Sharma S, Jalali S, Adiraju M V, Gopinathan U, Das T
Devchand Nagardas Jhaveri Microbiology Centre, L.V. Prasad Eye Institute, Hyderabad, India.
Retina. 1996;16(6):525-9. doi: 10.1097/00006982-199616060-00010.
Forty-seven consecutive patients with endophthalmitis were prospectively studied to: 1) compare the undiluted vitreous biopsy culture and membrane filter culture of vitrectomy cassette fluid; 2) determine the sensitivity and specificity of initial smear examinations in relation to final culture; and 3) characterize vitreous cytology in culture positive and negative endophthalmitis.
Examinations included smears (Gram stains, Diff Quik [Bacto Laboratories Pvt. Ltd., Liverpool, Australia] and unstained) and aerobic/anaerobic culture of undiluted vitreous biopsy specimens and diluted vitreous collected in the cassette. The cassette fluid was passed through 5-microns polycarbonate filter for cytology and a 0.22-microns polyvinylidene difluoride millipore filter for culture.
By either method culture results were positive in 27 (57.4%) patients. Culture positive of the vitreous biopsy alone was 44.6% and cassette fluid alone was 49% (P > 0.05). In the initial smear examination the sensitivity and specificity of the Gram stain were 66.6% and 84.2%, respectively. comparatively, Diff Quik provided lower sensitivity and specificity at 40.7% and 80.9% respectively. Examination of wet film of vitreous samples did not provide any useful information. Although polymorphs were seen in large numbers in all cultures that yielded positive results on examination, they also were seen in 80% of the sterile samples. There was no significant difference in the quantity of macrophages observed in infected and noninfected samples.
Initial smear examination and cytology have limited roles in the diagnosis of infectious endophthalmitis. Obtaining cultures of both an undiluted vitreous biopsy sample and the vitrectomy cassette fluid has a significant advantage compared with culture of only one sample.
对47例连续性眼内炎患者进行前瞻性研究,以:1)比较未稀释的玻璃体活检培养与玻璃体切割器盒内液体的膜滤器培养;2)确定初始涂片检查相对于最终培养的敏感性和特异性;3)对培养阳性和阴性的眼内炎患者的玻璃体细胞学特征进行描述。
检查包括涂片(革兰氏染色、Diff Quik[澳大利亚利物浦Bacto Laboratories Pvt. Ltd.]及未染色涂片)以及未稀释的玻璃体活检标本和盒内收集的稀释玻璃体的需氧/厌氧培养。盒内液体通过5微米聚碳酸酯滤膜进行细胞学检查,通过0.22微米聚偏二氟乙烯微孔滤膜进行培养。
通过任何一种方法,27例(57.4%)患者的培养结果为阳性。仅玻璃体活检培养阳性率为44.6%,仅盒内液体培养阳性率为49%(P>0.05)。在初始涂片检查中,革兰氏染色的敏感性和特异性分别为66.6%和84.2%。相比之下,Diff Quik的敏感性和特异性较低,分别为40.7%和80.9%。玻璃体样本湿片检查未提供任何有用信息。尽管在所有检查结果为阳性的培养物中均可见大量多形核白细胞,但在80%的无菌样本中也可见到。在感染和未感染样本中观察到的巨噬细胞数量无显著差异。
初始涂片检查和细胞学检查在感染性眼内炎的诊断中作用有限。与仅培养一个样本相比,同时获取未稀释的玻璃体活检样本和玻璃体切割器盒内液体的培养物具有显著优势。