You are leaving Medscape Education
Cancel Continue
Log in to save activities Your saved activities will show here so that you can easily access them whenever you're ready. Log in here CME & Education Log in to keep track of your credits.
 

 

CME / ABIM MOC / CE

Medscape Now! Hot Topics in Family Medicine June 2023 Part 2

  • Authors: News Authors: Eve Bender, Megan Brooks and Pauline Anderson; CME Author: Hennah Patel, MPharm, RPh
  • CME / ABIM MOC / CE Released: 6/28/2023
  • Valid for credit through: 6/28/2024, 11:59 PM EST
Start Activity

  • Credits Available

    Physicians - maximum of 0.25 AMA PRA Category 1 Credit(s)™

    ABIM Diplomates - maximum of 0.25 ABIM MOC points

    Nurses - 0.25 ANCC Contact Hour(s) (0 contact hours are in the area of pharmacology)

    Pharmacists - 0.25 Knowledge-based ACPE (0.025 CEUs)

    Physician Assistant - 0.25 AAPA hour(s) of Category I credit

    IPCE - 0.25 Interprofessional Continuing Education (IPCE) credit

    You Are Eligible For

    • Letter of Completion
    • ABIM MOC points

Target Audience and Goal Statement

This activity is intended for primary care physicians (PCPs), physician assistants (PAs), nurse practitioners (NPs), nurses, pharmacists, and other healthcare professionals (HCPs) involved in patient care.

The goal of this activity is for learners to be better able to evaluate and implement emerging data and guidelines into patient care.

Upon completion of this activity, participants will:

  • Have increased knowledge regarding
    • Recent advances in family medicine that are improving patient care
    • Implications for the healthcare team 


Disclosures

Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated. Others involved in the planning of this activity have no relevant financial relationships.


News Authors

  • Eve Bender

    Freelance writer, Medscape 

    Disclosures

    Eve Bender has no relevant financial relationships. 

  • Megan Brooks

    Freelance writer, Medscape 

    Disclosures

    Megan Brooks has no relevant financial relationships. 

  • Pauline Anderson

    Freelance writer, Medscape 

    Disclosures

    Pauline Anderson has no relevant financial relationships. 

CME Author

  • Hennah Patel, MPharm, RPh

    Freelance Medical Writer

    Disclosures

    Hennah Patel, MPharm, RPh, has no relevant financial relationships.

Editor/Nurse Planner

  • Leigh Schmidt, MSN, RN, CNE, CHCP

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Leigh Schmidt, MSN, RN, CNE, CHCP, has no relevant financial relationships.

Compliance Reviewer

  • Esther Nyarko, PharmD, CHCP

    Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Esther Nyarko, PharmD, CHCP, has no relevant financial relationships.


Accreditation Statements

Medscape

Interprofessional Continuing Education

In support of improving patient care, Medscape, LLC is jointly accredited with commendation by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.

IPCE

This activity was planned by and for the healthcare team, and learners will receive 0.25 Interprofessional Continuing Education (IPCE) credit for learning and change.

    For Physicians

  • Medscape, LLC designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™ . Physicians should claim only the credit commensurate with the extent of their participation in the activity.

    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.25 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit. Aggregate participant data will be shared with commercial supporters of this activity.

    The European Union of Medical Specialists (UEMS)-European Accreditation Council for Continuing Medical Education (EACCME) has an agreement of mutual recognition of continuing medical education (CME) credit with the American Medical Association (AMA). European physicians interested in converting AMA PRA Category 1 Credit™ into European CME credit (ECMEC) should contact the UEMS (www.uems.eu).

    College of Family Physicians of Canada Mainpro+® participants may claim certified credits for any AMA PRA Category 1 credit(s)™, up to a maximum of 50 credits per five-year cycle. Any additional credits are eligible as non-certified credits. College of Family Physicians of Canada (CFPC) members must log into Mainpro+® to claim this activity.

