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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
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Enhancing Antibiotic Stewardship using a Natural Language Approach for
Better Feature Representation
Simon A. Lee 1 Trevor Brokowski 2 3 Jeffrey N. Chiang 1 4
Abstract
The rapid emergence of antibiotic-resistant bac-
teria is recognized as a global healthcare crisis,
undermining the efficacy of life-saving antibiotics.
This crisis is driven by the improper and overuse
of antibiotics, which escalates bacterial resistance.
In response, this study explores the use of clinical
decision support systems, enhanced through the
integration of electronic health records (EHRs),
to improve antibiotic stewardship. However, EHR
systems present numerous data-level challenges,
complicating the effective synthesis and utiliza-
tion of data. In this work, we transform EHR data
into a serialized textual representation and employ
pretrained foundation models to demonstrate how
this enhanced feature representation can aid in
antibiotic susceptibility predictions. Our results
suggest that this text representation, combined
with foundation models, provides a valuable tool
to increase interpretability and support antibiotic
stewardship efforts.
1. Introduction
The Centers for Disease Control and Prevention (CDC) has
declared the rapid emergence of resistant bacteria a global
healthcare crisis, threatening the efficacy of antibiotics that
have saved millions of lives (Ventola, 2015; Golkar et al.,
2014; Gould & Bal, 2013; Sengupta et al., 2013; Nature,
2013; Lushniak, 2014). This crisis is primarily driven by the
mishandling and overuse of these antibiotics, which leads to
bacteria developing resistance through repetitive exposure
(Viswanathan, 2014; Read & Woods, 2014). These resistant
bacteria impose significant clinical and financial burdens on
*Equal contribution 1Department of Computational Medicine,
UCLA 2Yale School of Medicine 3Biomedical Informatics & Data
Science, Yale University 4Department of Neurosurgery, UCLA.
Correspondence to: Simon A. Lee <simonlee711@g.ucla.edu>,
Jeffrey Chiang <njchiang@g.ucla.edu>.
Proceedings of the 41st International Conference on Machine
Learning, Vienna, Austria. PMLR 235, 2024. Copyright 2024 by
the author(s).
healthcare systems, as well as on patients and their families
worldwide (Bartlett et al., 2013).
Clinical decision support systems hold substantial poten-
tial to assist healthcare providers in adhering to antibiotic
stewardship practices. This potential is largely facilitated by
electronic health record (EHR) software, which allows for
the seamless integration of patient health histories in digital
form (Evans, 2016; Cowie et al., 2017; Hoerbst & Ammen-
werth, 2010). The integration with EHRs enables the use
of continuously updated and deployed machine learning
models for clinical decision-making. However, EHR data
in its raw form presents numerous challenges, such as data
ingestion and feature representation (Wu et al., 2010).
In this work, we present a methodology that converts EHR
data into a serialized text form called pseudo-notes to predict
antibiotic susceptibility. This conversion from tabular to text
format facilitates the creation of interpretable data inputs for
pretrained foundation models, known for their rich feature
representation. Our primary objective is to develop a predic-
tive model that incorporates this representation strategy in
conjunction with foundation models. This approach aims to
enhance decision support systems and accurately identify
the most suitable antibiotics for patients, thereby offering a
data-driven solution to combat antibiotic resistance.
2. Related Works
Medical Representation Learning Medical representa-
tion learning on Electronic Health Records (EHRs) has
emerged as a critical area in healthcare research, focusing
on transforming complex medical data for enhanced clinical
decision-making. Initially, this involved extensive feature
engineering to convert raw EHR data into formats suitable
for traditional machine learning models (Tang et al., 2020;
Ferrao et al., 2016). However, this approach can be labor-
intensive and varies significantly across research groups due
to the lack of a standard protocol.
