The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Intracranial pressure monitoring in children with single suture and complex craniosynostosis: a review
Abstract
Introduction One third of patients with craniofacial dysostosis syndromes and about 15-20% of children with single suture craniostenosis have a documented increase in intracranial pressure (ICP). The early detection of intracranial hypertension is important in order to reduce the risks for brain development and visual function. However, in children with craniosynostosis, the clinical manifestations of abnormally increased ICP are difficult to detect, as the majority of patients may have neither warning signs nor symptoms for a long period of time.Review Moreover, data from the literature suggest that neither fundoscopic nor radiological findings are necessarily related to intracranial pressure recordings in this type of pathology. In this context prolonged ICP monitoring seems actually to be the most valuable diagnostic tool. Extradural, subdural, and intraparenchymal devices have been used, and different softwares have been employed for PC storage and analysis of the data obtained. Most recent series consider mean ICP combined with plateaux waves as the most sensitive indicators in the final evaluation of the results.Conclusions The analysis of the literature demonstrates a significant difference in the prevalence of raised ICP preoperatively between non-syndromic and syndromic patients. Among the non-syndromic children, a direct relation between the number of sutures involved and raised ICP is documented. The analysis of plateaux waves seems to be particularly important in children with borderline mean ICP values. Persistent postoperative raised ICP has been described in 6-15% of patients with craniofacial dysostosis. It must be related to the multifactorial etiology of increased ICP in these patients, which includes cerebral venous congestion, upper airway obstruction, and hydrocephalus.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Environmental influences have also been proposed as contributing factors, particularly in non-syndromic cases. These include in utero mechanical constraints, maternal health conditions, medication exposure, and other prenatal risk factors [1, 2, 11, 22–25].”
From Genetics versus environment in the pathophysiology of sagittal synostosis (2026) · cites this paper as [24]
Citations
Cites
Intracranial pressure in craniostenosis
Renier, D., Sainte-Rose, C., Marchac, D., & Hirsch, J.-F. (1982) · Journal of neurosurgery · doi:10.3171/jns.1982.57.3.0370 · Cited by 591
Intracranial pressure and intracranial volume in children with craniosynostosis
Gault, D. T., Renier, D., Marchac, D., & Jones, B. M. (1992) · Plastic and Reconstructive Surgery · doi:10.1097/00006534-199209000-00003 · Cited by 309 · cited 1×
“[11] concluded that “restricted skull volume contributes to intracranial pressure, but this is not the only factor G.”
BackgroundTuite, G. F., Chong, W. K., Evanson, J., Narita, A., Taylor, D. S. I., Harkness, W. F. J., Jones, B. M., & Hayward, R. D. (1996) · Neurosurgery · doi:10.1097/00006123-199602000-00009 · Cited by 239
Intracranial Pressure in Single-Suture Craniosynostosis
Thompson, D. N. P., Malcolm, G. P., Jones, B. M., Harkness, W. F. J., & Hayward, R. D. (2008) · Pediatric Neurosurgery · doi:10.1159/000120907 · Cited by 234
Taylor, W. J., Hayward, R. D., Lasjaunias, P. L., Britto, J. A., Thompson, D. N. P., Jones, B. M., & Evans, R. D. (2001) · Journal of neurosurgery · doi:10.3171/jns.2001.94.3.0377 · Cited by 184
Subdural intracranial pressure monitoring in craniosynostosis: its role in surgical management
Thompson, D., Harkness, W., Jones, B., Gonsalez, S., Andar, U., & Hayward, R. (1995) · Child's Nervous System · doi:10.1007/bf00301758 · Cited by 152
Tuite, G. F., Evanson, J., Chong, W. K., Thompson, D. N. P., Harkness, W. F. J., Jones, B. M., & Hayward, R. D. (1996) · Neurosurgery · doi:10.1097/00006123-199610000-00007 · Cited by 136
Scientific Foundations and Surgical Treatment of Craniosynostosis
Nerad, J. A. (1989) · American Journal of Ophthalmology · doi:10.1016/0002-9394(89)90459-5 · Cited by 122
Results and Complications of Intracranial Pressure Monitoring in 303 Children
Pople, I. K., Muhlbauer, M. S., Sanford, R. A., & Kirk, E. (2008) · Pediatric Neurosurgery · doi:10.1159/000120938 · Cited by 113
Aetiology of Herniation of the Hindbrain in Craniosynostosis
Thompson, D. N. P., Harkness, W. F. J., Jones, B. M., & Hayward, R. D. (2008) · Pediatric Neurosurgery · doi:10.1159/000121208 · Cited by 89
Cited by
Sorted by citations
Neurodevelopment of children with single suture craniosynostosis: a review
Kapp‐Simon, K. A., Speltz, M. L., Cunningham, M. L., Patel, P. K., & Tomita, T. (2006) · Child s Nervous System · doi:10.1007/s00381-006-0251-z · Cited by 293
“In addition, there is a lack of consistency in the methods for assessing ICP (see [19, 119] for reviews), which makes interpretation of the available data extremely difficult.”
