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Published in: Graefe's Archive for Clinical and Experimental Ophthalmology 7/2019

01-07-2019 | Toxoplasmosis | Inflammatory Disorders

Monitoring of visual field over 6 months after active ocular toxoplasmosis

Published in: Graefe's Archive for Clinical and Experimental Ophthalmology | Issue 7/2019

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Abstract

Purpose

To prospectively report the perimetric defects during a 6-month follow-up (FU) in patients with initially active ocular toxoplasmosis (OT).

Methods

Twenty-four patients were studied, including 11 eyes with chorioretinal toxoplasmosis proven with a positive aqueous humor sample and 13 eyes with a biologically unproven, chorioretinal lesion. Automated 24-2 SITA-Standard visual fields were performed at baseline, at the first, and sixth months of FU. A composite clinical severity score was calculated from visual acuity (VA), severity of vitreitis, chorioretinal lesion size, location of the lesion in zone 1, the presence of an initial macular or papillary edema, and long-term scarring. This provided a relative cutoff level of severity. Nine eyes out of the 24 eyes were considered severe (3 unproven and 6 proven OT).

Results

Initial and final visual field parameters (mean deviation [MD] and pattern standard deviation [PSD]) were significantly correlated (r = 0.873; p < 0.001, and r = 0.890; p < 0.001, respectively). During FU, only foveal threshold [FT] was correlated with VA at baseline (r = 0.48; p = 0.01) and at the 6-month FU visit (r = 0.547; p = 0.004). The MD initial predictive value of clinical severity was 0.739 according to the ROC curve. At baseline, severe and nonsevere OT exhibited no significant difference in term of MD (p = 0.06) and PSD (p = 0.1). During the FU, taking into account all the data, MD, PSD, visual function index [VFI], and FT were associated with the severity of toxoplasmosis (p = 0.018, 0.05, 0.016, and 0.02, respectively): the unproven group had a faster recovery of MD during FU (p = 0.05).

