Cargando…

Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies

BACKGROUND: Most of the results regarding hydrogen (H(2)) therapy for acute cerebral ischemia are derived from in vitro studies and animal experiments, with only a few obtained from human trials with a limited number of subjects. Thus, there is a paucity of information regarding both the beneficial...

Descripción completa

Detalles Bibliográficos
Autores principales: Nagatani, Kimihiro, Nawashiro, Hiroshi, Takeuchi, Satoru, Tomura, Satoshi, Otani, Naoki, Osada, Hideo, Wada, Kojiro, Katoh, Hiroshi, Tsuzuki, Nobusuke, Mori, Kentaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694409/
https://www.ncbi.nlm.nih.gov/pubmed/23799921
http://dx.doi.org/10.1186/2045-9912-3-13
_version_ 1782274855959265280
author Nagatani, Kimihiro
Nawashiro, Hiroshi
Takeuchi, Satoru
Tomura, Satoshi
Otani, Naoki
Osada, Hideo
Wada, Kojiro
Katoh, Hiroshi
Tsuzuki, Nobusuke
Mori, Kentaro
author_facet Nagatani, Kimihiro
Nawashiro, Hiroshi
Takeuchi, Satoru
Tomura, Satoshi
Otani, Naoki
Osada, Hideo
Wada, Kojiro
Katoh, Hiroshi
Tsuzuki, Nobusuke
Mori, Kentaro
author_sort Nagatani, Kimihiro
collection PubMed
description BACKGROUND: Most of the results regarding hydrogen (H(2)) therapy for acute cerebral ischemia are derived from in vitro studies and animal experiments, with only a few obtained from human trials with a limited number of subjects. Thus, there is a paucity of information regarding both the beneficial therapeutic effects as well as the side effects of H(2) on acute cerebral ischemia in humans. We designed a pilot study to investigate single dose intravenous H(2)-administration in combination with edaravone, aiming to provide an initial estimate of the possible risks and benefits in select patients presenting with acute ischemic stroke. METHODS: An open-label, prospective, non-randomized study of intravenous H(2)-administration was performed in 38 patients hospitalized for acute ischemic stroke. All patients received an H(2)-enriched intravenous solution in addition to edaravone immediately after the diagnosis of acute ischemic stroke. Acute stroke patients within 3 h of onset received intravenous tissue plasminogen activator (t-PA) (0.6 mg/kg) treatment, and patients receiving t-PA had to commence the administration of the H(2)-enriched intravenous solution and edaravone before or at the same time as the t-PA was infused. RESULTS: Complications were observed in 2 patients (5.3%), which consisted of diarrhea in 1 patient (2.6%) and cardiac failure in 1 patient (2.6%). No deterioration in laboratory tests, urinary tests, ECG, or chest X-ray radiograms occurred in any patient in this study. In all patients, the mean National Institutes of Health Stroke Scale (NIHSS) scores at baseline, and 7, 30, and 90 d after admission were 8.2 ± 7.5, 5.6 ± 7.1, 4.9 ± 6.5, and 4.5 ± 6.3, respectively. The early recanalization was identified in 4 of 11 patients (36.4%) who received intravenous t-PA administration. Hemorrhagic transformation was observed in 2 patients (18.2%). None of the patients in this study that were treated with t-PA developed symptomatic intracranial hemorrhage. CONCLUSIONS: Data from the current study indicate that an H(2)-enriched intravenous solution is safe for patients with acute cerebral infarction, including patients treated with t-PA.
format Online
Article
Text
id pubmed-3694409
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-36944092013-06-28 Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies Nagatani, Kimihiro Nawashiro, Hiroshi Takeuchi, Satoru Tomura, Satoshi Otani, Naoki Osada, Hideo Wada, Kojiro Katoh, Hiroshi Tsuzuki, Nobusuke Mori, Kentaro Med Gas Res Case Report BACKGROUND: Most of the results regarding hydrogen (H(2)) therapy for acute cerebral ischemia are derived from in vitro studies and animal experiments, with only a few obtained from human trials with a limited number of subjects. Thus, there is a paucity of information regarding both the beneficial therapeutic effects as well as the side effects of H(2) on acute cerebral ischemia in humans. We designed a pilot study to investigate single dose intravenous H(2)-administration in combination with edaravone, aiming to provide an initial estimate of the possible risks and benefits in select patients presenting with acute ischemic stroke. METHODS: An open-label, prospective, non-randomized study of intravenous H(2)-administration was performed in 38 patients hospitalized for acute ischemic stroke. All patients received an H(2)-enriched intravenous solution in addition to edaravone immediately after the diagnosis of acute ischemic stroke. Acute stroke patients within 3 h of onset received intravenous tissue plasminogen activator (t-PA) (0.6 mg/kg) treatment, and patients receiving t-PA had to commence the administration of the H(2)-enriched intravenous solution and edaravone before or at the same time as the t-PA was infused. RESULTS: Complications were observed in 2 patients (5.3%), which consisted of diarrhea in 1 patient (2.6%) and cardiac failure in 1 patient (2.6%). No deterioration in laboratory tests, urinary tests, ECG, or chest X-ray radiograms occurred in any patient in this study. In all patients, the mean National Institutes of Health Stroke Scale (NIHSS) scores at baseline, and 7, 30, and 90 d after admission were 8.2 ± 7.5, 5.6 ± 7.1, 4.9 ± 6.5, and 4.5 ± 6.3, respectively. The early recanalization was identified in 4 of 11 patients (36.4%) who received intravenous t-PA administration. Hemorrhagic transformation was observed in 2 patients (18.2%). None of the patients in this study that were treated with t-PA developed symptomatic intracranial hemorrhage. CONCLUSIONS: Data from the current study indicate that an H(2)-enriched intravenous solution is safe for patients with acute cerebral infarction, including patients treated with t-PA. BioMed Central 2013-06-25 /pmc/articles/PMC3694409/ /pubmed/23799921 http://dx.doi.org/10.1186/2045-9912-3-13 Text en Copyright © 2013 Nagatani et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nagatani, Kimihiro
Nawashiro, Hiroshi
Takeuchi, Satoru
Tomura, Satoshi
Otani, Naoki
Osada, Hideo
Wada, Kojiro
Katoh, Hiroshi
Tsuzuki, Nobusuke
Mori, Kentaro
Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
title Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
title_full Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
title_fullStr Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
title_full_unstemmed Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
title_short Safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
title_sort safety of intravenous administration of hydrogen-enriched fluid in patients with acute cerebral ischemia: initial clinical studies
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694409/
https://www.ncbi.nlm.nih.gov/pubmed/23799921
http://dx.doi.org/10.1186/2045-9912-3-13
work_keys_str_mv AT nagatanikimihiro safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT nawashirohiroshi safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT takeuchisatoru safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT tomurasatoshi safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT otaninaoki safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT osadahideo safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT wadakojiro safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT katohhiroshi safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT tsuzukinobusuke safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies
AT morikentaro safetyofintravenousadministrationofhydrogenenrichedfluidinpatientswithacutecerebralischemiainitialclinicalstudies