| Literature DB >> 30524488 |
Jane Farr1, Emily McGarva1, Jenny Nij Bijvank2, Hans van Vliet3, Hinke Marijke Jellema3, Michael D Crossland1, Axel Petzold1,2.
Abstract
The Pulfrich phenomenon, originally described in normal observers, is a treatable disorder of the perception of movement in depth in cases of unilateral or asymmetric optic neuropathy. Treatment is highly bespoke and factors influencing treatment response and failure remain unclear. We assessed 25 adults with suspected Pulfrich phenomenon due to a range of conditions in two tertiary referral centres. Monocularly tinted spectacles were successful in reducing symptoms of the Pulfrich phenomenon under daylight conditions in nine subjects, eight of whom had optic neuritis. These spectacles were not effective at night and in patients with visual field defects due to ischaemic optic neuropathy, glaucoma, optic disc drusen or severe peripapillary retinal nerve fibre loss on optical coherence tomography.Entities:
Keywords: Pulfrich; Visual illusions; depth perception; optic neuritis; visual rehabilitation
Year: 2018 PMID: 30524488 PMCID: PMC6276950 DOI: 10.1080/01658107.2018.1446537
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107
Figure 1.(A) Illustration of the Pulfrich phenomenon and how the pendulum is perceived either closer or further away than it really is. (B) The Pulfrich phenomenon viewed obliquely. An object moving in the plane AB to the viewer’s left approaching the filtered eye is perceived as travelling along the plane CD towards that eye.
Figure 2.(A) Photograph of Pulfrich experimental test material at Moorfields Eye Hospital. A coloured jungle scene with a monkey (green arrow, still on this photograph) is shown. (B) Photograph of Pulfrich experiment at VU Medical Centre Amsterdam. A black and white tablecloth is shown with a swinging black ball (green arrow, in motion giving impression of a blur on this photograph).
Figure 3.Prototype of spectacles for the Pulfrich phenomenon.
Patient characteristics.
| Characteristic | Patient data |
| N | 25 (London 14, Amsterdam 11) |
| Female | 17 (68%)1 |
| Age (median, IQR) | 49 (44–51) |
| Diagnoses | Optic neuritis, |
| NAION, | |
| Glaucoma, | |
| Optic disc drusen, | |
| Diplopia, | |
| Retinopathy, | |
| Nonorganic,2 | |
| Affected eye | Right 10 (40%) |
| Left 9 (36%) | |
| Bilateral 4 (16%) | |
| None 2 (8%) | |
| LogMAR BCVA (median, IQR) | RE 0 (−0.10–0.0) |
| LE 0 (−0.04–0.10) | |
| Affected eye3 0 (0–0.10) | |
| Non-affected eye 0 (−0.10–0) | |
| RAPD | 12 (50%) |
| pRNFL (median, IQR) [µm] | Affected eye 73 (65–89) |
| Non-affected eye 92 (85–100) |
1Gender not known in one patient.
2This includes patients with suspected nonorganic pathology.
3In patients with unilateral pathology.