某教学机构牙科诊所复合树脂污染调查

S. Werle, Roberto Santos, P. P. Dotto
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引用次数: 4

摘要

目的:通过微生物学分析评价巴西圣玛丽亚市某教学机构三所牙科诊所复合树脂的污染情况,并探讨复合树脂污染与使用频率的关系。方法:首先进行调查,确定每个诊所实习的学生人数和他们参加的教学学期。在不同的诊所有100个样本可供研究,并对所有样本进行了分析。在门诊环境中,从每个复合树脂注射器中无菌收集2毫米的增量。将样品立即送到实验室,浸入含有5ml BHI(脑心输注)培养基的试管中。在37℃的细菌培养箱中培养24小时后,由经验丰富的审查员首次读取培养基浊度,48小时后进行最后一次读取。建立阴性对照组。培养基发生浑浊的样品被认为是污染的。结果:在所分析的复合树脂样品中,有51%的样品被污染,不同诊所的污染比例不同。在诊所实习的学生人数与污染百分比之间存在很强的相关性。结论:在修复过程中,学生发生了导致污染的失败。因此,存在交叉感染的风险,这就需要另一种方法来避免这种过程中的污染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contamination of Composite Resins in Dental Clinics of a Teaching Institution
Objective: To evaluate by microbiological analysis, the contamination of composite resins in three dental clinics of a teaching institution in the city of Santa Maria, RS, Brazil and to assess the correlation between contamination and usage frequency of the resins. Method: First, a survey was performed to determine how many students practiced in each clinic and the teaching semester they were attending. One hundred samples were available for the study in the different clinics and all of them were analyzed. Two-millimeter increments were aseptically collected from each composite resin syringe in the outpatient setting. The samples were immediately to the laboratory and immersed in test tubes containing 5 mL of BHI (Brain Heart Infusion) culture medium. After 24-hour incubation period in a bacteriological incubator at 37oC the first reading of the culture medium turbidity was made by an experienced examiner, and the last reading was made after 48 h. A negative control group was established. The samples in which turbidity of the culture medium occurred were considered as contaminated. Results: 51% of the analyzed composite resin samples were contaminated, with percentage varying among the clinics. A strong correlation was found between the number of students practicing in the clinic and the percentage of contamination. Conclusion: At some point in the restorative procedure performed by the students occurs a failure that results in contamination. Therefore, there is a risk of cross-infection, which requires an alternative way to avoid this contamination in the procedures.
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