Google
Trusted Resources: News & Events
Latest announcements and gatherings
Stigmatizing language in medical records affects patient care, study shows
Physicians who use stigmatizing language in their patients’ medical records could be affecting the care they receive for years to come, according to a new Johns Hopkins study.
Titled “Do Words Matter? Stigmatizing Language and the Transmission of Bias in the Medical Record,” and published in the Journal of General Internal Medicine, the study aimed to determine whether the language and descriptions used in patient records could perpetuate bias among doctors.
The study analyzed the notes and descriptions physicians had written during visits to a hypothetical patient at a large urban medical center. Researchers then assessed how the language used in the notes influenced the patient’s care and pain management.
Researchers at the Johns Hopkins School of Medicine used an experimental vignette study design, in which 413 residents and medical students were randomized to read one of two chart notes presenting medically identical information about a hypothetical 28-year-old patient with sickle cell disease (SCD) and chronic pain in his left hip.
+myBinderRelated Content
-
Minority Health Counts: Building a More Equitable Community SummitBy Supporters of Families with Sickle Ce...
-
Association Between Hospital Admissions and Healthcare Provider Communication for Individuals With Sickle Cell Disea...Objective: To test the hypothesis that ...
-
Sickle cell disease in the emergency departmentAcute painful episodes are the most comm...
-
Roland B. Scott Memorial Symposium: I Want Somebody to LoveRoland B. Scott Symposium on Sickle Cell...
-
Sickle Cell Disease in the Emergency Department: Confronting Barriers to Care“You’re too pretty to have a disease...
-
Sickle Cell Disease: Racism in the American Health Care SystemWednesday, June 28 1-4 pm EDT Massachu...
-
Christiana Care Sickle Cell ProgramChristiana Care is one of the country’...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.