Evaluation of efficacy of tacrolimus 0.1% in orabase and triamcinolone acetonide 0.1% in orabase in the management of symptomatic oral lichen planus randomized single blind control study

Objectives: Studies done on the management of oral lichen planus using tacrolimus are limited. The aim of the study is to compare the efficacy of tacrolimus with tramcinolone acetonide topically in the management of symptomatic oral lichen planus and also to evaluate adverse effects and opportunisti...

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Main Authors: Manjunatha M Revanappa (Author), Venkatesh G Naikmasur (Author), Atul P Sattur (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2012-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Manjunatha M Revanappa  |e author 
700 1 0 |a Venkatesh G Naikmasur  |e author 
700 1 0 |a Atul P Sattur  |e author 
245 0 0 |a Evaluation of efficacy of tacrolimus 0.1% in orabase and triamcinolone acetonide 0.1% in orabase in the management of symptomatic oral lichen planus randomized single blind control study 
260 |b Wolters Kluwer Medknow Publications,   |c 2012-01-01T00:00:00Z. 
500 |a 0972-1363 
500 |a 0975-1572 
500 |a 10.5005/jp-journals-10011-1311 
520 |a Objectives: Studies done on the management of oral lichen planus using tacrolimus are limited. The aim of the study is to compare the efficacy of tacrolimus with tramcinolone acetonide topically in the management of symptomatic oral lichen planus and also to evaluate adverse effects and opportunistic yeast infections. Materials and methods: A randomized controlled study was conducted on 60 patients with symptomatic lesions of oral lichen planus with biopsy proven who fulfilled the inclusion criteria. Study group comprised of 30 patients who received topical 0.1 tacrolimus in orabase therapy for 4 weeks. Control group comprised of 30 patients who received topical 0.1% triamcinolone acetonide in orabase for 4 weeks. Results: Significant improvement of symptoms (7.80 ΁ 1.90 to 1.2 ΁ 2.6) and clinical scores (3.1 ΁ 1.27 to 2.3 ΁ 1.1) in study group as compared to control group (7.60 ΁ 2.01 to 2.7 ΁ 2.5) and (2.73 ΁ 1.46 to 1.2 ΁ 1.4). No significant adverse effects were observed and no recurrence was noted during treatment and follow-up. Conclusion: Study group has shown significant clinical response (p = 0.002) when compared to control group. However, double-blind, controlled studies are needed to evaluate the efficacy of tacrolimus in the treatment of symptomatic oral lichen planus and to address the safety for long-term therapy. 
546 |a EN 
690 |a Oral lichen planus 
690 |a Tacrolimus 
690 |a Triamcinolone acetonide 
690 |a Orabase 
690 |a Dentistry 
690 |a RK1-715 
690 |a Medical physics. Medical radiology. Nuclear medicine 
690 |a R895-920 
655 7 |a article  |2 local 
786 0 |n Journal of Indian Academy of Oral Medicine and Radiology, Vol 24, Iss 4, Pp 269-273 (2012) 
787 0 |n http://www.jiaomr.in/article.asp?issn=0972-1363;year=2012;volume=24;issue=4;spage=269;epage=273;aulast=Revanappa 
787 0 |n https://doaj.org/toc/0972-1363 
787 0 |n https://doaj.org/toc/0975-1572 
856 4 1 |u https://doaj.org/article/aec41f7276bf40b2837179d090e1d050  |z Connect to this object online.