The topic of Group 3 was "Oral Medicine", which addressed the influence of both material- and anti-resorptive drug-associated factors on clinical and biological outcomes and complications in implant dentistry. Focused questions addressed the following 3 categories: (1) Implant materials other than titanium (alloys); (2) Transmucosal abutment materials other than titanium (alloys); (3) Medications affecting bone metabolism. After more than 2 years of preparation as well as 72 hours of lively debate between almost 100 experts in the field of implant dentistry, Group 3 defined the following statements and recommendations:
Zirconia is a valid alternative to titanium as a material for implants and transmucosal components, allowing soft and hard tissue integration with clinical outcomes comparable to titanium (up to 5 years) – identified by implant survival, marginal bone loss and peri-implant probing depths. However, the current state of evidence remains limited, especially for 2-piece implant designs. Based on expert opinion, zirconia transmucosal components might be preferred in the esthetic zone.
Administration of low-dose anti-resorptive drugs (ARD) did not show any negative impact on early implant outcomes, but careful follow-up and supportive care is recommended in order to prevent peri-implant medication-related osteonecrosis of the jaw and implant-related sequestration. However, existing dental implants without peri-implant pathology should not be removed. In addition, withholding anti-resorptive drugs (drug holiday) for implant placement is not recommended.
For further details, please refer to the 7th ITI Consensus Conference Group 3 Consensus Report and review articles that can be downloaded from the ITI website.