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比较直肠拭子和粪便样本在新型内部 PCR 检测中的应用。

Comparison of rectal swabs and fecal samples for the detection of infections with a new in-house PCR assay.

机构信息

Centre de recherche en infectiologie de l'Université Laval, Québec City, Canada.

Centre de recherche du Centre hospitalier universitaire de Québec-Université Laval, Québec City, Canada.

出版信息

Microbiol Spectr. 2024 Jun 4;12(6):e0022524. doi: 10.1128/spectrum.00225-24. Epub 2024 Apr 30.

Abstract

UNLABELLED

The detection of infections (CDI) relies on testing the stool of patients by toxin antigen detection or PCR methods. Although PCR and antigenic methods have significantly reduced the time to results, delays in stool collection can significantly add to the turnaround time. The use of rectal swabs to detect could considerably reduce the time to diagnosis of CDI. We developed a new rapid PCR assay for the detection of and evaluated this PCR assay on both stool and rectal swab specimens. We recruited a total of 623 patients suspected of infection. Stool samples and rectal swabs were collected from each patient and tested by our PCR assay. Stool samples were also tested by the cell cytotoxicity neutralization assay (CCNA) as a reference. The PCR assay detected in 60 stool specimens and 61 rectal swabs for the 64 patients whose stool samples were positive for by CCNA. The PCR assay detected an additional 35 and 36 stool and rectal swab specimens positive for , respectively, for sensitivity with stools and rectal swabs of 93.8% and 95.3%, specificity of 93.7% and 93.6%, positive predictive values of 63.2% and 62.9%, and negative predictive values of 99.2% and 99.4%. Detection of using PCR on stools or rectal swabs yielded reliable and similar results. The use of PCR tests on rectal swabs could reduce turnaround time for CDI detection, thus improving CDI management and control of transmission.

IMPORTANCE

infection (CDI) is the leading cause of healthcare-associated diarrhea, resulting in high morbidity, mortality, and economic burden. In clinical laboratories, CDI testing is currently performed on stool samples collected from patients with diarrhea. However, the diagnosis of CDI can be delayed by the time required to collect stool samples. Barriers to sample collection could be overcome by using a rectal swab instead of a stool sample. Our study showed that CDI can be identified rapidly and reliably by a new PCR assay developed in our laboratory on both stool and rectal swab specimens. The use of PCR tests on rectal swabs could reduce the time for the detection of CDI and improve the management of this infection. It should also provide a useful alternative for infection-control practitioners to better control the spread of .

摘要

未标注

感染(CDI)的检测依赖于通过毒素抗原检测或 PCR 方法对患者的粪便进行检测。虽然 PCR 和抗原方法显著缩短了结果的时间,但粪便采集的延迟会显著增加周转时间。使用直肠拭子检测 可以大大缩短 CDI 的诊断时间。我们开发了一种新的快速 PCR 检测方法来检测 ,并在粪便和直肠拭子标本上评估了该 PCR 检测方法。我们招募了总共 623 名疑似感染的患者。从每位患者中采集粪便样本和直肠拭子,并通过我们的 PCR 检测方法进行检测。粪便样本还通过细胞细胞毒性中和测定(CCNA)进行检测作为参考。PCR 检测方法在通过 CCNA 检测到 64 名患者的粪便样本阳性的 60 份粪便样本和 61 份直肠拭子中检测到 。PCR 检测方法分别检测到另外 35 份和 36 份粪便和直肠拭子标本为阳性,粪便和直肠拭子的灵敏度分别为 93.8%和 95.3%,特异性为 93.7%和 93.6%,阳性预测值分别为 63.2%和 62.9%,阴性预测值分别为 99.2%和 99.4%。使用粪便或直肠拭子上的 PCR 检测 可以获得可靠且相似的结果。在 CDI 检测中使用直肠拭子上的 PCR 检测可以缩短周转时间,从而改善 CDI 的管理和控制 传播。

重要性

感染(CDI)是医疗保健相关腹泻的主要原因,导致高发病率、死亡率和经济负担。在临床实验室中,目前对腹泻患者的粪便样本进行 CDI 检测。然而,采集粪便样本所需的时间可能会延迟 CDI 的诊断。通过使用直肠拭子代替粪便样本,可以克服样本采集的障碍。我们的研究表明,通过我们实验室开发的新 PCR 检测方法,可快速可靠地在粪便和直肠拭子标本上识别 CDI。使用直肠拭子上的 PCR 检测可以缩短 CDI 的检测时间,并改善这种感染的管理。它还应该为感染控制从业者提供有用的替代方法,以更好地控制 的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae3/11237655/0d4fdc2ec8d8/spectrum.00225-24.f001.jpg

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