نتایج جستجو برای: کینیدین quinidine

تعداد نتایج: 1687  

ژورنال: فیض 2019

Background: Dextromethorphan (DM) as a non-opioid anti-cough has neuroprotective effects. Combination of DM with quinidine decreases rapid metabolism of DM to dextrorphan (DX). This study aimed to examine the effects of acute administration of quinidine, DM and combination of dextromethorphan/quinidine (DM/Q) on pentylenetetrazole (PTZ)-induced clonic and tonic seizure thresholds in mice. Mater...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی تهران 1350

چکیده ندارد.

Journal: :The Journal of clinical investigation 1961
H L CONN R J LUCHI

The interaction of quinidine with various body proteins may well be the fundamental process through which quinidine exerts its many effects. For example, quinidine binding with membrane lipoprotein may lead to decreased membrane permeability to passive ion movement. This permeability change has been held responsible for the quinidine-induced alterations in sodium and potassium exchange in cardi...

Journal: :Circulation 1999
M F Fromm R B Kim C M Stein G R Wilkinson D M Roden

BACKGROUND Although quinidine is known to elevate plasma digoxin concentrations, the mechanism underlying this interaction is not fully understood. Digoxin is not extensively metabolized, but it is known to be transported by the drug efflux pump P-glycoprotein, which is expressed in excretory tissues (kidney, liver, intestine) and at the blood-brain barrier. Accordingly, we tested the hypothesi...

1999
Martin F. Fromm Richard B. Kim Michael Stein Dan M. Roden

Background—Although quinidine is known to elevate plasma digoxin concentrations, the mechanism underlying this interaction is not fully understood. Digoxin is not extensively metabolized, but it is known to be transported by the drug efflux pump P-glycoprotein, which is expressed in excretory tissues (kidney, liver, intestine) and at the blood-brain barrier. Accordingly, we tested the hypothesi...

Journal: :Circulation 1981
D Wu J S Hung C T Kuo K S Hsu W B Shieh

Electrophysiologic studies were performed in 14 patients with atrioventricular nodal reentrant paroxysmal tachycardia (PSVT) before and after oral administration of 1.2-1.6 g quinidine sulfate over a 24-hour period (0.3-0.4 g every 6 hours). Studies were performed after 0.5-1 mg i.v. atropine before and after quinidine. All 14 patients had induction of sustained PSVT before quinidine, with or w...

Journal: :Journal of the American College of Cardiology 2013
Sami Viskin Arthur A M Wilde Milton E Guevara-Valdivia Amin Daoulah Andrew D Krahn Douglas P Zipes Amir Halkin Kalyanam Shivkumar Noel G Boyle Arnon Adler Bernard Belhassen Edgardo Schapachnik Farhan Asrar Raphael Rosso

OBJECTIVES The aim of this study was to determine the availability of quinidine throughout the world. BACKGROUND Quinidine is the only oral medication that is effective for preventing life-threatening ventricular arrhythmias due to Brugada syndrome and idiopathic ventricular fibrillation. However, because of its low price and restricted indication, this medication is not marketed in many coun...

2005
Garrett Lee Robert P. Paone

vs 57% of the quinidine patients (p < 0.0001). Sixty-eight percent of the flecainide patients met the above criterion and also had complete suppression of couplets and beats of ventricular tachycardia, vs 33% of the quinidine patients (p < 0.0001). PR and QRS intervals were prolonged by flecainide without clinical consequence, but they were not substantially affected by quinidine (p < 0.0001). ...

Journal: :Circulation 1990
S Juul-Möller N Edvardsson N Rehnqvist-Ahlberg

This open, parallel-group study compares quinidine and sotalol treatment for maintenance of sinus rhythm after direct current conversion of patients with chronic atrial fibrillation. The patients from 15 centers in Sweden were randomized to sotalol (98 patients) or quinidine (85 patients) after 2 hours of sinus rhythm after direct current conversion. According to primary efficacy assessment, 52...

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