Bacteriology Laboratory, Division of Laboratory Medicine, Department of Diagnostics, Geneva University Hospitals, 4 rue Gabrielle-Perret-Gentil, 1205, Geneva, Switzerland.
Division of Laboratory Medicine, Department of Diagnostics, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
Eur J Clin Microbiol Infect Dis. 2021 Oct;40(10):2171-2176. doi: 10.1007/s10096-021-04233-2. Epub 2021 May 8.
The objective of this study was to evaluate the performances of the automated digital imaging of Gram-stained slides against manual microscopy. Four hundred forty-three identified Gram-stained slides were included in this study. When both methods agreed, we considered the results as correct, and no further examination was carried out. Whenever the methods gave discrepant results, we reviewed the digital images and the glass slides by manual microscopy to avoid incorrectly read smears. The final result was a consensus of multiple independent reader interpretations. Among the 443 slides analyzed in this study, 101 (22.8%) showed discrepant results between the compared methods. The rates of discrepant results according to the specimen types were 5.7% (9/157) for positive blood cultures, 42% (60/142) for respiratory tract specimens, and 22% (32/144) for sterile site specimens. After a subsequent review of the discrepant slides, the final rate of discrepancies dropped to 7.0% (31/443). The overall agreement between the compared methods and the culture results reached 78% (345/443) and 79% (349/443) for manual microscopy and automated digital imaging, respectively. According to culture results, the specificity for automated digital imaging and manual microscopy were 90.8% and 87.7% respectively. In contrast, sensitivity was 84.1% for the two compared methods. The discrepant results were mostly encountered with microorganism morphologies of rare occurrence. The results reported in this study emphasize that on-screen reading is challenging, since the recognition of morphologies on-screen can appear different as compared to routine manual microscopy. Monitoring of Gram stain errors, which is facilitated by automated digital imaging, remains crucial for the quality control of reported Gram stain results.
本研究旨在评估革兰氏染色玻片的自动化数字成像与人工显微镜检查的性能。本研究共纳入 443 张已鉴定的革兰氏染色玻片。当两种方法一致时,我们认为结果是正确的,无需进一步检查。只要两种方法的结果不一致,我们就会通过人工显微镜检查数字图像和载玻片,以避免误读涂片。最终结果是多位独立读者解释的共识。在本研究分析的 443 张载玻片上,有 101 张(22.8%)两种方法的结果不一致。根据标本类型,比较方法不一致的结果发生率分别为:阳性血培养物为 5.7%(9/157),呼吸道标本为 42%(60/142),无菌部位标本为 22%(32/144)。对不一致的载玻片进行后续复查后,不一致的最终发生率降至 7.0%(31/443)。两种比较方法与培养结果的总符合率分别为人工显微镜 78%(345/443)和自动化数字成像 79%(349/443)。根据培养结果,自动化数字成像和人工显微镜的特异性分别为 90.8%和 87.7%。相比之下,两种比较方法的敏感性分别为 84.1%。不一致的结果主要与罕见出现的微生物形态有关。本研究结果强调,屏幕阅读具有挑战性,因为屏幕上的形态识别与常规人工显微镜检查相比可能会有所不同。通过自动化数字成像来监测革兰氏染色错误对于报告的革兰氏染色结果的质量控制仍然至关重要。