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Featured researches published by Mari Amino.


Journal of Cardiovascular Pharmacology | 2010

Comparative Study of Nifekalant Versus Amiodarone for Shock-Resistant Ventricular Fibrillation in Out-of-Hospital Cardiopulmonary Arrest Patients

Mari Amino; Koichiro Yoshioka; Tobias Opthof; Seiji Morita; Shunryo Uemura; Kozo Tamura; Tomokazu Fukushima; Shigeo Higami; Hiroyuki Otsuka; Kazuki Akieda; Makiyoshi Shima; Daisuke Fujibayashi; Tadashi Hashida; Sadaki Inokuchi; Itsuo Kodama; Teruhisa Tanabe

Background: In Japan, intravenous nifekalant (NIF) was often used for direct current cardioversion-resistant ventricular fibrillation (VF), until the use of intravenous amiodarone (AMD) was approved in 2007. The defibrillatory efficacy of NIF and AMD has thus far not been compared for resuscitation. Methods and Results: Between August 2007 and April 2009, 403 consecutive out-of-hospital patients with cardiopulmonary arrest were transferred to the Emergency Medical Service of Tokai University. Of these, 30 patients with first defibrillation failure or VF recurrence were enrolled for this NIF/AMD study. The final defibrillation success (and hospital survival rate) was 67% (10/15) in the AMD and 47% (7/15) in the NIF group. The discharge survival rate was 53% (8/15) in the AMD and 21% (4/15) in the NIF group (P = 0.06). Notably, all 4 survivors in the NIF group could take up normal daily life again, whereas this was restricted to only 2 patients from the 11 survivors in the AMD group. The difference is probably partly attributable to longer time from AMD administration to defibrillation success compared with NIF. In the cases of defibrillation failure, VF continued in 4/8 by NIF, however, asystole or pulseless electrical activity occurred in 4/5 patients by AMD. Conclusions: AMD may be borderline superior over NIF to facilitate defibrillation in out-of-hospital patients with cardiopulmonary arrest. However, from the view point of preservation of brain function, NIF is not inferior to AMD for CPR.


American Journal of Physiology-heart and Circulatory Physiology | 2010

Year-long upregulation of connexin43 in rabbit hearts by heavy ion irradiation

Mari Amino; Koichiro Yoshioka; Daisuke Fujibayashi; Tadashi Hashida; Yoshiya Furusawa; Wojciech Zareba; Yuji Ikari; Etsuro Tanaka; Hidezo Mori; Sadaki Inokuchi; Itsuo Kodama; Teruhisa Tanabe

A previous study from our laboratory has shown that a single targeted heavy ion irradiation (THIR; 15 Gy) to rabbit hearts increases connexin43 (Cx43) expression for 2 wk in association with an improvement of conduction, a decrease of the spatial inhomogeneity of repolarization, and a reduction of vulnerability to ventricular arrhythmias after myocardial infarction. This study investigated the time- and dose-dependent effects of THIR (5-15 Gy) on Cx43 expression in normal rabbit hearts (n = 45). Five rabbits without THIR were used as controls. A significant upregulation of Cx43 protein and mRNA in the ventricular myocardium was recognized by immunohistochemistry, Western blotting, and real-time PCR from 2 wk up to 1 yr after a single THIR at 15 Gy. THIR > or =10 Gy caused a significant dose-dependent increase of Cx43 protein and mRNA 2 wk after THIR. Anterior, lateral, and posterior free wall of the left ventricle, interventricular septum, and right ventricular free wall were affected similarly by THIR in terms of Cx43 upregulation. The radiation-induced increase of immunolabeled Cx43 was observed not only at the intercalated disk region but also at the lateral surface of ventricular myocytes. The increase of immunoreactive Cx43 protein was predominant in the membrane fraction insoluble in Triton X-100, that is the Cx43 in the sarcolemma. In vivo examinations of the rabbits 1 yr after THIR (15 Gy) revealed no significant changes in ECGs and echocardiograms (left ventricular dimensions, contractility, and diastolic function), indicating no apparent late radiation injury. A single application of THIR causes upregulation and altered cellular distribution of Cx43 in the ventricles lasting for at least 1 yr. This long-lasting remodeling effect on gap junctions may open the pathway to novel therapy against life threatening ventricular arrhythmias in structural heart disease.


