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The latest stories from AHA Today.
Nearly 80% of prekindergarten through 12th grade teachers, school staff and child care workers had received at least their first COVID-19 shot by April, the Centers for Disease Control and Prevention announced yesterday.
Leaders from Henry Ford Health System and the Islamic Center of America discuss their collaboration to increase vaccinations in the Muslim community around Detroit, and the cultural and logistical factors they considered to make their effort successful.
The National Academy of Medicine today released a discussion paper examining the experiences of hospitals and health systems during the COVID-19 pandemic, and opportunities to leverage the lessons of COVID-19 to support performance improvements to the sector more broadly.
In a letter to the editor published today by the Washington Post, AHA President and CEO Rick Pollack responds to a recent article in the paper’s Business section, which suggested COVID-19 relief funds enriched “wealthy” hospital systems.
The Centers for Medicare & Medicaid Services late today issued a proposed rule for the inpatient psychiatric facility prospective payment system for fiscal year 2022.
The Centers for Medicare & Medicaid Services today issued a brief proposed rule for the inpatient rehabilitation facility prospective payment system for fiscal year 2022.
The U.S. Court of Appeals for the 10th Circuit yesterday affirmed a district court decision rejecting an Albuquerque physician practice’s claims that Presbyterian Healthcare Services engaged in exclusionary or anticompetitive conduct under the Sherman Act.
Health Facilities Management, the official magazine of AHA’s American Society for Health Care Engineering, looks at factors to consider when creating space for patient surges.
Learn how hospital and health system leaders such as Richard Bagley, senior vice president, chief supply chain officer, Penn State Health, are looking beyond the pandemic to address long-standing vulnerabilities in the health care supply chain during crisis situations.
The Food and Drug Administration authorized for emergency use the first prescription antibody test that allows individuals to collect a finger-stick dried blood sample at home for analysis at a Symbiotica laboratory when a health care provider deems it appropriate.