-
Something wrong with this record ?
Ranolazin v léčbě akutních koronárních syndromů
[Effect of ranolazine, an antianginal agent with novel electrophysiological properties, on the incidence of arrhythmias in patients with non ST-segment elevation acute coronary syndrome: results from the Metabolic Efficiency With Ranolazine for Less Ischemia in Non ST-Elevation Acute Coronary Syndrome Thrombolysis in Myocardial Infarction 36 (MERLIN-TIMI 36) randomized controlled trial]
Scirica BM, et al.
Language Czech Country Czech Republic
- MeSH
- Acetanilides adverse effects therapeutic use MeSH
- Acute Disease MeSH
- Angina Pectoris drug therapy physiopathology prevention & control MeSH
- Diabetic Angiopathies epidemiology MeSH
- Electrophysiology MeSH
- Electrocardiography MeSH
- Myocardial Infarction complications physiopathology MeSH
- Myocardial Ischemia drug therapy MeSH
- Coronary Disease drug therapy complications MeSH
- Middle Aged MeSH
- Humans MeSH
- Piperazines adverse effects therapeutic use MeSH
- Placebos MeSH
- Aged MeSH
- Arrhythmias, Cardiac epidemiology chemically induced MeSH
- Tachycardia epidemiology MeSH
- Thrombolytic Therapy MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
Ranolazine, a piperazine derivative, reduces ischemia via inhibition of the late phase of the inward sodium current (late I(Na)) during cardiac repolarization, with a consequent reduction in intracellular sodium and calcium overload. Increased intracellular calcium leads to both mechanical dysfunction and electric instability. Ranolazine reduces proarrhythmic substrate and triggers such as early afterdepolarization in experimental models. However, the potential antiarrhythmic actions of ranolazine have yet to be demonstrated in humans. METHODS AND RESULTS: The Metabolic Efficiency With Ranolazine for Less Ischemia in Non-ST-Elevation Acute Coronary Syndrome (MERLIN)-Thrombolysis in Myocardial Infarction (TIMI) 36 (MERLIN-TIMI 36) trial randomized 6560 patients hospitalized with a non-ST-elevation acute coronary syndrome to ranolazine or placebo in addition to standard therapy. Continuous ECG (Holter) recording was performed for the first 7 days after randomization. A prespecified set of arrhythmias were evaluated by a core laboratory blinded to treatment and outcomes. Of the 6560 patients in MERLIN-TIMI 36, 6351 (97%) had continuous ECG recordings that could be evaluated for arrhythmia analysis. Treatment with ranolazine resulted in significantly lower incidences of arrhythmias. Specifically, fewer patients had an episode of ventricular tachycardia lasting > or = 8 beats (166 [5.3%] versus 265 [8.3%]; P<0.001), supraventricular tachycardia (1413 [44.7%] versus 1752 [55.0%]; P<0.001), or new-onset atrial fibrillation (55 [1.7%] versus 75 [2.4%]; P=0.08). In addition, pauses > or = 3 seconds were less frequent with ranolazine (97 [3.1%] versus 136 [4.3%]; P=0.01). CONCLUSIONS: Ranolazine, an inhibitor of late I(Na), appears to have antiarrhythmic effects as assessed by continuous ECG monitoring of patients in the first week after admission for acute coronary syndrome. Studies specifically designed to evaluate the potential role of ranolazine as an antiarrhythmic agent are warranted.
Effect of ranolazine, an antianginal agent with novel electrophysiological properties, on the incidence of arrhythmias in patients with non ST-segment elevation acute coronary syndrome: results from the Metabolic Efficiency With Ranolazine for Less Ischemia in Non ST-Elevation Acute Coronary Syndrome Thrombolysis in Myocardial Infarction 36 (MERLIN-TIMI 36) randomized controlled trial
- 000
- 04702naa 2200505 a 4500
- 001
- bmc07506371
- 003
- CZ-PrNML
- 005
- 20111210122605.0
- 008
- 080708s2008 xr e cze||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a cze $b eng
- 044 __
- $a xr
- 100 1_
- $a Scirica, B. M.
- 245 10
- $a Ranolazin v léčbě akutních koronárních syndromů / $c Scirica BM, et al.
