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白内障摘除及人工晶状体植入术后近平滑念珠菌性眼内炎暴发。

Outbreak of Candida parapsilosis endophthalmitis after cataract extraction and intraocular lens implantation.

作者信息

McCray E, Rampell N, Solomon S L, Bond W W, Martone W J, O'Day D

出版信息

J Clin Microbiol. 1986 Oct;24(4):625-8. doi: 10.1128/jcm.24.4.625-628.1986.

DOI:10.1128/jcm.24.4.625-628.1986
PMID:3490490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC268984/
Abstract

Between November 1983 and January 1984, 13 cases of Candida parapsilosis endophthalmitis occurred in Florida, Georgia, and Tennessee in patients who had had an intraocular lens implantation (IOLI) or cataract extraction with an IOLI. This outbreak followed the introduction in July 1983 of a new brand of balanced salt solution (BSS) used as an intraoperative ophthalmic irrigation solution. This product was subsequently recalled because of intrinsic fungal contamination. A retrospective cohort study including 704 ophthalmology patients at risk for exposure to this brand of BSS revealed that definite exposure to that product was a significant risk factor for C. parapsilosis endophthalmitis (P less than 0.001, Fisher exact test). A retrospective case control study including 203 control patients with definite exposure to BSS suggested that exposure to systemic steroids (P = 0.007, Fisher exact test) was an additional risk factor for C. parapsilosis endophthalmitis. Treatment modalities among the 13 patients included topical, intraocular, or systemic antifungal therapy (or a combination of these modalities) in 13 patients and vitrectomy in 10 patients. No patients had systemic symptoms or complete visual loss. Laboratory investigations showed a 6.7% overall contamination of the product with C. parapsilosis. After recall of the product by the manufacturer, no patients having a cataract extraction or IOLI at the institutions studied are known to have developed C. parapsilosis endophthalmitis.

摘要

1983年11月至1984年1月期间,佛罗里达州、佐治亚州和田纳西州有13例近平滑念珠菌性眼内炎病例,患者均接受过人工晶状体植入术(IOLI)或白内障摘除联合IOLI手术。此次疫情爆发之前,1983年7月引入了一种新品牌的平衡盐溶液(BSS),用作术中眼科冲洗液。该产品随后因存在内在真菌污染而被召回。一项回顾性队列研究纳入了704名有接触该品牌BSS风险的眼科患者,结果显示明确接触该产品是近平滑念珠菌性眼内炎的一个重要危险因素(P<0.001,Fisher精确检验)。一项回顾性病例对照研究纳入了203名明确接触过BSS的对照患者,结果表明接触全身用类固醇(P = 0.007,Fisher精确检验)是近平滑念珠菌性眼内炎的另一个危险因素。13名患者的治疗方式包括13名患者采用局部、眼内或全身抗真菌治疗(或这些方式的联合)以及10名患者接受玻璃体切除术。没有患者出现全身症状或完全失明。实验室调查显示该产品总体近平滑念珠菌污染率为6.7%。制造商召回该产品后,在研究机构接受白内障摘除或IOLI手术的患者中,尚无已知发生近平滑念珠菌性眼内炎的病例。

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