The Clinical Problem Solvers

JANUARY 19, 2022

Elliot Tapper discusses a clinical unknown case presented by Dr. Jennifer Mundell Jennifer Mundell Jennifer Mundell, MD FACP is the associate program director for Ascension St Vincent Internal Medicine Residency Program. Vincent in 2016.

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PEMBlog

JUNE 18, 2025

Researchers conducted a retrospective cohort study across 30 US and 1 Canadian pediatric emergency departments, analyzing data from 5641 children (ages 6 months to 17 years) treated with epinephrine for an acute allergic reaction between 2016 and 2019. 4 hours 1.9% 6 hours 1.1% No respiratory or cardiovascular symptoms 105 (95% CI 54–135) 4.1%

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The Clinical Problem Solvers

MAY 29, 2019

[link] Episode description Dr. Janice Kwan presents a clinical unknown to Dan and Rabih Download CPSolvers App here Schema #1 Schema #2 Show Notes Dr. Janice Kwan Janice Kwan is a general internist and Assistant Professor of Medicine at the University of Toronto.

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The Clinical Problem Solvers

DECEMBER 16, 2020

Nwamaka Eneanya and Jennifer Tsai to discuss the limitations and harms of race-based medicine in clinical practice. Our guests explain how we can incorporate race-conscious medicine in clinical settings, medical education, and biomedical/epidemiological research to responsibly recognize and address the harms of racial inequality.

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Clinic Education Clinical Practice Patient-Centered 52

Louisville Lectures

SEPTEMBER 18, 2020

She then compares and contrasts hunger and food insecurity and describes the scope of the issue in Louisville/Jefferson County as well as in the clinic population. After, Dr. Olges describes the clinical implications of food insecurity and finally, reviews the process for accessing the food bank in the AIM clinic.

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Medical Xpress

FEBRUARY 24, 2023

Between 2016 and 2018, more than 22 percent of Massachusetts residents reported any prior cannabis use for medical or recreational reasons. However, little is known about cannabis use in patients who undergo surgery or interventional procedures, where cannabis use has important additional clinical implications.

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Louisville Lectures

NOVEMBER 7, 2019

She remained at Loyola University as an Assistant Professor in Hospital Medicine before moving back to Louisville in 2016. Clinically, she serves as an inpatient teaching attending at University Hospital. Learn more about her here.

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Internal Medicine Hospital Clinic Medical 52

The Medical Futurist

JUNE 17, 2025

Artificial intelligence Already, dentists employ software to get insights into clinical decision-making, but AI is changing the face of dentistry, just like it is in many other fields. But AR also found a home in dentistry for both educational and clinical purposes.

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Annals of Family Medicine

NOVEMBER 20, 2024

Context: After a Samoan patient from New Zealand (NZ) attended a PACE workshop at NAPCRG in 2016 with her general practitioner, she was inspired to set up a Pacific community group to work towards better health outcomes for Pacific people living in South Auckland, NZ.

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Common Sense Family Doctor

JANUARY 19, 2025

The American Academy of Family Physicians (AAFP) maintains that clinical privileges should be based on documented training and experience rather than the physician’s specialty. From 2016 to 2021, the percentage of screening colonoscopies performed by family physicians decreased from 11.3%

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Plum Health

MAY 11, 2023

Thomas graduated from Wayne State University School of Medicine in 2013 - thereafter, he completed his residence at Oakwood/Beaumont Family Medicine Residency Program, and then started Plum Health DPC in November 2016. Time flies when you’re practicing medicine - the days are long but the years are short.

Family Medicine 52

Family Medicine DO Community Education 52

California Academy of Family Physicians (CAFP)

MAY 14, 2025

Elimination of (State-Only) Prospective Payment System Rates to Federally Qualified Health Centers and Rural Health Clinics for Undocumented Immigrants – Eliminates Prospective Payment System rates to clinics for state-only-funded services provided to undocumented Individuals.

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The Medical Futurist

JUNE 21, 2025

In 2016, The Guardian reported that a blind woman suffering from this disease was fitted with the implant labelled “bionic eye” in the UK as part of a trial at the Oxford Eye Hospital. Experts even say the eye is an ideal place to start for the first clinical use of CRISPR. The drug helped decrease the initial healing from 5 days.

