Radiological Health Data And Reports
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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 | : |
Publisher | : |
Total Pages | : 850 |
Release | : 1967 |
Genre | : Radiation |
ISBN | : |
Author | : Curtis Langlotz |
Publisher | : |
Total Pages | : 254 |
Release | : 2015-11-02 |
Genre | : |
ISBN | : 9781515174080 |
An essential resource for medical imaging professionals, this book provides everything you need to create exceptional radiology reports. In an accessible and informal style, one of the foremost experts on radiology reporting gives you practical tips for precise image interpretation and clear communication. This book should be required reading for radiologists in training, and is destined to become an indispensable part of every radiologist's library. Topics include: * The virtues of "normal" * How to say "I don't know" * Building a rhetorical foundation * Spatial relationships * Making recommendations * Suggesting clinical correlation * The hedge * Severity straddling * Size matters * Eponyms in radiology * A summary of reporting best practices * How speech recognition works * Optimizing your speech recognition * Templates and macros * The history of radiology reporting * Structured reporting case study * Structured reporting: what you can do today * Standard terminology for the radiology report * How to think about imaging information * Logic, probability, and the radiology report * Decision making in radiology * The radiology report in 2025
Author | : Thomas E. Johnson |
Publisher | : Lippincott Williams & Wilkins |
Total Pages | : 1289 |
Release | : 2012-10-09 |
Genre | : Medical |
ISBN | : 1451154232 |
This text is an invaluable, comprehensive data reference for anyone involved in health physics or radiation safety. This new edition addresses the specific data requirements of health physicists, with data presented in large tables, including the latest NCRP recommendations, which are tabulated and given in both SI and traditional units for ease of use. Although portions of these data can be obtained from various internet sites, many are obscure, difficult to navigate and/or have conflicting information for even the most common data, such as specific gamma ray constants. This new edition compiles all essential data in this vast field into one user-friendly, authoritative source. It also offers a website with full-text search capability. Markets include radiation safety, medical physics and nuclear medicine
Author | : |
Publisher | : |
Total Pages | : |
Release | : 2020 |
Genre | : |
ISBN | : 9781944888244 |
"This Report extends the concepts and approaches discussed in NCRP Report No. 171 and Commentary No. 24 to further reduce uncertainty in radiation risk assessments at low doses and low dose rates, thereby enhancing the bases for radiation protection guidance"--
Author | : Committee to Assess Health Risks from Exposure to Low Levels of Ionizing Radiation |
Publisher | : National Academies Press |
Total Pages | : 422 |
Release | : 2006-03-23 |
Genre | : Science |
ISBN | : 0309133343 |
This book is the seventh in a series of titles from the National Research Council that addresses the effects of exposure to low dose LET (Linear Energy Transfer) ionizing radiation and human health. Updating information previously presented in the 1990 publication, Health Effects of Exposure to Low Levels of Ionizing Radiation: BEIR V, this book draws upon new data in both epidemiologic and experimental research. Ionizing radiation arises from both natural and man-made sources and at very high doses can produce damaging effects in human tissue that can be evident within days after exposure. However, it is the low-dose exposures that are the focus of this book. So-called “late” effects, such as cancer, are produced many years after the initial exposure. This book is among the first of its kind to include detailed risk estimates for cancer incidence in addition to cancer mortality. BEIR VII offers a full review of the available biological, biophysical, and epidemiological literature since the last BEIR report on the subject and develops the most up-to-date and comprehensive risk estimates for cancer and other health effects from exposure to low-level ionizing radiation.
