Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jul 29;50(1):134.
doi: 10.1186/s13052-024-01705-x.

Clinical characteristics and prognosis of paediatric respiratory syncytial virus-related encephalopathy

Affiliations

Clinical characteristics and prognosis of paediatric respiratory syncytial virus-related encephalopathy

Yushan He et al. Ital J Pediatr. .

Abstract

Background: To understand the clinical characteristics and prognosis of respiratory syncytial virus (RSV)-related encephalopathy in children.

Methods: A retrospective analysis of the data of children who were diagnosed with RSV-related encephalopathy and admitted to the paediatric intensive care unit (PICU) of Beijing Children's Hospital between November 2016 and November 2023 was performed.

Results: Four hundred and sixty-four children with RSV infection were treated in the PICU, and eight of these patients (1.7%) were diagnosed with RSV-related encephalopathy. The mean age of the patients was 24.89 (5.92 ∼ 36.86) months. Two patients had underlying diseases. The time from the onset of illness to impaired consciousness was 3 (1.88-3.75) days. Five patients had convulsions, and three patients had an epileptic status. The serum procalcitonin (PCT) level was 1.63 (0.24, 39.85) ng/ml for the eight patients, and the cerebrospinal fluid (CSF) protein level was 232 (163 ∼ 848) g/L. Among the 8 patients, four patients underwent electroencephalogram (EEG) monitoring or examination. One patient showed continuous low-voltage, nonresponsive activity, and another patient displayed persistent slow waves, the remaining two patients had negative results. One patient had a combination of acute necrotizing encephalopathy (ANE) and acute encephalopathy with biphasic seizures and late reduced diffusion (AESD). Additionally, one patient had ANE, and another had acute brain swelling (ABS). One patient died in the hospital, and the other seven patients were discharged with improvement. Routine follow-up was conducted for 4.58(0.5 ∼ 6.50) years, and all patients fully recovered.

Conclusions: RSV-related encephalopathy could have varying clinical manifestations, and some types, such as ANE and ABS, are dangerous and can lead to death.

Keywords: Acute brain swelling; Acute necrotizing encephalopathy; Encephalopathy; Respiratory syncytial virus.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
RSV-related encephalopathy inclusion and exclusion process
Fig. 2
Fig. 2
MRI results of Patient 5 One year and ten months old gairl, was admitted for “six days of cough, intermittent fever and convulsions for five days”. On the 8th day of the disease course, the brain MRI showed flaky long T1 (A) and long T2 (B) abnormal signals in the bilateral thalamus, T2 FLAIR (C) had a high signal, and small patchy diffusion restriction (D, E arrows) could be seen in the right thalamus lesion. Diffusion restriction (D ∼ F) could be observed in the bilateral cerebral hemisphere and subcortex, showing “bright tree signs”, indicating cytotoxicoedema. Re-examination of the brain by MRI on the 19th day of the disease showed brain atrophy-like changes in T2 FLAIR images (G), the abnormal signals in the bilateral thalamus had basically disappeared, and the apparent diffusion coefficient (ADC) (H) indicated that there was no restriction of diffusion in the brain

Similar articles

References

    1. Yu J, Liu C, Xiao Y, Xiang Z, Zhou H, Chen L, et al. Respiratory syncytial virus seasonality, Beijing, China, 2007–2015. Emerg Infect Dis. 2019;25(6):1127–35. 10.3201/eid2506.180532. PMID: 31107230; PMCID: PMC6537707. 10.3201/eid2506.180532 - DOI - PMC - PubMed
    1. Hon KL, Leung AKC, Wong AHC, Dudi A, Leung KKY. Respiratory syncytial virus is the most common causative agent of viral bronchiolitis in young children: an updated review. Curr Pediatr Rev. 2023;19(2):139–149. 10.2174/1573396318666220810161945. PMID: 35950255. - PubMed
    1. Griffiths C, Drews SJ, Marchant DJ. Respiratory syncytial virus: infection, detection, and new options for prevention and treatment. Clin Microbiol Rev. 2017;30(1):277–319. 10.1128/CMR.00010-16. PMID: 27903593; PMCID: PMC5217795. 10.1128/CMR.00010-16 - DOI - PMC - PubMed
    1. Li Y, Wang X, Blau DM, Caballero MT, Feikin DR, Gill CJ, et al. Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. Lancet. 2022;399(10340):2047–64. 10.1016/S0140-6736(22)00478-0. Epub 2022 May 19. PMID: 35598608; PMCID: PMC7613574. 10.1016/S0140-6736(22)00478-0 - DOI - PMC - PubMed
    1. Saravanos GL, King CL, Deng L, Dinsmore N, Ramos I, Takashima M, et al. Respiratory syncytial virus-associated neurologic complications in children: a systematic review and aggregated case series. J Pediatr. 2021;239:39–e499. 10.1016/j.jpeds.2021.06.045. Epub 2021 Jun 25. PMID: 34181989. 10.1016/j.jpeds.2021.06.045 - DOI - PubMed

LinkOut - more resources