Recently, the focus has shifted to advanced foundation mod-
els that learn to represent medical data by analyzing exten-
sive text corpora, including clinical notes, medical literature,
and records. These models, primarily based on the BERT
architecture, generate rich, contextual latent representations
1
arXiv:2405.20419v1 [cs.LG] 30 May 2024

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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
of patient histories, significantly reducing the manual effort
in feature engineering (Rasmy et al., 2021; Liu et al., 2021;
Alsentzer et al., 2019; Lee et al., 2020). Moreover, new
techniques have been developed to incorporate the longitu-
dinal nature of EHR data, leveraging a patients progression
to predict outcomes (Steinberg et al., 2023; Wornow et al.,
2024; Pang et al., 2021; Li et al., 2022).
Clinical Decision Support Machine learning enhances
clinical decision support systems by analyzing vast datasets
to provide evidence-based recommendations that improve
patient care outcomes (Sutton et al., 2020). Since the acces-
sibility to EHR systems, there have been numerous such use
cases in predicting diseases (Liu et al., 2018; Cheng et al.,
2016), and various other patient outcomes (Lee et al., 2024;
Suter et al., 1994; Churpek et al., 2014) across all institu-
tions within the healthcare system. Furthermore, the inte-
gration of predictive models into clinical workflows enables
researchers to preemptively manage chronic conditions and
mitigate potential health crises before they escalate (Li et al.,
2020; Goldstein et al., 2017; Hohman et al., 2023). By con-
tinuously learning from new data, these systems evolve to
provide more accurate assessments and recommendations,
which support ongoing improvements in medical practices
and patient management strategies. However, much work
remains to be done on addressing the generalization and bi-
ases prevalent in many of these predictive algorithms (Goetz
et al., 2024; Agniel et al., 2018).
3. Methods
EHR Electronic Health Records are digital versions of a
patient’s medical history, maintained over time by health-
care providers. These records are valuable but consist of
heterogeneous tabular datasets organized into separate ta-
bles such as diagnostics, demographics, and medication,
presenting numerous challenges for researchers.
The primary challenge with EHRs is the heterogeneous na-
ture of the data, which includes numerical, categorical, and
free-text formats that are difficult to integrate and convert
into machine-readable formats. Furthermore, categorical
data fields often contain a large number of classes, poten-
tially distorting their original representation. For instance,
employing feature engineering techniques such as dummy
coding for categorical variables can introduce collinearity,
increase dimensionality, and result in sparse data represen-
tations. These modifications can complicate simple table
readouts and require more memory capacity for statistical
models to function effectively.
Pseudo-notes: Clinical Notes Generation from Tabular
Data Recent research has introduced a methodology for
serializing tabular data into text using text templates (Hegsel-
mann et al., 2023). This approach significantly enhances our
work by enabling uniform representation of all data in the
EHR as human-readable and interpretable text, rather than
as a collection of merged tables. Moreover, it creates an
interface to use foundation models pre-trained on large text
corpora, facilitating rich feature representation. In our work,
we use a mapping function f : T → S that turns individual
tables into serialized text, where T stands for individual
tables and S for serialized text. For each patient, we convert
each of their N tables—which cover different aspects like
diagnostics, medications, and vitals—into text segments.
These segments are then joined to create a single, detailed
paragraph per patient. This method combines all pertinent
patient information from various sources into one unified
narrative, effectively transforming the data structure into
S = J
N
i=1 f(Ti), where Ti is the ith table row concerning
the patient.
Data Source and Inclusion Criteria We sourced data
from the Medical Information Mart for Intensive Care IV
(MIMIC-IV) and MIMIC-IV Emergency Department (ED)
databases (Johnson et al., 2020; 2023). This study focused
on ED patients presumed to have staph infections, selected
based on specific inclusion criteria. Eligible participants
included those with any microbiological culture testing posi-
tive for a staph-related organism, sourced from bodily fluids
such as blood, urine, cerebral spinal fluid, pleural cavity, or
joint fluid, accompanied by a prescribed antibiotic whose
susceptibility was subsequently tested (Tong et al., 2015;
Kwiecinski & Horswill, 2020). From these criteria, we
identified 5976 unique prescriptions in our database. Addi-
tionally, patients with multiple ED admissions that met the
criteria were analyzed separately but were grouped within
the same train/test divisions to prevent test set contamina-
tion. This cohort included 10 unique antibiotics, whose
prevalences are shown in Table 1. A demographic overview
of our cohort is presented in Appendix Section B.
