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H-ISAC TLP Green Daily Cyber Headlines - June 8, 2023
H-ISAC TLP Green Daily Cyber Headlines for June 8, 2023.
CDC data confirm third COVID-19 vaccine dose safe in young children
The first data on the safety of a third mRNA COVID-19 vaccine dose among young children show that a third dose is safe for children ages 6 months to 5 years old, similar to findings for doses one and two.
AHA comments on proposed retroactive rulemaking on Medicare DSH policy
The AHA continues to oppose the Centers for Medicare & Medicaid Services’ policy to include Medicare Advantage patient days when calculating the Medicare fraction of a hospital’s disproportionate patient percentage for the Medicare Disproportionate Share Hospital program, and objects to the agency’s Aug. 6 proposal to apply the policy retroactively, the association told the agency.
AHA Statement to the Senate Finance Committee on Consolidation in Health Care
American Hospital Association (AHA) statement for the record to the Senate Finance Committee to provide the hospital perspective on how hospital mergers and acquisitions can expand and preserve access to quality care.
Blog: What a Recent Health Affairs Piece Gets Wrong about Hospital Finances and Charity Care
The AHA is pushing back against a recent Health Affairs article that uses flawed, debunked methodology in an attempt to undermine hospitals through preconceived notions of how the field’s finances are managed.
AHA podcast: Strengthening Risk Communications in Rural Health Care Emergencies
Communicating information is critical during emergencies and disasters.
New AHA report examines factors driving physician practice acquisition
Escalating costs associated with managing their own practice coupled with burdensome insurer policies and regulatory requirements are some of the factors driving physicians to seek employment in other practice settings, according to a new report released by the AHA.
FDA authorizes first at-home COVID-19 test using traditional review pathway
The Food and Drug Administration authorized for marketing the first at-home over-the-counter test for COVID-19 using a traditional premarket review pathway rather than emergency use authorities.