Oral acyclovir in the suppression of recurrent non-genital herpes simplex virus infection

SUMMARY In a double‐blind, placebo‐controlled, cross‐over trial in 11 patients suffering eight or more episodes of recurrent non‐genital herpes simplex virus (HSV) infection per annum, only two patients experienced a recurrence during treatment with oral acyclovir (200 mg 4 times daily) for up to 12...

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Veröffentlicht in:British journal of dermatology (1951) 1985-12, Vol.113 (6), p.731-735
Hauptverfasser: THOMAS, R.H.MEYRICK, DODD, H.J., YEO, JANE M., KIRBY, J.D.T.
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container_end_page 735
container_issue 6
container_start_page 731
container_title British journal of dermatology (1951)
container_volume 113
creator THOMAS, R.H.MEYRICK
DODD, H.J.
YEO, JANE M.
KIRBY, J.D.T.
description SUMMARY In a double‐blind, placebo‐controlled, cross‐over trial in 11 patients suffering eight or more episodes of recurrent non‐genital herpes simplex virus (HSV) infection per annum, only two patients experienced a recurrence during treatment with oral acyclovir (200 mg 4 times daily) for up to 12 weeks, compared with nine during placebo treatment (P=0.016). Although lesion development was effectively suppressed in nine of the patients whilst taking acyclovir, the development of prodromal symptoms, and occasionally erythema, was reported by five. There was no difference between acyclovir and placebo in the time to the next recurrence following completion of treatment. No patient reported any side effects of either placebo or acyclovir therapy. It is believed that this is the first report of any form of oral therapy which is effective in suppressing recurrent non‐genital HSV infection in immunocompetent patients.
doi_str_mv 10.1111/j.1365-2133.1985.tb02409.x
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Although lesion development was effectively suppressed in nine of the patients whilst taking acyclovir, the development of prodromal symptoms, and occasionally erythema, was reported by five. There was no difference between acyclovir and placebo in the time to the next recurrence following completion of treatment. No patient reported any side effects of either placebo or acyclovir therapy. 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Although lesion development was effectively suppressed in nine of the patients whilst taking acyclovir, the development of prodromal symptoms, and occasionally erythema, was reported by five. There was no difference between acyclovir and placebo in the time to the next recurrence following completion of treatment. No patient reported any side effects of either placebo or acyclovir therapy. It is believed that this is the first report of any form of oral therapy which is effective in suppressing recurrent non‐genital HSV infection in immunocompetent patients.</description><subject>Acyclovir - administration &amp; dosage</subject><subject>Acyclovir - therapeutic use</subject><subject>Administration, Oral</subject><subject>Adult</subject><subject>Antibiotics. Antiinfectious agents. 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Antiinfectious agents. Antiparasitic agents</topic><topic>Antiviral agents</topic><topic>Biological and medical sciences</topic><topic>Clinical Trials as Topic</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Herpes Simplex - prevention &amp; control</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. 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ispartof British journal of dermatology (1951), 1985-12, Vol.113 (6), p.731-735
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Acyclovir - administration & dosage
Acyclovir - therapeutic use
Administration, Oral
Adult
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiviral agents
Biological and medical sciences
Clinical Trials as Topic
Double-Blind Method
Female
Herpes Simplex - prevention & control
Humans
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Recurrence
title Oral acyclovir in the suppression of recurrent non-genital herpes simplex virus infection
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