Oral acyclovir in treatment of pityriasis rosea

Authors

  • Nut Laorueangwatthana
  • Santhita Pimonbut
  • Sirinat Suriyachai
  • Papichaya Songtuntarax

Abstract

OBJECTIVE

To identify the efficacy of oral acyclovir in treatment of pityriasis rosea (PR).

 

METHODS

Four independent reviewers systematically searched through electronic databases without language restriction, included Pubmed, Cochrane library, Scopus, and Trip Database. We also  performed hand searching to find all relevant studies outside the databases. We assessed quality and risk of bias of the included studies using Jadad score and The Cochrane Collaboration’s Tool for Assessing Risk of Bias. We extracted data from the included studies. The meta-analysis was performed where appropriate.

 

RESULTS

There were four randomized controlled trials identified, involving 251 patients with PR. Using oral acyclovir comparing with placebo or no treatment was associated with 2.76 times higher response rate to treatment (95% confidence interval (CI), 1.86 to 4.09; P<0.001; I2=11%), 2.19 times higher response rate to treatment (95% CI, 1.73 to 2.78; P<0.001; I2=18%) at the first week and the second week, respectively, and 44% relative risk reduction (RR 0.56, 95% CI, 0.41 to 0.77; P=0.004; I2=21%) in occurrence rate of new skin lesion after following in the first week.

 

CONCLUSION

Oral acyclovir was superior to placebo or no treatment for treating patients with PR regarding response rate to treatment at the first and the second week as well as occurrence rate reduction of the new skin lesion in the first week after starting the treatment.

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43.4.2 Oral acyclovir in treatment of pityriasis rosea cover

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Published

2019-08-31

How to Cite

Laorueangwatthana, N., Pimonbut, S., Suriyachai, S., & Songtuntarax, P. (2019). Oral acyclovir in treatment of pityriasis rosea. The Clinical Academia, 43(4), 128–139. Retrieved from https://he02.tci-thaijo.org/index.php/theclinicalacademia/article/view/227062