PEMBlog

MAY 17, 2023

Why then do we persist with the “is it medical/organic or psych” question? In: Textbook of Pediatric Emergency Medicine, 5th, Fleisher GR, Ludwig S, Henretig FM (Eds), Lippincott Williams & Wilkins, Philadelphia 2006. Special thanks to Manpreet Singh, MD ( @MprizzleER ) for helping to put this collaboration together.

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Medical Xpress

DECEMBER 23, 2022

A new Japanese study reveals that the age-standardized incidence rates of end-stage kidney disease (ESKD) requiring renal replacement therapy (RRT) due to chronic glomerulonephritis and diabetic nephropathy has decreased, while rates due to nephrosclerosis have increased considerably between 2006 and 2020.

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FDA Law Blog

FEBRUARY 4, 2024

Mullen — On January 18, 2024, the director of FDA’s Center for Devices and Radiological Health and the chief medical officer and acting director of CMS’ Center for Clinical Standards and Quality issued a joint press release supporting FDA’s recent proposed rule regulating Laboratory Developed Tests (LDTs). By Steven J. Gonzalez & Gail H.

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FDA Law Blog

NOVEMBER 1, 2023

Lenz, Principal Medical Device Regulation Expert & Sophia R. Gibbs — For more than three decades, FDA has claimed that the Federal Food, Drug & Cosmetic (FD&C Act) gives the agency legal authority to regulate laboratory developed tests (LDTs) as medical devices (see our prior post here ). Gaulkin & Jeffrey N.

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FDA Law Blog

DECEMBER 12, 2022

The Refractive Surgery Council (RSC) and Society for Excellence in Eyecare (SEE) , the Medical Device Manufacturers Association (MDMA) , and even the Commonwealth of Kentucky’s attorney general (AG) all requested the draft guidance be withdrawn. Regulatory Analysis. These lasers were previously approved with patient information booklets.

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The Health Policy Exchange

MARCH 14, 2013

In this month's Georgetown University Health Policy seminar, we discussed the financial and political challenges that AHRQ and its predecessor, the Agency for Health Care Policy and Research (AHCPR) have faced while trying to improve outcomes and effectiveness of medical care since the latter's founding during the first Bush Administration.

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Permanente Medicine

JUNE 3, 2025

Assistant Regional Medical Director, Care Experience Southern California Permanente Medical Group Podcast transcript Transcript is autogenerated. I practice family and sports medicine as part of the Southern California Permanente Medical Group here in Fontana, California. I joined SCPMG straight from residency in 2006.

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Today's Hospitalist

JUNE 7, 2025

Because many medications can cause weight gain, doctors should consider more weight-neutral alternatives. Medical societies and hospitals are weighing in on periprocedural concerns in patients taking GLP-1s who need procedures or surgeries. These medications are truly life-changing for many patients.” Nor should they be.

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Physician's Weekly

JUNE 24, 2025

from Geisinger Medical Center in Danville, Pennsylvania, and colleagues examined changes in patients’ internalized weight stigma before and after MBS. Patients aged 18+ who underwent primary bariatric surgery from 2006 to 2019 were identified (5,749 patients). Justin Dhyani, M.D.,

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Holistic Care Patient-Centered Patients Medical 52

Permanente Medicine

APRIL 29, 2025

million men and women aged 50 to 75 examined the outcomes of a Kaiser Permanente Northern California initiative begun in 2006 to increase colorectal cancer screening rates. Levin, MD , a Kaiser Permanente Division of Research scientist and gastroenterologist with The Permanente Medical Group. The study of 1.1

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GeriPal

MARCH 2, 2023

2006 Transcript Eric: Welcome to the GeriPal Podcast. It’s not a controlled substance medication. Eric: So I heard gabapentin is the 10th most commonly prescribed medication in the US. In psychiatry, a lot of the anti-epileptic medications, we call them mood stabilizers and are used in bipolar disorder.

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FDA Law Blog

MARCH 15, 2023

By Véronique Li, Senior Medical Device Regulation Expert — Earlier this month, FDA published a final rule to update the mammography regulations, issued under the Mammography Quality Standards Act of 1992 (MQSA) and the Federal Food, Drug, and Cosmetic Act (FD&C Act). It authorized FDA oversight over mammography facilities.

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GeriPal

JUNE 22, 2023

Summary Transcript Summary In the early 1990’s, California Medical Facility (CMF) created one of the nation’s first licensed hospice units inside a prison. Alex: We are in the California Medical Facility and we will ask our guest about that. I’ve known Michele a long time, since the Joint Medical Program. Michele: Yep.

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FDA Law Blog

FEBRUARY 4, 2025

As our readers may already know, FDA maintained three PRV programs to incentivize the development of therapies for underfunded diseases: the RPD PRV program, which sunset last month, the Medical Countermeasures (MCM) PRV Program, which sunset in October 2023, and the Tropical Disease PRV Program.

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Physician's Weekly

JUNE 12, 2025

It led to revocation of the elder Geier’s medical license and disciplinary action for David Geier for practicing medicine without a license. The two had access to the CDC database in 2004 and 2006. They also created a now-rejected treatment involving a hormone-blocking drug.

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GeriPal

JULY 6, 2023

Started as a direct case manager, worked in a variety of different places including the state legislature and I’ve been with the state office now since 2006. 60% of all medical costs have nothing to do with your health diagnosis. Eric: And Susan? But bottom line, it’s really trying to work across our different departments.

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GeriPal

MAY 1, 2025

And I graduated from medical school in the early 80s. And I was working at the time at Yale in New Haven, and I became medical director of a facility which was initially created in New Haven as a hospice like facility for people with HIV, which is in late 1995 and in 1996 when the Protease inhibitors came along. Meredith 09:33 Yes.

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GeriPal

DECEMBER 21, 2023

So IU, we have been able to convert our paper, Chris Callahan paper that was published in 2006, the first clinical trial that was positive. But for other- Diane: And it’s on the medical side. Some of these models I think include more medication management, some of them don’t. And the MIND at Home at Hopkins.

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Common Sense Family Doctor

MARCH 23, 2025

Please join me and hundreds of medical organizations in standing with AHRQ and preserving its vital contributions to the health of all Americans. ** For the past 30 years, a little-known U.S. Now the Department of Government Efficiency is trying again, threatening 90% staff reductions that would decimate the agency.

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FDA Law Blog

JUNE 9, 2021

As explained in CPG 440.100 and on FDA’s website , FDA adopted the “Unapproved Drug Initiative” (“UDI”) in 2006—later revised in 2011 —to remove unapproved drugs from the market using a risk-based approach both to ensure the safety and efficacy of all drug products on the market and the integrity of the drug approval process.

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