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老年人桩核冠修复前后龈沟内致龋菌变化的比较研究
引用本文:吕岩,徐心怡,郭斌,付敏,贾岳,郭小龙,陈媛媛,袁鹤.老年人桩核冠修复前后龈沟内致龋菌变化的比较研究[J].华西口腔医学杂志,2014,32(1):71-74.
作者姓名:吕岩  徐心怡  郭斌  付敏  贾岳  郭小龙  陈媛媛  袁鹤
作者单位:1.解放军总医院口腔医学研究所,北京 100853;
2.口腔疾病研究国家重点实验室华西口腔医院(四川大学),成都 610041
基金项目:四川省科技计划基金资助项目(2013SZ0008);解放军总医院临床扶持基金资助项目(项目编号:2012FC-TSYS-2003)
摘    要:目的 研究老年人桩核冠修复前后不同时期根面菌斑中主要致龋菌定植数量变化。方法 以单纯随机法选择下颌第一磨牙无咬合功能的患者30人,将一侧需行桩核冠修复的第一磨牙和对侧健康第一磨牙分为受试牙和对照牙。受试牙预备前、预备后 72 h、预备后 1周及冠修复后 1个月,分别采集受试牙与对照牙根面菌斑,然后进行厌氧培养、分离,通过菌落形态学检查、生化特征及聚合酶链反应( PCR)对其中变异链球菌、内氏放线菌和黏性放线菌进行鉴定和菌落计数。结果 受试牙变异链球菌预备前、预备后 72 h、预备后 1周、修复后 1个月菌落计数的变化差异有统计学意义( P<0.05)。受试牙黏性放线菌菌落计数在预备前、预备后 72 h、预备后 1周、修复后 1个月的变化差异有统计学意义( P<0.05)。受试牙内氏放线菌菌落计数在预备前、预备后 72 h及1周、修复后 1月的变化差异有统计学意义(P<0.05)。结论 变异链球菌、内氏放线菌及黏性放线菌在预备后1周菌落计数增加,修复后1个月菌落计数降低。以上结果提示在牙体预备后初期,应指导患者进行菌斑控制。

关 键 词:桩核冠  变异链球菌  放线菌  菌落形成单位  

Comparative studies on cariogenic bacteria of the root surface before and after post-core crown restoration in aged people
Lü Yan,Xu Xinyi,Guo Bin,Fu Min,Jia Yue,Guo Xiaolong,Chen Yuanyuan,Yuan He.Comparative studies on cariogenic bacteria of the root surface before and after post-core crown restoration in aged people[J].West China Journal of Stomatology,2014,32(1):71-74.
Authors:Lü Yan  Xu Xinyi  Guo Bin  Fu Min  Jia Yue  Guo Xiaolong  Chen Yuanyuan  Yuan He
Institution:1. Institute of Stoma-tology, General Hospital of Chinese PLA, Beijing 100853, China; 2. State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China
Abstract: Objective To investigate the changes in the quantity of colonizing Streptococcus mutans(S. mutans) and Acti-nomyces on the root surface plaque before and after post-core crown restoration of the mandibular first molars in the elderly patients. Methods  A total of 30 elderly patients, each with one post-core crown restoration of the mandibular first molar, were randomly chosen to participate in the studies. Patients with mandibular first molars with post-core crown restoration and those with healthy contralateral mandibular first molars were divided into the test and control groups, respectively. Root surface plaques of the two groups were collected before tooth preparation, 72 h after preparation, one week afterpreparation, and one month after restoration. S. mutans, Actinomyces naeslundii (A. naeslundii) and Actinomyces viscosus (A. viscosus), were identified using colony morphology, biochemical techniques, and polymerase chain reaction (PCR). Plaque count was measured usingmicrobial colony count. Results  The number of S. mutans and A. viscosus and A. naeslundii in the test group, whichwas statistically significant (P<0.05), increased 72 h after preparation. The quantities of S. mutans, A. viscosus, and A. naeslundii one week after preparation were significantly different (P<0.05). The plaque count of S. mutans, A. viscosus, and A. naeslundii in the test group decreased one month after restoration (P<0.05). Conclusion  The quantities of S. mutans, A. viscosus and A. naeslundii increase one week after preparation but decrease one month after restoration. The finding suggests that dentists shouldeducatepatientsabout plaquecontrol during the earlyperiod after tooth preparation.
Keywords:   postandcorecrown  Streptococcus mutans  Actinomycetes  colony-forming units
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