Evidence map›Paper›PMID 42709335›Full record

ArticleDermatology and therapy2026

Patient Experience and Preferences for Treatments in Atopic Dermatitis.

Diego Ruiz Dasilva, Joshua Burshtein, Jeffrey Weinberg, John Koo, Tina Bhutani-Jacques, Lenka V Hurton, Aaron S Farberg, Adam Friedman, Peter A Lio

Abstract read
PubMed Publisher
In one paragraph

Article in Dermatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Diego Ruiz DasilvaForefront Dermatology, Viriginia Beach, VA, USA.
Joshua BurshteinDepartment of Dermatology, University of Illinois-Chicago, Chicago, IL, USA.
Jeffrey WeinbergInfinity Dermatology, New York, NY, USA.
John KooDepartment of Dermatology, San Francisco School of Medicine, University of California, San Francisco, CA, USA.
Tina Bhutani-JacquesSynergy Dermatology, San Francisco, CA, USA.
Lenka V HurtonCastle Biosciences, Inc, 1500 W. Parkwood Dr., 4th Floor, Friendswood, TX, 77546, USA. lhurton@castlebiosciences.com.
Aaron S FarbergBaylor Scott & White Health System, Dallas, TX, USA.
Adam FriedmanDepartment of Dermatology, Medical Faculty Associates, George Washington University, Washington, DC, USA.
Peter A LioNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAlthough type 2 inflammatory pathway dysfunction is a hallmark of atopic dermatitis (AD), disease symptoms in many patients are also driven by other immune/inflammatory pathway dysfunctions, all of which lead to varied treatment response profiles of targeted systemic therapies for individual patients. Adding complexity to the process of identifying which systemic therapy to prescribe for an individual patient is that these treatments have varied safety profiles, routes of administration, monitoring requirements, and costs-all of which are reviewed during today's shared decision-making discussions.

methodsThis patient assessment study aimed to better understand patients' attitudes toward contemporary AD treatments, their experiences, and their perceptions of a molecular test to predict treatment response. A 32-question assessment tool, deemed eligible for IRB exemption, was made available to any attendees with AD at the 2024 Eczema Expo who wished to complete it.

resultsRegarding treatment objectives, results indicated the top three factors most important to respondents (n = 40) were itch control (70%), skin clearance (58%), and safety/side effects (50%). For respondents switching from their initial topical therapy due to lack of efficacy (n = 37), 38% switched to a systemic drug. Among respondents who had used targeted systemics (n = 22), 18% switched systemics, 4.5% added another systemic, 32% added topicals, and 45% did not modify their initial systemic treatment. The top two reasons for switching systemics or adding a topical treatment to their systemic were insufficient skin clearance and itch control. Of respondents open to taking a new systemic therapy, 94% showed interest in a test that would inform them about which targeted systemic therapy would work best for them.

conclusionThese findings highlight a clinical need for personalized therapeutic guidance in AD to improve patient care and treatment satisfaction.

Indexed as

Atopic dermatitisGEPItchMolecular testPrecision medicineQuality of lifeSystemic therapyTherapy cyclingUnmet need

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.