Long-term clinical evaluation of endodontically treated teeth by 15 F CO 2 laser microprobe: three years clinical follow-up of 1512 root canals--in-vivo study

1999 ◽  
Author(s):  
Gavriel Kesler ◽  
Rumelia Koren ◽  
Anat Kesler ◽  
Nissim Hay ◽  
Rivka Gal
2006 ◽  
Vol 15 (10) ◽  
pp. 1501-1510 ◽  
Author(s):  
El-hadi SariAli ◽  
Jean Philippe Lemaire ◽  
Hugues Pascal-Mousselard ◽  
Hélène Carrier ◽  
Waffa Skalli

2021 ◽  
Vol 21 (2) ◽  
pp. 78-85
Author(s):  
V.N. Germanova ◽  
◽  
E.V. Karlova ◽  
L.T. Volova ◽  
N.N. Sarbaeva ◽  
...  

Background: anti-inflammatory and antiproliferative agents are among tools to prevent postoperative scarring. Prolonged use of immunosuppressants characterized by a selective mechanism of action immediately at the surgical site. Aim: to assess the safety and efficacy of bio-resorptive drainage devices enriched with cyclosporine or everolimus in vivo. Patients and Methods: the study was conducted on 52 rabbit eyes. Before to the study, ocular surface disease provoked by the long-term use of preservative-containing IOP-lowering medications was simulated. The next step was the penetrating surgical procedure. The surgery involved implanting bio-resorptive drainage devices of polylactide enriched with cyclosporine or everolimus or control devices (neither cyclosporine nor everolimus). Postoperatively, all rabbits underwent regular ophthalmic exams and IOP measurements. Follow-up was 6 months. After 7 days, 1 month, and 6 months, the animals were slaughtered for the histology of surgical site. Results: better characteristics of filtering blebs and lower IOP values were seen among the animals who underwent surgical procedures with immunosuppressants compared to the control group even in the early post-op period. After 1 month, control filtering blebs stopped functioning and were characterized by the IBAGS H0 (height) and E0 (extent) in most animals. Meanwhile, in cyclosporine and everolimus groups, filtering blebs were characterized by the IBAGS Н1-Н2 and Е1-Е3 till the end of follow-up. After 6 months, mean IOP was 17.3±0.5 mm Hg in the control group and 13.0±0.4 mm Hg and 11.8±0.6 mm Hg in cyclosporine group and everolimus group, respectively. No significant differences between the groups were reported in terms of complications. Histology matched clinical data and illustrated the mechanism of increased outflow facility after the implantation of drainage devices enriched with immunosuppressants. Conclusion: in vivo experiment has demonstrated higher efficacy and similar safety of IOP-lowering surgery after the implantation of drainage devices enriched with selective immunosuppressants. Keywords: glaucoma surgery, immunosuppressants, cyclosporine, everolimus, drainage device, scarring, filtering bleb. For citation: Germanova V.N., Karlova E.V., Volova L.T. et al. Prolonged use of selective immunosuppressants in glacoma drainage surgery: experimental in vivo study. Russian Journal of Clinical Ophthalmology. 2021;21(2):78–85. DOI: 10.32364/2311-7729-2021-21-2-78-85.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1235
Author(s):  
Xiaohui Nan ◽  
Wenjia Lai ◽  
Dan Li ◽  
Jiesheng Tian ◽  
Zhiyuan Hu ◽  
...  

Derived from magnetotactic bacteria (MTB), magnetosomes consist of magnetite crystals enclosed within a lipid bilayer membrane and are known to possess advantages over artificially synthesized nanoparticles because of the narrow size distribution, uniform morphology, high purity and crystallinity, single magnetic domain, good biocompatibility, and easy surface modification. These unique properties have increasingly attracted researchers to apply bacterial magnetosomes (BMs) in the fields of biology and medicine as MRI imaging contrast agents. Due to the concern of biosafety, a long-term follow-up of the distribution and clearance of BMs after entering the body is necessary. In this study, we tracked changes of BMs in major organs of mice up to 135 days after intravenous injection using a combination of several techniques. We not only confirmed the liver as the well-known targeted organs of BMs, but also found that BMs accumulated in the spleen. Besides, two major elimination paths, as well as the approximate length of time for BMs to be cleared from the mice, were revealed. Together, the results not only confirm that BMs have high biocompatibility, but also provide a long-term in-vivo assessment which may further help to forward the clinical applications of BMs as an MRI contrast agent.


