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一项评估聚合酶链反应(PCR)作为疑似皮肤癣菌病患者诊断工具的初步研究。

A Pilot Study for the Evaluation of PCR as a Diagnostic Tool in Patients with Suspected Dermatophytoses.

作者信息

Sharma Robin, Gupta Samiksha, Asati Dinesh P, Karuna T, Purwar Shashank, Biswas Debasis

机构信息

Department of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.

Department of Dermatology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.

出版信息

Indian Dermatol Online J. 2017 May-Jun;8(3):176-180. doi: 10.4103/idoj.IDOJ_138_16.

Abstract

CONTEXT

The conventional diagnostic tools for dermatophytoses suffer from several limitations including low sensitivity, specificity, and long turn-around-time.

AIMS

The present study was, therefore, performed to evaluate the performance of a polymerase chain reaction (PCR)-based method for the diagnosis of this condition.

SETTINGS AND DESIGN

The study was conducted in the Dermatology outpatient department of a tertiary care teaching hospital in central India over a period of 3 months from July to September 2015.

MATERIALS AND METHODS

Forty participants, including 25 cases and 15 controls, were recruited in this observational study. Direct microscopy and fungal culture were performed from skin scrapings and nail clippings collected from the participants. PCR was also performed to amplify the chitin synthase 1 and internal transcribed spacer 2 genes from DNA samples extracted from the same clinical materials, using the method reported by Brillowska-Dabrowska et al. The diagnostic performance of fungal culture and PCR was compared using OpenEpi software.

RESULTS

We observed a significant male predominance among patients with dermatophytoses. The sensitivity of fungal culture and dermatophyte PCR to diagnose dermatophytoses was 24% and 48%, respectively, whereas the specificity of the two assays was 100% and 93.3%, respectively. The likelihood ratio of a positive PCR assay was 7.2 and the negative likelihood ratio was 0.5. PCR assay also delivered a significant shortening of the time-to-diagnosis, with the mean turn-around-time being 8 hours and 14 days for PCR and culture, respectively.

CONCLUSION

This study, thus, highlights the potential merits of the dermatophyte PCR assay in achieving a rapid diagnosis of dermatophytoses and underscores its utility as a complementary test to improve the sensitivity of the conventional diagnostic tools for this condition, as well as to reliably differentiate this condition from other similar skin conditions.

摘要

背景

皮肤癣菌病的传统诊断工具存在多种局限性,包括敏感性低、特异性低和周转时间长。

目的

因此,本研究旨在评估基于聚合酶链反应(PCR)的方法对这种疾病的诊断性能。

设置与设计

该研究于2015年7月至9月在印度中部一家三级护理教学医院的皮肤科门诊进行,为期3个月。

材料与方法

本观察性研究招募了40名参与者,包括25例病例和15名对照。从参与者收集的皮肤刮屑和指甲剪屑中进行直接显微镜检查和真菌培养。还使用Brillowska-Dabrowska等人报道的方法进行PCR,以从同一临床材料提取的DNA样本中扩增几丁质合酶1和内转录间隔区2基因。使用OpenEpi软件比较真菌培养和PCR的诊断性能。

结果

我们观察到皮肤癣菌病患者中男性占显著优势。真菌培养和皮肤癣菌PCR诊断皮肤癣菌病的敏感性分别为24%和48%,而两种检测方法的特异性分别为100%和93.3%。PCR检测阳性的似然比为7.2,阴性似然比为0.5。PCR检测还显著缩短了诊断时间,PCR和培养的平均周转时间分别为8小时和14天。

结论

因此,本研究突出了皮肤癣菌PCR检测在快速诊断皮肤癣菌病方面的潜在优点,并强调了其作为补充检测的效用,以提高这种疾病传统诊断工具的敏感性,以及可靠地区分这种疾病与其他类似皮肤疾病。

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