BackgroundMathijssen, I. M. J. (2015) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000002016 · Cited by 232
van der Meulen, J. (2012) · Child s Nervous System · doi:10.1007/s00381-012-1803-z · Cited by 169
“Levels of 8 to 20 % of elevated ICP in single-suture synostosis have been reported [27, 32, 78, 92].”
BackgroundDerderian, C. A., & Seaward, J. R. (2012) · Seminars in Plastic Surgery · doi:10.1055/s-0032-1320064 · Cited by 152
The Increase of Metopic Synostosis
van der Meulen, J., van der Hulst, R. R. W. J., van Adrichem, L. N. A., Arnaud, É., Chin-Shong, D., Duncan, C. A., Claessens, E. A. W. M. H., Hinojosa, J., Mathijssen, I. M. J., May, P. L., et al. (2009) · Journal of Craniofacial Surgery · doi:10.1097/scs.0b013e31818436be · Cited by 145
Fearon, J. A. (2014) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000000093 · Cited by 146
Genetic advances in craniosynostosis
Lattanzi, W., Barba, M., Di Pietro, L., & Boyadjiev, S. A. (2017) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.38159 · Cited by 129
Nowinski, D., Rocco, F. D., Rénier, D., SainteRose, C., Leikola, J., & Arnaud, É. (2012) · Child's Nervous System · doi:10.1007/s00381-012-1809-6 · Cited by 111
“Several mechanisms have been identified in the pathophysiology of intracranial hypertension in syndromic craniosynostosis [37].”
BackgroundThe clinical manifestations, molecular mechanisms and treatment of craniosynostosis
Stanton, E. W., Urata, M. M., Chen, J.-F., & Chai, Y. (2022) · Disease Models & Mechanisms · doi:10.1242/dmm.049390 · Cited by 117
Sylvian fissure arachnoid cysts: a survey on their diagnostic workout and practical management
Tamburrini, G., Fabbro, M. D., & Rocco, C. D. (2008) · Child s Nervous System · doi:10.1007/s00381-008-0585-9 · Cited by 111
Self-citationRaised Intracranial Pressure in Apert Syndrome
Marucci, D., Dunaway, D., Jones, B., & Hayward, R. (2008) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0b013e31818458f0 · Cited by 99
Craniofacial Syndromes and Surgery
Forrest, C. R., & Hopper, R. A. (2012) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0b013e318272c12b · Cited by 99
Recurrence of Synostosis following Surgical Repair of Craniosynostosis
Foster, K. A., Frim, D. M., & McKinnon, M. (2008) · Plastic & Reconstructive Surgery · doi:10.1097/01.prs.0000299393.36063.de · Cited by 90
Evaluation and management of nonsyndromic craniosynostosis
Ursitti, F., Fadda, T., Papetti, L., Pagnoni, M., Nicita, F., Iannetti, G., & Spalice, A. (2011) · Acta Paediatrica · doi:10.1111/j.1651-2227.2011.02299.x · Cited by 80
“Recent data using prolonged recording of intracranial pressure have suggest that increased pressure may also occur in an occasional patient with single suture fused (27).”
BackgroundIsolated sagittal craniosynostosis: definition, classification, and surgical indications
Massimi, L., Caldarelli, M., Tamburrini, G., Paternoster, G., & Di Rocco, C. (2012) · Child s Nervous System · doi:10.1007/s00381-012-1834-5 · Cited by 76
“In our experience with seven patients with isolated craniosynostosis undergone preoperative prolonged invasive recording, children with SC (three cases) and posterior brachicephaly (two cases) showed normal preoperative intracranial pressure values, differently from those with anterior brachicephaly (two cases) [43].”
