Skip to main content
Top
Published in: Japanese Journal of Ophthalmology 3/2014

01-05-2014 | Clinical Investigation

Effect of axial length reduction after trabeculectomy on the development of hypotony maculopathy

Authors: Yoshiko Matsumoto, Masashi Fujihara, Akiyasu Kanamori, Yuko Yamada, Makoto Nakamura

Published in: Japanese Journal of Ophthalmology | Issue 3/2014

Login to get access

Abstract

Purpose

To measure changes in axial length before and after trabeculectomy with noncontact, partial coherence laser interferometry and identify patient factors that lead to the development of hypotony maculopathy and axial length shortening in 25 eyes with intraocular pressure (IOP) ≤6 mmHg at 4 weeks after mitomycin C-augmented trabeculectomy.

Methods

A retrospective comparative case series. Hypotony maculopathy was identified with both ophthalmoscopy and spectral-domain optical coherence tomography. Axial length and IOP were serially measured pre- and postoperatively. Logistic regression analysis was performed to identify factors associated with the presence of hypotony maculopathy at 4 weeks after trabeculectomy and multiple regression analysis to identify factors associated with axial length changes.

Results

Ten eyes exhibited hypotony maculopathy, whereas the remaining 15 did not. Patients with hypotony maculopathy were significantly younger (47.7 ± 6.2 years) compared with those without it (63.3 ± 9.6 years, P = 0.0002, unpaired t test). The percent reduction of axial length after trabeculectomy was significantly larger in the former group (5.91 ± 2.76 %) compared with the latter group (1.51 ± 0.91 %) (P = 0.0001, Mann–Whitney U test). Multivariate analyses showed that only age was associated with the presence of hypotony maculopathy, with an odds ratio of 0.82 (P = 0.0075), when age, sex, type of glaucoma, lens status, percent changes in axial length and IOP before and after trabeculectomy, and central corneal thickness were included as independent variables (R 2 = 0.543, P = 0.003).

