Department of Pediatric Dentistry, Damascus University, Damascus, Syrian Arab Republic.
Clin Exp Dent Res. 2023 Oct;9(5):764-771. doi: 10.1002/cre2.755. Epub 2023 Jun 21.
This study aimed to compare and evaluate the efficacy of topical use of povidone-iodine (PVP-I) solution and chlorhexidine (CHX) gel on dental plaque regrowth after 3 and 7 days in toddlers aged 24-36 months.
A randomized controlled trial that included 45 healthy toddlers aged 24-36 months, who were randomly assigned to three groups. The first group received a placebo (distilled water (DW)) (negative control). The second group received topical CHX gel (0.2% w/v) (positive control). The third group received topical PVP-I solution (10% w/v). Plaque accumulation was measured at the baseline (t ), after 3 days (t ) and after 7 days (t ) using the Turesky-modified Quigley-Hein plaque index (TMQHPI). Oral hygiene practices were prohibited during the trial period. The trial ID is ACTRN12623000567628.
In the DW group, the mean of the TMQHPI score was 1.89 ± 0.67 at t and decreased to 1.45 ± 0.66 at t (p = .028). Similarly, in the CHX group, the mean of the TMQHPI score was 1.83 ± 1.06 at t and decreased to 1.02 ± 0.99 at t (p = .033). Regarding the PVP-I group, the mean of the TMQHPI score went from 1.84 ± 0.85 to 1.01 ± 0.61 at t and then increased to 1.57 ± 0.74 at t . Those changes were statistically significant (p = .001) and (p = .002), respectively. No statistically significant difference was noted between TMQHPI scores at t (p = .789). Regarding t and t , no statistically significant difference was found between the three groups (p > .05).
CHX and PVP-I efficacy lasted only for 3 days, and PVP-I was not superior to CHX in terms of plaque control in toddlers. However, further studies are needed to determine the long-term efficacy of these antiplaque agents in toddlers.
本研究旨在比较和评估 24-36 个月大的幼儿使用聚维酮碘(PVP-I)溶液和洗必泰(CHX)凝胶局部应用后 3 天和 7 天对牙菌斑再生长的疗效。
这是一项随机对照试验,纳入了 45 名 24-36 个月大的健康幼儿,他们被随机分为三组。第一组接受安慰剂(蒸馏水(DW))(阴性对照)。第二组给予局部 CHX 凝胶(0.2%w/v)(阳性对照)。第三组给予局部 PVP-I 溶液(10%w/v)。使用改良的 Turesky-Queigley-Hein 菌斑指数(TMQHPI)在基线(t )、第 3 天(t )和第 7 天(t )时测量菌斑堆积量。试验期间禁止进行口腔卫生措施。试验 ID 为 ACTRN12623000567628。
在 DW 组,TMQHPI 评分的平均值在 t 时为 1.89±0.67,在 t 时降至 1.45±0.66(p=0.028)。同样,在 CHX 组中,TMQHPI 评分的平均值在 t 时为 1.83±1.06,在 t 时降至 1.02±0.99(p=0.033)。关于 PVP-I 组,TMQHPI 评分的平均值从 t 时的 1.84±0.85降至 t 时的 1.01±0.61,然后在 t 时增加至 1.57±0.74。这些变化具有统计学意义(p=0.001)和(p=0.002)。t 时 TMQHPI 评分无统计学差异(p=0.789)。关于 t 和 t ,三组之间无统计学差异(p>0.05)。
CHX 和 PVP-I 的疗效仅持续 3 天,PVP-I 在控制幼儿牙菌斑方面并不优于 CHX。然而,需要进一步的研究来确定这些抗菌斑剂在幼儿中的长期疗效。