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CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy

BACKGROUND: Cytomegalovirus (CMV) infection is endemic worldwide. Although CMV reactivation often becomes a serious problem in immunocompromised patients, the prevalence of CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy has yet to be determined. METHOD: Among 175...

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Autores principales: Sato, Yusuke, Motoyama, Satoru, Maruyama, Kiyotomi, Yoshino, Key, Sasaki, Tomohiko, Wakita, Akiyuki, Ogawa, Jun-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101544/
http://dx.doi.org/10.1007/s10388-012-0316-x
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author Sato, Yusuke
Motoyama, Satoru
Maruyama, Kiyotomi
Yoshino, Key
Sasaki, Tomohiko
Wakita, Akiyuki
Ogawa, Jun-ichi
author_facet Sato, Yusuke
Motoyama, Satoru
Maruyama, Kiyotomi
Yoshino, Key
Sasaki, Tomohiko
Wakita, Akiyuki
Ogawa, Jun-ichi
author_sort Sato, Yusuke
collection PubMed
description BACKGROUND: Cytomegalovirus (CMV) infection is endemic worldwide. Although CMV reactivation often becomes a serious problem in immunocompromised patients, the prevalence of CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy has yet to be determined. METHOD: Among 175 consecutive patients with thoracic squamous cell esophageal cancer who underwent esophagectomy with extensive lymph node dissection at Akita University Hospital between 2007 and 2010, 11 patients (6.3 %) diagnosed with ARDS during the acute phase of esophagectomy were enrolled and treated with steroid pulse therapy, high-dose (15–20 mg/kg/day) administration and tapering in this retrospective study. RESULTS: Seven of the 11 patients (63.6 %) were diagnosed with CMV reactivation based on CMV antigenemia assayed 19.1 days after the start of methylprednisolone administration and were treated with ganciclovir for 39.6 days. Six of the 7 patients (85.7 %) diagnosed with CMV reactivation were administered a total methylprednisolone dose of more than 4,000 mg. Though there was no significant difference between patients with and without CMV reactivation, there was a tendency that patients with CMV reactivation showed a lower minimum number of lymphocytes during the acute phase of esophagectomy (p = 0.051, Student’s t test, average 223.3 and 298.0/μl, respectively). CONCLUSION: Though the number of study patients is small, the prevalence of CMV reactivation caused by high-dose methylprednisolone therapy for ARDS after esophagectomy is remarkably high. This result strikes a note of warning concerning the management of these patients and suggests the importance of screenings for CMV reactivation so as to make an accurate diagnosis and initiate treatment in a timely manner.
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spelling pubmed-71015442020-03-31 CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy Sato, Yusuke Motoyama, Satoru Maruyama, Kiyotomi Yoshino, Key Sasaki, Tomohiko Wakita, Akiyuki Ogawa, Jun-ichi Esophagus Original Article BACKGROUND: Cytomegalovirus (CMV) infection is endemic worldwide. Although CMV reactivation often becomes a serious problem in immunocompromised patients, the prevalence of CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy has yet to be determined. METHOD: Among 175 consecutive patients with thoracic squamous cell esophageal cancer who underwent esophagectomy with extensive lymph node dissection at Akita University Hospital between 2007 and 2010, 11 patients (6.3 %) diagnosed with ARDS during the acute phase of esophagectomy were enrolled and treated with steroid pulse therapy, high-dose (15–20 mg/kg/day) administration and tapering in this retrospective study. RESULTS: Seven of the 11 patients (63.6 %) were diagnosed with CMV reactivation based on CMV antigenemia assayed 19.1 days after the start of methylprednisolone administration and were treated with ganciclovir for 39.6 days. Six of the 7 patients (85.7 %) diagnosed with CMV reactivation were administered a total methylprednisolone dose of more than 4,000 mg. Though there was no significant difference between patients with and without CMV reactivation, there was a tendency that patients with CMV reactivation showed a lower minimum number of lymphocytes during the acute phase of esophagectomy (p = 0.051, Student’s t test, average 223.3 and 298.0/μl, respectively). CONCLUSION: Though the number of study patients is small, the prevalence of CMV reactivation caused by high-dose methylprednisolone therapy for ARDS after esophagectomy is remarkably high. This result strikes a note of warning concerning the management of these patients and suggests the importance of screenings for CMV reactivation so as to make an accurate diagnosis and initiate treatment in a timely manner. Springer Japan 2012-04-27 2012 /pmc/articles/PMC7101544/ http://dx.doi.org/10.1007/s10388-012-0316-x Text en © The Japan Esophageal Society and Springer 2012 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Sato, Yusuke
Motoyama, Satoru
Maruyama, Kiyotomi
Yoshino, Key
Sasaki, Tomohiko
Wakita, Akiyuki
Ogawa, Jun-ichi
CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy
title CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy
title_full CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy
title_fullStr CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy
title_full_unstemmed CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy
title_short CMV reactivation caused by methylprednisolone therapy for ARDS after esophagectomy
title_sort cmv reactivation caused by methylprednisolone therapy for ards after esophagectomy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101544/
http://dx.doi.org/10.1007/s10388-012-0316-x
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