Annals of Family Medicine

NOVEMBER 20, 2024

Context: The COVID pandemic disrupted global healthcare, impacting Academic Medical Centers (AMCs) in the United States, necessitating a comprehensive understanding of its effects on healthcare delivery and utilization. Study Design: This retrospective case series analysis utilizes Vizient’s clinical database data.

Patient-Centered 130

Patient-Centered Medical Utilities Patients 130

Annals of Family Medicine

NOVEMBER 20, 2024

Context: The COVID pandemic disrupted global healthcare, impacting academic medical centers (AMCs) in the United States, necessitating a comprehensive understanding of its effects on healthcare delivery and utilization. Study Design: This retrospective case series analysis utilizes Vizient’s clinical database data.

Utilities 130

Utilities Healthcare Patient-Centered Illness 130

Annals of Family Medicine

NOVEMBER 20, 2024

Many proposed methods for measuring continuity utilize an aggregation of patient visits. We modeled the odds of 2019 patient visits being with their PCP using a binomial generalized linear mixed model with a random PCP intercept. These patients had 54% of 2019 visits with their PCP.

PCP 130

PCP PCP Finance Nurse Practitioner 130

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.

Clinic 52

Clinic Education Clinical Practice Patient-Centered 52

Annals of Family Medicine

NOVEMBER 20, 2024

from Oct 2019 to Dec 2023. Study Design: This retrospective case series analysis utilizes Vizient’s clinical database data. The study is divided into three periods: pre-COVID (Oct 2019 to Mar 2020), COVID (Apr 2020 to May 2023), and post-COVID (Jun 2023 to Dec 2023). Mixed models were used for analysis.

Patient-Centered 130

Patient-Centered Patients Medical Illness 130

Today's Hospitalist

MAY 9, 2025

Yet this expansion has come with a significant administrative burden, particularly that of clinical documentation. This isn’t about replacing your clinical judgment. Ambient dictation, or ambient clinical documentation, represents a paradigm shift. This isn’t about replacing your clinical judgment. The result?

Patient-Centered 52

Patient-Centered Telemedicine Clinic Electronics 52

FDA Law

MAY 13, 2024

FDA has even gone so far as to maintain that the “real-life clinical performance of a medical product might be more clearly demonstrated through RWD/RWE because a controlled clinical trial often cannot evaluate all applications of a product in clinical practice across the full range of potential users.”

Medical 111

Medical Clinic Patients IT 111

FDA Law

FEBRUARY 28, 2022

address common questions and misconceptions about collecting and submitting to FDA patient engagement information regarding the design and conduct of a medical device clinical study.”. What would be the potential benefits if companies prospectively design medical device clinical studies with input from diverse patient advisors?

Patients 52

Patients Clinic Medical Patient-Centered 52

CDOCS

MARCH 15, 2021

Patients depend on our clinical knowledge as well as our recommendations and relationships with our specialist partners.</span></span></p> By the utilization of patient financing strategies, we can help to facilitate a means of affordability for the everyday patient.</span></span></p>

Patients 52

Patients Finance Education Utilities 52

FDA Law

AUGUST 4, 2022

On June 27, 2019, Pfizer sought an OIG advisory opinion to ensure that its proposal would not run afoul of federal law. Further, “there is little utility in comparing the language of the BIS to that of the AKS.”. The Lesson of this Case.

Manufacturing 98

Manufacturing Medical Government IT 98

FDA Law

SEPTEMBER 11, 2023

More recently, in 2019, FDA announced a push for predicate modernization ( link ) following a 2018 plan to modernize the 510(k) program by eliminating use of old predicates, sunsetting older predicates, and establishing the Safety and Performance Based Pathway ( link ).

Medical 64

Medical Electronics Manufacturing Utilities 64

FDA Law

FEBRUARY 2, 2023

Since 1962, the FD&C Act has authorized FDA to require that sponsors of clinical trials submit data from “preclinical tests (including tests on animals)” in order to demonstrate that their drug is safe enough to advance to testing in humans. adequate to justify the proposed clinical testing.” 21 U.S.C. § 355(i)(1)(A). 42 U.S.C. §

Clinic 64

Clinic IT Utilities Government 64

FDA Law

OCTOBER 14, 2021

Rather, FDA seems intent on regulating RAS devices almost as if they were therapeutics responsible for long term clinical outcomes. It is well out of bounds for FDA to regulate them as if they were a determinant of long term clinical outcomes. Gone are the days of tool type indications for this type of device. 21 U.S.C. §

Patient-Centered 52

Patient-Centered Healthcare Manufacturing Provider 52

Annals of Family Medicine

NOVEMBER 20, 2024

Study Design and Analysis: This is a retrospective observational study of primary care visits during the 2019-2022 study period. Population Studied: Patients with ≥1 visit between January 2018 and December 2019 and who remained in the cohort until at least May 2020. Measurements.

