Ozturk Taylan, Oner Hakan, Saatci Ali Osman, Kaynak Suleyman
Department of Ophthalmology, Dr. Behçet Uz Children's Hospital, Izmir, Turkey.
Int J Ophthalmol. 2012;5(3):377-83. doi: 10.3980/j.issn.2222-3959.2012.03.25. Epub 2012 Jun 18.
To compare the efficacy of low-fluence photodynamic therapy (PDT) combinations in the treatment of age-related macular degeneration (AMD).
Forty-five previously untreated eyes of 45 patients with exudative AMD whose best-corrected visual acuity (BCVA) was ≥0.3 (Snellen) were enrolled. 15 patients in Group I underwent low-fluence PDT (25J/cm(2)-300mW/cm(2)-83sec) and intravitreal pegaptanib combination, 15 patients in Group II underwent PDT (50J/cm(2)-600mW/cm(2)-83sec) and intravitreal pegaptanib combination while, 15 patients in Group III underwent intravitreal pegaptanib monotherapy. Complete ophthalmologic examinations were performed in pre and post treatment visits, and the results were statistically analised. A clinical activity score (CAS) was calculated by using changes in lesion size, amount of hemorrhage, staining pattern in FA and OCT measurement of intra/subretinal fluid. ≤ 3 logMAR lines of decrease in BCVA and decrease in CAS were considered as successful treatment.
The mean age of 19 female (42.2%) and 26 male (57.8%) patients was 72.82±8.02 years. Mean follow-up was 13.93±5.87 months. Lesion type was occult in 28 eyes (62.2%). Treatment success rates according to BCVA assessments were 86.7%, 80%, 60% and mean BCVA decrease were 0.3, 1.0, 2.2 logMAR lines in Group I, II and III, respectively (P>0.05). According to the changes in central macular thickness and CAS, no difference was found among the study groups (P=0.850 and P=0.811, respectively). Patients treated with combination regimens had lower intravitreal injection frequencies (P=0.015).
Combination regimen with intravitreal pegaptanib and low-fluence PDT seems to be safe and effective in stabilizing the clinical activity and BCVA in exudative AMD.
比较低能量光动力疗法(PDT)联合用药治疗年龄相关性黄斑变性(AMD)的疗效。
纳入45例渗出性AMD患者的45只未经治疗的眼睛,其最佳矫正视力(BCVA)≥0.3(斯内伦视力表)。I组15例患者接受低能量PDT(25J/cm² - 300mW/cm² - 83秒)联合玻璃体内注射培加替尼,II组15例患者接受PDT(50J/cm² - 600mW/cm² - 83秒)联合玻璃体内注射培加替尼,III组15例患者接受玻璃体内注射培加替尼单药治疗。在治疗前后进行完整的眼科检查,并对结果进行统计学分析。通过病变大小、出血量、荧光素血管造影(FA)染色模式和视网膜内/下液的光学相干断层扫描(OCT)测量的变化计算临床活动评分(CAS)。BCVA下降≤3个对数最小分辨角(logMAR)行和CAS下降被视为治疗成功。
19例女性(42.2%)和26例男性(57.8%)患者的平均年龄为72.82±8.02岁。平均随访时间为13.93±5.87个月。28只眼睛(62.2%)的病变类型为隐匿性。根据BCVA评估,I组、II组和III组的治疗成功率分别为86.7%、80%、60%,平均BCVA下降分别为0.3、1.0、2.2个logMAR行(P>0.05)。根据中心黄斑厚度和CAS的变化,各研究组之间未发现差异(分别为P = 0.850和P = 0.811)。联合治疗方案的患者玻璃体内注射频率较低(P = 0.015)。
玻璃体内注射培加替尼与低能量PDT联合方案在稳定渗出性AMD的临床活动和BCVA方面似乎是安全有效的。