Updated on 2025/12/11

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写真a

 
Kenichi Masui
 
Organization
Graduate School of Medicine Department of Medicine Anesthesiology Associate Professor
School of Medicine Medical Course
Title
Associate Professor
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Degree

  • 博士(医学) ( 山梨大学 )

Research Interests

  • pharmacodynamics

  • anesthetic pharmacology

  • pharmacokinetics

  • pharmacometrics

  • computer simulation

  • 筋弛緩薬

  • collagen disease

  • opioid

  • intravenous anesthetics

Research Areas

  • Life Science / Anesthesiology

  • Life Science / Clinical pharmacy

Education

  • Yamanashi Medical University

    1991 - 1997

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    Country: Japan

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Research History

  • Yokohama City University   Associate Professor

    2022

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  • Yokohama City University

    2021 - 2022

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  • Showa University   Lecturer

    2017 - 2021

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  • 防衛医科大学校   麻酔学講座   講師

    2010 - 2017

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  • 防衛医科大学校   麻酔学講座   助教

    2007 - 2010

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  • ゲント大学(ベルギー)   麻酔科学講座   研究員

    2007 - 2008

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  • 防衛医科大学校   麻酔学講座   助手

    2005 - 2007

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  • 諏訪中央病院   麻酔科   医長

    2004 - 2005

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  • Yamanashi Medical University   Research Associate

    2002 - 2004

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  • 諏訪中央病院   麻酔科   医師

    2000 - 2002

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  • Yamanashi Medical University   Research Associate

    1997 - 2000

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Professional Memberships

  • Japanese Society of Pediatric Anesthesiology

    2022.9

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  • American Socciety of Anesthesiologists

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  • THE JAPAN SOCIETY FOR CLINICAL ANESTHESIA

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  • 日本静脈麻酔学会

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  • 日本麻酔集中治療テクノロジー学会

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  • 日本麻酔科学会

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Committee Memberships

  • International Society of Anesthetic Pharmacology   Director  

    2025.10   

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  • 日本神経麻酔集中治療学会   評議員  

    2025.7   

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  • World Society of Intravenous Anaesthesia   Director  

    2025.4   

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  • 日本麻酔・集中治療テクノロジー学会   選任理事  

    2024.10   

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  •   日本麻酔科学会, 事務局委員  

    2024.7 - 2025.6   

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  • 日本小児麻酔学会   臨床研究推進委員会 委員  

    2023.10   

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  • 日本麻酔科学会   代議員  

    2023.6   

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  •   Scientific Reports, Editorial Board  

    2022.11 - 2024.3   

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  • JA Clinical Report   Section Editor  

    2021.3   

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    Committee type:Academic society

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  • 日本静脈麻酔学会   理事  

    2019.11   

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  • 日本麻酔科学会   学術研究審査委員会  

    2017.6 - 2023.6   

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  • 日本麻酔科学会   学術委員会  

    2017.6 - 2021.6   

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    Committee type:Academic society

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  • Journal of Anesthesia   Section Editor  

    2017.3   

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    Committee type:Academic society

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  • British Journal of Anaesthesia   Associate Editorial Board  

    2012.2 - 2020.9   

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  • 日本麻酔集中治療テクノロジー学会   評議員  

    2006.12   

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  • 日本静脈麻酔学会   評議員  

    2005.12 - 2019.11   

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Papers

  • Anesthetic induction drugs during tracheal intubation in critically ill patients: a systematic review Reviewed

    Tomoaki Yatabe, Kenichi Masui, Tomonori Takazawa, Moritoki Egi

    Journal of Anesthesia   2025.12

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    Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.1007/s00540-025-03636-1

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    Other Link: https://link.springer.com/article/10.1007/s00540-025-03636-1/fulltext.html

  • Clinical characteristics, management strategies, and outcomes in patients with preoperative venous thromboembolism who underwent surgery: survey data from 2020 to 2022 by the Japanese Society of Anesthesiologists Reviewed

    Chikashi Takeda, Yugo Yamashita, Kenichi Masui, Motoi Sugimura, Satoru Fujita, Manabu Kakinohana, Takashi Kita, Mitsutaka Edanaga, Tetsufumi Sato, Naoyuki Fujimura, Naoto Yamamoto, Masataka Ikeda, Ryuji Kawaguchi, Reiko Neki

    Journal of Anesthesia   2025.12

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    Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.1007/s00540-025-03635-2

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    Other Link: https://link.springer.com/article/10.1007/s00540-025-03635-2/fulltext.html

  • General anesthesia/general anesthetics: Journal of Anesthesia symposium 2025. Reviewed

    Kenichi Masui, Kotoe Kamata, Ayako Tojo, Michiyoshi Sanuki, Yoshiki Nakajima, Shuya Kiyama

    Journal of anesthesia   2025.10

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    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    Key interventions for anesthesia patients include administering drugs, infusing fluids and blood, and providing artificial ventilation. As general anesthetics are always administered to patients undergoing general anesthesia, anesthetists need to be familiar with the fundamentals and the latest issues of general anesthesia/anesthetics. The Journal of Anesthesia symposium 2025 aimed to discuss fundamental topics and environmental issues related to general anesthesia and anesthetics. In this symposium, we had following topics: (1) patient outcomes of general anesthesia observed outside the operating room after the surgery, (2) updated information on the benefits and limitations of intravenous and inhalational anesthesia, (3) the environmental impact and recommended actions, and (4) potential reasons for not selecting intravenous anesthesia despite its apparent benefits for anesthetized patients.

    DOI: 10.1007/s00540-025-03591-x

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  • Appropriate use of a pharmacokinetic model for remimazolam target-controlled infusion. Reviewed International journal

    Kenichi Masui

    European journal of anaesthesiology   42 ( 8 )   758 - 760   2025.8

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    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1097/EJA.0000000000002178

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  • Umbilical analgesic concentrations after labour analgesia with programmed intermittent epidural bolus: a prospective observational study. Reviewed International journal

    Arisa Ijuin, Masaki Sato, Nagayoshi Umehara, Shoichiro Amari, Jumpei Saito, Mayuko Abe, Wataru Matsunaga, Yoko Yamashita, Yasuyuki Suzuki, Kenichi Masui

    Canadian journal of anaesthesia = Journal canadien d'anesthesie   2025.6

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    Authorship:Lead author, Last author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    PURPOSE: The umbilical analgesic concentrations after using programmed intermittent epidural bolus (PIEB) and patient-controlled epidural analgesia (PCEA) without continuous infusion are unknown. We aimed to characterize umbilical ropivacaine and fentanyl concentrations and examine their influence on neonatal conditions at delivery. METHODS: We prospectively studied 50 parturients with singleton pregnancies who received combined spinal-epidural analgesia using PIEB (7 mL every 45 min) and PCEA (7 mL per bolus; lockout interval: 15 min) with 0.08% ropivacaine and 2 μg·mL-1 fentanyl, with clinician-administered boluses as necessary. We evaluated the umbilical venous analgesic concentrations and neonatal characteristics. RESULTS: The median [interquartile range (IQR)] hourly ropivacaine and fentanyl doses were 13 [11-15] mg·hr-1 and 39 [30-50] µg·hr-1, respectively. The ropivacaine and fentanyl concentrations were 77 [56-98] ng·mL-1 and 0.125 [0.125-0.20] ng·mL-1 at delivery, respectively. The umbilical analgesic concentrations were correlated with the labour duration and total dose. In parturients given clinician-administered boluses within 1 hr before delivery, the ropivacaine and fentanyl concentrations were similar to those without (81 [54-104] vs 77 [54-96] ng·mL-1 and 0.20 [0.125-0.20] vs 0.125 [0.05-0.20] ng·mL-1, respectively). The umbilical arterial pH was > 7.2 and the Apgar score at 5 min was ≥ 8 for all neonates. No neonates exhibited systemic local anesthetic toxicity. Respiratory support was required for 14 neonates. CONCLUSIONS: Umbilical analgesic concentrations at delivery were low after labour analgesia using a regimen of PIEB with PCEA for up to 19 hr. An intermittent bolus dosing regimen may contribute to a decrease in umbilical analgesic concentrations.

    DOI: 10.1007/s12630-025-02975-7

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  • Remimazolam anesthesia in pediatric patients undergoing cardiac catheterization for congenital heart disease: a retrospective observational study. Reviewed

    Maiko Hosokawa, Yurie Takahashi, Takahiro Ueno, Katsunori Oe, Kenichi Masui

    Journal of anesthesia   2024.8

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    BACKGROUND: Benzodiazepines are used in pediatric patients with congenital heart disease (CHD) because of their mild hemodynamic depressant effects. A novel short-acting benzodiazepine, remimazolam, is expected to be suitable for these patients. We examined the characteristics of remimazolam anesthesia in pediatric patients with CHD undergoing cardiac catheterization. METHODS: This single-center retrospective study included pediatric patients undergoing cardiac catheterization for CHD. The primary outcome was the remimazolam dose for loss of consciousness. Secondary outcomes included the mean maintenance remimazolam dose, recovery time from anesthesia, predicted remimazolam concentration at emergence, decrease in blood pressure and heart rate, vasopressor administration during anesthesia, electroencephalogram index (bispectral index: BIS or patient state index: PSI), and life-threatening adverse events. RESULTS: Thirty-nine patients, aged 2 months to 16 years, were included. Thirty-three patients received a median [interquartile] midazolam dose of 0.10 [0.10-0.10] mg.kg-1 in the pre-anesthesia room. The remimazolam dose for loss of consciousness was 0.34 [0.26-0.45] mg.kg-1. The mean maintenance dose was 1.0 [0.8-1.4] mg.kg-1.h-1. The recovery time was 15 [12-17] min. The predicted remimazolam concentration at emergence was 0.4-1.2 µg.ml-1 in 3-6-year-old patients. Blood pressure and heart rate decreased by 30% in 15 and 6 patients, respectively. Vasopressors were administered as a bolus in 8 patients. The BIS or PSI did not fall ≤ 60 or ≤ 50, respectively, in 51% of patients before tracheal intubation. No life-threatening adverse events were reported. CONCLUSIONS: Remimazolam is a good alternative anesthetic agent for pediatric patients undergoing cardiac catheterization for CHD.

    DOI: 10.1007/s00540-024-03395-5

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  • Remimazolam: its clinical pharmacology and evolving role in anesthesia and sedation practice. Invited Reviewed International journal

    Kenichi Masui

    Current opinion in anaesthesiology   37 ( 4 )   344 - 351   2024.8

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    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Ovid Technologies (Wolters Kluwer Health)  

    Purpose of review

    Remimazolam is a novel benzodiazepine anesthetic/sedative, designed as a rapidly metabolized carboxylic acid. Since its recent launch, the role of remimazolam in modern anesthesia and sedation practice is still evolving. This review aims to outline the clinical pharmacology and clinical utility of remimazolam to elucidate its potential advantages and limitations.

    Recent findings

    Remimazolam is “short-acting” but not ultra-short-acting compared with propofol based on context-sensitive decrement times. But compared to propofol, the availability of the benzodiazepine antagonist, flumazenil, is considered an advantage, particularly in certain emergency situations such as in patients with difficult airways. However, because flumazenil is shorter acting than remimazolam when remimazolam accumulates or is present in a high concentration, the reappearance of remimazolam sedation may occur after the initial reversal of anesthesia/sedation from flumazenil administration. Although it is beneficial that remimazolam causes less respiratory depression and hypotension than propofol, serious respiratory depression and hypotension can still occur. Remimazolam administration causes minimal or no pain on injection. Remimazolam is associated with less postoperative nausea and vomiting than inhaled anesthetics, but propofol is clearly superior in this regard. The anesthetic/sedative effects may be prolonged by severe hepatic impairment; remimazolam tolerance can occur in long-term benzodiazepine users.

    Summary

    Remimazolam may be beneficial to use in procedural sedation and general anesthesia for patients with difficult airways or hemodynamic instability. Further clinical studies with remimazolam are warranted to identify the potential benefits in other settings and patient populations.

    DOI: 10.1097/ACO.0000000000001384

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  • Hypotension after general anaesthesia induction using remimazolam or propofol in geriatric patients undergoing sevoflurane anaesthesia with remifentanil: a single-centre, double-blind, randomised controlled trial. Reviewed International journal

    Ryuki Takaki, Masashi Yokose, Takahiro Mihara, Yusuke Saigusa, Hiroyuki Tanaka, Natsuhiro Yamamoto, Kenichi Masui, Takahisa Goto

    British journal of anaesthesia   133 ( 1 )   24 - 32   2024.7

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    BACKGROUND: The occurrence of hypotension after induction of general anaesthesia is common in geriatric patients, and should be prevented to minimise perioperative complications. Compared with propofol, remimazolam potentially has a lower incidence of hypotension. This study aimed to compare the incidence of hypotension after general anaesthesia induction with remimazolam or propofol in geriatric patients. METHODS: This single-centre, double-blind, randomised trial enrolled 90 patients aged ≥80 yr who received general anaesthesia for scheduled surgery. Patients were randomised to receive remimazolam (12 mg kg-1 h-1) or propofol (0.025 mg kg-1 s-1) for anaesthesia induction, with remifentanil and sevoflurane. The presence or absence of hypertension on the ward served as the stratification factor. The incidence of hypotension after the induction of general anaesthesia, defined as a noninvasive mean arterial pressure of <65 mm Hg measured every minute from initiation of drug administration to 3 min after tracheal intubation, was the primary outcome. Subgroup analysis was performed for the primary outcome using preoperative ward hypertension, clinical frailty scale, Charlson Comorbidity Index, and age. RESULTS: Three subjects were excluded before drug administration, and 87 subjects were included in the analysis. The incidence of hypotension was 72.1% (31/43) and 72.7% (32/44) with remimazolam or propofol, respectively. No statistically significant differences (adjusted odds ratio, 0.96; 95% confidence interval, 0.37-2.46; P=0.93) were observed between groups. Subgroup analysis revealed no significant differences between groups. CONCLUSIONS: Compared with propofol, remimazolam did not reduce the incidence of hypotension after general anaesthesia induction in patients aged ≥80 yr. CLINICAL TRIAL REGISTRATION: UMIN000042587.

    DOI: 10.1016/j.bja.2024.04.013

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  • What are standard monitoring devices for anesthesia in future? Reviewed

    Shinju Obara, Naoyuki Hirata, Satoshi Hagihira, Keisuke Yoshida, Yoshifumi Kotake, Shunichi Takagi, Kenichi Masui

    Journal of anesthesia   2024.5

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    Monitoring the patient's physiological functions is critical in clinical anesthesia. The latest version of the Japanese Society of Anesthesiologists' Guidelines for Safe Anesthesia Monitoring, revised in 2019, covers various factors, including electroencephalogram monitoring, oxygenation, ventilation, circulation, and muscle relaxation. However, with recent advances in monitoring technologies, the information provided has become more detailed, requiring practitioners to update their knowledge. At a symposium organized by the Journal of Anesthesia in 2023, experts across five fields discussed their respective topics: anesthesiologists need to interpret not only the values displayed on processed electroencephalogram monitors but also raw electroencephalogram data in the foreseeable future. In addition to the traditional concern of preventing hypoxemia, monitoring for potential hyperoxemia and the effects of mechanical ventilation itself will become increasingly important. The importance of using AI analytics to predict hypotension, assess nociception, and evaluate microcirculation may increase. With the recent increase in the availability of neuromuscular monitoring devices in Japan, it is important for anesthesiologists to become thoroughly familiar with the features of each device to ensure its effective use. There is a growing desire to develop and introduce a well-organized, integrated "single screen" monitor.

