Publications by authors named "Stanley M Huff"

There are over 8 million central venous access devices inserted each year, many in patients with chronic conditions who rely on central access for life-preserving therapies. Central venous access device-related complications can be life-threatening and add tens of billions of dollars to health care costs, while their incidence is most likely grossly mis- or underreported by medical institutions. In this communication, we review the challenges that impair retention, exchange, and analysis of data necessary for a meaningful understanding of critical events and outcomes in this clinical domain.

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Article Synopsis
  • Delivering optimal care in clinical settings is complicated by limited evidence from costly clinical trials, leaving many healthcare questions unanswered.
  • Underserved regions often struggle to access and implement advanced evidence-based guidelines due to a lack of resources and training for care providers.
  • The use of eActions, or validated clinical decision support systems, could enhance decision-making in busy healthcare environments, but requires overcoming technical and cultural challenges, as well as better data management systems.
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Background And Objective: Logical Observation Identifiers Names and Codes (LOINC) is a universal standard for identifying laboratory tests and clinical observations. It facilitates a smooth information exchange between hospitals, locally and internationally. Although it offers immense benefits for patient care, LOINC coding is complex, resource-intensive, and requires substantial domain expertise.

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  • - The study investigates the limitations of genetic lab test report formats, which often restrict data accessibility for clinical decision support systems, and evaluates the potential of the HL7 FHIR CG IG standard to improve interoperability.
  • - Researchers analyzed sample reports from four genetic tests, identifying 36 common key data elements (KDEs) that were mapped to the FHIR CG IG, suggesting further enhancements for standard development.
  • - While the FHIR CG IG covers most identified KDEs, the study proposes additional extensions to better represent certain data, emphasizing the need for ongoing contributions from the clinical genetics community to refine the standard.
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  • - The study investigates how genetic testing laboratories in the U.S. view the implementation of health-care interoperability (HC) standards, particularly their utility in genetic test reports towards clinical information systems.
  • - Researchers gathered insights through surveys and interviews, identifying 24 key themes from 9 labs, highlighting challenges like genetic knowledge complexity, and motivations like competitive advantage and financial incentives.
  • - Findings suggest that labs see potential benefits in adopting HC standards, driven by competition and incentives, which could enhance quality control, research, and the overall health system's learning ability.
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  • This study explores how U.S. genetic testing labs manage their information processing for better integration with electronic health records (EHRs).
  • Researchers conducted interviews and discussions with representatives from ten labs to analyze their information flow and workflow models.
  • The findings revealed three common lab system types, highlighting that many labs use non-standard methods for sharing genetic test data, which hinders effective clinical use and public health improvements.
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  • Clinical decision-making often relies on clinicians' knowledge and experience, but this can lead to biases and variations in care, complicating the goal of providing only the right care.
  • Current electronic health records (EHRs) mostly serve administrative purposes and contribute to clinician stress, lacking robust decision-support tools that could enhance personalized patient care.
  • The proposed solution is "eActions," which are computer protocols designed to help clinicians make consistent, evidence-based decisions for patients, thereby improving healthcare quality and reducing unwarranted variations in treatment.
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Context.—: The Logical Observation Identifiers Names and Codes (LOINC) system is supposed to facilitate interoperability, and it is the federally required code for exchanging laboratory data.

Objective.

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Objective: This article describes lessons learned from the collaborative creation of logical models and standard Health Level Seven (HL7) Fast Healthcare Interoperability Resources (FHIR) profiles for family planning and reproductive health. The National Health Service delivery program will use the FHIR profiles to improve federal reporting, program monitoring, and quality improvement efforts.

Materials And Methods: Organizational frameworks, work processes, and artifact testing to create FHIR profiles are described.

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Health care and biomedical research are awash in data. Traditional data warehouse methodologies do not scale to this challenge; nor do their schema match the variety of analytic use cases. An alternative model, which shreds data into well-formed constituent data elements, conformant with the emerging CIMI-FHIR standards and stored together with the complete, raw, source data using modern and scalable data utilities such as Hadoop and its derivatives, affords the creation of pluripotent data repositories.

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In this study we developed a Fast Healthcare Interoperability Resources (FHIR) profile to support exchanging a full pedigree based family health history (FHH) information across multiple systems and applications used by clinicians, patients, and researchers. We used previously developed clinical element models (CEMs) that are capable of representing the FHH information, and derived essential data elements including attributes, constraints, and value sets. We analyzed gaps between the FHH CEM elements and existing FHIR resources.

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Objective: The objective of the Strategic Health IT Advanced Research Project area four (SHARPn) was to develop open-source tools that could be used for the normalization of electronic health record (EHR) data for secondary use--specifically, for high throughput phenotyping. We describe the role of Intermountain Healthcare's Clinical Element Models ([CEMs] Intermountain Healthcare Health Services, Inc, Salt Lake City, Utah) as normalization "targets" within the project.

Materials And Methods: Intermountain's CEMs were either repurposed or created for the SHARPn project.

