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一种新研发的单剂量眼科溶液滴注辅助器的有效性

Effectiveness of a Newly Developed Instillation Aid for Unit-Dose Ophthalmic Solutions.

作者信息

Takahashi Airi, Kasai Yuka, Sakamoto Masako, Matsuda Yuji, Ito Yuka, Haro Hirotaka, Kashiwagi Kenji

机构信息

Department of Ophthalmology, Faculty of Medicine, University of Yamanashi, Yamanashi 409-3898, Japan.

Division of Rehabilitation, University of Yamanashi Hospital, Yamanashi 409-3898, Japan.

出版信息

J Clin Med. 2025 Jul 24;14(15):5243. doi: 10.3390/jcm14155243.

Abstract

To evaluate the effectiveness and limitations of a newly developed unit-dose eye drop instillation aid in patients with glaucoma. Hospitalized adult glaucoma patients at the University of Yamanashi were enrolled if they had self-administered glaucoma eye drops for at least six months, had no upper limb impairments or cognitive decline, and had corrected visual acuity of ≥20/200 in at least one eye. This study used 0.1% hyaluronic acid mini-ophthalmic drops. Eye drop instillation was performed in the following order: without aid in the sitting position, with aid in the sitting position, without aid in the supine position, and with aid in the supine position. One practice trial with the device was conducted beforehand. Successful instillation was defined as delivery of a drop into the conjunctival sac without contact with the ocular surface, eyelashes, or face. Patients were also surveyed regarding the perceived usefulness of the device. Sixty-three patients (37 males, 26 females; mean age 71.3 ± 11.2 years) participated. In the sitting position, the success rate improved significantly from 70.3% without the aid to 89.1% with the aid ( = 0.0005). Success rates decreased with age but improved more markedly in older patients. In the supine position, the rate was 76.6% without the aid and 100% with the aid ( < 0.0001). Unit-dose eye drop aids significantly increase the success rate of instillation, especially among elderly patients, and may contribute to better adherence and treatment outcomes in glaucoma care.

摘要

评估一种新开发的单位剂量眼药水滴注辅助装置在青光眼患者中的有效性和局限性。如果山梨大学的成年住院青光眼患者自行使用青光眼眼药水至少六个月,无上肢损伤或认知功能下降,且至少一只眼睛的矫正视力≥20/200,则纳入研究。本研究使用0.1%透明质酸微型眼药水。眼药水滴注按以下顺序进行:坐姿无辅助、坐姿有辅助、仰卧位无辅助、仰卧位有辅助。事先对该装置进行了一次练习试验。成功滴注定义为一滴眼药水滴入结膜囊且未接触眼表、睫毛或面部。还对患者进行了关于该装置感知有用性的调查。63名患者(37名男性,26名女性;平均年龄71.3±11.2岁)参与了研究。在坐姿下,成功率从无辅助时的70.3%显著提高到有辅助时的89.1%(P = 0.0005)。成功率随年龄下降,但老年患者提高更为明显。在仰卧位,无辅助时的成功率为76.6%,有辅助时为100%(P < 0.0001)。单位剂量眼药水辅助装置显著提高了滴注成功率,尤其是在老年患者中,可能有助于改善青光眼护理中的依从性和治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55df/12346924/e9cf10a1e9b3/jcm-14-05243-g001.jpg

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