Oswaldo Ferreira Moura Brasil1; Maria Vitoria Moura Brasil3; Marcelo Palis Ventura3; Hugo Soares Maia1
DOI: 10.1590/S0004-27492010000200018
ABSTRACT
Cystoid macular edema is an uncommon, but well known, side effect of latanoprost. Two cases of bilateral and simultaneous cystoid macular edema associated with latanoprost use are described, which complete resolution of the edema is observed upon drug discontinuation.
Keywords: Macula lutea; Macular edema; Glaucoma; Prostaglandin F; Case Reports; Human; Adult
RESUMO
O edema macular cistóide é um efeito colateral incomum, porém bem conhecido, do latanoprost. São descritos dois casos de edema macular cistóide bilateral e simultâneo associado ao uso de latanoprost, em que foi observada completa resolução do edema após a suspensão da droga.
Descritores: Mácula lútea; Edema macular; Glaucoma; Prostaglandina F; Relatos de casos; Humanos; Adultos
CASE REPORTS
Bilateral and simultaneous cystoid macular edema associated with latanoprost use: report of two cases
Edema macular cistóide bilateral e simultâneo associado com o uso de latanoprost: relato de dois casos
Oswaldo Ferreira Moura BrasilI; Maria Vitoria Moura BrasilII; Marcelo Palis VenturaIII; Hugo Soares MaiaIV
IRetina and Vitreous Service, Instituto Brasileiro de Oftalmologia - IBOL, Rio de Janeiro (RJ) - Brazil. Instituto da Visão, Universidade Federal de São Paulo UNIFESP -São Paulo (SP) - Brazil
IIGlaucoma Service, Instituto Brasileiro de Oftalmologia - IBOL - Rio de Janeiro (RJ) - Brazil. Instituto da Visão, UNIFESP - São Paulo (SP) - Brazil
IIIGlaucoma Service, Instituto Brasileiro de Oftalmologia -IBOL - Hospital Universitário Antônio Pedro, Universidade Federal Fluminense - HUAP - UFF - Rio de Janeiro (RJ) - Brazil
IVRetina and Vitreous Service, Instituto Brasileiro de Oftalmologia - IBOL -Rio de Janeiro (RJ) - Brazil
ABSTRACT
Cystoid macular edema is an uncommon, but well known, side effect of latanoprost. Two cases of bilateral and simultaneous cystoid macular edema associated with latanoprost use are described, which complete resolution of the edema is observed upon drug discontinuation.
Keywords: Macula lutea; Macular edema; Glaucoma; Prostaglandin F, synthetic; Case Reports; Human; Adult
RESUMO
O edema macular cistóide é um efeito colateral incomum, porém bem conhecido, do latanoprost. São descritos dois casos de edema macular cistóide bilateral e simultâneo associado ao uso de latanoprost, em que foi observada completa resolução do edema após a suspensão da droga.
Descritores: Mácula lútea; Edema macular; Glaucoma; Prostaglandina F, synthetic; Relatos de casos ; Humanos; Adultos
INTRODUCTION
Latanoprost is a prostaglandin analogue that reduces intraocular pressure by increasing uveoscleral outflow. Since its introduction in 1996 it has been widely used to treat glaucoma and ocular hypertension, and several ocular side effects have been reported including hypertrichosis, increased eyelash pigmentation, hypotony, choroidal effusion, iritis, anterior uveitis and cystoid macular edema (CME). Nevertheless, latanosprost is rarely discontinued due to one of its side effects(1).
The prostaglandin analogues may be associated with retinal bloodbarrier breakdown and CME has been reported as a side effect of latanoprost in numerous case reports, usually in association with risk factors such as aphakia and opened posterior capsule. The incidence of CME associated with latanoprost therapy is considered to be very low(2).
Two cases of bilateral and simultaneous CME associated with latanoprost are described, which complete resolution of the macular edema is observed following discontinuation of the drug.