    DOI: 10.1007/s00540-024-03347-z

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  • Anesthesia management for thoracoscopic resection of a huge intrathoracic meningocele: a case report. Reviewed International journal

    Ryosuke Nakazawa, Kenichi Masui, Takahisa Goto

    JA clinical reports   10 ( 1 )   14 - 14   2024.2

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    BACKGROUND: Diagnosed intrathoracic meningocele is an uncommon complication of neurofibromatosis type 1. We report an anesthesia management for a rare case undergoing thoracoscopic resection of a huge intrathoracic meningocele. CASE PRESENTATION: A 51-year-old woman was scheduled for thoracoscopic meningectomy under general anesthesia. We monitored intrathecal pressure during anesthesia to prevent a decrease in intrathecal pressure. During surgery, the intrathecal pressure occasionally increased by around 5 cmH2O immediately after the insertion of the drainage tube and occasionally decreased by up to 10 cmH2O during the careful slow aspiration of the cerebrospinal fluid (CSF). The pressure rapidly recovered after the interruption of the procedures. She was discharged on postoperative day 4 without major complications. CONCLUSIONS: The CSF pressure was fluctuated by procedures during thoracoscopic resection of a huge meningocele. A CSF pressure monitoring was useful to detect the sudden change of CSF pressure immediately, which can cause intracranial hemorrhage.

    DOI: 10.1186/s40981-024-00697-1

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  • Monitored Anesthesia Care Under a Combination of Low-Dose Remimazolam Infusion and Flumazenil Antagonism: A Case Report

    Kotoe Kamata, Kenichi Masui

    Cureus   2023.10

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    Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.7759/cureus.46728

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  • Reply to "Re-sedation after a large dose of flumazenil". Reviewed

    Kenichi Masui

    Journal of anesthesia   37 ( 1 )   162 - 163   2023.2

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    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.1007/s00540-022-03123-x

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    Other Link: https://link.springer.com/article/10.1007/s00540-022-03123-x/fulltext.html

  • Equilibration rate constant, ke0, to determine effect-site concentration for the Masui remimazolam population pharmacokinetic model in general anesthesia patients. Reviewed

    Kenichi Masui, Satoshi Hagihira

    Journal of anesthesia   36 ( 6 )   757 - 762   2022.12

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    Effect-site concentration is widely used to determine drug dosage in anesthesia practice. To obtain effect-site concentration, a pharmacokinetic model with a corresponding equilibration rate constant between plasma and effect-site, ke0, is necessary. Remimazolam, a novel short-acting benzodiazepine, has been approved as anesthetic/sedative. Recently, a remimazolam pharmacokinetic model has been published using a large dataset including wide range of subject characteristics (416 males and 246 females, age 18-93 years, total body weight 34-149 kg, height 133-204 cm, body mass index 14-61 kg m-2, ASA physical status: I-IV, and Asian, White, American African, and 2 other races). This Masui model can be applicable to various patients, but a pharmacodynamic model including ke0 was not developed simultaneously. A previous article has indicated that the time to peak effect of drug after its bolus should be used to determine ke0 for a pharmacokinetic model without simultaneous development of corresponding pharmacodynamic model. The ke0 value can be calculated using numerical analysis but not algebraic solution. We provide the detail method of the numerical analysis and a tool to have ke0 value easily for the Masui remimazolam PK model. Additionally, we provide a multiple regression model to have ke0 value for the PK model.

    DOI: 10.1007/s00540-022-03099-8

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  • Caution!! Reappearance of remimazolam effect after a flumazenil bolus: a larger bolus of flumazenil and a lower total remimazolam clearance are higher risks. Reviewed

    Kenichi Masui

    Journal of anesthesia   2022.9

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    DOI: 10.1007/s00540-022-03107-x

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  • Hypotension after general anesthesia induction using remimazolam in geriatric patients: Protocol for a double-blind randomized controlled trial. Reviewed International journal

    Masashi Yokose, Ryuki Takaki, Takahiro Mihara, Yusuke Saigusa, Natsuhiro Yamamoto, Kenichi Masui, Takahisa Goto

    PloS one   17 ( 9 )   e0275451   2022.9

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    INTRODUCTION: In geriatric patients, hypotension is often reported after general anesthesia induction using propofol. Remimazolam is a novel short-acting sedative. However, the incidence of hypotension after general anesthesia induction using remimazolam in geriatric patients remains unclear. This study aims to compare the incidence of hypotension associated with remimazolam and propofol in patients aged ≥80 years. METHODS: This single-center, double-blind, randomized, two-arm parallel group, standard treatment-controlled, interventional clinical trial will include 90 patients aged ≥80 years undergoing elective surgery under general anesthesia who will be randomized to receive remimazolam or propofol for induction. The primary outcome is the incidence of hypotension after general anesthesia induction, occurring between the start of drug administration and 3 min after intubation. We define hypotension as mean blood pressure <65 mmHg. The primary outcome will be analyzed using the full analysis set. The incidence of hypotension in the two groups will be compared using the Mantel-Haenszel χ2 test. Subgroup analysis of the primary outcome will be performed based on the Charlson comorbidity index, clinical frailty scale, hypertension in the ward, and age. Secondary outcomes will be analyzed using the Fisher's exact test, Student's t test, and Mann-Whitney U test, as appropriate. Logistic regression analysis will be performed to explore the factors associated with the incidence of hypotension after anesthesia induction. DISCUSSION: Our trial will determine the efficacy of remimazolam in preventing hypotension and provide evidence on the usefulness of remimazolam for ensuring hemodynamic stability during general anesthesia induction in geriatric patients. TRIAL REGISTRATION: The study has been registered with UMIN Clinical Trials Registry (UMIN000042587), on June 30, 2021.

    DOI: 10.1371/journal.pone.0275451

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  • A population pharmacokinetic model of remimazolam for general anesthesia and consideration of remimazolam dose in clinical practice. Reviewed

    Kenichi Masui, Thomas Stöhr, Marija Pesic, Tomohiro Tonai

    Journal of anesthesia   2022.6

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    BACKGROUND: Remimazolam besylate is a novel short-acting benzodiazepine. An appropriate pharmacokinetic model of remimazolam is desirable in anesthesia practice. The aim of the study was to develop a pharmacokinetic model using plasma samples from patients anesthetized with remimazolam. Influence of patient characteristics, context-sensitive decrement-times, and dose regimens were also examined. METHODS: Data were obtained from four trials on patients, and seven trials on healthy volunteers. The characteristics of 416 male and 246 female subjects were as follows: age, 18-93 years; body weight, 34-149 kg; and American Society of Anesthesiologists physical status (ASA-PS), I-IV. 2231 arterial and 3200 venous samples were used for the final model. The equilibration rate constant between arterial plasma and effect-site was estimated using the concept of time to peak effect. The final model was used to generate context-sensitive decrement times and dose regimens for general anesthesia. RESULTS: A three-compartment model plus virtual venous compartment with allometric scaling of adjusted body weight (ABW), age, sex, and ASA-PS as covariates were selected as the final model. Elimination clearance was lower in males, and in subjects with higher ABW and ASA-PS scores. Approximately 10% or 20% higher dose rate was necessary in females than in males or ASA-PS I/II than III/IV patient. The context-sensitive half-time for effect-site concentration in a 55-year-old, 70-kg, 170-cm male or female ASA-PS I/II patient after > 6-h infusion was 16.7 or 15.9 min. CONCLUSION: Remimazolam pharmacokinetic model for general anesthesia was successfully developed. ABW, ASA-PS, and sex has a considerable impact on the remimazolam concentration.

    DOI: 10.1007/s00540-022-03079-y

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  • Mortality Risk Stratification Using Cluster Analysis in Patients With Myositis-Associated Interstitial Lung Disease Receiving Initial Triple-Combination Therapy Reviewed International journal

    Takahisa Gono, Kenichi Masui, Shinji Sato, Masataka Kuwana

    Frontiers in Medicine   9   883699 - 883699   2022.5

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Frontiers Media SA  

    Objective

    To stratify patients with polymyositis/dermatomyositis-associated interstitial lung disease (ILD) who were initially treated with an intensive regimen consisting of high-dose corticosteroids, a calcineurin inhibitor, and intravenous cyclophosphamide (triple-combo therapy) into subgroups based on mortality outcomes by a cluster analysis using a large-scale multicenter retrospective cohort of Japanese patients with myositis-associated ILD (JAMI).

    Methods

    Two-step cluster analysis of preclustering and subsequent hierarchical clustering was conducted in 185 patients who received triple-combo therapy in an unbiased manner. Initial predictors for mortality previously reported in patients with myositis-associated ILD were used as variables and included age, sex, disease duration, classification of myositis, requirement of supplemental oxygen, anti-aminoacyl tRNA synthetase (ARS) antibody, anti-melanoma differentiation-associated gene 5 (MDA5) antibody, and serum levels of C-reactive protein (CRP) and Krebs von den Lungen-6 (KL-6). The cluster model was further applied to 283 patients who received conventional regimens consisting of corticosteroids with or without a single immunosuppressive agent (dual-combo therapy or monotherapy). Cumulative survival rates were compared using Kaplan-Meier analysis, and the log-rank test was used to test for significant differences between two groups.

    Results

    We developed a cluster model consisting of 6 clusters, which were categorized by age at onset, clinically amyopathic dermatomyositis, CRP, KL-6, requirement of supplemental oxygen, anti-ARS antibody, and anti-MDA5 antibody. This model was judged to be of good quality based on the silhouette measure of cohesion and separation of 0.6. These clusters were regrouped into three subsets based on low (&amp;lt;10%), moderate (10-50%), and high (&amp;gt;50%) mortality rates. The performance of the clustering was generally replicated in patients who received initial dual-combo therapy or monotherapy. Survival benefits of triple-combo therapy over dual-combo therapy or monotherapy were not observed in any of the clusters.

    Conclusion

    We successfully developed a cluster model that stratified patients with myositis-associated ILD who were treated with initial triple-combo therapy into subgroups with different prognoses, although this model failed to identify a patient subgroup that showed survival benefits from triple-combo therapy over dual-combo therapy or monotherapy.

    DOI: 10.3389/fmed.2022.883699

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  • Lateral position for difficult intubation in a patient with history of hemiglossectomy and flap reconstruction: a case report. Reviewed International journal

    Fumiko Yokogawa, Katsunori Oe, Maiko Hosokawa, Kenichi Masui

    JA clinical reports   8 ( 1 )   16 - 16   2022.3

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    BACKGROUND: Reconstructive head and neck surgery can alter upper airway anatomy. We report a difficult intubation in a patient with a history of hemiglossectomy and reconstruction. CASE PRESENTATION: A 65-year-old female patient, who had undergone hemiglossectomy with the flap reconstruction, underwent video-assisted thoracoscopic esophagectomy for esophageal cancer. After the loss of consciousness during anesthesia induction, we failed to perform direct and oral fiberoptic intubation using a video laryngoscope and nasal fiberoptic intubation without or with video laryngoscope assistance in the supine position. Finally, shifting the patient to the left-lateral position allowed successful nasal fiberoptic intubation. Postoperatively, we were informed that she was unable to sleep in the supine position because of airway obstruction and therefore always slept on her side. CONCLUSION: Preanesthetic evaluation of the influence of body position on the airway patency during sleep or sedation may aid in airway management.

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  • Remimazolam Tolerance in Long-term Benzodiazepine Users: A Case Report of 2 Cases. Reviewed International journal

    Haruka Yoshikawa, Maiko Hosokawa, Yuki Kashima, Sayaka Oki, Kenichi Masui

    A&A practice   15 ( 5 )   e01460   2021.5

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    A 60-year-old woman with a 5-year history of anxiolytic use, a diazepam-equivalent daily dose of 15 mg, was scheduled for esophageal stent removal. She was given remimazolam (0.5 mg/kg) but remained fully alert. She only lost consciousness with propofol (40 mg). A 61-year-old man with a 1-year history of anxiolytic use, diazepam-equivalent daily dose of 20 mg, was scheduled for hand tumor resection. He was given remimazolam (0.3 mg/kg) but remained fully alert. He only lost consciousness after desflurane inhalation. In a patient with a history of long-term benzodiazepine use, anesthetic or sedative agents aside from remimazolam should be considered.

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  • Propofol infusions using a human target controlled infusion (TCI) pump in chimpanzees (Pan troglodytes). Reviewed International journal

    T Miyabe-Nishiwaki, A Kaneko, A Yamanaka, N Maeda, J Suzuki, M Tomonaga, T Matsuzawa, K Muta, R Nishimura, I Yajima, D J Eleveld, A R Absalom, K Masui

    Scientific reports   11 ( 1 )   1214 - 1214   2021.1

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    Chimpanzees are genetically and physiologically similar to humans. Several pharmacokinetic models of propofol are available and target controlled infusion (TCI) of propofol is established in humans, but not in chimpanzees. The purpose of this study was to investigate if human pharmacokinetic models can accurately predict propofol plasma concentration (Cp) in chimpanzees and if it is feasible to perform TCI in chimpanzees. Ten chimpanzees were anaesthetized for regular veterinary examinations. Propofol was used as an induction or maintenance agent. Blood samples were collected from a catheter in a cephalic vein at 3-7 time points between 1 and 100 min following the propofol bolus and/or infusion in five chimpanzees, or TCI in six chimpanzees. Cp was measured using high-performance liquid chromatography. The Marsh, Schnider and Eleveld human pharmacokinetic models were used to predict Cp for each case and we examined the predictive performances of these models using the Varvel criteria Median PE and Median APE. Median PE and Median APE for Marsh, Schnider and Eleveld models were within or close to the acceptable range. A human TCI pump was successfully maintained propofol Cp during general anesthesia in six chimpanzees. Human propofol pharmacokinetic models and TCI pumps can be applied in chimpanzees.

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  • Pharmacokinetics and effects on clinical and physiological parameters following a single bolus dose of propofol in common marmosets (Callithrix jacchus). Reviewed International journal

    Kanako Muta, Takako Miyabe-Nishiwaki, Kenichi Masui, Isao Yajima, Tomoya Iizuka, Akihisa Kaneko, Ryohei Nishimura

    Journal of veterinary pharmacology and therapeutics   44 ( 1 )   18 - 27   2021.1

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    The objectives of this study were (a) to establish a population pharmacokinetic model and (b) to investigate the clinical and physiological effects of a single bolus dose of propofol in common marmosets. In Study 1, pharmacokinetic analysis was performed in six marmosets under sevoflurane anaesthesia. 8 mg/kg of propofol was administrated at a rate of 4 mg kg-1  min-1 . Blood samples were collected 2, 5, 15, 30, 60, 90, 120 or 180 min after starting propofol administration. Plasma concentration was measured, and population pharmacokinetic modelling was performed. A two-compartment model was selected as the final model. The population pharmacokinetic parameters were as follows: V1  = 1.14 L, V2  = 77.6 L, CL1  = 0.00182 L/min, CL2  = 0.0461 L/min. In Study 2, clinical and physiological parameters were assessed and recorded every 2 min after 12 mg/kg of propofol was administrated at a rate of 4 mg kg-1  min-1 . Immobilization was sustained for 5 min following propofol administration without apparent bradycardia. While combination of propofol and sevoflurane caused apnoea in Study 1, apnoea was not observed following single administration of propofol in Study 2. These data provide bases for further investigation on intravenous anaesthesia using propofol in common marmosets.

