Evidence map›Paper›PMID 40541663›Full record

ReviewThe ocular surface2025

Attribution of causality in Stevens-Johnson syndrome/toxic epidermal necrolysis.

Asha Parvathaneni, Liliya Benchetrit, Derek Metcalfe, James T Kwan, Yandong Bian, Tavé Van Zyl, Hajirah N Saeed, James Chodosh

Abstract readReview
In one paragraph

Review in The ocular surface, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

8 authors.

Asha ParvathaneniUniversity of Missouri-Kansas City School of Medicine, Kansas City, MO, USA.
Liliya BenchetritDepartment of Otolaryngology-Head and Neck Surgery Boston University Medical Center Boston, Massachusetts, USA.
Derek MetcalfeDepartment of Ophthalmology and Visual Sciences, UMass Chan Medical School, Worcester, MA, USA.
James T KwanNew England Eye Center, Department of Ophthalmology, Tufts University School of Medicine, Boston, MA, USA.
Yandong BianMass Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA, USA.
Tavé Van ZylDepartment of Ophthalmology & Visual Science, Yale School of Medicine, New Haven, CT, USA.
Hajirah N SaeedIllinois Eye and Ear Infirmary, Department of Ophthalmology & Visual Sciences, University of Illinois College of Medicine, Chicago, IL, USA.
James ChodoshDepartment of Ophthalmology and Visual Sciences, University of New Mexico School of Medicine, Albuquerque, NM, USA. Electronic address: jchodosh@salud.unm.edu.

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MCANANY, JAMES JASON · 1985 to 2025
$14.8M
Identification of genetic polymorphisms in Stevens Johnson syndrome and toxic epidermal necrolysisK23EY028230 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SAEED, HAJIRAH · 2018 to 2022
$1.3M
NEI NIH HHS K23 EY028230NEI NIH HHS P30 EY001792
6 · The paper itself

Abstract

Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is an acute, severe immunobullous disorder of skin and mucous membranes that is most commonly induced by exposure to drugs. Causation of SJS/TEN is most often determined by the "algorithm of drug causality for epidermal necrolysis" (ALDEN) tool. However, concerns remain regarding the precision of ALDEN and causality assessment tools, potentially impacting ongoing studies attempting to link specific genotypes with specific drug classes as causes. To determine whether a standard of care exists in attribution of causation in SJS/TEN, we performed a narrative review of current concepts on causation in SJS/TEN, and available clinical and laboratory assessment tools for attributing causation. We found that current SJS/TEN causality attribution tools, including ALDEN, are somewhat limited by underlying assumptions. The utility of ex vivo tests proposed for determining causation in SJS/TEN, specifically the lymphocyte transformation test and cytokine stimulation assays, remain under investigation and are either not tractable for acute SJS/TEN or are not yet validated. In summary, a critical unmet need exists in the care of SJS/TEN patients, namely the difficulty in determining a precise cause in any specific individual. This shortfall limits the clinician's ability to discontinue only the causal agent in the acute phase, confounds studies of pathogenesis, and leaves affected patients in the chronic phase without knowing which drug or drug class is safe to use in the future. Further studies are needed to close this critical gap in the care of this devastating disease.

Indexed as

Stevens-Johnson SyndromeHumansCausationStevens Johnson syndromeToxic epidermal necrolysis

Identifiers

PMID40541663
PMCPMC12238975

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.