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Episode 354: Antiracism in Medicine – Episode 25 – Live from SGIM 2024: Best of Antiracism Research at the Society of General Internal Medicine’s 2024 Annual Meeting

The Clinical Problem Solvers

Cooper September 19, 2024 Summary : This episode highlights a selection of antiracism research presentations at a live recording of the podcast at the 2024 SGIM Annual Meeting. Clinician Response to Patient Medication Prices Displayed in the Electronic Health Record. During this episode, we hear from Dr. S. link] Sinaiko, A.

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You don’t need X-Rays in a child with bronchiolitis, croup, asthma, or first time wheezing

PEMBlog

Special thanks to Todd Florin, MD, MSCE who contributed to this post – he is also an expert on respiratory and infectious emergencies. A common phenomenon in EDs around the country, this scenario is only made worse by typical spikes in patient volumes during respiratory viral seasons.

Asthma 52
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Be The Market: How Doctors Should Invest Their Money

The Motivated MD

You spend your life dedicated to patient care while still hoping to leave work and have the energy to be mentally and physically present for your families and friends. I am not liable for any loss of profit or any other commercial damages, including but not limited to special, incidental, consequential, or other damages.

Finance 52
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I Finally Matched and I'm Going to be a Plastic Surgeon!!!!

Aspiring Minority Doctor

I emailed my personal application packet which is literally 43 pages long and includes everything from my CV to score reports, letters of recommendation, credentials/certifications, and case logs from my previous program in addition to my downloaded official Electronic Residency Application Service (ERAS) application.

IT 52
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Mastering Responses to FDA 510(k) AI Letters: A Strategic Approach

FDA Law Blog

We will then present an effective strategy to address FDA’s AI request in a timely manner. Understanding the Traditional 510(k) Review Timeline There are three types of Premarket Notification 510(k)s: Traditional , Special , and Abbreviated. In this presentation, FDA suggested the following tips.

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New Draft Guidance Provides Detailed (and Burdensome) Recommendations for Chemical Assessments to Support Medical Device Biocompatibility

FDA Law Blog

In addition, the recommendation to test the device after maximum reprocessing cycles appears counterintuitive to the other recommendations in the guidance, which focus on the toxicological concern of chemical additives or manufacturing process aids, including cohort of concern compounds, present on the device that can be extracted.

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Screening for Dementia: A Podcast with Anna Chodos, Joseph Gaugler and Soo Borson

GeriPal

I heard this beautiful thing the other day, which was to an electronic medical record, I am not a whole person. Joe 18:38 Yeah, you know, it’s interesting, Soo, I’m doing a county by county visit here in Minnesota where I actually give a presentation on the basics of dementia and Alzheimer’s disease. I’m busy.

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