探索非典型拔除第三下磨牙后牙槽骨愈合优化的细胞学问题

M.А. Mugalbayeva, U.R. Mirzakulova, G.B. Zaitenova, Z.S. Uglanov
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摘要

本研究旨在探讨非典型拔除下第三磨牙后牙槽骨愈合的细胞学特征,利用骨整形合成材料与富含血小板因子的血小板凝胶和血浆相结合,增强局部骨生成。材料与方法 在这项比较临床研究中,在非典型拔除下第三磨牙后收集了牙槽内容物涂片。对细胞元素进行量化,以便进行细胞学分析。数据收集使用 Microsoft Excel 16.34 版开发的模板。统计处理使用 RStudio 2023.03.1 Build 446(Posit Software,PBC)进行。涂片风干后,用 1:1 的酒精和丙酮混合液固定 5 分钟,先用 May-Grünwald 亚甲基蓝染色(15 分钟),然后用 Romanowsky-Giemsa 天青-伊红染色(30 分钟)。涂片图像由 Leica morpho 密度测定复合仪采集:DM 1000显微镜和DFC-320相机,以400倍放大率获得jpg格式的图像。结果 该研究包括 30 名患者,分为对照组和实验组。细胞学分析分别在术后第 2 天、第 5 天和第 10 天进行。两组患者术后第 2 天的肺泡涂片均显示有红细胞(6 个)和中性粒细胞(2 个)。第 5 天,实验组出现中性粒细胞(3 个)和大量球菌(6 个)。第 10 天,上皮细胞(n = 8)主要表现为增殖。结论 所获结果表明,在非典型拔除第三磨牙后,采用骨整形合成材料与富含血小板因子的血小板凝胶和血浆相结合,可有效增强局部骨生成。与对照组相比,这种方法明显提高了上皮化活性、成纤维活性和修复过程的其他指标。
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EXPLORING CYTOLOGICAL ASPECTS OF SOCKET HEALING OPTIMIZATION AFTER ATYPICALREMOVAL OF THE THIRD LOWER MOLAR
This study aims to investigate the cytological characteristics of socket healing after atypical removal of the lower third molar, utilizing osteoplastic synthetic material in conjunction with platelet-rich gel and plasma enriched with thrombocyte factors, to enhance local osteogenesis. Materials and Methods For this comparative clinical study, smears of alveolar content were collected following atypical extraction of the lower third molar. Cell elements were quantified for cytological analysis. Data collection utilized a template developed in Microsoft Excel version 16.34. Statistical processing was performed using RStudio 2023.03.1 Build 446 (Posit Software, PBC). Smears were air-dried, fixed in a 1:1 mixture of alcohol and acetone for 5 minutes, stained first with May-Grünwald’s methylene blue (15 minutes), followed by Romanowsky-Giemsa’s azure-eosin stain (30 minutes). Smear images were captured with the Leica morpho densitometric complex: DM 1000 microscope, DFC-320 camera, images were obtained in jpg format at 400x magnification. Results The study encompassed 30 patients divided into control and experimental groups. Cytological analysis was conducted on the 2nd, 5th, and 10th days of post- operation. In both groups, on the 2nd day, alveolar smears showed the presence of erythrocytes (n = 6) and neutrophils (n = 2). On the 5th day, the experimental group exhibited neutrophils (n = 3) and abundant cocci microflora (n = 6). On the 10th day, epitheliocytes (n = 8) primarily indicated proliferation. Conclusions The obtained results underscore the effectiveness of employing osteoplastic synthetic material in combination with plateletrich gel and plasma enriched with thrombocyte factors for enhancing local osteogenesis following atypical removal of the third molar. This approach demonstrates significant elevation in epithelialization activity, fibroblastic activity, and other markers of the reparative process in comparison to the control group.
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