首页> 美国卫生研究院文献>International Journal of Environmental Research and Public Health >Effect of Chinese Propolis as an Intracanal Medicament on Post-Operative Endodontic Pain: A Double-Blind Randomized Controlled Trial
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Effect of Chinese Propolis as an Intracanal Medicament on Post-Operative Endodontic Pain: A Double-Blind Randomized Controlled Trial

机译:蜂胶作为根管内药物对术后牙髓痛的影响:双盲随机对照试验

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摘要

Propolis is a potent anti-microbial and natural anti-inflammatory by-product obtained from the beehive. Studies have demonstrated the superior biocompatibility and anti-microbial properties of propolis as compared to calcium hydroxide. However, its effect on postoperative endodontic pain is unknown. Therefore, this study aimed to investigate the impact of Chinese propolis paste as an intracanal medicament on postoperative endodontic pain intensities compared with calcium hydroxide (control) at different time intervals in necrotic teeth with periapical radiolucency. Eighty patients with single-rooted necrotic teeth with visible periapical radiolucency were recruited and randomly allocated to either the calcium hydroxide or propolis groups. After chemo-mechanical preparation and intracanal medicament insertion, patients were given the VAS (visual analogue scale) to record pain scores. Inter-group data were compared and analyzed using two-way repeated measure ANOVA (Bonferroni test). A -value of < 0.025 was considered significant. In total, >78% of the patients experienced no or only mild post-operative pain in both the groups at all time intervals, without any significant difference in pain scores between the two groups ( > 0.025). An overall flare-up rate of 14.8% was found. The results suggest that either of these medicaments can be used as an inter-appointment medication for the prevention of postoperative pain in necrotic cases.
机译:蜂胶是从蜂箱中获得的有效的抗菌和天然消炎副产品。研究表明,与氢氧化钙相比,蜂胶具有出色的生物相容性和抗微生物特性。但是,其对术后牙髓痛的作用尚不清楚。因此,本研究旨在研究不同时间间隔的根尖周透性坏死牙龈牙膏作为根管内药物与氢氧化钙(对照组)在不同时间间隔对牙髓痛强度的影响。招募了80名具有根尖周透照性的单根坏死牙齿的患者,并将其随机分配至氢氧化钙或蜂胶组。在进行化学机械准备和插入腔内药物后,给患者提供VAS(视觉模拟评分)以记录疼痛评分。使用两次重复测量方差分析(Bonferroni检验)对组间数据进行比较和分析。 <0.025的-值被认为是重要的。总体而言,两组中的> 78%的患者在所有时间间隔内均未经历或仅有轻微的术后疼痛,两组之间的疼痛评分无显着差异(> 0.025)。发现整体爆发率为14.8%。结果表明,这些药物中的任何一种都可以用作预防坏死病例术后疼痛的预约药物。

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