Cochrane Database Syst Rev. 2015 Mar 31;3:CD008694. doi: 10.1002/14651858.CD008694.pub2.
BACKGROUND: 
Comforting
 behaviours, such as the use of pacifiers (dummies, soothers), blankets 
and finger or thumb sucking, are common in babies and young 
children. These comforting habits, which can be referred to collectively
 as 'non-nutritive sucking habits' (NNSHs), tend to stop as children get
 older, under their own impetus or with support from parents and 
carers. However, if the habit continues whilst the permanent dentition 
is becoming established, it can contribute to, or cause, development of a
 malocclusion (abnormal bite). A diverse variety of approaches has been 
used to help children with stopping a NNSH. These include advice, 
removal of the comforting object, fitting an orthodontic appliance to 
interfere with the habit, application of an aversive taste to the digit 
or behaviour modification techniques. Some of these interventions are 
easier to apply than others and less disturbing for the child and their 
parent; some are more applicable to a particular type of habit.
OBJECTIVES: 
The
 primary objective of the review was to evaluate the effects of 
different interventions for cessation of NNSHs in children. The 
secondary objectives were to determine which interventions work most 
quickly and are the most effective in terms of child and parent- or 
carer-centred outcomes of least discomfort and psychological distress 
from the intervention, as well as the dental measures of malocclusion 
(reduction in anterior open bite, overjet and correction of posterior 
crossbite) and cost-effectiveness.
SEARCH METHODS: 
We
 searched the following electronic databases: the Cochrane Oral Health 
Group Trials Register (to 8 October 2014), the Cochrane Central Register
 of Controlled Trials (CENTRAL) (The Cochrane Library 2014, Issue 9), 
MEDLINE via OVID (1946 to 8 October 2014), EMBASE via OVID (1980 to 8 
October 2014), PsycINFO via OVID (1980 to 8 October 2014) and CINAHL via
 EBSCO (1937 to 8 October 2014), the US National Institutes of Health 
Trials Register (Clinical Trials.gov) (to 8 October 2014) and the WHO 
International Clinical Trials Registry Platform (to 8 October 2014). 
There were no restrictions regarding language or date of publication in 
the searches of the electronic databases. We screened reference lists 
from relevant articles and contacted authors of eligible studies for 
further information where necessary.
SELECTION CRITERIA: 
Randomised
 or quasi-randomised controlled trials in children with a non-nutritive 
sucking habit that compared one intervention with another intervention 
or a no-intervention control group. The primary outcome of interest was 
cessation of the habit.
DATA COLLECTION AND ANALYSIS: 
We
 used standard methodological procedures expected by The Cochrane 
Collaboration. Three review authors were involved in screening the 
records identified; two undertook data extraction, two assessed risk of 
bias and two assessed overall quality of the evidence base. Most of the 
data could not be combined and only one meta-analysis could be carried 
out.
MAIN RESULTS: 
We
 included six trials, which recruited 252 children (aged two and a half 
to 18 years), but presented follow-up data on only 246 children. Digit 
sucking was the only NNSH assessed in the studies. Five studies compared
 single or multiple interventions with a no-intervention or waiting list
 control group and one study made a head-to-head comparison. All the 
studies were at high risk of bias due to major limitations in 
methodology and reporting. There were small numbers of participants in 
the studies (20 to 38 participants per study) and follow-up times ranged
 from one to 36 months. Short-term outcomes were observed under one year
 post intervention and long-term outcomes were observed at one year or 
more post intervention. Orthodontics appliance (with or without 
psychological intervention) versus no treatmentTwo trials that assessed 
this comparison evaluated our primary outcome of cessation of habit. One
 of the trials evaluated palatal crib and one used a mix of palatal 
cribs and arches. Both trials were at high risk of bias. The orthodontic
 appliance was more likely to stop digit sucking than no treatment, 
whether it was used over the short term (risk ratio (RR) 6.53, 95% 
confidence interval (CI) 1.67 to 25.53; two trials, 70 participants) or 
long term (RR 5.81, 95% CI 1.49 to 22.66; one trial, 37 participants) or
 used in combination with a psychological intervention (RR 6.36, 95% CI 
0.97 to 41.96; one trial, 32 participants). Psychological intervention 
versus no treatmentTwo trials (78 participants) at high risk of bias 
evaluated positive reinforcement (alone or in combination with gaining 
the child's co-operation) or negative reinforcement compared with no 
treatment. Pooling of data showed a statistically significant difference
 in favour of the psychological interventions in the short term (RR 
6.16, 95% CI 1.18 to 32.10; I(2) = 0%). One study, with data from 57 
participants, reported on the long-term effect of positive and negative 
reinforcement on sucking cessation and found a statistically significant
 difference in favour of the psychological interventions (RR 6.25, 95% 
CI 1.65 to 23.65). Head-to-head comparisonsOnly one trial demonstrated a
 clear difference in effectiveness between different active 
interventions. This trial, which had only 22 participants, found a 
higher likelihood of cessation of habit with palatal crib than palatal 
arch (RR 0.13, 95% CI 0.03 to 0.59).
AUTHORS' CONCLUSIONS: 
This
 review found low quality evidence that orthodontic appliances (palatal 
arch and palatal crib) and psychological interventions (including 
positive and negative reinforcement) are effective at improving sucking 
cessation in children. There is very low quality evidence that palatal 
crib is more effective than palatal arch. This review has highlighted 
the need for high quality trials evaluating interventions to stop 
non-nutritive sucking habits to be conducted and the need for a 
consolidated, standardised approach to reporting outcomes in these 
trials.