Conclusions

Age-dependent axial length reduction is a risk factor for the development of hypotony maculopathy after trabeculectomy.
Literature
1.
go back to reference Gass JDM. Hypotony maculopathy. In: Bellows JG, editor. Contemporary ophthalmology. Honoring Sir Stewart Duke-Elder. Baltimore: Williams & Wilkins; 1972. p. 343–66. Gass JDM. Hypotony maculopathy. In: Bellows JG, editor. Contemporary ophthalmology. Honoring Sir Stewart Duke-Elder. Baltimore: Williams & Wilkins; 1972. p. 343–66.
3.
go back to reference Suñer IJ, Greenfield DS, Miller MP, Nicolela MT, Palmberg PF. Hypotony maculopathy after filtering surgery with mitomycin C. Incidence and treatment. Ophthalmology. 1997;104:207–14.PubMedCrossRef Suñer IJ, Greenfield DS, Miller MP, Nicolela MT, Palmberg PF. Hypotony maculopathy after filtering surgery with mitomycin C. Incidence and treatment. Ophthalmology. 1997;104:207–14.PubMedCrossRef
4.
go back to reference Jampel HD, Pasquale LR, Dibernardo C. Hypotony maculopathy following trabeculectomy with mitomycin C. Arch Ophthalmol. 1992;110:1049–50.PubMedCrossRef Jampel HD, Pasquale LR, Dibernardo C. Hypotony maculopathy following trabeculectomy with mitomycin C. Arch Ophthalmol. 1992;110:1049–50.PubMedCrossRef
5.
go back to reference Stamper RL, McMenemy MG, Lieberman MF. Hypotonous maculopathy after trabeculectomy with subconjunctival 5-fluorouracil. Am J Ophthalmol. 1992;114:544–53.PubMed Stamper RL, McMenemy MG, Lieberman MF. Hypotonous maculopathy after trabeculectomy with subconjunctival 5-fluorouracil. Am J Ophthalmol. 1992;114:544–53.PubMed
6.
go back to reference Fannin LA, Schiffman JC, Budenz DL. Risk factors for hypotony maculopathy. Ophthalmology. 2003;110:1185–91.PubMedCrossRef Fannin LA, Schiffman JC, Budenz DL. Risk factors for hypotony maculopathy. Ophthalmology. 2003;110:1185–91.PubMedCrossRef
7.
go back to reference Cashwell LF, Martin CA. Axial length decrease accompanying successful glaucoma filtration surgery. Ophthalmology. 1999;106:2307–11.PubMedCrossRef Cashwell LF, Martin CA. Axial length decrease accompanying successful glaucoma filtration surgery. Ophthalmology. 1999;106:2307–11.PubMedCrossRef
8.
go back to reference Kook MS, Kim HB, Lee SU. Short-term effect of mitomycin-C augmented trabeculectomy on axial length and corneal astigmatism. J Cataract Refract Surg. 2001;27:518–23.PubMedCrossRef Kook MS, Kim HB, Lee SU. Short-term effect of mitomycin-C augmented trabeculectomy on axial length and corneal astigmatism. J Cataract Refract Surg. 2001;27:518–23.PubMedCrossRef
9.
go back to reference Nemeth J, Horoczi Z. Changes in the ocular dimensions after trabeculectomy. Int Ophthalmol. 1992;16:355–7.PubMedCrossRef Nemeth J, Horoczi Z. Changes in the ocular dimensions after trabeculectomy. Int Ophthalmol. 1992;16:355–7.PubMedCrossRef
10.
go back to reference Drexler W, Findl O, Menapace R, Rainer G, Vass C, Hitzenberger CK, et al. Partial coherence interferometry: a novel approach to biometry in cataract surgery. Am J Ophthalmol. 1998;126:524–34.PubMedCrossRef Drexler W, Findl O, Menapace R, Rainer G, Vass C, Hitzenberger CK, et al. Partial coherence interferometry: a novel approach to biometry in cataract surgery. Am J Ophthalmol. 1998;126:524–34.PubMedCrossRef
11.
go back to reference Francis BA, Wang M, Lei H, Du LT, Minckler DS, Green RL, et al. Changes in axial length following trabeculectomy and glaucoma drainage device surgery. Br J Ophthalmol. 2005;89:17–20.PubMedCentralPubMedCrossRef Francis BA, Wang M, Lei H, Du LT, Minckler DS, Green RL, et al. Changes in axial length following trabeculectomy and glaucoma drainage device surgery. Br J Ophthalmol. 2005;89:17–20.PubMedCentralPubMedCrossRef
12.
go back to reference Pederson JE. Ocular hypotony. In: Ritch R, Shields MB, Krupin T, editors. The glaucomas. 2nd ed. St. Louis: Mosby; 1996. p. 385–95. Pederson JE. Ocular hypotony. In: Ritch R, Shields MB, Krupin T, editors. The glaucomas. 2nd ed. St. Louis: Mosby; 1996. p. 385–95.
13.
go back to reference Goodkin ML, Grewal DS, Greenfield DS. Three-dimensional high-speed optical coherence tomography for diagnosis of hypotony maculopathy following glaucoma filtration surgery. J Glaucoma. 2010;19:349–55.PubMedCentralPubMedCrossRef Goodkin ML, Grewal DS, Greenfield DS. Three-dimensional high-speed optical coherence tomography for diagnosis of hypotony maculopathy following glaucoma filtration surgery. J Glaucoma. 2010;19:349–55.PubMedCentralPubMedCrossRef
14.
go back to reference Lima VC, Prata TS, Castro DP, Castro LC, De Moraes CG, Mattox C, et al. Macular changes detected by Fourier-domain optical coherence tomography in patients with hypotony without clinical maculopathy. Acta Ophthalmol. 2011;89:e274–7.PubMedCrossRef Lima VC, Prata TS, Castro DP, Castro LC, De Moraes CG, Mattox C, et al. Macular changes detected by Fourier-domain optical coherence tomography in patients with hypotony without clinical maculopathy. Acta Ophthalmol. 2011;89:e274–7.PubMedCrossRef
15.
go back to reference Klink T, Lieb WE, Gobel W. Early and late optical coherence tomography (OCT) findings in patients with postoperative hypotony. Ophthalmologe. 2000;97:353–8 (in German).PubMedCrossRef Klink T, Lieb WE, Gobel W. Early and late optical coherence tomography (OCT) findings in patients with postoperative hypotony. Ophthalmologe. 2000;97:353–8 (in German).PubMedCrossRef