    Through an agreement between the Accreditation Council for Continuing Medical Education and the Royal College of Physicians and Surgeons of Canada, medical practitioners participating in the Royal College MOC Program may record completion of accredited activities registered under the ACCME’s “CME in Support of MOC” program in Section 2 of the Royal College’s MOC Program.

    Contact This Provider

    For Nurses

  • Awarded 0.25 contact hour(s) of nursing continuing professional development for RNs and APNs; 0.00 contact hours are in the area of pharmacology.

    Contact This Provider

    For Pharmacists

  • Medscape designates this continuing education activity for 0.25 contact hour(s) (0.025 CEUs) (Universal Activity Number: JA0007105-0000-23-274-H01-P).

    Contact This Provider

  • For Physician Assistants

    Medscape, LLC has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with AAPA CME Criteria. This activity is designated for 0.25 AAPA Category 1 CME credits. Approval is valid until 06/28/2024. PAs should only claim credit commensurate with the extent of their participation.

For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]


Instructions for Participation and Credit

There are no fees for participating in or receiving credit for this online educational activity. For information on applicability and acceptance of continuing education credit for this activity, please consult your professional licensing board.

This activity is designed to be completed within the time designated on the title page; physicians should claim only those credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 75% on the post-test.

Follow these steps to earn CME/CE credit*:

  1. Read about the target audience, learning objectives, and author disclosures.
  2. Study the educational content online or print it out.
  3. Online, choose the best answer to each test question. To receive a certificate, you must receive a passing score as designated at the top of the test. We encourage you to complete the Activity Evaluation to provide feedback for future programming.

You may now view or print the certificate from your CME/CE Tracker. You may print the certificate, but you cannot alter it. Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period, you can print out the tally as well as the certificates from the CME/CE Tracker.

*The credit that you receive is based on your user profile.

CME / ABIM MOC / CE

Medscape Now! Hot Topics in Family Medicine June 2023 Part 2

Authors: News Authors: Eve Bender, Megan Brooks and Pauline Anderson; CME Author: Hennah Patel, MPharm, RPhFaculty and Disclosures

CME / ABIM MOC / CE Released: 6/28/2023

Valid for credit through: 6/28/2024, 11:59 PM EST

processing....

The field of family medicine is continuously advancing, making it challenging for members of the interprofessional team to stay aware of key developments. This article focuses on recent updates in neurology and gastroenterology, which may impact the management of patients by family medicine practitioners.

REGULAR NAPPING LINKED TO GREATER BRAIN VOLUME

Napping during the day is common among young children, but less so after the age of 6 and into adulthood. However, daytime napping may be beneficial to cognitive function.[1] In a new study, researchers at University College London, United Kingdom, and the University of the Republic of Uruguay, Montevideo, aimed to explore the relationship between regular daytime napping, brain structure and cognition in adults.

They found that daily napping may help preserve brain health and that individuals genetically predisposed to regular napping had larger total brain volume, a surrogate of better cognitive health.[1]

"Our results suggest that napping may improve brain health," first author Valentina Paz, MSc, a PhD candidate at the University of the Republic of Uruguay in Montevideo told Medscape Medical News. "Specifically, our work revealed a 15.8 cubic cm increase in total brain volume with more frequent daytime napping," she said.

The findings were published online June 19 in Sleep Health.[1]

Higher Brain Volume

Previous studies examining the potential link between napping and cognition in older adults have yielded conflicting results.

