2013
DOI: 10.1097/ico.0b013e318288ad4d
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Cocaine-Assisted Epithelial Debridement for the Treatment of Anterior Basement Membrane Dystrophy

Abstract: Topical cocaine-assisted epithelial debridement offers a simple and inexpensive method for treating patients with ABMD who experience recurrent corneal erosions and/or irregular astigmatism resulting in decreased visual acuity.

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Cited by 11 publications
(10 citation statements)
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“…The cohort was too small to provide meaningful conclusions. Sayegh et al applied cocaine to the cornea – in a manner similar to alcohol – to facilitate ED 71. Benitez-del-Castillo et al combined 250 µg/mL of substance P-derived peptide with 1 µg/mL of insulin-like growth factor that they applied as an eye drop four times a day to a single patient for 2 months 72.…”
Section: Introductionmentioning
confidence: 99%
“…The cohort was too small to provide meaningful conclusions. Sayegh et al applied cocaine to the cornea – in a manner similar to alcohol – to facilitate ED 71. Benitez-del-Castillo et al combined 250 µg/mL of substance P-derived peptide with 1 µg/mL of insulin-like growth factor that they applied as an eye drop four times a day to a single patient for 2 months 72.…”
Section: Introductionmentioning
confidence: 99%
“…Firstly, an abnormal or deficient basal membrane caused by corneal melting due to local inflammation hindered epithelial healing, resulting in defective cellular adhesion and recurrent breakdown of the epithelium [10]. Secondly, the inflammatory cells and stromal keratocytes in a distinct, preexisting inflammatory microenvironment restrained epithelial healing by secreting proinflammatory cytokines and proteolytic enzymes [3].…”
Section: Discussionmentioning
confidence: 99%
“…The opacities could lead to the disruption of visual acuity, but their location and severity determine the final outcomes. [ 12 ] The onset seems to be earlier in homozygote than in heterozygote patients. [ 13 ] GCD2 is related to TGFB1 gene mutation, is mapped to chromosome 5q, and has an autosomal dominant pattern.…”
Section: Introductionmentioning
confidence: 99%
“…[ 13 ] GCD2 is related to TGFB1 gene mutation, is mapped to chromosome 5q, and has an autosomal dominant pattern. [ 12 ] Histologically, GCD2 patients have both superficial hyaline granular deposits and deep amyloid lattice deposits. The hyaline granules and amyloid lattice lines are stained with Masson’s trichrome and Congo red, respectively.…”
Section: Introductionmentioning
confidence: 99%
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