PMID- 16329058 OWN - NLM STAT- MEDLINE DCOM- 20060131 LR - 20190917 IS - 1120-6721 (Print) IS - 1120-6721 (Linking) VI - 15 IP - 6 DP - 2005 Nov-Dec TI - Conventional perimetry, short-wavelength automated perimetry, frequency-doubling technology, and visual evoked potentials in the assessment of patients with multiple sclerosis. PG - 730-8 AB - PURPOSE: To evaluate the diagnostic power of conventional, achromatic, automated perimetry (CAP), short-wavelength automated perimetry (SWAP), frequency-doubling technology (FDT) perimetry, and visual evoked potentials (VEP) in a group of patients with multiple sclerosis (MS) with or without a history of optic neuritis. METHODS: Thirty eyes of 15 patients (5 male, 10 female, average age 38+/-7 years) with confirmed diagnosis of MS underwent CAP, SWAP (Humphrey 750-II VFA, program central 30-2, full-threshold strategy), FDT perimetry (program N-30), and pattern VEPs. Sixteen eyes (53.3%) had no history of ocular involvement and a negative ophthalmologic examination. They were matched with a control group of 10 healthy volunteers (4 male, 6 female, average age 31+/-10 years). The mean deviation (MD) and the pattern standard deviation (PSD) of the two groups were compared (t-test). Fourteen eyes (46.7%) had, on the contrary, a history of optic neuritis. Inside this group, the MD and the PSD of the three techniques were correlated (Spearman's rank test), in order to investigate whether any significant differences might be revealed by these techniques in pointing out the total amount of visual field damage. RESULTS: When comparing MS patients without signs or symptoms of ocular involvement and a control group, no significant differences were found for CAP MD, CAP PSD, and FDT PSD. Significant differences were found, on the contrary, for SWAP MD (p=0.0014), SWAP PSD (p=0.0001), and FDT MD (p=0.0001). When considering the MD and the PSD of the three techniques in the group of MS patients who had a history of optic neuritis, a significant correlation was found only between CAP MD and SWAP MD (r=0.0057), with a tendency by SWAP to reveal a higher rate of visual field loss. The other correlations were not significant. According to predefined criteria, the group of asymptomatic subjects had abnormal CAP in 1 eye (6.25%), abnormal SWAP in 9 (56.2%), abnormal FDT in 11 (68.7%), and abnormal VEPs in 7 (43.7%). The combined use of all techniques allowed us to identify silent optic nerve impairment in 15 (93.7%) eyes. CONCLUSIONS: Short-wavelength automated perimetry and FDT perimetry are two non-conventional perimetric techniques that were mainly developed for the early detection of glaucomatous damage. The results of this study demonstrate their efficacy also in detecting early visual field deficits in MS patients without clinical signs of optic neuropathy. Frequency doubling perimetry, in particular, proved to be an easy, fast, and sensitive technique in the assessment of patients with MS. Our results also suggest that subclinical visual involvement in MS can be better diagnosed using multiple (neurophysiologic and psychophysical) tests. FAU - Corallo, G AU - Corallo G AD - Eye Clinic, Dept. of Neurosciences, Ophthalmology and Genetics, University of Genova, Genova, Italy. Guido.Corallo@unige.it FAU - Cicinelli, S AU - Cicinelli S FAU - Papadia, M AU - Papadia M FAU - Bandini, F AU - Bandini F FAU - Uccelli, A AU - Uccelli A FAU - Calabria, G AU - Calabria G LA - eng PT - Comparative Study PT - Journal Article PL - United States TA - Eur J Ophthalmol JT - European journal of ophthalmology JID - 9110772 SB - IM MH - Adult MH - *Evoked Potentials, Visual MH - Female MH - Humans MH - Male MH - Multiple Sclerosis/*diagnosis MH - Optic Neuritis/*diagnosis MH - Sensitivity and Specificity MH - Vision Disorders/*diagnosis MH - Visual Field Tests/*methods MH - *Visual Fields EDAT- 2005/12/06 09:00 MHDA- 2006/02/01 09:00 CRDT- 2005/12/06 09:00 PHST- 2005/12/06 09:00 [pubmed] PHST- 2006/02/01 09:00 [medline] PHST- 2005/12/06 09:00 [entrez] AID - 10.1177/112067210501500612 [doi] PST - ppublish SO - Eur J Ophthalmol. 2005 Nov-Dec;15(6):730-8. doi: 10.1177/112067210501500612.