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  • Interpretation of laboratory tests for prevention of the SARS-CoV-2 transmission. Reviewed

    Kenichi Masui

    Journal of anesthesia   2020.11

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    With the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), medical providers should take care to prevent the transmission of SARS-CoV-2 in hospitals including super-spreading. Understanding super-spreading would be useful to reduce future transmission. Some publications have shown clusters of SARS-CoV-2 such as at choir practice and in hospitals. Aerosol can be considered as a primary transmission route. As SARS-CoV-2 stability in aerosol is similar to SARS-CoV-1 with the higher reproductive number of SARS-CoV-2 than SARS-CoV-1, another factor causes rapidly spread-out, e.g. a higher discharge ratio from infected people or a higher viral intake ratio to human body. A basic research suggests higher infectivity of SARS-CoV-2 in the nose than the peripheral lung. Universal masking would be important to prevent the exposure of SARS-CoV-2 droplet to uninfected people. To detect SARS-CoV-2 infection, laboratory tests such as reverse transcription polymerase chain reaction and enzyme-linked immunosorbent assays are applied. Although sensitivity and specificity are provided for the ability of the test, positive or negative prediction values are useful to indicate the possiblity of infection or non-infection in clinical practice. We have to realize that the positive and negative prediction values depend on the sensitivity, specificity, and infection probability of the patient.

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  • Risk prediction modeling based on a combination of initial serum biomarkers in myositis-associated interstitial lung disease. Reviewed International journal

    Takahisa Gono, Kenichi Masui, Naoshi Nishina, Yasushi Kawaguchi, Atsushi Kawakami, Kei Ikeda, Yohei Kirino, Yumiko Sugiyama, Yoshinori Tanino, Takahiro Nunokawa, Yuko Kaneko, Shinji Sato, Katsuaki Asakawa, Taro Ukichi, Shinjiro Kaieda, Taio Naniwa, Yutaka Okano, Masataka Kuwana

    Arthritis & rheumatology (Hoboken, N.J.)   73 ( 4 )   677 - 686   2020.10

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    OBJECTIVE: To establish predictive models for mortality in patients with polymyositis/dermatomyositis (PM/DM)-associated interstitial lung disease (ILD) using a combination of initial serum biomarkers. METHODS: A multicenter JAMI cohort database of 497 incident cases of PM/DM-ILD was used as a derivation cohort, and 111 cases were additionally collected as a validation cohort. Risks for predicting all-cause mortality were identified by univariate and multivariable Cox regression analyses using candidate serum biomarkers as explanatory variables. The predictive models for mortality were generated in patients with and without anti-melanoma differentiation-associated gene 5 (MDA5) antibody, using a combination of risk factors. Cumulative survival rates were assessed using Kaplan-Meier analysis, and were compared between the subgroups with Breslow test. RESULTS: In a derivation cohort, C-reactive protein (CRP) and Krebs von den Lungen-6 (KL-6) were identified as independent risk factors for mortality in both anti-MDA5-positive and negative patients. We then developed a prediction model termed MCK (MDA5, CRP, and KL-6) model, identifying patients at low (<15%), moderate (15-50%), or high risk (≥50%) of mortality, based on the number of risk factors. The MCK model successfully differentiated cumulative survival rates in anti-MDA5-positive patients (P < 0.01 between low and moderate risk and P = 0.03 between moderate and high risk) and in anti-MDA5-negative patients (P < 0.001 between low and moderate risk). Utility of the MCK model was replicated in the validation cohort. CONCLUSION: The evidence-based risk prediction model using CRP and KL-6 combined with anti-MDA5 antibody might be useful for predicting prognosis in patients with PM/DM-ILD.

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  • Propofol suppresses the His-ventricular conduction in paediatric patients. Reviewed International journal

    Mayuka Matsushima, Seishi Kimura, Atsuhiro Kitaura, Shinichi Hamasaki, Tatsushige Iwamoto, Takashi Mino, Kenichi Masui, Shinichi Nakao

    Journal of clinical pharmacy and therapeutics   46 ( 2 )   433 - 439   2020.10

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    WHAT IS KNOWN AND OBJECTIVE: Propofol is the most commonly used intravenous anaesthetic worldwide and is considered to be safe for all ages. However, there have been some reports that propofol induces severe atrioventricular (AV) blocks in humans and some studies demonstrated that propofol suppressed the cardiac conduction system in animals. A precise mechanism by which the block is induced has not been elucidated yet in humans. The objective of this study was to investigate the effects of propofol on the cardiac conduction system and the cardiac autonomic nervous balance in children. METHODS: We enrolled 23 paediatric patients (age: 6-15 years; males: 16, females: 7) who were scheduled to undergo radiofrequency catheter ablation (RFCA) under general anaesthesia. Anaesthesia was induced with 2 mg/kg propofol and 0.5 µg/kg/min remifentanil, and tracheal intubation was performed with the aid of 1 mg/kg rocuronium. Anaesthesia was maintained with 5-7 mg/kg/h propofol and 0.2 µg/kg/min remifentanil during the RFCA. After the completion of the RFCA, anaesthesia was further maintained with 5 mg/kg/h propofol and 0.2 µg/kg/min remifentanil for at least 10 min (LC: low propofol concentration state), followed by the injection of 2 mg/kg propofol and the infusion of 10 mg/kg/h propofol for 10 min (HC: high propofol concentration state). The sinus node recovery time (SNRT), sinoatrial conduction time (SACT), atrial-His (AH) interval and the His-ventricular (HV) interval were measured at the end of both the LC and HC. Cardiac autonomic regulation was simultaneously assessed based on heart rate variability. RESULTS AND DISCUSSION: Propofol significantly suppressed intrinsic cardiac HV conduction, but did not affect the SNRT, SACT or the AH interval. As HV blocks, which occur below the His bundle, are often life-threatening, the HV conduction delay may be a cause of severe AV blocks induced by propofol. Propofol directly suppressed parasympathetic nerve activity, and sympathetic nerve activity was also suppressed. WHAT IS NEW AND CONCLUSION: These results indicate that propofol suppresses the HV conduction and might help to elucidate the mechanism by which propofol causes lethal AV blocks.

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  • Severe hyponatremia with seizures and confirmed mild brain edema by hysteroscopic myomectomy: a case report. Reviewed International journal

    Haruko Okazaki, Norikazu Miura, Yuki Kashima, Ryoichi Miyashita, Katsunori Oe, Keiko Kawakami, Tetsuya Ishikawa, Kenichi Masui

    JA clinical reports   6 ( 1 )   74 - 74   2020.10

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    BACKGROUND: Hyponatremia can be developed during hysteroscopic surgery with electrolyte-free irrigation fluid. We experienced severe hyponatremia with postoperative seizures and confirmed mild brain edema. CASE PRESENTATION: A quadragenarian female patient underwent a 2-h hysteroscopic myomectomy with electrolyte-free fluid for uterine distension under general anesthesia. Plasma sodium level of 84.1 mmol/L 100 min after the start of surgery indicated excessive absorption of the irrigation fluid. Acute severe hyponatremia was diagnosed with significant edema in the conjunctiva, lip, and extremities. She was treated with a continuous infusion of hypertonic saline. However, seizures and cerebral edema developed 7 h later. The patient recovered without neurological deficits at postoperative day 2. CONCLUSION: The electrolyte-free irrigation fluid can be absorbed rapidly during hysteroscopic surgery. Its interruption with hyponatremia should be considered against prolonged surgery. Especially under general anesthesia, caution should be exercised because the typical symptoms of hyponatremia such as nausea and confusion are blinded.

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  • 小児のプロポフォール予測濃度の基礎 Reviewed

    増井 健一

    日本小児麻酔学会誌   26 ( 1 )   100 - 104   2020.10

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  • Suspected propofol infusion syndrome during normal targeted propofol concentration. Reviewed

    Taku Ichikawa, Keiko Okuyama, Kotoe Kamata, Kenichi Masui, Makoto Ozaki

    Journal of anesthesia   34 ( 4 )   619 - 623   2020.8

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    To this day, the pathophysiology and risk factors of propofol infusion syndrome (PRIS) remain unknown. Moreover, there is no widely accepted definition of PRIS, even though it is a potentially fatal condition. While many suspected cases of PRIS have been reported in both pediatric and adult populations, the actual propofol plasma concentration (Cp) has never been clarified. In this clinical report, we described the first suspected PRIS case in which the propofol Cp was measured 25 min after 226 min of propofol infusion (7.2 µg/mL), which was 12 times higher than the predicted value (0.6 µg/mL). In the presented case, we observed gradually progressive uncontrollable hypercapnia and tachycardia, followed by severe lactic acidosis during surgical anesthesia based on the target-controlled infusion of propofol. Levels of liver enzymes were slightly elevated which suggests little or no liver damage though propofol is mainly metabolized by the liver. Meanwhile, renal impairment, a common secondary feature of PRIS, occurred concomitantly when hypercapnia and metabolic acidosis were manifested. In this case, low or delayed propofol clearance might have been a triggering factor causing severe lactic acidosis.

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  • Individual pharmacometric analysis for sugammadex reversal and re-administration of neuromuscular blockade. Reviewed

    Yuki Kashima, Kenichi Masui

    Journal of anesthesia   2020.7

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    Sugammadex is an innovative reversal agent for neuromuscular blockade (NMB) induced by rocuronium. Although there is a case that re-paralysis is necessary after sugammadex administration, limited reports can be found on the sugammadex dosage for reversal from profound paralysis after induction and immediate re-paralysis following such reversal in detail. We experienced a case in which NMB reversal was required in a short period after paralysis for induction due to the discovery of anisocoria. We successfully re-induced general anesthesia with tracheal intubation soon after. To examine the validity of the dosing, we performed a pharmacometric analysis. A pharmacokinetic-pharmacodynamic model was developed for the patient based on a published pharmacokinetic-pharmacodynamic model for rocuronium and sugammadex. The developed model appropriately describes the train of four ratio observed. In this case, the dose of approximately 8 mg/kg sugammadex but not the conventional dose of 16 mg/kg would be enough for immediate reversal after induction. For the re-paralysis 30 min after NMB reversal, not 1.4 mg/kg but 2.2 mg/kg rocuronium was an adequate dose. Taking individual differences including given dose and time intervals in consideration, NMB monitoring should be used to determine the necessary dose of rocuronium and sugammadex in such situations.

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  • Seasonal and residential clustering at disease onset of anti-MDA5-associated interstitial lung disease. Reviewed International journal

    Naoshi Nishina, Shinji Sato, Kenichi Masui, Takahisa Gono, Masataka Kuwana

    RMD open   6 ( 2 )   2020.6

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    OBJECTIVES: To investigate whether the onset of polymyositis (PM)/dermatomyositis (DM)-associated interstitial lung disease (ILD) is influenced by season and residence in the context of myositis-specific autoantibodies. METHODS: For patients with PM/DM-associated ILD enrolled in a multicentre cohort, 365 and 481 patients were eligible for seasonal and geographical analysis, respectively, based on the availability of reliable clinical information. The patients were divided into three groups: (1) anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive patients, (2) anti-aminoacyl tRNA synthetase (anti-ARS) antibody-positive patients and (3) patients negative for those antibodies. Seasonality was assessed by the Rayleigh test. Distance from residence to the nearest waterfront was measured on Google Map and was compared between groups by the exact Wilcoxon rank-sum test. RESULTS: In anti-MDA5-positive patients, the disease developed more frequently in October-March (p=0.03), whereas a seasonal relationship was not found in the remaining two patient groups. Residence at disease onset in anti-MDA5-positive patients was significantly closer to the waterfront, especially to freshwater, compared with that in anti-ARS-positive or anti-MDA5-/ARS-negative patients (p=0.003 and 0.006, respectively). CONCLUSIONS: Anti-MDA5-associated ILD occurred predominantly from October to March in individuals residing near freshwater, suggesting an environmental influence on the onset of this disease subset.

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  • Remimazolam besilate, a benzodiazepine, has been approved for general anesthesia!! Reviewed

    Kenichi Masui

    Journal of anesthesia   2020.3

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    DOI: 10.1007/s00540-020-02755-1

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  • The efficacy of acute normovolemic hemodilution for preventing perioperative allogeneic blood transfusion in gynecological cancer patients. Reviewed International journal

    Junichi Saito, Kenichi Masui, Satoko Noguchi, Kishiko Nakai, Yoshiko Tamai, Yoko Midorikawa, Hirotaka Kinoshita, Noriko Mikami, Masato Kitayama, Hiroshi Hashimoto, Kazuyoshi Hirota

    Journal of clinical anesthesia   60   42 - 43   2020.3

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    DOI: 10.1016/j.jclinane.2019.08.025

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  • Clinical characteristics of cancer-associated myositis complicated by interstitial lung disease: a large-scale multicentre cohort study. Reviewed International journal

    Yuko Kaneko, Takahiro Nunokawa, Yoshinori Taniguchi, Yukie Yamaguchi, Takahisa Gono, Kenichi Masui, Atsushi Kawakami, Yasushi Kawaguchi, Shinji Sato, Masataka Kuwana

    Rheumatology (Oxford, England)   59 ( 1 )   112 - 119   2020.1

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    OBJECTIVE: To clarify the incidence, risk factors, and impact of malignancy in patients with PM/DM-associated interstitial lung disease (ILD). METHODS: This study used data from 497 patients with PM/DM-associated ILD enrolled in a multicentre, retrospective and prospective cohort of incident cases. Cancer-associated myositis (CAM) was defined as malignancy diagnosed within 3 years before or after PM/DM diagnosis. Demographic and clinical information was recorded at the time of diagnosis, and data about the occurrence of mortality and malignancy was collected. RESULTS: CAM was identified in 32 patients with PM/DM-associated ILD (6.4%). Patients with CAM were older (64 vs 55 years, P < 0.001), presented with arthritis less frequently (24% vs 49%, P = 0.01), and showed a lower level of serum Krebs von den Lungen-6 (687 vs 820 IU/l, P = 0.03) than those without CAM. The distribution of myositis-specific autoantibodies, including anti-melanoma differentiation-associated gene 5, anti-aminoacyl tRNA synthetase, and anti-transcriptional intermediary factor 1-γ antibodies, did not differ between the groups. Survival analysis demonstrated that CAM patients had a poorer survival than non-CAM patients (P = 0.006), primarily due to excess deaths by concomitant malignancy, while mortality due to ILD-related respiratory failure was similar between the groups (P = 0.51). CONCLUSION: Concomitant malignancy can occur in patients with PM/DM-associated ILD, and has significant impact on mortality. Older age, lack of arthritis, and a lower level of serum Krebs von den Lungen-6 at diagnosis are predictors of concomitant malignancy.

