May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Comparing Efficacy of XalacomTM and CosoptTM on Intraocular Pressure and Optic Nerve Head Perfusion in Glaucoma Patients: A Randomized Cross–Over Trial
Author Affiliations & Notes
  • C.P. Jonescu–Cuypers
    Ophthalmology,
    Univ Cologne, Cologne, Germany
  • G. Roessler
    Ophthalmology,
    Univ Cologne, Cologne, Germany
  • M. Hellmich
    Biostatistics and Epidemiology,
    Univ Cologne, Cologne, Germany
  • M. Diestelhorst
    Ophthalmology,
    Univ Cologne, Cologne, Germany
  • Footnotes
    Commercial Relationships  C.P. Jonescu–Cuypers, None; G. Roessler, None; M. Hellmich, None; M. Diestelhorst, None.
  • Footnotes
    Support  The study was supported in part by Pharmacia/Pfizer, Germany. The authors have no financial interest
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 2461. doi:
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      C.P. Jonescu–Cuypers, G. Roessler, M. Hellmich, M. Diestelhorst; Comparing Efficacy of XalacomTM and CosoptTM on Intraocular Pressure and Optic Nerve Head Perfusion in Glaucoma Patients: A Randomized Cross–Over Trial . Invest. Ophthalmol. Vis. Sci. 2005;46(13):2461.

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

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Abstract
 
Abstract:
 

Blood flow may play a major role in the development of open angle glaucoma. It is important to know the effect of a drug on intraocular pressure (IOP) and peripapillary retinal perfusion used in the treatment of the disease. The aim of this study was to compare the effects of XalacomTM (q.d.) and CosoptTM (bid.) on intraocular hemodynamics and IOP in glaucoma patients and ocular hypertensives.

 

 

Following a 3 weeks run–in period with timolol 0.5% bid (baseline), patients were randomly assigned to CosoptTM b.i.d. administered at 8.00 and 20.00 hours in group I and XalacomTM q.d. at 8.00 hours in group II. After 6 weeks all patients continued with the other medication for another 6 weeks. Measurements included visual acuity, slit–lamp examination, retinal blood flow with the Heidelberg Retina Flowmeter (HRF) using the standard measurement window and IOP. Data from paired eyes were averaged.

 

We included 30 eyes of 16 patients (8 females, 8 males; mean age: 64.7 ± 8.5 years).

 

 

*I: Cosopt–Xalacom; II: Xalacom–Cosopt

 

Analysis of covariance revealed a statistically significant (p=0.003) difference of mean IOP reduction in favor of XalacomTM q.d. treatment. The difference of mean retinal blood flow reduction was only borderline statistically significant (p=0.057). We found tendencies of retinal blood flow reduction from CosoptTM b.i.d. (p=0.156) and slight increase from XalacomTM q.d. (p=0.395).

 

The study results suggest a retinal blood flow reduction following fixed combination treatment with CosoptTM after pre–treatment with timolol 0.5% b.i.d. for 3 weeks. The HRF data do not reveal a significant increase of retinal blood flow from XalacomTM eye drops. The significantly better IOP reduction from XalacomTM treatment was confirmed.

 

 
Keywords: optic flow • optic disc • pharmacology 
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