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玻璃体切除术后细菌眼内炎患眼持续性囊样黄斑水肿应用玻璃体内注射地塞米松植入物的中期安全性和有效性。

Mid-term safety and effectiveness of intravitreal dexamethasone implant to treat persistent cystoid macular edema in vitrectomized eyes for bacterial endophthalmitis.

机构信息

Department of Medical Science, Neuroscience and Sense Organs, Eye Clinic, University of Bari, 70124, Bari, Italy.

Eye Clinic, Hospital "SS Annunziata", ASL Taranto, Via F. Bruno, 1, 74010, Taranto, Italy.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2022 Aug;260(8):2703-2710. doi: 10.1007/s00417-022-05615-8. Epub 2022 Mar 7.

Abstract

PURPOSE

To evaluate the mid-term safety and effectiveness of intravitreal dexamethasone implant (DEX-i) for treating unresponsive to medical therapy cystoid macular edema (CME) in vitrectomized eyes for endophthalmitis.

METHODS

Retrospective and interventional case series study conducted on vitrectomized eyes for endophthalmitis that developed a CME that did not adequately respond to medical therapy, who underwent 0.7-mg DEX-i. Main outcome measures were changes in central retinal thickness (CRT) and best corrected visual acuity (BCVA).

RESULTS

Eleven eyes were included in the study. Microbiological findings of vitreous biopsies were 7 (63.6%) staphylococcus epidermidis; 3 (27.3%) Pseudomonas aeruginosa; and 1 (9.1%) Propionibacterium acnes. Median (interquartile range, IqR) duration of CME was 4.0 (3.0-4.0) months. Median (IqR) time between vitrectomy and DEX-i was 9.0 (9.0-11.0) months. Median CRT was significantly decreased from 548.0 (412.8-572.5) µm at baseline to 308.0 (281.3-365.5) µm at month 6 (p = 0.0009, Friedman test). Median BCVA significantly improved from 38.0 (30.5-44.8) letters at baseline to 50.0 (46.8-53.0) letters at month 6 (p < 0.0001, Friedman), with 9 (81.8%) eyes gaining ≥ 10 letters. Elevation of intraocular pressure was observed in one (9.1%) eye, which was successfully controlled with medical therapy. No recurrence of endophthalmitis or other complications was observed. Eight (72.7%) eyes required an additional DEX-i, while 3 (27.3%) were successfully controlled with only one DEX-i. CME recurrence occurred in 5 (62.5%) Gram-positive and 3 (100.0%) Gram-negative bacteria (p = 0.2357).

CONCLUSION

In vitrectomized eyes for endophthalmitis affected by CME unresponsive to medical therapy, DEX-i had an acceptable safety profile and achieved favorable outcomes. The possibility of suppressing mechanisms for infection control should be taken into account, although correct management of endophthalmitis and long time without reactivation before DEX-i reduce the risk.

摘要

目的

评估玻璃体内注射地塞米松植入物(DEX-i)治疗对治疗性反应不佳的内眼炎玻璃体切除术后伴囊样黄斑水肿(CME)的中期安全性和有效性。

方法

回顾性和干预性病例系列研究纳入了玻璃体切除术后发生 CME 的内眼炎患者,这些患者对药物治疗反应不佳,并接受了 0.7mg DEX-i 治疗。主要观察指标为视网膜中央厚度(CRT)和最佳矫正视力(BCVA)的变化。

结果

本研究纳入了 11 只眼。玻璃体活检的微生物学结果为 7 只眼(63.6%)为表皮葡萄球菌;3 只眼(27.3%)为铜绿假单胞菌;1 只眼(9.1%)为痤疮丙酸杆菌。CME 的中位(四分位距,IQR)持续时间为 4.0(3.0-4.0)个月。玻璃体切除术后至 DEX-i 的中位(IQR)时间为 9.0(9.0-11.0)个月。CRT 从基线时的 548.0(412.8-572.5)µm 显著降低至 6 个月时的 308.0(281.3-365.5)µm(p=0.0009,Friedman 检验)。BCVA 从基线时的 38.0(30.5-44.8)个字母显著提高至 6 个月时的 50.0(46.8-53.0)个字母(p<0.0001,Friedman),其中 9 只眼(81.8%)提高了≥10 个字母。一只眼(9.1%)出现眼压升高,经药物治疗成功控制。未观察到内眼炎复发或其他并发症。8 只眼(72.7%)需要再次注射 DEX-i,3 只眼(27.3%)仅用一次 DEX-i 即可成功控制。5 只革兰阳性菌(62.5%)和 3 只革兰阴性菌(100.0%)发生 CME 复发(p=0.2357)。

结论

对于药物治疗反应不佳的内眼炎玻璃体切除术后伴 CME 的患者,DEX-i 具有可接受的安全性,并获得了良好的结果。尽管正确的内眼炎管理和 DEX-i 治疗前长时间没有再激活可以降低风险,但应考虑抑制感染控制机制的可能性。

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