Evidence map›Paper›PMID 36778654›Full record

ArticleCase reports in immunology2023

Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome in a Child with Cystic Fibrosis.

Ahmed Abushahin, Haneen Toma, Sara G Hamad, Mutasim Abu-Hasan

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In one paragraph

Article in Case reports in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

4 authors.

Ahmed AbushahinDepartment of Pediatrics, Pulmonology Division, Sidra Medicine, P.O. Box 26999, Doha, Qatar.
Haneen TomaDepartment of Pediatrics, Pulmonology Division, Sidra Medicine, P.O. Box 26999, Doha, Qatar.
Sara G HamadDepartment of Pediatrics, Pulmonology Division, Sidra Medicine, P.O. Box 26999, Doha, Qatar.ORCID https://orcid.org/0000-0002-8292-2011
Mutasim Abu-HasanDepartment of Pediatrics, Pulmonology Division, Sidra Medicine, P.O. Box 26999, Doha, Qatar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Drug reaction with eosinophilia and systemic symptoms (DRESSs) syndrome is an idiosyncratic drug-induced reaction that rarely occurs in children but can lead to serious complications. It manifests most commonly with fever, extensive skin eruptions, and eosinophilia. Symptoms typically develop two to six weeks after the initiation of the inciting drug. Visceral organ involvement especially the liver can also occur and if not recognized early and the inciting drug is not stopped immediately, it can lead to liver failure. Therefore, early diagnosis is important but can be very challenging because of disease rarity, lack of a diagnostic test, and its overlap with other common pediatric allergic and infectious conditions. Conclusion: Our case demonstrates the importance of early recognition of the DRESS syndrome in children who develop fever and skin rashes with eosinophilia while undergoing long-term antibiotic treatment. Prompt discontinuation of the offending drug is the cornerstone therapy and results in the resolution of symptoms and prevention of serious complications.

Identifiers

PMID36778654
PMCPMC9911254

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