Table 1. Antibiotic Prevalence in MIMIC IV Cohort
ANTIBIOTIC
TRAIN
TEST
TOTAL PREVALENCE (%)
CLINDAMYCIN
2645
624
54.69%
DAPTOMYCIN
1815
425
37.51%
ERYTHROMYCIN
2626
639
54.59%
GENTAMICIN
4549
1127
94.89%
LEVOFLOXACIN
2866
715
60.00%
OXACILLIN
2702
667
56.32%
RIFAMPIN
1929
459
39.96%
TETRACYCLINE
3747
909
76.57%
TRIMETHOPRIM/SUL
3671
908
71.66%
VANCOMYCIN
2529
611
52.53%
To motivate our experimental setup, we examine the infor-
mation available about a patient at their time of arrival in the
emergency department. To predict antibiotic use, we utilize
2

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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
Figure 1. Area under the Receiver Operating Characteristic (AUROC) curves for each antibiotic classification shows that, despite the
nuances, BioMegatron performs the best.
six clinical modalities from the MIMIC ED Database. These
EHR modalities include arrival and triage information, med-
ication reconciliation (medrecon), diagnostic codes (ICD-
9/10), vital signs, and Pyxis data. All these data points are
linked to antibiotic labels from the MIMIC database using
a patient ID, visit, and Hospital Admission ID (Hadm id),
allowing us to accurately identify the patients and their tests
in which certain antibiotics were effective.
Experiments In this work, we benchmark different rep-
resentation strategies of EHR to identify the most effective
method for predicting antibiotic susceptibility. We approach
this problem as a multilabel binary classification, where
we train the same base model (Light Gradient Boosted Ma-
chines) using various representation startegies of the input.
These representations include: raw tabular data; EHR-shot
(Wornow et al., 2024), a foundation model for tabular EHR;
and three text-based representations: word2vec, a generic
language model, and a medical language model, BioMega-
tron (Shin et al., 2020). Additionally, we conduct a clus-
tering of our pseudonotes using the BERTopic algorithm
(Grootendorst, 2022) to determine if these embeddings can
naturally cluster patients. Identifying these clusters can pro-
vide insights into their potential performance in settings like
zero-shot learning and provide insights into the decision
making process.
4. Results
Antibiotic Susceptibility Prediction In our analysis of
antibiotic prediction, we measure the Area Under the Re-
ceiver Operating Characteristic curve (AUROC) and Area
Under the Precision-Recall Curve (AUPRC). Additionally,
we bootstrap 1,000 times to generate 95% confidence in-
tervals. Our AUROC and AUPRC results are displayed
in Figures 1 and 2. We also measure additional F1 scores
and Matthews correlation coefficients, with a whole table
readout which are included in the appendix.
Clustering Experiment In our clustering experiments,
we aim to identify clusters using the BERTopic algorithm.
By identifying clusters based on embeddings, we believe
this approach can form the basis for zero-shot applications
across various clinical tasks. Additionally, finding similar
embeddings could provide insights into decision-making
processes in these black-box models. We showcase the
similarity matrix of our patient clusters in Figure 3.
5. Discussion
Clinical Notes with Foundation Models Provide the best
representation and interpretability From Figures 1 and
2, we observe that the foundation models operating on our
pseudo-notes method provide the best overall performance
across most of the antibiotics. While a generic founda-
tion model and EHR-shot excel with some antibiotics, the
clinical foundation model consistently shows superior per-
formance across both AUROC and AUPRC metrics.
Beyond enhanced predictive abilities, an advantage of our
pseudo-notes method over EHR foundation models and
tabular representations is its interpretability. Compared to
the specific structuring required by EHR-shot, our method
offers a simpler and more effective interface to understand
the data that is being modeled which can improve the trust
between AI and healthcare professionals.
Interoperability Another advantage of pseudo-notes over
EHR foundation models is their interoperability with pro-
prietary healthcare systems. Our method offers a straight-
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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
Figure 2. Area under the Precision Recall Curve (AUPRC) curves for each antibiotic classification shows that, despite the nuances,
BioMegatron performs the best.