Journal of Cardiovascular Pharmacology | 2015

Nifekalant Hydrochloride and Amiodarone Hydrochloride Result in Similar Improvements for 24-Hour Survival in Cardiopulmonary Arrest Patients: The SOS-KANTO 2012 Study.

Mari Amino; Sadaki Inokuchi; Ken Nagao; Yoshihide Nakagawa; Koichiro Yoshioka; Yuji Ikari; Hiraku Funakoshi; Katsura Hayakawa; Masakazu Matsuzaki; Atsushi Sakurai; Yoshio Tahara; Naohiro Yonemoto; Arino Yaguchi; Naoto Morimura

Background: Amiodarone (AMD), nifekalant (NIF), and lidocaine (LID) hydrochlorides are widely used for ventricular tachycardia/fibrillation (VT/VF). This study retrospectively investigated the NIF potency and the differential effects of 2 initial AMD doses (⩽150 mg or 300 mg) in the Japanese SOS-KANTO 2012 study population. Methods and Results: From 16,164 out-of-hospital cardiac arrest cases, 500 adult patients using a single antiarrhythmic drug for shock-resistant VT/VF were enrolled and categorized into 4 groups (73 LID, 47 NIF, 173 AMD-⩽150, and 207 AMD-300). Multivariate analyses evaluated the outcomes of NIF, AMD-⩽150, or AMD-300 groups versus LID group. Odds ratios (ORs) for survival to admission were 3.21 [95% confidence interval (CI): 1.38–7.44, P < 0.01] in NIF and 3.09 (95% CI: 1.55–6.16, P < 0.01) in AMD-⩽150 groups and significantly higher than those of the LID group. However, the OR was 1.78 (95% CI: 0.90–3.51, P = 0.10) in AMD-300 group and was not significant than LID group. ORs for 24-hour survival were 6.68 in NIF, 4.86 in AMD-⩽150, and 2.97 in AMD-300, being significantly higher in these groups. Conclusions: NIF and AMD result in similar improvements for 24-hour survival in cardiopulmonary arrest patients, and this suggest the necessity of a randomized control study.


Clinical Toxicology | 2010

A case of torsades de pointes induced by severe QT prolongation after an overdose of eperisone and triazolam in a patient receiving nifedipine.

Takeshi Yamagiwa; Mari Amino; Seiji Morita; Rie Yamamoto; Takeshi Saito; Sadaki Inokuchi

Introduction. Eperisone hydrochloride is a centrally acting muscle relaxant, and triazolam is a short-acting benzodiazepine. Although commonly prescribed, cardiotoxicity induced by a single overdose of either drug is comparatively rare. A patient receiving nifedipine developed torsades de pointes (TdP) because of prolongation of the corrected QT (QTc) interval after an overdose of eperisone hydrochloride and triazolam. Case report. A 60-year-old man receiving nifedipine was admitted in a comatose condition 3 h after ingesting 5,000 mg of eperisone and 2.5 mg of triazolam. Electrocardiogram showed sinus rhythm with prolongation of the QTc interval (820 ms). The serum electrolyte levels were as follows: potassium, 3.8 mEq/L; magnesium, 2.4 mg/dL. The serum drug concentrations were high: eperisone, 15,360 ng/mL; triazolam, 110.8 ng/mL. A temporary cardiac pacemaker was implanted immediately after the development of TdP, 11 h after the ingestion. The serum triazolam concentration normalized on day 2. The QTc interval and eperisone concentration normalized on day 6. Conclusion. Eperisone and triazolam overdose can cause life-threatening cardiotoxicity. Electrocardiographic monitoring and serial determination of QTc interval are likely the best way to observe these patients and evaluate the risk of cardiotoxicity.


