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急性白内障术后眼内炎玻璃体腔内注射莫西沙星:疗效和安全性。

Intravitreal moxifloxacin injections in acute post-cataract surgery endophthalmitis: Efficacy and safety.

机构信息

Department of Ophthalmology, Shri Jagdamba Charitable Eye Hospital, Andh Vidhalaya Campus, Sri Ganganagar, Rajasthan, India.

出版信息

Indian J Ophthalmol. 2021 Feb;69(2):326-330. doi: 10.4103/ijo.IJO_587_20.

Abstract

PURPOSE

The aim of this study was to evaluate the efficacy and safety of intravitreal moxifloxacin injections in the treatment of acute post-cataract surgery endophthalmitis with visual acuity equal to or greater than hand movements.

METHODS

Fifty two patients with post-cataract surgery endophthalmitis who presented within 6 weeks with visual acuity equal to or greater than hand movements received two intravitreal moxifloxacin injections 48 h apart. Patients with prior history of ocular disease or treatment were excluded. Patients were followed up to 3 months either for resolution of endophthalmitis or worsening of disease. Number of patients who achieved visual acuity equal to or better than 20/40 and 20/200 at the third-month follow-up visit were compared with the number of patients at presentation, using Chi-square test. In addition, pretreatment LogMAR visual acuity at the time of presentation was compared with posttreatment visual acuity at end of third month using paired t test.

RESULTS

Fifty (96.15%) patients showed complete resolution of endophthalmitis while three patients required vitrectomy. Forty-one (78.85%) and 49 (94.23%) patients achieved visual acuity equal to or better than 20/40 and 20/200, respectively, at the third-month follow-up visit as compared to eight (15.38%) and 13 (25%) patients, respectively, at presentation (P < 0.05). In addition, mean LogMAR visual acuity at the time of presentation was 0.755 which improved to 0.307 at the third-month follow-up visit (P < 0.05). None of the patients developed hypersensitivity reactions to intravitreal moxifloxacin.

CONCLUSION

Intravitreal moxifloxacin injections showed promising results in acute post-cataract surgery endophthalmitis.

摘要

目的

本研究旨在评估玻璃体腔内注射莫西沙星治疗术后 6 周内视力等于或优于手动的急性白内障术后眼内炎的疗效和安全性。

方法

52 例白内障术后眼内炎患者,发病后 6 周内视力等于或优于手动,每 48 小时行玻璃体腔内注射莫西沙星 2 次。排除有眼部疾病史或治疗史的患者。随访 3 个月,观察眼内炎的缓解或加重情况。采用卡方检验比较第 3 个月随访时视力达到或优于 20/40 和 20/200 的患者数与发病时的患者数。另外,采用配对 t 检验比较发病时的 LogMAR 视力与第 3 个月末的治疗后视力。

结果

50 例(96.15%)患者眼内炎完全缓解,3 例需行玻璃体切除术。41 例(78.85%)和 49 例(94.23%)患者在第 3 个月随访时的视力分别达到或优于 20/40 和 20/200,而发病时的分别为 8 例(15.38%)和 13 例(25%)(P<0.05)。此外,发病时的平均 LogMAR 视力为 0.755,第 3 个月随访时改善至 0.307(P<0.05)。所有患者均未对玻璃体腔内注射莫西沙星产生过敏反应。

结论

玻璃体腔内注射莫西沙星治疗急性白内障术后眼内炎疗效显著。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6501/7933854/774af148ac80/IJO-69-326-g001.jpg

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