Experimental Evaluation of a Novel Device to Quantify Canal Cleanliness: An In Vitro Study

Oral Pub Date : 2024-04-07 DOI:10.3390/oral4020013
Lorenzo Arcuri, G. Gambarini, Alessio Zanza, L. Testarelli, Claudio Arcuri, Randolph Cross, Massimo Galli
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Abstract

Endodontic treatments are performed to avoid extractions and maintain the natural dentition. Root canal treatments are undertaken to eliminate or prevent an infection within the root canal system. Chemical and mechanical root canal debridement are the main methods used in endodontics to remove necrotic tissue, microorganisms, and microbial byproducts from the canal. However, to date there is no objective method to clinically determine the proper root canal disinfection level and thus proceed with the obturation. Clinicians just rely on their experience and habits or can trust in empirical methods such as the insertion of paper cones inside the canal and then check their appearance after the removal. Even in the in vitro and ex vivo scientific studies there is no objective method to analyze and compare the efficacy of different endodontic chemo-mechanical techniques and materials. The most frequently used method is to visually analyze some areas with a scanning electron microscope (SEM), even if the resulting images are hardly quantifiable and could greatly vary according to the analyzed area. A new device to clinically test the cleanliness of a root canal and display the result in an objective score was recently developed. The device analyzes the luminescence generated by an enzyme cycling method that process the adenosine triphosphate (ATP), adenosine diphosphate (ADP) and adenosine monophosphate (AMP) present in organic residues. The aim of the present in vitro study was to test the efficacy and reliability of this novel device (Endocator) in a controlled in vitro environment, before using it in clinical practice. The device sensitivity was tested on 5 single canal resin blocks. Three consecutive sampling were executed by one operator for each block to test the device repeatability. Results were recorded according to Endoscore (ES) and relative light unit (RLU) scales. Descriptive analysis and comparison between the 5 resin blocks and the 3 consecutive sampling were performed. Only the comparison between the first and third measurements both for ES (p = 0.00115999) and RLU (p = 0.00532749) resulted significant. Endocator was able to determine small variations of canal contamination in a controlled laboratory environment, showing high sensitivity and repeatability.
对一种新型设备进行实验评估,以量化管腔清洁度:体外研究
进行牙髓治疗是为了避免拔牙和保持天然牙列。根管治疗是为了消除或预防根管系统内的感染。化学和机械根管清创是根管治疗中用于清除根管中坏死组织、微生物和微生物副产品的主要方法。然而,迄今为止,临床上还没有一种客观的方法来确定适当的根管消毒程度,从而进行封髓。临床医生只能依靠自己的经验和习惯,或者相信经验性的方法,比如将纸锥插入根管,然后在取出后检查纸锥的外观。即使在体外和体内科学研究中,也没有客观的方法来分析和比较不同的牙髓化学机械技术和材料的功效。最常用的方法是用扫描电子显微镜(SEM)对某些区域进行直观分析,尽管所得到的图像很难量化,而且会因分析区域的不同而有很大差异。最近开发了一种新设备,用于临床检测根管的清洁度,并以客观分数显示结果。该设备通过酶循环方法分析有机残留物中的三磷酸腺苷 (ATP)、二磷酸腺苷 (ADP) 和单磷酸腺苷 (AMP) 所产生的荧光。本体外研究的目的是在将这种新型装置(Endocator)用于临床实践之前,在受控体外环境中测试其功效和可靠性。该装置的灵敏度在 5 个单管树脂块上进行了测试。每个树脂块由一名操作员连续取样三次,以测试设备的可重复性。测试结果按照内窥镜评分(ES)和相对光单位(RLU)进行记录。对 5 个树脂块和 3 次连续取样进行了描述性分析和比较。只有第一次和第三次测量的 ES 值(p = 0.00115999)和 RLU 值(p = 0.00532749)之间的比较具有显著性。Endocator 能够在受控的实验室环境中确定牙管污染的微小变化,显示出较高的灵敏度和可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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