BackgroundSelf-citationEvidence-Based Medicine: Nonsyndromic Craniosynostosis
Tahiri, Y. H., Bartlett, S. P. P., & Gilardino, M. S. (2017) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000003473 · Cited by 74
Neuroendoscopic treatment of arachnoid cysts of the quadrigeminal cistern: a series of 14 cases
Cinalli, G., Spennato, P., Columbano, L., Ruggiero, C., Aliberti, F., Trischitta, V., Buonocore, M. C., & Cianciulli, E. (2010) · Journal of Neurosurgery Pediatrics · doi:10.3171/2010.8.peds08491 · Cited by 71
Papilledema in Isolated Single-Suture Craniosynostosis: Prevalence and Predictive Factors
Florisson, J. M. G., van Veelen, M.-L. C., Bannink, N., van Adrichem, L. N. A., van der Meulen, J. J. N. M., Bartels, M. C., & Mathijssen, I. M. J. (2010) · Journal of Craniofacial Surgery · doi:10.1097/scs.0b013e3181c3465e · Cited by 71
Arko, L., Swanson, J. W., Fierst, T. M., Henn, R. E., Chang, D., Storm, P. B., Bartlett, S. P., Taylor, J. A., & Heuer, G. G. (2015) · Neurosurgical FOCUS · doi:10.3171/2015.3.focus153 · Cited by 67
Early Frontofacial Symmetry After Correction of Unilateral Coronal Synostosis
Tan, S. P. K., Proctor, M. R., Mulliken, J. B., & Rogers, G. F. (2013) · Journal of Craniofacial Surgery · doi:10.1097/scs.0b013e318299742e · Cited by 67
“Frontoorbital advancement also expands cranial volume, thus reducing potential elevation in intracranial pressure, which can occur in a small percentage of these patients.(12) Nevertheless, FOA is associated with significant blood loss, a 4- to 5-day hospitalization, and the potential for major complications.”
BackgroundCranial Ultrasound as a First-Line Imaging Examination for Craniosynostosis
Rozovsky, K., Udjus, K., Wilson, N., Barrowman, N. J., Simanovsky, N., & Miller, E. (2016) · Pediatrics · doi:10.1542/peds.2015-2230 · Cited by 64
Tamburrini, G., Caldarelli, M., Massimi, L., Gasparini, G. M., Pelo, S., & Rocco, C. D. (2012) · Child s Nervous System · doi:10.1007/s00381-012-1819-4 · Cited by 58
“The detection of elevated intracranial pressure cannot be easy [52, 65].”
BackgroundInfluentialSelf-citationIsaac, K. V., MacKinnon, S. E., Dagi, L. R., Rogers, G. F., Meara, J. G., & Proctor, M. R. (2018) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000005383 · Cited by 57
Hankinson, T. C., Fontana, E. J., Anderson, R. C. E., & Feldstein, N. A. (2010) · Journal of Neurosurgery Pediatrics · doi:10.3171/2010.5.peds09313 · Cited by 56
A late complication of CSF shunting: acquired Chiari I malformation
Caldarelli, M., Novegno, F., & Rocco, C. D. (2008) · Child s Nervous System · doi:10.1007/s00381-008-0760-z · Cited by 56
“Only three patients (cases 14, 15, and 16) underwent prolonged ICP recordings (48, 72, and 144 h, respectively) utilizing an ad hoc personally devised computerized system, already described in previous papers [7, 21, 22 ].”
MethodSelf-citationPapilledema in Patients With Apert, Crouzon, and Pfeiffer Syndrome
Bannink, N., Joosten, K. F. M., van Veelen, M. C., Bartels, M. C., Tasker, R. C., van Adrichem, L. N. A., van der Meulen, J. J. N. M., Vaandrager, J. M., de Jong, T. H. R., & Mathijssen, I. M. J. (2008) · Journal of Craniofacial Surgery · doi:10.1097/scs.0b013e31815f4015 · Cited by 56
“Information on the frequency of this problem, however, is limited.(9) Clinically, it is difficult to recognize significantly elevated ICP in these children because symptoms can be vague.”
BackgroundIntraoperative intracranial pressure monitoring in the pediatric craniosynostosis population
Judy, B. F., Swanson, J. W., Yang, W., Storm, P. B., Bartlett, S. P. P., Taylor, J. A., Heuer, G. G., & Lang, S. (2018) · Journal of Neurosurgery Pediatrics · doi:10.3171/2018.5.peds1876 · Cited by 56
“23,28,29 Tuite et al. 28 hypothesized that papilledema in the young may be decreased due to the greater compliance of the unfused sutures, which may afford protection for the optic nerve from the effects of ICP.”
BackgroundResultInfluentialNeurodevelopmental Problems in Non-Syndromic Craniosynostosis
Shim, K., Park, E.-K., Kim, J.-S., Kim, Y. O., & Kim, D.-S. (2016) · Journal of Korean Neurosurgical Society · doi:10.3340/jkns.2016.59.3.242 · Cited by 53
First Vault Expansion in Apert and Crouzon-Pfeiffer Syndromes: Front or Back?
