Evidence map›Paper›PMID 39406204›Full record

GuidelineDermatology (Basel, Switzerland)2024

Systemic Therapy for Atopic Dermatitis in Children and Adolescents: A US Expert Consensus.

Lawrence F Eichenfield, Mark Boguniewicz, Christine T Lauren, Donald Y M Leung, Moise L Levy, Lynda C Schneider, Elaine C Siegfried, Wynnis L Tom, Amy S Paller

Abstract readConsensus StatementPractice Guideline
In one paragraph

Guideline in Dermatology (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Celiac Disease and Skin Diseases: A Bidirectional Mendelian Randomization Study.Clinical, cosmetic and investigational dermatology · 2025
    Article
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.

Lawrence F EichenfieldDepartments of Dermatology and Pediatrics, University of California San Diego, La Jolla, California, USA.
Mark BoguniewiczDivision of Allergy-Immunology, Department of Pediatrics, National Jewish Health, Denver, Colorado, USA.
Christine T LaurenDepartments of Dermatology and Pediatrics, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA.
Donald Y M LeungDivision of Allergy-Immunology, Department of Pediatrics, National Jewish Health, Denver, Colorado, USA.
Moise L LevyDepartments of Pediatrics and Internal Medicine (Dermatology), Dell Medical School at The University of Texas at Austin, Austin, Texas, USA.
Lynda C SchneiderDivision of Immunology, Boston Children's Hospital, Boston, Massachusetts, USA.
Elaine C SiegfriedDepartment of Pediatrics, Saint Louis University, St. Louis, Missouri, USA.
Wynnis L TomDepartments of Dermatology and Pediatrics, University of California San Diego, La Jolla, California, USA.
Amy S PallerDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atopic dermatitis (AD) is a chronic, type-2 mediated, inflammatory skin disease characterized by intense pruritus, disruption of skin barrier function, and immune dysregulation. Management strategies for AD are routinely determined based on disease severity. First-line treatment begins with basic skin care and topical anti-inflammatory medication, which is typically sufficient for the management of mild-to-moderate disease. For those patients with moderate-to-severe disease, systemic therapy is often required. This can involve off-label treatment with conventional immunosuppressant medications. However, this approach is limited by a lack of robust clinical trial data and safety concerns that necessitate close monitoring. The emergence of novel targeted biologics and small molecules to treat AD presents an opportunity to optimize AD management and patient outcomes by offering greater efficacy than traditional immunosuppressants and a favorable safety profile. As the treatment landscape shifts, clinicians can benefit from a standardized process of patient assessment and treatment, along with resources to help maintain contemporary knowledge of available therapeutic options. This US-based, expert-led consensus used a modified Delphi process to develop core recommendations for the use of systemic medications for the management of pediatric patients <18 years of age with moderate-to-severe AD.

Indexed as

ConsensusDermatitis, AtopicImmunosuppressive AgentsAdolescentChildDelphi TechniqueDermatologic AgentsHumansSeverity of Illness IndexUnited StatesDermatologic AgentsImmunosuppressive AgentsAlternative systemic therapyConventional systemic therapyPediatric atopic dermatitisSystemic therapyTopical therapy

Identifiers

PMID39406204
PMCPMC11651338

What OpenQuestion holds

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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.