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The Clinical Problem Solvers

APRIL 24, 2025

Dr. Benton mentors clinical and research physicians, fellows, and postdoctoral trainees. Clinically, he cares for youth and families through the Department of Psychiatry & Behavioral Sciences and the new Division of Addiction Medicine at Boston Children’s Hospital. Child and Adolescent Psychiatric Clinics of North America.

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Mental Health Community Hospital Appointment 52

The Medical Futurist

MAY 18, 2025

Clinical use is already accepted, new FDA approvals and new trials are underway targeting new niches, like pediatric surgeries. They have started a large-scale clinical trial involving 10,000 patients, expected to last two years, with plans to obtain CE marking by the end of 2024. Since then, the concept has become a reality.

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Healthcare Hospital Medical Patient-Centered 64

The Clinical Problem Solvers

MARCH 14, 2025

Dr. Benton mentors clinical and research physicians, fellows, and postdoctoral trainees. Clinically, he cares for youth and families through the Department of Psychiatry & Behavioral Sciences and the new Division of Addiction Medicine at Boston Children’s Hospital. Child and Adolescent Psychiatric Clinics of North America.

Mental Health 52

Mental Health Community Patient-Centered Hospital 52

NPR Health

DECEMBER 20, 2024

She's been on dialysis for four hours a day, three days a week since 2016. So the Food and Drug Administration made an exception to its usual clinical study requirements to allow Looney this new kind of pig kidney. Towana is a 53-year-old grandmother from Gadsden, Ala. Her immune system would reject a human kidney.

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FDA Law Blog

OCTOBER 10, 2022

Javitt — On September 28, 2022, the FDA issued the long anticipated final Clinical Decision Support Software Guidance (CDS Guidance), which replaces the revised draft guidance document from 2019. Other medical information.

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Clinic Medical Provider Patients 52

Physician's Weekly

JUNE 24, 2025

So, in 2016, she celebrated her 60th birthday at her local CVS. A connection to dementia will require further research, and Geldsetzer is trying to raise philanthropic funding for a clinical trial. Her doctor and several pharmacies turned her down because she was below the recommended age at the time, which was 60.

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Vaccination Illness Hospital Patient-Centered 52

PEMBlog

OCTOBER 17, 2023

The diagnosis can be made clinically. Clinical Pediatric Dermatology 5 th ed, Elsevier, 2016, 382-401. The Mayo Clinic Experience With Psychogenic Purpura (Gardner-Diamond Syndrome). Patients often describe a sensation of burning or stinging pain rather than itching. References Paller, AS, Mancini, AJ. Gu SL, Jorizzo JL.

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FDA Law Blog

SEPTEMBER 6, 2022

This Draft Guidance, when finalized, will replace the Final Guidance issued just six years ago (the 2016 Guidance). Changes from the 2016 Guidance. The Draft Guidance covers charging in a clinical trial or in one of the expanded access settings and the differences between them. What’s new in the new Draft Guidance?

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Clinic Manufacturing Patients IT 52

FDA Law Blog

JUNE 3, 2025

The assertion that prescribing immediate-release opioids longer than two or three months is a red flag may have originated with the Center for Disease Control and Prevention (CDC) 2022 Clinical Practice Guideline for Prescribing Opioids for Pain. Deborah Dowell et al., 1, Recommendation 3. Recommendation 1.

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Clinical Practice Patient-Centered Patients Clinic 59

PEMBlog

JUNE 14, 2023

Children’s Mental Health Emergency Department Visits: 2007-2016. Characteristics, Clinical Care, and Disposition Barriers for Mental Health Patients Boarding in the Emergency Department. Pediatrics. 2020 Jun;145(6):e20191536. doi: 10.1542/peds.2019-1536. Epub 2020 May 11. PMID: 32393605.

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Mental Health Management Patient-Centered Finance 98

FDA Law Blog

JANUARY 15, 2024

In 2016, FDA determined that e-cigarettes and their component parts fell under the term “new tobacco products,” requiring manufacturers of such products to submit PMTAs for FDA review before the Agency would issue a marketing order permitting the legal sale of the product. FDA failed on each count.

