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基于五年临床经验评估 16S 和 18S rRNA 基因靶向的下一代测序的诊断准确性和临床实用性。

Evaluating the diagnostic accuracy and clinical utility of 16S and 18S rRNA gene targeted next-generation sequencing based on five years of clinical experience.

机构信息

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Department of Clinical Microbiology, Aalborg University Hospital, Aalborg, Denmark.

出版信息

Infect Dis (Lond). 2023 Nov;55(11):767-775. doi: 10.1080/23744235.2023.2241550. Epub 2023 Aug 3.

Abstract

BACKGROUND

The use of 16S/18S rRNA targeted next-generation sequencing (tNGS) has improved microbial diagnostics, however, the use of tNGS in a routine clinical setting requires further elucidation. We retrospectively evaluated the diagnostic accuracy and clinical utility of 16S/18S tNGS, routinely used in the North Denmark Region between 2017 and 2021.

METHODS

We retrieved 544 tNGS results from 491 patients hospitalised with suspected infection (e.g. meningitis, pneumonia, intraabdominal abscess, osteomyelitis and joint infection). The tNGS assays was performed using the Illumina MiSeq desktop sequencer, and BION software for annotation. The patients' diagnosis and clinical management was evaluated by medical chart review. We calculated sensitivity and specificity, and determined the diagnostic accuracy of tNGS by defining results as true positive, true negative, false positive, and false negative.

RESULTS

Overall, tNGS had a sensitivity of 56% and a specificity of 97%. tNGS was more frequently true positive compared to culture (32% vs 18%), and tNGS detected a greater variety of bacteria and fungi, and was more frequently polymicrobial. However, the total diagnostic turnaround time was 16 days, and although 73% of tNGS results were true positive or true negative, only 4.4% of results led to changes in clinical management.

CONCLUSIONS

As a supplement to culture, tNGS improves identification of pathogenic microorganisms in a broad range of clinical specimens. However, the long turnaround time of tNGS in our setting may have contributed to a limited clinical utility. An improved turnaround time can be the key to improved clinical utility in a future setting.

摘要

背景

16S/18S rRNA 靶向下一代测序(tNGS)的使用提高了微生物诊断水平,然而,在常规临床环境中使用 tNGS 还需要进一步阐明。我们回顾性评估了 16S/18S tNGS 在 2017 年至 2021 年期间在丹麦北部地区常规使用的诊断准确性和临床实用性。

方法

我们从 491 名疑似感染(如脑膜炎、肺炎、腹腔脓肿、骨髓炎和关节感染)住院患者中检索了 544 份 tNGS 结果。tNGS 检测使用 Illumina MiSeq 台式测序仪和 BION 软件进行注释。通过病历回顾评估患者的诊断和临床管理。我们计算了敏感性和特异性,并通过将结果定义为真阳性、真阴性、假阳性和假阴性来确定 tNGS 的诊断准确性。

结果

总的来说,tNGS 的敏感性为 56%,特异性为 97%。tNGS 比培养更常为真阳性(32% 比 18%),tNGS 检测到更多种类的细菌和真菌,且更常为混合感染。然而,总诊断周转时间为 16 天,尽管 73%的 tNGS 结果为真阳性或真阴性,但只有 4.4%的结果导致临床管理的改变。

结论

作为培养的补充,tNGS 提高了对广泛临床标本中病原体微生物的识别。然而,在我们的环境中,tNGS 的长周转时间可能导致其临床实用性有限。在未来的环境中,提高周转时间可能是提高临床实用性的关键。

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