PubMed Essentials, Mastering the Worlds Health Research Database PDF Download
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Author: Bengt Edhlund
Publisher: Lulu.com
ISBN: 1312289457
Category : Science
Languages : en
Pages : 186
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Book Description
A user's guide to smarter searching of medical information, 'PubMed Essentials' is the complete and concise guide on how to navigate your way through and perfect your use of PubMed. This book explains in detail the general features, the Medical Subject Headings (MeSH), different search strategies, logical filters and how to communicate PubMed records between colleagues. My NCBI is descibed as a powerful alert service with your choice of logical filters and how you build and store your own collection of records in PubMed. Since then this service has developed and its functionality and reliability have improved. Today, PubMed is the most popular database out of this system of NCBI databases. PubMed is the essential tool for health researchers worldwide, handling millions of queries per day.
Author: Bengt Edhlund
Publisher: Lulu.com
ISBN: 1312289457
Category : Science
Languages : en
Pages : 186
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Book Description
A user's guide to smarter searching of medical information, 'PubMed Essentials' is the complete and concise guide on how to navigate your way through and perfect your use of PubMed. This book explains in detail the general features, the Medical Subject Headings (MeSH), different search strategies, logical filters and how to communicate PubMed records between colleagues. My NCBI is descibed as a powerful alert service with your choice of logical filters and how you build and store your own collection of records in PubMed. Since then this service has developed and its functionality and reliability have improved. Today, PubMed is the most popular database out of this system of NCBI databases. PubMed is the essential tool for health researchers worldwide, handling millions of queries per day.
Author: Leonid Kalinichenko
Publisher: Springer
ISBN: 3319571354
Category : Computers
Languages : en
Pages : 286
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Book Description
This book constitutes the refereed proceedings of the 28th International Conference on Data Analytics and Management in Data Intensive Domains, DAMDID/RCDL 2016, held in Ershovo, Moscow, Russia, in October 2016. The 16 revised full papers presented together with one invited talk and two keynote papers were carefully reviewed and selected from 57 submissions. The papers are organized in topical sections on semantic modeling in data intensive domains; knowledge and learning management; text mining; data infrastructures in astrophysics; data analysis; research infrastructures; position paper.
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309164257
Category : Medical
Languages : en
Pages : 267
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Book Description
Healthcare decision makers in search of reliable information that compares health interventions increasingly turn to systematic reviews for the best summary of the evidence. Systematic reviews identify, select, assess, and synthesize the findings of similar but separate studies, and can help clarify what is known and not known about the potential benefits and harms of drugs, devices, and other healthcare services. Systematic reviews can be helpful for clinicians who want to integrate research findings into their daily practices, for patients to make well-informed choices about their own care, for professional medical societies and other organizations that develop clinical practice guidelines. Too often systematic reviews are of uncertain or poor quality. There are no universally accepted standards for developing systematic reviews leading to variability in how conflicts of interest and biases are handled, how evidence is appraised, and the overall scientific rigor of the process. In Finding What Works in Health Care the Institute of Medicine (IOM) recommends 21 standards for developing high-quality systematic reviews of comparative effectiveness research. The standards address the entire systematic review process from the initial steps of formulating the topic and building the review team to producing a detailed final report that synthesizes what the evidence shows and where knowledge gaps remain. Finding What Works in Health Care also proposes a framework for improving the quality of the science underpinning systematic reviews. This book will serve as a vital resource for both sponsors and producers of systematic reviews of comparative effectiveness research.
Author: Gina S. Lovasi
Publisher:
ISBN: 0190885300
Category : Medical
Languages : en
Pages : 385
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Book Description
Urban Public Health grapples with the complexity of the urban setting as a physical and social space while also providing an abundance of global and local examples of current urban health practices.