16.
go back to reference Karasheva G, Goebel W, Klink T, Haigis W, Grehn F. Changes in macular thickness and depth of anterior chamber in patients after filtration surgery. Graefe’s Arch Clin Exp Ophthalmol. 2003;241:170–5.CrossRef Karasheva G, Goebel W, Klink T, Haigis W, Grehn F. Changes in macular thickness and depth of anterior chamber in patients after filtration surgery. Graefe’s Arch Clin Exp Ophthalmol. 2003;241:170–5.CrossRef
17.
go back to reference Dellaporta A. Fundus changes in postoperative hypotony. Am J Ophthalmol. 1955;40:781–5.PubMed Dellaporta A. Fundus changes in postoperative hypotony. Am J Ophthalmol. 1955;40:781–5.PubMed
18.
go back to reference Miglior S, Brigatti L, Valati P, Balestreri C, Rossetti L, Bujtar E, et al. Relationship between morphometric optic disc parameters, gender and axial length. Curr Eye Res. 1994;13:119–24.PubMedCrossRef Miglior S, Brigatti L, Valati P, Balestreri C, Rossetti L, Bujtar E, et al. Relationship between morphometric optic disc parameters, gender and axial length. Curr Eye Res. 1994;13:119–24.PubMedCrossRef
19.
go back to reference Fotedar R, Wang JJ, Burlutsky G, Morgan IG, Rose K, Wong TY, et al. Distribution of axial length and ocular biometry measured using partial coherence laser interferometry (IOL Master) in an older white population. Ophthalmology. 2010;117:417–23.PubMedCrossRef Fotedar R, Wang JJ, Burlutsky G, Morgan IG, Rose K, Wong TY, et al. Distribution of axial length and ocular biometry measured using partial coherence laser interferometry (IOL Master) in an older white population. Ophthalmology. 2010;117:417–23.PubMedCrossRef
20.
go back to reference Kakutani Y, Nakamura M, Nagai-Kusuhara A, Kanamori A, Negi A. Marked cup reversal presumably associated with scleral biomechanics in a case of adult glaucoma. Arch Ophthalmol. 2010;128:139–41.PubMedCrossRef Kakutani Y, Nakamura M, Nagai-Kusuhara A, Kanamori A, Negi A. Marked cup reversal presumably associated with scleral biomechanics in a case of adult glaucoma. Arch Ophthalmol. 2010;128:139–41.PubMedCrossRef
21.
go back to reference Mochizuki H, Lesley AG, Brandt JD. Shrinkage of the scleral canal during cupping reversal in children. Ophthalmology. 2011;118:2008–13.PubMedCrossRef Mochizuki H, Lesley AG, Brandt JD. Shrinkage of the scleral canal during cupping reversal in children. Ophthalmology. 2011;118:2008–13.PubMedCrossRef
22.
go back to reference Rada JA, Achen VR, Penugonda S, Schmidt RW, Mount BA. Proteoglycan composition in the human sclera during growth and aging. Invest Ophthalmol Vis Sci. 2000;41:1639–48.PubMed Rada JA, Achen VR, Penugonda S, Schmidt RW, Mount BA. Proteoglycan composition in the human sclera during growth and aging. Invest Ophthalmol Vis Sci. 2000;41:1639–48.PubMed
23.
go back to reference Pallikaris IG, Kymionis GD, Ginis HS, Kounis GA, Tsilimbaris MK. Ocular rigidity in living human eyes. Invest Ophthalmol Vis Sci. 2005;46:409–14.PubMedCrossRef Pallikaris IG, Kymionis GD, Ginis HS, Kounis GA, Tsilimbaris MK. Ocular rigidity in living human eyes. Invest Ophthalmol Vis Sci. 2005;46:409–14.PubMedCrossRef
24.
go back to reference Geraghty B, Jones SW, Rama P, Akhtar R, Elsheikh A. Age-related variations in the biomechanical properties of human sclera. J Mech Behav Biomed Mater. 2012;16:181–91.PubMedCrossRef Geraghty B, Jones SW, Rama P, Akhtar R, Elsheikh A. Age-related variations in the biomechanical properties of human sclera. J Mech Behav Biomed Mater. 2012;16:181–91.PubMedCrossRef
25.
go back to reference Coudrillier B, Tian J, Alexander S, Myers KM, Quigley HA, Nguyen TD. Biomechanics of the human posterior sclera: age- and glaucoma-related changes measured using inflation testing. Invest Ophthalmol Vis Sci. 2012;53:1714–28.PubMedCentralPubMedCrossRef Coudrillier B, Tian J, Alexander S, Myers KM, Quigley HA, Nguyen TD. Biomechanics of the human posterior sclera: age- and glaucoma-related changes measured using inflation testing. Invest Ophthalmol Vis Sci. 2012;53:1714–28.PubMedCentralPubMedCrossRef
26.
go back to reference McBrien NA, Cornell LM, Gentle A. Structural and ultrastructural changes to the sclera in a mammalian model of high myopia. Invest Ophthalmol Vis Sci. 2001;42:2179–87.PubMed McBrien NA, Cornell LM, Gentle A. Structural and ultrastructural changes to the sclera in a mammalian model of high myopia. Invest Ophthalmol Vis Sci. 2001;42:2179–87.PubMed
27.
go back to reference Sergienko NM, Shargorogska I. The scleral rigidity of eyes with different refractions. Graefes Arch Clin Exp Ophthalmol. 2012;250:1009–12.PubMedCrossRef Sergienko NM, Shargorogska I. The scleral rigidity of eyes with different refractions. Graefes Arch Clin Exp Ophthalmol. 2012;250:1009–12.PubMedCrossRef
Metadata
Title
Effect of axial length reduction after trabeculectomy on the development of hypotony maculopathy
Authors
Yoshiko Matsumoto
Masashi Fujihara
Akiyasu Kanamori
Yuko Yamada
Makoto Nakamura
Publication date
01-05-2014
Publisher
Springer Japan
Published in
Japanese Journal of Ophthalmology / Issue 3/2014
Print ISSN: 0021-5155
Electronic ISSN: 1613-2246
DOI
https://doi.org/10.1007/s10384-014-0312-x

Other articles of this Issue 3/2014

Japanese Journal of Ophthalmology 3/2014 Go to the issue