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A caries vaccine is a vaccine to prevent and protect against tooth decay. [1] Streptococcus mutans ( S. mutans ) has been identified as the major etiological agent of human dental caries. The development of a vaccine for tooth decay has been under investigation since the 1970s.
It does not resorb, and is biocompatible, forming a seal against the tooth material that minimizes leakage. [1] Originally, MTA was dark gray in color, but white versions have been on the market since 2002. Bismuth oxide, which was added as a radioopacifier (to make the filling stand out on X-rays), [citation needed] can discolour the teeth. [3]
The majority of clinical studies indicate the annual failure rates (AFRs) are between 1% and 3% with tooth colored fillings on back teeth. Root canaled (endodontically) treated teeth have AFRs between 2% and 12%. The main reasons for failure are cavities that occur around the filling and fracture of the real tooth.
On Thursday, the companies filed for full approval of their COVID-19 vaccine with the U.S. Food and Drug Administration to include adolescents aged 12 to 15. Pfizer to test third dose of COVID-19 ...
Traditionally teeth are shaved down to make room for the crown but, more recently, stainless steel crowns have been used to seal decay into the tooth and stop it progressing. This is known as the Hall Technique and works by depriving the bacteria in the decay of nutrients and making their environment less favorable for them.
T-cell immunity might outlast antibody immunity—at least in some patients. Soon, you can find out your truth for yourself.
Dental pulpal testing is a clinical and diagnostic aid used in dentistry to help establish the health of the dental pulp within the pulp chamber and root canals of a tooth. . Such investigations are important in aiding dentists in devising a treatment plan for the tooth being test
Vaccine manufacturers do not receive licensing until a complete clinical cycle of development and trials proves the vaccine is safe and has long-term effectiveness, following scientific review by a multinational or national regulatory organization, such as the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA). [105] [106]