The federal medical privacy rule is commonly known as the "HIPAA privacy rule." However, it actually holds the title, "Standards for Privacy of Individually Identifiable Health Information."
ST. PAUL, Minn.—Earlier this summer, government health IT coordinators announced the formation of a 10-year electronic health records (EHR) interoperability plan that will allow even more government agencies access to Americans’ private medical data—all in the name of better patient care.
There’s triple trouble with electronic health records: patient safety, medical privacy, and data security. And there are at least eight hazards. But much taxpayer money has been thrown at the highly speculative, untested EHR for political and profit purposes.
Citizens’ Council for Health Freedom Says Far from Preventing Fraud, Health Care System is Contributing to It
ST. PAUL, Minn.—More problems with Obamacare abound—this time with inconsistent data for those who have enrolled.
ST. PAUL, Minn.—The blue and white “H” signs signifying a nearby hospital should be symbols of safety and help for those in need of medical care. But increased privacy intrusions, growing threats to parental rights, and encroaching government regulations that diminish quality of care have all contributed to making our nation’s health care system an increasingly unsafe place for Americans.
ST. PAUL, Minn.—The U.S. House of Representatives will vote on Tuesday on the Newborn Screening Saves Lives Reauthorization Act of 2014 (H.R.1281), which would extend for five years the funding program that allows states to collect and store newborn DNA without parental consent.
The federal government is planning to eliminate privacy protections for medical records regarding treatment for alcohol and drug abuse and treatment for mental health conditions. The Substance Abuse and Mental Health Services Administration (SAMHSA) will hold a public listening session on Wednesday, June 11, 2014, to solicit public comments on this proposal.
Federal officials are defending an unconscionable act. Between 2005 and 2009, the National Institutes of Health (NIH) supported research on 1,316 premature newborns without requiring parents to be told their baby could die and the baby’s oxygen monitor would not show their child’s true oxygen level.