12 (7, 21)<0.001
    FFP4 (2, 7)8 (4, 15)<0.001
    PLT5 (0, 8)7 (4, 15)<0.001
    Cryo0 (0, 0)0 (0, 2)<0.001
AIS Body Region, median (IQR)
    Head1 (0, 3)2 (0, 3)<0.001
    Face0 (0, 1)0 (0, 1)<0.001
    Thorax2 (0, 3)3 (2, 4)<0.001
    Abdomen1 (0, 2)3 (2, 4)<0.001
    Extremity2 (0, 3)3 (2, 4)<0.001
ISS, median (IQR)21 (10, 33)34 (26, 45)<0.001
Hemorrhage Control Procedures in 4 h, n (%)
    Laparotomy12,045 (12.1%)373 (46.5%)<0.001
    Thoracotomy/Sternotomy2256 (2.3%)90 (11.2%)<0.001
    Extremity vascular2900 (2.9%)34 (4.2%)0.026
    Preperitoneal pelvic packing1880 (1.9%)99 (12.3%)<0.001
    External fixation of pelvis147 (0.1%)19 (2.4%)<0.001
    Angioembolization of pelvis1868 (1.9%)122 (15.2%)<0.001
Comorbidities, n (%)
    Alcoholism8657 (8.8%)42 (5.4%)<0.001
    Bleeding disorder3028 (3.1%)10 (1.3%)0.004
    CHF4121 (4.2%)7 (0.9%)<0.001
    Smoker17,240 (17.5%)101 (13.1%)0.001
    CKD1751 (1.8%)5 (0.6%)0.017
    Diabetes11,619 (11.8%)54 (7.0%)<0.001
    MI1138 (1.2%)4 (0.5%)0.097
    PAD709 (0.7%)3 (0.4%)0.28
    HTN26,725 (27.2%)106 (13.7%)<0.001
    COPD6899 (7.0%)19 (2.5%)<0.001
    Steroid use802 (0.8%)2 (0.3%)0.086
    Cirrhosis2043 (2.1%)14 (1.8%)0.61
    Substance abuse4522 (4.6%)41 (5.3%)0.35
Abbreviations: RBC: red blood cell, FFP: fresh frozen plasma, PLT: platelet, Cryo: cryoprecipitate, AIS: Abbreviated Injury Score, ISS: Injury Severity Score, CHF: congestive heart failure, CKD: chronic kidney disease, MI: myocardial infarction, PAD: peripheral artery disease, HTN: hypertension, COPD: chronic obstructive pulmonary disease. Bold text refers to the overall category of following sub-categories.
Table 3. Outcomes of REBOA versus No REBOA patients. In our study, we emphasize only 24 h mortality as our primary outcome.
Table 3. Outcomes of REBOA versus No REBOA patients. In our study, we emphasize only 24 h mortality as our primary outcome.
No REBOAREBOAp-Value
N (%)99,812 (99.2%)803 (0.8%)
Hospital complications, n (%)
    CAUTI732 (0.7%)13 (1.6%)0.003
    CLABSI336 (0.3%)5 (0.6%)0.16
    Superficial SSI649 (0.7%)4 (0.5%)0.6
    Deep SSI779 (0.8%)18 (2.3%)<0.001
    Organ space SSI561 (0.6%)4 (0.5%)0.81
    Sepsis1598 (1.6%)30 (3.8%)<0.001
    Pressure ulcer2426 (2.4%)36 (4.5%)<0.001
    DVT2126 (2.1%)42 (5.3%)<0.001
    PE1387 (1.4%)20 (2.5%)0.008
    Compartment syndrome455 (0.5%)20 (2.5%)<0.001
    Cardiac arrest7043 (7.1%)175 (21.8%)<0.001
    MI581 (0.6%)3 (0.4%)0.44
    ARDS2796 (2.8%)28 (3.5%)0.24
    VAP4975 (5.0%)30 (3.8%)0.11
    AKI3211 (3.2%)80 (10.0%)<0.001
    Unplanned intubation3131 (3.1%)24 (3.0%)0.82
    Unplanned return to OR2184 (2.2%)61 (7.6%)<0.001
    Unplanned ICU admission2745 (2.8%)25 (3.1%)0.52
Ventilator days, median (IQR)1 (0, 4)2 (1, 7)<0.001
ICU LOS, median (IQR)2 (0, 8)2 (0, 12)0.019
24 h mortality, n (%)20,828 (20.9%)377 (46.9%)<0.001
In-hospital mortality, n (%)30,706 (30.8%)496 (61.8%)<0.001
Abbreviations: CAUTI: catheter-associated urinary tract infection, CLABSI: central line-associated bloodstream infection, SSI: surgical site infection, DVT: deep vein thrombosis, PE: pulmonary embolism, MI: myocardial infarction, ARDS: acute respiratory distress syndrome, VAP: ventilator-associated pneumonia, AKI: acute kidney injury, OR: operating room, ICU: intensive care unit, LOS: length of stay. Bold text refers to category description for following sub-categories.
Table 4. Terminal leaf level absolute risk reduction (ARR) of original vs. prescribed REBOA treatment on 24 h mortality. We observe a consistent reduction in mortality rate across different leaves.
Table 4. Terminal leaf level absolute risk reduction (ARR) of original vs. prescribed REBOA treatment on 24 h mortality. We observe a consistent reduction in mortality rate across different leaves.
Leaf #OriginalPrescribedARRARR (%)
50.9590.8790.0807.984
60.7190.7180.0010.080
70.4060.4060.0000.000
90.8480.8340.0151.477
120.9190.8880.0313.059
130.8880.8880.0000.005
140.8200.8190.0010.087
170.7400.6850.0545.438
180.1900.1820.0080.831
190.1230.1210.0020.153
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Bokenkamp, M.; Ma, Y.; Dorken-Gallastegi, A.; Proaño-Zamudio, J.A.; Gebran, A.; Velmahos, G.C.; Bertsimas, D.; Kaafarani, H.M.A. Can Artificial Intelligence Improve the Appropriate Use and Decrease the Misuse of REBOA? Bioengineering 2025, 12, 1025. https://doi.org/10.3390/bioengineering12101025

AMA Style

Bokenkamp M, Ma Y, Dorken-Gallastegi A, Proaño-Zamudio JA, Gebran A, Velmahos GC, Bertsimas D, Kaafarani HMA. Can Artificial Intelligence Improve the Appropriate Use and Decrease the Misuse of REBOA? Bioengineering. 2025; 12(10):1025. https://doi.org/10.3390/bioengineering12101025

Chicago/Turabian Style

Bokenkamp, Mary, Yu Ma, Ander Dorken-Gallastegi, Jefferson A. Proaño-Zamudio, Anthony Gebran, George C. Velmahos, Dimitris Bertsimas, and Haytham M. A. Kaafarani. 2025. "Can Artificial Intelligence Improve the Appropriate Use and Decrease the Misuse of REBOA?" Bioengineering 12, no. 10: 1025. https://doi.org/10.3390/bioengineering12101025

APA Style

Bokenkamp, M., Ma, Y., Dorken-Gallastegi, A., Proaño-Zamudio, J. A., Gebran, A., Velmahos, G. C., Bertsimas, D., & Kaafarani, H. M. A. (2025). Can Artificial Intelligence Improve the Appropriate Use and Decrease the Misuse of REBOA? Bioengineering, 12(10), 1025. https://doi.org/10.3390/bioengineering12101025

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