article thumbnail

Assessment of Project ECHO(R) Opioid Use Disorder Sessions for Primary Care Teams [Education and training]

Annals of Family Medicine

Intervention: 12 monthly online OUD sessions held from April 2023 to March 2024. 4 expert faculty members developed session curriculum: screening and diagnosis, using behavioral health/counseling, addressing harm reduction, among others. Setting: 20 PC practices located in various regions across the US.

article thumbnail

Machine learning models for atrial fibrillation detection in primary care using electronic health records: systematic review [Cardiovascular disease]

Annals of Family Medicine

Context: Atrial fibrillation (AFib) significantly impacts patient morbidity and mortality, despite existing screening practices. We searched seven databases from inception to May 2023. Two independent reviewers screened and extracted data using Covidence® with disagreements resolved by a third reviewer.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

Pain-Related Medication in Adults with Intellectual Disability: a systematic review [Pain management]

Annals of Family Medicine

Search strategy developed for six medical databases (2000-March 2023), key terms of ID, pain, analgesia, medication. Following removal of duplicates 20,425 titles, 2,716 abstracts, 341 full-text articles were screened; 28 articles were eligible for inclusion. Study Design and Analysis: Systematic review (PROSPERO CRD42023415051).

article thumbnail

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.” Published 2023 Jan 6. Prenatal Diagnosis.

article thumbnail

Rare Diseases: Pathways to accelerating diagnoses 

Myriad Genetics

Which one of those 17 doctors ultimately was able to pull together the pieces of Alex’s health picture and suggest a diagnosis? 1 Besides harnessing technology, doctors and families have two other tools they can use much earlier in their journeys to help them diagnose a rare disease: Newborn screenings and genetic carrier screens.

article thumbnail

Feasibility and Acceptability of Implementing a Digital Cognitive Assessment for Alzheimer Disease and Related Dementias in Primary Care [Original Research]

Annals of Family Medicine

PURPOSE We assessed the feasibility and acceptability of implementing a digital cognitive assessment (DCA) for Alzheimer disease and related dementias (ADRD) screening into primary care. We also assessed the prevalence of positive screens and measured diagnostic and care outcomes after a positive DCA result.

article thumbnail

More than the rule of 2s: All about Meckel Diverticulum

PEMBlog

STAT Pearls, 2023 Wrap Up Meckel diverticulum is a congenital anomaly of the small intestine that can present with various clinical manifestations, including rectal bleeding and obstruction. The Diagnosis of Meckel’s Diverticulum: A Continuing Challenge. Updated 2023 Jan 30]. ” An et. Clin Radiol. J R Soc Med.