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Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study

BACKGROUND: Vitamin C is an immune-relevant micronutrient, which is depleted in viral infections and this deficiency seems to play a critical role in the pathogenesis of herpes infections and in the development of postherpetic neuralgia. The objective of this observational multicenter study was to e...

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Autores principales: Schencking, Martin, Vollbracht, Claudia, Weiss, Gabriele, Lebert, Jennifer, Biller, Andreas, Goyvaerts, Birgit, Kraft, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560828/
https://www.ncbi.nlm.nih.gov/pubmed/22460093
http://dx.doi.org/10.12659/MSM.882621
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author Schencking, Martin
Vollbracht, Claudia
Weiss, Gabriele
Lebert, Jennifer
Biller, Andreas
Goyvaerts, Birgit
Kraft, Karin
author_facet Schencking, Martin
Vollbracht, Claudia
Weiss, Gabriele
Lebert, Jennifer
Biller, Andreas
Goyvaerts, Birgit
Kraft, Karin
author_sort Schencking, Martin
collection PubMed
description BACKGROUND: Vitamin C is an immune-relevant micronutrient, which is depleted in viral infections and this deficiency seems to play a critical role in the pathogenesis of herpes infections and in the development of postherpetic neuralgia. The objective of this observational multicenter study was to evaluate the utilization, safety and efficacy of intravenously administrated vitamin C in patients with shingles. MATERIAL/METHODS: Between April 2009 and December 2010 16 general practitioners recorded data of 67 participants with symptomatic herpes zoster who received vitamin C intravenously (Pascorbin(®) 7.5 g/50 ml) for approximately 2 weeks in addition to standard treatment. The assessment of pain (VAS) and the dermatologic symptoms of shingles such as hemorrhagic lesions and the number of efflorescences were investigated in a follow-up observation phase of up to 12 weeks. RESULTS: Mean declines of pain scores (VAS), number of affected dermatomes and efflorescences, and the presence of hemorrhagic vesicles between the baseline and follow-up assessments at 2 and 12 weeks were statistically significant. Overall, 6.4% of the participants experienced post-herpetic neuralgia. Common complaints such as general fatigue and impaired concentration also improved during the study. The effects and the tolerability of the treatment were evaluated positively by the physicians. The risk of developing PHN was reduced. CONCLUSIONS: The data presented here provide evidence that concomitant use of intravenously administered ascorbic acid may have beneficial effects on herpes zoster-associated pain, dermatologic findings and accompanying common complaints. To confirm our findings, randomized, placebo-controlled clinical studies are necessary.
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spelling pubmed-35608282013-04-24 Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study Schencking, Martin Vollbracht, Claudia Weiss, Gabriele Lebert, Jennifer Biller, Andreas Goyvaerts, Birgit Kraft, Karin Med Sci Monit Clinical Research BACKGROUND: Vitamin C is an immune-relevant micronutrient, which is depleted in viral infections and this deficiency seems to play a critical role in the pathogenesis of herpes infections and in the development of postherpetic neuralgia. The objective of this observational multicenter study was to evaluate the utilization, safety and efficacy of intravenously administrated vitamin C in patients with shingles. MATERIAL/METHODS: Between April 2009 and December 2010 16 general practitioners recorded data of 67 participants with symptomatic herpes zoster who received vitamin C intravenously (Pascorbin(®) 7.5 g/50 ml) for approximately 2 weeks in addition to standard treatment. The assessment of pain (VAS) and the dermatologic symptoms of shingles such as hemorrhagic lesions and the number of efflorescences were investigated in a follow-up observation phase of up to 12 weeks. RESULTS: Mean declines of pain scores (VAS), number of affected dermatomes and efflorescences, and the presence of hemorrhagic vesicles between the baseline and follow-up assessments at 2 and 12 weeks were statistically significant. Overall, 6.4% of the participants experienced post-herpetic neuralgia. Common complaints such as general fatigue and impaired concentration also improved during the study. The effects and the tolerability of the treatment were evaluated positively by the physicians. The risk of developing PHN was reduced. CONCLUSIONS: The data presented here provide evidence that concomitant use of intravenously administered ascorbic acid may have beneficial effects on herpes zoster-associated pain, dermatologic findings and accompanying common complaints. To confirm our findings, randomized, placebo-controlled clinical studies are necessary. International Scientific Literature, Inc. 2012-04-01 /pmc/articles/PMC3560828/ /pubmed/22460093 http://dx.doi.org/10.12659/MSM.882621 Text en © Med Sci Monit, 2012 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
spellingShingle Clinical Research
Schencking, Martin
Vollbracht, Claudia
Weiss, Gabriele
Lebert, Jennifer
Biller, Andreas
Goyvaerts, Birgit
Kraft, Karin
Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study
title Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study
title_full Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study
title_fullStr Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study
title_full_unstemmed Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study
title_short Intravenous Vitamin C in the treatment of shingles: Results of a multicenter prospective cohort study
title_sort intravenous vitamin c in the treatment of shingles: results of a multicenter prospective cohort study
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560828/
https://www.ncbi.nlm.nih.gov/pubmed/22460093
http://dx.doi.org/10.12659/MSM.882621
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