Legislation Proposed to Improve the Accuracy of Patient Matching
New legislation has been introduced that seeks to establish standards and protocols to improve the matching of patients with their medical records and promote interoperability without increasing the burdens on providers and health systems. Adding patient data to the medical records of incorrect recipients can have serious consequences and it has been a problem that has plagued the healthcare industry for years. There have been many cases where incorrect matching has resulted in denied claims, medical errors, and even patient deaths. Patients with mismatched records often have to undergo unnecessary repeated medical tests, the cost of which can be considerable. Each instance of mismatched records costs an average of $1,950 per patient inpatient stay, and more than $1,700 per emergency department visit, and 35% of all denied claims are due to inaccurate patient identification. The HIPAA Journal was recently contacted by one patient who has been plagued by mismatching problems with her healthcare provider due to her having the same name and date of birth as another patient. The other...
Empress Ambulance Service Settles Class Action Lawsuit for $1.05 Million
Empress Ambulance Service, an ambulance company that operates in many regions of New York as Empress EMS, has proposed a $1.05 million settlement to resolve claims it failed to implement appropriate cybersecurity safeguards to protect the sensitive data of patients. Empress EMS suffered a Hive ransomware attack in July 2022, in which files were encrypted and sensitive patient data was stolen. The Hive group published some of the data on its data leak site; however, Empress EMS paid the ransom, and the data was removed from the leak site. The forensic investigation confirmed the protected health information of 318,558 patients was compromised in the attack. Several lawsuits were filed in response to the data breach and a settlement has been proposed to resolve the claims, with no admission of wrongdoing by Empress EMS. Under the terms of the settlement, class members – individuals who were notified about the data breach by Empress EMS – are entitled to submit claims for up to $10,000 for reimbursement of documented expenses incurred as a result of the data breach, such as tax and...
Guide to the FDA Regulation of Medical Devices
The FDA regulation of medical devices is conducted via the Administration’s Center for Devices and Radiological Health (CDRH), which not only regulates firms that manufacture, repackage, relabel, and import medical devices, but also regulates radiation-emitting products such as x-ray systems and ultrasound equipment throughout their product lifecycles. To simplify medical device regulation, CDRH has classified approximately 1,700 generic types of medical devices and grouped them into sixteen medical specialties or “panels” (see 21 CFR Chapter I, Subchapter H). Each type of generic device is assigned to one of three regulatory classes depending on the level of risk the device poses to the patient or user and the level of control necessary to assure the safety and effectiveness of the device. Class I Devices Under the FDA regulation of medical devices, Class I Devices are most often devices not intended to support or sustain life and that are unlikely to pose a significant risk of illness or injury. Examples include elastic bandages, manual stethoscopes, surgical masks, and tongue...
January 2024 Healthcare Data Breach Report
In January, 61 data breaches of 500 or more records were reported to the U.S. Department of Health and Human Services (HHS) Office for Civil Rights (OCR), which is a 22% month-over-month reduction in reported data breaches, with data breaches falling to two below the monthly average of 63 data breaches a month. While the reduction in data breaches is good news, January is typically a relatively quiet month for healthcare data breaches, and January’s figures are 45% higher than January 2023. For the second consecutive month, there was a fall in the number of breached records with 8,800,875 healthcare records breached in January. As with the number of reported breaches, the reduction is good news but the number of breached records is much higher than in previous years. Further, in January 2024, 4 cyberattacks were reported to OCR where the total number of records involved has yet to be determined. To meet the reporting requirements of the HIPAA Breach Notification Rule – which requires data breaches to be reported within 60 days of discovery – those four data breaches were reported...
What are the HHS OIG Anti-Kickback Regulations?
The HHS OIG anti-kickback regulations prohibit the remuneration of individuals or organizations in Federal healthcare programs when the purpose of the remuneration is to induce referrals – or is in return for referrals – for items or services reimbursable by a Federal healthcare program. Individuals and organizations that violate the regulations can be fined, imprisoned, and/or excluded from all federal healthcare programs. The HHS OIG anti-kickback regulations were introduced in 1972 as a safeguard against fraud and abuse in federal healthcare programs such as Medicare and Medicaid. Originally only relating to financial transactions, the HHS OIG anti-kickback regulations have been subsequently extended to include any form of monetary or “in-kind” remuneration offered, solicited, paid, or received in exchange for items or services billable to a federal healthcare program. According to its November 2023 interpretation of remuneration, HHS OIG states “remuneration includes anything of value, whether in cash, in kind, or other form. […] Remuneration may take the form of cash,...



