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猫用0.1%和1%阿托品滴眼液的评估:耐受性、稳定性和疗效的比较研究。

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

作者信息

Handel Karin W, Ofri Ron, Goncharov Yulia, Arad Dikla, Sebbag Lionel

机构信息

Koret School of Veterinary Medicine, The Hebrew University of Jerusalem, Rehovot, Israel.

出版信息

Vet Ophthalmol. 2025 Jul;28(4):714-721. doi: 10.1111/vop.13268. Epub 2024 Aug 22.

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.

摘要

目的

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。

步骤

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/12274123/e6e3f3ff0a81/VOP-28-714-g002.jpg

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