Wills Eye Hospital, Mid Atlantic Retina, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Wills Eye Hospital, Mid Atlantic Retina, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Am J Ophthalmol. 2021 Feb;222:194-201. doi: 10.1016/j.ajo.2020.08.013. Epub 2020 Sep 2.
To evaluate the effect of physician face mask use on rates and outcomes of postinjection endophthalmitis.
Retrospective, comparative cohort study.
Setting: Single-center. StudyPopulation: Eyes receiving intravitreal anti-vascular endothelial growth factor injections from July 1, 2013, to September 1, 2019.
Cases were divided into "Face Mask" group if face masks were worn by the physician during intravitreal injections or "No Talking" group if no face mask was worn but a no-talking policy was observed during intravitreal injections. MainOutcomeMeasures: Rate of endophthalmitis, visual acuity, and microbial spectrum.
Of 483,622 intravitreal injections administered, 168 out of 453,460 (0.0371%) cases of endophthalmitis occurred in the No Talking group, and 9 out of 30,162 (0.0298%) cases occurred in the Face Mask group (odds ratio, 0.81; 95% confidence interval, 0.41-1.57; P = .527). Sixteen cases of oral flora-associated endophthalmitis were found in the No Talking group (1 in 28,341 injections), compared to none in the Face Mask group (P = .302). Mean logMAR visual acuity at presentation in cases that developed culture-positive endophthalmitis was significantly worse in the No Talking group compared to the Face Mask group (17.1 lines lost from baseline acuity vs 13.4 lines lost; P = .031), though no difference was observed at 6 months after treatment (P = .479).
Physician face mask use did not influence the risk of postinjection endophthalmitis compared to a no-talking policy. However, no cases of oral flora-associated endophthalmitis occurred in the Face Mask group. Future studies are warranted to assess the role of face mask use to reduce endophthalmitis risk, particularly attributable to oral flora.
评估医生戴口罩对注射后眼内炎发生率和结局的影响。
回顾性、比较队列研究。
地点:单中心。研究人群:2013 年 7 月 1 日至 2019 年 9 月 1 日接受玻璃体内抗血管内皮生长因子注射的眼睛。
如果医生在玻璃体内注射时戴口罩,则将病例分为“戴口罩”组,如果不戴口罩但在玻璃体内注射时遵守“不说话”政策,则将病例分为“不说话”组。主要观察指标:眼内炎发生率、视力和微生物谱。
在 483622 次玻璃体内注射中,168 例(0.0371%)发生在“不说话”组,9 例(0.0298%)发生在“戴口罩”组(比值比,0.81;95%置信区间,0.41-1.57;P=.527)。在“不说话”组发现 16 例口腔菌群相关眼内炎(1 例/28341 次注射),而在“戴口罩”组未发现(P=.302)。发生培养阳性眼内炎的病例在就诊时的平均 logMAR 视力明显较“戴口罩”组差(从基线视力丧失 17.1 行 vs 丧失 13.4 行;P=.031),但治疗 6 个月后无差异(P=.479)。
与不说话政策相比,医生戴口罩使用并未影响注射后眼内炎的风险。然而,在“戴口罩”组未发生口腔菌群相关眼内炎。需要进一步研究来评估戴口罩使用以降低眼内炎风险的作用,特别是归因于口腔菌群。