Dental Caries in Children
Conditions
Keywords
Er:YAG laser, Caries removal, Dental anxiety, Acceptability
Brief summary
The aim of this study is to evaluate the acceptance of pediatric patiens using Er: YAG laser in comparison with the conventional techniques for caries removal. The study was carried out on 100 children between the ages of 9-12, who had class 1 occlusal caries in one of their permanent first molars. The patients were divided into two groups; conventional technical group and laser group. Rotary handpieces was used in conventional technique group, Er:YAG laser was used in the laser group for caries removal. The heart rate of each patient was measured during the caries removal procedure at 30 seconds intervals. The pain during the procedure was determined by VAS. CFSS-DS scale was used to determine the anxiety level of the patients before and after the procedure. FIS was used to determine how patients are disturbed from the smell, taste, sound, vibration and sight of the devices after the procedure. The video segments were collected from the patients during the caries removal and the procedural pain were evaluated by the FLACC scale.
Detailed description
Based our results, ın the laser group, the patients were found to experience less pain and discomfort compared to conventional technique according to the VAS and FLACC scores. The rate of patients with dental anxiety decreased significantly in the laser group compared with the conventional group according to CFSS-DS performed after the procedure. According to the sensory survey, the laser group had good acceptability compared to the conventional technique group in terms of vibration and sight. The laser group showed a lower percentage increase in heart rate comparsion between beginning and end of procedure. It was observed that the cavity preparation time was longer in the laser group.
Interventions
DEVICERotary handpieces
Dental Caries removal
DEVICEEr:YAG laser
Dental Caries removal
Sponsors
Cukurova University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
9 Years to 12 Years
Healthy volunteers
Yes
Inclusion criteria
* patients age between 9-12 years old * Having no systemic condition and ASA 1 healty status * Having lower permanent first molar teeth with occlusal caries (class 1) * having no laser treatment before
Exclusion criteria
* having spontaneous tooth pain * having high dental anxiety * having no restorative treatment before * teeth with periapical pathology, a root filling or non-vital teeth.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Comfort | through study completion, an average of 6 months | Units on a Scale ( Patient comfort was evaluated with Facial Image Scale after treatment. Patients signed from 1 to 5 score for treatment comfort.The data were collected and statistically analysed using by the numerical data. In this study, 1 and 2 scores are considered as better outcome. Patients who signed these scores described as good comfortable. The worst outcome is considered as the patients signed 4-5. Each scale range for each time interval evaluated as count of patient and presented as percentage.) |
| Dental anxiety | through study completion, an average of 6 months | Units on a Scale (Dental anxiety was evaluated with Dental Subscale of the Children's Fear Survey Schedule after treatment. The patients signed from 0 to 38 score for dental anxiety after the treatment.The data were collected and statistically analysed using by the numerical data. In this study, 0-38 scores are considered as better outcome. Patients who were have these scores described no dental anxiety for treatment. The worst outcome is considered as the patients have \>38. Each scale range for each time interval evaluated as count of patient and presented as percentage.) |
| Changes in pain | through study completion, an average of 6 months | Units on a Scale (Changes in pain was evaluated with Legs, Activity, Cry, Consolability scale after treatment. Observer signed from 0 to 3 score for treatment pain during the treatment.The data were collected and statistically analysed using by the numerical data. In this study, 0 and 1 scores are considered as better outcome. Patients who were signed these scores described as no pain for treatment. The worst outcome is considered as the patients signed 2-3. Each scale range for each time interval evaluated as count of patient and presented as percentage.) |
Countries
Turkey (Türkiye)
Outcome results
None listed