Smt. Kanuri Santhamma Center for Vitreoretinal Diseases, Kallam Anji Reddy Campus, LV Prasad Eye Institute, Hyderabad, India.
Retina and Uveitis Department, GMR Varalaxmi Campus, LV Prasad Eye Institute, Visakhapatnam, India.
Am J Ophthalmol. 2019 Jan;197:53-58. doi: 10.1016/j.ajo.2018.09.007. Epub 2018 Sep 19.
To describe the clinical presentations, diagnosis, and management outcomes of Nocardia endophthalmitis.
Retrospective, interventional, multicenter case series.
The study was conducted in a multicentric institutional practice setup and included 25 eyes of 25 patients with culture-proven Nocardia endophthalmitis. Anterior chamber fluid and/or vitreous and/or intraocular lens were submitted for microbiological evaluation in all cases. Patients with non-Nocardia etiology and those that were culture negative were excluded. Case records were studied and data regarding demography, clinical presentations, interventions received, and final visual and anatomic outcomes were noted. The main outcome measures were final visual outcomes and factors determining them.
The mean age of the patients was 54.7 ± 22.9 years. By the etiology of infection, 18 (75%) eyes were post-cataract surgery (operated elsewhere), 3 (12.5%) eyes were posttrauma, and 3 (12.5%) eyes were endogenous. The final follow-up was a mean of 14.25 ± 30.35 months, median 2 months. The odds of a favorable outcome were 42.5 (95% confidence interval [CI] 3.15 to 571.84, P = .0047) when the vision was more than hand motions at presentation, 9.42 (95% CI 0.92 to 95.89, P = .05) in male sex, 21 (95% CI 0.9 to 489.7, P = .05) when presentation was within 48 hours, and 2.5 (95% CI 0.23 to 26.48, P = .44) with primary vitrectomy instead of a biopsy. The in vitro susceptibility was poor for vancomycin and was best for amikacin.
The visual outcome in Nocardia endophthalmitis is very guarded when presenting vision is poor. On diagnostic confirmation or high index of suspicion, intravitreal amikacin is preferred.
描述诺卡氏菌眼内炎的临床表现、诊断和治疗结果。
回顾性、介入性、多中心病例系列。
该研究在一个多中心机构实践环境中进行,纳入了 25 例 25 只眼经培养证实的诺卡氏菌眼内炎患者。所有病例均行前房液和/或玻璃体和/或眼内晶状体微生物学评估。排除了非诺卡氏菌病因和培养阴性的病例。研究病例记录,记录人口统计学资料、临床表现、接受的干预措施以及最终的视力和解剖学结果。主要观察指标是最终的视力结果和影响视力的因素。
患者的平均年龄为 54.7 ± 22.9 岁。根据感染病因,18 只(75%)眼为白内障术后(在其他地方手术),3 只(12.5%)眼为外伤后,3 只(12.5%)眼为内源性。平均随访时间为 14.25 ± 30.35 个月,中位数为 2 个月。当就诊时视力优于手动视力时,良好结局的可能性为 42.5(95%置信区间[CI] 3.15 至 571.84,P=0.0047),男性时为 9.42(95%CI 0.92 至 95.89,P=0.05),就诊时间在 48 小时内时为 21(95%CI 0.9 至 489.7,P=0.05),行玻璃体切除术而不是活检时为 2.5(95%CI 0.23 至 26.48,P=0.44)。万古霉素的体外敏感性较差,阿米卡星的敏感性最好。
当就诊时视力较差时,诺卡氏菌眼内炎的视力预后非常差。一旦确诊或高度怀疑,应首选玻璃体内注射阿米卡星。