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To develop CigStopper, a real-time, automated medical billing prototype designed to identify eligible tobacco cessation care codes, thereby reducing administrative workload while improving billing accuracy.

We analyzed interoperability-related Real World Testing results to identify whether developers are providing meaningful results with the appropriate context to enable stakeholders to understand the Certified Health IT conformance and interoperability when deployed in production environments.

In response to requests from several Rapid Acceleration of Diagnostics-Underserved Populations (RADx-UP) community-engaged research projects to include Long COVID common data elements (CDEs) in the existing RADx-UP CDEs, the RADx-UP Coordination and Data Collection Center (CDCC) leadership formed the Long COVID CDEs Task Force.

Little is known about how clinical decision support (CDS) tools can support care teams in changing clinical decisions to account for patients' social risks. We piloted a suite of electronic health record (EHR)-based CDS tools designed to facilitate social risk-informed care decisions to assess how the tools were used in practice and how they could be improved.

Usage of autotext or "dotphrases" is ubiquitous among provider workflows in electronic health records (EHRs). Yet, little is known about the impact of these tools in inpatient settings and among resident physicians. We aimed to evaluate the association between autotext usage and documentation time among resident physicians in an academic medical center using the Cerner EHR.

Delirium is a severe condition, often underreported and linked to adverse outcomes such as increased mortality and prolonged hospitalization. Despite its significance, delirium prediction is often hindered by underreporting and inconsistent labeling, highlighting the need for models trained on reliably labeled data (ground truth). This review examines (i) practices for determining labels in delirium prediction models and (ii) how study designs affect label quality, aiming to identify key considerations for [...]

This work aims to provide a specialized template for integrating diverse study data types with varying sharing restrictions specific to NIH HEAL Initiative chronic pain and substance use research.

Telemedicine for specialty medical care is evolving from a COVID-19 pandemic-era requirement to an option for patients and clinicians alike, requiring evidence to guide optimal use of virtual specialty care. Heterogeneity across medical specialties complicates this evidence generation. To address this gap in the literature, we present an approach to evaluation of telehealth across specialties with the potential to generate findings generalizable across specialties and health systems.

Congenital heart disease (CHD) patients with single ventricle physiology (SVP) have heterogeneous characteristics that challenge cohort classification. We aim to develop a phenotyping algorithm that accurately identifies SVP patients using electronic health record (EHR) data.

Diagnosis codes documented in electronic health records (EHR) are often relied upon to clinically phenotype patients for biomedical research. However, these diagnoses can be incomplete and inaccurate, leading to false negatives when searching for patients with phenotypes of interest. This study aims to determine whether PheMAP, a comprehensive knowledgebase integrating multiple clinical terminologies beyond diagnosis to capture phenotypes, can effectively identify patients lacking relevant EHR diagnosis codes.