How States Report Medical Errors to the Public: Issues and Barriers
This paper explores how data from mandatory reporting systems are (or can be) disclosed to the public. Based upon detailed interviews with states that have mandatory reporting systems, NASHP identified critical junctures in the design of reporting systems that influence the ultimate use of data. By examining and mapping out these critical junctures, the parameters of existing reporting systems can be better understood, and the intent of new reporting systems can be made more explicit and viable.
This report examines the protection and disclosure of mandatory reported data with a focus on:
• When and how states publicly disclose reported data,
• When and how states protect reported data,
• The perceived relationship between reporting and malpractice litigation, and
• Other factors relevant to data disclosure.
| reporting_medical_errors.pdf | 306.5 KB |

For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