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With the objective of increasing electronic death registration, Intermountain Healthcare and the Utah Office of Vital Records and Statistics have developed a system enabling death certification from within Intermountain's electronic medical record (EMR), consisting of an EMR module and an HL7 interface. Comparison of post-intervention death certification at Intermountain Healthcare against a baseline study found a slight increase in the percentage of deaths certified electronically (73% pre vs. 77% post).

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Background And Objective: Intermountain Healthcare has a long history of using coded terminology and detailed clinical models (DCMs) to govern storage of clinical data to facilitate decision support and semantic interoperability. The latest iteration of DCMs at Intermountain is called the clinical element model (CEM). We describe the lessons learned from our CEM efforts with regard to subjective decisions a modeler frequently needs to make in creating a CEM.

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Natural language processing (NLP) technologies provide an opportunity to extract key patient data from free text documents within the electronic health record (EHR). We are developing a series of components from which to construct NLP pipelines. These pipelines typically begin with a component whose goal is to label sections within medical documents with codes indicating the anticipated semantics of their content.

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Research Objective: To develop scalable informatics infrastructure for normalization of both structured and unstructured electronic health record (EHR) data into a unified, concept-based model for high-throughput phenotype extraction.

Materials And Methods: Software tools and applications were developed to extract information from EHRs. Representative and convenience samples of both structured and unstructured data from two EHR systems-Mayo Clinic and Intermountain Healthcare-were used for development and validation.

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A semantic lexicon which associates words and phrases in text to concepts is critical for extracting and encoding clinical information in free text and therefore achieving semantic interoperability between structured and unstructured data in Electronic Health Records (EHRs). Directly using existing standard terminologies may have limited coverage with respect to concepts and their corresponding mentions in text. In this paper, we analyze how tokens and phrases in a large corpus distribute and how well the UMLS captures the semantics.

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With increasing adoption of electronic health records (EHRs), the need for formal representations for EHR-driven phenotyping algorithms has been recognized for some time. The recently proposed Quality Data Model from the National Quality Forum (NQF) provides an information model and a grammar that is intended to represent data collected during routine clinical care in EHRs as well as the basic logic required to represent the algorithmic criteria for phenotype definitions. The QDM is further aligned with Meaningful Use standards to ensure that the clinical data and algorithmic criteria are represented in a consistent, unambiguous and reproducible manner.

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The clinical element model (CEM) is an information model designed for representing clinical information in electronic health records (EHR) systems across organizations. The current representation of CEMs does not support formal semantic definitions and therefore it is not possible to perform reasoning and consistency checking on derived models. This paper introduces our efforts to represent the CEM specification using the Web Ontology Language (OWL).

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Article Synopsis
  • The study aimed to create and validate quality metrics for detailed clinical models (DCMs) using the ISO/IEC 9126 software evaluation model.
  • A two-round Delphi survey with 9 international experts was conducted to assess the metrics' face and content validity, resulting in 8 evaluation domains and 29 quality metrics.
  • The metrics received a high reliability score (kappa of 0.73), indicating they are robust tools that can help DCM developers and clinical users make informed decisions.
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Federal authorities have recently signaled that they would consider delaying some aspects of implementation of the newest version of the International Classification of Diseases, known as ICD-10-CM, a coding system used to define health care charges and diagnoses. Some industry groups have reacted with dismay, and many providers with relief. We are concerned that adopting this new classification system for reimbursement will be disruptive and costly and will offer no material improvement over the current system.

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The Strategic Health IT Advanced Research Projects (SHARP) Program, established by the Office of the National Coordinator for Health Information Technology in 2010 supports research findings that remove barriers for increased adoption of health IT. The improvements envisioned by the SHARP Area 4 Consortium (SHARPn) will enable the use of the electronic health record (EHR) for secondary purposes, such as care process and outcomes improvement, biomedical research and epidemiologic monitoring of the nation's health. One of the primary informatics problem areas in this endeavor is the standardization of disparate health data from the nation's many health care organizations and providers.

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The Clinical Element Model (CEM) is a strategy designed to represent logical models for clinical data elements to ensure unambiguous data representation, interpretation, and exchange within and across heterogeneous sources and applications. The current representations of CEMs have limitations on expressing semantics and formal definitions of the structure and the semantics. Here we introduce our initial efforts on representing the CEM in OWL, so that the enrichment with OWL semantics and further semantic processing can be achieved in CEM.

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LOINC codes are seeing increased use in many organizations. In this study, we examined the barriers to semantic interoperability that still exist in electronic data exchange of laboratory results even when LOINC codes are being used as the observation identifiers. We analyzed semantic interoperability of laboratory data exchanged using LOINC codes in three large institutions.

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SHARPn is a collaboration among 16 academic and industry partners committed to the production and distribution of high-quality software artifacts that support the secondary use of EMR data. Areas of emphasis are data normalization, natural language processing, high-throughput phenotyping, and data quality metrics. Our work avails the industrial scalability afforded by the Unstructured Information Management Architecture (UIMA) from IBM Watson Research labs, the same framework which underpins the Watson Jeopardy demonstration.

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