Department of Laboratory Medicine and Pathology, University of Washingtongrid.34477.33grid.471394.cgrid.34477.33 School of Medicine, Seattle, Washington, USA.
Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
J Clin Microbiol. 2021 Oct 19;59(11):e0095521. doi: 10.1128/JCM.00955-21. Epub 2021 Aug 18.
Broad-range fungal PCR is a powerful tool for identifying pathogens directly from patient specimens; however, reported estimates of clinical utility vary and costs discourage universal testing. We investigated the diagnostic and clinical utility of broad-range fungal PCR by examining 9 years of results from sinonasal specimens, hypothesizing that this anatomic location would identify immunocompromised patients at high risk for invasive fungal disease. We retrospectively identified 644 PCRs and 1,446 fungal cultures from sinus sites. To determine the relative performance of each testing modality, we performed chart review on 52 patients having specimens submitted for culture and PCR on the same day. Positivity rates were significantly higher for PCR (37.1%) than culture (13.7%) but similar for formalin-fixed and fresh tissues (42.3% versus 34.6%). Relative to culture, PCR had significantly faster turnaround time to both preliminary (94.5 versus 108.8 h) and final positive (137.9 versus 278.5 h) results. Among chart-reviewed patients, 88% were immunocompromised, 65% had proven or probable fungal disease, and testing sensitivities for culture and PCR (67.5% and 85.0%) were not statistically different. Nevertheless, PCR identified pathogens not recovered by culture in 14.9% of cases and informed clinical decision-making in 16.7% of all reviewed cases, and sensitivity of PCR combined with culture (90.0%) was higher than that of culture alone. We conclude that broad-range fungal PCR is frequently informative for patients at risk of serious fungal disease and is complementary to and has faster turnaround time than culture. Formalin-fixed tissue does not adversely affect diagnostic yield, but anatomic site may impact assay positivity rates.
广谱真菌 PCR 是一种从患者标本中直接鉴定病原体的强大工具;然而,报告的临床实用性估计各不相同,成本也阻碍了普遍检测。我们通过检查 9 年来鼻腔鼻窦标本的结果,研究了广谱真菌 PCR 的诊断和临床实用性,假设该解剖位置可以识别出患有侵袭性真菌病风险高的免疫功能低下患者。我们回顾性地确定了 644 例 PCR 和 1446 例鼻窦部位的真菌培养物。为了确定每种检测方式的相对性能,我们对 52 名同一天同时提交培养物和 PCR 标本的患者进行了图表回顾。PCR 的阳性率(37.1%)明显高于培养(13.7%),但福尔马林固定和新鲜组织的阳性率相似(42.3%与 34.6%)。与培养相比,PCR 初步(94.5 与 108.8 小时)和最终阳性(137.9 与 278.5 小时)结果的周转时间明显更快。在图表回顾的患者中,88%为免疫功能低下,65%患有已证实或可能的真菌感染,培养和 PCR 的检测敏感性(67.5%和 85.0%)无统计学差异。然而,PCR 在 14.9%的病例中鉴定出培养未回收的病原体,并在 16.7%的所有回顾病例中影响临床决策,PCR 与培养相结合的敏感性(90.0%)高于单独培养的敏感性。我们得出的结论是,广谱真菌 PCR 经常为患有严重真菌感染风险的患者提供信息,与培养相辅相成,并且比培养的周转时间更快。福尔马林固定组织不会对诊断结果产生不利影响,但解剖部位可能会影响检测阳性率。