Data-driven AI is establishing itself at the center of evidence-based medicine. However, reports of shortcomings and unexpected behavior are growing due to AI's reliance on association-based learning. A major reason for this behavior: latent bias in machine learning datasets can be amplified during training and/or hidden during testing. We present a data modality-agnostic auditing framework for generating targeted hypotheses about sources of bias which we refer to as Generalized Attribute Utility and Detectability-Induced bias Testing (G-AUDIT) for datasets. Our method examines the relationship between task-level annotations and data properties including protected attributes (e.g., race, age, sex) and environment and acquisition characteristics (e.g., clinical site, imaging protocols). G-AUDIT automatically quantifies the extent to which the observed data attributes may enable shortcut learning, or in the case of testing data, hide predictions made based on spurious associations. We demonstrate the broad applicability and value of our method by analyzing large-scale medical datasets for three distinct modalities and learning tasks: skin lesion classification in images, stigmatizing language classification in Electronic Health Records (EHR), and mortality prediction for ICU tabular data. In each setting, G-AUDIT successfully identifies subtle biases commonly overlooked by traditional qualitative methods that focus primarily on social and ethical objectives, underscoring its practical value in exposing dataset-level risks and supporting the downstream development of reliable AI systems. Our method paves the way for achieving deeper understanding of machine learning datasets throughout the AI development life-cycle from initial prototyping all the way to regulation, and creates opportunities to reduce model bias, enabling safer and more trustworthy AI systems.

Large language models with a transformer-based encoder/decoder architecture, such as T5, have become standard platforms for supervised tasks. To bring these technologies to the clinical domain, recent work has trained new or adapted existing models to clinical data. However, the evaluation of these clinical T5 models and comparison to other models has been limited. Are the clinical T5 models better choices than FLAN-tuned generic T5 models? Do they generalize better to new clinical domains that differ from the training sets? We comprehensively evaluate these models across several clinical tasks and domains. We find that clinical T5 models provide marginal improvements over existing models, and perform worse when evaluated on different domains. Our results inform future choices in developing clinical LLMs.

Clinical Question Answering (QA) systems enable doctors to quickly access patient information from electronic health records (EHRs). However, training these systems requires significant annotated data, which is limited due to the expertise needed and the privacy concerns associated with clinical data. This paper explores generating Clinical QA data using large language models (LLMs) in a zero-shot setting. We find that naive prompting often results in easy questions that do not reflect the complexity of clinical scenarios. To address this, we propose two prompting strategies: 1) instructing the model to generate questions that do not overlap with the input context, and 2) summarizing the input record using a predefined schema to scaffold question generation. Experiments on two Clinical QA datasets demonstrate that our method generates more challenging questions, significantly improving fine-tuning performance over baselines. We compare synthetic and gold data and find a gap between their training efficacy resulting from the quality of synthetically generated answers.

The third ML4H symposium was held in person on December 10, 2023, in New Orleans, Louisiana, USA. The symposium included research roundtable sessions to foster discussions between participants and senior researchers on timely and relevant topics for the \ac{ML4H} community. Encouraged by the successful virtual roundtables in the previous year, we organized eleven in-person roundtables and four virtual roundtables at ML4H 2022. The organization of the research roundtables at the conference involved 17 Senior Chairs and 19 Junior Chairs across 11 tables. Each roundtable session included invited senior chairs (with substantial experience in the field), junior chairs (responsible for facilitating the discussion), and attendees from diverse backgrounds with interest in the session's topic. Herein we detail the organization process and compile takeaways from these roundtable discussions, including recent advances, applications, and open challenges for each topic. We conclude with a summary and lessons learned across all roundtables. This document serves as a comprehensive review paper, summarizing the recent advancements in machine learning for healthcare as contributed by foremost researchers in the field.

Diabetic eye disease is a major cause of blindness worldwide. The ability to monitor relevant clinical trajectories and detect lapses in care is critical to managing the disease and preventing blindness. Alas, much of the information necessary to support these goals is found only in the free text of the electronic medical record. To fill this information gap, we introduce a system for extracting evidence from clinical text of 19 clinical concepts related to diabetic eye disease and inferring relevant attributes for each. In developing this ophthalmology phenotyping system, we are also afforded a unique opportunity to evaluate the effectiveness of clinical language models at adapting to new clinical domains. Across multiple training paradigms, we find that BERT language models pretrained on out-of-distribution clinical data offer no significant improvement over BERT language models pretrained on non-clinical data for our domain. Our study tempers recent claims that language models pretrained on clinical data are necessary for clinical NLP tasks and highlights the importance of not treating clinical language data as a single homogeneous domain.