Janulevičienė Ingrida, Derkač Irmante, Grybauskiene Lina, Paulauskaitė Ruta, Gromnickaite Ruta, Kuzmienė Loreta
Eye Clinic of Kaunas Medical Academy of Lithuanian University of Health Sciences, Kaunas, Lithuania.
Clin Ophthalmol. 2012;6:103-9. doi: 10.2147/OPTH.S28104. Epub 2012 Jan 12.
To compare the effects on tolerability, tear osmolarity, and intraocular pressure (IOP)-lowering effect of switching from benzalkonium chloride (BAK) containing prostaglandin analog (PGA) latanoprost to preservative-free tafluprost.
Thirty patients with open-angle glaucoma (N = 60 eyes), 26 women (87%) and four men (13%) aged 64.1 (SD 14.1) years, showing abnormal values of tear osmolarity, corneal fluorescein staining, tear film break-up time (TBUT), or subjective discomfort with current latanoprost treatment were included. After tear osmolarity (TearLab™ Osmolarity System), TBUT, corneal fluorescein staining, and baseline IOP (Goldmann tonometer) measurements and the completion of Ocular Surface Disease Index and Ocular Surface Symptoms in Glaucoma Scale questionnaires, patients were assigned to preservative-free tafluprost treatment. Measurements were repeated 2, 6 and 12 weeks after change of medication.
No statistically significant differences in IOP were observed 2, 6, and 12 weeks after switching to preservative-free tafluprost. Mean IOP at baseline was 16.4 mmHg (SD 2.9), after 2 weeks 16.2 mmHg (2.8), after 6 weeks 16.2 (2.6), and after 12 weeks 16.3 mmHg (2.3). Mean tear osmolarity decreased significantly from 315.7 mOsm/L (SD 15.1) at baseline to 308.0 ± 14.4 mOsm/L (P = 0.002), 301.7 ± 14.5 mOsm/L (P < 0.001), and 302.0 ± 9.9 mOsm/L (P < 0.001) 2, 6, and 12 weeks after changing medication to preservative-free tafluprost, respectively. Tear osmolarity was lower in 37 eyes (61.7%) after 2 weeks, in 46 eyes (76.7%) after 6 weeks, and in 49 eyes (81.7%) after 12 weeks (P < 0.005; t-test). At baseline corneal fluorescein staining was observed in 43 eyes (71.7%), after 2 weeks in 34 eyes (56.7%), after 6 weeks in 12 eyes (20.0%), and after 12 weeks in 7 eyes (11.7%) (P < 0.005; McNemar test). Mean TBUT increased from 3.7 seconds (SD 1.1) at baseline to 4.1 seconds (SD 1.0) at week 2, 5.2 seconds (SD 1.5) at week 6, and 6.5 seconds (SD 1.5) at week 12 (P < 0.001; t-test). The number of patients expressing discomfort with latanoprost diminished from 30 (100%) at baseline, to 19 (63.3%) after week 2, and to 11 (36.6%) (P < 0.05; McNemar test) after 12 weeks.
Preservative-free tafluprost is better tolerated than BAK-containing latanoprost, showing lower tear osmolarity levels while maintaining effective IOP control.
比较从含苯扎氯铵(BAK)的前列腺素类似物(PGA)拉坦前列素转换为无防腐剂他氟前列素对耐受性、泪液渗透压和降低眼压(IOP)效果的影响。
纳入30例开角型青光眼患者(共60只眼),其中26例女性(87%),4例男性(13%),年龄64.1(标准差14.1)岁,这些患者泪液渗透压、角膜荧光素染色、泪膜破裂时间(TBUT)值异常,或当前使用拉坦前列素治疗时存在主观不适。在测量泪液渗透压(TearLab™渗透压系统)、TBUT、角膜荧光素染色和基线眼压(Goldmann眼压计),并完成眼表疾病指数和青光眼眼表症状量表问卷后,患者开始接受无防腐剂他氟前列素治疗。在更换药物后2周、6周和12周重复进行测量。
转换为无防腐剂他氟前列素后2周、6周和12周,眼压未观察到统计学上的显著差异。基线时平均眼压为16.4 mmHg(标准差2.9),2周后为16.2 mmHg(2.8),6周后为16.2(2.6),12周后为16.3 mmHg(2.3)。平均泪液渗透压从基线时的315.7 mOsm/L(标准差15.1)显著下降至更换药物为无防腐剂他氟前列素后2周的308.0±14.4 mOsm/L(P = 0.002)、6周的301.7±14.5 mOsm/L(P < 0.001)和12周的302.0±9.9 mOsm/L(P < 0.001)。2周后37只眼(61.7%)、6周后46只眼(76.7%)和12周后49只眼(81.7%)的泪液渗透压降低(P < 0.005;t检验)。基线时43只眼(71.7%)观察到角膜荧光素染色,2周后34只眼(56.7%),6周后12只眼(20.0%),12周后7只眼(11.7%)(P < 0.005;McNemar检验)。平均TBUT从基线时的3.7秒(标准差1.1)增加至第2周的4.1秒(标准差1.0)、第6周的5.2秒(标准差1.5)和第12周的6.5秒(标准差1.5)(P < 0.001;t检验)。表示对拉坦前列素不适的患者数量从基线时的30例(100%)减少至第2周后的19例(63.3%),12周后减少至11例(36.6%)(P < 0.05;McNemar检验)。
无防腐剂他氟前列素比含BAK的拉坦前列素耐受性更好,在维持有效眼压控制的同时,泪液渗透压水平更低。