Senneby Anna, Mejàre Ingegerd, Sahlin Nils-Eric, Svensäter Gunnel, Rohlin Madeleine
Faculty of Odontology, Malmö University, 205 06 Malmö, Sweden.
The Swedish Council on Technology Assessment in Health Care, Box 3657, 103 59 Stockholm, Sweden.
J Dent. 2015 Dec;43(12):1385-93. doi: 10.1016/j.jdent.2015.10.011. Epub 2015 Oct 19.
To evaluate the accuracy of different methods used to identify individuals with increased risk of developing dental coronal caries.
Studies on following methods were included: previous caries experience, tests using microbiota, buffering capacity, salivary flow rate, oral hygiene, dietary habits and sociodemographic variables. QUADAS-2 was used to assess risk of bias. Sensitivity, specificity, predictive values, and likelihood ratios (LR) were calculated. Quality of evidence based on ≥3 studies of a method was rated according to GRADE.
PubMed, Cochrane Library, Web of Science and reference lists of included publications were searched up to January 2015.
From 5776 identified articles, 18 were included. Assessment of study quality identified methodological limitations concerning study design, test technology and reporting. No study presented low risk of bias in all domains. Three or more studies were found only for previous caries experience and salivary mutans streptococci and quality of evidence for these methods was low. Evidence regarding other methods was lacking. For previous caries experience, sensitivity ranged between 0.21 and 0.94 and specificity between 0.20 and 1. Tests using salivary mutans streptococci resulted in low sensitivity and high specificity. For children with primary teeth at baseline, pooled LR for a positive test was 3 for previous caries experience and 4 for salivary mutans streptococci, given a threshold ≥10(5) CFU/ml.
Evidence on the validity of analysed methods used for caries risk assessment is limited. As methodological quality was low, there is a need to improve study design.
Low validity for the analysed methods may lead to patients with increased risk not being identified, whereas some are falsely identified as being at risk. As caries risk assessment guides individualized decisions on interventions and intervals for patient recall, improved performance based on best evidence is greatly needed.
评估用于识别患牙冠龋风险增加个体的不同方法的准确性。
纳入了关于以下方法的研究:既往龋病经历、使用微生物群的检测、缓冲能力、唾液流速、口腔卫生、饮食习惯和社会人口统计学变量。采用QUADAS-2评估偏倚风险。计算敏感性、特异性、预测值和似然比(LR)。根据对一种方法≥3项研究的证据质量,依据GRADE进行评级。
检索了截至2015年1月的PubMed、Cochrane图书馆、科学网以及纳入出版物的参考文献列表。
从5776篇已识别的文章中,纳入了18篇。对研究质量的评估发现了有关研究设计、检测技术和报告方面的方法学局限性。没有研究在所有领域均呈现低偏倚风险。仅在既往龋病经历和唾液变形链球菌方面发现了三项或更多研究,且这些方法的证据质量较低。缺乏关于其他方法的证据。对于既往龋病经历,敏感性在0.21至0.94之间,特异性在0.20至1之间。使用唾液变形链球菌进行检测的敏感性较低而特异性较高。对于基线时有乳牙的儿童,在阈值≥10⁵CFU/ml时,既往龋病经历阳性检测的合并LR为3,唾液变形链球菌为4。
用于龋病风险评估的分析方法有效性的证据有限。由于方法学质量较低,需要改进研究设计。
分析方法的有效性较低可能导致未识别出风险增加的患者,而一些患者被错误地识别为有风险。由于龋病风险评估指导着关于干预措施和患者复诊间隔的个体化决策,因此迫切需要基于最佳证据提高评估性能。