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CDOCS

MARCH 4, 2024

<p>According to the Dental Assisting National Board, dental assistant job satisfaction has declined every year since 2016, and currently only 50% feel valued by their employer. Within the last year, feeling under appreciated is now the second highest reason dental assistants are leaving the dental field.</p> </p>

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FDA Law Blog

MAY 3, 2021

On April 28, FDA issued its first Notice of Noncompliance for failure to submit required clinical trial results information to ClinicalTrials.gov. The ClinicalTrials.gov database is a public database of clinical studies administered by the U.S. The notice was given to Acceleron Pharma, Inc., National Library of Medicine. 42 U.S.C. §

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Clinic Patient-Centered IT Provider 52

FDA Law Blog

JANUARY 18, 2022

In May 2016, FDA released a draft guidance document titled “Technical Considerations for Additive Manufactured Devices” (see our blog post on the draft guidance here ), which was finalized in 2018 (see our blog post on the final guidance here ).

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FDA Law Blog

FEBRUARY 29, 2024

A surrogate endpoint is a marker, such as a laboratory measurement, radiographic image, physical sign or other measure that is thought to predict clinical benefit but is not itself a measure of clinical benefit. Drug companies are still required to conduct studies to confirm the anticipated clinical benefit. That did not happen.

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Clinic IT Provider Patient-Centered 59

FDA Law Blog

NOVEMBER 1, 2023

Regulating LDTs: A Long and Winding Road In what might sound to some like protesting too much, the PR invokes FDA’s longstanding assertion that IVDs “manufactured” by laboratories are medical devices and that clinical laboratories that develop tests are acting as manufacturers. FDA’s position is, however, only one side of the story.

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Manufacturing Hospital Healthcare Medical 81

FDA Law Blog

JANUARY 18, 2022

In May 2016, FDA released a draft guidance document titled “Technical Considerations for Additive Manufactured Devices” (see our blog post on the draft guidance here ), which was finalized in 2018 (see our blog post on the final guidance here ).

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Medical Manufacturing Healthcare Government 75

FDA Law Blog

MAY 3, 2021

Butler — On April 28, FDA issued its first Notice of Noncompliance for failure to submit required clinical trial results information to ClinicalTrials.gov. The ClinicalTrials.gov database is a public database of clinical studies administered by the U.S. The notice was given to Acceleron Pharma, Inc., National Library of Medicine.

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Clinic Patient-Centered IT Provider 40

FDA Law Blog

APRIL 20, 2021

Certain types of clinical decision-support software. Calculator/Data Processing Module for Clinical Use. Remove non-device software functions intended for transferring, storing, converting formats, or displaying clinical laboratory test or other device data and results. By McKenzie E. 21 C.F.R.). Device Type. Modification.

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Electronics Medical Management Clinic 40

CDOCS

MARCH 31, 2021

Take clinical photos (7)<br /> 4. Send materials to the lab with clinical photos.</span></p> National Director, Clinical Technology Solutions of MicroDental Laboratories. February 23, 2016). Take an impression of upper/lower and bite<br /> 2. MicroDental Laboratories.</span></span></span></li>

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FDA Law Blog

JUNE 23, 2021

I have witnessed it inform whether clinical trial results are clinically meaningful (or not) as well as the selection and even development of primary endpoints. What Dr. Cavazzoni lays out is the traditional way in which patients have informed drug benefit-risk decision-making: by setting the “clinical context” of the disease.

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Patients Patient-Centered Clinic IT 52

FDA Law Blog

JUNE 29, 2022

It explains that “FDA typically gives greater weight to trials that are conducted in larger populations, use a well-understood and widely accepted, well-constructed clinical endpoint, and incorporate certain design features (e.g., randomization, blinding).” Fiscal Year. Total Requests Received. Granted .

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FDA Law Blog

NOVEMBER 20, 2024

Since the first issuance of FDA’s guidance Use of International Standard ISO 10993-1, “Biological evaluation of medical devices – Part 1: Evaluation and testing within a risk management process” in 2016, sponsors submitting premarket submissions to FDA have had the option of using these techniques to evaluate certain biocompatibility endpoints.

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PEMBlog

SEPTEMBER 24, 2024

Most patients are afebrile by the third day of treatment and clinically improved within two weeks. doi: 10.1128/microbiolspec.TNMI7-0032-2016. An important point from this case is to consider CT imaging when a child has persistent or recurrent pneumonia. 2018 Jul;48(3):247-250. doi: 10.1177/0049475518765305. Epub 2018 Apr 6.

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