Articles Tagged With:
-
Applicant looks great on paper? He or she might be a terrible fit for access
During an interview for a patient access position, one applicant confided that she had difficulty working the second shift on her last job. “And she was applying for a second shift position! That was a red flag waving in the wind,” says Lolita M. Tyree, CHAM, MSW, patient access manager in the ED at Riverside Regional Medical Center in Newport News, VA.
-
Avoidable no-authorization denials cut by 60% — Avoid postponing procedure at your hospital
Is there a problem with an authorization that will result in a denied claim? Good communication with providers and office staff about this issue has reduced avoidable authorization denials by 60% at LCMC Health in New Orleans, according to Stacy Calvaruso, CHAM, system assistant vice president of patient access services.
-
Pending coverage, no authorization, or high out-of-pocket?
A patient is scheduled for an MRI in three days, but the payer says it could take five business days to obtain the required authorization.
-
Big data is at every IRB’s fingertips — but can you use it?
Research institutions increasingly are investing in electronic systems that have the capability of collecting and storing big data.
-
Overhauling processes is a major HRPP challenge
IRBs have accumulated a lot of responsibilities and processes over the years, and some of it is not necessary or not really part of the IRB’s role, experts say.
-
Using QI to improve electronic and other systems or processes
Many IRBs have had quality improvement processes and electronic IRB systems in place for a number of years now, but are they working optimally?
-
Here’s a short version of the criteria for approval
Title 45, part 46.111 of the U.S. Department of Health and Human Services’ Protection of Human Subjects, revised in 2009, contains a very short, but important list of criteria for IRB approval of research.
-
VoICE Project fills education gap in informed consent process
Research institutions should make certain the responsibility for a successful informed consent process is primarily that of the researcher and not the potential participant.
-
Strategies for providing IC to very large subject pools
Newborn blood-sample screening has been going on for decades, but ethical considerations have evolved in recent years, and this is changing research informed consent.
-
Informed consent flexibility on fed side results in creative IC
In recent years, IRBs have witnessed federal regulators becoming more flexible in applying regulations regarding informed consent — a shift resulting in more creative and practical IC methods, including electronic, short form, and video consent.