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  • Evaluation of usefulness in surfactant protein D as a predictor of mortality in myositis-associated interstitial lung disease. Reviewed International journal

    Shinjiro Kaieda, Takahisa Gono, Kenichi Masui, Naoshi Nishina, Shinji Sato, Masataka Kuwana

    PloS one   15 ( 6 )   e0234523   2020

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    OBJECTIVE: Surfactant protein D (SP-D) is considered a serum biomarker of various forms of interstitial lung disease (ILD). In this study, we examined the utility of SP-D as a predictive biomarker for mortality in patients with ILD associated with polymyositis/dermatomyositis (PM/DM) using large-scale multicentre cohort data. METHODS: We enrolled 381 patients with incident PM/DM-associated ILD in a multicentre retrospective cohort based on the availability of serum SP-D at the baseline. Demographic and clinical characteristics as well as the presence of autoantibodies to melanoma differentiation-associated gene 5 (MDA5) and aminoacyl tRNA synthetase were measured at the time of diagnosis, and follow-up survival data were collected prospectively. RESULTS: Seventy-eight patients died during the median observation period of 18 months, and the majority of patients died of ILD. The SP-D levels at baseline were significantly lower (P = 0.02) in a non-survivor subset than in a survivor subset among the entire enrolled patients. However, the SP-D levels were higher in the non-survivor subset than in the survivor subset based on the stratification by anti-MDA5-positive, anti-ARS-positive and, double-negativity, although there was an only statistically significant difference (P = 0.01) in the double-negative group. Surprisingly, the SP-D levels were within the upper limit of normal, 110 ng/mL, in 54 (87%) of 62 anti-MDA5-positive patients who died. In the double-negative group, the mortality rates were significantly higher (P = 0.002) in a subset with SP-D ≥127.6 ng/mL, the cut-off value for mortality calculated by the receiver operating characteristic curve, than the other subset. All of patients with SP-D <127.6 ng/mL survived. CONCLUSION: Serum SP-D levels behave differently among patients with stratified by anti-MDA5 antibody, anti-ARS antibody and both negativity in PM/DM-associated ILD. Its use in clinical practice should be applied with caution on the basis of the presence or absence of anti-MDA5 antibody or anti-ARS antibody.

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  • Rocuronium pharmacodynamic models for published five pharmacokinetic models: age and sex are covariates in pharmacodynamic models. Reviewed

    Kenichi Masui, Sayaka Ishigaki, Atsuko Tomita, Hiroshi Otake

    Journal of anesthesia   32 ( 5 )   709 - 716   2018.10

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  • Comparison of plasma propofol concentration for apnea, response to mechanical ventilation, and airway device between endotracheal tube and supraglottic airway device in Beagles. Reviewed

    Tomoya Iizuka, Kenichi Masui, Hideko Kanazawa, Ryohei Nishimura

    The Journal of veterinary medical science   80 ( 9 )   1420 - 1423   2018.9

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    The relationships between propofol plasma concentrations and the pharmacodynamic endpoints may differ according to a type of airway device. To clarify these relationships in different airway devices would be useful to avoid the complication such as apnea and intraoperative awareness. The aim of this study was to investigate the influence of difference of airway device on propofol requirement during maintenance of anesthesia in dogs. We compared the influence of airway devices on the plasma propofol concentrations for apnea, response to mechanical ventilation, and response to airway device between endotracheal tube (ETT) and supraglottic airway device (SGAD) in Beagles. The pharmacodynamic effects were repeatedly assessed at varying propofol concentrations. The plasma concentrations (mean ± SD) of propofol in the ETT and SGAD groups were 10.2 ± 1.8 and 10.9 ± 2.4 µg/ml for apnea (P=0.438), 7.9 ± 1.2 and 7.4 ± 1.5 µg/ml for response to mechanical ventilation (P=0.268), and 5.2 ± 0.7 and 5.4 ± 1.5 µg/ml for response to airway device (P=0.580), respectively. Required propofol concentration during maintenance of anesthesia may be similar between ETT and SGAD. Without moderate to strong stimuli such as airway device insertion or painful stimulation during surgery, the type of airway device may have little impact on required propofol concentration during maintenance of anesthesia in dogs.

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  • Calcineurin Inhibitor for the Treatment of Myositis-Associated Interstitial Lung Disease: Comparison between Cyclosporine and Tacrolimus Reviewed

    Gono Takahisa, Masui Kenichi, Nishina Naoshi, Sato Shinji, Kuwana Masataka

    ARTHRITIS & RHEUMATOLOGY   70   2018.9

  • Initial predictors of poor survival in myositis-associated interstitial lung disease: a multicentre cohort of 497 patients. Reviewed International journal

    Shinji Sato, Kenichi Masui, Naoshi Nishina, Yasushi Kawaguchi, Atsushi Kawakami, Maasa Tamura, Kei Ikeda, Takahiro Nunokawa, Yoshinori Tanino, Katsuaki Asakawa, Yuko Kaneko, Takahisa Gono, Taro Ukichi, Shinjiro Kaieda, Taio Naniwa, Masataka Kuwana

    Rheumatology (Oxford, England)   57 ( 7 )   1212 - 1221   2018.7

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    DOI: 10.1093/rheumatology/key060

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  • Size of uterine leiomyoma is a predictor for massive haemorrhage during caesarean delivery. Reviewed International journal

    Kiguna Sei, Kenichi Masui, Hidenori Sasa, Kenichi Furuya

    European journal of obstetrics, gynecology, and reproductive biology   223   60 - 63   2018.4

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    DOI: 10.1016/j.ejogrb.2018.02.014

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  • Clinical Utility of Intraoperative Motor-Evoked Potential Monitoring to Prevent Postoperative Spinal Cord Injury in Thoracic and Thoracoabdominal Aneurysm Repair: An Audit of the Japanese Association of Spinal Cord Protection in Aortic Surgery Database. Reviewed International journal

    Kenji Yoshitani, Kenichi Masui, Masahiko Kawaguchi, Mikito Kawamata, Manabu Kakinohana, Shinya Kato, Kyoko Hasuwa, Michiaki Yamakage, Yusuke Yoshikawa, Kimitoshi Nishiwaki, Tadashi Aoyama, Yoshimi Inagaki, Kazumasa Yamasaki, Mishiya Matsumoto, Kazuyoshi Ishida, Atsuo Yamashita, Katsuhiro Seo, Shinichi Kakumoto, Hironobu Hayashi, Yuu Tanaka, Satoshi Tanaka, Takashi Ishida, Hiroyuki Uchino, Takayasu Kakinuma, Yoshitsugu Yamada, Yoshiteru Mori, Shunsuke Izumi, Kunihiro Nishimura, Michikazu Nakai, Yoshihiko Ohnishi

    Anesthesia and analgesia   126 ( 3 )   763 - 768   2018.3

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  • Propofol-fentanyl interaction in Beagles - Apnea, response to mechanical ventilation, endotracheal tube, and tetanic stimulation Reviewed

    T. Iizuka, K. Masui, T. Miyabe-Nishiwaki, H. Kanazawa, R. Nishimura

    RESEARCH IN VETERINARY SCIENCE   115   34 - 42   2017.12

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    DOI: 10.1016/j.rvsc.2017.01.021

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  • Predictive Modeling of Mortality in Polymyositis/Dermatomyositis Patients with Interstitial Lung Disease Based on Combination of Serum Myositis-Specific Autoantibodies and Conventional Biomarkers Reviewed

    Takahisa Gono, Kenichi Masui, Yasushi Kawaguchi, Kei Ikeda, Atsushi Kawakami, Maasa Tamura, Yoshinori Tanino, Takahiro Nunokawa, Yuko Kaneko, Shinji Sato, Katsuaki Asakawa, Naoshi Nishina, Masataka Kuwana

    ARTHRITIS & RHEUMATOLOGY   69   2017.10

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  • Influence of maternal remifentanil concentration on fetal-to-maternal ratio in pregnant ewes. Reviewed

    Masaki Sato, Kenichi Masui, Borjigin Sarentonglaga, Mio Yamaguchi, Rika Fukumori, Yoshikazu Nagao, Haruhiko Sago, Hiroyuki Sumikura

    Journal of anesthesia   31 ( 4 )   517 - 522   2017.8

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    DOI: 10.1007/s00540-017-2332-4

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  • In Reply. Reviewed International journal

    Kenichi Masui, Sayako Itakura

    Anesthesiology   126 ( 5 )   986 - 986   2017.5

  • In Response. Reviewed International journal

    Kenichi Masui, Sayaka Ishigaki

    Anesthesia and analgesia   124 ( 2 )   695 - 696   2017.2

  • Influence of preoperative oral rehydration on arterial plasma rocuronium concentrations and neuromuscular blocking effects: A randomised controlled trial. Reviewed International journal

    Sayaka Ishigaki, Takahiro Ogura, Ayana Kanaya, Yu Miyake, Kenichi Masui, Tomiei Kazama

    European journal of anaesthesiology   34 ( 1 )   16 - 21   2017.1

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    DOI: 10.1097/EJA.0000000000000526

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  • Systematic review of motor evoked potentials monitoring during thoracic and thoracoabdominal aortic aneurysm open repair surgery: a diagnostic meta-analysis. Reviewed

    Yuu Tanaka, Masahiko Kawaguchi, Yoshinori Noguchi, Kenji Yoshitani, Mikito Kawamata, Kenichi Masui, Takeo Nakayama, Yoshitugu Yamada

    Journal of anesthesia   30 ( 6 )   1037 - 1050   2016.12

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    DOI: 10.1007/s00540-016-2242-x

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  • Influence of Season and Residential Environment on Development of Anti-Melanoma Differentiation-Associated Gene 5 Antibody-Positive Dermatomyositis with Interstitial Lung Disease Reviewed

    Naoshi Nishina, Shinji Sato, Yasushi Kawaguchi, Atsushi Kawakami, Maasa Tamura, Kei Ikeda, Takahiro Nunokawa, Yoshinori Tanino, Katsuaki Asakawa, Yuko Kaneko, Takahisa Gono, Kenichi Masui, Masataka Kuwana

    ARTHRITIS & RHEUMATOLOGY   68   2016.10

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  • Initial Predictors of Short-Term Poor Survival Rates in Patients with Polymyositis/Dermatomyositis-Associated Interstitial Lung Disease Reviewed

    Shinji Sato, Kenichi Masui, Naoshi Nishina, Yasushi Kawaguchi, Atsushi Kawakami, Maasa Tamura, Kei Ikeda, Takahiro Nunokawa, Yoshinori Tanino, Katsuaki Asakawa, Yuko Kaneko, Takahisa Gono, Masataka Kuwana

    ARTHRITIS & RHEUMATOLOGY   68   2016.10

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  • The predictive ability of six pharmacokinetic models of rocuronium developed using a single bolus: evaluation with bolus and continuous infusion regimen. Reviewed

    Tomoki Sasakawa, Kenichi Masui, Tomiei Kazama, Hiroshi Iwasaki

    Journal of anesthesia   30 ( 4 )   620 - 7   2016.8

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    DOI: 10.1007/s00540-016-2174-5

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  • Rapid Infusion of Hydroxyethyl Starch 70/0.5 but not Acetate Ringer's Solution Decreases the Plasma Concentration of Propofol during Target-controlled Infusion. Reviewed International journal

    Sayako Itakura, Kenichi Masui, Tomiei Kazama

    Anesthesiology   125 ( 2 )   304 - 12   2016.8

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    DOI: 10.1097/ALN.0000000000001184

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  • The Pharmacokinetics of Atomized Lidocaine Administered via the Trachea: A Randomized Trial. Reviewed International journal

    Yumiko Takaenoki, Kenichi Masui, Yutaka Oda, Tomiei Kazama

    Anesthesia and analgesia   123 ( 1 )   74 - 81   2016.7

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    DOI: 10.1213/ANE.0000000000001317

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  • Saline Flush After Rocuronium Bolus Reduces Onset Time and Prolongs Duration of Effect: A Randomized Clinical Trial. Reviewed International journal

    Sayaka Ishigaki, Kenichi Masui, Tomiei Kazama

    Anesthesia and analgesia   122 ( 3 )   706 - 11   2016.3

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    DOI: 10.1213/ANE.0000000000001094

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  • Pulse wave transit time measurements of cardiac output in patients undergoing partial hepatectomy: a comparison of the esCCO system with thermodilution. Reviewed International journal

    Masato Tsutsui, Yoshiyuki Araki, Kenichi Masui, Tomiei Kazama, Yoshihiro Sugo, Thomas L Archer, Gerard R Manecke Jr

    Anesthesia and analgesia   117 ( 6 )   1307 - 12   2013.12

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    DOI: 10.1213/ANE.0b013e3182a44c87

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  • Utility Of Autoantibody Testing For Predicting Risk Of Pulmonary Arterial Hypertension: A Retrospective Analysis In Routine Autoantibody Laboratory Reviewed

    Masataka Kuwana, Yuichiro Shirai, Hidekata Yasuoka, Tsutomu Takeuchi, Kenichi Masui

    ARTHRITIS AND RHEUMATISM   65   S1098 - S1099   2013.10

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  • Evaluation of the predictive performance of a pharmacokinetic model for propofol in Japanese macaques (Macaca fuscata fuscata) Reviewed

    T. Miyabe-Nishiwaki, K. Masui, A. Kaneko, K. Nishiwaki, T. Nishio, H. Kanazawa

    Journal of Veterinary Pharmacology and Therapeutics   36 ( 2 )   169 - 173   2013.4

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    DOI: 10.1111/j.1365-2885.2012.01404.x

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  • Neonatal desflurane exposure induces more robust neuroapoptosis than do isoflurane and sevoflurane and impairs working memory. Reviewed International journal

    Mitsuyoshi Kodama, Yasushi Satoh, Yukiko Otsubo, Yoshiyuki Araki, Ryuji Yonamine, Kenichi Masui, Tomiei Kazama

    Anesthesiology   115 ( 5 )   979 - 91   2011.11

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    DOI: 10.1097/ALN.0b013e318234228b

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  • Effect of fentanyl on ischemic depolarization and ischemic neuronal damage of hippocampal CA1 in the gerbil. Reviewed

    Kensuke Shiraishi, Yoshimasa Takeda, Kenichi Masui, Hideki Taninishi, Toshihiro Sasaki, Tetsuya Danura, Kiyoshi Morita

    Journal of anesthesia   25 ( 4 )   540 - 8   2011.8

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    DOI: 10.1007/s00540-011-1143-2

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  • Awareness during anesthesia: the results of a questionnaire survey in Japan. Reviewed

    Yasuhiro Morimoto, Yuko Nogami, Kaori Harada, Tsunehisa Tsubokawa, Kenichi Masui

    Journal of anesthesia   25 ( 1 )   72 - 7   2011.2

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    DOI: 10.1007/s00540-010-1050-y

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  • Hypnotic effects and pharmacokinetics of a single bolus dose of propofol in Japanese macaques (Macaca fuscata fuscata). [corrected]. Reviewed International journal

    Takako Miyabe-Nishiwaki, Kenichi Masui, Akihisa Kaneko, Koki Nishiwaki, Etsuko Shimbo, Hideko Kanazawa

    Veterinary anaesthesia and analgesia   37 ( 6 )   501 - 10   2010.11

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    DOI: 10.1111/j.1467-2995.2010.00564.x

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  • The performance of compartmental and physiologically based recirculatory pharmacokinetic models for propofol: a comparison using bolus, continuous, and target-controlled infusion data. Reviewed International journal

    Kenichi Masui, Richard N Upton, Anthony G Doufas, Johan F Coetzee, Tomiei Kazama, Eric P Mortier, Michel M R F Struys

