Niederman Richard
Department of Epidemiology and Health Promotion, New York University College of Dentistry, New York, New York, USA.
Evid Based Dent. 2013 Dec;14(4):107-8. doi: 10.1038/sj.ebd.6400966.
The PubMed and Embase databases were searched together with hand searching of the Journal of Periodontology, Journal of Periodontal Research and Journal of Clinical Periodontology. The reference lists of identified articles were also searched.
Prospective cohort or cross-sectional studies assessing the effect of pregnancy on gingival inflammation evaluated by the gingival index and/or bleeding on probing were included. Study quality was assessed using the Newcastle-Ottawa scale (NOS).
Study assessment and data extraction were carried out independently by two reviewers, with disputes resolved by a third reviewer. Mean values of primary and secondary outcomes were directly pooled and analysed with weighted mean differences (WMDs) and 95% confidence intervals (CIs), considering independently each study design (cohort and cross-sectional). Study specific estimates were pooled with both the fixed- and random-effect models.
Forty-four articles representing 33 studies (14 cohort and 19 cross-sectional) were included. Meta-analyses revealed a significantly lower GI in pregnant women in the first term compared with those in their second or third term of pregnancy; a lower mean GI score in post-partum women compared with women in their second [WMD = 0.143; 95% CI (0.031; 0.255); p = 0.012] or third term [WMD = 0.256; 95% CI (0.151; 0.360); p < 0.001] of pregnancy, when considering cohort studies; non-pregnant women had lower mean GI values than women in their second or third term of pregnancy. Small changes in plaque levels were reported.
The results of this systematic review confirm that gingival inflammation is significantly increased throughout pregnancy and when comparing pregnant versus post-partum or non-pregnant women, without a concomitant increase in plaque levels. However, this information should be considered with caution, due to the small number of studies included in the meta-analyses, the low quality of the included studies, differences in study design, absence of a periodontal diagnosis at baseline and performance of periodontal treatment in some cases. No conclusions could be drawn regarding secondary outcomes such as microbiological, immunological and patient-centred data, because no meta-analyses were possible for these factors. Future studies with higher quality should be designed to answer these questions.
对PubMed和Embase数据库进行了检索,并人工检索了《牙周病学杂志》《牙周病研究杂志》和《临床牙周病学杂志》。还检索了已识别文章的参考文献列表。
纳入前瞻性队列研究或横断面研究,这些研究通过牙龈指数和/或探诊出血评估妊娠对牙龈炎症的影响。使用纽卡斯尔-渥太华量表(NOS)评估研究质量。
由两名审阅者独立进行研究评估和数据提取,如有争议则由第三名审阅者解决。主要和次要结局的均值直接合并,并采用加权均值差(WMD)和95%置信区间(CI)进行分析,分别考虑每种研究设计(队列研究和横断面研究)。采用固定效应模型和随机效应模型合并研究的具体估计值。
纳入了代表33项研究的44篇文章(其中队列研究14项,横断面研究19项)。荟萃分析显示,与妊娠第二或第三期的女性相比,妊娠第一期的孕妇牙龈指数显著更低;在队列研究中,产后女性的平均牙龈指数得分低于妊娠第二期[WMD = 0.143;95% CI(0.031;0.255);p = 0.012]或第三期[WMD = 0.256;95% CI(0.151;0.360);p < 0.001]的女性;非孕妇的平均牙龈指数值低于妊娠第二或第三期孕妇。报告了菌斑水平的微小变化。
本系统评价的结果证实,在整个孕期以及比较孕妇与产后或非孕妇时,牙龈炎症显著增加,且菌斑水平没有相应增加。然而,由于荟萃分析纳入的研究数量较少、纳入研究质量较低、研究设计存在差异、基线时未进行牙周诊断以及某些情况下进行了牙周治疗,应谨慎看待这些信息。对于微生物学、免疫学和以患者为中心的数据等次要结局,无法得出结论,因为无法对这些因素进行荟萃分析。应设计更高质量的未来研究来回答这些问题。