Cochrane · intervention · CD010743
Xylitol‐containing products for preventing dental caries in children and adults
Riley, P, Moore, D, Ahmed, F, et al. · Cochrane Database of Systematic Reviews · 2015 · Cochrane Library
Full textEvery question was extracted from the full review (methods and results), not only its Summary of Findings table.
Questions
17
current version
GRADE rated
7
No studies
1
Included studies
10
as reported
No studies 1 · 5.9%Ungraded 9 · 52.9%Very low 3 · 17.6%Low 4 · 23.5%Moderate 0 · 0%High 0 · 0%
Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.
Review question
| Element | Planned (methods) | Found (results) |
|---|---|---|
| Population | Children and adults. Exclusion: majority of participants undergoing fixed or removable orthodontic treatment; intervention provided for less than one year; participants selected on the basis of having underlying health conditions | 7969 participants randomised (5903 analysed) across 10 studies (n=10); 1 study in adults (n=1), 9 studies in children aged 1 month to 13 years (n=9) |
| Intervention | Xylitol-containing products compared with placebo or no intervention (which includes routine care), provided for at least 1 year. Appropriate comparators: non-cariogenic placebos (e.g. sorbitol) or no intervention | Xylitol lozenges (n=669); Xylitol candy (n=252); Xylitol syrup 8 g/day (n=94); Xylitol sucking tablets (n=118); Fluoride toothpaste with 10% xylitol (n=4216); Xylitol tablets via pacifier (n=62); Xylitol wipes (n=44) |
| Comparison | Placebo or no intervention (which includes routine care); non-cariogenic placebo (e.g. sorbitol); or another xylitol-containing product. Cariogenic sweeteners (sucrose, glucose, fructose) and anti-cariogenic agents (e.g. erythritol) were inappropriate comparators | Control lozenges (sucralose placebo) (n=669); Control (sorbitol) candy (n=252); Control (low-dose 2.67 g/day xylitol) syrup (n=94); No treatment (children/infants); Fluoride toothpaste (n=4216); Control (sorbitol) tablets (n=62); Control wipes (n=44) |
| Outcomes | Primary: Change in dental caries increment (DFT/DFS or DMFT/DMFS for permanent teeth; dmfs/d(e)fs, dmft/d(e)ft for deciduous teeth; permanent and deciduous analysed separately); Number of participants with and without dental caries increment. Secondary: Quality of life (QOL); Patient satisfaction; Cost; Adverse effects (e.g. gastrointestinal complaints, discolouration of teeth, pain and discomfort) | Caries increment / caries in primary teeth (n=10 studies); Number of participants with a caries increment (n=4 studies); Adverse effects (n=7 studies mentioned, mostly not in a usable format) |
| Study designs | Randomised controlled trials (RCTs), including cluster randomised trials but excluding cross-over trials | Randomised controlled trials (8 parallel, 2 cluster-randomised) (n=10) |
| Timing | Interventions provided for at least 1 year; longest-term data (follow-up nearest to 3 years) preferred | 1 to 3 years |
Search date: 2014-08. Databases: Cochrane Oral Health Group's Trials Register; Cochrane Central Register of Controlled Trials (CENTRAL); MEDLINE via OVID; EMBASE via OVID; CINAHL via EBSCOhost; Web of Science Conference Proceedings; ProQuest Dissertations and Theses
Questions and results
Current version onlyXylitol lozenges (5 g/day) vs Control lozenges (sucralose-sweetened placebo, no xylitol)
Population: Adults
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Caries increment (DFS) 33 months | PF 0.08 [-0.03, 0.20] -0.64 [-1.58, 0.30] DFS (mean difference in caries increment) | 1 study · 669 participants | Low Downgraded: imprecision |
Adverse effects (sores in the mouth, cramps, bloating, constipation, flatulence, loose stool or diarrhoea) 33 months | Patterns of adverse effects (sores in the mouth, cramps, bloating, constipation, flatulence, and loose stool or diarrhoea) were similar for both groups. Bader 2013. | 1 study · 669 participants | Ungraded |
Xylitol candy (7.5 g/day) vs Control (sorbitol) candy
Population: Children (mixed dentition; baseline about 8 years)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Adverse effects 36 months | The authors reported that there were no adverse effects for either group. Honkala 2014. | 1 study · 252 participants | Ungraded |
Caries increment (dmfs, primary and permanent teeth combined) 36 months | One study (252 children) compared xylitol (7.5 g/day) candy with control (sorbitol) candy over 36 months. The data could not be used in analysis because the authors combined primary/deciduous and permanent teeth and… | 1 study · 252 participants | Ungraded |
Xylitol lozenges (4.7 g/day) vs No treatment
