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Dive into the research topics where Akiko Kanaya is active.

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Featured researches published by Akiko Kanaya.


European Journal of Pharmacology | 1998

Enhancement of serotonergic neural activity contributes to cyclosporine-induced tremors in mice.

Hideki Shuto; Yasufumi Kataoka; Akiko Kanaya; Kazuhisa Matsunaga; Masanori Sueyasu; Ryozo Oishi

A single cyclosporine injection (50 mg/kg, i.p.) significantly enhanced harmine- but not oxotremorine-induced tremors in mice. This potentiation became more apparent when cyclosporine (50 mg/kg, i.p.) was administered once a day for seven days. These findings suggest an involvement of monoaminergic mechanisms in cyclosporine-induced tremors. The effects of cyclosporine were examined on the dynamics of noradrenaline, dopamine and serotonin in the mouse brain. Both single and repeated treatment with cyclosporine significantly facilitated the serotonin turnover as estimated from the probenecid-induced accumulation of 5-hydroxyindoleacetic acid, but either mode of treatment failed to change the contents of monoamines and their metabolites or the turnover of noradrenaline and dopamine. Therefore, the cyclosporine-enhanced activity of serotonin neurons may be interpreted as producing adverse central effects, including tremors.


Respiration | 2007

Effects of Salmeterol in Patients with Persistent Asthma Receiving Inhaled Corticosteroid plus Theophylline

Hiromasa Inoue; Masashi Komori; Takafumi Matsumoto; Satoru Fukuyama; Mikiko Matsumura; Takako Nakano; Miyuki Tsuda; Koichiro Matsumoto; Akiko Kanaya; Atsushi Moriwaki; Hisamichi Aizawa; Makoto Yoshida; Yoichi Nakanishi

Background: Patients with severe asthma require multiple therapies to improve lung function and reduce symptoms. The use of long-acting inhaled β2-agonists plus theophylline in addition to high doses of inhaled corticosteroids (ICSs) for the treatment of severe asthma has not been extensively studied. Objective: The purpose of this study was to investigate the efficacy and safety of salmeterol combined with high-dose ICSs plus theophylline in severe asthma. Methods: We undertook a randomized, placebo-controlled, crossover study to compare the effect of a single dose of inhaled salmeterol (50 µg) or a placebo in patients with severe asthma whose conditions were not being adequately controlled by therapies with high-dose ICSs plus oral theophylline with or without leukotriene receptor antagonists. Results: Twenty patients took part in the trial. Compared with the placebo, the inhalation of salmeterol significantly increased the FEV1. Even in the 9 patients treated with high-dose ICSs plus theophylline plus a leukotriene receptor antagonist, the FEV1 increased significantly more after salmeterol than after the placebo. Conclusion: Patients with severe asthma receiving high-dose ICSs plus theophylline may benefit from the addition of salmeterol.


Journal of Pharmaceutical Health Care and Sciences | 2015

Relationship between incident types and impact on patients in drug name errors: a correlational study

Toshikazu Tsuji; Toshihiro Irisa; Shunichi Ohata; Chiyo Kokubu; Akiko Kanaya; Masanori Sueyasu; Nobuaki Egashira; Satohiro Masuda

BackgroundThere are many reports regarding various medical institutions’ attempts at incident prevention, but the relationship between incident types and impact on patients in drug name errors has not been studied. Therefore, we analyzed the relationship between them, while also assessing the relationship between preparation and inspection errors. Furthermore, the present study aimed to clarify the incident types that lead to severe patient damage.MethodsThe investigation object in this study was restricted to “drug name errors”, preparation and inspection errors in them were classified into three categories (similarity of drug efficacy, similarity of drug name, similarity of drug appearance) or two groups (drug efficacy similarity (+) group, drug efficacy similarity (−) group). Then, the relationship between preparation and inspection errors was investigated in three categories, the relationship between incident types and impact on patients was examined in two groups.ResultsThe frequency of preparation errors was liable to be caused by the following order: similarity of drug efficacy > similarity of drug name > similarity of drug appearance. In contrast, the rate of inspection errors was liable to be caused by the following order: similarity of drug efficacy < similarity of drug name < similarity of drug appearance. In addition, the number of preparation errors in the drug efficacy similarity (−) group was fewer than that in the drug efficacy similarity (+) group. However, the rate of inspection errors in the drug efficacy similarity (−) group was significantly higher than that in the drug efficacy similarity (+) group. Furthermore, the occupancy rate of preparation errors, incidents more than Level 0, 1, and 2 in the drug efficacy similarity (−) group increased gradually according to the rise of patient damage.ConclusionsOur results suggest that preparation errors caused by the similarity of drug appearance and/or drug name are likely to lead to the incidents (inspection errors), and these incidents are likely to cause severe damage to patients subsequently.