CASE REPORTS
Case 1
A 60 year-old male with severe primary open-angle glaucoma treated with dorzolamide-timolol solution (CosoptTM) in both eyes (OU). The patient had history of cataract surgery with intraocular lens (IOL) implantation 3 years before and yag-laser capsulotomy 1 year later in OU. Bestcorrected visual acuity was 20/40 in the right eye (OD) and 20/150 in the left eye (OS). Intraocular pressure (IOP) was 20/21 mmHg. Latanoprost (XalatanTM) was then added to the treatment and IOP was reduced to 12/13 mmHg one month later. Three months after starting latanoprost the patient complained of reduced vision in OU, and best-corrected visual acuity was 20/100 in OD and 20/400 in OS. IOP was 6/8 mmHg at this time. Fluorescein angiography disclosed CME in OU (Figure 1A and 1B) and latanoprost was discontinued, being replaced by brimonidine (Alphagan-PTM). One month later vision improved to 20/40 in OD and 20/150 in OS, which was equal to baseline. IOP raised to 14/15 mmHg and remained stable throughout the follow-up. A few months later a control fluorescein angiography was performed and the CME was gone (Figure 1C and D).
Case 2
A 85 year-old female came in for a second opinion about glaucoma diagnosis. She had been diagnosed with primary open-angle glaucoma for 30 years, but was not currently using any anti-glaucomatous medication. The patient had previous cataract surgery with IOL implantation 10 years before and yag-laser capsulotomy 1 year later in OU. Bestcorrected visual acuity was 20/30 in OD and 20/25 in OS. IOP was 22/28 mmHg. Latanoprost (XalatanTM) was started and 1 month later IOP was reduced to 18/17 mmHg. However, the patient complained of reduced visual acuity, which was 20/50 in OD and 20/40 in OS. Fluorescein angiography disclosed CME in OU (Figure 2A and B) and latanoprost was discontinued. Dorzolamide-timolol solution (CosoptTM) was started instead. After 1 month, vision returned to baseline values (20/30 in OD and 20/25 in OS) and IOP was 15/15 mmHg. Further in the follow-up a new fluorescein angiography did not show CME (Figure 2C and D).
DISCUSSION
In phases I and II studies of latanoprost, there was no reported case of CME in 380 patients whereas in phase III studies there were 2 reported cases of CME in 300 patients(3). In addition, 120 cases of CME associated with latanoprost have been spontaneously reported to Pharmacia as of June 1999, during which time an estimated 1.700.000 patients had been treated with the drug(3). Sum up to that several anecdotal case reports such as the ones we have described. The overall conclusion is that if there is an association between latanoprost use and CME it is certainly infrequent, even if it is underestimated, since many cases might have not been reported.
The rationale for development of CME due to latanoprost use is that the drug may lead to the disruption of the bloodaqueous barrier, and this barrier's breakdown, as measured by aqueous laser flare meter, has been significantly associated with development of CME in aphakic and pseudophakic eyes using latanoprost(4-5). Interestingly, concurrent administration of nonsteroidal eyedrops seemed to prevent development of CME associated with latanoprost use in early postoperative pseudophakias(4).
Even tough the incidence of CME that could be attributable to latanoprost use is expected to be very low, it is known that aphakic and pseudophakic eyes, particularly those with open posterior capsule, are more likely to develop the side effect(3,6-8). Furthermore, some investigators failed to show CME development in patients with normally functioning blood-ocular barrier(9).
In case 1 hypotony maculopathy was discarded since it typically follows filtration surgery and is characterized by vision loss, retinal striae, choroidal folds, and no evidence of vascular leakage. In this case, there were no other clinical features of hypotony, such as shallow anterior chamber, Descemet's membrane striae, or serous choroidal detachment.
In the described cases, bilateral and simultaneous visually significant CME that could be attributable to latanoprost eyedrops were observed. Discontinuation of the drug led to improvement of vision to baseline values as well as to documented angiographic resolution of the CME in both cases. We believe it is important to raise awareness of this uncommon side effect in order to prevent any further vision loss in our glaucoma patients.
REFERENCES
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Correspondence Address:
Oswaldo Ferreira Moura Brasil
Praia de Botafogo, 206 - Rio de Janeiro (RJ)
CEP 22250-040
E-mail: [email protected]
Recebido para publicação em 27.10.2008
Última versão recebida em 08.10.2009
Aprovação em 17.12.2009
Work carried out at Instituto Brasileiro de Oftalmologia (IBOL) - Rio de Janeiro.