Spruijt, B., Rijken, B., den Ottelander, B. D., Joosten, K., Lequin, M., Loudon, S., van Veelen, M. V., & Mathijssen, I. (2016) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0000000000001894 · Cited by 51
A National Study on Craniosynostosis Surgical Repair
Nguyen, C. P., Hernandez‐Boussard, T., Khosla, R. K., & Curtin, C. M. (2012) · The Cleft Palate-Craniofacial Journal · doi:10.1597/11-324 · Cited by 50
Eley, K., Johnson, D. W., Wilkie, A. O., Jayamohan, J., Richards, P., & Wall, S. (2012) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0b013e318267d5ae · Cited by 43
Bonfield, C. M., Lee, P. S., Adamo, M. A., & Pollack, I. F. (2014) · Journal of Cranio-Maxillofacial Surgery · doi:10.1016/j.jcms.2014.01.036 · Cited by 46
“The prevalence of elevated ICP has been estimated to be as high as 20% in single suture synostosis (Tamburrini et al., 2005).”
BackgroundBlount, J. P., Louis, R. G., Tubbs, R. S., & Grant, J. H. (2007) · Child s Nervous System · doi:10.1007/s00381-007-0362-1 · Cited by 46
“[47] found that among nonsyndromic children with craniosynostosis, there is a direct relation between the number of sutures involved and the raised intracranial pressure documented.”
BackgroundSimanovsky, N., Hiller, N., Koplewitz, B. Z., & Rozovsky, K. (2008) · European Radiology · doi:10.1007/s00330-008-1193-5 · Cited by 42
“Even in cases of single-suture synostosis, there is significant risk of increased ICP due to a variety of mechanisms, including cerebral venous congestion, upper airway obstruction, and hydrocephalus [4].”
BackgroundMa, L., Chang, Q., Pei, F., Liu, M., Zhang, W., Hong, Y., Chai, Y., & Chen, J. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.09.012 · Cited by 41
Revisiting Crouzon syndrome: reviewing the background and management of a multifaceted disease
Helman, S. N., Badhey, A. K., Kadakia, S., & Myers, E. (2014) · Oral and Maxillofacial Surgery · doi:10.1007/s10006-014-0467-0 · Cited by 43
“Early on in the course of this syndrome, acute treatment prioritizes airway management and offsetting elevated ICP.”
InfluentialCraniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical Problems
Choi, J. W., Lim, S.-Y., & Shin, H.-J. (2016) · Journal of Korean Neurosurgical Society · doi:10.3340/jkns.2016.59.3.197 · Cited by 39
Intracranial Volume and Head Circumference in Children with Unoperated Syndromic Craniosynostosis
Breakey, R. W., Knoops, P. G., Borghi, A., Rodríguez-Flórez, N., O'Hara, J., James, G., Dunaway, D., Schievano, S., & Jeelani, N. U. O. (2018) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0000000000004843 · Cited by 41
Intracranial Volume and Whole Brain Volume in Infants with Unicoronal Craniosynostosis
Hill, C. A., Vaddi, S., Moffitt, A. J., Kane, A. A., Marsh, J. L., Panchal, J., Richtsmeier, J. T., & Aldridge, K. J. (2010) · The Cleft Palate-Craniofacial Journal · doi:10.1597/10-051 · Cited by 39
“The link between decreased ICV and elevated ICP is tenuous; a strong relationship between ICP and ICV has yet to be identified in infants with either syndromic or nonsyndromic craniosynostosis (Fok et al., 1992; Gault et al., 1992; Tamburrini et al., 2005).”
BackgroundLevitt, M. R., Niazi, T. N., Hopper, R. A., Ellenbogen, R. G., & Ojemann, J. G. (2012) · Journal of Neurosurgery Pediatrics · doi:10.3171/2011.11.peds11268 · Cited by 38
Occipital plagiocephaly: unilateral lambdoid synostosis versus positional plagiocephaly
Linz, C., Collmann, H., Meyer‐Marcotty, P., Böhm, H., Krauß, J., Müller-Richter, U. D. A., Ernestus, R., Wirbelauer, J., Kübler, A. C., & Schweitzer, T. (2014) · Archives of Disease in Childhood · doi:10.1136/archdischild-2014-305944 · Cited by 36
Diagnosis of infant synostotic and nonsynostotic cranial deformities: a review for pediatricians
Ghizoni, E., Denadai, R., Raposo‐Amaral, C. A., Joaquim, A. F., Tedeschi, H., & Raposo-Amaral, C. E. (2016) · Revista Paulista de Pediatria (English Edition) · doi:10.1016/j.rppede.2016.02.005 · Cited by 36
Ghali, G. Z., Ghali, M. G. Z., Ghali, E. Z., Srinivasan, V. M., Wagner, K. M., Rothermel, A. T., Taylor, J. A., Johnson, J. N., Kan, P., Lam, S. K., et al. (2018) · World Neurosurgery · doi:10.1016/j.wneu.2018.07.260 · Cited by 35
Jaszczuk, P., Rogers, G. F., Guzman, R. G., & Proctor, M. R. (2015) · Child s Nervous System · doi:10.1007/s00381-015-2934-9 · Cited by 35
“[25].”
