Forgie A H, Paterson M, Pine C M, Pitts N B, Nugent Z J
Dental Public Health and Health Psychology Section, Dundee Dental Hospital and School, Dundee, Scotland, UK.
Caries Res. 2000 Sep-Oct;34(5):432-9. doi: 10.1159/000016619.
A professionally applied two-stage chlorhexidine varnish, Chlorzoin((R)), was developed to achieve sustained release and minimise the problems of staining and bad taste associated with chlorhexidine mouthrinses. The primary aim of this randomised controlled clinical trial was to assess the efficacy of Chlorzoin in reducing the caries increment in high-caries-risk adolescents. Secondary aims included investigating the effect of compliance upon caries increment, the effect of Chlorzoin upon salivary mutans streptococci levels and assessing the benefit of individual dental health advice by dental auxiliaries in a community setting. 1,240 children, initially aged 11-13 years, assessed to be at high caries risk were recruited into the trial. The trial design involved four arms: an observational group, a control group, an active (Chlorzoin) varnish group and a placebo varnish group. All subjects were examined annually by a calibrated examiner who was blind to the group allocation. Three-year caries increments were calculated using clinical, clinical and fibre-optic transillumination, and clinical and bitewing data sets. The results indicated that the use of Chlorzoin had an initial effect on mutans streptococci levels but that no long-term reduction in caries increment or mutans streptococci infection could be detected. One reason for this lack of efficacy may have been the regimen of reduced frequency of varnish applications after the initial period. Children who followed the protocol and, therefore, were seen regularly by dental auxiliaries had a lower caries increment than those who did not. This finding was independent of varnish allocation. In summary, under this regimen, Chlorzoin has been found to be effective in decreasing salivary mutans streptococci but ineffective as a caries-preventive agent in high-risk Scottish children when applied pragmatically in a community setting.
一种专业应用的两阶段洗必泰清漆Chlorzoin((R))被研发出来,以实现持续释放,并将与洗必泰漱口水相关的染色和不良味道问题降至最低。这项随机对照临床试验的主要目的是评估Chlorzoin在降低高龋齿风险青少年龋齿增量方面的疗效。次要目的包括研究依从性对龋齿增量的影响、Chlorzoin对唾液变形链球菌水平的影响,以及评估社区环境中牙科辅助人员提供的个人口腔健康建议的益处。1240名最初年龄在11至13岁、被评估为高龋齿风险的儿童被纳入该试验。试验设计包括四个组:一个观察组、一个对照组、一个活性(Chlorzoin)清漆组和一个安慰剂清漆组。所有受试者每年由一名对分组情况不知情的经过校准的检查人员进行检查。使用临床、临床和光纤透照以及临床和咬合翼片数据集计算三年的龋齿增量。结果表明,使用Chlorzoin对变形链球菌水平有初始影响,但未检测到龋齿增量或变形链球菌感染的长期降低。疗效不佳的一个原因可能是初始阶段后清漆应用频率降低的方案。遵循方案并因此定期接受牙科辅助人员检查的儿童的龋齿增量低于未遵循方案的儿童。这一发现与清漆分配无关。总之,在这种方案下,已发现Chlorzoin在降低唾液变形链球菌方面有效,但在社区环境中实际应用时,作为高危苏格兰儿童的防龋剂无效。