Registries for Evaluating Patient Outcomes PDF Download
Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download Registries for Evaluating Patient Outcomes PDF full book. Access full book title Registries for Evaluating Patient Outcomes by Agency for Healthcare Research and Quality/AHRQ. Download full books in PDF and EPUB format.
Author: Agency for Healthcare Research and Quality/AHRQ Publisher: Government Printing Office ISBN: 1587634333 Category : Medical Languages : en Pages : 396
Book Description
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: Agency for Healthcare Research and Quality/AHRQ Publisher: Government Printing Office ISBN: 1587634333 Category : Medical Languages : en Pages : 396
Book Description
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: M. Beth Shanholtzer Publisher: McGraw-Hill Education ISBN: 9781260082265 Category : Medical Languages : en Pages : 304
Book Description
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: ISBN: Category : Electronic government information Languages : en Pages :
Book Description
Addresses many issues concerning electronic records access, and provides a state-by-state summary of key issues regarding electronic information.
Author: Publisher: ISBN: Category : Court administration Languages : en Pages : 162
Book Description
"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: Christa Grammas Carter Publisher: ISBN: Category : Languages : en Pages :
Book Description
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.
Author: National Research Council Publisher: National Academies Press ISBN: 0309096960 Category : Computers Languages : en Pages : 112
Book Description
The federal government generates and increasingly saves a large and growing fraction of its records in electronic form. In 1998, the National Archives and Record Administration (NARA) launched its Electronic Archives (ERA) program to create a system to preserve and provide access to federal electronic records. To assist in this project, NARA asked the NRC to conduct a two-phase study to provide advice as it develops the ERA program. The first two reports (phase one) provided recommendations on design, engineering, and related issues facing the program. This report (phase two) focuses on longer term, more strategic issues including technology trends that will shape the ERA system, archival processes of the ERA, and future evolution of the system. It also provides an assessment of technical and design issues associated with record integrity and authenticity.
Author: Agency for Healthcare Research and Quality/AHRQ
Author: Agency for Healthcare Research and Quality/AHRQ
Author: DIANE Publishing Company
Author: James E. Houpt
Author: M. Beth Shanholtzer
Author: Lucy A. Dalglish
Author: 
Author: Christa Grammas Carter
Author: National Research Council
Author: 
Author: Washington (State). Governor (1997-2005 : Locke)