Journal of Trauma-injury Infection and Critical Care | 2009

Two Cases in Which Myocardial Injury Could Be Only Evaluated by Nuclear Medicine Studies on Electric Shock Patients Whose Electrocardiogram and Myocardial Enzyme Levels Were Normal

Mari Amino; Koichiro Yoshioka; Seiji Morita; Takeshi Yamagiwa; Hiroyuki Otsuka; Kazuki Akieda; Shinichi Iizuka; Shigetaka Kanda; Yuji Ikari; Seiji Nasu; Kenji Hatakeyama; Itsuo Kodama; Sadaki Inokuchi; Teruhisa Tanabe

Heart injury due to electric shock is currently diagnosed based on electrocardiogram (ECG) changes or elevated levels of myocardial enzymes or both. However, the rate at which ECG detects abnormalities is very low; thus, the estimated rate of the diagnosis of myocardial damage due to electric shock is lower than the actual rate. The method of nuclear medicine study of the heart is superior with regard to evaluating transient ischemia, such as angina pectoris, in patients whose ECG and myocardial enzyme levels are normal. Therefore, we attempted to diagnose transient myocardial damage in electric shock patients by using nuclear medicine study of the heart.


Annals of Noninvasive Electrocardiology | 2009

Circadian Distribution of Paroxysmal Atrial Fibrillation in Patients with and without Structural Heart Disease in Untreated State

Yoshiaki Deguchi; Mari Amino; Kumiko Adachi; Atsushi Matsuzaki; Osamu Iwata; Koichiro Yoshioka; Eiichi Watanabe; Teruhisa Tanabe

Background: This study aimed to compare the circadian distribution of the onset, maintenance and termination of paroxysmal atrial fibrillation (PAF) between structural and non‐structural heart diseases (SHD and NSHD, respectively) in the untreated state.


Journal of Trauma-injury Infection and Critical Care | 2009

One-Year Follow-Up and Convalescence Evaluated by Nuclear Medicine Studies and 24-Hour Holter Electrocardiogram in 11 Patients With Myocardial Injury Due to a Blunt Chest Trauma

Mari Amino; Koichiro Yoshioka; Seiji Morita; Shinichi Iizuka; Hiroyuki Otsuka; Rie Yamamoto; Hiromichi Aoki; Toru Aizawa; Yuji Ikari; Seiji Nasu; Kenji Hatakeyama; Misako Iino; Itsuo Kodama; Sadaki Inokuchi; Teruhisa Tanabe

BACKGROUND There are few reports on long-term convalescence with regard to cardiac injury caused by blunt chest trauma. Nuclear medicine study of the heart (NMSH) in the early stages of injury is reportedly superior to detect the correlation between injury and fatal arrhythmia. Therefore, we prospectively performed NMSH and Holter electrocardiogram (ECG) in the early and chronic stages for a cardiac injury patient, and we longitudinally examined the recovery process and the occurrence of fatal arrhythmia. METHODS AND RESULTS A total of 202 patients with blunt chest trauma were admitted to our hospital between April 2006 and January 2007. Of 65 patients who were diagnosed with cardiac injury by ECG, a myocardial enzyme, or cardiac ultrasonography, 11 were enrolled in this study because they agreed to outpatient visiting for regular examinations for 1 year. NMSH showed positive findings in 6 of the 11 patients in the acute period of <1 month. Twelve months later, five patients improved but still exhibited protracted cardiac damage without complete recovery. Among the six patients in whom NMSH showed positive findings, Holter ECG indicated an abnormal finding in two patients in the acute period and in four patients in the chronic period, and detected one patient with a nonsustained ventricular tachycardia in the chronic period. CONCLUSION Cardiac injuries may exacerbate cardiac functions and lead to fatal arrhythmia during the chronic period. Therefore, evaluating recovery for at least 12 months after myocardial damage is necessary to prevent sudden cardiac death.