Effectiveness and Safety of Independent Pediatric Nurse Practitioners in Evaluating Plagiocephaly
Kuang, A. A., Bergquist, C. S., Crupi, L., Oliverio, M., & Selden, N. R. W. (2013) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0b013e3182958a89 · Cited by 34
Update in Management of Craniosynostosis
Xue, A. S., Buchanan, E. P., & Hollier, L. H. (2022) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000009046 · Cited by 34
Implications of a Vertex Bulge following Modified Strip Craniectomy for Sagittal Synostosis
Marucci, D. D., Johnston, C. P., Anslow, P., Jayamohan, J., Richards, P. G., Wilkie, A. O. M., & Wall, S. A. (2008) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0b013e3181774240 · Cited by 35
Management of Facial Asymmetry
Sándor, G. K. B., McGuire, T. P., Ylikontiola, L. P., Serlo, W. S., & Pirttiniemi, P. M. (2007) · Oral and Maxillofacial Surgery Clinics of North America · doi:10.1016/j.coms.2007.05.001 · Cited by 33
Zhang, R. S., Wes, A. M., Naran, S., Hoppe, I. C., Sun, J. J., Mazzaferro, D. M., Bartlett, S. P. P., & Taylor, J. A. (2018) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000004230 · Cited by 33
“Nonsyndromic patients with multisutural involvement are more prone to developing increased ICP, and the frequency doubles after 1 year of age.(4,12) Debate regarding optimal timing of surgery continues, although delayed intervention is associated with increased morbidity.”
Study, T. N. B. D. P., Justice, C. M., Cuellar, A., Bala, K., Sabourin, J., Cunningham, M. L., Crawford, K. L., Phipps, J. M., Zhou, Y., Cilliers, D. D., et al. (2020) · Human Genetics · doi:10.1007/s00439-020-02157-z · Cited by 32
Self-citationSurgical Correction of Nonsyndromic Sagittal Craniosynostosis
Simpson, A. M., Wong, A. L., & Bezuhly, M. (2016) · Annals of Plastic Surgery · doi:10.1097/sap.0000000000000713 · Cited by 33
Management of Craniosynostosis at an Advanced Age
Iyengar, R. J., Klinge, P. M., Chen, W. S., Boxerman, J. L., Sullivan, S. R., & Taylor, H. O. B. (2016) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000002725 · Cited by 32
“%) underwent ICP measurements either at the time of surgery (epidural monitoring) or prior to surgery (intraparenchymal monitoring), and 3 of these patients (30% of total, and 75% of those measured) had documented elevations in ICP.”
BackgroundInfluentialHaredy, M. M., Zuccoli, G., Tamber, M. S., Davis, A. A., Nischal, K. K., & Goldstein, J. A. (2018) · Child s Nervous System · doi:10.1007/s00381-018-3728-7 · Cited by 32
“Intracranial hypertension has been estimated to affect 15 to 20% of patients with single suture craniosynostosis [2, 3] and 50 to 75% of those with multisutural craniosynostosis”
BackgroundSwanson, J. W., Xu, W., Ying, G., Pan, W., Lang, S., Heuer, G. G., Bartlett, S. P. P., & Taylor, J. A. (2019) · Child s Nervous System · doi:10.1007/s00381-019-04448-x · Cited by 30
Elevated Intracranial Pressure in Patients with Craniosynostosis by Optical Coherence Tomography
Kalmar, C. L., Humphries, L. S., McGeehan, B., Ying, G., Heuer, G. G., Liu, G. T., Avery, R. A., Bartlett, S. P. P., Taylor, J. A., Lang, S., et al. (2022) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000008821 · Cited by 30
Flanagan, M. F. (2015) · Neurology Research International · doi:10.1155/2015/794829 · Cited by 29
Endoscopic-assisted osteotomies for the treatment of craniosynostosis
Hinojosa, J., Esparza, J., & Muñoz, M. J. (2007) · Child s Nervous System · doi:10.1007/s00381-007-0473-8 · Cited by 30
“Concern of parents and the fact understood by pediatricians that some of these cases may be followed by increased intracranial pressure when left uncorrected [24, 25] have led to a rising awareness in the follow-up and treatment of these children.”
BackgroundCraniosynostosis and hydrocephalus: relevance and treatment modalities
Frassanito, P., Palombi, D., & Tamburrini, G. (2021) · Child s Nervous System · doi:10.1007/s00381-021-05158-z · Cited by 29
“Therefore, careful monitoring of intracranial pressure and ventricular size in the pre- and postoperative period is a diagnostic mainstay [29].”