To clarify this association Paz and colleagues used Mendelian randomization to study DNA samples, cognitive outcomes, and functional magnetic resonance imaging (fMRI) data in participants from the ongoing UK Biobank Study.[1]  

Starting with data from 378,932 study participants (mean age 57), investigators compared measures of brain health and cognition of those who are more genetically programmed to nap with people who did not have these genetic variations. More specifically, the investigators examined 97 sections of genetic code previously linked to the likelihood of regular napping and correlated these results with fMRI and cognitive outcomes between those genetically predisposed to take regular naps and those who were not.[1]

Study outcomes included total brain volume, hippocampal volume, reaction time, and visual memory. The final study sample included 35,080 with neuroimaging, cognitive assessment, and genotype data.[1]

The researchers estimated that the average difference in brain volume between individuals genetically programmed to be habitual nappers and those who were not was equivalent to 15.8 cubic cm, or 2.6 to 6.5 years of aging. However, there was no difference in the other 3 outcomes — hippocampal volume, reaction time, and visual processing — between the 2 study groups.[1]

Since investigators did not have information on the length of time participants napped, Paz suggested that "taking a short nap in the early afternoon may help cognition in those needing it." However, she added, the study's findings need to be replicated before any firm conclusions can be made. More work is needed to examine the associations between napping and cognition, and the replication of these findings using other datasets and methods," she said.

The investigators note that the study's findings augment the knowledge of the "impact of habitual daytime napping on brain health which is essential to understanding cognitive impairment in the aging population. The lack of evidence for an association between napping and hippocampal volume and cognitive outcomes (eg, alertness) may be affected by habitual daytime napping and should be studied in the future."

Strengths, Limitations

Commenting on the findings for Medscape Medical News, Tara Spires-Jones, PhD, president of the British Neuroscience Association and group leader at the UK Dementia Research Institute, said, "the study shows a small but significant increase in brain volume in people who have a genetic signature associated with taking daytime naps."

Spires-Jones, who was not involved in the research, noted that while the study is well-conducted, it has limitations. Because Mendelian randomization uses a genetic signature, she noted, outcomes depend on the accuracy of the signature. "The napping habits of UK Biobank participants were self-reported, which might not be entirely accurate, and the 'napping' signature overlapped substantially with the signature for cognitive outcomes in the study, which makes the causal link weaker," she said. "Even with those limitations, this study is interesting because it adds to the data indicating that sleep is important for brain health," said Spires-Jones.

Implications for the Interprofessional Healthcare Team

• The interprofessional healthcare team should stay aware of the latest data regarding brain health

• The team should communicate the latest evidence regarding napping and brain health to patients, particularly adults, where relevant

NO LINK BETWEEN PPIS AND DEMENTIA IN NEW STUDY

Proton pump inhibitors (PPIs) are a class of medicines used in the treatment of a variety of stomach acid-related conditions. They are most commonly prescribed for conditions such as esophagitis, reflux disease, peptic ulcers, Helicobacter pylori infection, and to prevent drug-induced ulcers caused by nonsteroidal anti-inflammatory drugs (NSAIDs)[2] In addition, histamine-2 receptor antagonists (H2RAs) are widely used for the treatment of common gastrointestinal conditions such as acid-peptic disease, ulcers, reflux disease and heartburn.[3] Some studies have suggested that use of PPIs can increase the risk of dementia. As such, investigators from the US conducted a post-hoc analysis of the ASPirin in Reducing Events in the Elderly (ASPREE) trial to determine the association between PPIs and H2RAs with dementia and cognitive decline.[4]

TOPLINE:

A new study provides reassurance about the long-term safety of PPI and H2RA use in older adults, finding no increased risk for dementia or cognitive changes.[4]

METHODOLOGY:

  • Post hoc observational study within the ASPREE clinical trial[5]
  • 18,934 adults aged 65+ from the US and Australia without dementia at baseline
  • 4667 (25%) PPI users and 368 (2%) H2RA users at baseline
  • PPI and H2RA use, dementia incidence, and cognitive changes were tracked

TAKEAWAY:

  • In multivariable analysis, baseline PPI use was not associated with incident dementia (hazard ratio [HR], 0.88) or cognitive impairment (HR, 1.00)
  • PPI use was not linked to changes in overall cognitive test scores over time (β -0.002)
  • No associations were found between H2RA use and cognitive endpoints

IN PRACTICE:

"Long-term use of PPIs in older adults is unlikely to have negative effects on cognition," the study team concludes.

