From the Department of Ophthalmology, University of Virginia, Charlottesville, Virginia, USA.
From the Department of Ophthalmology, University of Virginia, Charlottesville, Virginia, USA.
Am J Ophthalmol. 2024 Jun;262:97-106. doi: 10.1016/j.ajo.2024.01.018. Epub 2024 Jan 26.
To evaluate factors that inform systemic antifungal choices in patients with endogenous fungal endophthalmitis (EFE).
Single-institution retrospective case series.
Charts of EFE patients from 2010 to 2023 were reviewed. Patients treated systemically for EFE with a minimum of 14 days of follow-up were included. Outcome measures included time to improvement in vitritis or chorioretinitis, systemic therapy modification, and need for surgical intervention.
A total of 20 eyes of 16 patients were included. Candida species were most common (43.8%), followed by culture-negative EFE (37.5%) and Aspergillus species (18.8%). In all, 90% of eyes had vitritis and/or macula-involving chorioretinitis. The majority of Candida infections (60%) or culture-negative EFE (75%) were treated initially with oral antifungals. Patients with a history of immune compromise, positive fungal culture, or positive Fungitell assay were more likely to be treated with early intravenous (IV) antifungal therapy. Two patients required systemic antifungal therapy modification because of worsening chorioretinitis, in 1 case due to voriconazole-resistant Aspergillosis that demonstrated chorioretinal lesion growth despite intravitreal amphotericin B injections and systemic voriconazole, and in the second case due to worsening chorioretinitis from Candida dubliniensis infection that regressed upon switch from oral to IV fluconazole.
Initial systemic treatment decisions in patients with EFE were driven by systemic culture positivity, systemic symptoms, or comorbidities. Intravitreal antifungal therapy may be insufficient to arrest progression of chorioretinal lesions in some cases. Larger studies are needed to determine whether visible end-organ damage in the form of chorioretinitis may be useful for guiding systemic therapy changes.
评估内生真菌性眼内炎(EFE)患者全身抗真菌治疗选择的影响因素。
单中心回顾性病例系列研究。
回顾了 2010 年至 2023 年 EFE 患者的病历。纳入接受至少 14 天随访的 EFE 患者,接受全身治疗。观察指标包括玻璃体炎或脉络膜视网膜炎改善时间、全身治疗药物改变和手术干预需求。
共纳入 16 例患者的 20 只眼。最常见的病原体是念珠菌(43.8%),其次是培养阴性的 EFE(37.5%)和曲霉菌(18.8%)。所有眼均有玻璃体炎和/或累及黄斑的脉络膜视网膜炎。60%的念珠菌感染或 75%的培养阴性 EFE 患者最初接受口服抗真菌药物治疗。有免疫功能受损史、真菌培养阳性或 Fungitell 检测阳性的患者更可能接受早期静脉(IV)抗真菌治疗。有 2 例患者因脉络膜视网膜炎恶化而需要更改全身抗真菌治疗方案,1 例为曲霉菌属感染,尽管玻璃体腔注射两性霉素 B 和全身伏立康唑治疗,但伏立康唑耐药性曲霉菌的眼内和眼外病变仍进展,另 1 例为 Candida dubliniensis 感染,在口服氟康唑改为静脉用氟康唑后,脉络膜视网膜炎好转。
EFE 患者的初始全身治疗决策取决于全身培养阳性、全身症状或合并症。在某些情况下,玻璃体内抗真菌治疗可能不足以阻止脉络膜视网膜炎病变的进展。需要进行更大规模的研究,以确定脉络膜视网膜炎等眼内终末器官损害是否有助于指导全身治疗药物的改变。