Author: Adam Bohr
Publisher: Academic Press
ISBN: 0128184396
Category : Computers
Languages : en
Pages : 385
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Book Description
Artificial Intelligence (AI) in Healthcare is more than a comprehensive introduction to artificial intelligence as a tool in the generation and analysis of healthcare data. The book is split into two sections where the first section describes the current healthcare challenges and the rise of AI in this arena. The ten following chapters are written by specialists in each area, covering the whole healthcare ecosystem. First, the AI applications in drug design and drug development are presented followed by its applications in the field of cancer diagnostics, treatment and medical imaging. Subsequently, the application of AI in medical devices and surgery are covered as well as remote patient monitoring. Finally, the book dives into the topics of security, privacy, information sharing, health insurances and legal aspects of AI in healthcare. - Highlights different data techniques in healthcare data analysis, including machine learning and data mining - Illustrates different applications and challenges across the design, implementation and management of intelligent systems and healthcare data networks - Includes applications and case studies across all areas of AI in healthcare data
Author: Mildred L. Patten
Publisher: Taylor & Francis
ISBN: 1351969757
Category : Psychology
Languages : en
Pages : 229
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Book Description
• Designed for students who are getting lost in the details of research methods and not getting the big picture, this short book provides an overview of the essential concepts traditionally covered in a research methods class. •Lively examples on contemporary topics stimulate students’ interest and show the relevance of research methods to their everyday lives. •Divided into short sections, this book makes it easy for you to give customized assignments. Assign only the sections your students need. •Shows students how to interpret statistics without computations. •Factual Questions at the end of each section allow students to check their comprehension. •Questions for Discussion stimulate classroom dialogue. • New to this edition: Five new sections on in-text citations and reference lists have been added. Numerous changes have also been made for consistency with the latest editions of the APA and ASA Style manuals, and new examples have been added.
Author: Rebecca Skloot
Publisher: Crown
ISBN: 0307589382
Category : Science
Languages : en
Pages : 386
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Book Description
#1 NEW YORK TIMES BESTSELLER • “The story of modern medicine and bioethics—and, indeed, race relations—is refracted beautifully, and movingly.”—Entertainment Weekly NOW A MAJOR MOTION PICTURE FROM HBO® STARRING OPRAH WINFREY AND ROSE BYRNE • ONE OF THE “MOST INFLUENTIAL” (CNN), “DEFINING” (LITHUB), AND “BEST” (THE PHILADELPHIA INQUIRER) BOOKS OF THE DECADE • ONE OF ESSENCE’S 50 MOST IMPACTFUL BLACK BOOKS OF THE PAST 50 YEARS • WINNER OF THE CHICAGO TRIBUNE HEARTLAND PRIZE FOR NONFICTION NAMED ONE OF THE BEST BOOKS OF THE YEAR BY The New York Times Book Review • Entertainment Weekly • O: The Oprah Magazine • NPR • Financial Times • New York • Independent (U.K.) • Times (U.K.) • Publishers Weekly • Library Journal • Kirkus Reviews • Booklist • Globe and Mail Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor Southern tobacco farmer who worked the same land as her slave ancestors, yet her cells—taken without her knowledge—became one of the most important tools in medicine: The first “immortal” human cells grown in culture, which are still alive today, though she has been dead for more than sixty years. HeLa cells were vital for developing the polio vaccine; uncovered secrets of cancer, viruses, and the atom bomb’s effects; helped lead to important advances like in vitro fertilization, cloning, and gene mapping; and have been bought and sold by the billions. Yet Henrietta Lacks remains virtually unknown, buried in an unmarked grave. Henrietta’s family did not learn of her “immortality” until more than twenty years after her death, when scientists investigating HeLa began using her husband and children in research without informed consent. And though the cells had launched a multimillion-dollar industry that sells human biological materials, her family never saw any of the profits. As Rebecca Skloot so brilliantly shows, the story of the Lacks family—past and present—is inextricably connected to the dark history of experimentation on African Americans, the birth of bioethics, and the legal battles over whether we control the stuff we are made of. Over the decade it took to uncover this story, Rebecca became enmeshed in the lives of the Lacks family—especially Henrietta’s daughter Deborah. Deborah was consumed with questions: Had scientists cloned her mother? Had they killed her to harvest her cells? And if her mother was so important to medicine, why couldn’t her children afford health insurance? Intimate in feeling, astonishing in scope, and impossible to put down, The Immortal Life of Henrietta Lacks captures the beauty and drama of scientific discovery, as well as its human consequences.
Author:
Publisher:
ISBN:
Category : Medical policy
Languages : en
Pages : 132
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Book Description
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
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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: World Health Organization
Publisher: World Health Organization
ISBN: 9241562811
Category : Law
Languages : en
Pages : 162
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Book Description
This book reviews the current state of health research and concludes that: more investment is needed, research need to be managed more effectively to help strengthen health systems and build public confidence in science; stronger emphasis should be placed on translating knowledge into action. There are five sections: learning to improve health, gives an overview and some historical perspective; towards a scientific basis for health systems; strengthening health research systems; linking research to action; and recommendations and an action plan.