Figure 3. Identifying clusters from our patient embeddings is indi-
cated by the squares forming along the diagonal of our similarity
matrix.
forward interface for converting any EHR tabular data from
tables to text. Our conversion also facilitates the use of
off-the-shelf open-source foundation models. As improved
models are continually developed, this data format provides
an easy interface to adapt and swap the backbone for im-
proved representation of our clinical text. Additionally,
EHR foundation models do not operate on non-OMOP vo-
cabularies, which limits its effectiveness on datasets like
MIMIC-IV that utilize these specialized vocabularies.
Patient Similarity One final advantage of our pseudo-
notes is illustrated in Figure 3, which demonstrates the
capability to perform a similarity search on our patient em-
beddings. From this analysis, we identified clusters related
to sepsis, diabetes, stomach acid issues, anxiety, painkillers,
respiratory conditions, and antidepressants. This opens up
potential use cases for this data representation strategy to
be used in zero-shot learning studies and offers insights
into decision-making processes based on the embeddings.
Further research is needed to explore both of these areas.
6. Conclusion
In this work, we introduced a methodology called pseudo-
notes, which converts EHR tabular data into text to achieve
an optimal representation strategy. We discovered that
pseudo-notes outperformed various representation strategies
and remains a highly flexible framework, compatible with
the ongoing development of foundation model backbones,
which could further enhance its performance. Additionally,
we found that pseudo-notes can identify patient clusters
within the EHR, opening up promising avenues for future
studies in zero-shot learning and model interpretation.
From an application perspective, we demonstrated how a
straightforward data transformation has emerged as an easy
interface for making EHR data synergized before integrat-
ing it into machine learning models. We think that this
strategy could be a better way to work with EHR data for
future research and help build trust due to its interpretabil-
ity. Particularly in this study, we illustrated its potential by
identifying suitable antibiotics for patients arriving at the
ED, where timely and accurate decisions are critical. We as
4

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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
a group have highlighted the importance of improving an-
tibiotic stewardship and showcase the impact of data-driven
strategies in addressing pressing healthcare challenges.
Impact Statement
The goal of this work is to advance the field of Machine
Learning in Healthcare, and thus presents a novel potential
interface between modern NLP (Foundation models) and
clinical data.
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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
A. Appendix
A.1. Additional Commentary
Limitations Some limitations of this work include the variability in patients’ histories and the 512 sequence length
limitation imposed by the DistilBERT (Sanh et al., 2019) and BioMegatron models (Shin et al., 2020). Consequently,
portions of a patient’s medical history may be truncated depending on the length of that history. Tokenization strategies (e.g.,
sub-word tokenization) can significantly influence how we handle the analysis.
Future Work Future work in our group, from a methodological perspective, aims to explore how these notes can enhance
studies in model interpretability and zero-shot or few-shot frameworks. From an application standpoint, we are interested in
applying this methodology across various departments and applications. We plan to collaborate with clinicians throughout
our institution to determine the types of clinical decision support models that are most needed and to assess how AI can
benefit these healthcare facilities.
Additionally, future work will include benchmarking the plethora of foundation models available on the Huggingface
Platform (Wolf et al., 2019). This will help us identify the best foundation model for specific tasks and determine whether
these embeddings are task-agnostic.
B. Dataset Characteristics
B.1. Patient Demographics
Table 2. MIMIC IV Cohort Data Overview
DESCRIPTION
CATEGORY
TRAIN
TEST
TOTALS
PRESCRIPTION, N
TOTAL
4803
1173
5976
UNIQUE ID, N
TOTAL
3283
878
4161
AGE MEAN (SD)
59 (17) 58 (17)
SEX %
FEMALE
1341
351
1692
MALE
1942
527
2469
RACE/ETHNICITY %
WHITE
2212
583
2795
BLACK
416
119
535
OTHER
401
96
497
HISPANIC/LATINO
150
55
205
ASIAN
88
20
108
UNABLE
12
3
15
NATIVE HAWAIIAN
4
2
6
B.2. Clinical Modalities
Table 3. Overview of Clinical Modalities in Emergency Department Visits
Modality Name
Description
Arrival Information
Records patient demographics, time of arrival, and mode of arrival
(e.g., ambulance, walk-in).