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 318 |
Release | : 2011-11-25 |
Genre | : Medical |
ISBN | : 0309212421 |
Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In recent years, individuals and organizations have expressed concern that the 510(k) process is neither making safe and effective devices available to patients nor promoting innovation in the medical-device industry. Several high-profile mass-media reports and consumer-protection groups have profiled recognized or potential problems with medical devices cleared through the 510(k) clearance process. The medical-device industry and some patients have asserted that the process has become too burdensome and is delaying or stalling the entry of important new medical devices to the market. At the request of the FDA, the Institute of Medicine (IOM) examined the 510(k) process. Medical Devices and the Public's Health examines the current 510(k) clearance process and whether it optimally protects patients and promotes innovation in support of public health. It also identifies legislative, regulatory, or administrative changes that will achieve the goals of the 510(k) clearance process. Medical Devices and the Public's Health recommends that the U.S. Food and Drug Administration gather the information needed to develop a new regulatory framework to replace the 35-year-old 510(k) clearance process for medical devices. According to the report, the FDA's finite resources are best invested in developing an integrated premarket and postmarket regulatory framework.
Author | : United States. Public Health Service. Division of Radiological Health |
Publisher | : |
Total Pages | : 560 |
Release | : 1962 |
Genre | : Radioactive pollution |
ISBN | : |
Author | : Olga R. Brook |
Publisher | : Thieme |
Total Pages | : 368 |
Release | : 2021-04-21 |
Genre | : Medical |
ISBN | : 1684201527 |
A practical guide for radiologists on providing high yield disease-specific reports Multiple studies show that referring physicians have a clear preference for structured radiology reports due to clarity and ease of interpretation, yet a one-size-fits all approach does not address disease complexities. Concurrently, the use of structured radiology templates has increased, driven in part by the need to comply with big data and artificial intelligence as well as reimbursement. Standardization of reporting is one of the first essential steps in the transformation of radiology from "the art of imaging" to a robust data science. Radiology Structured Reporting Handbook: Disease-Specific Templates and Interpretation Pearls by Professors Olga R. Brook, Wieland H. Sommer, and esteemed colleagues is a highly practical guide on structured reporting for every major area of radiology. Featuring disease-specific templates, the book is organized in six sections and 53 chapters. Section one covers core foundation topics, from different definitions of structured reporting and pros and cons to change management and how to build templates. Five disease-specific sections encompass specific cancers and a variety of abdominal, thoracic, neurological, and cardiovascular diseases and conditions. Key Highlights Downloadable disease-specific templates for a variety of clinical entities including cardiovascular, thoracic, abdominal, oncological, and neuroradiology Essential interpretation pearls for specific diseases from top experts in a bullet format, accompanied by relevant figures and tables Together, the templates and pearls provide an essential and unique practice resource for optimal and clinically relevant reporting. The book also serves as a succinct educational tool for radiology trainees and practicing radiologists who may not interpret specific highly specialized types of studies on a daily basis.
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 321 |
Release | : 1996-03-25 |
Genre | : Medical |
ISBN | : 0309175674 |
Does radiation medicine need more regulation or simply better-coordinated regulation? This book addresses this and other questions of critical importance to public health and safety. The issues involved are high on the nation's agenda: the impact of radiation on public safety, the balance between federal and state authority, and the cost-benefit ratio of regulation. Although incidents of misadministration are rare, a case in Pennsylvania resulting in the death of a patient and the inadvertent exposure of others to a high dose of radiation drew attention to issues concerning the regulation of ionizing radiation in medicine and the need to examine current regulatory practices. Written at the request from the Nuclear Regulatory Commission (NRC), Radiation in Medicine reviews the regulation of ionizing radiation in medicine, focusing on the NRC's Medical Use Program, which governs the use of reactor-generated byproduct materials. The committee recommends immediate action on enforcement and provides longer term proposals for reform of the regulatory system. The volume covers: Sources of radiation and their use in medicine. Levels of risk to patients, workers, and the public. Current roles of the Nuclear Regulatory Commission, other federal agencies, and states. Criticisms from the regulated community. The committee explores alternative regulatory structures for radiation medicine and explains the rationale for the option it recommends in this volume. Based on extensive research, input from the regulated community, and the collaborative efforts of experts from a range of disciplines, Radiation in Medicine will be an important resource for federal and state policymakers and regulators, health professionals involved in radiation treatment, developers and producers of radiation equipment, insurance providers, and concerned laypersons.