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THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA

BACKGROUND: Pityriasis Rosea (PR) is an acute inflammatory and self-limiting skin disorder, sometimes with troublesome symptoms. To date, there are few treatments available for this disorder. AIM: Compare the traditional treatment with erythromycin to a newly introduced antiviral treatment acyclovir...

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Autores principales: Ehsani, Amirhooshang, Esmaily, Nafiseh, Noormohammadpour, Pedram, Toosi, Siavash, Hosseinpour, Alireza, Hosseini, Mahbobeh, Sayanjali, Shima
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965909/
https://www.ncbi.nlm.nih.gov/pubmed/21063515
http://dx.doi.org/10.4103/0019-5154.70672
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author Ehsani, Amirhooshang
Esmaily, Nafiseh
Noormohammadpour, Pedram
Toosi, Siavash
Hosseinpour, Alireza
Hosseini, Mahbobeh
Sayanjali, Shima
author_facet Ehsani, Amirhooshang
Esmaily, Nafiseh
Noormohammadpour, Pedram
Toosi, Siavash
Hosseinpour, Alireza
Hosseini, Mahbobeh
Sayanjali, Shima
author_sort Ehsani, Amirhooshang
collection PubMed
description BACKGROUND: Pityriasis Rosea (PR) is an acute inflammatory and self-limiting skin disorder, sometimes with troublesome symptoms. To date, there are few treatments available for this disorder. AIM: Compare the traditional treatment with erythromycin to a newly introduced antiviral treatment acyclovir for PR. MATERIALS AND METHODS: Patients with clinically confirmed diagnosis of PR, matching our exclusion criteria, were enrolled. They were randomized in two groups that received high-dose oral acyclovir or erythromycin. The participants were evaluated two, four, and eight weeks after commencement of the study and followed for one year. RESULTS: A total of 30 patients including 15 males and 15 females completed the study. After eight weeks, 13 patients in the acyclovir group experienced complete response, while in the erythromycin group only six patients had complete response (P < 0.05). Also, patients in the acyclovir group experienced faster resolution of pruritus in comparison with the erythromycin group (not significant). No adverse drug reaction was detected in both groups. CONCLUSION: It seemed that a high-dose of oral acyclovir was a safe and effective therapy for PR, although this remained to be confirmed in larger studies.
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spelling pubmed-29659092010-11-09 THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA Ehsani, Amirhooshang Esmaily, Nafiseh Noormohammadpour, Pedram Toosi, Siavash Hosseinpour, Alireza Hosseini, Mahbobeh Sayanjali, Shima Indian J Dermatol Therapeutic Round BACKGROUND: Pityriasis Rosea (PR) is an acute inflammatory and self-limiting skin disorder, sometimes with troublesome symptoms. To date, there are few treatments available for this disorder. AIM: Compare the traditional treatment with erythromycin to a newly introduced antiviral treatment acyclovir for PR. MATERIALS AND METHODS: Patients with clinically confirmed diagnosis of PR, matching our exclusion criteria, were enrolled. They were randomized in two groups that received high-dose oral acyclovir or erythromycin. The participants were evaluated two, four, and eight weeks after commencement of the study and followed for one year. RESULTS: A total of 30 patients including 15 males and 15 females completed the study. After eight weeks, 13 patients in the acyclovir group experienced complete response, while in the erythromycin group only six patients had complete response (P < 0.05). Also, patients in the acyclovir group experienced faster resolution of pruritus in comparison with the erythromycin group (not significant). No adverse drug reaction was detected in both groups. CONCLUSION: It seemed that a high-dose of oral acyclovir was a safe and effective therapy for PR, although this remained to be confirmed in larger studies. Medknow Publications 2010 /pmc/articles/PMC2965909/ /pubmed/21063515 http://dx.doi.org/10.4103/0019-5154.70672 Text en © Indian Journal of Dermatology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Therapeutic Round
Ehsani, Amirhooshang
Esmaily, Nafiseh
Noormohammadpour, Pedram
Toosi, Siavash
Hosseinpour, Alireza
Hosseini, Mahbobeh
Sayanjali, Shima
THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA
title THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA
title_full THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA
title_fullStr THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA
title_full_unstemmed THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA
title_short THE COMPARISON BETWEEN THE EFFICACY OF HIGH DOSE ACYCLOVIR AND ERYTHROMYCIN ON THE PERIOD AND SIGNS OF PITIRIASIS ROSEA
title_sort comparison between the efficacy of high dose acyclovir and erythromycin on the period and signs of pitiriasis rosea
topic Therapeutic Round
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965909/
https://www.ncbi.nlm.nih.gov/pubmed/21063515
http://dx.doi.org/10.4103/0019-5154.70672
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