Triage Information
Documents vital signs, severity of condition using scales like ESI,
and initial chief complaints upon arrival.
Medication Reconciliation
Details previous and current medications the patient is taking, in-
cluding dosages and frequency.
Patient Vitals
Ongoing measurements throughout the ED visit including heart rate,
blood pressure, temperature, etc.
Diagnosis Codes
ICD-9/10 codes used to classify and record diagnoses during the
visit.
Pyxis Information
Information on medications administered during the ED stay via the
Pyxis system, including timing and dosage.
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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
C. Results
Table 4. Performance Metrics for Clindamycin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.7179 ± 0.032
0.7719 ± 0.019
0.7737 ± 0.031
0.7786 ± 0.015
0.7689 ± 0.029
MCC
0.0914 ± 0.011
0.4162 ± 0.0624
0.3561 ± 0.026
0.3772 ± 0.028
0.3379 ± 0.022
ROC-AUC
0.6029 ± 0.044
0.7664 ± 0.020
0.7263 ± 0.023
0.7443 ± 0.030
0.7244 ± 0.034
PRC-AUC
0.6427 ± 0.010
0.7859 ± 0.026
0.7660 ± 0.013
0.7684 ± 0.015
0.7653 ± 0.019
Table 5. Performance Metrics for Daptomycin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.2667 ± 0.032
0.3704 ± 0.069
0.3333 ± 0.050
0.3529 ± 0.012
0.3529 ± 0.035
MCC
0.2867 ± 0.065
0.3584 ± 0.022
0.3943 ± 0.041
0.4586 ± 0.058
0.4587 ± 0.034
ROC-AUC
0.6107 ± 0.063
0.6651 ± 0.065
0.60223 ± 0.070
0.5211 ± 0.060
0.6708 ± 0.062
PRC-AUC
0.1107 ± 0.006
0.1679 ± 0.015
0.2323 ± 0.004
0.2319 ± 0.005
0.2474 ± 0.006
Table 6. Performance Metrics for Erythromycin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.5495 ± 0.030
0.6575 ± 0.023
0.6394 ± 0.038
0.6592 ± 0.020
0.6473 ± 0.025
MCC
0.1306 ± 0.021
0.3807 ± 0.029
0.3209 ± 0.042
0.3702 ± 0.037
0.3406 ± 0.028
ROC-AUC
0.5879 ± 0.044
0.7590 ± 0.022
0.7320 ± 0.025
0.7597 ± 0.023
0.7600 ± 0.025
PRC-AUC
0.4530 ± 0.017
0.6718 ± 0.024
0.6754 ± 0.016
0.6872 ± 0.012
0.6964 ± 0.014
Table 7. Performance Metrics for Gentamicin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.9762 ± 0.030
0.9775 ± 0.065
0.9776 ± 0.040
0.9766 ± 0.045
0.9776 ± 0.032
MCC
0.2521 ± 0.055
0.3634 ± 0.021
0.3953 ± 0.030
0.3969 ± 0.065
0.3667 ± 0.035
ROC-AUC
0.6158 ± 0.089
0.6310 ± 0.047
0.6727 ± 0.047
0.6777 ± 0.042
0.6523 ± 0.039
PRC-AUC
0.9706 ± 0.036
0.9672 ± 0.004
0.9675 ± 0.002
0.9713 ± 0.002
0.9678 ± 0.011
Table 8. Performance Metrics for Levofloxacin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.7641 ± 0.028
0.8386 ± 0.017
0.8088 ± 0.012
0.8034 ± 0.013
0.8066 ± 0.013
MCC
0.1766 ± 0.025
0.5094 ± 0.015
0.4302 ± 0.025
0.4260 ± 0.017
