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Chiari malformation (CM) is a type of disease in which the cerebellar tonsils extend downward due to abnormal development of the hindbrain. Still, recent bibliometric studies on CM are a blind spot. We conducted a bibliometric analysis of research over the past decade to explore the hot spots and trends in this field. We used VOSviewer, CiteSpace and Bibliometrix to perform a global bibliometric analysis of the articles from 2013 to 2022 on CM in the web of science (WOS) core collection. The query identified 2155 articles, of which most were published in the USA. Institutions like Akron University and the University of Washington published the most articles and were widely cited. Loth Francis and R. Shane Tubbs were the most productive authors on this topic. Besides, the top-cited article was also published by R.Shane Tubbs in J NEUROSURG-PEDIATR (2011). A great number of relevant studies focused on syringomyelia and surgical technique such as posterior fossa decompression. The CM field is still heating up and will continue to grow in popularity. Our findings offer a panoramic view of this research field for new researchers and policymakers.
Mahazou I, Choukri M, Parker F, et al. Cerebellar syringocephaly following surgery for chiari malformation. Neurology. 2021;97(1):38–39.
Taylor DG, Chatrath A, Mastorakos P, et al. Cerebrospinal fluid area and syringogenesis in Chiari malformation type Ⅰ. J Neurosurg. 2020;134(3):825–830.
Rogers JM, Savage G, Stoodley MA. A systematic review of cognition in chiari I malformation. Neuropsychol Rev. 2018;28(2):176–187.
Rosenblum JS, Pomeraniec IJ, Heiss JD. Chiari malformation (update on diagnosis and treatment). Neurol Clin. 2022;40(2):297–307.
Granata T, Valentini LG. Epilepsy in type 1 chiari malformation. Neurol Sci. 2011;32(3):303–306.
Antonucci MU, Drohan A. Dynamic cerebellar tonsils in chiari malformation. J Pediatr. 2019;206:295.
Bastianon Santiago R, Kaye B, Hagerty V, et al. Chiari malformation type 1 and semi-sitting position-a suitable alternative for patients with high BMI. World Neurosurg. 2023;S1878eS8750(23), 00836–7.
Meadows J, Kraut M, Guarnieri M, et al. Asymptomatic Chiari Type I malformations identified on magnetic resonance imaging. J Neurosurg. 2000;92(6):920–926.
Arnautovic A, Splavski B, Boop FA, et al. Pediatric and adult Chiari malformation Type I surgical series 1965–2013: a review of demographics, operative treatment, and outcomes. J Neurosurg Pediatr. 2015;15(2):161–177.
Bianchi F, Montedoro B, Frassanito P, Massimi L, Tamburrini G. Chiari I malformation: management evolution and technical innovation. Childs Nerv Syst. 2023;39(10):2757–2769.
Qin Y, Zhang Q, Liu YR. Analysis of knowledge bases and research focuses of cerebral ischemia-reperfusion from the perspective of mapping knowledge domain. Brain Res Bull. 2020;156:15–24.
Zarcone TJ. Neuroscience and actometry: an example of the benefits of the precise measurement of behavior. Brain Res Bull. 2022;185:86–90.
Eck NJ, Waltman L. Software survey: VOSviewer, a computer program for bibliometric mapping. Scientometrics. 2010;84(2):523–538.
Chen C. CiteSpace: A Practical Guide for Mapping Scientific Literature. Incorporated: Nova Science Publishers; 2016.
Dervi H. Bibliometric analysis using bibliometrix an R package. J Scientometr Res. 2020;8(3):156–160.
Ohsawa Y, Iwafuchi M, Uchiyama M, et al. Surgical treatment and problem of massive small intestinal resection in childrendassessment of background diseases and actual management. Nihon Geka Gakkai Zasshi. 1988;89(9):1378–1381.
Albert GW. Chiari malformation in children. Pediatr Clin. 2021;68(4):783–792.
Atallah O, Wolff Fernandes F, Krauss JK. The chiari malformations: a bibliometric analysis of the 100 most cited articles. World Neurosurg. 2023;175: e754–e768.
Dyste GN, Menezes AH. Presentation and management of pediatric chiari malformations without myelodysplasia. Neurosurgery. 1988;23(5):589–597.
Dyste GN, Menezes AH, VanGilder JC. Symptomatic chiari malformations. J Neurosurg. 1989;71(2):159–168.
Greenlee JDW, Donovan KA, Hasan DM, et al. Chiari I malformation in the very young child: the spectrum of presentations and experience in 31 children under age 6 years. Pediatrics. 2002;110(6):1212–1219.
Menezes AH. Primary craniovertebral anomalies and the hindbrain herniation syndrome (Chiari I): data base analysis. Pediatr Neurosurg. 1995;23(5):260–269.
Eppelheimer MS, Nwotchouang BST, Heidari Pahlavian S, et al. Cerebellar and brainstem displacement measured with DENSE MRI in chiari malformation following posterior Fossa decompression surgery. Radiology. 2021;301(1):187–194.
Tubbs RS, Yan H, Demerdash A, et al. Sagittal MRI often overestimates the degree of cerebellar tonsillar ectopia: a potential for misdiagnosis of the Chiari I malformation. Childs Nerv Syst. 2016;32:1245–1248.
Williams G, Thyagaraj S, Fu A, et al. In vitro evaluation of cerebrospinal fluid velocity measurement in type Ⅰ Chiari malformation: repeatability, reproducibility, and agreement using 2D phase contrast and 4D flow MRI. Fluids Barriers CNS. 2021;18(1):12.
Lu CL, Ma LB, Yuan CH, et al. Phenotypes and prognostic factors of syringomyelia in single-center patients with chiari I malformation: moniliform type as a special configuration. Neurospine. 2022;19(3):816–827.
Yuan CH, Guan J, Du YQ, et al. Repeat craniocervical decompression in patients with a persistent or worsening Syrinx: a preliminary report and early results. World Neurosurg. 2020;138:e95–e105.
Vandertop WP. Syringomyelia. Neuropediatrics. 2014;45(1):3–9.
Holste KG, Muraszko KM, Maher CO. Epidemiology of chiari I malformation and syringomyelia. Neurosurg Clin. 2023;34(1):9–15.
Wawrzyniak A, Lubiatowski P. Shoulder arthropathy secondary to syringomyelia: systematic review. EFORT Open Rev. 2023;8(1):26–34.
Spazzapan P, Bosnjak R, Prestor B, et al. Chiari malformations in children: an overview. World J Clin Cases. 2021;9(4):764–773.
Blount JP, Hopson BD, Johnston JM, et al. What has changed in pediatric neurosurgical care in spina bifida? A 30-year UAB/Children's of Alabama observational overview. Childs Nerv Syst. 2023;39(7):1791–1804.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).