- 246 11
- $a Effect of ranolazine, an antianginal agent with novel electrophysiological properties, on the incidence of arrhythmias in patients with non ST-segment elevation acute coronary syndrome: results from the Metabolic Efficiency With Ranolazine for Less Ischemia in Non ST-Elevation Acute Coronary Syndrome Thrombolysis in Myocardial Infarction 36 (MERLIN-TIMI 36) randomized controlled trial
- 314 __
- $a TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston
- 520 9_
- $a Ranolazine, a piperazine derivative, reduces ischemia via inhibition of the late phase of the inward sodium current (late I(Na)) during cardiac repolarization, with a consequent reduction in intracellular sodium and calcium overload. Increased intracellular calcium leads to both mechanical dysfunction and electric instability. Ranolazine reduces proarrhythmic substrate and triggers such as early afterdepolarization in experimental models. However, the potential antiarrhythmic actions of ranolazine have yet to be demonstrated in humans. METHODS AND RESULTS: The Metabolic Efficiency With Ranolazine for Less Ischemia in Non-ST-Elevation Acute Coronary Syndrome (MERLIN)-Thrombolysis in Myocardial Infarction (TIMI) 36 (MERLIN-TIMI 36) trial randomized 6560 patients hospitalized with a non-ST-elevation acute coronary syndrome to ranolazine or placebo in addition to standard therapy. Continuous ECG (Holter) recording was performed for the first 7 days after randomization. A prespecified set of arrhythmias were evaluated by a core laboratory blinded to treatment and outcomes. Of the 6560 patients in MERLIN-TIMI 36, 6351 (97%) had continuous ECG recordings that could be evaluated for arrhythmia analysis. Treatment with ranolazine resulted in significantly lower incidences of arrhythmias. Specifically, fewer patients had an episode of ventricular tachycardia lasting > or = 8 beats (166 [5.3%] versus 265 [8.3%]; P<0.001), supraventricular tachycardia (1413 [44.7%] versus 1752 [55.0%]; P<0.001), or new-onset atrial fibrillation (55 [1.7%] versus 75 [2.4%]; P=0.08). In addition, pauses > or = 3 seconds were less frequent with ranolazine (97 [3.1%] versus 136 [4.3%]; P=0.01). CONCLUSIONS: Ranolazine, an inhibitor of late I(Na), appears to have antiarrhythmic effects as assessed by continuous ECG monitoring of patients in the first week after admission for acute coronary syndrome. Studies specifically designed to evaluate the potential role of ranolazine as an antiarrhythmic agent are warranted.
- 650 _2
- $a acetanilidy $x škodlivé účinky $x terapeutické užití $7 D000083
- 650 _2
- $a akutní nemoc $7 D000208
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a angina pectoris $x farmakoterapie $x patofyziologie $x prevence a kontrola $7 D000787
- 650 _2
- $a srdeční arytmie $x epidemiologie $x chemicky indukované $7 D001145
- 650 _2
- $a koronární nemoc $x farmakoterapie $x komplikace $7 D003327
- 650 _2
- $a diabetické angiopatie $x epidemiologie $7 D003925
- 650 _2
- $a elektrokardiografie $7 D004562
- 650 _2
- $a elektrofyziologie $7 D004594
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a infarkt myokardu $x komplikace $x patofyziologie $7 D009203
- 650 _2
- $a ischemická choroba srdeční $x farmakoterapie $7 D017202
- 650 _2
- $a piperaziny $x škodlivé účinky $x terapeutické užití $7 D010879
- 650 _2
- $a placebo $7 D010919
- 650 _2
- $a tachykardie $x epidemiologie $7 D013610
- 650 _2
- $a trombolytická terapie $7 D015912
- 773 0_
- $w MED00012706 $t Clinical cardiology alert $g Roč. 2, č. 1 (2008), s. 2 $x 1213-2586
- 910 __
- $a ABA008 $b B 2242 $c 407 a $y 1
- 990 __
- $a 20080708110723 $b ABA008
- 991 __
- $a 20081212122547 $b ABA008
- 999 __
- $a ok $b bmc $g 621996 $s 474429
- BAS __
- $a 3
- BMC __
- $a 2008 $b 2 $c 1 $d 2 $i 1213-2586 $m Clinical Cardiology Alert $x MED00012706
- LZP __
- $a 2008-7/mkme