0.4261 ± 0.017
ROC-AUC
0.6326 ± 0.034
0.7972 ± 0.017
0.7787 ± 0.021
0.7974 ± 0.018
0.7937 ± 0.021
PRC-AUC
0.7324 ± 0.013
0.8290 ± 0.014
0.8157 ± 0.011
0.8459 ± 0.012
0.8449 ± 0.014
Table 9. Performance Metrics for Oxacillin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.7264 ± 0.027
0.8229 ± 0.024
0.7899 ± 0.018
0.7790 ± 0.023
0.7975 ± 0.014
MCC
0.2012 ± 0.015
0.4955 ± 0.017
0.4456 ± 0.021
0.4028 ± 0.020
0.4674 ± 0.018
ROC-AUC
0.5607 ± 0.027
0.7996 ± 0.016
0.7688 ± 0.017
0.7692 ± 0.013
0.7723 ± 0.015
PRC-AUC
0.6069 ± 0.011
0.8408 ± 0.018
0.7847 ± 0.019
0.7807 ± 0.018
0.7960 ± 0.017
8

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Enhancing Antibiotic Stewardship using a Natural Language Approach for Better Feature Representation
Table 10. Performance Metrics for Rifampin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.5619 ± 0.026
0.6250 ± 0.024
0.6582 ± 0.012
0.6455 ± 0.017
0.6434 ± 0.018
MCC
≥0.0000 ± 0.000
0.4136 ± 0.027
0.3907 ± 0.012
0.3599 ± 0.017
0.3583 ± 0.021
ROC-AUC
0.5083 ± 0.026
0.7634 ± 0.015
0.7691 ± 0.015
0.7553 ± 0.016
0.7644 ± 0.015
PRC-AUC
0.4082 ± 0.002
0.6927 ± 0.011
0.7017 ± 0.013
0.6940 ± 0.011
0.6999 ± 0.012
Table 11. Performance Metrics for Tetracycline
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.8950 ± 0.025
0.9009 ± 0.024
0.9028 ± 0.027
0.9035 ± 0.023
0.9049 ± 0.021
MCC
0.1657 ± 0.025
0.3805 ± 0.012
0.3696 ± 0.015
0.3795 ± 0.017
0.3865 ± 0.021
ROC-AUC
0.5822 ± 0.035
0.6908 ± 0.018
0.6843 ± 0.023
0.6843 ± 0.025
0.6933 ± 0.023
PRC-AUC
0.8467 ± 0.004
0.8571 ± 0.005
0.8717 ± 0.005
0.8760 ± 0.003
0.8822 ± 0.002
Table 12. Performance Metrics for Trimethoprim/sulfa
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.8835 ± 0.018
0.8856 ± 0.027
0.9080 ± 0.032
0.9080 ± 0.024
0.9100 ± 0.025
MCC
≥ 0.0000 ± 0.000
0.3785 ± 0.023
0.4070 ± 0.031
0.4162 ± 0.023
0.4321 ± 0.032
ROC-AUC
0.5393 ± 0.031
0.7026 ± 0.016
0.7025 ± 0.018
0.6946 ± 0.027
0.7122 ± 0.026
PRC-AUC
0.8159 ± 0.017
0.8707 ± 0.015
0.8748 ± 0.004
0.8742 ± 0.004
0.8815 ± 0.008
Table 13. Performance Metrics for Vancomycin
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
F1
0.6786 ± 0.021
0.7201 ± 0.016
0.7227 ± 0.015
0.7244 ± 0.014
0.7287 ± 0.023
MCC
0.1433 ± 0.026
0.3342 ± 0.023
0.3382 ± 0.026
0.3370 ± 0.025
0.3555 ± 0.024
ROC-AUC
0.5431 ± 0.020
0.7566 ± 0.014
0.7449 ± 0.011
0.7542 ± 0.012
0.7610 ± 0.013
PRC-AUC
0.5537 ± 0.005
0.7781 ± 0.018
0.7676 ± 0.015
0.7754 ± 0.019
0.7708 ± 0.006
Table 14. Number of Winning Metrics
METRIC
TABULAR
EHR-SHOT
WORD2VEC
DISTILBERT
BIOMEGATRON
TOTAL
NUMBER
0
13
3
7
17
40
9
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