    Anesthesia and analgesia   111 ( 2 )   368 - 79   2010.8

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    DOI: 10.1213/ANE.0b013e3181bdcf5b

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  • Effects of a short-acting [beta]1 receptor antagonist landiolol on hemodynamics and tissue injury markers in patients with subarachnoid hemorrhage undergoing intracranial aneurysm surgery. Reviewed International journal

    Masahiko Kawaguchi, Kouji Utada, Kenji Yoshitani, Hiroyuki Uchino, Yoshimasa Takeda, Kenichi Masui, Takefumi Sakabe

    Journal of neurosurgical anesthesiology   22 ( 3 )   230 - 9   2010.7

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    DOI: 10.1097/ANA.0b013e3181d0c2e4

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  • Early phase pharmacokinetics but not pharmacodynamics are influenced by propofol infusion rate. Reviewed International journal

    Kenichi Masui, Marimo Kira, Tomiei Kazama, Satoshi Hagihira, Eric P Mortier, Michel M R F Struys

    Anesthesiology   111 ( 4 )   805 - 17   2009.10

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    DOI: 10.1097/ALN.0b013e3181b799c1

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  • [Pharmacokinetic simulations of remifentanil]. Reviewed

    Kenichi Masui, Tomiei Kazama

    Masui. The Japanese journal of anesthesiology   56 ( 11 )   1287 - 95   2007.11

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    Remifentanil has short half-lives: the values of alpha and beta decay are about 2 and 15 min, respectively. Therefore, the time for remifentanil concentration to reach its steady state concentration (Css) is shorter than those of other anesthetic drugs such as propofol and fentanyl. The Css and the time course of plasma concentration as well as effect-site concentration (Ce) during the continuous infusion of remifentanil could be helpful in our clinical practice. Css is strongly affected by weight and age with Minto's pharmacokinetic parameters of remifentanil. Css increases by a factor of 1.8 when the weight doubles, and Css in a 75-year-old is 1.5 times higher than Css in a 25-year-old. We tried to simulate the time courses of remifentanil Ce and fentanyl Ce during induction, maintenance, and emergence phases of anesthesia. Because of the short half-lives, remifentanil concentration could be well-controlled. However, remifentanil concentration does not reach the Css immediately with constant rate infusion. For example, it will take about 5 min for remifentanil effect-site concentration to decrease from Css to a half of Css. It is considered that anesthetic management with remifentanil is superior to that without it.

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  • On-line monitoring of end-tidal propofol concentration in anesthetized patients. Reviewed International journal

    Akira Takita, Kenichi Masui, Tomiei Kazama

    Anesthesiology   106 ( 4 )   659 - 64   2007.4

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    DOI: 10.1097/01.anes.0000264745.63275.59

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  • [Comparison of pentazocine and fentanyl in total intravenous anesthesia using propofol]. Reviewed

    Akihiko Nonaka, Satomi Suzuki, Fumiaki Abe, Kenichi Masui

    Masui. The Japanese journal of anesthesiology   55 ( 8 )   983 - 7   2006.8

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    BACKGROUND: Pentazocine may be an alternative for fentanyl during total intravenous anesthesia (TIVA) using propofol. The authors compared the efficacy and safety of pentazocine for analgesics in TIVA using propofol. METHODS: Eighty-nine patients scheduled for mastectomy were analyzed retrospectively. Patients were classified into two groups by used analgesics; pentazocine (Group P, n = 34) and fentanyl (Group F, n = 55). Anesthesia was induced with propofol, using target controlled infusion method, and ketamine 20-50 mg, and was maintained with propofol infusion and increments of fentanyl or single dose of pentazocine with 40% oxygen in air. Postoperative pain was assessed using a visual analogue pain scale (VAS). RESULTS: There were no differences in the patient background between both groups. Systolic as well as diastolic blood pressure and heart rate were not different between both groups during surgery. The maintenance dose of propofol was not different between the two groups. Awakening time in about 80% of patients was within 15 minutes and is not different between the two groups. There were no differences between the two groups regarding VAS. There are no severe complications. Incidence of nausea and vomiting was not different between the two groups. CONCLUSIONS: The results suggest that pentazocine would provide a stable hemodynamic state, rapid recovery and an effective postoperative pain relief to the same degree as with fentanyl in TIVA with propofol.

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  • Isoflurane and sevoflurane during reperfusion prevent recovery from ischaemia in mitochondrial KATP channel blocker pretreated hearts Reviewed

    K. Masui, S. Kashimoto, A. Furuya, T. Oguchi

    European Journal of Anaesthesiology   23 ( 2 )   123 - 129   2006.2

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    DOI: 10.1017/S0265021505002024

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  • [Refractory generalized convulsions in a patient undergoing brain tumor resection during propofol anesthesia]. Reviewed

    Hisashi Fukushima, Tadahiko Ishiyama, Takeshi Oguchi, Kenichi Masui, Takashi Matsukawa, Teruo Kumazawa

    Masui. The Japanese journal of anesthesiology   53 ( 6 )   691 - 2   2004.6

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    Propofol has been used to treat convulsions, while the drug is known to induce convulsions. We described a case of generalized convulsions during brain tumor resection under propofol anesthesia. A 24-year-old man was scheduled to undergo brain tumor resection. He had no history of epilepsy. Anesthesia was induced and maintained with propofol and fentanyl. During the craniotomy, the patient developed generalized convulsions. Diazepam, thiamylal, and phenytoin were given intravenously and the seizure activity resolved. Generalized convulsions recurred three times during the operation. Postoperative course was uneventful. On the 16 th postoperative day, the patient underwent ventriculoperitoneal shunt under general anesthesia using sevoflurane, nitrous oxide and oxygen. Convulsions were not noted intra- and postoperatively. Because convulsions did not occur during sevoflurane anesthesia and the patient had no history of epilepsy, propofol may have induced a generalized convulsions on the first operation.

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  • Sevoflurane reduces dysrhythmias during reperfusion in the working rat heart Reviewed

    T. Oguchi, S. Kashimoto, T. Yamaguchi, K. Masui, T. Kumazawa

    Journal of Anesthesia   15 ( 1 )   22 - 28   2001

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    DOI: 10.1007/s005400170047

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Books

  • 日めくり麻酔科エビデンスアップデート5

    榎本夕里亜, 菅沼進也, 増井健一( Role: Joint authorロボット麻酔システム)

    2025.12  ( ISBN:9784771906242

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  • 麻酔科学の最新知見

    増井健一( Role: Joint authorシプロフォール(Ciprofol))

    2025.12  ( ISBN:9784771906235

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  • 麻酔科学レビュー : 最新主要文献とガイドラインでみる

    増井健一( Role: Joint author新しい全身麻酔薬レミマゾラム)

    総合医学社  2025.6  ( ISBN:9784883784929

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  • 麻酔科薬剤ノート : 周術期の麻酔・救急対応薬の使用のポイント

    増井健一( Role: Joint author降圧薬/冠血管拡張薬)

    羊土社  2025.6  ( ISBN:9784758111263

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    Total pages:334, 1p   Language:Japanese  

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    Other Link: https://webview.isho.jp/book/detail/abs/10.18958/9784758111263

  • 麻酔科研修ノート

    増井 健一( Role: Joint author麻酔関連偶発症例調査)

    診断と治療社  2024.12  ( ISBN:9784787826343

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    Total pages:xxviii, 718p   Language:Japanese  

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  • 麻酔科学レビュー2024 : 最新主要文献とガイドラインでみる

    増井 健一( Role: Joint author新しい全身麻酔薬レミマゾラム)

    総合医学社  2024.6  ( ISBN:9784883784820

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  • 臨床麻酔薬理学書

    増井 健一( Role: Joint author1章薬物動態学、2章薬力学)

    中山書店  2023.12  ( ISBN:9784521750699

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    Total pages:xii, 379p   Language:Japanese  

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  • 理解して使いこなす麻酔科機器 : モニター・ICU機器・ペースメーカー

    増井 健一( Role: Joint author呼気プロポフォール濃度分析)

    文光堂  2023.11  ( ISBN:9784830628580

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    Total pages:212p   Language:Japanese  

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  • 麻酔科学レビュー2023 : 最新主要文献とガイドラインでみる

    増井 健一( Role: Joint author新しい全身麻酔薬レミマゾラム)

    総合医学社  2023.5  ( ISBN:9784883784721

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    Total pages:357p   Language:Japanese  

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  • 麻酔科学レビュー 2022: 最新主要文献とガイドラインでみる

    増井 健一( Role: Joint author新しい全身麻酔薬レミマゾラム)

    総合医学社  2022.6  ( ISBN:9784883787487

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    Total pages:335p   Language:Japanese  

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  • 麻酔における気道管理の手技と知識を知る

    増井 健一( Role: Joint author第6章-1 麻酔導入法の種類)

    日本医事新報社  2022.6  ( ISBN:9784784959365

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  • レミマゾラムQ&A : 明日からの臨床麻酔が広がる

    増井 健一( Role: Joint authorQ9 覚醒する効果部位濃度はどの程度でしょうか? レミマゾラムのcontext-sensitive decrement timeについても教えてください;Q17 麻薬性鎮痛薬の併用方法は?プロポフォールと同様でよいのでしょうか?)

    克誠堂出版  2022.5  ( ISBN:9784771905627

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    Total pages:xi, 305p   Language:Japanese  

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  • 読んでおきたい麻酔科学論文

    増井 健一( Role: Joint author第2章 静脈麻酔)

    克誠堂出版  2022.2 

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  • 神経麻酔最前線 すべては患者の機能維持・向上のために

    増井 健一( Role: Joint author5. ベンゾジアゼピン系薬物; column 3 新薬レミマゾラムのこの領域における可能性)

    中外医学社  2021.6  ( ISBN:9784498055483

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  • 麻酔科学レビュー2021

    増井 健一( Role: Joint author新しい全身麻酔薬レミマゾラム)

    総合医学社  2021.6  ( ISBN:9784883787425

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  • 高齢者麻酔のポイント50

    増井 健一( Role: Joint author若年・壮年と比べた高齢者の薬物動態・薬力学の特徴について教えてください)

    克誠堂出版  2021.6  ( ISBN:9784771905504

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  • 新臨床麻酔スタンダード

    増井 健一( Role: Joint author新しい全身麻酔薬レミマゾラム)

    克誠堂出版  2020.5  ( ISBN:9784771905337

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    Total pages:vii, 434p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2019

    ( Role: Joint authorAI・人工知能 EXPO で見つけたテクノロジー)

    日本麻酔・集中治療テクノロジー学会  2020.3 

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  • 一歩進んだ麻酔管理 : 常識は常に真実か?

    増井 健一( Role: Joint author全身麻酔薬と麻薬の相乗作用; BISモニターは術中覚醒を予防しない?)

    克誠堂出版  2019.5  ( ISBN:9784771905160

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    Total pages:xiv, 294p   Language:Japanese  

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  • 医学系研究、論文投稿上のQ&A : すべての医療従事者が知りたい!

    増井 健一( Role: Joint authorQ33 研究対象者数はなぜ事前に決める必要があるのですか?; Q34 研究対象者数はどのように決めるのですか?; Q35 研究開始前に決めておくべき統計事項は何ですか?; Q37 データは何を収集・記録・保存しておく必要がありますか?; Q39 データはどう解析すればよいですか?)

    日本医事新報社  2017.8  ( ISBN:9784784946358

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    Total pages:173p   Language:Japanese  

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  • 麻酔偶発症A to Z

    増井 健一( Role: Joint authorプロポフォールの有害作用; 麻薬性オピオイド全身投与による呼吸抑制,過鎮静,悪心・嘔吐,瘙痒感,尿閉,便秘)

    文光堂  2017.6  ( ISBN:9784830628450

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    Total pages:15, 660 p   Language:Japanese  

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  • Total Intravenous Anesthesia and Target Controlled Infusions: A Comprehensive Global Anthology

    Kenichi Masui( Role: Joint authorHow to Select a PK/PD Model)

    Springer International Publishing  2017.3 

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    ISBN: 9783319476060(hard cover)

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  • エビデンスで読み解く小児麻酔

    増井 健一( Role: Joint author小児の発達薬理学とPK・PD)

    克誠堂出版  2016.11  ( ISBN:9784771904729

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    Total pages:vii, 286p   Language:Japanese  

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  • 臨床の疑問に答える静脈麻酔Q&A99

    増井 健一( Role: Joint authorQ28 麻酔維持中のプロポフォール目標濃度は一定でよいのでしょうか?; column薬物血中濃度に対する心拍出量の影響; Q29 レミフェンタニルとフェンタニルの併用時に効果部位濃度を加算して考えてよいのでしょうか?; Q82 生理学的モデルとは何ですか?; Q84 コンパートメントモデルの各パラメータ(Vi,kijなど)の意味を教えてください; Q89 Context-sensitive half-time(CSHT)とは何を表すものですか?; Q90 鎮痛薬と鎮静薬の相互作用について教えてください; Q91 Response Surfaceの見方について教えてください; Q92 薬物動態モデルを利用した濃度予測はあらゆる患者に適用できるのでしょうか?; Q93 薬物動態モデルの精度はどのような方法で評価するのでしょうか?; Q94 LBMが使われている薬物動態モデルの問題を教えてください; column3-コンパートメントモデルの微分方程式; column薬物動態モデル・薬力学的モデルの作成方法; 付録② 薬物動態モデル一覧; 付録③ 静脈麻酔を理解するための用語集)

    羊土社  2015.11  ( ISBN:9784758111140

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    Total pages:243p   Language:Japanese  

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  • 鎮静と術中覚醒

    増井 健一( Role: Joint authorIsolated Forearm Technique)

    真興交易医書出版部  2015.10  ( ISBN:9784880039008

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    Total pages:132p   Language:Japanese  

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  • 周術期管理の謎22

    増井 健一( Role: Joint authorレミフェンタニルの1μg/kg/min の投与に意味はあるのか?)

