April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
The International Collaborative Exfoliation Syndrome Treatment (ICEST) Study: Results
Author Affiliations & Notes
  • A. Angelilli
    Ophthalmology, New York Eye and Ear Infirmary, New York, New York
  • R. Ritch
    Ophthalmology, New York Eye and Ear Infirmary, New York, New York
  • T. Krupin
    Ophthalmology, Northwestern University Medical Center, Chicago, Illinois
  • A. G. P. Konstas
    Ophthalmology, AHEPA Hospital, Thessaloniki, Greece
  • J. M. Liebmann
    Ophthalmology, New York Eye and Ear Infirmary, New York, New York
  • E. Ilitchev
    Ophthalmology, New York Eye and Ear Infirmary, New York, New York
  • M. Marmor
    Ophthalmology, New York University Medical Center, New York, New York
  • ICEST Study Group
    Ophthalmology, New York Eye and Ear Infirmary, New York, New York
  • Footnotes
    Commercial Relationships  A. Angelilli, None; R. Ritch, None; T. Krupin, None; A.G.P. Konstas, None; J.M. Liebmann, None; E. Ilitchev, None; M. Marmor, None.
  • Footnotes
    Support  Unlimited grant from Pfizer
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 2474. doi:
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    • Get Citation

      A. Angelilli, R. Ritch, T. Krupin, A. G. P. Konstas, J. M. Liebmann, E. Ilitchev, M. Marmor, ICEST Study Group; The International Collaborative Exfoliation Syndrome Treatment (ICEST) Study: Results. Invest. Ophthalmol. Vis. Sci. 2009;50(13):2474.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To compare the effect of treatment with latanoprost plus pilocarpine vs timolol or fixed combination timolol/dorzolamide (T/D) in eyes with exfoliation syndrome (XFS) and elevated IOP.

Methods: : A randomized, prospective, international, 12-center, two-year, open-label clinical trial was conducted. XFS patients aged 50-80 years with untreated IOP ≥22 mmHg and open angles with or without mild to moderate glaucomatous damage were included. One eligible eye per patient was randomly assigned to latanoprost and pilocarpine qhs to increase aqueous outflow and inhibit pupillary movement (group I), or to decrease aqueous production with timolol or T/D bid as needed for IOP control (group II). IOP, tonographic outflow facility, and trabecular pigmentation were measured every 6 months.

Results: : 277 (146 male) patients (mean age 69.1±6.8 yr, range 50-80 yr)` were enrolled between October 2000 and July 2003. XFS was unilateral in 118 (42.6%) and bilateral in 159 (57.4%) patients. Baseline TM pigmentation at the 6:00 angle was significantly associated with IOP (p=0.01). IOP reduction was 1.3 mmHg greater in Group I (n=145) than in Group II (n=132) (p=0.0003). Mean increase in outflow facility in Group I was 0.005 µl/mmHg/min vs 0 µl/mmHg/min in Group II (p<0.001). TM pigmentation at the 6:00 position at 24 months decreased from baseline more frequently in Group I than in Group II [34(26%) vs 20(16%)] and increased from baseline more frequently in Group II than in Group I [31(25%) vs 24(18%)].

Conclusions: : Subjects in Group I had lower IOP, improved outflow facility and decreased TM pigmentation. Initial therapy to increase aqueous outflow and interfere with dispersion of exfoliation material and iris pigment by inhibiting pupillary movement is preferable to reducing aqueous secretion, which may be deleterious as primary treatment in this disorder.

Clinical Trial: : www.clinicaltrials.gov 00.24

Keywords: clinical (human) or epidemiologic studies: treatment/prevention assessment/controlled clinical trials • drug toxicity/drug effects • aqueous 
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