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The DOI matches its Crossref record; 12 of the 13 references it cites were found in a registry or an index; none of the 8 sources its claims cite is checked for support yet.

Paroxysmal Sympathetic Hyperactivity in Pediatric Acquired Brain Injury: An Under-Recognized Entity

Open access
Kamate, Mahesh, Koppad, Bhavna, Thanuja, Basavanagowda·2025·Annals of Indian Academy of Neurology

Abstract

Paroxysmal sympathetic hyperactivity (PSH) is a less-known neurologic emergency that can be life-threatening. It is a form of extreme autonomic dysregulation leading to multiple episodes of sympathetic hyperactivity. The pathogenesis of this interesting entity is yet to be fully understood. It presents as unexplained tachycardia, hypertension, and sometimes hyperthermia. Poor awareness of this fact leads to unnecessary workup to look for the cause of fever and interventions such as change of antibiotics. If it is not treated adequately, it can even cause complications like arrhythmias that can be fatal at times. PSH secondary to acquired brain injury is better known in adults, but there are scarce reports in children. We describe six cases of PSH in children with acquired brain injury – four secondary to traumatic brain injury and two secondary to neurologic infection (one with bacterial meningitis and the other one with viral meningoencephalitis). PSH can be seen in non-traumatic brain injury cases like meningitis. Due to a lack of awareness about this common but under-recognized entity, it is seldom diagnosed and treated. Early detection and treatment can be life-saving and improve patient outcomes. Earlier onset may be associated with poorer outcomes and mortality.

Overview

CoChat Summary

TL;DR

This case series describes six children with paroxysmal sympathetic hyperactivity (PSH) after acquired brain injury, including four with traumatic brain injury and two with neurologic infection. It argues that PSH is under-recognized in children, can occur within the first week, and that earlier onset may be associated with poorer outcomes and mortality.

Key findings

  • Six children aged 10 months to 17 years (two male, four female) were diagnosed with PSH: four had traumatic brain injury, one had staphylococcal meningitis, and one had herpes simplex virus-1 encephalitis. All had tachycardia, five of six had hypertension, four had dystonia, and all had PSH onset within the first week of illness.
  • PSH-AM scores ranged from 11 to 16, all within the “possible” PSH range (8–16). Both children with onset on day 2 died by the end of the first ICU week, with death attributed to cardiovascular instability–PSH; the other four improved.
  • CRP was checked in four cases and was normal in three, with a declining trend in the fourth, suggesting that a normal CRP during fever may help differentiate PSH from infectious fever.
  • PSH occurred after non-traumatic acquired brain injury such as meningitis and encephalitis, not only after traumatic brain injury.

Methods

  • Case series of six children enrolled from January 2022 to June 2024; MRI was performed in all cases, and the PSH-assessment measure (PSH-AM) was applied to each case.
  • The authors assessed number of symptoms per child, number of episodes per day, and outcome; written parental consent and institutional ethics committee approval were obtained.

Limitations

  • Stated: there is a lack of pediatric PSH data, no comparative drug trials exist, treatment is not standardized, diagnostic criteria are not firmly established, and future studies with larger sample sizes are needed.
  • Evident: this is a six-patient case series without a control group, so the suggested association between earlier onset and mortality cannot establish causality; treatment was heterogeneous (gabapentin, baclofen, propranolol, clonidine), limiting comparison.
  • Evident: the text inconsistently reports hypertension frequency, stating “five out of six” in the results/abstract but “four of the five children” in the discussion.

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Integrity signals

Registry

Crossref · 10.4103/aian.aian_549_24

Cites

12 of 13 references verified0 citation errors · 1 not checkable

Statistics

Nothing to recompute.

Figures

Figure 1 MRI of the brain of case 5 and case 6. (a and b) Case 5: T2-weighted axial images showing hyperintensities in the subcortical white matter (bold arrow) and bilateral thalami (arrow). (c and d) Case 6: Diffusion-weighted axial imaging showing hyperintensitites involving bilateral thalami (*) and temporal regions (double-headed white arrow). (e and f) Case 6: Apparent diffusion coefficient maps showing hypo-intense signals in areas corresponding to (c) and (d), respectively (double-headed white arrow). MRI: magnetic resonance imaging
Figure 1 MRI of the brain of case 5 and case 6. (a and b) Case 5: T2-weighted axial images showing hyperintensities in the subcortical white matter (bold arrow) and bilateral thalami (arrow). (c and d) Case 6: Diffusion-weighted axial imaging showing hyperintensitites involving bilateral thalami (*) and temporal regions (double-headed white arrow). (e and f) Case 6: Apparent diffusion coefficient maps showing hypo-intense signals in areas corresponding to (c) and (d), respectively (double-headed white arrow). MRI: magnetic resonance imagingCC BY-NC-SA · PubMed Central

Verification

Claims the paper makes

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Self-check

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Citations

Cites

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Metadata

Authors
Kamate, M., Koppad, B., & Thanuja, B.
Affiliations
  • Jawaharlal Nehru Medical College (IN)
  • Department of Pediatric Neurology, Karnataka Lingayat Education Academy of Higher Education and Research University’s Jawaharlal Nehru Medical College, Belagavi, Karnataka, India
Corresponding author
Kamate, Mahesh
Venue
Annals of Indian Academy of Neurology
Published
2025-01
Volume
28
Issue
1
Pages
99-103
ISSN
  • 0972-2327 (ISSN-L)
  • 1998-3549
OpenAlex
W4406436770
Cited by
1
References
12
Citations by year
2026: 1
FWCI
0.50
Type
journal article
Language
en
Open access
Locations
  • Annals of Indian Academy of Neurology (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
  • Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury Research
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Takotsubo Cardiomyopathy and Associated Phenomena
Keywords
paroxysmal sympathetic hyperactivity, acquired brain injury, pediatric patients, traumatic brain injury, bacterial meningitis, viral meningoencephalitis, autonomic dysfunction, tachycardia, hypertension, hyperthermia, cardiac arrhythmias, neurological emergencies, under-recognition

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This page
CoChat. (2026). Citation check: Paroxysmal Sympathetic Hyperactivity in Pediatric Acquired Brain Injury: An Under-Recognized Entity. https://app.cochat.ai/papers/10.4103/aian.aian_549_24
The paper
Kamate, M., Koppad, B., & Thanuja, B. (2025). Paroxysmal Sympathetic Hyperactivity in Pediatric Acquired Brain Injury: An Under-Recognized Entity. Annals of Indian Academy of Neurology. https://doi.org/10.4103/aian.aian_549_24

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.