    克誠堂出版  2015.6  ( ISBN:9784771904460

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    Total pages:vii, 216p   Language:Japanese  

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  • 麻酔科医のための周術期の薬物使用法

    増井 健一( Role: Joint authorレミフェンタニル;フェンタニル)

    中山書店  2015.5  ( ISBN:9784521737126

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    Total pages:523p   Language:Japanese  

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  • 改訂版 麻酔科薬剤ノート : 周術期の麻酔・救急対応薬の使用のポイント

    増井 健一( Role: Joint author降圧薬/冠血管拡張薬)

    羊土社  2014.11  ( ISBN:9784758111119

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    Total pages:308p   Language:Japanese  

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  • 麻酔科医のための知っておきたいワザ22

    増井 健一( Role: Joint authorTCIポンプを使いこなす)

    克誠堂出版  2014.5  ( ISBN:9784771904293

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    Total pages:vii, 280p   Language:Japanese  

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  • 静脈麻酔

    増井 健一( Role: Joint author大量出血を伴う手術や長時間手術の麻酔)

    克誠堂出版  2014.5  ( ISBN:9784771904262

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    Total pages:xv, 367p   Language:Japanese  

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  • 周術期モニタリング徹底ガイド : 臨床に役立つ機器のしくみと活用法 : 基本からピットフォールまで

    増井 健一( Role: Joint authorTCIポンプ(プロポフォール血中濃度))

    羊土社  2013.11  ( ISBN:9784758111096

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    Total pages:329p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2012

    増井 健一( Role: Joint authorExcel上でRを使う)

    日本麻酔・集中治療テクノロジー学会  2013.10 

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  • あらゆる科で役立つ!麻酔科で学びたい技術 : 手にとるようにわかる,麻酔の基本概念と手技・周術期管理のポイント,知っておくべき病態の知識

    増井 健一( Role: Joint authorTIVAによる麻酔法)

    羊土社  2013.6  ( ISBN:9784758105507

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    Total pages:261p   Language:Japanese  

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  • オピオイド : 基礎を知って臨床で使いこなす

    増井 健一( Role: Joint authorオピオイドのPK/PD)

    克誠堂出版  2012.6  ( ISBN:9784771903968

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    Total pages:vii, 209p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2009

    萩平哲, 増井健一, 高階雅紀, 内田整, 森隆比古( Role: Joint author薬物をボーラス投与した時の薬物動態モデル)

    日本麻酔・集中治療テクノロジー学会  2012.4 

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  • 麻酔・集中治療とテクノロジー2011

    増井健一, 萩平哲, 風間富栄( Role: Joint author薬物をボーラス投与した時の薬物動態モデル)

    日本麻酔・集中治療テクノロジー学会  2012.4 

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  • 麻酔科薬剤ノート : 周術期の麻酔・救急対応薬の使用のポイント

    増井 健一( Role: Joint author降圧薬/冠血管拡張)

    羊土社  2010.6  ( ISBN:9784758111010

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  • 麻酔・集中治療とテクノロジー2006

    増井 健一( Role: Joint authorExcel でデータ入力から基本統計まで)

    日本麻酔・集中治療テクノロジー学会  2009.9 

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  • 麻酔の現況と展望 : 研修医と指導医のための質問317

    増井 健一( Role: Joint authorオピオイド(麻薬))

    総合医学社  2009.5  ( ISBN:9784883786008

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    Total pages:278p   Language:Japanese  

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  • 今日から実践できるTIVA [2]

    増井 健一(レミフェンタニルを用いた麻酔導入)

    真興交易医書出版部  2008.4  ( ISBN:9784880038100

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  • 麻酔・集中治療とテクノロジー2005

    増井 健一( Role: Joint authorExcel のグラフ機能を使いこなす)

    日本麻酔・集中治療テクノロジー学会  2006.11 

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  • 麻酔・集中治療とテクノロジー2004

    増井 健一( Role: Joint author統計データの正しい解釈のために)

    日本麻酔・集中治療テクノロジー学会  2006.9 

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  • 今日から実践できるTIVA

    増井 健一( Role: Joint author総論Ⅱ Goog risk 症例におけるTIVA の実際-調節するにはプロポフォールか?オピオイドか?-)

    真興交易医書出版部  2006.6  ( ISBN:9784880037677

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  • コ・メディカルのための統計学入門 : これさえあれば,論文作成・学会発表なんか怖くない!

    増井 健一( Role: Joint authorメタ・アナリシス)

    日本放射線技師会出版会  2005.11  ( ISBN:4861570069

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    Total pages:199p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2003

    増井 健一( Role: Joint author活用しようPDF 利用〜作成〜論文投稿)

    日本麻酔・集中治療テクノロジー学会  2004.12 

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  • ここからはじめるメタ・アナリシス : Excelを使って簡単に

    増井 健一( Role: Sole author)

    真興交易医書出版部  2003.6  ( ISBN:4880037001

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    Total pages:135p   Language:Japanese  

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  • 静脈麻酔/TCIソフトウェアガイドブック : 研修医からエキスパートまで

    増井 健一( Role: Joint authorBeConSim)

    克誠堂出版  2003.5  ( ISBN:4771902623

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    Total pages:168p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2002

    増井 健一( Role: Joint author再利用可能なBIS センサーの試作)

    2003.2 

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  • 手術室,ICUにおけるLANのノウハウ

    増井 健一( Role: Joint authorパーソナルコンピュータでシリンジポンプを操作する―通信ソフトウェア開発のために―)

    真興交易(株)医書出版部  2003.2  ( ISBN:4880036900

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    Total pages:279p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2001

    増井 健一( Role: Joint authorソフトウェアのユーザーインターフェイス ー 使いやすさを考える ー; 年齢によるpharmacodynamics の影響を取り入れたTCI ソフトウェア)

    日本麻酔・集中治療テクノロジー学会  2002.7 

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  • ドクター,ナースのためのPalm活用ガイド

    増井 健一( Role: Joint author辞書ソフトKDIC の使用方法; ビューワJ-Doc Reader の使用方法)

    南江堂  2002.5  ( ISBN:4524235485

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    Total pages:ix, 148p   Language:Japanese  

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  • 麻酔・集中治療とテクノロジー2000

    増井 健一( Role: Joint authorWindows95/98 で動くプロポフォール薬物動態シミュレーションソフトの試作)

    日本麻酔・集中治療テクノロジー学会  2001.1 

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  • The hypertrophied heart

    Kenichi Masui, Takeshi Oguchi, Satoshi Kashimoto( Role: Joint authorEffects of melatonin on cardiac function and metabolism in the ischemic working rat heart)

    Kluwer Academic Publishers  2000.9  ( ISBN:0792377419

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  • Characteristics of the novel anesthetic/sedative remimazolam and its cautionary notes Invited

    294 ( 3 )   214 - 219   2025.7

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    J-GLOBAL

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  • Improved Survival in Patients with Myositis-Associated Interstitial Lung Disease (ILD) During the Period 2011 to 2023: Comparative and Integrative Analysis of Three Multicenter Cohorts in Japan

    Masataka Kuwana, Kenichi Masui, Atsushi Kawakami, Takafumi Suda, Shinji Sato, Yasushi Kawaguchi, Takeshi Johkoh, Tomoaki Hoshino, Naoki Shimada, Yasuhiro Kondoh, Yoshinori Tanino, Tohru Takeuchi, Yoshiyuki Abe, Naoki Kimura, Yasushi Inoue, Keisuke Tomii, Toru Arai, Kunihiro Yamaoka, Kaneshige Sasaki, Taio Naniwa, Ran Nakashima, Kenjiro Shima, Osamu Nishiyama, Yuko Waseda, Hiroshi Mukae, Hirofumi Chiba, Keigo Ikeda, Kazuya Ichikado, Yohei Kirino, Koichi Amano, Takashi Nawata, Tomoo Kishaba, Daisuke Asatori, Daisuke Kobayashi, Takahisa Gono

    ARTHRITIS & RHEUMATOLOGY   76   2381 - 2383   2024.9

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  • プロポフォールTIVA Invited Reviewed

    増井健一, 波平めぐみ, 末廣かれん, 佐藤澪令, 倉富秀之, 川畑慶一郎, 堀田直志, 後藤隆久

    臨床麻酔   47 ( 8 )   1152 - 1160   2023.10

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  • 【レミマゾラムを使いこなそう!】レミマゾラム投与に関連する副作用

    増井 健一

    臨床麻酔   47 ( 8 )   955 - 962   2023.9

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  • 【高齢者準緊急手術の周術期管理】高齢者の麻酔薬薬物動態・薬力学

    増井 健一

    麻酔   72 ( 9 )   855 - 861   2023.9

  • レミマゾラム 特徴と展望

    増井 健一

    臨床麻酔   46 ( 臨増 )   243 - 251   2022.3

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  • レミマゾラム リスク社会を担う新しい麻酔薬を使うために

    増井 健一

    日本臨床麻酔学会誌   41 ( 6 )   S167 - S167   2021.10

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  • Neo-TIVA時代へようこそ レミマゾラムを通して識るプロポフォールの姿

    増井 健一

    日本臨床麻酔学会誌   41 ( 4 )   352 - 358   2021.7

  • 【レミマゾラム】レミマゾラムの薬物動態学

    増井 健一

    LiSA   28 ( 6 )   608 - 613   2021.6

  • 【最新主要文献とガイドラインでみる 麻酔科学レビュー 2021】新しい全身麻酔薬レミマゾラム

    増井 健一

    麻酔科学レビュー   2021   331 - 338   2021.5

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  • 【麻酔薬体内動態・薬力学back-to-basics】薬物相互作用を理解する

    増井 健一

    麻酔   70 ( 3 )   256 - 263   2021.3

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  • ロボットを利用した術前外来支援システムの開発

    今井桃花, 加島有紀, 眞一弘士, 眞一弘士, 山下咲良, 増井健一

    日本麻酔・集中治療テクノロジー学会プログラム・抄録集(Web)   38th   2021

  • レミマゾラムの予測血中濃度シミュレーション

    合田廷大, 増井健一

    日本麻酔・集中治療テクノロジー学会プログラム・抄録集(Web)   38th   2021

  • 甲状腺機能亢進症を伴う高度るいそう患者のプロポフォール麻酔での高維持濃度・高覚醒濃度の経験

    古谷 未央子, 大川 浩文, 増井 健一

    日本臨床麻酔学会誌   40 ( 6 )   S304 - S304   2020.10

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  • 小児のプロポフォール予測濃度の基礎

    増井 健一

    日本小児麻酔学会誌   26 ( 1 )   100 - 104   2020.10

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  • 医学における自然言語処理と専門辞書の重要性

    眞一 弘士, 増井 健一

    麻酔   69 ( 4 )   443 - 449   2020.4

  • AI・人工知能EXPOで見つけたテクノロジー

    増井健一

    麻酔・集中治療とテクノロジー   2019   2020

  • REPORT OF MADAGASCAR CLEFT LIP AND PALATE MEDICAL COOPERATIVE DISPATCH-FROM AN ANESTHETIST’S POINT OF VIEW-

    加島有紀, 増井健一, 三浦倫一, 大嶽浩司

    昭和学士会雑誌(Web)   80 ( 5 )   2020

  • 小児麻酔のためのファーマコメトリクス

    増井健一

    日本麻酔科学会学術集会(Web)   67th   2020

  • レミマゾラムを通して識るプロポフォールの姿

    増井健一

    日本臨床麻酔学会誌   40 ( 6 )   2020

  • 小児麻酔におけるプロポフォールの使用 小児のプロポフォール予測濃度の基礎

    増井 健一

    日本小児麻酔学会誌   25 ( Suppl. )   62 - 62   2019.11

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  • 【ビッグデータ:麻酔領域発展のための活用】麻酔科領域が持つビッグデータの種類とその活用

    増井 健一

    麻酔   68 ( 11 )   1168 - 1175   2019.11

  • ロクロニウムのファーマコメトリクス 薬物動態力学モデルによる予測濃度を利用しよう

    増井 健一

    臨床麻酔   43 ( 5 )   673 - 679   2019.5

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    筋弛緩薬による筋弛緩効果を適切にコントロールするには、筋弛緩モニターが必須である。また薬物動態力学モデルによる予測濃度はそれを単独で使うのではなく、脳波モニターなどによって効果の評価を行ったうえで、濃度と効果の関係を把握して使うことが肝要である。ロクロニウムとスガマデクスの薬物動態力学モデルの知見など、筋弛緩でもファーマコメトリクスが活用できる知見を紹介した。

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  • チンパンジーにおけるプロポフォール静脈麻酔法の検討-ヒト薬物動態モデルでチンパンジーの血中濃度を予測できるか?

    宮部貴子, 兼子明久, 山中淳史, 石上暁代, 前田典彦, 鈴木樹理, 友永雅己, 松沢哲郎, 牟田佳那子, 西村亮平, 矢島功, Douglas Eleveld, Anthony Absalom, 増井健一

    SAGA21 (熊本)   2018.11

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  • 【麻酔科学の領域の広がり】薬物動態力学を臨床麻酔へ

    増井 健一

    昭和学士会雑誌   78 ( 5 )   434 - 439   2018.10

  • 神経筋伝達に関する研究 単回ボーラス投与により開発したロクロニウムの薬物動態学的な6モデルの予測能 ボーラスと持続点滴レジメンによる評価(The predictive ability of six pharmacokinetic models of rocuronium developed using a single bolus: evaluation with bolus and continuous infusion regimen)

    笹川 智貴, 増井 健一

    日本臨床麻酔学会誌   38 ( 6 )   S122 - S122   2018.10

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  • rSO2とSpMetを術中管理指標に用いた先天性メトヘモグロビン血症患者の全身麻酔経験

    木村 真也, 岩光 麗美, 増井 健一, 大嶽 浩司

    日本臨床麻酔学会誌   38 ( 6 )   S256 - S256   2018.10

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  • Evaluation of the predictive performance of human pharmacokinetic models of propofol in chimpanzees

    Takako Miyabe-Nishiwaki, Akihisa Kaneko, Atsushi Yamanaka, Akiyo Ishigami, Norihiko Maeda, Juri Suzuki, Masaki Tomonaga, Tetsuro Matsuzawa, Kanako Muta, Ryohei Nishimura, Douglas Eleveld, Anthony Absalom, Isao Yajima, Kenichi Masui

    13th World Congress of Veterinary Anaesthesiology (Italy)   2018.9

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  • スガマデクスを投与した直後ロクロニウムを再投与した場合の筋弛緩効果の検討 シミュレーションスタディ

    石原 大雅, 増井 健一, 大嶽 浩司

    麻酔科学サマーセミナー   15回   47 - 47   2018.6

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  • Artificial Intelligence and Automatic Assist Anesthesia

    増井健一

    日本臨床麻酔学会誌   38 ( 3 )   410 - 414   2018.5

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    &lt;p&gt;In 2016, there were many news reports concerning artificial intelligence learning by itself. For example, AlphaGo(Google DeepMind)won a Go match against a professional high-level player, and an automatic driving bus ran for a test on public road. In the area of anesthesiology, automated anesthesia is associated with artificial intelligence. There are currently a number of automated systems which maintain drug concentrations of anesthetics. Another automated anesthesia system, which administers an anesthetic drug to maintain these pharmacodynamic effects, requires appropriate electroencephalographic monitoring and continuous measurement of the actual drug concentration. Computer-assisted anesthetic management can compensate for shortcomings of anesthesiologists and improve medical quality in daily practice.&lt;/p&gt;

    DOI: 10.2199/jjsca.38.410

    J-GLOBAL

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  • プロポフォールの維持濃度をどうやって決めるか?覚醒濃度を予測してから維持濃度を決める方法

    増井健一

    Lisa別冊   25   131‐139   2018.4

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    J-GLOBAL

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  • 【2018のシェヘラザードたち】 (第二十一夜)プロポフォールの維持濃度をどうやって決めるか? 覚醒濃度を予測してから維持濃度を決める方法

    増井 健一

    LiSA 別冊   25 ( 別冊'18春号 )   131 - 139   2018.4

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  • プロポフォールの維持濃度をどうやって決めるか? : 覚醒濃度を予測してから維持濃度を決める方法 (2018のシェヘラザードたち)

    増井 健一

    LiSA. 別冊   131 - 139   2018

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  • 犬における薬物動態モデルを用いたプロポフォールの予測血中濃度の精度検討

    飯塚智也, 増井健一, 長久保大, 牟田佳那子, 鎌田正利, 西村亮平

    日本獣医麻酔外科学雑誌   48 ( Supplement 2 )   211   2017.11

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    J-GLOBAL

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  • 犬における薬物動態モデルを用いたプロポフォールの予測血中濃度の精度検討

