Handel Karin W, Ofri Ron, Goncharov Yulia, Arad Dikla, Sebbag Lionel
Koret School of Veterinary Medicine, The Hebrew University of Jerusalem, Rehovot, Israel.
Vet Ophthalmol. 2025 Jul;28(4):714-721. doi: 10.1111/vop.13268. Epub 2024 Aug 22.
Investigate the tolerance, stability, and efficacy of topical 0.1% and 1% atropine in cats.
Six cats underwent two trials separated by a 2-week washout period. One drop of artificial tears was placed in one randomly selected eye (control), and one drop of either 0.1% atropine (Trial I) or 1% atropine (Trial II) was placed in the other eye. Immediate adverse effects were recorded for severity (0-3) and duration (seconds). Horizontal pupil diameter (HPD), pupillary light reflexes (PLRs), intraocular pressure (IOP), Schirmer tear test-1 (STT-1), and heart rate (HR) were monitored at baseline then 8 h post-administration. PLRs were assessed for a total of 72 h. Stability was assessed weekly for 1 month in room temperature and refrigerated conditions, evaluating solution clarity, pH, and drug concentrations.
Adverse effects had a significantly lower severity score and shorter duration with 0.1% versus 1% atropine (severity 1.2 ± 0.4 vs. 2.5 ± 0.5, p = .010; duration 107.5 ± 53.3 vs. 293.3 ± 106.5 s, p = .009). HPD was significantly greater than baseline measurements as early as 40 min for both atropine formulations. Pupils were non-responsive for a significantly shorter duration with 0.1% versus 1% atropine (median 7 h vs. 47.5 h, p = .031). Compared with control eyes, IOP was significantly elevated by 1% atropine (p = .021) but not 0.1% atropine (p = .502). No significant differences were noted in STT-1 and HR measurements. Both solutions were stable in room temperature and refrigerated conditions for 1 month.
Diluted 0.1% atropine was stable and better tolerated by cats, offering a potential alternative to feline patients that experience adverse effects from topical 1% atropine.
研究局部应用0.1%和1%阿托品对猫的耐受性、稳定性和疗效。
六只猫进行了两项试验,中间间隔2周的洗脱期。在一只随机选择的眼睛中滴入一滴人工泪液(对照),在另一只眼睛中滴入一滴0.1%阿托品(试验I)或1%阿托品(试验II)。记录即刻不良反应的严重程度(0 - 3级)和持续时间(秒)。在基线时以及给药后8小时监测水平瞳孔直径(HPD)、瞳孔对光反射(PLR)、眼压(IOP)、泪液分泌试验-1(STT-1)和心率(HR)。对PLR进行总共72小时的评估。在室温及冷藏条件下每周评估一次稳定性,持续1个月,评估溶液的清晰度、pH值和药物浓度。
与1%阿托品相比,0.1%阿托品的不良反应严重程度评分显著更低,持续时间更短(严重程度1.2±0.4对2.5±0.5,p = 0.010;持续时间107.5±53.3对293.3±106.5秒,p = 0.009)。两种阿托品制剂在给药后40分钟时,HPD就显著大于基线测量值。与1%阿托品相比,0.1%阿托品使瞳孔无反应的持续时间显著更短(中位数7小时对47.5小时,p = 0.031)。与对照眼相比,1%阿托品使IOP显著升高(p = 0.021),但0.1%阿托品未使其显著升高(p = 0.502)。在STT-1和HR测量中未发现显著差异。两种溶液在室温及冷藏条件下均稳定1个月。
稀释的0.1%阿托品稳定,猫对其耐受性更好,为因局部应用1%阿托品出现不良反应的猫科动物患者提供了一种潜在的替代选择。