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Universal molecular Clostridioides difficile screening and overtreatment in solid organ transplant recipients.普遍的分子梭状芽胞杆菌艰难梭菌筛选和实体器官移植受者的过度治疗。
Transpl Infect Dis. 2020 Oct;22(5):e13375. doi: 10.1111/tid.13375. Epub 2020 Jul 1.
2
Host Immune Markers Distinguish Clostridioides difficile Infection From Asymptomatic Carriage and Non-C. difficile Diarrhea.宿主免疫标志物可区分艰难梭菌感染与无症状携带和非艰难梭菌性腹泻。
Clin Infect Dis. 2020 Mar 3;70(6):1083-1093. doi: 10.1093/cid/ciz330.
3
In Search of the (Clostridium difficile) Holy Grail.寻找(艰难梭菌)圣杯
Clin Infect Dis. 2020 Mar 3;70(6):1094-1095. doi: 10.1093/cid/ciz333.
4
Healthcare provider diagnostic testing practices for identification of Clostridioides (Clostridium) difficile in children: an Emerging Infections Network survey.医疗机构对儿童艰难梭菌(梭状芽孢杆菌)检测的诊断实践:一项新兴传染病网络调查。
Infect Control Hosp Epidemiol. 2019 Mar;40(3):276-280. doi: 10.1017/ice.2018.347. Epub 2019 Feb 15.
5
Frequency of Positive Enzyme Immunoassay for Toxin in Stool of Asymptomatic Carriers of Clostridium difficile.艰难梭菌无症状携带者粪便中毒素酶免疫测定阳性率
Clin Infect Dis. 2019 Feb 1;68(4):711. doi: 10.1093/cid/ciy701.
6
Comparison of Clostridioides difficile Stool Toxin Concentrations in Adults With Symptomatic Infection and Asymptomatic Carriage Using an Ultrasensitive Quantitative Immunoassay.采用超敏定量免疫法比较有症状感染和无症状携带的成人艰难梭菌粪便毒素浓度。
Clin Infect Dis. 2019 Jan 1;68(1):78-86. doi: 10.1093/cid/ciy415.
7
Clinical Practice Guidelines for Clostridium difficile Infection in Adults and Children: 2017 Update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA).临床实践指南:成人和儿童艰难梭菌感染:美国传染病学会(IDSA)和美国医疗保健流行病学学会(SHEA)2017 年更新。
Clin Infect Dis. 2018 Mar 19;66(7):987-994. doi: 10.1093/cid/ciy149.
8
Screening for Clostridium difficile colonization on admission to a hematopoietic stem cell transplant unit may reduce hospital-acquired C difficile infection.入院时对造血干细胞移植病房的艰难梭菌定植进行筛查可能会降低医院获得性艰难梭菌感染。
Am J Infect Control. 2018 Apr;46(4):459-461. doi: 10.1016/j.ajic.2017.10.009. Epub 2017 Nov 21.
9
Reclassification of Clostridium difficile as Clostridioides difficile (Hall and O'Toole 1935) Prévot 1938.艰难梭菌重新分类为艰难梭杆菌(霍尔和奥图尔,1935年)普雷沃,1938年。
Anaerobe. 2016 Aug;40:95-9. doi: 10.1016/j.anaerobe.2016.06.008. Epub 2016 Jun 28.
10
Using Multiplex Molecular Testing to Determine the Etiology of Acute Gastroenteritis in Children.使用多重分子检测确定儿童急性胃肠炎的病因
J Pediatr. 2016 Sep;176:50-56.e2. doi: 10.1016/j.jpeds.2016.05.068. Epub 2016 Jun 18.

两步法检测艰难梭菌在区分儿童感染与定植方面并不充分。

Two-step Testing for Clostridioides Difficile is Inadequate in Differentiating Infection From Colonization in Children.

作者信息

Parnell Jacob M, Fazili Irtiqa, Bloch Sarah C, Lacy D Borden, Garcia-Lopez Valeria A, Bernard Rachel, Skaar Eric P, Edwards Kathryn M, Nicholson Maribeth R

机构信息

Department of Medicine, Vanderbilt University Medical Center, Nashville.

University of Tennessee Health Science Center, Memphis.

出版信息

J Pediatr Gastroenterol Nutr. 2021 Mar 1;72(3):378-383. doi: 10.1097/MPG.0000000000002944.

DOI:10.1097/MPG.0000000000002944
PMID:32925555
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7870537/
Abstract

OBJECTIVES

Recent Infectious Disease Society of America guidelines recommend multistep testing algorithms to diagnose Clostridioides difficile infection (CDI), including a combination of nucleic acid amplification-based testing (NAAT) and toxin enzyme immunoassay (EIA). The use of these algorithms in children, including the ability to differentiate between C. difficile colonization and CDI, however, has not been evaluated.

METHODS

We prospectively enrolled asymptomatic pediatric patients with cancer, cystic fibrosis (CF), or inflammatory bowel disease (IBD) and obtained a stool sample for NAAT testing. If positive by NAAT (colonized), EIA was performed. In addition, children with symptomatic CDI who tested positive by NAAT via the clinical laboratory were enrolled, and EIA was performed on residual stool. A functional cell cytotoxicity neutralization assay (CCNA) was also applied to stool samples from both the colonized and symptomatic cohorts.

RESULTS

Of the 225 asymptomatic children enrolled in the study, 47 (21%) were colonized with C. difficile including 9/59 (15.5%) with cancer, 30/92 (32.6%) with CF, and 8/74 (10.8%) with IBD. An additional 41 children with symptomatic CDI were enrolled. When symptomatic and colonized children were compared, neither EIA positivity (44% vs 26%, P = 0.07) nor CCNA positivity (49% vs 45%, P = 0.70) differed significantly or were able to predict disease severity in the symptomatic cohort.

CONCLUSIONS

Use of a multistep testing algorithm with NAAT followed by EIA failed to differentiate symptomatic CDI from asymptomatic colonization in our pediatric cohort. As multistep algorithms are moved into clinical care, the pediatric provider will need to be aware of their limitations.

摘要

目的

美国传染病学会近期发布的指南推荐采用多步骤检测算法来诊断艰难梭菌感染(CDI),包括基于核酸扩增的检测(NAAT)和毒素酶免疫测定(EIA)相结合的方法。然而,这些算法在儿童中的应用,包括区分艰难梭菌定植和CDI的能力,尚未得到评估。

方法

我们前瞻性纳入了患有癌症、囊性纤维化(CF)或炎症性肠病(IBD)的无症状儿科患者,并获取粪便样本进行NAAT检测。如果NAAT检测呈阳性(定植),则进行EIA检测。此外,纳入通过临床实验室NAAT检测呈阳性的有症状CDI儿童,并对剩余粪便进行EIA检测。还对定植和有症状队列的粪便样本应用了功能性细胞毒性中和试验(CCNA)。

结果

在纳入研究的225名无症状儿童中,47名(21%)被艰难梭菌定植,其中包括9/59名(15.5%)癌症患儿、30/92名(32.6%)CF患儿和8/74名(10.8%)IBD患儿。另外纳入了41名有症状CDI儿童。比较有症状和定植儿童时,EIA阳性率(44%对26%,P = 0.07)和CCNA阳性率(49%对45%,P = 0.70)均无显著差异,也无法预测有症状队列中的疾病严重程度。

结论

在我们的儿科队列中,采用先NAAT后EIA的多步骤检测算法未能区分有症状CDI和无症状定植。随着多步骤算法应用于临床护理,儿科医疗服务提供者需要意识到其局限性。