Quality & Patient Safety
Medtronic has recalled more than 204,000 devices used to assist hospital and other patients with end-stage heart failure due to the potential for power source interruptions, the Food and Drug Administration reported Friday.
The Food and Drug Administration this week issued a safety communication reminding health care professionals of factors that increase the risk of surgical fires on or near a patient and offering recommendations to reduce these fires from occurring.
Innovation Leadership Challenge: Collaborating to Improve Hospital Flow, Save Lives and Reduce Costs
Date: July 25, 2018
Time: 8:00- 5:00 p.m. PT
The Missouri Hospital Association (MHA) is the 2018 recipient of the Dick Davidson Quality Milestone Award for Allied Association Leadership for its work to improve health care quality, the American Hospital Association (AHA) announced today.
The AHA today submitted comments on the Food and Drug Administration’s Medical Device Safety Action Plan.
The Institute for Healthcare Improvement today convened a national steering committee, whose members include the AHA, to create a national plan to accelerate patient safety progress across the care continuum.
Watch the video
AHA Chair Nancy Howell Agee yesterday said that the health care field needs “to transform” and “find ways to deliver care that provides value and is affordable.”
In her investiture address at the AHA Annual Membership Meeting, Agee spoke about the AHA’s Value Initiative and…
Humana Inc. has launched a national program that will compensate hospitals for improving patient experience, safety and outcomes based on certain quality measures from The Joint Commission’s Integrated Care Certification and hospital-based Palliative Care Coordination Certification programs.
Thirteen states participating in a regional collaborative to improve birth outcomes in the South decreased early elective deliveries by an average 22% between 2011 and 2014, compared with 14% in other regions.
Health care providers should not use endoscope connectors labeled for use without reprocessing between patients because they carry a risk of cross-contamination, the Food and Drug Administration announced today.