Using spectral-domain optical coherence tomography to detect optic neuropathy in patients with craniosynostosis

Dagi, Linda R.; Tiedemann, Laura M.; Heidary, Gena; Robson, Caroline D.; Hall, Amber M.; Zurakowski, David

doi:10.1016/j.jaapos.2014.07.177

Cited by 23 publications

(24 citation statements)

References 26 publications

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“…Sun studied 36 patients with scaphocephaly treated with a minimally invasive technique with spring distraction. 35 At a mean age of 3.9 months (range 1.9 -9.2 months), the age at surgery strongly related to the change in cranial index: for each additional month in age the change in CI decreased by 1.3 (p ¼ 0.03).…”

Section: A) Sagittal Suture Synostosismentioning

confidence: 92%

“…34 Other authors have described similar results. 35,36 Dagi describes 54 patients with a wide variety of types of isolated and syndromic craniosynostosis. 35 The sensitivity of OCT to detect papilledema was 60% and the specificity 90%.…”

Section: Conclusion ---mentioning

confidence: 99%

“…35,36 Dagi describes 54 patients with a wide variety of types of isolated and syndromic craniosynostosis. 35 The sensitivity of OCT to detect papilledema was 60% and the specificity 90%. In the study by Swanson, 40 patients with craniosynostosis received an OCT, 5 patients with hydrocephalus and increased ICP and 34 healthy controls.…”

Section: Conclusion ---mentioning

confidence: 99%

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Updated Guideline on Treatment and Management of Craniosynostosis

Mathijssen

2020

Journal of Craniofacial Surgery

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Working Group Guideline Craniosynostosis Contents Chapter 1. Introduction Chapter 2. Methodology for guideline development Chapter 3. Referral and diagnostics Chapter 4. Perioperative care Chapter 5. Surgical treatment of isolated, non-syndromic craniosynostosis Chapter 6. Surgical treatment of multisuture and syndromic craniosynostosis-the cranial vault Chapter 7. Surgical treatment of syndromic craniosynostosis-FACE Chapter 8. Increased intracranial pressure Chapter 9. Hydrocephalus Chapter 10. Chiari Chapter 11. Visual, refractive and motility impairments Chapter 12. Respiratory disorders Chapter 13. Hearing impairments and speech/language development Chapter 14. Dentofacial abnormalities Chapter 15. (Neuro)cognitive, socio-emotional and behavioural functioning Chapter 16. Psychosocial functioning Chapter 17. Criteria for craniosynostosis expertise center and team members From the Chair of the working group Guideline Craniosynostosis,

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Section: A) Sagittal Suture Synostosismentioning

confidence: 92%

Section: Conclusion ---mentioning

confidence: 99%

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Updated Guideline on Treatment and Management of Craniosynostosis

Mathijssen

2020

Journal of Craniofacial Surgery

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“…Allerdings wird nur bei einem Teil der Kinder mit Optikusatrophie eine vorangehende Stauungspapille beobachtet. Möglicherweise können gering ausgeprägte Nervenfaserödeme durch die OCT sensitiver erfasst werden (26).…”

Section: Kraniosynostosenunclassified

Veränderungen der Papilla nervi optici im Kindesalter

Tegetmeyer¹

2018

Kinder- und Jugendmedizin

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ZusammenfassungDie Papilla nervi optici ist mithilfe der ophthalmoskopischen Untersuchung der visuellen Inspektion zugänglich. Dadurch ist es möglich, bereits im Säuglings- und frühen Kindesalter Papillenveränderungen zu erkennen, die mit angeborenen Fehlbildungen des Gehirns einhergehen können oder durch Tumoren, akute Erkrankungen des Sehnerven oder des Zentralnervensystems verursacht werden. Zur Dokumentation, Quantifizierung und Verlaufsbeobachtung der Papillenveränderungen stehen verschiedene bildgebende Verfahren zur Verfügung. Die Einteilung der Papillenveränderungen in angeborene Anomalien, in Papillenveränderungen mit Papillenprominenz und in atrophische Veränderungen im Rahmen einer Optikusatrophie hat sich für die Differenzialdiagnose möglicher Ursachen bewährt. Daraus lassen sich in Kooperation zwischen Pädiatern und Ophthalmologen gezielt weiterführende diagnostische und therapeutische Maßnahmen ableiten.

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“…4). By providing a detailed examination of the retina and optic nerve head, equivalent in many ways to an in vivo, noninvasive biopsy, OCT has been shown to be a valuable tool in the diagnosis and monitoring of a number of pathologies, including glaucoma [50,51], macular degeneration [52], papilledema [53], and optic neuropathy in older children with craniosynostosis [54].…”

Section: Optical Coherence Tomography (Oct)mentioning

confidence: 99%

Noninvasive methods of detecting increased intracranial pressure

Gerety

Alemán

et al. 2016

Childs Nerv Syst

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The detection of elevated intracranial pressure (ICP) is of paramount importance in the diagnosis and management of a number of neurologic pathologies. The current gold standard is the use of intraventricular or intraparenchymal catheters; however, this is invasive, expensive, and requires anesthesia. On the other hand, diagnosing intracranial hypertension based on clinical symptoms such as headaches, vomiting, and visual changes lacks sensitivity. As such, there exists a need for a noninvasive yet accurate and reliable method for detecting elevated ICP. In this review, we aim to cover both structural modalities such as computed tomography (CT), magnetic resonance imaging (MRI), ocular ultrasound, fundoscopy, and optical coherence tomography (OCT) as well as functional modalities such as transcranial Doppler ultrasound (TCD), visual evoked potentials (VEPs), and near-infrared spectroscopy (NIRS).

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Using spectral-domain optical coherence tomography to detect optic neuropathy in patients with craniosynostosis

Cited by 23 publications

References 26 publications

Updated Guideline on Treatment and Management of Craniosynostosis

Updated Guideline on Treatment and Management of Craniosynostosis

Veränderungen der Papilla nervi optici im Kindesalter

Noninvasive methods of detecting increased intracranial pressure

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