In-vivo high resolution imaging of optic nerve head drusen using spectral-domain Optical Coherence Tomography
© Murthy et al; licensee BioMed Central Ltd. 2010
Received: 8 January 2010
Accepted: 7 June 2010
Published: 7 June 2010
Optic nerve head drusen (ONHD) are white calcareous deposits, seen either superficially on the optic nerve head or buried within it. Diagnosis of ONHD is made by one or more ways: clinical exam, autofluorescence, ultrasound of the optic nerve, CT scan and/or visual field examination. The present study describes features of ONHD based on another diagnostic modality, the spectral-domain OCT (Spectralis).
This is a retrospective case series of 5 patients with bilateral ONHD with a best-corrected visual acuity of 20/20 and no other posterior segment pathology. All the patients underwent fundus photography, fundus autofluorescence, B-scan ultrasonography, Spectralis OCT and Humphrey 30-2 threshold visual fields.
All 5 patients had surface ONHD which were autofluorescent and echodense on B-scan ultrasonography. Spectralis OCT findings in the corresponding areas include 'scattered spots with high reflectivity' casting a shadow underneath. The reflectivity can be distinctly differentiated from the blood vessels on the optic nerve. Two patients had an arcuate scotoma on the Humphrey visual fields. No correlation was found between the changes on Spectralis OCT with that of visual field.
Spectralis OCT is another useful ancillary investigation in the diagnosis of ONHD and we describe the features in the present study.
Optic Nerve Head Drusen (ONHD) are white calcareous deposits that are generally asymptomatic and are bilateral in 66-85% of cases . They are characteristically found in the pre-laminar region of the ONH and are believed to arise from the debris due to long standing axonal stasis in the nerve fibre layer . Histopathologically, the drusen contain multiple deposits of calcium crystals that vary in size (5 to 1000 microns) [2, 3]. These crystals mechanically compress the overlying nerve fibre layer resulting in progressive visual field defects .
The diagnosis of ONHD is based upon a strong index of suspicion and confirmed by B-scan ultrasound of the posterior segment, which shows echodense structure with acoustic shadowing. CT scan may be required in the rare case when ultrasound is inconclusive [1–3]. Time-domain Stratus OCT has been used in recent years to document the nerve fibre layer changes associated with drusen . However, the poor resolution of time-domain OCT prevents the visualization of changes seen as a result of mechanical compression due to the drusen.
Spectral-domain Optical Coherence Tomography (SD-OCT) by its ability to acquire 40000 A-scans per second provides high resolution images of the Optic nerve head . In this case series we describe SD-OCT findings in 5 cases of ONHD.
This is a retrospective case series report of 5 patients with ONHD in whom changes seen on spectral domain OCT (SD-OCT) were documented. Approval for this study was obtained from the University of Florida Institutional Review Board-03 (Reference number: 2008-003). Five patients with bilateral ONHD with best corrected visual acuity 20/20 and no other posterior segment pathology were included in this series. All the patients underwent a detailed ocular examination, posterior segment digital fundus photography (Zeiss FF450, Carl Zeiss, US), fundus angiography to document autofluorescence (Spectralis, Heidelberg Engineering, Germany) and B-scan ultrasonography of the posterior segment (Sonomed Inc, US).
Optic nerve head scans, using the Spectralis OCT (Heidelberg Engineering, Germany) were done on all the patients by an experienced operator using the raster lines protocol. The area scanned was 4 mm by 4 mm at 50 micron intervals. Cross-sectional images, one per second, were obtained with a longitudinal resolution of 7 μm. Patient's fixation was monitored by asking the patient to look at an internal fixation or by guiding through an infrared monitoring camera.
Results and Discussion
SD-OCT by its ability to acquire 100 times more number of A-scans as compared to Stratus OCT provides high resolution images of the cross section of the optic nerve head, a close approximation to the histopathological section [6–9]. In our case, the SD-OCT showed dense spots within the nerve fibre layer of the ONH causing shadowing underneath, corresponding to the calcium content of the drusen. In areas corresponding to the drusen, lacunar areas with a single spot of high reflectivity was noted, which we describe as a 'cap' sign. These probably correspond to the nidus of calcification seen histopathologically in the early stages of the formation of drusen. This feature helps in differentiating circular areas of decreased reflectivity seen as the major blood vessels cast an optical shadow underneath. In addition, SD-OCT is useful in detecting the buried drusen which are not obvious on clinical examination.
Visual field changes described in cases of ONHD are characteristically arcuate scotomas corresponding to the nerve fibre layer defects arising out of mechanical compression due to the drusen . In our series, two patients had an arcuate scotoma on the Humphrey visual fields. However, these changes could not be correlated as there were no corresponding baseline scans available. These changes are also commonly seen in surface rather than buried drusen which was the case in two of our patients. Further study of a larger population of patients with serial follow up is required to validate the use of spectral-domain OCT in the management of patients with ONHD.
In summary, SD-OCT is a useful ancillary investigation in the diagnosis of optic nerve head drusen and in documenting the changes seen in retinal nerve fibre layer due to the compressive effects of the drusen.
List of abbreviations
Optic Nerve Head Drusen
Spectral-domain Optical Coherence Tomography.
Financial Interests: The authors declare that they have no financial interests
Funding source: None
Written consent for publication was obtained from the patients included in the study
Presented as a poster in ARVO meeting, Fort Lauderdale, May 2009
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- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2342/10/11/prepub