Fibrin clot adherence on cleaned and decontaminated titanium abutment surfaces: An in vitro study.

Habibe Öztürk Ulusoy, Esra Ercan, Orhan Özatik, Mustafa Tunalı
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Abstract

Statement of problem: Osseointegration is now primarily established, but soft tissue integration is still susceptible to failure and problematic on implant surfaces. So, implant dentistry is increasingly focusing on improving peri-implant soft tissue integration.

Purpose: The present study aimed to evaluate the blood fibrin clot formation and adhesion on the abutment after cleaning and decontamination and determine the suitable abutment surface associated with fibrin clot attachment.

Materials and methods: Forty-two abutments (14 per group) were used in the present study: a brand-new (BN), contaminated with biofilm (CO) and decontaminated with an enzymatic cleaner and autoclave sterilization (DEC). For a fibrin clot, 9 mL of whole human blood and abutments was centrifuged at 2700 rpm for 12 min. Clots were divided into two parts for histomorphometry and scanning electron microscopy (SEM) analysis. Twelve abutments disconnected from the clot and two not treated with blood were observed under SEM.

Results: Residual debris and biofilm were observed on the abutment surface in the CO group but not in other groups. Healthy and organized fibrin clots formed on all abutments. The fibrin extension areas are distributed uniformly in BN and DEC groups but irregularly in CO. The surface percentage of the fibrin clot extensions was 41.76% ± 6.73, 26.99% ± 6.40, and 37.83% ± 9.72 for the BN, CON, and DEC groups, respectively. The blood clot-attached areas in the CO group were statistically lower than the other groups. No difference was observed between the BN and DEC groups.

Conclusions: This study confirmed that surface contamination could influence blood clot attachment on the abutment surfaces. Cleaning and sterilization can have a favorable effect on soft tissue healing on abutment surfaces.

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纤维蛋白凝块在清洁和去污钛基台表面的附着力:体外研究
问题陈述:骨结合目前已基本确立,但软组织结合仍容易失败,种植体表面的软组织结合也存在问题。目的:本研究旨在评估清洁和去污后基台表面血纤维蛋白凝块的形成和附着情况,并确定与纤维蛋白凝块附着相关的合适基台表面:本研究使用了 42 个基台(每组 14 个):全新的(BN)、被生物膜污染的(CO)和用酶清洗剂和高压灭菌器消毒的(DEC)。对于纤维蛋白凝块,9 毫升的全人类血液和基台在 2700 转/分的转速下离心 12 分钟。凝块被分成两部分,用于组织形态测量和扫描电子显微镜(SEM)分析。在扫描电子显微镜下观察了 12 个与血块分离的基台和两个未用血液处理的基台:结果:在 CO 组的基台表面观察到残留碎屑和生物膜,而在其他组则没有。所有基台上都形成了健康有序的纤维蛋白凝块。纤维蛋白扩展区在 BN 组和 DEC 组分布均匀,但在 CO 组分布不规则。BN组、CON组和DEC组纤维蛋白凝块扩展区的表面百分比分别为41.76%±6.73、26.99%±6.40和37.83%±9.72。据统计,CO 组的血凝块附着面积低于其他组。结论:这项研究证实,表面污染会影响基台表面的血凝块附着。清洁和消毒可以对基台表面软组织的愈合产生有利影响。
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