Evidence map›Paper›PMID 40103891›Full record

ArticlePakistan journal of medical sciences2025

Comparative analysis of Mycoplasma Pneumoniae and Drug-induced Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis in Children.

Xiaoyuan Wu, Lei Kang, Yanhong Jia, Li Jia, Fang Guo

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Article in Pakistan journal of medical sciences, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiaoyuan WuXiaoyuan Wu Department of Infectious Diseases, Hebei Children's Hospital, 133 Jianhua South Street, Shijiazhuang 050000, Hebei Province, China.
Lei KangLei Kang Department of Pediatric Intensive Care Unit, Hebei Children's Hospital, 133 Jianhua South Street, Shijiazhuang 050000, Hebei Province, China.
Yanhong JiaYanhong Jia Department of Infectious Diseases, Hebei Children's Hospital, 133 Jianhua South Street, Shijiazhuang 050000, Hebei Province, China.
Li JiaLi Jia Department of Infectious Diseases, Hebei Children's Hospital, 133 Jianhua South Street, Shijiazhuang 050000, Hebei Province, China.
Fang GuoFang Guo Department of Infectious Diseases, Hebei Children's Hospital, 133 Jianhua South Street, Shijiazhuang 050000, Hebei Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To compare the differences between clinical characteristics, therapeutic management, and prognosis of mycoplasma pneumonia (MP) and drug-induced Stevens-Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN) in children. Methods: This was a retrospective study. The clinical data of SJS and TEN patients admitted to Hebei Children's Hospital from 2014-2024 were retrospectively analyzed and divided into the MP group and the drug group based on laboratory findings and the ALDEN algorithm for comparative study. Results: A total of 42 cases were included in the study. Among them, 20 cases were in the MP group and 22 cases were in the drug group. The median age of MP group was 108.0 (54.0, 129.0) months, which was greater than drug group with 42.0 (22.5, 75.0) months, and the difference was statistically significant (P < 0.05). Ten cases (50.0%) in the MP group had chest CT suggestive of consolidation of lung/pleural effusion, which was higher than the two cases (9.1%) in the drug group, with a statistically significant difference (P<0.05). Both groups were given systemic corticosteroids (Cs) treatment, and the proportion of children receiving Cs shock therapy combined with intravenous immunoglobulin (IVIG) in the MP group was significantly lower than that in the drug group, with a statistically significant difference (P<0.05). When SCORTEN score ≧3, the proportion of the MP group receiving Cs shock therapy and IVIG application increased. The median SCORTEN score in both groups was two, corresponding to a predicted mortality rate of 12.2%, whereas all children in the MP group survived and three died in the drug group, with an actual mortality rate of 13.6%. Conclusion: MP infection and drugs constitute the predominant triggers of SJS/TEN in children, with non-steroidal anti-inflammatory drugs (NSAIDs) and Chinese patent medicines (CPMs) as the main sensitizing drugs. For those with SCORTEN≦2 points, macrolides combined with conventional dose Cs may be the first-line treatment option for them.

Indexed as

ChildrenMcoplasma pnemanimeStevens-Johnson syndromeToxic epidermal necrolysis

Identifiers

PMID40103891
PMCPMC11911766

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