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Blue light-filtering intraocular lenses and post-operative mood: a pilot clinical study

机译:滤蓝光人工晶状体与术后情绪:一项临床试验研究

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摘要

The purpose of the study was to determine if implantation of blue-filtering intraocular lenses (IOLs) affects post-operative mood, inducing more depression, compared to patients undergoing implantation with conventional IOLs. The study was conducted at the Angers University Hospital, France. This was a prospective with a lowercase pilot study, including consecutive patients planned to undergo cataract surgery in both eyes within 1 week. The same type of IOL was used in both eyes of each patient. The choice of IOL was not randomized but driven by the habits and experience of each participating surgeon. Cognitively healthy patients (an MMSE score higher than 25) were assessed before and after surgery, using the 30-item geriatric depression scale (GDS) to seek symptoms of depression. Univariate and multiple logistic regressions were used to examine the association between the type of IOL and the 30-item GDS score improvement during the 3 months after lens implantation, while adjusting for participants’ characteristics (age, visual acuity). Blue-filtering IOLs were used in 16 patients (mean ± standard deviation, 75.6 ± 7.5 years; 75 % female), and untinted IOLs in 18 patients (77.3 ± 6.9 years; 77.8 %female). Pre-operatively visual acuity and GDS scores were comparable in the two groups. The post-operative GDS score was improved by 1.91 ± 3.10 points in the whole sample (P = 0.002), as well as in each subgroup of patients. Three months after surgery, the mean change in GDS score did not differ between groups (P = 0.365), nor did the mean visual acuity (P = 0.198).
机译:这项研究的目的是确定与接受传统IOL植入的患者相比,植入蓝色滤光型人工晶状体(IOL)是否会影响术后情绪,并导致更多的抑郁症。该研究在法国昂热大学医院进行。这是一项针对小写字母的前瞻性研究的前瞻性研究,包括计划在1周内用双眼进行白内障手术的连续患者。每个患者的两只眼睛都使用相同类型的IOL。 IOL的选择不是随机的,而是由每个参与手术的外科医生的习惯和经验决定的。在手术前后,使用30个项目的老年抑郁量表(GDS)评估抑郁症的认知健康患者(MMSE评分高于25)。单因素和多元logistic回归用于检查晶状体植入后3个月内IOL类型与30项GDS评分改善之间的关系,同时调整参与者的特征(年龄,视敏度)。滤蓝的IOLs用于16例患者(平均±标准差,75.6±7.5岁;女性75%),未染色的IOLs用于18例患者(77.3±6.9岁;女性77.8%)。两组的术前视敏度和GDS评分相当。整个样本以及每个患者亚组中,术后GDS评分均提高了1.91±3.10分(P = 0.002)。术后三个月,两组间GDS评分的平均变化无差异(P = 0.365),平均视力也无差异(P = 0.198)。

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