Integrated Care News by CFHA

MAY 1, 2025

Reclaiming Time and Attention Primary care professionals may log more than eleven hours a day, over half of it in the electronic health record (Menchaca, 2025). Evidence‑informed care was literally at his fingertips. Administrative overload fuels burnout and pushes us away from our patients.

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A Country Doctor Writes

JUNE 21, 2025

I thought of it the other day when I put together a presentation about Galileo’s way of interacting with patients. Six years ago, I wrote the essay below about an article I read in the New England Journal of Medicine. Its basic argument was that it isn’t sustainable to only see patients one by one in traditional doctor visits.

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Medical Xpress

FEBRUARY 27, 2023

An electronic medical record (EMR) alert is effective for reducing food allergy panel ordering among pediatric and adult patients, according to a study presented at the annual meeting of the American Academy of Allergy, Asthma & Immunology, held from Feb. 24 to 27 in San Antonio.

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Integrated Care News by CFHA

MAY 8, 2025

Protocols and Reminders Reminder and recall systems (mail, phone, text, apps, other media, and electronic health records) to identify and remind or notify individuals or parents when vaccines are due to have shown evidence of increasing vaccine uptake, and they are often combined with other strategies.

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Integrated Care News by CFHA

MAY 19, 2025

MBC is presented not simply as data collection, but as a dynamic, evidence-based clinical process that enhances outcomes, promotes equity, and strengthens team-based care. Health technology tools, such as electronic health records with embedded MBC capabilities, digital platforms for automated symptom tracking, data analytics (e.g.,

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The Clinical Problem Solvers

JUNE 26, 2023

Calac June 22, 2023 Summary : This episode highlights a selection of antiracism research presentations at a live recording of the podcast at the 2023 SGIM Annual Meeting. Identify strategies to mitigate bias and stigma in the electronic health record as a trainee and medical practitioner.

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Electronics Internal Medicine Patient-Centered Healthcare 52

FDA Law Blog

NOVEMBER 29, 2021

Currently, DEA regulations do not address transfer of controlled substance prescriptions — whether paper or electronic — between pharmacies for the initial filling of the prescription. At present, a pharmacy that receives an EPCS that it is unable to fill can only notify the patient that the prescription cannot be filled. DEA-637).

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Physician's Weekly

JUNE 19, 2025

Patients with documented mental illness or substance use disorders (SUDs) continue to encounter a mixed—sometimes starkly divergent—quality of emergency department (ED) care when they present with chest pain, abdominal pain, or other non‑psychiatric complaints, according to a patient‑interview study published in Health Services Research.

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Physician's Weekly

JUNE 14, 2025

Clinical and demographic data were collected during the study visit and from electronic medical records. Abnormal lung function was present in 51.9% Quantitative analyses of the right ventricular (RV) function were performed retrospectively. The results showed that 52 children with CDH, 17 with EICLM, and 12 with GO were studied.

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Physician's Weekly

JUNE 23, 2025

Authors of an abstract presented at the American Diabetes Association’s 85th Scientific Sessions called for a holistic, chronic treatment model to support children and young adults with obesity. The retrospective analysis incorporated data from Optum MarketClarity claims and electronic medical records.

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Physician's Weekly

JUNE 17, 2025

As rates of obesity continue to rise alongside new therapeutic options, a team of researchers at the 85th Scientific Sessions of the American Diabetes Association (ADA) will present findings from PATHWEIGH , a pragmatic clinical trial designed to embed evidence-based obesity care directly into primary care workflows.

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FDA Law Blog

AUGUST 9, 2023

Houck — If a patient presents a paper prescription for a controlled substance to a pharmacy and the pharmacy cannot fill it, the patient can take that prescription to another pharmacy. Transfer of Electronic Prescriptions for Schedule II-V Controlled Substances Between Pharmacies for Initial Filling, 88 Fed. By Larry K.

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Maine Academy of Family Physicians

JULY 6, 2023

In Maine, Anopheles mosquito vectors are present. All confirmed and suspected patients with malaria must be reported to Maine CDC by electronic laboratory reporting, fax at 800-293-7534, or by phone at 800-821-5821. While the risk in Maine remains low, it is possible for local mosquitoes to acquire Plasmodium spp.

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Medical Xpress

FEBRUARY 2, 2023

Analysis of 20 years of electronic health records across the U.S.

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Complication Electronics 97

Physician's Weekly

JUNE 16, 2025

Upshaw, MD , and colleagues developed an anonymous electronic survey they emailed to 12 academic medical systems, three US lymphoma cooperative groups, and two community hospitals, and distributed at one international lymphoma meeting. Respondents were also asked about their real-world use of cardioprotective strategies over the past 5 years.

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Routine Screenings Patient-Centered Screening Provider 52

Annals of Family Medicine

NOVEMBER 20, 2024

In 2022, Bunce et al embedded "card" questions into an electronic health record (EHR) with responses saved to the EHR database. In this presentation, we will show participants details of how we configured the Epic and REDCap tools, making it relatively easy to replicate the process for other card studies.

