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Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children

OBJECTIVES: To determine the efficacy of methylprednisolone pulse therapy for children with Mycoplasma pneumoniae pneumonia (MP) that is refractory to antibiotic treatment. METHODS: Refractory patients were defined as cases showing clinical and radiological deterioration despite appropriate antibiot...

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Autores principales: Tamura, Akihiro, Matsubara, Kousaku, Tanaka, Takayuki, Nigami, Hiroyuki, Yura, Kazuo, Fukaya, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Infection Society. Published by Elsevier Ltd. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112643/
https://www.ncbi.nlm.nih.gov/pubmed/18656264
http://dx.doi.org/10.1016/j.jinf.2008.06.012
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author Tamura, Akihiro
Matsubara, Kousaku
Tanaka, Takayuki
Nigami, Hiroyuki
Yura, Kazuo
Fukaya, Takashi
author_facet Tamura, Akihiro
Matsubara, Kousaku
Tanaka, Takayuki
Nigami, Hiroyuki
Yura, Kazuo
Fukaya, Takashi
author_sort Tamura, Akihiro
collection PubMed
description OBJECTIVES: To determine the efficacy of methylprednisolone pulse therapy for children with Mycoplasma pneumoniae pneumonia (MP) that is refractory to antibiotic treatment. METHODS: Refractory patients were defined as cases showing clinical and radiological deterioration despite appropriate antibiotic therapy for 7 days or more. We identified 6 such children (male/female: 3/3) aged 3–9 years who were treated between 1998 and 2006. During the same period, 190 children with MP were admitted to our institution. RESULTS: Common laboratory findings of the patients included cytopenia, elevated serum lactate dehydrogenase and ferritin levels, and elevated urine β(2)-microglobulin levels, suggesting complication of hypercytokinemic condition. We initiated intravenous methylprednisolone at a dose of 30 mg/kg on 10.2 ± 2.8 clinical days and administered it once daily for 3 consecutive days. Fever subsided 4–14 h after initiation of steroid pulse therapy in all patients. This dramatic effect was accompanied by rapid improvement of radiological abnormalities including infiltrates and pleural effusion, followed by improvement of laboratory abnormalities. There were no adverse events of steroid therapy. CONCLUSIONS: This is the first case-series study showing an effect of 3-day methylprednisolone pulse therapy on refractory MP in children. This therapy is apparently an efficacious and well-tolerated treatment for refractory MP.
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spelling pubmed-71126432020-04-02 Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children Tamura, Akihiro Matsubara, Kousaku Tanaka, Takayuki Nigami, Hiroyuki Yura, Kazuo Fukaya, Takashi J Infect Article OBJECTIVES: To determine the efficacy of methylprednisolone pulse therapy for children with Mycoplasma pneumoniae pneumonia (MP) that is refractory to antibiotic treatment. METHODS: Refractory patients were defined as cases showing clinical and radiological deterioration despite appropriate antibiotic therapy for 7 days or more. We identified 6 such children (male/female: 3/3) aged 3–9 years who were treated between 1998 and 2006. During the same period, 190 children with MP were admitted to our institution. RESULTS: Common laboratory findings of the patients included cytopenia, elevated serum lactate dehydrogenase and ferritin levels, and elevated urine β(2)-microglobulin levels, suggesting complication of hypercytokinemic condition. We initiated intravenous methylprednisolone at a dose of 30 mg/kg on 10.2 ± 2.8 clinical days and administered it once daily for 3 consecutive days. Fever subsided 4–14 h after initiation of steroid pulse therapy in all patients. This dramatic effect was accompanied by rapid improvement of radiological abnormalities including infiltrates and pleural effusion, followed by improvement of laboratory abnormalities. There were no adverse events of steroid therapy. CONCLUSIONS: This is the first case-series study showing an effect of 3-day methylprednisolone pulse therapy on refractory MP in children. This therapy is apparently an efficacious and well-tolerated treatment for refractory MP. The British Infection Society. Published by Elsevier Ltd. 2008-09 2008-07-25 /pmc/articles/PMC7112643/ /pubmed/18656264 http://dx.doi.org/10.1016/j.jinf.2008.06.012 Text en Copyright © 2008 The British Infection Society. Published by Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Tamura, Akihiro
Matsubara, Kousaku
Tanaka, Takayuki
Nigami, Hiroyuki
Yura, Kazuo
Fukaya, Takashi
Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children
title Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children
title_full Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children
title_fullStr Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children
title_full_unstemmed Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children
title_short Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children
title_sort methylprednisolone pulse therapy for refractory mycoplasma pneumoniae pneumonia in children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112643/
https://www.ncbi.nlm.nih.gov/pubmed/18656264
http://dx.doi.org/10.1016/j.jinf.2008.06.012
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