BackgroundSelf-citationCurrent Controversies in Metopic Suture Craniosynostosis
Jaskolka, M. S. (2017) · Oral and Maxillofacial Surgery Clinics of North America · doi:10.1016/j.coms.2017.07.003 · Cited by 29
van der Meulen, J., van der Vlugt, J., Okkerse, J. M. E., & Albert Hofman, D. (2008) · Journal of Neurosurgery Pediatrics · doi:10.3171/ped-08/01/025 · Cited by 29
Shruthi, N. M., & Gulati, S. (2022) · Journal of Pediatric Neurosciences · doi:10.4103/jpn.jpn_25_22 · Cited by 27
Kunz, M., Lehner, M., Heger, A., Armbruster, L., Weigand, H., Mast, G., & Peraud, A. (2014) · Child's Nervous System · doi:10.1007/s00381-013-2340-0 · Cited by 30
Langvatn, E. A., Frič, R., Due‐Tønnessen, B. J., & Eide, P. K. (2019) · Journal of Neurosurgery Pediatrics · doi:10.3171/2019.2.peds18767 · Cited by 25
Rattani, A., Riordan, C. P., Meara, J. G., & Proctor, M. R. (2020) · Journal of Neurosurgery Pediatrics · doi:10.3171/2020.2.peds19522 · Cited by 26
Park, D. H., Chung, J., & Yoon, S. H. (2010) · Pediatric Neurosurgery · doi:10.1159/000319005 · Cited by 25
Craniofacial reconstruction as a treatment for elevated intracranial pressure
Baird, L. C., Gonda, D. D., Cohen, S. R., Evers, L. H., LeFloch, N., Levy, M. L., & Meltzer, H. S. (2011) · Child s Nervous System · doi:10.1007/s00381-011-1615-6 · Cited by 25
“Others have argued that this scale is not relevant in the setting of craniosynostosis [24].”
BackgroundInfluentialNormocephalic Pancraniosynostosis Resulting in Late Presentation of Elevated Intracranial Pressures
Foo, R., Whitáker, L. A., & Bartlett, S. P. P. (2010) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0b013e3181d62b48 · Cited by 24
Cranial Fossa Volume and Morphology Development in Apert Syndrome
Lu, X., Forte, A. J., Wilson, A. T., Steinbacher, D. M., Alperovich, M. A., Alonso, N., & Persing, J. A. (2020) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000006679 · Cited by 22
Frame-based cranial reconstruction
Hochfeld, M. S., Lamecker, H., Thomale, U., Schulz, M., Stefan Zachow, A., & Haberl, H. (2014) · Journal of Neurosurgery Pediatrics · doi:10.3171/2013.11.peds1369 · Cited by 22
Airway anomalies in patients with craniosynostosis
Mathews, F., Shaffer, A. D., Georg, M. W., Ford, M. D., Goldstein, J. A., Jabbour, N., & Simons, J. P. (2018) · The Laryngoscope · doi:10.1002/lary.27589 · Cited by 21
Trigonocephaly: Long-term results after surgical correction of metopic suture synostosis
Wójcicki, P., & Prudel, B. (2019) · Advances in Clinical and Experimental Medicine · doi:10.17219/acem/90763 · Cited by 21
Posterior calvarial distraction for complex craniosynostosis and cerebellar tonsillar herniation
Lo, W. B., Thant, K. Z., Kaderbhai, J., White, N., Nishikawa, H., Dover, M. S., Evans, M., & Rodrigues, D. (2020) · Journal of Neurosurgery Pediatrics · doi:10.3171/2020.4.peds19742 · Cited by 21
Kunz, A., & Iliadis, C. (2007) · Child s Nervous System · doi:10.1007/s00381-007-0468-5 · Cited by 21
“For example, in sagittal synostosis, there is the well-known compression of the superior sagittal sinus [29], and in craniosynostosis-related syndromes or the non-syndromic multiple suture synostosis, a stenotic or no-flow of the sigmoid-jugular sinus complex is seen, again producing this hypertensive state [30].”
BackgroundSpruijt, B., Mathijssen, I., Bredero-Boelhouwer, H., Cherian, P., Corel, L., van Veelen, M. V., Hayward, R., Tasker, R., & Joosten, K. (2016) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0000000000002741 · Cited by 22
Rufai, S. R., Jeelani, O., & McLean, R. J. (2020) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000006771 · Cited by 20
“Direct intraparenchymal measurement represents the gold standard, but involves hospital admission and carries risks of infection, bleeding, and device failure.(6) Noninvasive methods such as ophthalmoscopy,(9) transorbital ultrasound,(10) and radiography(11) deliver inadequate sensitivity to be used for screening.”