Conclusion

Visual field parameters better reflected the chorioretinal destruction related to the toxoplasmosis lesion and the functional repercussions than VA alone. Interestingly, MD at presentation could be a discriminating factor of severity in active OT, and each visual field parameter follow-up could be a support to manage patients with active OT, especially in the severe group.
Literature
1.
2.
go back to reference Furtado JM, Winthrop KL, Butler NJ et al (2013) Ocular toxoplasmosis I: parasitology, epidemiology and public health: ocular toxoplasmosis. Clin Exp Ophthalmol 41(1):82–94CrossRef Furtado JM, Winthrop KL, Butler NJ et al (2013) Ocular toxoplasmosis I: parasitology, epidemiology and public health: ocular toxoplasmosis. Clin Exp Ophthalmol 41(1):82–94CrossRef
3.
go back to reference Holland GN (2003) Ocular toxoplasmosis: a global reassessment. Am J Ophthalmol 136(6):973–988CrossRef Holland GN (2003) Ocular toxoplasmosis: a global reassessment. Am J Ophthalmol 136(6):973–988CrossRef
4.
go back to reference Holland GN (2004) Ocular toxoplasmosis: a global reassessment. Am J Ophthalmol 137(1):1–17PubMed Holland GN (2004) Ocular toxoplasmosis: a global reassessment. Am J Ophthalmol 137(1):1–17PubMed
5.
go back to reference Pleyer U, Schlüter D, Mänz M (2014) Ocular toxoplasmosis: recent aspects of pathophysiology and clinical implications. Ophthalmic Res 52(3):116–123CrossRef Pleyer U, Schlüter D, Mänz M (2014) Ocular toxoplasmosis: recent aspects of pathophysiology and clinical implications. Ophthalmic Res 52(3):116–123CrossRef
6.
go back to reference Weiss LM, Dubey JP (2009) Toxoplasmosis: a history of clinical observations. Int J Parasitol 39(8):895–901CrossRef Weiss LM, Dubey JP (2009) Toxoplasmosis: a history of clinical observations. Int J Parasitol 39(8):895–901CrossRef
7.
go back to reference Wilder HC (1952) Toxoplasma chorioretinitis in adults. Arch Ophthalmol 48(2):127–136CrossRef Wilder HC (1952) Toxoplasma chorioretinitis in adults. Arch Ophthalmol 48(2):127–136CrossRef
8.
go back to reference Dodds EM, Holland GN, Stanford MR et al (2008) Intraocular inflammation associated with ocular toxoplasmosis: relationships at initial examination. Am J Ophthalmol 146(6):856–865.e2CrossRef Dodds EM, Holland GN, Stanford MR et al (2008) Intraocular inflammation associated with ocular toxoplasmosis: relationships at initial examination. Am J Ophthalmol 146(6):856–865.e2CrossRef
9.
go back to reference Martin WG, Brown GC, Parrish RK et al (1980) Ocular toxoplasmosis and visual field defects. Am J Ophthalmol 90(1):25–29CrossRef Martin WG, Brown GC, Parrish RK et al (1980) Ocular toxoplasmosis and visual field defects. Am J Ophthalmol 90(1):25–29CrossRef
10.
go back to reference Schlaegel TF, Weber JC (1984) The macula in ocular toxoplasmosis. Arch Ophthalmol 102(5):697–698CrossRef Schlaegel TF, Weber JC (1984) The macula in ocular toxoplasmosis. Arch Ophthalmol 102(5):697–698CrossRef
11.
go back to reference Stanford MR (2005) The visual field in toxoplasmic retinochoroiditis. Br J Ophthalmol 89(7):812–814CrossRef Stanford MR (2005) The visual field in toxoplasmic retinochoroiditis. Br J Ophthalmol 89(7):812–814CrossRef
12.
go back to reference Scherrer J, Iliev ME, Halberstadt M et al (2007) Visual function in human ocular toxoplasmosis. Br J Ophthalmol 91(2):233–236CrossRef Scherrer J, Iliev ME, Halberstadt M et al (2007) Visual function in human ocular toxoplasmosis. Br J Ophthalmol 91(2):233–236CrossRef
13.
go back to reference Delair E, Latkany P, Noble AG et al (2011) Clinical manifestations of ocular toxoplasmosis. Ocul Immunol Inflamm 19(2):91–102CrossRef Delair E, Latkany P, Noble AG et al (2011) Clinical manifestations of ocular toxoplasmosis. Ocul Immunol Inflamm 19(2):91–102CrossRef
14.
go back to reference Commodaro AG, Belfort RN, Rizzo LV et al (2009) Ocular toxoplasmosis: an update and review of the literature. Mem Inst Oswaldo Cruz 104(2):345–350CrossRef Commodaro AG, Belfort RN, Rizzo LV et al (2009) Ocular toxoplasmosis: an update and review of the literature. Mem Inst Oswaldo Cruz 104(2):345–350CrossRef
15.
go back to reference Garweg JG, de Groot-Mijnes JDF, Montoya JG (2011) Diagnostic approach to ocular toxoplasmosis. Ocul Immunol Inflamm 19(4):255–261CrossRef Garweg JG, de Groot-Mijnes JDF, Montoya JG (2011) Diagnostic approach to ocular toxoplasmosis. Ocul Immunol Inflamm 19(4):255–261CrossRef
16.
go back to reference Goldmann H, Witmer R (1954) Antikörper im Kammerwasser. Ophthalmologica 127(4–5):323–330CrossRef Goldmann H, Witmer R (1954) Antikörper im Kammerwasser. Ophthalmologica 127(4–5):323–330CrossRef
17.
