Journals / Glokom Katarakt / 2010 / Cilt: 5 - Sayı: 1

Short term effects of topical latanoprost 0.005%) on tear film

Topikal latanoprostun (%0.005) gözyaşı filmine kısa dDönem etkileri

Pages
38–42
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusion: Topical latanoprost (0.005%) may increase tear break-up time in short term use.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Purpose: To investigate effects of topical latanoprost (0.005%) on tear film.
📊
Key Findings & Data:Material and Methods: 20 eyes of 20 patients who had been diagnosed as primary open angle glaucoma and undergone anti-glaucoma treatment, were included in this study.
💡
Conclusion & Impact:Conclusion: Topical latanoprost (0.005%) may increase tear break-up time in short term use.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Purpose: To investigate effects of topical latanoprost (0.005%) on tear film. Material and Methods: 20 eyes of 20 patients who had been diagnosed as primary open angle glaucoma and undergone anti-glaucoma treatment, were included in this study. Basal Schirmer test, tear break-up time, Rose Bengal, and ocular surface disease index were applied for all of the cases before topical latanoprost therapy. All of the tests were repeated in 1st, 2nd and 3rd month of the treatment. All results were evaluated with nonparametric Wilcoxon test by SPSS 13.0. Results: Mean age was 51.8±6.4 (SD) (12\8 Female\Male). Mean scores were established as Schirmer 9.5±3.3 mm, tear break-up time 12.4±3 sec, Rose Bengal 3.85±2, ocular surface disease index 49.53±20 before the terapy. There’s no significant changes in Schirmer, Rose Bengal and ocular surface disease index score in 1st, 2nd and 3rd month of the treatment but a significant increase was observed in tear break-up time 13.6±2 (p=0.007) at the 2nd and 13.9±1.8 (p=0.004) 3rd month. Conclusion: Topical latanoprost (0.005%) may increase tear break-up time in short term use.

Özet

Amaç: Topikal latanoprostun (%0.005) kullanımının gözyaşı filmine etkilerini araştırmak. Gereç ve Yöntem: Çalışmaya primer açık açılı glokom tanısı yeni koyulup tedaviye başlanan 20 olgunun 20 gözü dahil edildi. Topikal latanoprost (%0.005) tedavisi başlamadan önce tüm olgulara bazal schirmer, gözyaşı kırılma zamanı, rose bengal testi ve oküler yüzey hastalığı indeksi skorlaması yapıldı. Tedavinin devamında 1, 2 ve 3. aylarda aynı testler tekrar yapıldı. Tüm sonuçlar SPSS 13.0 ile non parametrik Wilcoxon testi ile değerlendirildi. Bulgular: Olguların yaş ortalaması 51.8±6.4 (SD) (12\8 Kadın\ Erkek) idi. Tedavi başlamadan önce olguların ortalama Schirmer 9.5±3.3 mm, gözyaşı kırılma zamanı 12.4±3 sn, Rose Bengal skoru 3.85 ±2, oküler yüzey hastalığı indeksi skoru 49.53±20 olarak saptandı. Olguların 1, 2 ve 3. ayda yapılan takiplerinde schirmer testi, Rose Bengal ve oküler yüzey hastalığı indeksi skorunda anlamlı bir bulgu tespit edilemedi. Göz yaşı kırılma zamanında ise anlamlı bir artış olduğu [2. ay 13.6±2 (p=0.007), 3. ay 13.9±1.8 (p=0.004)] gözlemlendi. Sonuç: Topikal latanoprostun (%0.005) kısa dönem kullanımı gözyaşı kırılma zamanının uzamasına neden olabilmektedir.

🔖

Cite This Article

YILDIZ, A. A., BARDAK, Y., TIĞ, U. Ş. (2010). Short term effects of topical latanoprost 0.005%) on tear film. Glokom Katarakt, Cilt: 5 - Sayı: 1, 38–42. https://ajindex.com/articles/226571

References (16)

  1. Huq F.: Molecular modelling analysis of the metabolism of latanoprost. J Pharmacol. and Toxicol. 2007;2:359-365
  2. Diestelhorst M, Roters S, Krieglstein GK.: The effect of latanoprost 0.005%once daily versus 0.0015%twice daily on intraocular pressure and aqueous humour protein concentration in glaucoma patients. A randomized, double-masked comparison with timolol 0.5%.Graefes Arch Clin Exp Ophthalmol. 1997;235:20- 26
  3. Product Monograph: Xalatan (Latanoprost ophthalmic solution) 50 μgml Prostaglandine F2a analogue. Pfizer Canada Inc 2003
  4. Özçetin H, Şener AB: Miyopi ve tedavisi. Nobel Tıp Kitabevleri. 2002;14-20
  5. Kanski JJ.: Clinical Ophthalmology. Butterworth-Hellnemann. 1989;88-120. 6. van Bijsterveld OP.: Diagnostic test in the sicca syndrome. Arch Ophthalmol. 1969;82:10-14
  6. Bengisu Ü.: Göz Hastalıkları. Palme Yayıncılık 4. Basım. 1998;39- 50
  7. Özcura F, Aydin S, Helvaci MR.: Ocular surface disease index for the diagnosis of dry eye syndrome. Ocul Immunol Inflamm. 2007;15:389-393
  8. Aragona P, Candella V, Caputi AP et al.: Effects of a stable analogue of PGE2 [11-deoxy-13,14 dehydro-16 (S)- methylester methyl PGE2; FCE 20700] on the secretory processes of conjunctival goblet cells of the rabbit. Exp. Eye Res. 1987:45;647-654
  9. Özer F, Yosunkaya Ş.: Astım ve lökotrienler: Genel Tıp Derg. 2005;15:91-99
  10. Rang HP, Dale MM, Ritter JM et al.: Pharmacology Churchill Livingstone. 2003;5:234
  11. Kowalewski MP, Beceriklisoy HB, Aslan S et al.: Time related changes in luteal prostaglandin synthesis and steroidogenic capacity during pregnancy, normal and antiprogestin induced luteolysis in the bitch. Anim Reprod Sci. 2009;116:129-138
  12. Ishida N, Odani-Kawabata N, Shimazaki A et al.: Prostanoids in the therapy of glaucoma. Cardiovasc Drug Rev. 2006;24:1-10
  13. Cao W, Harnett KM, Behar J et al.: PGF(2alpha)-induced contraction of cat esophageal and lower esophageal sphincter circular smooth muscle. Am J Physiol Gastrointest Liver Physiol. 2002;283:282-291
  14. Scott G, Jacobs S, Leopardi S et al.: Effects of PGF2 alpha on human melanocytes and regulation of the FP receptor by ultraviolet radiation. Exp Cell Res. 2005;304:407-416
  15. Stefan C, Dumitrica DM.: Ocular surface disfunction in glaucoma. Oftalmologia. 2008;52:114-119
  16. Thygesen J, Aaen K, Theodorsen F et al.: Short-term effect of latanoprost and timolol eye drops on tear fluid and the ocular surface in patients with primary open-angle glaucoma and ocular hypertension. Acta O