    飯塚 智也, 増井 健一, 長久保 大, 牟田 佳那子, 鎌田 正利, 西村 亮平

    日本獣医麻酔外科学雑誌   48 ( Suppl.2 )   211 - 211   2017.11

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  • 【最新の輸液・栄養・麻酔管理II】 術前麻酔管理

    増井 健一

    消化器外科   40 ( 10 )   1427 - 1437   2017.9

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  • 筋弛緩薬の薬物動態シミュレーション

    笹川智貴, 国沢卓之, 増井健一

    臨床麻酔(真興交易)   41 ( 8 )   1087 - 1095   2017.8

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  • 複数モデルの同時シミュレーションに対応したAndroid端末薬物動態シミュレータ

    中島 陽平, 増井 健一, 風間 富栄

    麻酔・集中治療とテクノロジー   2016   100 - 100   2017.3

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  • コモンマーモセットにおけるプロポフォールの薬物動態解析

    牟田佳奈子, 宮部貴子, 増井健一, 矢島功, 飯塚智也, 兼子明久, 西村亮平

    第6回日本マーモセット研究会   2016.12

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  • 人工知能と自動麻酔

    増井健一

    日本臨床麻酔学会誌   36 ( 6 )   S221   2016.10

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  • 静脈麻酔のパラダイムシフト 「自動麻酔」の時代に備える 人工知能と自動麻酔

    増井 健一

    日本臨床麻酔学会誌   36 ( 6 )   S221 - S221   2016.10

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  • チンパンジーにおける静脈麻酔薬プロポフォール投与法の検討

    宮部貴子, 兼子明久, 山中淳史, 石上暁代, 前田典彦, 鈴木樹理, 松沢哲郎, 矢島功, 増井健一

    日本野生動物医学会大会・講演要旨集   22nd   78   2016

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  • 【麻酔薬の薬物動態・薬力学と年齢】 プロポフォールの薬物動態・薬力学と年齢

    増井 健一

    臨床麻酔   39 ( 9 )   1231 - 1238   2015.9

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  • プロポフォール再考 小児麻酔に生かそう プロポフォールPK/PD

    増井 健一

    日本小児麻酔学会誌   21 ( 1 )   57 - 57   2015.8

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  • 【術中覚醒】 Isolated Forearm Technique

    増井 健一

    臨床麻酔   39 ( 3 )   451 - 456   2015.3

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  • 術前経口補水患者では麻酔導入時のロクロニウムの血漿濃度が低い

    三宅裕, 石垣さやか, 増井健一, 金谷綾奈, 荒木義之, 小倉敬浩

    防衛衛生   62 ( 別冊 )   72 - 72   2014.12

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  • 近未来の小児のTIVA:Open TCIと薬物動態モデル

    増井健一

    日本臨床麻酔学会誌   34 ( 6 )   S159   2014.10

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  • 小児のopenTCIに向けて 近未来の小児のTIVA Open TCIと薬物動態モデル

    増井 健一

    日本臨床麻酔学会誌   34 ( 6 )   S159 - S159   2014.10

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  • 大血管手術と運動誘発電位、脳脊髄液ドレナージ 多施設共同研究とマニュアル作成に向けて MEPTRIAL 後ろ向き研究の結果

    増井 健一

    Cardiovascular Anesthesia   18 ( Suppl. )   147 - 147   2014.9

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  • 強皮症における病因解明と根治的治療法の開発 リウマチ膠原病外来受診例における肺動脈性肺高血圧症(PAH)リスク因子の評価

    桑名正隆, 白井悠一郎, 安岡秀剛, 増井健一

    強皮症における病因解明と根治的治療法の開発 平成25年度 総括・分担研究報告書   169 - 175   2014

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  • 老年患者におけるオピオイドのPKPD

    増井健一

    日本老年麻酔学会プログラム・抄録集   26th   32   2014

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  • 【open TCI:PK-PD学ぶなら今でしょ】 吸入麻酔薬の理論的なTIVAへの併用 SimTAnを使ってビジュアルで知識を整理しよう

    三條 芳光, 増井 健一, 風間 富栄

    LiSA   20 ( 11 )   1092 - 1097   2013.11

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  • 【open TCI:PK-PD学ぶなら今でしょ】 麻酔管理に直結するPK-PDモデルの違い PKモデルは血中濃度に,PDモデルは効果部位濃度に影響を及ぼす

    増井 健一

    LiSA   20 ( 11 )   1064 - 1067   2013.11

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  • Excel上でRを使う

    増井健一

    麻酔・集中治療とテクノロジー   2012   105 - 107   2013.10

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  • Smart Pilot View―アイソボログラムの理論的背景

    増井健一

    日本臨床麻酔学会誌   33 ( 6 )   S193   2013.10

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  • Smart Pilot View アイソボログラムの理論的背景

    増井 健一

    日本臨床麻酔学会誌   33 ( 6 )   S193 - S193   2013.10

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  • 【あらゆる科で役立つ!麻酔科で学びたい技術 手にとるようにわかる、麻酔の基本概念と手技・周術期管理のポイント、知っておくべき病態の知識】 (第1章)現代の麻酔の概念の理解を目指す TIVAによる麻酔法

    増井 健一

    レジデントノート   15 ( 5 )   785 - 793   2013.6

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  • The Management of Intravenous Patient-controlled Analgesia with Simulations Based on the Pharmacokinetics and Pharmacodynamics of Fentanyl

    林和子, 槌田圭一郎, 増井健一, 佐和貞治

    日本臨床麻酔学会誌   32 ( 5 )   814 - 820   2012.9

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    &amp;nbsp;&amp;nbsp;The effect site concentration of fentanyl during postoperative day 1 was simulated with a linear 3-compartment model, and an IV-PCA (intravenous patient-controlled analgesia) menu was created on the basis of the simulation result. The relation between postoperative effect site concentration and analgesic effect was then reviewed. The simulation indicates that the intravenous administration of 300 &amp;mu;g fentanyl accompanied with basal administration of 25 &amp;mu;g/h fentanyl, at 2h before the emergence, maintains a stable effect site concentration of 1.0 ng/m&lt;I&gt;l&lt;/I&gt; in a 50-kg patient. The effect site concentrations of fentanyl, 1.4 ng/m&lt;I&gt;l&lt;/I&gt; in the emergent period and 1.0 ng/m&lt;I&gt;l&lt;/I&gt; in postoperative period, are useful in postoperative analgesia in non-abdominal surgery.

    DOI: 10.2199/jjsca.32.814

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  • Hypnotic effects and pharmacokinetics of a single bolus dose of propofol in Japanese macaques (Macaca fsucata fsucata) (vol 37, pg 501, 2010)

    T. Miyabe-Nishiwaki, K. Masui, A. Kaneko, K. Nishiwaki, E. Shimbo, H. Kanazawa

    VETERINARY ANAESTHESIA AND ANALGESIA   39 ( 4 )   435 - 435   2012.7

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  • 薬物をボーラス投与した時の薬物動態モデル

    萩平哲, 増井健一, 高階雅紀, 内田整, 森隆比古

    麻酔・集中治療とテクノロジー   2009   77 - 80   2012.4

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  • 薬物をボーラス投与した時の薬物動態モデル―Gauss曲線を元にした初期相モデルとTransitモデルの比較―

    増井健一, 萩平哲, 風間富栄

    麻酔・集中治療とテクノロジー   2011   88 - 90   2012.4

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  • Lag timeはコンパートメントモデルの予測正確性を改善するか?

    増井健一, 風間富栄

    麻酔・集中治療とテクノロジー   2009   134   2012.4

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  • 薬物をボーラス投与した時の薬物動態モデル Gauss曲線を元にした初期相モデルとTransitモデルの比較

    増井 健一, 萩平 哲, 風間 富栄

    麻酔・集中治療とテクノロジー   2011   88 - 90   2012.4

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    Gauss曲線を元にした薬物動態モデルと、Transitモデル(連続した複数のコンパートメントによるモデルで、なだらかな濃度上昇を表現できる)を比較し、NONMEMでモデリングが可能なコンパートメントモデルでの濃度変化曲線の表現の可能性を検討した。Lag+Transitモデル、TransitモデルともNONMEMで扱えるため、population pharmacokinetics modelに組み込むことができるが、Transitモデルは曲線の形状の表現に大きな制約があり、Lag+Transitモデルの方が濃度の表現に向いていることが示唆された。しかし、lagモデルを組み込むかどうかに関わりなく、Transitモデルを表す式には、Gauss曲線を元にしたモデルの式よりも制約があることが示唆された。

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  • 薬物をボーラス投与した時の薬物動態モデル

    萩平 哲, 増井 健一, 高階 雅紀, 内田 整, 森 隆比古

    麻酔・集中治療とテクノロジー   2009   77 - 80   2012.4

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  • 全静脈麻酔のための薬物動態力学の基礎

    増井 健一

    日本臨床麻酔学会誌   31 ( 6 )   S187 - S187   2011.10

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  • 効果的な星状神経節ブロックのための影響因子についての検討

    坂本英治, 梅田英一郎, 増井健一, 湯舟晋也, 児玉光厳, 雫石正明, 高松功, 池田健彦, 風間富栄

    日本ペインクリニック学会誌   17 ( 4 )   517   2010.9

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  • プロポフォール静脈麻酔の至適鎮静量に対する術前不安の影響

    坂本 英治, 増井 健一, 大坪 由紀子, 梅田 英一郎, 田村 響子, 佐藤 大介, 三條 芳光, 風間 富栄

    日本歯科麻酔学会雑誌   38 ( 4 )   479 - 479   2010.9

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  • 効果的な星状神経節ブロックのための影響因子についての検討

    坂本 英治, 梅田 英一郎, 増井 健一, 湯舟 晋也, 児玉 光厳, 雫石 正明, 高松 功, 池田 健彦, 風間 富栄

    日本ペインクリニック学会誌   17 ( 4 )   517 - 517   2010.9

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  • コンピュータ 薬物動態シミュレーションと薬物動態モデル

    増井健一, 風間富栄

    臨床麻酔(真興交易)   34 ( 臨増 )   445 - 455   2010.3

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  • 【術中覚醒記憶】 モニタリングは術中覚醒を防ぐか?

    増井 健一

    LiSA   16 ( 11 )   1026 - 1031   2009.11

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  • フェンタニルとミダゾラムが就眠時プロポフォール濃度に及ぼす影響

    増井健一, 風間富栄

    麻酔・集中治療とテクノロジー   2007   57 - 58   2009.9

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  • フェンタニルとミダゾラムが就眠時プロポフォール濃度に及ぼす影響

    増井 健一, 風間 富栄

    麻酔・集中治療とテクノロジー   2007   57 - 58   2009.9

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  • Excelでデータ入力から基本統計まで

    増井 健一

    麻酔・集中治療とテクノロジー   2006   95 - 95   2009.9

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  • 【麻酔の現況と展望 研修医と指導医のための質問317】 麻酔で使う薬剤 オピオイド(麻薬)

    増井 健一

    麻酔科学レクチャー   1 ( 1 )   143 - 148   2009.5

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  • Anesthetic effects and pharmacokinetics of a bolus dose of propofol in Japanese macaques (Macaca fsucata fsucata) Reviewed

    Miyabe-Nishiwaki T, Masui K, Kaneko A, Nishiwaki K, Shimbo E, Kanazawa H

    10th World Congress of Veterinary Anaesthesiology, (2009/9/1-4 Glasgow, UK)   2009

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  • ニホンザルにおけるプロポフォールTCI導入についての検討

    宮部 貴子, 兼子 明久, 西脇 弘樹, 神保 江津子, 増井 健一, 金澤 秀子

    獣医麻酔外科学雑誌   39 ( Suppl.1 )   200 - 200   2008.6

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  • 気管挿管によるBISおよびエントロピーの変化に及ぼすレミフェンタニルによる影響

    川口慎憲, 高松功, 増井健一, 風間富栄

    J Anesth   22 ( Supplement (CD-ROM) )   P1-24-03   2008

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  • 【新しいオピオイドを迎えて、わが国の麻酔管理はどう変わるか】 レミフェンタニル投与の血中濃度シミュレーション

    増井 健一, 風間 富栄

    麻酔   56 ( 11 )   1287 - 1295   2007.11

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  • Simulation and Clinical Anesthesia with Pharmacokinetic Multi Compartment Model.

    増井健一, 風間富栄

    シミュレーション   26 ( 3 )   145 - 151   2007.9

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    Multi compartment model is one of pharmacokinetic models. The model is widely used for calculating predicted blood concentration of intravenous anesthetics in clinical practice. The model provides anesthesiologists not only to see the time course of drug concentration but also one technique for continuous drug infusion, target-controlled infusion (TCI). When an intravenous drug is infused to patient constantly, the concentration of the drug will increase gradually. Effect of drug is determined by the drug concentration and its sensitivity to patient. TCI for intravenous drugs can maintain predicted blood concentration to be constant. Today, Diprifusor[○!R], that is infusion pump for TCI, is used for clinical anesthesia.

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  • 気管挿管によるBISおよびエントロピーの変化

    川口慎憲, 高松功, 増井健一, 風間富栄

    J Anesth   21 ( Supplement (CD-ROM) )   P1-07-03   2007

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  • Excelのグラフ機能を使いこなす

    増井 健一

    麻酔・集中治療とテクノロジー   2005   158 - 161   2006.11

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  • コンパートメントモデルを表す微分方程式の一般解から、静脈麻酔薬投与中止後の効果部位濃度減少曲線を考える

    増井 健一

    麻酔・集中治療とテクノロジー   2005   124 - 124   2006.11

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  • ボーラス投与のプロポフォールが効果を発現するために必要な時間の検討

    白神麻依子, 増井健一, 風間富栄

    日本臨床麻酔学会誌   26 ( 6 )   S363   2006.10

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  • 難治性顔面神経麻痺に鍼治療が有効であった一例

    平野昌人, 増井健一, 風間富栄

    日本臨床麻酔学会誌   26 ( 6 )   S393   2006.10

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  • 難治性顔面神経麻痺に鍼治療が有効であった一例

    平野 昌人, 増井 健一, 風間 富栄

    日本臨床麻酔学会誌   26 ( 6 )   S393 - S393   2006.10

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  • ボーラス投与のプロポフォールが効果を発現するために必要な時間の検討

    白神 麻依子, 増井 健一, 風間 富栄

    日本臨床麻酔学会誌   26 ( 6 )   S363 - S363   2006.10

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  • 統計データの正しい解釈のために

    増井 健一

    麻酔・集中治療とテクノロジー   2004   95 - 96   2006.9

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  • プロポフォールを用いた全静脈麻酔法 ペンタゾシンとフェンタニルの比較

    野中 明彦, 鈴木 聡美, 阿部 文明, 増井 健一

    麻酔   55 ( 8 )   983 - 987   2006.8

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    2003〜2004年にプロポフォールを用いた全静脈麻酔法で管理した乳癌手術患者89例を対象とし,併用する鎮痛薬ペンタゾシンとフェンタニルを比較検討した.対象はペンタゾシン34例,フェンタニル55例であり,麻酔記録と回診記録から薬物投与量,循環動態,覚醒状況,術後鎮痛,合併症を調査した.その結果,麻酔時中のプロポフォールの目標血中濃度は両群間で有意差はなく,術後の循環動態,覚醒の状況,術後疼痛の程度,悪心・嘔吐の頻度に両群間で有意差はなかった.プロポフォールを用いた全静脈麻酔法に併用する鎮痛薬として,ペンダゾシンとフェンタニルは同程度に有用であることが示唆された

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  • 防衛医大病院におけるBLS&AED推進プロジェクト

    清住 哲郎, 白尾 聡子, 小林 裕幸, 澤田 喜代子, 増井 健一, 木村 一生, 鈴木 洋司, 玉井 誠一

    防衛衛生   53 ( 別冊 )   112 - 112   2006.1

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  • 多経路多単位仮説による薬物相乗効果の解析

    上農喜朗, 増井健一, 多田羅恒雄, 太城力良, KAMAYA Hiroshi

    J Anesth   20 ( Supplement (CD-ROM) )   Q05-01   2006

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  • An Analysis of Incident Reporting in 1999 and 2004

    石山忠彦, 増井健一, 熊沢光生

    日本臨床麻酔学会誌   25 ( 7 )   684 - 688   2005.11

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    &amp;nbsp; Incident reports provide information about the things that went wrong, and have the potential to improve the quality of patient&#039;s care. We compared incident reporting identified in 1999 and 2004 to elucidate how it works. Our evaluation mainly concerned the incidental total number, anesthesia machine, and drugs. There were 59 and 33 incidents reported in 1999 and 2004, respectively. Critical incidents were markedly decreased in 2004. Incidents related to the anesthesia machine decreased from 10 to 5, however, the same incidents occurred repeatedly. On the other hand, incidents associated with drugs increased from 7 to 10. Decrease of critical incidents may have resulted from awareness of mishaps and thus infomation sharing that have been highlighted by incident reporting. Nevertheless, incidents involving anesthesia machine occurred repeatedly and incidents of drugs increased. Because human factors should be closely involved in incidents associated with the anesthesia machine and drugs, and incidents are mainly caused by human error, some mechanical preventive strategies should be provided to lessen the risk in anesthetic practice.

