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Intracranial pressure in craniostenosis
Abstract
In this study, intracranial pressure (ICP) was recorded with an epidural sensor for periods of 12 to 24 hours in 92 cases of craniosynostosis. Pre- and postoperative recordings were performed in 23 patients, and 55 children underwent preoperative psychometric testing. The ICP was found to be normal in one-third of the cases, was obviously elevated in one-third, and was borderline in one-third. Waves of increased ICP were recorded during rapid eye movement (REM) sleep. After surgery, ICP decreased progressively and returned to normal in several weeks. A significant statistical relationship was found between the patients' ICP and their mental level: the higher the ICP the lower the mental level. The regression curve of ICP as a function of age shows that ICP is maximal at the age of 6 years and decreases later. The significance of these results is discussed. The authors recommend that ICP be recorded in cases of craniosynostosis since it is of some help in deciding whether patients should undergo surgery.
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“Increased intracranial pressure not only leads to visual problems but also to a delay in neurocognitive development.”
From Isolated Sagittal Craniosynostosis: A Comprehensive Review (2024) · cites this paper as [26]
In the citing paper
“A number of pathophysiological factors, alone or in combination, may explain the occurrence of neurocognitive problems associated with ISS:increased intracranial pressure [26],deformation of the brain as a result of deformation of the skull [27],problems with the normal development of the brain,compression of the venous sinuses with resulting impairment of venous outflow [14,28].”
From Isolated Sagittal Craniosynostosis: A Comprehensive Review (2024) · cites this paper as [26]
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Hayward, R. D., Britto, J. A., Dunaway, D. J., Evans, R. D., Jeelani, O., & Thompson, D. N. P. (2015) · Journal of Neurosurgery Pediatrics · doi:10.3171/2014.11.peds14625 · Cited by 15
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“An older study identified that for the first 6 years of life, ICP increased with age [115, 116].”
BackgroundComplications related to cranial vault surgery
Greensmith, A. L., Meara, J. G., Holmes, A. D., & Lo, P. A. (2004) · Oral and Maxillofacial Surgery Clinics of North America · doi:10.1016/j.coms.2004.07.001 · Cited by 14
“[37] Renier D, Sainte-Rose C, Marchac D, Hirsch J.”
BackgroundUpper Facial Asymmetries Resulting from Unilateral Coronal Synostosis
Posnick, J. C. (1996) · Atlas of the Oral and Maxillofacial Surgery Clinics · doi:10.1016/s1061-3315(18)30107-0 · Cited by 14
Papilledema in unicoronal synostosis: a rare finding.
van de Beeten, S. D. C., Cornelissen, M., van Seeters, R. M., van Veelen, M. V., Versnel, S., Loudon, S., & Mathijssen, I. (2019) · Journal of Neurosurgery: Pediatrics · doi:10.3171/2019.3.peds18624 · Cited by 9
Le pronostic mental des scaphocéphalies
Arnaud, É., Rénier, D., Marchac, D., Brunet, L., & Pierre‐Kahn, A. (1996) · Archives de Pédiatrie · doi:10.1016/s0929-693x(96)80003-0 · Cited by 14
Cerebrospinal fluid collections in sagittal suture synostosis
Usami, K., Nicolini, F., Arnaud, E., & Di Rocco, F. (2016) · Child s Nervous System · doi:10.1007/s00381-015-3011-0 · Cited by 13
Intracranial Volume in 15 Children with Bilateral Coronal Craniosynostosis
Tovetjärn, R., Maltese, G., Wikberg, E., Bernhardt, P., Kölby, L., & Tarnow, P. (2014) · Plastic & Reconstructive Surgery Global Open · doi:10.1097/gox.0000000000000216 · Cited by 13
Magnéli, S., Howells, T. P., Saiepour, D., Nowinski, D. J., Enblad, P., & Nilsson, P. (2016) · Child s Nervous System · doi:10.1007/s00381-016-3023-4 · Cited by 13
“The risk of raised ICP is greatest in multi-suture cases where the incidence has been reported to be between 47 and 67 % [5, 6], but it also exists in single suture synostosis where the incidence is between 4 and 44 % [5–8].”
BackgroundPart 1: Surgical Correction in 231 Trigonocephaly Patients – The Alder Hey Experience
Hennedige, A. A., Richardson, D., Duncan, C. A., Parks, C., Sinha, A., Ellenbogen, J. R., & Robertson, B. (2021) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000007475 · Cited by 13
Payner, T. D., Prenger, E. C., Berger, T. S., & Crone, K. R. (1994) · Neurosurgery · doi:10.1097/00006123-199403000-00007 · Cited by 13
Heart rate variability during plateau waves of intracranial pressure: A pilot descriptive study
Luís, A. S., Santos, A. S., Dias, C., Almeida, R., & Rocha, A. P. (2015) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2015.7319794 · Cited by 12
“craniosynostosis [9], idiopathic intracranial pressure [7,10], leptomeningeal carcinomatosis and encephalitis [11].”
BackgroundPhysiological Changes and Clinical Implications of Syndromic Craniosynostosis
Sakamoto, H., Matsusaka, Y., Kunihiro, N., & Imai, K. (2016) · Journal of Korean Neurosurgical Society · doi:10.3340/jkns.2016.59.3.204 · Cited by 12
Identification and Management of Cranial Anomalies in Perinatology.
