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三种用于鉴定牙周病原体的商用分子诊断测试的组内和组间一致性

Inter- and intra-test agreement of three commercially available molecular diagnostic tests for the identification of periodontal pathogens.

作者信息

Untch Martin, Schlagenhauf Ulrich

机构信息

Private Dental Practice, Bahnhofstr. 9, 63654, Buedingen, Germany.

Department of Periodontology, University Hospital Wuerzburg, Pleicherwall 2, 97070, Wuerzburg, Germany.

出版信息

Clin Oral Investig. 2015 Nov;19(8):2045-52. doi: 10.1007/s00784-015-1418-3. Epub 2015 Feb 15.

Abstract

OBJECTIVE

The aim of the study was to compare the agreement and reproducibility of three test kits (IAI Pado Test 4⋅5®, micro-IDent®, and Carpegen® Perio Diagnostik) regarding the detection of Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, and Aggregatibacter actinomycetemcomitans.

MATERIALS AND METHODS

Periodontal plaque samples from 20 patients suffering from severe chronic or aggressive periodontitis were split into two identical batches. Samples of batch 1 were evaluated immediately. Samples of batch 2 were analyzed after a storage period of 2 weeks at 4 °C.

RESULTS

The conformity of results obtained by the evaluated test kits as well as the concordant detection rate of periodontopathogens proved to be low. The agreement of the detection rate depends on the chosen test kit. The intra-test reproducibility of the qualitative analysis of identical plaque samples was perfect only for Carpegen® Perio Diagnostik. The quantitative analysis of the results expressed as n-fold difference of the test results revealed an only poor inter-test agreement between the test systems.

CONCLUSIONS

Results of test kits for the identification of periodontopathogens are significantly influenced by the detection technology applied. The most advanced technology tended to give the most reliable results.

CLINICAL RELEVANCE

As microbiological test results are supposed to be used for the planning of subsequent treatment strategies, clinicians should be aware of the limitations of results obtained by the different test systems and should use the results only in conjunction with clinical data for subsequent therapeutic decisions.

摘要

目的

本研究旨在比较三种检测试剂盒(IAI Pado Test 4⋅5®、micro-IDent®和Carpegen® Perio Diagnostik)在检测牙龈卟啉单胞菌、福赛坦氏菌、具核梭杆菌和伴放线聚集杆菌方面的一致性和可重复性。

材料与方法

将20例重度慢性或侵袭性牙周炎患者的牙周菌斑样本分成两个相同批次。批次1的样本立即进行评估。批次2的样本在4℃下保存2周后进行分析。

结果

经评估的检测试剂盒所获得结果的一致性以及牙周病原体的一致检出率较低。检出率的一致性取决于所选用的检测试剂盒。仅Carpegen® Perio Diagnostik对相同菌斑样本的定性分析在检测内具有完美的可重复性。以检测结果的n倍差异表示的结果定量分析显示,各检测系统之间的检测间一致性较差。

结论

用于鉴定牙周病原体的检测试剂盒的结果受所应用检测技术的显著影响。最先进的技术往往能给出最可靠的结果。

临床意义

由于微生物检测结果应用于后续治疗策略的规划,临床医生应意识到不同检测系统所获结果的局限性,并且在后续治疗决策中应仅将这些结果与临床数据结合使用。

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