    DOI: 10.2199/jjsca.25.684

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  • 全身麻酔中の患者にプロポフォールを動注した1症例

    三谷 茂樹, 石山 忠彦, 増井 健一, 奥山 克巳, 熊澤 光生

    麻酔   54 ( 10 )   1188 - 1189   2005.10

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  • 「論文発表のための統計学入門」第8回 メタ・アナリシス

    増井健一

    日本放射線技師会雑誌   52 ( 3 )   1329 - 1335   2005.3

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  • 犬における全静脈麻酔の現状と今後の展望

    長浜正太郎, 西村亮平, 増井健一, 望月学, 佐々木伸雄

    日本獣医学会学術集会講演要旨集   139回   147 - 147   2005.3

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  • 無作為割付支援ソフトウェア

    増井健一

    J Anesth   19 ( Supplement (CD-ROM) )   X1.03   2005

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  • 硬膜外PCAによる術後とう痛管理:胃切除術後症例の検討

    市川学, 飯嶋哲也, 石山忠彦, 樫本温, 熊沢光生, 増井健一

    J Anesth   19 ( Supplement (CD-ROM) )   P2-32.11   2005

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  • 活用しようPDF 利用〜作成〜論文投稿

    増井 健一

    麻酔・集中治療とテクノロジー   2003   83 - 85   2004.12

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  • プロポフォール麻酔下の脳腫瘍摘出術中に起きた難治性の全身痙攣

    福島 久史, 石山 忠彦, 小口 健史, 増井 健一, 松川 隆, 熊澤 光生

    麻酔   53 ( 6 )   691 - 692   2004.6

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    24歳男.脳室内腫瘍に対して全身麻酔下での腫瘍摘出術を施行した.酸素6l・min-1マスク下にプロポフォール90mgとフェンタニル150μgで急速導入し,ベクロニウム6mgで気管挿管を行った.空気-酸素混合で吸入酸素濃度を33%とし,麻酔維持はプロポフォール7mg・kg-1・h-1とフェンタニル125μg・h-1による全静脈麻酔で行い,ベクロニウム1mg・h-1を投与した.手術開始50分後,開頭操作中に血圧の低下と心拍数の増加を認め,その直後に全身性痙攣が出現した.プロポフォール100mg,ジアゼパム10mg,チアミラール200mgの投与を行い,痙攣はいったん消失したが,手術開始10時間後,11時間30分後,17時間後に再発した.手術後に痙攣は認めなかった.16日後に脳室-腹腔短絡術が行われた際には導入薬にチアミラールを用いて亜酸化窒素-酸素-セボフルランで維持し,術中・術後を通して痙攣は発生しなかった

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  • 補助薬投与法としてのTCI レミフェンタニルのTCI

    増井 健一

    LiSA   11 ( 6 )   572 - 576   2004.6

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  • 犬におけるプロポフォールのTarget Controlled Infusion法の検討

    長浜正太郎, 佐野忠士, 西村亮平, 増井健一, 望月学, 佐々木伸雄

    日本獣医学会学術集会講演要旨集   137回   141 - 141   2004.3

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  • Free radical scavenger with inhalation anesthetic prevents recovery from ischemia in rat hearts

    K Masui, S Kashimoto, A Furuya, T Oguchi, T Kumazawa

    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY   35 ( 11 )   A34 - A34   2003.11

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  • プロポフォールTCIによる麻酔管理(応用)

    増井健一

    日本臨床麻酔学会誌   23 ( 8 )   S221   2003.9

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  • TCIを活用しよう 初心者から上級者まで 薬物動態学を考慮した薬物投与 プロポフォールTCIによる麻酔管理(応用)

    増井 健一

    日本臨床麻酔学会誌   23 ( 8 )   S221 - S221   2003.9

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  • プロポフォール麻酔下での脳腫瘍摘出術中に頻繁に痙攣発作をきたした1症例

    福島 久史, 石山 忠彦, 小口 健史, 増井 健一, 樫本 温, 熊澤 光生, 杉田 正夫

    麻酔   52 ( 7 )   804 - 804   2003.7

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  • Inhalation Anesthetics during Reperfusion Prevent Recovery from Ischemia in the Mitochondrial KATP channel Blocker Pretreated Hearts

    American Society of Anesthesiologists 2003 Annual Meeting   2003

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  • 再利用可能なBISセンサーの試作

    増井 健一, 樫本 温, 熊澤 光生

    麻酔・集中治療とテクノロジー   2002   33 - 36   2002.12

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    麻酔科医は血行動態の変化により鎮静レベルの判断を行ってきたが,Aspect社製BISモニタA-1050の登場により,血行動態のみでは鎮静レベルの判断を行い難いことが明確になった.しかし,Aspect社製BISセンサー(既製BISセンサー)は高価かつディスポーザブルであるため,BISモニタを全身麻酔症例全例に使用すると病院の経営を圧迫してしまう.そこで,再使用可能なA-1050用BISセンサーを試作した.再利用可能なBISセンサーを,心電図電極,心電図誘導コード,シリアルオスコネクタを用い試作した.BISモニタのインピーダンスチェックを通過し使用可能であった

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  • 汎用ソフトと特化ソフトの組み合わせ

    増井健一

    日本臨床麻酔学会誌   22 ( 8 )   S136   2002.9

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  • コンピュータ発達と臨床麻酔の質的向上 現状と未来 汎用ソフトと特化ソフトに組み合わせ

    増井 健一

    日本臨床麻酔学会誌   22 ( 8 )   S136 - S136   2002.9

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  • 硫酸モルヒネ徐放製剤投与中の母体から出生した新生児例

    畑 園子, 飯島 純, 武井 義親, 池田 仁恵, 平岡 正人, 増井 健一, 河内 敏行

    日本小児科学会雑誌   106 ( 4 )   575 - 575   2002.4

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  • プロポフォール急速静脈内投与における予測濃度の検討

    日本静脈麻酔・Infusion Technology 研究会第9回大会   2002

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  • 年齢によるpharmacodynamicsの影響を取り入れたTCIソフトウェア

    増井健一, 野中明彦, 樫本温, 熊沢光生

    麻酔・集中治療とテクノロジー   2001   45 - 47   2001.11

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  • ソフトウェアのユーザーインターフェースと使用者に対する教育 ソフトウェアのユーザーインターフェース 使いやすさを考える

    増井 健一

    麻酔・集中治療とテクノロジー   2001   81 - 84   2001.11

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  • 年齢によるpharmacodynamicsの影響を取り入れたTCIソフトウェア

    増井 健一, 野中 明彦, 樫本 温, 熊沢 光生

    麻酔・集中治療とテクノロジー   2001   45 - 47   2001.11

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  • Windows95/98で動くプロポフォール薬物動態シミュレーションソフトの試作

    増井 健一, 野中 明彦, 樫本 温, 熊澤 光生

    麻酔・集中治療とテクノロジー   2000   28 - 31   2001.1

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  • Propofol with New Effect Compartment-Controlled Target-Controlled Infusion Algorithm Induces Minimal Hemodynamic Changes after Tracheal Intubation

    American Society of Anesthesiologists 2001 Annual Meeting   2001

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  • 人工膝関節置換術後リハビリにおける硬膜外PCAは入院期間を短縮するか

    飯嶋 哲也, 山口 敏昭, 奥山 克巳, 熊澤 光生, 岩本 竜一, 増井 健一

    ペインクリニック   21 ( 8 )   1219 - 1219   2000.12

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  • 小児心臓外科手術 当院における1999年のトピックス

    鈴木 章司, 吉井 新平, 保坂 茂, Samuel Abraham, 大澤 宏, 多田 祐輔, 杉山 央, 丹 哲士, 角野 敏恵, 駒井 孝行, 矢内 淳, 奥山 克巳, 石山 忠彦, 川村 淳夫, 増井 健一, 樋口 浩二

    山梨医学   28   80 - 85   2000.10

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    山梨医科大学付属病院において1999年に施行された小児心臓外科手術は43例(開心術37例,非開心術6例)で,在院死亡は2例,遠隔死亡なしであった.この間のトピックスとして,遠心ポンプ脱血小型人工心肺回路modified ultrafiltration(MUF)の導入,minimally invasive cardiac surgery(MICS)の適応拡大,経右房経肺動脈アプローチによるファロー四徴症根治術,fenestrated one &amp; a half repair,extracardiac TCPC(total cavopulmonary connection)の導入,低体重の左心低形成症候群症例に対する両側肺動脈絞扼術と右室肺動脈間人工血管間置法によるmodified Norwood手術,乳児期早期の人工弁置換術,等があり,医療の質的な向上がもたらされた

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  • Effects of nicorandil on myocardial function and metabolism in the ischemic heart with or without inhalation anesthetics

    A Furuya, S Kashimoto, T Oguchi, K Masui, T Kumazawa

    ANESTHESIOLOGY   93 ( 3A )   U170 - U170   2000.9

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  • Age-related propofol effects on myocardial contraction and intracellular Ca2+ dynamics of isolated rat hearts

    T Oguchi, T Yamaguchi, S Kashimoto, A Furuya, K Masui

    ANESTHESIOLOGY   93 ( 3A )   U171 - U171   2000.9

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  • 薬剤部と協力した術後疼痛管理システムの構築(硬膜外PCAを中心に)

    飯嶋 哲也, 山口 敏昭, 奥山 克巳, 岩本 竜一, 増井 健一, 熊澤 光生

    日本臨床麻酔学会誌   20 ( 8 )   S425 - S425   2000.9

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  • Eisenmenger Syndromeを合併した消化管穿孔症例の麻酔管理

    川村 淳夫, 増井 健一, 石山 忠彦, 樫本 温, 熊澤 光生

    蘇生   18 ( 3 )   268 - 268   1999.9

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  • ニトログリセリン静注にて蘇生し得た冠攣縮の1症例

    増井 健一, 長田 満, 前田 宜包, 田中 行夫, 駒井 孝行, 熊澤 光生

    蘇生   18 ( 3 )   232 - 232   1999.9

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  • 胸腺内副甲状腺腫瘍摘出術後の抜管直後に両側気胸を発症した1症例

    増井 健一, 石山 忠彦, 熊澤 光生

    麻酔   48 ( 6 )   652 - 653   1999.6

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  • 胸腺内副甲状腺腫瘍摘出術での抜管直後に両側気胸を発症した1例

    増井 健一, 石山 忠彦, 熊澤 光生

    蘇生   17 ( 3 )   192 - 192   1998.9

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Awards

  • Joint 1st place

    2024.9   Association of Anaesthetists Annual Meeting 2024   Machine learning model for predicting arterial pressure using drug concentrations

    Kenichi Masui. Hroshi Makazu

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  • JSIVA賞

    2020.11   第27回日本静脈麻酔学会  

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  • 第26回日本静脈麻酔学会JSIVA賞

    2019.11  

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  • 第6回MSD Award

    2018   日本臨床麻酔学会  

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  • ベストプレゼンテーション 優秀賞

    2018   第15回麻酔科学サマーセミナー  

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  • JSIVA賞

    2015   第22回日本静脈麻酔学会  

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  • JSIVA賞

    2013   第20回日本静脈麻酔学会  

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  • JSIVA賞

    2012   日本静脈麻酔学会  

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  • JSIVA賞

    2010   第17回日本静脈麻酔学会  

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  • Three Best Abstracts

    2010   13th EuroSIVA Annual Scientific Meeting  

    MASUI Kenichi

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  • JSIVA賞

    2009   第16回日本静脈麻酔学会  

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  • 日本麻酔科学会ソフトウェアコンテスト優秀賞

    2007  

    増井 健一

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  • 日本麻酔科学会ソフトウェアコンテスト優秀賞

    2001  

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  • The excellent prize of Sotware Contest of the Japanese Society of Anesthesialogists

    2001  

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  • The utility prize of Software Contest of Japanese Society of Anesthesiologists

    2000  

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  • 日本麻酔科学会ソフトウェアコンテスト実用賞

    2000  

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Research Projects

  • 全身麻酔を施行する小児手術患者におけるレミマゾラムの有効性、安全性および薬物動態を検討するための第III相医師主導治験

    2023.4 - 2027.3

    国立研究開発法人日本医療研究開発機構  臨床研究・治験推進研究事業 

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    Authorship:Principal investigator  Grant type:Competitive

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  • 機械学習・統計解析・薬物動態力学解析を組み合わせた麻酔薬理研究

    Grant number:22K09030  2022.4 - 2025.3

    日本学術振興会  科学研究費助成事業 基盤研究(C)  基盤研究(C)

    増井 健一

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    Grant amount:\4160000 ( Direct Cost: \3200000 、 Indirect Cost:\960000 )

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  • 統合レジストリによる多発性筋炎/皮膚筋炎関連間質性肺疾患の個別化医療基盤の構築

    2021 - 2024

    国立研究開発法人日本医療研究開発機構  難治性疾患実用化研究事業 

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    Authorship:Coinvestigator(s)  Grant type:Competitive

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  • 呼気プロポフォール連続測定の臨床使用のための基盤研究

    2018 - 2022

    文部科学省  科学研究費助成事業 

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    Authorship:Principal investigator 

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  • 術中覚醒を減少させるための麻酔関連薬剤の薬物動態力学研究

    2011 - 2014

    文部科学省  科学研究費補助金 

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Social Activities

  • 第9回 マダガスカル口唇口蓋裂医療協力

    昭和大学  2019.11 - 2019.12

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    Type:Other

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