2005 ◽  
Vol 53 (5) ◽  
pp. 278-284 ◽  
Author(s):  
Nara Branco ◽  
Ivy Lee ◽  
Hongbo Zhai ◽  
Howard I. Maibach

2015 ◽  
Vol 17 (2) ◽  
pp. 43
Author(s):  
Rodolfo Zeledón DDS, Esp ◽  
Carolina Ballestero DDS, Esp ◽  
Erick Hernández DDS. Esp ◽  
Tatiana Ramírez DDS, MSD ◽  
Marianela Benavides DDS, Esp ◽  
...  

The objective of this clinical study was to evaluate by polymerase chain reaction (PCR) the antimicrobial efficacy and the outcome of an endodontic protocol treatment (EPT) performed by under-graduated dental students on infected root canals associated with periapical lesions. Fifty-six patients attending for treatment of pulp necrosis and apical periodontitis were included. A specific EPT approach was performed and DNA extracts were taken at the baseline (S1), after a disinfection-neutralization procedure (S2), post-chemomechanical preparation (S3) and after Intracanal medication (S4) for the presence of specific bacteria. The outcome of the EPT was assessed radiographically using the Periapical Index-system (PAI) after 18-month follow-up. An intergroup evaluation shows that when comparing S1 to S3, S1 to S4, S2 to S3, and S2 to S4, the presence of bacteria were significantly reduced (P < 0.05). Finally, S4 was not significantly reduced when compared with S3 (P > 0.05). The most prevalent species in their respect order were Actinomyces Israelii > Enterococcus Faecalis > Fusobacterium Nucleatum/Prevotella Nigrescens > Phorphyromonas Endodontalis. After the 18-month follow-up, the overall success rate of root canal – treated teeth was of 88% (PAI 1 or 2). This In Vivo study demonstrated that EPT significantly reduced the number of cases with positive results for the studied bacteria, showing a profound positive impact in the outcome of endodontic treatment of teeth diagnosed with Pulp Necrosis and Apical Periodontitis. 


2017 ◽  
Vol 43 (4) ◽  
pp. 511-516
Author(s):  
Joel Hanhart ◽  
Yishay Weill ◽  
Yaakov Rozenman

2016 ◽  
Vol 2 (1) ◽  
pp. 27
Author(s):  
PoojaRavindra Shivasharan ◽  
AKatge Farhin ◽  
MayurManohar Wakpanjar ◽  
Ashveeta Shetty

1990 ◽  
pp. 369-371
Author(s):  
C. Arienta ◽  
M. Caroli ◽  
S. Balbi ◽  
A. Parma ◽  
E. Calappi ◽  
...  

1998 ◽  
Vol 16 (5) ◽  
pp. 263-267 ◽  
Author(s):  
GAVRIEL KESLER ◽  
RUMELIA KOREN ◽  
ANAT KESLER ◽  
NISSIM HAY ◽  
RIVKA GAL

Diagnostics ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 210 ◽  
Author(s):  
Rico Rutkowski ◽  
Georg Daeschlein ◽  
Thomas von Woedtke ◽  
Ralf Smeets ◽  
Martin Gosau ◽  
...  

Despite increasing knowledge gained based on multidisciplinary research, plasma medicine still raises various questions regarding specific effects as well as potential risks. With regard to significant statements about in vivo applicability that cannot be prognosticated exclusively based on in vitro data, there is still a deficit of clinical data. This study included a clinical follow-up of five probands who had participated five years previously in a study on the influence of cold atmospheric pressure plasma (CAP) on the wound healing of CO2 laser-induced skin lesions. The follow-up included a complex imaging diagnostic involving dermatoscopy, confocal laser scanning microscopy (CLSM) and hyperspectral imaging (HSI). Hyperspectral analysis showed no relevant microcirculatory differences between plasma-treated and non-plasma-treated areas. In summary of all the findings, no malignant changes, inflammatory reactions or pathological changes in cell architecture could be detected in the plasma-treated areas. These unique in vivo long-term data contribute to a further increase in knowledge about important safety aspects in regenerative plasma medicine. However, to confirm these findings and secure indication-specific dose recommendations, further clinical studies are required.


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