IADR Abstract Archives

Mineral trioxide aggregate as a pulpotomy medicament: An evidence-based assessment

Objective: The principles of evidence-based dentistry were used to compare the clinical and radiographic successes of four pulpotomy medicaments in human primary molars. Methods: Electronic databases were searched and sieved for randomised clinical trials comparing the clinical and radiographic successes of mineral trioxide aggregate (MTA), formocresol (FC), ferric sulfate (FS) and calcium hydroxide (CH) pulpotomies. Data were extracted and common odds ratios (CORs) were derived by fixed effects meta-analysis (MA). Results: Direct MA found MTA was significantly more successful clinically (COR = 3.11; 95% CI = 1.09 – 8.85; p = 0.03) and radiographically (COR = 4.50; CI = 1.78 – 11.42; p = 0.002) than FC. Indirect MAs found MTA was significantly more successful radiographically (COR = 4.69; CI = 1.70 – 12.95; p = 0.003) than FS, and significantly more successful clinically (COR = 6.48; CI = 1.75 – 24.0; p = 0.005) and radiographically (COR = 10.47; CI = 3.35 – 32.76; p = 0.00005) than CH. Conclusions: Current evidence suggests MTA compared with FC and CH as a pulpotomy medicament results in significantly higher clinical and radiographic successes in all time periods up to exfoliation. Mineral trioxide aggregate compared with FS as a pulpotomy medicament results in significantly higher radiographic success in all time periods up to exfoliation. (This study was supported by a grant from the The University of Melbourne School of Dental Science Research Committee.)
Division: Australian/New Zealand Division Meeting
Meeting: 2007 Australian/New Zealand Division Meeting (Adelaide, Australia)
Location: Adelaide, Australia
Year: 2007
Final Presentation ID:
Abstract Category|Abstract Category(s): Scientific Groups
Authors
  • Ng, Fiona Kwee Hwa  ( University of Melbourne, Melbourne VIC, N/A, Australia )
  • Messer, Louise Brearley  ( University of Melbourne, Melbourne VIC, N/A, Australia )
  • SESSION INFORMATION
    Oral Session
    Pulp Biology