Evaluation of 0.1% and 1% atropine eyedrops in cats: A comparative study of tolerance, stability, and efficacy.

IF 1.7 4区 农林科学 Q2 VETERINARY SCIENCES Veterinary ophthalmology Pub Date : 2024-08-22 DOI:10.1111/vop.13268
Karin W Handel, Ron Ofri, Yulia Goncharov, Dikla Arad, Lionel Sebbag
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Abstract

Objective: Investigate the tolerance, stability, and efficacy of topical 0.1% and 1% atropine in cats.

Procedures: 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.

Results: 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.

Conclusions: 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.

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猫用 0.1% 和 1% 阿托品眼药水的评估:耐受性、稳定性和疗效比较研究。
目的: 研究猫对局部 0.1%和 1%阿托品的耐受性、稳定性和疗效:调查猫对 0.1% 和 1% 阿托品外用药的耐受性、稳定性和疗效:六只猫进行了两次试验,中间间隔了两周的清洗期。在随机选取的一只眼睛(对照组)中滴入一滴人工泪液,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)。记录即时不良反应的严重程度(0-3)和持续时间(秒)。用药后 8 小时,监测瞳孔水平直径 (HPD)、瞳孔对光反射 (PLR)、眼压 (IOP)、Schirmer 泪液测试-1 (STT-1) 和心率 (HR)。在室温和冷藏条件下,连续 1 个月每周进行稳定性评估,评估溶液的透明度、pH 值和药物浓度:结果:0.1%阿托品与 1%阿托品相比,不良反应的严重程度明显降低,持续时间明显缩短(严重程度 1.2 ± 0.4 vs. 2.5 ± 0.5,p = .010;持续时间 107.5 ± 53.3 vs. 293.3 ± 106.5 秒,p = .009)。两种阿托品配方的 HPD 早在 40 分钟时就明显高于基线测量值。使用 0.1% 和 1% 阿托品时,瞳孔无反应的时间明显更短(中位数分别为 7 小时和 47.5 小时,p = .031)。与对照组相比,1% 阿托品能显著升高眼压(p = .021),而 0.1% 阿托品则不能(p = .502)。STT-1 和 HR 测量结果无明显差异。两种溶液在室温和冷藏条件下均可稳定使用 1 个月:稀释后的 0.1%阿托品对猫的稳定性和耐受性更好,为局部使用 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品。
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来源期刊
Veterinary ophthalmology
Veterinary ophthalmology 农林科学-兽医学
CiteScore
2.70
自引率
37.50%
发文量
82
审稿时长
12-24 weeks
期刊介绍: Veterinary Ophthalmology is a peer-reviewed, international journal that welcomes submission of manuscripts directed towards academic researchers of veterinary ophthalmology, specialists and general practitioners with a strong ophthalmology interest. Articles include those relating to all aspects of: Clinical and investigational veterinary and comparative ophthalmology; Prospective and retrospective studies or reviews of naturally occurring ocular disease in veterinary species; Experimental models of both animal and human ocular disease in veterinary species; Anatomic studies of the animal eye; Physiological studies of the animal eye; Pharmacological studies of the animal eye.
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