Primary Care 130

Primary Care Patients Diagnosis Family Practice 130

PEMBlog

SEPTEMBER 27, 2023

The diagnosis of a virus illness is generally made clinically with a history and clinical exam and does not require confirmatory testing. We understand many families request this test and we urge you to talk with them about these recommendations so we can move to reducing the number of clinical tests that will not change management.

Patients 52

Patients Illness Hospital Management 52

Physician's Practice

JUNE 25, 2025

Dr. Baum is Professor of Clinical Urology at Tulane Medical School in New Orleans, Louisiana. Dr. Baum is the author of Marketing Your Clinical Practice-Ethically, Effectively, and Economicall y, which is in its 4th edition, has sold over 175,000 copies and has been translated into Spanish. About Neil Baum, M.D.

Patients 52

Patients Private Practice Management Healthcare 52

FDA Law

JUNE 7, 2021

Subpart H) pathway in 2014, then issued it as final guidance in January 2019. However, the FDA guidance goes on to say in some cases, additional context is needed by specifically inserting a sentence in the indications statement that: no clinical benefit has been established.

Clinic 98

Clinic IT Private Practice Utilities 98

Physician's Weekly

JUNE 22, 2025

0.97], P = 0.02). Investigators concluded that sex differences in testing rates and urinary mediator levels highlighted the necessity of considering sex when optimizing the diagnostic utility of these mediators. 1.25], P < 0.001) and lower levels in non-atopic females (M/F ratio 0.86, [95% CI: 0.76–0.97],

Asthma 52

Asthma Utilities Clinic Individual 52

The Clinical Problem Solvers

FEBRUARY 8, 2023

Between 2007 – 2019, Black individuals experienced a higher death rate for opioid overdose deaths than any other racial or ethnic group. Dr. Jordan then questions the utility and continued operation of methadone clinics, especially as the United States largely moves on from the COVID-19 pandemic.

Community 52

Community Patient-Centered Mental Health Board-Certified 52

The Clinical Problem Solvers

APRIL 5, 2022

Published April 5, 2019. January 18, 2019. The Clinical Problem Solvers Podcast. Calac, Victor A. link] Homeless community in San Diego resists police terror and demands safe housing – Liberation News Lopez, M., Rothstein, R. Segregated by Design. Silkworm Studio. Accessed April 3, 2022. link] Swift, C. Community Access.

Community 52

Community Patient-Centered Emergency Room Medical 52

FDA Law

SEPTEMBER 30, 2024

CMS did not finalize the price verification survey, which would have required manufacturers of 10 costly drugs selected annually to provide clinical information as well as information on production, distribution, research, and marketing costs, revenue and profit, and ex-U.S. pricing, among other things. See 42 U.S.C. 1396r-8(b)(3)(C)(iii).

Manufacturing 59

Manufacturing Utilities Provider IT 59

GeriPal

AUGUST 25, 2022

And yet, we know little about the clinical experience of people with dementia in hospice. My interest in this paper and this topic goes back a long time and is based on my clinical experience as a hospice nurse, where I was taking care of what I felt like and what we’ve confirmed with research is about half of my patients.

Families 106

Families Family IT Patients 106

PEMBlog

APRIL 26, 2023

Today, we are going to discuss firearm safety and ways to screen for it in both the ED and clinic settings. From 2019 to 2020, the rate of firearm related deaths among children increased by 30%. Carney and I am a pediatric resident at Cincinnati Children’s Hospital Medical Center. I’m here with my co-resident, Dr. Humphrey.

Families 52

Families Family Mental Health Healthcare 52

FDA Law

JUNE 2, 2023

For 10 high-cost single source covered outpatient drugs selected annually by CMS, manufacturers would be required to respond to a so-called “price verification survey” by providing not only clinical and utilization information about the drug, but also costs of production, distribution, research, and marketing; revenue and profit; and ex-U.S.

Manufacturing 59

Manufacturing Vaccination Government Diagnosis 59

FDA Law

SEPTEMBER 13, 2021

A May 2019 CMS final rule that would have required drug TV advertisements to disclose the WAC of the drug was challenged by a group of pharmaceutical companies and vacated on statutory grounds by the D.C. Medicare negotiation authority; encourage biosimilars and generic drug utilization).

Manufacturing 98

Manufacturing Supply Chain Patient-Centered Utilities 98