Electronic Records Access
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Author | : Agency for Healthcare Research and Quality/AHRQ |
Publisher | : Government Printing Office |
Total Pages | : 385 |
Release | : 2014-04-01 |
Genre | : Medical |
ISBN | : 1587634333 |
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author | : James E. Houpt |
Publisher | : |
Total Pages | : 34 |
Release | : 1990 |
Genre | : Public records |
ISBN | : |
Author | : M. Beth Shanholtzer |
Publisher | : McGraw-Hill Education |
Total Pages | : 304 |
Release | : 2020-06-11 |
Genre | : Medical |
ISBN | : 9781260082265 |
Developed as a comprehensive learning resource, this hands-on course for Integrated Electronic Health Records is offered through McGraw Hill's Connect. Connect uses the latest technology and learning techniques to better connect professors to their students, and students to the information and customized resources they need to master a subject. Both the worktext and the online course include coverage of EHRclinic, an education-based EHR solution for online electronic health records, practice management applications, and interoperable physician-based functionality. EHRclinic will be used to demonstrate the key applications of electronic health records. Attention is paid to providing the "why"behind each task, so that the reader can accumulate transferable skills. The coverage is focused on using an EHR program in a doctor's office, while providing additional information on how tasks might also be completed in a hospital setting.
Author | : Lucy A. Dalglish |
Publisher | : |
Total Pages | : |
Release | : 2003 |
Genre | : Electronic government information |
ISBN | : |
Addresses many issues concerning electronic records access, and provides a state-by-state summary of key issues regarding electronic information.
Author | : MIT Critical Data |
Publisher | : Springer |
Total Pages | : 435 |
Release | : 2016-09-09 |
Genre | : Medical |
ISBN | : 3319437429 |
This book trains the next generation of scientists representing different disciplines to leverage the data generated during routine patient care. It formulates a more complete lexicon of evidence-based recommendations and support shared, ethical decision making by doctors with their patients. Diagnostic and therapeutic technologies continue to evolve rapidly, and both individual practitioners and clinical teams face increasingly complex ethical decisions. Unfortunately, the current state of medical knowledge does not provide the guidance to make the majority of clinical decisions on the basis of evidence. The present research infrastructure is inefficient and frequently produces unreliable results that cannot be replicated. Even randomized controlled trials (RCTs), the traditional gold standards of the research reliability hierarchy, are not without limitations. They can be costly, labor intensive, and slow, and can return results that are seldom generalizable to every patient population. Furthermore, many pertinent but unresolved clinical and medical systems issues do not seem to have attracted the interest of the research enterprise, which has come to focus instead on cellular and molecular investigations and single-agent (e.g., a drug or device) effects. For clinicians, the end result is a bit of a “data desert” when it comes to making decisions. The new research infrastructure proposed in this book will help the medical profession to make ethically sound and well informed decisions for their patients.
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 36 |
Release | : 2003-07-31 |
Genre | : Medical |
ISBN | : 0309185432 |
Commissioned by the Department of Health and Human Services, Key Capabilities of an Electronic Health Record System provides guidance on the most significant care delivery-related capabilities of electronic health record (EHR) systems. There is a great deal of interest in both the public and private sectors in encouraging all health care providers to migrate from paper-based health records to a system that stores health information electronically and employs computer-aided decision support systems. In part, this interest is due to a growing recognition that a stronger information technology infrastructure is integral to addressing national concerns such as the need to improve the safety and the quality of health care, rising health care costs, and matters of homeland security related to the health sector. Key Capabilities of an Electronic Health Record System provides a set of basic functionalities that an EHR system must employ to promote patient safety, including detailed patient data (e.g., diagnoses, allergies, laboratory results), as well as decision-support capabilities (e.g., the ability to alert providers to potential drug-drug interactions). The book examines care delivery functions, such as database management and the use of health care data standards to better advance the safety, quality, and efficiency of health care in the United States.
Author | : |
Publisher | : |
Total Pages | : 162 |
Release | : 2000 |
Genre | : Court administration |
ISBN | : |
"This manual provides PACER users with a better understanding of what PACER is and how it works ... The United States Courts designed an electronic public access system called PACER (Public Access to Court Electronic Records) for the U.S. District Courts, the U.S. Bankruptcy Courts, and the U.S. Circuit Courts of Appeals. PACER systems are beneficial for quickly tracking or retrieving accurate information about current federal cases."--Page 1
Author | : Bruce I. Ambacher |
Publisher | : Rowman & Littlefield |
Total Pages | : 212 |
Release | : 2003 |
Genre | : Electronic records |
ISBN | : 0810847698 |
As the institution with the oldest, largest, and most actively managed program in the world, the U.S. National Archives and Records Administration (NARA) encompasses thirty years of experience in appraising, accessioning, preserving, describing and providing access to archival electronic records. In this collection of essays, twelve contributors, each of whom has been involved in NARA's development, discuss the application of archival theory and practice in NARA's development of these functions and trace how they evolved over time. The result is a fascinating and awesome amalgam of achievement, anecdote, and aspiration.
Author | : National Academies of Sciences, Engineering, and Medicine |
Publisher | : National Academies Press |
Total Pages | : 335 |
Release | : 2020-01-02 |
Genre | : Medical |
ISBN | : 0309495474 |
Patient-centered, high-quality health care relies on the well-being, health, and safety of health care clinicians. However, alarmingly high rates of clinician burnout in the United States are detrimental to the quality of care being provided, harmful to individuals in the workforce, and costly. It is important to take a systemic approach to address burnout that focuses on the structure, organization, and culture of health care. Taking Action Against Clinician Burnout: A Systems Approach to Professional Well-Being builds upon two groundbreaking reports from the past twenty years, To Err Is Human: Building a Safer Health System and Crossing the Quality Chasm: A New Health System for the 21st Century, which both called attention to the issues around patient safety and quality of care. This report explores the extent, consequences, and contributing factors of clinician burnout and provides a framework for a systems approach to clinician burnout and professional well-being, a research agenda to advance clinician well-being, and recommendations for the field.
Author | : Christa Grammas Carter |
Publisher | : |
Total Pages | : |
Release | : 2008 |
Genre | : |
ISBN | : |
ABSTRACT: Governments at the local, state and federal levels are using electronic-storage technology for their document and record management. Benefits of this technology include the ability to 1) expeditiously search and retrieve documents and 2) remotely access, deliver, and transfer documents. While these benefits help government act more efficiently, they have not yet been used to make public records more accessible to the public. Ironically, some states' public records laws are so difficult to interpret and apply that they complicate the very process that seeks to open up the public records system with electronic access. My study examined the state laws that regulate access to electronic public records. The results were compared with those of a similar study published in 2000. The contrast and comparison between the current state of the law and that of eight years ago provides a nation-wide evaluation of changes in the level of access that the public has to electronic records.