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Accelerate adoption of clinical research technology that obtains electronic health record (EHR) data through HL7 Fast Healthcare Interoperability Resources (FHIR).

Despite the rapid development of AI in clinical medicine, reproducibility and methodological limitations hinder its clinical utility. In response, MINimum Information for Medical AI Reporting (MINIMAR) standards were introduced to enhance publication standards and reduce bias, but their application remains unexplored. In this review, we sought to assesses the quality of reporting in AI/ML studies of cardiac amyloidosis (CA) an increasingly important cause of heart failure.

Severe maternal morbidity and mortality are higher in the United States than in other high-income countries, and unacceptable disparities persist. To facilitate research on these outcomes, we developed a standardized approach for extracting perinatal data from electronic health records (EHRs).

The Bridge2AI program is establishing rules of practice for creating ethically sourced health data repositories to support the effective use of ML/AI in biomedical and behavioral research. Given the initially undefined nature of ethically sourced data, this work concurrently developed definitions and guidelines alongside repository creation, grounded in a practical, operational framework.

Electronic Health Records (EHRs) sampled from different populations can introduce unwanted biases, limit individual-level data sharing, and make the data and fitted model hardly transferable across different population groups. In this context, our main goal is to design an effective method to transfer knowledge between population groups, with computable guarantees for suitability, and that can be applied to quantify treatment disparities.

Risk prediction models are used in hospitals to identify pediatric patients at risk of clinical deterioration, enabling timely interventions and rescue. The objective of this study was to develop a new explainer algorithm that uses a patient's clinical notes to generate text-based explanations for risk prediction alerts.

In real-world data (RWD), defining the observation period-the time during which a patient is considered observable-is critical for estimating incidence rates (IRs) and other outcomes. Yet, in the absence of explicit enrollment information, this period must often be inferred, introducing potential bias.

Real-world data (RWD) analyses primarily rely on structured clinical documentation collected through routine clinical care or driven by medical billing requirements. Patient-reported outcome measures (PROMs), integrated into electronic health records (EHRs), are an additional data source that could offer valuable insights into a patient's perspective and contribute to a more comprehensive understanding of health outcomes in RWD studies. This study aims to characterize agreement between PROMs symptoms and structured clinical [...]

Evaluate the association between telemedicine intensity and ambulatory physician electronic health record (EHR) use following the COVID-19 pandemic.

To explore the performance of 4 large language model (LLM) chatbots for the analysis of 2 of the most commonly used tools for the advanced analysis of systematic reviews (SRs) and meta-analyses.