Research Paper (postgraduate) from the year 2015 in the subject Health - Public Health, grade: 1, Northeastern University of Boston, language: English, abstract: Data breaches in U.S. healthcare have become ubiquitous with modern hackers honing in on healthcare data due to its lucrative economic value. Cyber crooks regard medical identity theft as ‘The triple crown of stolen data’ as it’s worth more than a Social Security Number or credit card number in the internet black market. The black market rate for each partial EHR is $50 as compared to $1 for a stolen Social Security Number or credit card number. With 44% of data breaches that healthcare organizations contribute to, this report analyzes for the evolving security measures and trends in the healthcare industry to protect data from cyber crooks. An infographic study was carried out to explore the ways by which data is lost, states accounting the most and least number of medical data breaches, and the location of breached information. Outcome of this infographics study is expected to pave the way for possibility of future research and scholarly debate. Potential of cloud computing in healthcare has been taken into account and was analyzed for its benefits of adoption and use, obstacles, and its forecast in the near future. At the outset, this report is a snapshot of U.S. healthcare’s defensive preparation and strategy against the level of cyber-attacks that will be coming at them, statistical analysis on types of breach impacting healthcare organizations the most, state-wise percentage analysis of medical data breach, and cloud computing as a defensive solution to protect the data from cyber-attacks, and insider threat - disgruntled employees and patient-record snoopers.

This book pinpoints current and impending threats to the healthcare industry's data security.

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.

This report sets out the results of a study of consumer attitudes toward data breaches, notifications of those breaches, and company responses to such events.

In the realm of health care, privacy protections are needed to preserve patients' dignity and prevent possible harms. Ten years ago, to address these concerns as well as set guidelines for ethical health research, Congress called for a set of federal standards now known as the HIPAA Privacy Rule. In its 2009 report, Beyond the HIPAA Privacy Rule: Enhancing Privacy, Improving Health Through Research, the Institute of Medicine's Committee on Health Research and the Privacy of Health Information concludes that the HIPAA Privacy Rule does not protect privacy as well as it should, and that it impedes important health research.

Protect Your Organization Against Massive Data Breaches and Their Consequences Data breaches can be catastrophic, but they remain mysterious because victims don’t want to talk about them. In Data Breaches, world-renowned cybersecurity expert Sherri Davidoff shines a light on these events, offering practical guidance for reducing risk and mitigating consequences. Reflecting extensive personal experience and lessons from the world’s most damaging breaches, Davidoff identifies proven tactics for reducing damage caused by breaches and avoiding common mistakes that cause them to spiral out of control. You’ll learn how to manage data breaches as the true crises they are; minimize reputational damage and legal exposure; address unique challenges associated with health and payment card data; respond to hacktivism, ransomware, and cyber extortion; and prepare for the emerging battlefront of cloud-based breaches. Understand what you need to know about data breaches, the dark web, and markets for stolen data Limit damage by going beyond conventional incident response Navigate high-risk payment card breaches in the context of PCI DSS Assess and mitigate data breach risks associated with vendors and third-party suppliers Manage compliance requirements associated with healthcare and HIPAA Quickly respond to ransomware and data exposure cases Make better decisions about cyber insurance and maximize the value of your policy Reduce cloud risks and properly prepare for cloud-based data breaches Data Breaches is indispensable for everyone involved in breach avoidance or response: executives, managers, IT staff, consultants, investigators, students, and more. Read it before a breach happens! Register your book for convenient access to downloads, updates, and/or corrections as they become available. See inside book for details.

Miscellaneous facts and ideas are interconnected and represented in a visual format, a "visual miscellaneum," which represents "a series of experiments in making information approachable and beautiful" -- from p.007