go back to reference Fekkar A, Bodaghi B, Touafek F et al (2008) Comparison of immunoblotting, calculation of the Goldmann-Witmer coefficient, and real-time PCR using aqueous humor samples for diagnosis of ocular toxoplasmosis. J Clin Microbiol 46(6):1965–1967CrossRef Fekkar A, Bodaghi B, Touafek F et al (2008) Comparison of immunoblotting, calculation of the Goldmann-Witmer coefficient, and real-time PCR using aqueous humor samples for diagnosis of ocular toxoplasmosis. J Clin Microbiol 46(6):1965–1967CrossRef
18.
go back to reference Villard O, Filisetti D, Roch-Deries F et al (2003) Comparison of enzyme-linked immunosorbent assay, immunoblotting, and PCR for diagnosis of Toxoplasmic chorioretinitis. J Clin Microbiol 41(8):3537–3541CrossRef Villard O, Filisetti D, Roch-Deries F et al (2003) Comparison of enzyme-linked immunosorbent assay, immunoblotting, and PCR for diagnosis of Toxoplasmic chorioretinitis. J Clin Microbiol 41(8):3537–3541CrossRef
19.
go back to reference Fardeau C, Romand S, Rao NA et al (2002) Diagnosis of toxoplasmic retinochoroiditis with atypical clinical features. Am J Ophthalmol 134(2):196–203CrossRef Fardeau C, Romand S, Rao NA et al (2002) Diagnosis of toxoplasmic retinochoroiditis with atypical clinical features. Am J Ophthalmol 134(2):196–203CrossRef
20.
go back to reference Cunningham ET (2011) Proportionate topographic areas of retinal zones 1, 2, and 3 for use in describing infectious retinitis. Arch Ophthalmol 129(11):1507CrossRef Cunningham ET (2011) Proportionate topographic areas of retinal zones 1, 2, and 3 for use in describing infectious retinitis. Arch Ophthalmol 129(11):1507CrossRef
21.
go back to reference European Glaucoma Society (ed) (2014) Terminology and guidelines for glaucoma, 4th edn. PubliComm, Savona, p 195 European Glaucoma Society (ed) (2014) Terminology and guidelines for glaucoma, 4th edn. PubliComm, Savona, p 195
22.
go back to reference Standardization of Uveitis Nomenclature for Reporting Clinical Data (2005) Results of the first international workshop. Am J Ophthalmol 140(3):509–516CrossRef Standardization of Uveitis Nomenclature for Reporting Clinical Data (2005) Results of the first international workshop. Am J Ophthalmol 140(3):509–516CrossRef
23.
go back to reference Ouyang Y, Pleyer U, Shao Q et al (2014) Evaluation of cystoid change phenotypes in ocular toxoplasmosis using optical coherence tomography. PLoS One 9(2):e86626CrossRef Ouyang Y, Pleyer U, Shao Q et al (2014) Evaluation of cystoid change phenotypes in ocular toxoplasmosis using optical coherence tomography. PLoS One 9(2):e86626CrossRef
24.
go back to reference Diniz B, Regatieri AR et al (2011) Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis. Clin Ophthalmol:645–647 Diniz B, Regatieri AR et al (2011) Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis. Clin Ophthalmol:645–647
25.
go back to reference Monnet D (2009) Optical coherence tomography in ocular toxoplasmosis. Int J Med Sci:137–138 Monnet D (2009) Optical coherence tomography in ocular toxoplasmosis. Int J Med Sci:137–138
26.
go back to reference Smith JR, Cunningham ET (2002) Atypical presentations of ocular toxoplasmosis. Curr Opin Ophthalmol 13(6):387–392CrossRef Smith JR, Cunningham ET (2002) Atypical presentations of ocular toxoplasmosis. Curr Opin Ophthalmol 13(6):387–392CrossRef
27.
go back to reference Song A, Scott IU, Davis JL et al (2002) Atypical anterior optic neuropathy caused by toxoplasmosis. Am J Ophthalmol 133(1):162–164CrossRef Song A, Scott IU, Davis JL et al (2002) Atypical anterior optic neuropathy caused by toxoplasmosis. Am J Ophthalmol 133(1):162–164CrossRef
28.
go back to reference Mets MB, Holfels E, Boyer KM et al (1997) Eye manifestations of congenital toxoplasmosis. Am J Ophthalmol 123(1):1–16CrossRef Mets MB, Holfels E, Boyer KM et al (1997) Eye manifestations of congenital toxoplasmosis. Am J Ophthalmol 123(1):1–16CrossRef
29.
go back to reference Maenz M, Schlüter D, Liesenfeld O et al (2014) Ocular toxoplasmosis past, present and new aspects of an old disease. Prog Retin Eye Res 39:77–106CrossRef Maenz M, Schlüter D, Liesenfeld O et al (2014) Ocular toxoplasmosis past, present and new aspects of an old disease. Prog Retin Eye Res 39:77–106CrossRef
30.
go back to reference Riemslag FCC, Brinkman CJJ, Lunel HFEV et al (1992) Analysis of the electroretinogram in toxoplasma retinochorioiditis. Doc Ophthalmol 82(1–2):57–63CrossRef Riemslag FCC, Brinkman CJJ, Lunel HFEV et al (1992) Analysis of the electroretinogram in toxoplasma retinochorioiditis. Doc Ophthalmol 82(1–2):57–63CrossRef
Metadata
Title
Monitoring of visual field over 6 months after active ocular toxoplasmosis
Publication date
01-07-2019
Published in
Graefe's Archive for Clinical and Experimental Ophthalmology / Issue 7/2019
Print ISSN: 0721-832X
Electronic ISSN: 1435-702X
DOI
https://doi.org/10.1007/s00417-019-04313-2

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