BackgroundThe Risk of Psychopathology in Children with Craniosynostosis
van der Vlugt, J., van der Meulen, J., Creemers, H., Willemse, S. P., Lequin, M. L., & Okkerse, J. (2009) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0b013e3181bcf2dc · Cited by 16
Kadakia, S., Helman, S. N., Healy, N. J., Saman, M., & Wood‐Smith, D. (2014) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000001121 · Cited by 20
“Conclusions: This study collates surgical management data from CS and other related syndromes as a means of establishing a cohesive approach to the surgical treatment of CS. Key Words: Carpenter syndrome, craniofacial surgery, acrocephalopolysyndactyly, craniosynostosis, craniofacial reconstruction, syndactyly/brachyd…”
BackgroundInfluentialMa, R., Rowland, D., Judge, A., Calisto, A., Jayamohan, J., Johnson, D., Richards, P., Magdum, S. A., & Wall, S. A. (2018) · Journal of Neurosurgery Pediatrics · doi:10.3171/2017.9.peds17360 · Cited by 20
Pellicer, E., Siebold, B. S., Birgfeld, C. B., & Gallagher, E. R. (2018) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000004180 · Cited by 20
Brookes, C. D., Golden, B. A., & Turvey, T. A. (2014) · Atlas of the Oral and Maxillofacial Surgery Clinics · doi:10.1016/j.cxom.2014.04.001 · Cited by 20
“Venous congestion, hydrocephalus, and upper airway obstruction likely all contribute to intracranial hypertension.(16,59)”
BackgroundKuta, V., Curry, L. C., McNeely, D., Walling, S. A., Chorney, J. M. L., & Bezuhly, M. (2020) · BMJ Open · doi:10.1136/bmjopen-2019-033403 · Cited by 19
Sader, N., Mehta, V., Hart, S., Bliss, L., Moore, H., DaSilva, M., Rashid, R., & Riva-Cambrin, J. (2021) · Journal of Neurosurgery Pediatrics · doi:10.3171/2021.5.peds2136 · Cited by 20
Electrophysiological and fundoscopic detection of intracranial hypertension in craniosynostosis
Rufai, S. R., Marmoy, O. R., Thompson, D., van de Lande, L. S., Breakey, R. W. F., Bunce, C., Panteli, V., Schwiebert, K., Mohamed, S., Proudlock, F. A., et al. (2022) · Eye · doi:10.1038/s41433-021-01839-w · Cited by 18
“IH occurs in 30–40% [4, 5] of the syndromic cases, most commonly in patients diagnosed with Apert (71%) [6], Crouzon (61%) [7] and Pfeiffer (60%) [8] syndromes.”
BackgroundCognitive Development in Single-Suture Craniosynostosis – A Systematic Review
Olsson, K., Engman, J. H., Nowinski, D. J., Ramklint, M., & Frick, M. A. (2023) · Developmental Neuropsychology · doi:10.1080/87565641.2023.2225662 · Cited by 18
“There is a well-known risk for raised intracranial pressure in some forms of CS, particularly in certain genetic syndromes such as Crouzon and Apert (Tamburrini et al., 2005).”
BackgroundPitfalls for the Pediatrician: Positional Molding or Craniosynostosis?
Komotar, R. J., Zacharia, B. E., Ellis, J. A., & Feldstein, N. A. (2006) · Pediatric Annals · doi:10.3928/0090-4481-20060501-08 · Cited by 18
Saethre–Chotzen syndrome: long‐term outcome of a syndrome‐specific management protocol
den Ottelander, B. K., van Veelen, M. C., de Goederen, R., van de Beeten, S. D. C., Dremmen, M. H. G., Loudon, S. E., Versnel, S. L., van den Ouweland, A. M., van Dooren, M. F., Joosten, K. F. M., et al. (2020) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.14670 · Cited by 17
“The latest available test results were evaluated, since papilledema may have a long-term effect on vision.(13) Confounding caused by strabismus and/or amblyopia was minimalized by using the eye with the best visual acuity.”
MethodRufai, S. R., Bowman, R. J. C., Bunce, C., Panteli, V., McLean, R. J., Teli, S., Gottlob, I., Thomas, M. G., Jeelani, O., & Proudlock, F. A. (2021) · Translational Vision Science & Technology · doi:10.1167/tvst.10.8.24 · Cited by 16
Fronto-Orbital Advancement for Metopic and Unilateral Coronal Craniosynostoses
Massenburg, B. B., Tolley, P. D., Lee, A., & Susarla, S. M. (2022) · Oral and Maxillofacial Surgery Clinics of North America · doi:10.1016/j.coms.2022.01.001 · Cited by 16
The genetic overlap between osteoporosis and craniosynostosis
Kague, É., Medina‐Gómez, C., Boyadjiev, S. A., & Rivadeneira, F. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1020821 · Cited by 16
“Thus, affected children may experience ongoing medical complications, such as increased intracranial pressure (66, 67), vision problems (optic neuropathy secondary to elevated intracranial pressure, strabismus, refracture errors, exposure keratopathy from exorbitism) (68), and learning disabilities (69–71).”
