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A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts

OBJECTIVES: To evaluate and compare the efficacy of MMR vaccine and MIP vaccine for resolution of Cutaneous warts (Cw). METHODS: The hospital-based prospective randomized interventional study was done where a total of 60 patients of Cw were divided into two groups of 30 patients each: Group A receiv...

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Autores principales: Kaur, Amandeep, Brar, Balvinder Kaur, Kumar, Sumir, Brar, Sukhmani Kaur, Boparai, Amarbir Singh, Puri, Neerja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208270/
https://www.ncbi.nlm.nih.gov/pubmed/34188270
http://dx.doi.org/10.4103/ijd.IJD_700_20
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author Kaur, Amandeep
Brar, Balvinder Kaur
Kumar, Sumir
Brar, Sukhmani Kaur
Boparai, Amarbir Singh
Puri, Neerja
author_facet Kaur, Amandeep
Brar, Balvinder Kaur
Kumar, Sumir
Brar, Sukhmani Kaur
Boparai, Amarbir Singh
Puri, Neerja
author_sort Kaur, Amandeep
collection PubMed
description OBJECTIVES: To evaluate and compare the efficacy of MMR vaccine and MIP vaccine for resolution of Cutaneous warts (Cw). METHODS: The hospital-based prospective randomized interventional study was done where a total of 60 patients of Cw were divided into two groups of 30 patients each: Group A received 0.1 ml of intralesional injection of MIP vaccine and Group B received 0.5 ml of MMR vaccine. The treatment protocol involved three intralesional injection of vaccines at intervals of 3 weeks (maximum of three injections). The follow-up was done every 4 weeks for at least 24 weeks for the comparison of the two groups. The primary outcomes were the decrease in size of the wart or clearance of primary warts. The secondary outcomes were the improvement in the distant warts and any complications related to the use of vaccines. The data were entered in MS Excel and analyzed using SPSS 17.0 version. A P value of <0.05 was considered statistically significant. RESULTS: The baseline demographic and wart characteristics were comparable between the two groups (P > 0.05). As compared to MMR, MIP showed an early (9.41 vs 11.71 weeks, P = 0.027), and a significantly higher complete response (90% vs 76.67%) with P < 0.05. The less duration of the warts was significantly associated with the higher complete response (P < 0.05) in both the groups. The common side effects were erythema/inflammation [19 (63.34%)] in Group A and pain during the injection [19 (63.34%)] in Group B with P < 0.0001. CONCLUSION: In conclusion, MIP intralesional injections have a quicker response and are more efficacious compared to MMR in the treatment of Cw, though each vaccine carries its own sets of side effects.
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spelling pubmed-82082702021-06-28 A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts Kaur, Amandeep Brar, Balvinder Kaur Kumar, Sumir Brar, Sukhmani Kaur Boparai, Amarbir Singh Puri, Neerja Indian J Dermatol Original Article OBJECTIVES: To evaluate and compare the efficacy of MMR vaccine and MIP vaccine for resolution of Cutaneous warts (Cw). METHODS: The hospital-based prospective randomized interventional study was done where a total of 60 patients of Cw were divided into two groups of 30 patients each: Group A received 0.1 ml of intralesional injection of MIP vaccine and Group B received 0.5 ml of MMR vaccine. The treatment protocol involved three intralesional injection of vaccines at intervals of 3 weeks (maximum of three injections). The follow-up was done every 4 weeks for at least 24 weeks for the comparison of the two groups. The primary outcomes were the decrease in size of the wart or clearance of primary warts. The secondary outcomes were the improvement in the distant warts and any complications related to the use of vaccines. The data were entered in MS Excel and analyzed using SPSS 17.0 version. A P value of <0.05 was considered statistically significant. RESULTS: The baseline demographic and wart characteristics were comparable between the two groups (P > 0.05). As compared to MMR, MIP showed an early (9.41 vs 11.71 weeks, P = 0.027), and a significantly higher complete response (90% vs 76.67%) with P < 0.05. The less duration of the warts was significantly associated with the higher complete response (P < 0.05) in both the groups. The common side effects were erythema/inflammation [19 (63.34%)] in Group A and pain during the injection [19 (63.34%)] in Group B with P < 0.0001. CONCLUSION: In conclusion, MIP intralesional injections have a quicker response and are more efficacious compared to MMR in the treatment of Cw, though each vaccine carries its own sets of side effects. Wolters Kluwer - Medknow 2021 /pmc/articles/PMC8208270/ /pubmed/34188270 http://dx.doi.org/10.4103/ijd.IJD_700_20 Text en Copyright: © 2021 Indian Journal of Dermatology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Kaur, Amandeep
Brar, Balvinder Kaur
Kumar, Sumir
Brar, Sukhmani Kaur
Boparai, Amarbir Singh
Puri, Neerja
A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts
title A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts
title_full A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts
title_fullStr A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts
title_full_unstemmed A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts
title_short A Randomized Comparative Study of MIP and MMR Vaccine for the Treatment of Cutaneous Warts
title_sort randomized comparative study of mip and mmr vaccine for the treatment of cutaneous warts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208270/
https://www.ncbi.nlm.nih.gov/pubmed/34188270
http://dx.doi.org/10.4103/ijd.IJD_700_20
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