1995
DOI: 10.1007/bf00241474
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Anterior chamber inflammation after transconjunctival cryosurgery

Abstract: Transconjunctival cryosurgery caused mild inflammation in the anterior chamber of the eye for 3 weeks. The inflammation was not affected by the presence of retinal break or limited retinal detachment, the degree of myopia, or the extent of the treatment area.

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Cited by 8 publications
(10 citation statements)
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“…In a study on the treatment of peripheral retinal degeneration with retinal cryocoagulation, an increase in aqueous flare 1, 2, and 3 weeks after surgery was found; however, 4 weeks after treatment the flare values returned to normal [32]. Peak values were reached 2 weeks after cryo (6.7 photon counts/ms).…”
Section: Discussionmentioning
confidence: 68%
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“…In a study on the treatment of peripheral retinal degeneration with retinal cryocoagulation, an increase in aqueous flare 1, 2, and 3 weeks after surgery was found; however, 4 weeks after treatment the flare values returned to normal [32]. Peak values were reached 2 weeks after cryo (6.7 photon counts/ms).…”
Section: Discussionmentioning
confidence: 68%
“…On the other hand, a breakdown of the blood-aqueous and blood-retinal barriers has been reported to occur after retinal cryocoagulation, which has for many years caused this treatment modality to be regarded as somewhat questionable [5,6,23,30,32]. Other disadvantages, such as tractional retinal detachment and even overfreeze, added to the generally negative impression, but these were eventually found to be related to an outdated cryo application technique with a 360°peritomy, cryo application without visualization of the retina by indirect ophthalmoscopy, or even disinsertion of the rectus muscles [15,16,20,25].…”
Section: Discussionmentioning
confidence: 99%
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“…Consequently, the production of angiogenic factors and hence the formation of anterior retinal neovascularizations are decreased. The increased risk of hemorrhage in our study might be due to a cryotherapy-induced blood-retinal barrier breakdown, which might have stimulated the release of inflammatory and angiogenic mediators such as vascular endothelial growth factor [5,22]. These elements potentially might aggravate the development and/or progression of fibrovascular tissue, and hence increase the risk of recurrent VH.…”
Section: Discussionmentioning
confidence: 69%