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Hearing Screening in Private Family Practice Medicine Using Tablet Applications [Original Research]

Annals of Family Medicine

The present study evaluated the acceptability and the feasibility of hearing screening for patients consulting in private family practice medicine. Among the screened patients, 161 (74%) had negative test results, while 59 (27%) had positive results indicating hearing loss.

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Evaluating effectiveness of educational intervention on syphilis screening and interpretation in a Family Medicine Residency [Infectious diseases (not respiratory tract)]

Annals of Family Medicine

Improved interpretation and management of syphilis screening results after intervention Results: Survey questions assessing knowledge had variable performance with net poor discrimination after the educational intervention. Post-hoc power analysis for appropriate versus inappropriate diagnosis and management was very low (2.7%

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Patient Advocacy Group Leaders Perceptions on Primary Cares Role in Caring for Patients with a History of Breast Cancer [Health care services, delivery, and financing]

Annals of Family Medicine

Context Patient advocacy groups engage patients, families, and caregivers in navigating the cancer landscape, focusing on early detection/screening, as well as psychosocial and financial support during treatment. As these groups have grown, they have major influences over their communities, funding, and policy.

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A New Outlook: How Carrier Screening Shaped One Family’s Future

Myriad Genetics

When Ashley Pantier and her husband decided to start a family, they were young, healthy, and filled with a sense of joyful optimism. We went through the pediatrician, the physical therapist, and none of those people brought up carrier screening. Ashley’s journey to a diagnosis for Christopher probably felt like forever to their family.

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Outcomes associated with timing of screening for gestational diabetes [Women's health]

Annals of Family Medicine

Context: Screening for gestational diabetes (GDM) at recommended times, based on a pregnant woman’s risk for GDM, is important in order to initiate and optimize the management of GDM as early as possible, thus mitigating the risk of several adverse outcomes for both pregnant women and their offspring.

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AMPLIFY™ Technology Enhances Prenatal Screening for 22q11.2 Microdeletion

Myriad Genetics

Less invasive options like prenatal cell-free DNA (cfDNA) screens can also be used to help identify the microdeletion. According to a study in Genes (Basel) , cfDNA screens have “a 70–83% detection rate and a 40–50% positive predictive value (PPV) for most associated 22q microdeletions.” We observed 100% PPV. DiGeorge syndrome (22q11.2

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Rare Diseases: Pathways to accelerating diagnoses 

Myriad Genetics

Many of us have seen stories in the news about American families on diagnostic odysseys for their children with rare diseases. Which one of those 17 doctors ultimately was able to pull together the pieces of Alex’s health picture and suggest a diagnosis? None of them. It was the AI program ChatGPT.