Journal of Cardiovascular Pharmacology | 2016

Does Antiarrhythmic Drug during Cardiopulmonary Resuscitation Improve the One-month Survival: The SOS-KANTO 2012 Study

Mari Amino; Sadaki Inokuchi; Koichiro Yoshioka; Yoshihide Nakagawa; Yuji Ikari; Hiraku Funakoshi; Katsura Hayakawa; Masakazu Matsuzaki; Atsushi Sakurai; Yoshio Tahara; Naohiro Yonemoto; Ken Nagao; Arino Yaguchi; Naoto Morimura

Background: Antiarrhythmic drugs (AAD) are often used for fatal ventricular arrhythmias during cardiopulmonary resuscitation (CPR). However, the efficacy of initial AAD administration during CPR in improving long-term prognosis remains unknown. This study retrospectively evaluated the effect of AAD administration during CPR on 1-month prognosis in the SOS-KANTO 2012 study population. Methods and Results: Of the 16,164 out-of-hospital cardiac arrest cases, 1350 shock-refractory patients were included: 747 patients not administered AAD and 603 patients administered AAD. Statistical adjustment for potential selection bias was performed using propensity score matching, yielding 1162 patients of whom 792 patients were matched (396 pairs). The primary outcome was 1-month survival. The secondary outcome was the proportion of patients with favorable neurological outcome at 1 month. Logistic regression with propensity scoring demonstrated an odds ratio (OR) for 1-month survival in the AAD group of 1.92 (P < 0.01), whereas the OR for favorable neurological outcome at 1 month was 1.44 (P = 0.26). Conclusions: Significantly greater 1-month survival was observed in the AAD group compared with the non-AAD group. However, the effect of ADD on the likelihood of a favorable neurological outcome remains unclear. The findings of the present study may indicate a requirement for future randomized controlled trials evaluating the effect of ADD administration during CPR on long-term prognosis.


Journal of Arrhythmia | 2014

Systematic review of the use of intravenous amiodarone and nifekalant for cardiopulmonary resuscitation in Japan

Mari Amino; Koichiro Yoshioka; Shigetaka Kanda; Yoshiaki Deguchi; Mari Nakamura; Yoshinori Kobayashi; Sadaki Inokuchi; Teruhisa Tanabe; Yuji Ikari

Intravenous amiodarone is considered to be the first‐line drug for the treatment of ventricular tachycardia or fibrillation. However, in Japan, nifekalant had been used before the introduction of amiodarone; therefore, most clinical studies on amiodarone use have been small‐scale studies. The aim of the present study was to review the literature concerning the actual use of amiodarone and nifekalant in order to evaluate the effects of both drugs and the most appropriate mode of administration.


American Journal of Emergency Medicine | 2014

Serum concentration of eperisone hydrochloride correlates with QT interval

Takeshi Yamagiwa; Seiji Morita; Mari Amino; Naoya Miura; Takeshi Saito; Sadaki Inokuchi

BACKGROUND Eperisone hydrochloride is a centrally acting muscle relaxant prescribed for muscle stiffness that acts by depressing the activities of α and γ efferent neurons in the spinal cord and supraspinal structures. Although a case of eperisone-induced severe QT prolongation had been reported, the relationship between serum eperisone concentration and QT interval remains obscure. OBJECTIVE The aim of this study was to investigate the relationship between serum eperisone concentration and QT interval. METHODS Four patients who overdosed on eperisone were admitted to our hospital between January 2010 and December 2011. We took simultaneous serial measurements of serum eperisone concentration and QT interval in the intensive care unit. In total, 22 measurement points were plotted for these patients. We analyzed the correlation between the serum eperisone concentration and corrected QT (QTc) interval. RESULTS Three men and one woman (mean age, 50 years) overdosed on eperisone with an average dose of 3087.5 mg (therapeutic dose, 150 mg/day). The mean QTc interval at arrival was 592 ms (range, 444-825 ms), and the mean serum eperisone concentration at arrival was 1257.5 ng/mL (range, 14.5-4120.0 ng/mL). The correlation coefficient was 0.833 between serum eperisone concentration and QTc interval (P < .001). CONCLUSION Serum eperisone concentration correlates with QTc interval in patients who overdose on eperisone.

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