Journal of Pharmaceutical Health Care and Sciences | 2015

Differences in recognition of similar medication names between pharmacists and nurses: a retrospective study

Toshikazu Tsuji; Toshihiro Irisa; Shinji Tagawa; Takehiro Kawashiri; Hiroaki Ikesue; Chiyo Kokubu; Akiko Kanaya; Nobuaki Egashira; Satohiro Masuda

BackgroundDifferences in error rates between pharmacists and nurses in terms of drug confirmation have not been studied. The purpose of this study was to analyze differences in error rates between pharmacists and nurses from the viewpoint of error categories, and to clarify differences in recognition regarding drug name similarity.MethodsIn this study, preparation errors and incidents were classified into three categories (drug strength errors, drug name errors, and drug count errors) to investigate the influence of error categories on pharmacists and nurses. In addition, errors in two categories (drug strength errors and drug name errors) were reclassified into another two error groups, to investigate the influence of drug name similarity on pharmacists and nurses: a “drug name similarity (−) group” and a “drug name similarity (+) group”. Then, differences in error rates of pharmacists and those of nurses were analyzed respectively within three categories and two groups. Furthermore, differences in error rates between pharmacists and nurses were analyzed in each of the three categories and two groups.ResultsError rates of pharmacists for both drug strength errors and drug name errors were significantly higher than that for drug count errors, and similar results were obtained for nurses (P < 0.05). However, there were no significant differences in error rates between pharmacists and nurses in each of the three categories. Furthermore, error rate of nurses was significantly higher than that of pharmacists in the drug name similarity (+) group (P < 0.05), while there was no significant difference in error rates between pharmacists and nurses in the drug name similarity (−) group.ConclusionsThese results suggest that in contrast to pharmacists, nurses are easily affected by similarities in drug names. Therefore, pharmacists should offer information on medications having plural strengths or similar names to nurses, in order to minimize damage to patients resulting from errors.


Pulmonary Pharmacology & Therapeutics | 2013

Effects of tiotropium on lung function in severe asthmatics with or without emphysematous changes

Makoto Yoshida; Takako Nakano; Satoru Fukuyama; Takafumi Matsumoto; Miyuki Eguchi; Atsushi Moriwaki; Shohei Takata; Kentaro Machida; Akiko Kanaya; Koichiro Matsumoto; Yoichi Nakanishi; Hiromasa Inoue


Japanese Journal of Pharmaceutical Health Care and Sciences | 2013

Estimation of Risk Ratio in Classification of Dispensing Incident

Toshikazu Tsuji; Narumi Kakoki; Toshihiro Irisa; Chiyo Kokubu; Akiko Kanaya; Yoshihiro Hirakawa; Masanori Sueyasu; Makoto Kawashige; Nobuaki Egashira; Ryozo Oishi


Japanese Journal of Pharmaceutical Health Care and Sciences | 2006

Questionnaire Survey of Physicians to Assess Their Appreciation of Clinical Research and Evaluate CRC Practice in Kyushu University Hospital

Toshikazu Tsuji; Yoko Wakasugi; Akiko Kanaya; Masayo Yamasaki; Tomoko Nishida; Keiko Kikutake; Shuko Okumura; Yuko Tsutsumi; Mieko Inada; Seiichi Yamada; Naoka Kojo; Kanae Hamada; Manabu Yoshikawa; Yoichi Nakanishi; Ryozo Oishi


Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan | 2016

The relationship between occurrence timing of dispensing errors and subsequent danger to patients under the situation according to the classification of drugs by efficacy

Toshikazu Tsuji; Kenichiro Nagata; Takehiro Kawashiri; Takaaki Yamada; Toshihiro Irisa; Yuko Murakami; Akiko Kanaya; Nobuaki Egashira; Satohiro Masuda


Japanese Journal of Pharmaceutical Health Care and Sciences | 2016

Development and Utility Evaluation of a Compatibility Chart of Injections Commonly Used in the Intensive Care Unit

Shigeru Ishida; Maki Takeda; Rie Ogawa; Takafumi Nakashima; Hiroaki Ikesue; Hiroyuki Watanabe; Akiko Kanaya; Nobuaki Egashira; Satohiro Masuda


Respiration | 2007

Contents Vol. 74, 2007

Emmanuel Weitzenblum; Leandro G. Fritscher; Simone Canani; Cláudio C. Mottin; Carlos C. Fritscher; Diovane Berleze; Kenneth R. Chapman; José M. Chatkin; Romain Kessler; Min Xie; Xian-Sheng Liu; Matthieu Canuet; Koichiro Matsumoto; Akiko Kanaya; Atsushi Moriwaki; Hisamichi Aizawa; Makoto Yoshida; Yoichi Nakanishi; Ignacio Aranda; Santiago Romero; I. Mayeux; V. Jounieaux; Anne-Cécile Métivier; Encarnacion Barroso; Luis Hernandez; Joan Gil; Raquel Garcia; Jens Schreiber; Christel Schreiber; Tiberiu Shulimzon

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