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Atraumatic restorative treatment compared to the Hall Technique for occluso-proximal carious lesions in primary molars; 36-month follow-up of a randomised control trial in a school setting

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Background: Atraumatic Restorative Treatment (ART) and the Hall Technique (HT) are both minimally invasive, non-aerosol generating procedures (non-AGPs). They seem to have never been directly compared, nor has the HT been studied in a non-clinical setting. This study compared the HT and ART restorations placed in a school setting after 36 months.

Methods: Children (5–10 yo) who had a primary molar with a dentinal occluso-proximal, cavitated carious lesion were allocated to the ART (selective removal) or HT arms. Primary outcome: restoration survival over 36-months (using Kaplan–Meier survival analysis, log rank test, and Cox regression). Secondary outcomes: (1) occlusal vertical dimension (OVD) (1, 2, 3, 4 weeks) and (2) child self-reported discomfort; (3) treatment acceptability (immediately following interventions); (4) Child Oral Health Related Quality of Life (OHRQoL), before treatment and after 6 months and (5) a post hoc analysis of time to tooth exfoliation (1, 6, 12, 18, 24, 30, 36 months).

Results: One-hundred and thirty-one children (ART = 65; HT = 66) were included (mean age = 8.1 ± 1.2). At 36 months, 112 (85.5%) children were followed-up. Primary outcome: restoration survival rates ART = 32.7% (SE = 0.08; 95% CI 0.17–0.47); HT = 93.4% (0.05; 0.72–0.99), p < 0.001; Secondary outcomes: (1) OVD returned to pre-treatment state within 4 weeks; (2) treatment discomfort was higher for the HT (p = 0.018); (3) over 70% of children and parents showed a high acceptability for treatments, with crown aesthetics being a concern for around 23% of parents; (4) Child OHRQoL improved after 6 months; and (5) teeth treated with the HT exfoliated earlier than those in the ART group (p = 0.007).

Conclusions: Both ART and the HT were acceptable to child participants and their parents and all parents thought both restorations protected their child’s tooth. However, the crown appearance concerned almost a quarter of parents in the HT arm. Children experienced less discomfort in the ART group. Although both treatments can be performed in a non-clinical setting and have the advantage of being non-aerosol generating procedures (non-AGPs), the HT had almost three times higher survival rates (93.4%) for restoring primary molar occluso-proximal cavities compared to ART (32.7%).

Trial registration: This trial was registered in ClinicalTrials.gov (NCT02569047), 5th October 2015. https://clinicaltrials.gov/ct2/show/study/NCT02569047?cond=Hall+Technique+Atraumatic+Rest orative+Treatment&draw=2&rank=2.

Original languageEnglish
Article number318
Pages (from-to)1-18
Number of pages18
JournalBMC Oral Health
Volume20
Issue number1
Early online date11 Nov 2020
DOIs
Publication statusPublished - Dec 2020

Funding

We would like to thank the municipality of the city of Tietê, the schoolchildren, their parents, schools and the health service of Tietê, especially, Enio Saccon and Ana Paula Forlevize for making this trial possible to be carried out in the local schools, with the help of all the school managers participating in this trial; the GC Europe (Leuven, BE) for donating the glass ionomer cements used in this trial (EQUIA Forte and Fuji I), the 3M ESPE (St. Paul, USA) for donating the Stainless Steel Crowns used to perform the Hall Technique; and the students from the Academisch Centrum Tandheelkunde Amsterdam (ACTA, Netherlands), Daniella Pool and Mirjiam Huveneers who act as two of the operators of this trial. GC Europe and 3M ESPE had no role in the study design, interventions, data collection, data analysis, data interpretation or manuscript writing. The main author (MPA) was granted a Fellowship from the São Paulo Research Foundation (Fundação de Amparo à Pesquisa do Estado de São Paulo—FAPESP) to carry out this trial (Process Number 2015/18098-2). Resources necessary for the trial procedures and research team were supported by the University of São Paulo (USP), the Academic Centre for Dentistry Amsterdam (ACTA) and the University of Dundee (UoD), with the help of two other Brazilian funding agencies (Conselho Nacional de Desenvolvimento Científico e Tecnológico—CNPq and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—CAPES). Neither the funding body nor the Sponsors had any role in the design of the study, the collection, analysis, and interpretation of data and in writing this manuscript. Acknowledgements

FundersFunder number
3M Espe
Academic Centre for Dentistry Amsterdam
Academisch Centrum Tandheelkunde Amsterdam
Daniella Pool and Mirjiam Huveneers
University of Dundee
GC Europe
Fundação de Amparo à Pesquisa do Estado de São Paulo2015/18098-2
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Universidade de São Paulo

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