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Medical Xpress

MARCH 7, 2023

Doctors who received customized electronic health record (EHR) alerts for specific patients were 2.5

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The Clinical Problem Solvers

SEPTEMBER 22, 2020

[link] Episode Description Dr. Joshua Inglis presents a Human Dx case to Sharmin , Vivek Nair and Joshua Morris. His academic interests include clinical reasoning, drug allergy and the electronic health record. Human Dx Case Link Download CPSolvers App here Patreon website Schema Want to test your learning? Take our Episode Quiz here.

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Today's Hospitalist

MAY 9, 2025

By removing the need to constantly look at a screen or type notes, we can be more present and engaged, fostering stronger therapeutic relationships and improving patient satisfaction. Metrics for assessing physician activity using electronic health record log data. Healthcare (Basel). 2022;10(7):1286. Nuance Communications.

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FDA Law Blog

DECEMBER 12, 2022

Please check out FDA’s presentation on this very topic – Is My Product a Medical Device? See here for the slides, here for the recording of the presentation, and here for the transcript.). Step 4: Is the software function intended to serve as electronic patient records?

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The Clinical Problem Solvers

SEPTEMBER 19, 2024

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. link] Sinaiko, A. T., & Goss, F. link] Sloan, C.

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FDA Law Blog

AUGUST 8, 2023

The new final guidance, by its own terms, establishes “a recommended framework for predicting the mutagenic and carcinogenic potential of nitrosamine drug substance-related impurities (NDSRIs) that could be present in drug products and recommends acceptable intake (AI) limits for NDSRIs.”

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FDA Law Blog

AUGUST 13, 2023

The information is presented in a Q&A format. FDA is developing an electronic portal for registration and listing submissions that will be available in October 2023. Although FDA strongly encourages electronic registration, it is developing a paper form as an alternative to electronic registration.

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FDA Law Blog

APRIL 25, 2024

This Revised Draft Guidance provides considerations for manufacturers, packers or distributors (dubbed “firms”) of prescription biological reference products, biosimilar products, and interchangeable biosimilar products presenting data and information about such products in promotional materials in a truthful and non-misleading way.

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FDA Law Blog

OCTOBER 24, 2022

These data are routinely collected from a variety of sources, such as electronic health records, providing information on health and healthcare in actual patients, rather than in the controlled environment of a clinical trial. This value is potentially even greater for rare diseases, where there are limited sources of data.

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FDA Law Blog

DECEMBER 4, 2023

12, 2012). “[W]hen the circumstances surrounding the presentation of a prescription would give rise to suspicion in a ‘reasonable professional,’ there is a duty to question the prescription.” Holiday CVS, L.L.C. d/b/a CVS/Pharmacy, Nos. 219 and 5195; Decision and Order , 77 Fed. 62,316, 62,342 (Oct. Holiday CVS , 77 Fed. Complaint ¶ 62.

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FDA Law Blog

OCTOBER 24, 2023

Mullen — As of October 1, 2023, all 510(k) submissions, unless exempted, must be submitted to FDA using the electronic Submission Template And Resource ( eSTAR ). On September 29, 2023, FDA released a draft guidance on Electronic Submission Template for Medical Device De Novo Requests.

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PEMBlog

AUGUST 30, 2023

Many of the children you will evaluate during your shift are among the estimated 10 million United States (US) ED visits made by children with asthma, bronchiolitis, and croup, the most common pediatric respiratory conditions presenting to acute care settings.

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FDA Law Blog

SEPTEMBER 22, 2024

To request an FEI Number, laboratories will need to provide a long list of identifying information to FDA via email ( feiportal@fda.hhs.gov ) ( see slide 23 of the FDA’s presentation for the complete list). Of note, laboratories will need to provide a comprehensive list of activities conducted at the laboratory site.

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FDA Law Blog

SEPTEMBER 17, 2023

Inside Building 66 Upon arriving at Building 66, all visitors must present government-issued photo identification for check-in. Additionally, recent visitors did not have to scan their identification cards through an electronic machine. The video equipment dynamically followed the speakers and presented them on the screen.

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FDA Law Blog

JUNE 27, 2023

FDA could present this information in a Frequently Asked Questions (FAQ) section, like it uses on other webpages describing its programs. Ways to Minimize Burden of Information Collection FDA currently accepts voluntary submission of allegations of regulatory misconduct through electronic form , email, or regular mail.

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FDA Law Blog

MARCH 7, 2023

Lenz, Principal Medical Device Regulation Expert — As we discussed in our prior post , the electronic Submission Template And Resource (eSTAR) template will take getting used to in terms of form. By Adrienne R. It is also going to take some getting used to in terms of process.

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FDA Law Blog

JULY 10, 2023

We will then present an effective strategy to address FDA’s AI request in a timely manner. However, the strategy of addressing the AI request presented in the next section of this blog post applies to all three types of 510(k)s. In this presentation, FDA suggested the following tips.

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The Motivated MD

OCTOBER 10, 2024

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. You are already a hardworking professional. You deserve your hard-earned income to work for you consistently, with little mental bandwidth needed.

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Finance Individual Management IT 52

Aspiring Minority Doctor

MARCH 26, 2021

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.

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FDA Law Blog

SEPTEMBER 27, 2023

The biggest changes are the addition of Type D and Initial Targeted Engagement for Regulatory Advice on CDER and CBER ProducTs (INTERACT) meetings to the four types already present (Types A, B, B (end of phase), and C), and the addition of additional meeting formats.

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GeriPal

JULY 19, 2024

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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