National Partnership Staff
Survey finds patients increasingly value EHRs—even those whose doctors use paper records  – Clinical Innovation+Technology

A debate over end-of-life care – 12

In a third essay, Debra L. Ness, of the National Partnership for Women and Families, and Beverley H. Johnson, of the Institute for Patient- and Family-Centered Care, urge that end-of-life care be considered a partnership among patient, family, and medical team, a collaboration, more responsive as needs change.

Insurers “must reimburse for social support as well as clinical care and must be flexible enough to evolve as care plans change,” they write.

Survey finds patients increasingly value EHRs—even those whose doctors use paper records  – Clinical Innovation+Technology

Sick leave discussion takes off in city halls, statehouses across U.S. – Pittsburgh Tribune-Review

As of November, 16 cities and three states have paid sick leave ordinances, according to a report from the Philadelphia Mayor’s Task Force on Paid Sick Leave. But some states are passing pre-emption laws that prohibit municipalities from establishing sick leave policies — up to 11 from 2011 through 2014, according to the National Partnership for Women and Families.

Survey finds patients increasingly value EHRs—even those whose doctors use paper records  – Clinical Innovation+Technology

Dying in America: Report sets off discussion in Annals of Internal Medicine – Washington Post

“There may be no truer test of a health-care system than how it supports persons with advanced illness or at the end of life and the loved ones who care for them. In that regard, most would agree that our health-care system struggles and often fails,” said Debra L. Ness, president of the National Partnership for Women and Families, and Beverley H. Johnson, president of the Institute for Patient-and Family-Centered Care.

Survey finds patients increasingly value EHRs—even those whose doctors use paper records  – Clinical Innovation+Technology

Where’s HIT Headed in 2015? – For The Record

“Access to one’s own health information is a right guaranteed to all patients by HIPAA but it’s not well understood, even within the provider community,” says Erin Mackay, associate director of HIT programs for the National Partnership for Women & Families. “One of the great potentials for technology is the ability to put that information at the fingertips of patients — particularly as more individuals become caregivers to their children and, increasingly, to their parents as well.”