Population: Children (permanent teeth; baseline 8 to 10 years)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Adverse effects 24 months (48-month follow-up) | There were no usable data presented for adverse effects. Lenkkeri 2012. | 1 study | Ungraded |
Caries increment (DMFS) 24 months (48-month follow-up) | PF -0.10 [-0.59, 0.39] 0.28 [-0.99, 1.55] DMFS (mean difference in caries increment; higher with xylitol) | 1 study · 200 participants | Very low Downgraded: risk of bias, imprecision |
Number of children with a caries increment 24 months (48-month follow-up) | RR 1.02 [0.83, 1.26] | 1 study · 200 participants | Ungraded |
Xylitol syrup (high dose, 8 g/day) vs Control (low-dose xylitol, 2.67 g/day) syrup
Population: Infants (primary teeth; baseline about 9 to 15 months)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Caries in primary teeth (mean number of decayed primary teeth) 12 months | PF 0.58 [0.33, 0.83] -1.10 [-2.03, -0.18] decayed primary teeth (mean difference in number) | 1 study · 94 participants | Low Downgraded: imprecision |
Adverse effects (loose stools, diarrhoea) 12 months | Adverse effects were not reported in a usable format, but the reported rates of loose stools and diarrhoea were very similar between groups. There were no serious adverse effects during the study. Milgrom 2009. | 1 study · 94 participants | Ungraded |
Xylitol sucking tablets (1 g/day) vs No treatment
Population: Infants/young children (primary teeth; baseline about 1 to 3 years)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Number of infants with a caries increment 18 months (24-month follow-up) | RR 0.72 [0.35, 1.45] | 1 study · 118 participants | Ungraded |
Caries increment (dmfs) 18 months (24-month follow-up) | PF 0.53 [0.001, 1.04] -0.42 [-1.12, 0.28] dmfs (mean difference in caries increment) | 1 study · 118 participants | Very low Downgraded: risk of bias, imprecision |
Fluoride toothpaste containing 10% xylitol vs Fluoride toothpaste (fluoride-only, no xylitol)
Population: Children with permanent teeth (schoolchildren)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Adverse effects 2.5 to 3 years | Adverse effects: both studies reported that there were no adverse effects in either the xylitol or control group. | 2 studies · 4216 participants | Ungraded |
Caries increment (DFS), prevented fraction at 2.5 to 3 years 2.5 to 3 years | PF 0.13 [0.08, 0.18] -0.28 [-0.42, -0.14] DFS (mean caries increment; fewer with xylitol) | 2 studies · 4216 participants | Low Downgraded: risk of bias, indirectness |
Xylitol tablets (200 to 600 mg/day) via slow-release pacifier/dummy vs Control (sorbitol) tablets
Population: Infants (primary teeth; from about 1 month of age)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Number of infants with a caries increment (dmfs) 24 months (48-month follow-up) | RR 3.08 [0.69, 13.65] | 1 study · 62 participants | Very low Downgraded: risk of bias, imprecision |
Xylitol wipes (4.2 g/day) vs Control wipes (no xylitol)
Population: Infants (primary teeth)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Number of infants with a caries increment (dmfs) 12 months | RR 0.14 [0.02, 1.07] | 1 study · 44 participants | Low Downgraded: imprecision |
Adverse effects 12 months | The authors reported that there were no adverse effects for either group. Zhan 2012. | 1 study · 44 participants | Ungraded |
Xylitol chewing gum vs No treatment or non-cariogenic control
Population: Children and adults
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year | It was surprising that there were no eligible randomised trials testing xylitol chewing gums against either no treatment or a non-cariogenic control. | 0 studies | No studies |
Xylitol-containing products (gels, toothpastes, varnishes, mouthrinses, chewing gums or sprays), provided for at least one year vs Placebo or no intervention (which includes routine care)
Population: Children and adolescents below 18 years of age (permanent or deciduous teeth, or both)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year | Protocol only; no results reported. Planned comparison of xylitol-containing products versus placebo or no intervention for preventing dental caries. | 0 studies | No studies |
One xylitol-containing product (gel, toothpaste, varnish, mouthrinse, chewing gum or spray) vs Another xylitol-containing product
Population: Children and adolescents below 18 years of age (permanent or deciduous teeth, or both)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year | Protocol only; no results reported. Planned head-to-head comparison of one xylitol-containing product versus another. | 0 studies | No studies |