STUDY DETAILS:

The study was led by Raaj Mehta, MD, PhD, with Massachusetts General Hospital and Harvard Medical School in Boston. The study was published online June 12 in Gastroenterology.[4] Funding was provided by grants from the National Institute on Aging, the National Cancer Institute, and other institutions.

LIMITATIONS:

Potential for residual confounding and underestimation of PPI and H2RA use, lack of data on medication dose and duration, and the absence of APOE4 allele status.

Implications for the Interprofessional Healthcare Team

• The interprofessional healthcare team should be cognizant of new evidence regarding the use of PPIs and H2RAs to treat common gastroenterological conditions

• The team should incorporate the latest evidence and guidance into clinical decision making for these diseases

INFLAMMATORY BOWEL DISEASE TIED TO INCREASED STROKE RISK

Studies have shown that individuals with inflammatory bowel disease (IBD) have an increased risk for thromboembolic events. However, evidence on long-term risk is lacking. In a new study, researchers looked into the relationships between confirmed IBD and long-term stroke risk in more than 85,000 patients.[6]

TOPLINE:

Patients with IBD are at increased risk for stroke, especially ischemic stroke, for at least 25 years after diagnosis.

METHODOLOGY:

  • IBD, which causes chronic intestinal inflammation, encompasses Crohn's disease (CD), ulcerative colitis (UC), and IBD-unclassified (IBD-U)
  • The population-based cohort study included 85,006 patients with biopsy-confirmed IBD between 1969 and 2019, a matched reference group drawn from the general population and IBD-free siblings
  • Covariates included country of birth, socioeconomic status, healthcare-seeking behavior, and cardiovascular-related comorbidities and medication use prior to the index date
  • The primary outcome was incident overall stroke; secondary outcomes were incident ischemic and hemorrhagic stroke (including intracranial hemorrhage and subarachnoid hemorrhage)

TAKEAWAY:

  • During a median follow-up of about 12 years, there were 3720 incident strokes in IBD patients (incidence rate [IR] 32.6 per 10,000 person-years) compared with 15,599 in the reference individuals (IR, 27.7)
  • After multivariable adjustment, IBD patients were at increased risk for overall stroke (adjusted hazard ratio [aHR], 1.13; 95% CI, 1.08, 1.17) and ischemic stroke (aHR, 1.14; 95% CI: 1.09, 1.18), but not hemorrhagic stroke (aHR, 1.06; 95% CI: 0.97, 1.15)
  • The aHR for overall stroke remained increased even 25 years after diagnosis, corresponding to one additional stroke case per 93 IBD patients until then
  • Individuals with different subtypes of IBD were also at significantly increased risk for overall stroke
  • The sibling comparison also showed IBD patients had significantly higher risk for overall stroke and ischemic stroke but not hemorrhagic stroke
  • In subgroup analyses, the aHR for overall stroke was higher in women (1.20, vs 1.06 in men), in those with younger onset IBD, and those diagnosed from 2010 to 2019

IN PRACTICE:

These results along with earlier data "indicate that ischemic stroke is one of the most clinically important CVD-related outcomes in IBD patients" write the authors, who urged screening and management of stroke risk factors in IBD patients and development of relevant guidelines.

STUDY DETAILS:

The study was conducted by Jiangwei Sun, PhD, Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden, and colleagues. It was published online June 14 in the journal Neurology.[6]

LIMITATIONS:

The matched references may have included patients with undiagnosed stroke, which may dilute the real association. Changes in the diagnostic criteria for IBD and stroke over the study period may affect the associations. The study lacked complete data on all protective and stroke risk factors, such as diet and other lifestyle factors, that may confound the association, and data on inflammatory markers.

Implications for the Interprofessional Healthcare Team

• The interprofessional healthcare team should be aware of the long-term stroke risk among patients with IBD

• The team should screen for and manage risk of stroke among patients with IBD, where clinically appropriate

 

Earn Credit

  • Print