BackgroundMarupudi, N. I., Sood, S., Rozzelle, A. A., & Ham, S. D. (2016) · Journal of Neurosurgery Pediatrics · doi:10.3171/2016.1.peds15569 · Cited by 16
Telemetric Intracranial Pressure Monitoring in Syndromic Craniosynostosis
Beez, T., O’Kane, R., Piper, I., Koppel, D. A., & Sangra, M. (2016) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000002556 · Cited by 16
“This risk is highest in patients of syndromic craniosynostosis involving multiple sutures, with 90% of patients having raised ICP.2 However, children with single suture craniosynostosis can also be affected and the incidence of raised Copyright © 2016 Mutaz B. Habal, MD. Unautho # 2016 Mutaz B. Habal, MD ICP in this s…”
MethodInfluentialThe role of ICP overnight monitoring (ONM) in children with suspected craniostenosis
Zipfel, J., Jager, B., Collmann, H., Czosnyka, Z. H., Schuhmann, M. U., & Schweitzer, T. (2019) · Child s Nervous System · doi:10.1007/s00381-019-04288-9 · Cited by 16
Rufai, S. R., Hisaund, M., Jeelani, O., & McLean, R. J. (2021) · BMJ Open · doi:10.1136/bmjopen-2020-046935 · Cited by 15
Rojas-Peña, M. L., Olivares‐Navarrete, R., Hyzy, S. L., Arafat, D., Schwartz, Z., Boyan, B. D., Williams, J. K., & Gibson, G. C. (2014) · Journal of Genomics · doi:10.7150/jgen.8833 · Cited by 15
“Atypical growth of the cranium could be related to aberrant mechanical pressure on the developing skull in utero, compromising cerebral blood flow (11).”
BackgroundDifferential spatial regulation of BMP molecules is associated with single-suture craniosynostosis
Whitton, A., Hyzy, S. L., Britt, C., Williams, J. K., Boyan, B. D., & Olivares‐Navarrete, R. (2016) · Journal of Neurosurgery Pediatrics · doi:10.3171/2015.12.peds15414 · Cited by 15
Normalization of Speech Processing After Whole-Vault Cranioplasty in Sagittal Synostosis
Chuang, C., Rolison, M. J., Yang, J. F., Brooks, E. D., Hashim, P. W., Travieso, R., Terner, J. S., Steinbacher, D. M., Landi, N., Stavropoulos, K. K. M., et al. (2018) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000004474 · Cited by 15
Yokote, A., Aihara, Y., Eguchi, S., & Okada, Y. (2013) · Child s Nervous System · doi:10.1007/s00381-013-2049-0 · Cited by 15
Letter to the Editor: Raised intracranial pressure and nonsyndromic sagittal craniosynostosis
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
Haredy, M. M., Liasis, A. C., Fu, V. L. N., Davis, A. A., Pollack, I. F., Losee, J. E., Saied, S. M. A., Nischal, K. K., & Goldstein, J. A. (2019) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000005935 · Cited by 14
van Nunen, D. P. F., Stubenitsky, B. M., Woerdeman, P. A., Han, K. S., Breugem, C. C., van der Molen, A. B. M., & de Graaff, J. C. (2016) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000003072 · Cited by 14
Metadata
- Authors
- Tamburrini, G., Caldarelli, M., Massimi, L., Santini, P., & Di Rocco, C.
- Affiliations
- Agostino Gemelli University Polyclinic (IT)
- Corresponding author
- Tamburrini, G.
- Venue
- Child's Nervous System
- Published
- 2005-05-03
- Volume
- 21
- Issue
- 10
- Pages
- 913-921
- ISSN
- 0256-7040 (ISSN-L)
- 1433-0350
- OpenAlex
- W2044133352
- Cited by
- 261
- References
- 36
- Citations by year
- 2026: 14 · 2025: 8 · 2024: 19 · 2023: 11 · 2022: 23 · 2021: 21 · 2020: 21 · 2019: 17 · 2018: 19 · 2017: 12 · 2016: 16 · 2015: 12 · 2014: 13 · 2013: 6 · 2012: 12
- FWCI
- 2.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Child s Nervous System (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 monitoring, craniosynostosis, single-suture craniosynostosis, intracranial hypertension, cerebral venous congestion, upper airway obstruction, hydrocephalus, children
- MeSH terms
- Cerebrospinal Fluid Shunts, Child, Child, Preschool, Cranial Sutures, Craniosynostoses, Craniotomy, Humans, Intracranial Pressure, Monitoring, Physiologic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
