| Literature DB >> 21731252 |
Grace Tara Paul1, M Hemalata, Mohamed Faizuddin.
Abstract
INTRODUCTION: It is a well established fact that periodontitis is caused by a group of highly specific microorganisms, organized as a bio-film on the tooth surface. Hence, therapeutic modalities are directed against elimination or adequate suppression of these organisms. Thorough debridement of these sites is possible mainly by scaling and root planing (SRP) and open- flap debridement in deeper sites. Open- flap debridement includes conventional surgical procedures such as the modified Widman flap procedure. Surgical procedures, however, have a number of disadvantages and hence efforts have been on at improving various non-surgical approaches, which are directed more specifically at the microbial nature of periodontal disease. Use of local drug-delivery devices is one such approach. The combined therapy of SRP and local drug delivery has been showing promising results in improving all the parameters in periodontal disease.Entities:
Keywords: Controlled release drug delivery device; modified Widman flap; non-surgical management
Year: 2010 PMID: 21731252 PMCID: PMC3118077 DOI: 10.4103/0972-124X.76932
Source DB: PubMed Journal: J Indian Soc Periodontol ISSN: 0972-124X
Figure 1Experimental site and control site at baseline
Figure 2SRP and chlorhexidine chip placed at experimental site and modified widman flap procedure done in control site
Figure 3Experimental site and control site at the end of 9 months
Figure 4Microbiological profile assessed under dark-field microscopy (×400) at the experimental and control sites; at baseline
Figure 5Microbiological profile assessed under dark-field microscopy (×400) at the experimental and control sites; at the end of 3 months
Figure 6Microbiological profile assessed under dark-field microscopy (×400) at the experimental and control sites; at the end of 9 months
Mean values with standard deviation for different clinical variables
Mean values with standard deviation for different microbiological variables (×400 magnification) at the experimental and control sites; at the end of 9
Figure 7Depicting total motile organisms in experimental and control groups
Figure 8Depicting total non-motile organisms in experimental and control groups