Vargo, J., Hasan, A., & Andrews, B. (2018) · Clinics of Perinatology · doi:10.1016/j.clp.2018.07.008 · Cited by 13
Current Treatment of Craniosynostosis and Future Therapeutic Directions
Wan, D. C., Kwan, M. D., Lorenz, H. P., & Longaker, M. T. (2008) · KARGER eBooks · doi:10.1159/000115043 · Cited by 12
Current Management of Craniosynostosis
Adamo, M. A., & Pollack, I. F. (2009) · Neurosurgery Quarterly · doi:10.1097/wnq.0b013e3181a32e1e · Cited by 12
Chromosome 17: Gene Mapping Studies of Cleft Lip With or Without Cleft Palate in Chinese Families
Peanchitlertkajorn, S., Cooper, M. E., Liu, Y.-E., Field, L. L., & Marazita, M. L. (2003) · The Cleft Palate-Craniofacial Journal · doi:10.1597/1545-1569(2003)040 · Cited by 24
Steady-state lumbar infusion tests in the management of children with craniosynostosis
Lundar, T., & NORNES, H. (1991) · Child s Nervous System · doi:10.1007/bf00263830 · Cited by 12
“Previous studies have demonstrated the value of ICP monitor ing in the management of children with craniosynostosis [9].”
ResultHersh, D. S., & Hughes, C. D. (2021) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2021.09.008 · Cited by 13
Bukowska‐Olech, E., Sowińska‐Seidler, A., Larysz, D., Gawliński, P., Koczyk, G., Popiel, D., Gurba-Bryśkiewicz, L., Materna‐Kiryluk, A., Adamek, Z., Szczepankiewicz, A., et al. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.865494 · Cited by 11
“Consequently, affected patients present with facial dysmorphism, cortex lesion, seizures, intellectual disability, visual and hearing impairments, or breathing difficulties that are all secondary to CS (Renier et al., 1982; Thompson et al., 1995; Tubbs et al., 2001; Gupta et al., 2003; Mathijssen and Arnaud, 2007; Chi…”
BackgroundKirman, C. N., Tran, B. W., Sanger, C., Railean, S., Glazier, S. S., & David, L. R. (2011) · Journal of Craniofacial Surgery · doi:10.1097/scs.0b013e31821cc50c · Cited by 11
“Delayed or absent surgical intervention can further result in marked visual impairment and developmental delay that may result in permanent deficits.(18,19) Our patient had evidence of chronically elevated ICP as seen on CT scan by extensive scalloping of the inner skull table and optic nerve atrophy.”
BackgroundLambdoid synostosis and occipital plagiocephaly: clinical decision rules for surgical intervention
Carson, B. S., James, C. S., VanderKolk, C. A., & Guarnieri, M. (1997) · Neurosurgical FOCUS · doi:10.3171/foc.1997.2.2.11 · Cited by 11
“Intracranial pressure may not be readily apparent on imaging studies or from clinical signs or symptoms.[9,58,67,76] Several groups”
BackgroundBlindness From Late Presenting Undiagnosed Pancraniosynostosis Mimicking Pseudotumor Cerebri
Bonfield, C. M., Tamber, M. S., & Losee, J. E. (2013) · Journal of Child Neurology · doi:10.1177/0883073813495307 · Cited by 11
“If left untreated, craniosynostosis is a potentially dangerous condition, which can lead to complications resulting from increased intracranial pressure.(2) Increased intracranial pressure usually presents with a constellation of symptoms including nausea, vomiting, headache, lethargy, and visual loss.”
BackgroundSowińska‐Seidler, A., Bukowska‐Olech, E., Socha, M., Larysz, D., & Jamsheer, A. (2018) · Journal of Applied Genetics · doi:10.1007/s13353-018-0447-4 · Cited by 11
“Consequently, increased risk for cortex lesion with intellectual disability or visual and hearing impairment is observed (Renier et al. 1982; Morriss-Kay and Wilkie 2005).”
BackgroundSensory morbidity after palatal flap surgery--fact or fiction?
Magennis, P. (1990) · PubMed · Cited by 11
Le retentissement fonctionnel des craniosténoses
Rénier, D., Arnaud, É., & Marchac, D. (2006) · Neurochirurgie · doi:10.1016/s0028-3770(06)71220-6 · Cited by 11
Metadata
- Authors
- Renier, D., Sainte-Rose, C., Marchac, D., & Hirsch, J.-F.
- Venue
- Journal of neurosurgery
- Published
- 1982-09
- Volume
- 57
- Issue
- 3
- Pages
- 370-377
- ISSN
- 0022-3085 (ISSN-L)
- OpenAlex
- W2032830902
- Cited by
- 591
- References
- 21
- Citations by year
- 2026: 18 · 2025: 9 · 2024: 28 · 2023: 23 · 2022: 29 · 2021: 34 · 2020: 21 · 2019: 23 · 2018: 31 · 2017: 28 · 2016: 20 · 2015: 19 · 2014: 18 · 2013: 19 · 2012: 17
- FWCI
- 3.23
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of neurosurgery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Craniofacial Disorders and Treatments
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Health Sciences › Medicine › Clinical Neurology › Cerebral Venous Sinus Thrombosis
- Keywords
- intracranial pressure, craniosynostosis, REM sleep, mental status, craniosynostosis surgery, pediatric patients
- MeSH terms
- Adolescent, Child, Child, Preschool, Craniosynostoses, Female, Humans, Infant, Intelligence, Intracranial Pressure, Male, Postoperative Period, Sleep, Sleep, REM
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