Evidence map›Paper›PMID 41622169›Full record

SynthesisOrphanet journal of rare diseases2026

Clinical features of Infantile Epileptic Spasms Syndrome: a systematic review.

Xiao Meng, Danielle S Takacs, Yashaswini Kelagere, Zihan Zhang, Sanjanaa Seshadri, Jiyeon Cha, Ming Li, Lei-Shih Chen

Abstract readSystematic Review
In one paragraph

Synthesis in Orphanet journal of rare diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Xiao MengDepartment of Health Behavior, School of Public Health, Texas A&M University, College Station, USA.
Danielle S TakacsDivision of Neurology and Developmental Neuroscience, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, USA.
Yashaswini KelagereDivision of Neurology and Developmental Neuroscience, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, USA.
Zihan ZhangDepartment of Health Behavior, School of Public Health, Texas A&M University, College Station, USA.
Sanjanaa SeshadriDepartment of Health Behavior, School of Public Health, Texas A&M University, College Station, USA.
Jiyeon ChaDepartment of Health Behavior, School of Public Health, Texas A&M University, College Station, USA.
Ming LiDepartment of Health Sciences, Towson University, Maryland, USA.
Lei-Shih ChenDepartment of Health Behavior, School of Public Health, Texas A&M University, College Station, USA. lacechen@tamu.edu.ORCID http://orcid.org/0000-0001-5320-6350

Funding

Texas A&M University Health Science Center Texas A&M University Health Science Center
6 · The paper itself

Abstract

introductionInfantile Epileptic Spasms Syndrome (IESS) is a severe epilepsy in children between one month and two years of age. Urgent referral of possible IESS cases from pediatricians and family physicians who care for children to neurologists for diagnosis and treatment has been shown to significantly improve patient health outcomes. Yet, a comprehensive list of IESS clinical features is lacking. We conducted a systematic review of studies to report IESS clinical features.

methodsArticles from the MEDLINE Complete and Embase databases were searched from the earliest years of databases availability (1979) to July 31, 2024. We followed the Preferred Reporting for Systematic Reviews and Meta-Analysis guidelines to conduct this systematic review with 140 articles, all of which were descriptive studies.

resultsWe identified 25 clinical features among the 3,786 children with IESS who were included in 140 studies. No single clinical descriptor was reported in over half of the children. The six most commonly reported clinical features included flexor spasms (48.28%), mixed spasms (30.19%), extensor spasms (10.49%), symmetric spasms (8.49%), asymmetric/focal spasms (6.50%), and head nodding (2.48%).

conclusionsThere were a wide variety of IESS presentation descriptions. This review will help future researchers to develop an IESS screening tool that can assist pediatricians and family physicians who care for children in making urgent referrals.

Indexed as

Spasms, InfantileChild, PreschoolHumansInfantClinical featuresInfantile Epileptic Spasms SyndromePediatriciansSystematic review

Identifiers

PMID41622169
PMCPMC12955028

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.