Direkt zum Inhalt
Merck
  • Triple subconjunctival bevacizumab injection for early corneal recurrent pterygium: one-year follow-up.

Triple subconjunctival bevacizumab injection for early corneal recurrent pterygium: one-year follow-up.

Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics (2014-11-05)
Angel Nava-Castañeda, Isabel Ulloa-Orozco, Lilia Garnica-Hayashi, Joaquín Hernandez-Orgaz, Maria Carmen Jimenez-Martinez, Yonathan Garfias
ZUSAMMENFASSUNG

The aim of the study was to evaluate the effect of 3 subconjunctival bevacizumab injections in patients with an early corneal pterygium recurrence. This study was a nonrandomized single center trial. Patients with an early corneal pterygium recurrence were selected. All patients received 3 subconjunctival bevacizumab (2.5 mg/0.1 mL) injections (basal, 2 and 4 weeks) in the recurrence area of the pterygium. The corneal and corneal-conjunctival neovascularization areas and the corneal opacification area of each pterygium were determined using digital slit lamp pictures. Thirty-eight patients were enrolled into the study; all patients were injected within 3 months of the diagnosed pterygium recurrence. Interestingly, the bevacizumab injections had a significant effect (P<0.05) on the reduction of corneal, corneal-conjunctival area of neovascularization determined as pixels and on the corneal opacification area determined as mm(2) when comparing the basal values, to the values obtained after 15 days, 1 month, 3 months, 6 months, and 12 months after injections. The vascularized area in all recurrent pterygia and the corneal opacification area with this triple regimen of subconjunctival bevacizumab injections were reduced, which remained until the end of the study. These results suggest that bevacizumab subconjunctival injections could be useful to treat recurrent pterygium.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Dexamethason, powder, BioReagent, suitable for cell culture, ≥97%
Sigma-Aldrich
Dexamethason, ≥98% (HPLC), powder
Sigma-Aldrich
Dexamethason, powder, γ-irradiated, BioXtra, suitable for cell culture, ≥80% (HPLC)
Sigma-Aldrich
Tobramycin, Aminoglycoside antibiotic
USP
Dexamethason, United States Pharmacopeia (USP) Reference Standard
Supelco
Dexamethason, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Tetracain -hydrochlorid, ≥99%
USP
Tobramycin, United States Pharmacopeia (USP) Reference Standard
Supelco
Tobramycin, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Dexamethason, meets USP testing specifications
USP
Tetracain -hydrochlorid, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Dexamethason, tested according to Ph. Eur.
Supelco
Tetracain -hydrochlorid, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Dexamethason, VETRANAL®, analytical standard
Dexamethason, European Pharmacopoeia (EP) Reference Standard
Tobramycin, European Pharmacopoeia (EP) Reference Standard
Dexamethason für die Systemeignung, European Pharmacopoeia (EP) Reference Standard
Tetracain -hydrochlorid, European Pharmacopoeia (EP) Reference Standard
Dexamethason, British Pharmacopoeia (BP) Assay Standard
Dexamethason für die Peakidentifizierung, European Pharmacopoeia (EP) Reference Standard
Tetracain für die Systemeignung, European Pharmacopoeia (EP) Reference Standard